Imaging

Soft-tissue sarcomas are quite rare, with an annual incidence of 20 to 30 per 1,000,000 persons in the United States.¹ Because of their heterogeneous presentation, they remain a diagnostic challenge and are often initially confused for more common, benign disorders.² Chronic expanding hematoma, first described by Friedlander and colleagues³ in 1968, is a rare entity that is particularly difficult to distinguish from soft-tissue malignancy.^3-5 Chronic expanding hematoma is defined as a hematoma that gradually expands over 1 month or longer, is absent of neoplastic change on histologic sections, and does not occur in the setting of coagulopathy.⁶

Typically associated with remote trauma, these lesions often present as a slowly growing mass on the anterior or lateral thigh, calf, or buttock.^3-4,7-9 They have been reported to persist as long as 46 years, with sizes ranging from 3 to 55 cm in maximum diameter.⁷ On imaging, they have a cystic appearance with a dense fibrous capsule.^7-8 Most cases resolve uneventfully after drainage or marginal excision, although some cases require repeated intervention.⁷ This case report describes a morbidly obese patient with a chronic expanding hematoma in the distal posterior thigh whose definitive treatment was delayed 6 months because of her pregnancy status and inability to lie prone for open biopsy. The patient provided written informed consent for print and electronic publication of this case report.

Case Report

A 27-year-old morbidly obese woman, who was pregnant at 12 weeks gestation, was seen in an orthopedic oncology clinic with a 1-month history of a slowly growing, painful posterior thigh mass. She had no history of cancer or bleeding disorder, and denied a history of trauma or constitutional symptoms consistent with malignancy. Coagulation studies were normal. Magnetic resonance imaging (MRI) obtained 2 weeks prior in the emergency room showed a cystic lesion with mass-like components in the posterior compartment of the distal right thigh, measuring 17 cm longitudinally. The lesion was located adjacent to, but not involving, the sciatic nerve and femoral vasculature. On initial examination, the large soft-tissue mass was evident and moderately painful to palpation; no skin changes were noted, and the patient had a normal sensorimotor examination. Fine-needle aspiration was performed, which resulted in amorphous debris consistent with hematoma.

Repeat MRI 2 months later showed increased size of the lesion (9.5×10.5 cm axial, 22.0 cm craniocaudal). Although most findings of a more extensive imaging protocol, including precontrast and postcontrast sequences, were consistent with hematoma, the lesion also had several characteristics that indicated soft-tissue sarcoma. Specifically, findings suggestive of chronic hematoma included the hyperintense short tau inversion recovery (STIR) T1/T2 signal of the cystic component consistent with proteinaceous fluid and the low STIR TI/T2 signal of the periphery consistent with a rim of hemosiderin (Figure 1). Additionally, the cystic component of the lesion had multiple fine septations that are atypical for a hematoma (Figure 1), and several lymph nodes greater than 1.7 cm in short axis were noted in the anterior thigh and hemipelvis that were suspicious of metastatic lymphadenopathy. The encapsulated appearance of the lesion with a sharply defined margin and short transition zone were also reassuring findings for a benign lesion (Figures 1, 2A, 2B). However, several findings were identified that suggested soft-tissue sarcoma, including a nodular soft-tissue component on the medial wall of the lesion that had heterogeneous enhancement with contrast (Figure 2B). We, therefore, proceeded with ultrasound-guided core needle biopsy of the mass and cytologic sampling of the fluid components, which were again consistent with hematoma; no evidence of internal vascular flow was noted on Doppler ultrasound. Ultrasound-guided right inguinal lymph node biopsy was also performed and was negative for malignancy. Because of her large body habitus and pregnancy status, it was agreed that open biopsy should be delayed until after delivery to avoid placing the patient in a prone position.

The patient visited the emergency room several times during the following months because of intermittent exacerbations of her lower extremity pain, swelling, and occasional paresthesias. About 6 months after initial presentation, repeat MRI again showed increased size of the mass (13.5×13.5 cm axial, 28 cm craniocaudal). There was also increased displacement of the adjacent neurovascular structures but no evidence of deep vein thrombosis. Because of concerns about the increased symptomatology of her thigh mass and possible sampling error of the previous biopsies, an elective cesarean section was performed at 35 weeks gestation. One week later, after clearance by her obstetrician, we proceeded with open biopsy of the mass in prone position. Initial sampling was negative for malignancy on frozen section; then, we expressed 1.75 L of brown fluid and solidified blood products, irrigated copiously, and placed a surgical drain. The permanent histologic specimens were again consistent with hematoma, and microbial cultures were negative. A week later, the patient accidentally removed her drain, and she presented with a fever (101°F) on postoperative day (POD) 15. Computed tomography showed reaccumulation of fluid; duplex ultrasound was negative. She was placed on cephalexin and underwent ultrasound-guided replacement of the drain with removal of an additional 750 mL fluid on POD 20. She drained an additional 150 to 200 mL/d for 1 month, with marked improvement in her leg swelling and knee range of motion. The drainage decreased during the next 3 weeks, and the drain was removed on POD 75.

 

Discussion

The presence of a hematoma in the extremities is usually a straightforward diagnosis. However, the unusual circumstances of this case highlight all the indications for investigation for possible soft-tissue sarcoma when a patient presents with what appears to be a benign condition.

Hematomas are rare in the absence of trauma or coagulopathy, with chronic expansion of hematomas rarer still.^4,7,10-11 The patient had no evidence of coagulopathy because of her ability to have an uncomplicated pregnancy and elective cesarean section. She denied a history of trauma, and the location of her hematoma at the posterior distal thigh is an uncommon site of injury. In this setting, fine-needle aspiration and serial imaging to assess for progressive increase in lesion size were indicated to rule out malignancy.²

MRI is the gold-standard imaging modality for distinguishing soft-tissue masses from hematomas.^5,12-14 Unlike the typical appearance of a hematoma, sarcomas of the soft-tissue extremities are often complex cystic lesions with multiple septations, internal soft-tissue components, and relatively ill-defined margins.^15-17 However, as a hematoma becomes chronic, it can develop a fibrinous capsule, and the contents can manifest an atypical, heterogeneous appearance from scattered, progressive accumulation of blood products that is essentially indistinguishable from sarcomas on imaging.⁵

Because of the expansion of the hematoma and the atypical appearance of the mass on imaging, repeated core biopsy and, eventually, open biopsy were indicated, despite a preliminary negative diagnosis based on fine-needle aspiration. This resulted from the possibility of sampling error that is particularly relevant to cystic sarcomas, because only portions of the mass may be composed of malignant cells.² An unusual aspect of this case is the regional lymphadenopathy noted on MRI, because regional lymphatic spread is a known mechanism of metastasis in soft-tissue sarcomas.¹⁸ However, the inguinal biopsies showed a chronic inflammatory infiltrate and were negative for malignancy, and enlarged nodes were not seen on imaging several months later. It is possible that the lymphadenopathy resulted from an unrelated process; alternatively, it may have been secondary to impaired lymphatic drainage because of mass effect from the hematoma, which also caused temporary lower extremity swelling.

The distal posterior thigh is an unreported location for a chronic expanding hematoma. Our patient developed slowly progressive lower-limb swelling and, eventually, paresthesias because of displacement of the neurovasculature, an unusual sequela that was recently reported in a similar case of an acute spontaneous hematoma in a patient on warfarin.¹⁹ Rupture of a Baker cyst is a possible inciting factor in our patient, although the proximal location of the lesion and the clearly defined tissue plane on MRI between the hematoma and the popliteal region make this unlikely. Finally, the patient’s lesion showed no evidence of vascular flow on Doppler ultrasonography, although giant hematomas secondary to popliteal aneurysm rupture have been reported.^20-22

Conclusion

This case highlights the features of a chronic expanding hematoma that can suggest soft-tissue sarcoma and shows the recommended diagnostic steps to differentiate the 2 conditions. This case also describes an unreported location for a chronic expanding hematoma with resulting progressive neurovascular displacement caused by mass effect. We recommend careful monitoring of patients with similarly expansile lesions in this region for signs of neurovascular compromise.

Soft-tissue sarcomas are quite rare, with an annual incidence of 20 to 30 per 1,000,000 persons in the United States.¹ Because of their heterogeneous presentation, they remain a diagnostic challenge and are often initially confused for more common, benign disorders.² Chronic expanding hematoma, first described by Friedlander and colleagues³ in 1968, is a rare entity that is particularly difficult to distinguish from soft-tissue malignancy.^3-5 Chronic expanding hematoma is defined as a hematoma that gradually expands over 1 month or longer, is absent of neoplastic change on histologic sections, and does not occur in the setting of coagulopathy.⁶

Typically associated with remote trauma, these lesions often present as a slowly growing mass on the anterior or lateral thigh, calf, or buttock.^3-4,7-9 They have been reported to persist as long as 46 years, with sizes ranging from 3 to 55 cm in maximum diameter.⁷ On imaging, they have a cystic appearance with a dense fibrous capsule.^7-8 Most cases resolve uneventfully after drainage or marginal excision, although some cases require repeated intervention.⁷ This case report describes a morbidly obese patient with a chronic expanding hematoma in the distal posterior thigh whose definitive treatment was delayed 6 months because of her pregnancy status and inability to lie prone for open biopsy. The patient provided written informed consent for print and electronic publication of this case report.

Case Report

A 27-year-old morbidly obese woman, who was pregnant at 12 weeks gestation, was seen in an orthopedic oncology clinic with a 1-month history of a slowly growing, painful posterior thigh mass. She had no history of cancer or bleeding disorder, and denied a history of trauma or constitutional symptoms consistent with malignancy. Coagulation studies were normal. Magnetic resonance imaging (MRI) obtained 2 weeks prior in the emergency room showed a cystic lesion with mass-like components in the posterior compartment of the distal right thigh, measuring 17 cm longitudinally. The lesion was located adjacent to, but not involving, the sciatic nerve and femoral vasculature. On initial examination, the large soft-tissue mass was evident and moderately painful to palpation; no skin changes were noted, and the patient had a normal sensorimotor examination. Fine-needle aspiration was performed, which resulted in amorphous debris consistent with hematoma.

Repeat MRI 2 months later showed increased size of the lesion (9.5×10.5 cm axial, 22.0 cm craniocaudal). Although most findings of a more extensive imaging protocol, including precontrast and postcontrast sequences, were consistent with hematoma, the lesion also had several characteristics that indicated soft-tissue sarcoma. Specifically, findings suggestive of chronic hematoma included the hyperintense short tau inversion recovery (STIR) T1/T2 signal of the cystic component consistent with proteinaceous fluid and the low STIR TI/T2 signal of the periphery consistent with a rim of hemosiderin (Figure 1). Additionally, the cystic component of the lesion had multiple fine septations that are atypical for a hematoma (Figure 1), and several lymph nodes greater than 1.7 cm in short axis were noted in the anterior thigh and hemipelvis that were suspicious of metastatic lymphadenopathy. The encapsulated appearance of the lesion with a sharply defined margin and short transition zone were also reassuring findings for a benign lesion (Figures 1, 2A, 2B). However, several findings were identified that suggested soft-tissue sarcoma, including a nodular soft-tissue component on the medial wall of the lesion that had heterogeneous enhancement with contrast (Figure 2B). We, therefore, proceeded with ultrasound-guided core needle biopsy of the mass and cytologic sampling of the fluid components, which were again consistent with hematoma; no evidence of internal vascular flow was noted on Doppler ultrasound. Ultrasound-guided right inguinal lymph node biopsy was also performed and was negative for malignancy. Because of her large body habitus and pregnancy status, it was agreed that open biopsy should be delayed until after delivery to avoid placing the patient in a prone position.

The patient visited the emergency room several times during the following months because of intermittent exacerbations of her lower extremity pain, swelling, and occasional paresthesias. About 6 months after initial presentation, repeat MRI again showed increased size of the mass (13.5×13.5 cm axial, 28 cm craniocaudal). There was also increased displacement of the adjacent neurovascular structures but no evidence of deep vein thrombosis. Because of concerns about the increased symptomatology of her thigh mass and possible sampling error of the previous biopsies, an elective cesarean section was performed at 35 weeks gestation. One week later, after clearance by her obstetrician, we proceeded with open biopsy of the mass in prone position. Initial sampling was negative for malignancy on frozen section; then, we expressed 1.75 L of brown fluid and solidified blood products, irrigated copiously, and placed a surgical drain. The permanent histologic specimens were again consistent with hematoma, and microbial cultures were negative. A week later, the patient accidentally removed her drain, and she presented with a fever (101°F) on postoperative day (POD) 15. Computed tomography showed reaccumulation of fluid; duplex ultrasound was negative. She was placed on cephalexin and underwent ultrasound-guided replacement of the drain with removal of an additional 750 mL fluid on POD 20. She drained an additional 150 to 200 mL/d for 1 month, with marked improvement in her leg swelling and knee range of motion. The drainage decreased during the next 3 weeks, and the drain was removed on POD 75.

 

Discussion

The presence of a hematoma in the extremities is usually a straightforward diagnosis. However, the unusual circumstances of this case highlight all the indications for investigation for possible soft-tissue sarcoma when a patient presents with what appears to be a benign condition.

Hematomas are rare in the absence of trauma or coagulopathy, with chronic expansion of hematomas rarer still.^4,7,10-11 The patient had no evidence of coagulopathy because of her ability to have an uncomplicated pregnancy and elective cesarean section. She denied a history of trauma, and the location of her hematoma at the posterior distal thigh is an uncommon site of injury. In this setting, fine-needle aspiration and serial imaging to assess for progressive increase in lesion size were indicated to rule out malignancy.²

MRI is the gold-standard imaging modality for distinguishing soft-tissue masses from hematomas.^5,12-14 Unlike the typical appearance of a hematoma, sarcomas of the soft-tissue extremities are often complex cystic lesions with multiple septations, internal soft-tissue components, and relatively ill-defined margins.^15-17 However, as a hematoma becomes chronic, it can develop a fibrinous capsule, and the contents can manifest an atypical, heterogeneous appearance from scattered, progressive accumulation of blood products that is essentially indistinguishable from sarcomas on imaging.⁵

Because of the expansion of the hematoma and the atypical appearance of the mass on imaging, repeated core biopsy and, eventually, open biopsy were indicated, despite a preliminary negative diagnosis based on fine-needle aspiration. This resulted from the possibility of sampling error that is particularly relevant to cystic sarcomas, because only portions of the mass may be composed of malignant cells.² An unusual aspect of this case is the regional lymphadenopathy noted on MRI, because regional lymphatic spread is a known mechanism of metastasis in soft-tissue sarcomas.¹⁸ However, the inguinal biopsies showed a chronic inflammatory infiltrate and were negative for malignancy, and enlarged nodes were not seen on imaging several months later. It is possible that the lymphadenopathy resulted from an unrelated process; alternatively, it may have been secondary to impaired lymphatic drainage because of mass effect from the hematoma, which also caused temporary lower extremity swelling.

The distal posterior thigh is an unreported location for a chronic expanding hematoma. Our patient developed slowly progressive lower-limb swelling and, eventually, paresthesias because of displacement of the neurovasculature, an unusual sequela that was recently reported in a similar case of an acute spontaneous hematoma in a patient on warfarin.¹⁹ Rupture of a Baker cyst is a possible inciting factor in our patient, although the proximal location of the lesion and the clearly defined tissue plane on MRI between the hematoma and the popliteal region make this unlikely. Finally, the patient’s lesion showed no evidence of vascular flow on Doppler ultrasonography, although giant hematomas secondary to popliteal aneurysm rupture have been reported.^20-22

Conclusion

This case highlights the features of a chronic expanding hematoma that can suggest soft-tissue sarcoma and shows the recommended diagnostic steps to differentiate the 2 conditions. This case also describes an unreported location for a chronic expanding hematoma with resulting progressive neurovascular displacement caused by mass effect. We recommend careful monitoring of patients with similarly expansile lesions in this region for signs of neurovascular compromise.

Soft-tissue sarcomas are quite rare, with an annual incidence of 20 to 30 per 1,000,000 persons in the United States.¹ Because of their heterogeneous presentation, they remain a diagnostic challenge and are often initially confused for more common, benign disorders.² Chronic expanding hematoma, first described by Friedlander and colleagues³ in 1968, is a rare entity that is particularly difficult to distinguish from soft-tissue malignancy.^3-5 Chronic expanding hematoma is defined as a hematoma that gradually expands over 1 month or longer, is absent of neoplastic change on histologic sections, and does not occur in the setting of coagulopathy.⁶

Typically associated with remote trauma, these lesions often present as a slowly growing mass on the anterior or lateral thigh, calf, or buttock.^3-4,7-9 They have been reported to persist as long as 46 years, with sizes ranging from 3 to 55 cm in maximum diameter.⁷ On imaging, they have a cystic appearance with a dense fibrous capsule.^7-8 Most cases resolve uneventfully after drainage or marginal excision, although some cases require repeated intervention.⁷ This case report describes a morbidly obese patient with a chronic expanding hematoma in the distal posterior thigh whose definitive treatment was delayed 6 months because of her pregnancy status and inability to lie prone for open biopsy. The patient provided written informed consent for print and electronic publication of this case report.

Case Report

A 27-year-old morbidly obese woman, who was pregnant at 12 weeks gestation, was seen in an orthopedic oncology clinic with a 1-month history of a slowly growing, painful posterior thigh mass. She had no history of cancer or bleeding disorder, and denied a history of trauma or constitutional symptoms consistent with malignancy. Coagulation studies were normal. Magnetic resonance imaging (MRI) obtained 2 weeks prior in the emergency room showed a cystic lesion with mass-like components in the posterior compartment of the distal right thigh, measuring 17 cm longitudinally. The lesion was located adjacent to, but not involving, the sciatic nerve and femoral vasculature. On initial examination, the large soft-tissue mass was evident and moderately painful to palpation; no skin changes were noted, and the patient had a normal sensorimotor examination. Fine-needle aspiration was performed, which resulted in amorphous debris consistent with hematoma.

Repeat MRI 2 months later showed increased size of the lesion (9.5×10.5 cm axial, 22.0 cm craniocaudal). Although most findings of a more extensive imaging protocol, including precontrast and postcontrast sequences, were consistent with hematoma, the lesion also had several characteristics that indicated soft-tissue sarcoma. Specifically, findings suggestive of chronic hematoma included the hyperintense short tau inversion recovery (STIR) T1/T2 signal of the cystic component consistent with proteinaceous fluid and the low STIR TI/T2 signal of the periphery consistent with a rim of hemosiderin (Figure 1). Additionally, the cystic component of the lesion had multiple fine septations that are atypical for a hematoma (Figure 1), and several lymph nodes greater than 1.7 cm in short axis were noted in the anterior thigh and hemipelvis that were suspicious of metastatic lymphadenopathy. The encapsulated appearance of the lesion with a sharply defined margin and short transition zone were also reassuring findings for a benign lesion (Figures 1, 2A, 2B). However, several findings were identified that suggested soft-tissue sarcoma, including a nodular soft-tissue component on the medial wall of the lesion that had heterogeneous enhancement with contrast (Figure 2B). We, therefore, proceeded with ultrasound-guided core needle biopsy of the mass and cytologic sampling of the fluid components, which were again consistent with hematoma; no evidence of internal vascular flow was noted on Doppler ultrasound. Ultrasound-guided right inguinal lymph node biopsy was also performed and was negative for malignancy. Because of her large body habitus and pregnancy status, it was agreed that open biopsy should be delayed until after delivery to avoid placing the patient in a prone position.

The patient visited the emergency room several times during the following months because of intermittent exacerbations of her lower extremity pain, swelling, and occasional paresthesias. About 6 months after initial presentation, repeat MRI again showed increased size of the mass (13.5×13.5 cm axial, 28 cm craniocaudal). There was also increased displacement of the adjacent neurovascular structures but no evidence of deep vein thrombosis. Because of concerns about the increased symptomatology of her thigh mass and possible sampling error of the previous biopsies, an elective cesarean section was performed at 35 weeks gestation. One week later, after clearance by her obstetrician, we proceeded with open biopsy of the mass in prone position. Initial sampling was negative for malignancy on frozen section; then, we expressed 1.75 L of brown fluid and solidified blood products, irrigated copiously, and placed a surgical drain. The permanent histologic specimens were again consistent with hematoma, and microbial cultures were negative. A week later, the patient accidentally removed her drain, and she presented with a fever (101°F) on postoperative day (POD) 15. Computed tomography showed reaccumulation of fluid; duplex ultrasound was negative. She was placed on cephalexin and underwent ultrasound-guided replacement of the drain with removal of an additional 750 mL fluid on POD 20. She drained an additional 150 to 200 mL/d for 1 month, with marked improvement in her leg swelling and knee range of motion. The drainage decreased during the next 3 weeks, and the drain was removed on POD 75.

 

Discussion

The presence of a hematoma in the extremities is usually a straightforward diagnosis. However, the unusual circumstances of this case highlight all the indications for investigation for possible soft-tissue sarcoma when a patient presents with what appears to be a benign condition.

Hematomas are rare in the absence of trauma or coagulopathy, with chronic expansion of hematomas rarer still.^4,7,10-11 The patient had no evidence of coagulopathy because of her ability to have an uncomplicated pregnancy and elective cesarean section. She denied a history of trauma, and the location of her hematoma at the posterior distal thigh is an uncommon site of injury. In this setting, fine-needle aspiration and serial imaging to assess for progressive increase in lesion size were indicated to rule out malignancy.²

MRI is the gold-standard imaging modality for distinguishing soft-tissue masses from hematomas.^5,12-14 Unlike the typical appearance of a hematoma, sarcomas of the soft-tissue extremities are often complex cystic lesions with multiple septations, internal soft-tissue components, and relatively ill-defined margins.^15-17 However, as a hematoma becomes chronic, it can develop a fibrinous capsule, and the contents can manifest an atypical, heterogeneous appearance from scattered, progressive accumulation of blood products that is essentially indistinguishable from sarcomas on imaging.⁵

Because of the expansion of the hematoma and the atypical appearance of the mass on imaging, repeated core biopsy and, eventually, open biopsy were indicated, despite a preliminary negative diagnosis based on fine-needle aspiration. This resulted from the possibility of sampling error that is particularly relevant to cystic sarcomas, because only portions of the mass may be composed of malignant cells.² An unusual aspect of this case is the regional lymphadenopathy noted on MRI, because regional lymphatic spread is a known mechanism of metastasis in soft-tissue sarcomas.¹⁸ However, the inguinal biopsies showed a chronic inflammatory infiltrate and were negative for malignancy, and enlarged nodes were not seen on imaging several months later. It is possible that the lymphadenopathy resulted from an unrelated process; alternatively, it may have been secondary to impaired lymphatic drainage because of mass effect from the hematoma, which also caused temporary lower extremity swelling.

The distal posterior thigh is an unreported location for a chronic expanding hematoma. Our patient developed slowly progressive lower-limb swelling and, eventually, paresthesias because of displacement of the neurovasculature, an unusual sequela that was recently reported in a similar case of an acute spontaneous hematoma in a patient on warfarin.¹⁹ Rupture of a Baker cyst is a possible inciting factor in our patient, although the proximal location of the lesion and the clearly defined tissue plane on MRI between the hematoma and the popliteal region make this unlikely. Finally, the patient’s lesion showed no evidence of vascular flow on Doppler ultrasonography, although giant hematomas secondary to popliteal aneurysm rupture have been reported.^20-22

Conclusion

This case highlights the features of a chronic expanding hematoma that can suggest soft-tissue sarcoma and shows the recommended diagnostic steps to differentiate the 2 conditions. This case also describes an unreported location for a chronic expanding hematoma with resulting progressive neurovascular displacement caused by mass effect. We recommend careful monitoring of patients with similarly expansile lesions in this region for signs of neurovascular compromise.

VIENNA – Bedside echocardiography has become a key part of quickly assessing patients with acute heart failure to decide the best management strategy.

But bedside echo images often are challenging to interpret, so physicians performing an initial work-up of an acute heart failure patient need training in a basic echocardiography examination, Dr. Nuno Cardim said in an interview during the annual meeting of the European Association of Cardiovascular Imaging.

Known as Focused Cardiac Ultrasound (FoCUS), this triage-level exam is distinct from a comprehensive echocardiography assessment. Instead, FoCUS addresses some basic, yes-or-no, present-or-absent questions regarding systolic function, hypovolemia, tamponade, pleural effusion, and pulmonary embolus.

In a position paper and then in practice recommendations issued in 2014, the European Association of Cardiovascular Imaging acknowledged that use of FoCUS in acute heart failure patients was “irreversible,” said Dr. Cardim, professor and director of echocardiography and cardiac imaging at Hospital da Luz in Lisbon.

Cardiologists and echocardiography specialists need to make sure that FoCUS training is available to all physicians who might see suspected acute heart failure patients in emergency medicine settings, Dr. Cardim said.

Dr. Cardim had no disclosures.

[email protected]

On Twitter @mitchelzoler

VIENNA – Bedside echocardiography has become a key part of quickly assessing patients with acute heart failure to decide the best management strategy.

But bedside echo images often are challenging to interpret, so physicians performing an initial work-up of an acute heart failure patient need training in a basic echocardiography examination, Dr. Nuno Cardim said in an interview during the annual meeting of the European Association of Cardiovascular Imaging.

Known as Focused Cardiac Ultrasound (FoCUS), this triage-level exam is distinct from a comprehensive echocardiography assessment. Instead, FoCUS addresses some basic, yes-or-no, present-or-absent questions regarding systolic function, hypovolemia, tamponade, pleural effusion, and pulmonary embolus.

In a position paper and then in practice recommendations issued in 2014, the European Association of Cardiovascular Imaging acknowledged that use of FoCUS in acute heart failure patients was “irreversible,” said Dr. Cardim, professor and director of echocardiography and cardiac imaging at Hospital da Luz in Lisbon.

Cardiologists and echocardiography specialists need to make sure that FoCUS training is available to all physicians who might see suspected acute heart failure patients in emergency medicine settings, Dr. Cardim said.

Dr. Cardim had no disclosures.

[email protected]

On Twitter @mitchelzoler

VIENNA – Bedside echocardiography has become a key part of quickly assessing patients with acute heart failure to decide the best management strategy.

But bedside echo images often are challenging to interpret, so physicians performing an initial work-up of an acute heart failure patient need training in a basic echocardiography examination, Dr. Nuno Cardim said in an interview during the annual meeting of the European Association of Cardiovascular Imaging.

Known as Focused Cardiac Ultrasound (FoCUS), this triage-level exam is distinct from a comprehensive echocardiography assessment. Instead, FoCUS addresses some basic, yes-or-no, present-or-absent questions regarding systolic function, hypovolemia, tamponade, pleural effusion, and pulmonary embolus.

In a position paper and then in practice recommendations issued in 2014, the European Association of Cardiovascular Imaging acknowledged that use of FoCUS in acute heart failure patients was “irreversible,” said Dr. Cardim, professor and director of echocardiography and cardiac imaging at Hospital da Luz in Lisbon.

Cardiologists and echocardiography specialists need to make sure that FoCUS training is available to all physicians who might see suspected acute heart failure patients in emergency medicine settings, Dr. Cardim said.

Dr. Cardim had no disclosures.

[email protected]

On Twitter @mitchelzoler

Knee osteoarthritis (KOA), a common disabling disease with a high impact on quality of life, has a large societal cost. Yet no procedure halts progressive degeneration of the osteoarthritic knee joint.^1,2

According to Barry,³ mesenchymal stem cells (MSCs) differentiate into many different connective tissue cells, including cartilage. MSCs can be isolated from bone marrow, skeletal muscle, fat, and synovium. MSCs are multipotent cells with the capacity for self-renewal. Therefore, adult MSCs may regenerate tissues damaged by disease. In OA, the proliferative capacity and ability to differentiate are reduced in MSCs. Intra-articular injections of MSCs (MSC therapy) could repair progressively degenerated knee cartilage.

This review article summarizes the knowledge on the role of intra-articular injections of MSCs in the treatment of KOA, based on studies published in PubMed and the Cochrane Library. The article also reviews the methodology and results of the animal and clinical studies published so far on the topic.

Materials and Methods

PubMed (Medline) and the Cochrane Library were searched for literature on the role of MSC therapy in treating KOA. The key words used were stem cells and knee osteoarthritis. The period searched was from when these search engines began until January 31, 2014. One hundred thirty-five articles (including negative studies) were found, but only the 25 deeply focused on the topic were reviewed. The Figure shows the flow diagram of this study.

Results

Several experimental models of KOA have shown that MSC therapy can delay progressive degeneration of the knee joint (Appendix 1).^4-15 Using a rabbit massive meniscal defect model, Hatsushika and colleagues¹³ found that a single intra-articular injection of synovial MSCs into the knee adhered around the meniscal defect and promoted meniscal regeneration. Park and colleagues¹⁴ conducted an experimental study in dogs—the first demonstrating regional and systemic safety and systemic immunomodulatory effects of repeated local delivery of allogeneic MSCs in vivo. Regarding the observed systemic immunomodulatory effects, clinical and pathologic examinations revealed no severe consequences of repeated MSC transplantations. Results of mixed leukocyte reactions demonstrated suppression of T-cell proliferation after MSC transplantations.

Of the human studies published so far, only 3 were prospective randomized trials (level II evidence) included in the Cochrane Library (Appendix 2).^16-18 Varma and colleagues¹⁶ found that intra-articular injections of MSCs considerably improved overall KOA outcome scores. Fifty patients with mild to moderate KOA were divided into 2 groups. Group A underwent arthroscopic débridement, and group B had buffy coat (MSC concentrate) injection and arthroscopic débridement. Patients were assessed on the basis of their visual analog scale (VAS) pain scores and osteoarthritis outcome scores.

Wong and colleagues¹⁷ analyzed 56 knees in 56 patients (mean age, 51 years) with unicompartmental KOA and genu varum. Patients were randomly assigned to 2 groups, MSC and control. All patients underwent high tibial osteotomy (HTO) and microfracture. Patients in the MSC group received intra-articular injection of cultured MSCs with hyaluronic acid (HA) 3 weeks after surgery. Patients in the control group received only HA. The primary outcome measure was International Knee Documentation Committee (IKDC) score 6 months, 1 year, and 2 years after surgery. Secondary outcome measures were Tegner and Lysholm clinical scores and 1-year postoperative Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) scores. Both treatment arms achieved improvements in Tegner, Lysholm, and IKDC scores. After adjustment for age, baseline scores, and time of evaluation, the MSC group had significantly better scores. One year after surgery, magnetic resonance imaging (MRI) scans showed significantly better MOCART scores for the MSC group. Intra-articular injection of MSCs appeared to be effective in improving short-term clinical and MOCART outcomes in patients who underwent HTO and microfracture for varus knees with cartilage defects.

Saw and colleagues¹⁸ compared histologic and MRI evaluation of articular cartilage regeneration in patients with chondral lesions treated by arthroscopic subchondral drilling followed by postoperative intra-articular injections of HA with and without peripheral blood stem cells (PBSCs). Fifty patients (ages, 18-50 years) with International Cartilage Repair Society grades 3 and 4 lesions of the knee joint underwent arthroscopic subchondral drilling; 25 patients were randomized to the intervention group (HA + PBSC) and 25 to the control group (HA). Both groups received 5 weekly injections starting 1 week after surgery. Three additional injections of either HA + PBSC or HA only were given at weekly intervals 6 months after surgery. After arthroscopic subchondral drilling into grades 3 and 4 chondral lesions, postoperative intra-articular injections of autologous PBSC combined with HA resulted in improved quality of articular cartilage repair over the same treatment without PBSC.

The other human studies analyzed had a low level of evidence (grade IV, case series) but found that intra-articular injections of MSCs reduced pain and improved function in patients with KOA over the short term, 1 year (Appendix 3).^19-25

 

Discussion

This review aimed to define the role of MSC therapy in the treatment of KOA. MSC therapy has yielded encouraging outcomes in experimental models of KOA.^4-15 These experimental studies have suggested that MSCs can halt cartilage degeneration in KOA. So far, however, only 3 human studies with grade II evidence (randomized prospective trials) have been reported on the role of MSCs in KOA, but results of these studies have suggested that MSCs can reduce pain and improve function.^16-18

Previous reviews of the literature^1,2 have analyzed the role of MSC therapy in KOA. Barry and Murphy¹ reported that several early-stage clinical trials, initiated or under way in 2013, were testing MSC delivery as an intra-articular injection into the knee, but optimal dose and vehicle were yet to be established. Filardo and colleagues² reported that, despite growing interest in this biological approach to cartilage regeneration, knowledge on the topic is still preliminary, as shown by the prevalence of preclinical studies and the presence of low-quality clinical studies.

Study design weakness prevents effective comparison of the efficacy of MSC therapy with that of other treatments for relief of pain and other outcomes in KOA. The consistency of evidence of the clinical studies is low because of many uncontrolled variables.^1-3

Conclusion

The results of MSC therapy in KOA are encouraging. However, optimal dose and vehicle are yet to be established.¹ Knowledge on this topic is still preliminary. Many aspects have to be optimized, and further randomized controlled trials are needed to support the potential of this biological treatment for cartilage repair and to evaluate advantages and disadvantages with respect to the available treatments. The relative short duration of these studies is also a limitation for the technique at present.

Knee osteoarthritis (KOA), a common disabling disease with a high impact on quality of life, has a large societal cost. Yet no procedure halts progressive degeneration of the osteoarthritic knee joint.^1,2

According to Barry,³ mesenchymal stem cells (MSCs) differentiate into many different connective tissue cells, including cartilage. MSCs can be isolated from bone marrow, skeletal muscle, fat, and synovium. MSCs are multipotent cells with the capacity for self-renewal. Therefore, adult MSCs may regenerate tissues damaged by disease. In OA, the proliferative capacity and ability to differentiate are reduced in MSCs. Intra-articular injections of MSCs (MSC therapy) could repair progressively degenerated knee cartilage.

This review article summarizes the knowledge on the role of intra-articular injections of MSCs in the treatment of KOA, based on studies published in PubMed and the Cochrane Library. The article also reviews the methodology and results of the animal and clinical studies published so far on the topic.

Materials and Methods

PubMed (Medline) and the Cochrane Library were searched for literature on the role of MSC therapy in treating KOA. The key words used were stem cells and knee osteoarthritis. The period searched was from when these search engines began until January 31, 2014. One hundred thirty-five articles (including negative studies) were found, but only the 25 deeply focused on the topic were reviewed. The Figure shows the flow diagram of this study.

Results

Several experimental models of KOA have shown that MSC therapy can delay progressive degeneration of the knee joint (Appendix 1).^4-15 Using a rabbit massive meniscal defect model, Hatsushika and colleagues¹³ found that a single intra-articular injection of synovial MSCs into the knee adhered around the meniscal defect and promoted meniscal regeneration. Park and colleagues¹⁴ conducted an experimental study in dogs—the first demonstrating regional and systemic safety and systemic immunomodulatory effects of repeated local delivery of allogeneic MSCs in vivo. Regarding the observed systemic immunomodulatory effects, clinical and pathologic examinations revealed no severe consequences of repeated MSC transplantations. Results of mixed leukocyte reactions demonstrated suppression of T-cell proliferation after MSC transplantations.

Of the human studies published so far, only 3 were prospective randomized trials (level II evidence) included in the Cochrane Library (Appendix 2).^16-18 Varma and colleagues¹⁶ found that intra-articular injections of MSCs considerably improved overall KOA outcome scores. Fifty patients with mild to moderate KOA were divided into 2 groups. Group A underwent arthroscopic débridement, and group B had buffy coat (MSC concentrate) injection and arthroscopic débridement. Patients were assessed on the basis of their visual analog scale (VAS) pain scores and osteoarthritis outcome scores.

Wong and colleagues¹⁷ analyzed 56 knees in 56 patients (mean age, 51 years) with unicompartmental KOA and genu varum. Patients were randomly assigned to 2 groups, MSC and control. All patients underwent high tibial osteotomy (HTO) and microfracture. Patients in the MSC group received intra-articular injection of cultured MSCs with hyaluronic acid (HA) 3 weeks after surgery. Patients in the control group received only HA. The primary outcome measure was International Knee Documentation Committee (IKDC) score 6 months, 1 year, and 2 years after surgery. Secondary outcome measures were Tegner and Lysholm clinical scores and 1-year postoperative Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) scores. Both treatment arms achieved improvements in Tegner, Lysholm, and IKDC scores. After adjustment for age, baseline scores, and time of evaluation, the MSC group had significantly better scores. One year after surgery, magnetic resonance imaging (MRI) scans showed significantly better MOCART scores for the MSC group. Intra-articular injection of MSCs appeared to be effective in improving short-term clinical and MOCART outcomes in patients who underwent HTO and microfracture for varus knees with cartilage defects.

Saw and colleagues¹⁸ compared histologic and MRI evaluation of articular cartilage regeneration in patients with chondral lesions treated by arthroscopic subchondral drilling followed by postoperative intra-articular injections of HA with and without peripheral blood stem cells (PBSCs). Fifty patients (ages, 18-50 years) with International Cartilage Repair Society grades 3 and 4 lesions of the knee joint underwent arthroscopic subchondral drilling; 25 patients were randomized to the intervention group (HA + PBSC) and 25 to the control group (HA). Both groups received 5 weekly injections starting 1 week after surgery. Three additional injections of either HA + PBSC or HA only were given at weekly intervals 6 months after surgery. After arthroscopic subchondral drilling into grades 3 and 4 chondral lesions, postoperative intra-articular injections of autologous PBSC combined with HA resulted in improved quality of articular cartilage repair over the same treatment without PBSC.

The other human studies analyzed had a low level of evidence (grade IV, case series) but found that intra-articular injections of MSCs reduced pain and improved function in patients with KOA over the short term, 1 year (Appendix 3).^19-25

 

Discussion

This review aimed to define the role of MSC therapy in the treatment of KOA. MSC therapy has yielded encouraging outcomes in experimental models of KOA.^4-15 These experimental studies have suggested that MSCs can halt cartilage degeneration in KOA. So far, however, only 3 human studies with grade II evidence (randomized prospective trials) have been reported on the role of MSCs in KOA, but results of these studies have suggested that MSCs can reduce pain and improve function.^16-18

Previous reviews of the literature^1,2 have analyzed the role of MSC therapy in KOA. Barry and Murphy¹ reported that several early-stage clinical trials, initiated or under way in 2013, were testing MSC delivery as an intra-articular injection into the knee, but optimal dose and vehicle were yet to be established. Filardo and colleagues² reported that, despite growing interest in this biological approach to cartilage regeneration, knowledge on the topic is still preliminary, as shown by the prevalence of preclinical studies and the presence of low-quality clinical studies.

Study design weakness prevents effective comparison of the efficacy of MSC therapy with that of other treatments for relief of pain and other outcomes in KOA. The consistency of evidence of the clinical studies is low because of many uncontrolled variables.^1-3

Conclusion

The results of MSC therapy in KOA are encouraging. However, optimal dose and vehicle are yet to be established.¹ Knowledge on this topic is still preliminary. Many aspects have to be optimized, and further randomized controlled trials are needed to support the potential of this biological treatment for cartilage repair and to evaluate advantages and disadvantages with respect to the available treatments. The relative short duration of these studies is also a limitation for the technique at present.

Knee osteoarthritis (KOA), a common disabling disease with a high impact on quality of life, has a large societal cost. Yet no procedure halts progressive degeneration of the osteoarthritic knee joint.^1,2

According to Barry,³ mesenchymal stem cells (MSCs) differentiate into many different connective tissue cells, including cartilage. MSCs can be isolated from bone marrow, skeletal muscle, fat, and synovium. MSCs are multipotent cells with the capacity for self-renewal. Therefore, adult MSCs may regenerate tissues damaged by disease. In OA, the proliferative capacity and ability to differentiate are reduced in MSCs. Intra-articular injections of MSCs (MSC therapy) could repair progressively degenerated knee cartilage.

This review article summarizes the knowledge on the role of intra-articular injections of MSCs in the treatment of KOA, based on studies published in PubMed and the Cochrane Library. The article also reviews the methodology and results of the animal and clinical studies published so far on the topic.

Materials and Methods

PubMed (Medline) and the Cochrane Library were searched for literature on the role of MSC therapy in treating KOA. The key words used were stem cells and knee osteoarthritis. The period searched was from when these search engines began until January 31, 2014. One hundred thirty-five articles (including negative studies) were found, but only the 25 deeply focused on the topic were reviewed. The Figure shows the flow diagram of this study.

Results

Several experimental models of KOA have shown that MSC therapy can delay progressive degeneration of the knee joint (Appendix 1).^4-15 Using a rabbit massive meniscal defect model, Hatsushika and colleagues¹³ found that a single intra-articular injection of synovial MSCs into the knee adhered around the meniscal defect and promoted meniscal regeneration. Park and colleagues¹⁴ conducted an experimental study in dogs—the first demonstrating regional and systemic safety and systemic immunomodulatory effects of repeated local delivery of allogeneic MSCs in vivo. Regarding the observed systemic immunomodulatory effects, clinical and pathologic examinations revealed no severe consequences of repeated MSC transplantations. Results of mixed leukocyte reactions demonstrated suppression of T-cell proliferation after MSC transplantations.

Of the human studies published so far, only 3 were prospective randomized trials (level II evidence) included in the Cochrane Library (Appendix 2).^16-18 Varma and colleagues¹⁶ found that intra-articular injections of MSCs considerably improved overall KOA outcome scores. Fifty patients with mild to moderate KOA were divided into 2 groups. Group A underwent arthroscopic débridement, and group B had buffy coat (MSC concentrate) injection and arthroscopic débridement. Patients were assessed on the basis of their visual analog scale (VAS) pain scores and osteoarthritis outcome scores.

Wong and colleagues¹⁷ analyzed 56 knees in 56 patients (mean age, 51 years) with unicompartmental KOA and genu varum. Patients were randomly assigned to 2 groups, MSC and control. All patients underwent high tibial osteotomy (HTO) and microfracture. Patients in the MSC group received intra-articular injection of cultured MSCs with hyaluronic acid (HA) 3 weeks after surgery. Patients in the control group received only HA. The primary outcome measure was International Knee Documentation Committee (IKDC) score 6 months, 1 year, and 2 years after surgery. Secondary outcome measures were Tegner and Lysholm clinical scores and 1-year postoperative Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) scores. Both treatment arms achieved improvements in Tegner, Lysholm, and IKDC scores. After adjustment for age, baseline scores, and time of evaluation, the MSC group had significantly better scores. One year after surgery, magnetic resonance imaging (MRI) scans showed significantly better MOCART scores for the MSC group. Intra-articular injection of MSCs appeared to be effective in improving short-term clinical and MOCART outcomes in patients who underwent HTO and microfracture for varus knees with cartilage defects.

Saw and colleagues¹⁸ compared histologic and MRI evaluation of articular cartilage regeneration in patients with chondral lesions treated by arthroscopic subchondral drilling followed by postoperative intra-articular injections of HA with and without peripheral blood stem cells (PBSCs). Fifty patients (ages, 18-50 years) with International Cartilage Repair Society grades 3 and 4 lesions of the knee joint underwent arthroscopic subchondral drilling; 25 patients were randomized to the intervention group (HA + PBSC) and 25 to the control group (HA). Both groups received 5 weekly injections starting 1 week after surgery. Three additional injections of either HA + PBSC or HA only were given at weekly intervals 6 months after surgery. After arthroscopic subchondral drilling into grades 3 and 4 chondral lesions, postoperative intra-articular injections of autologous PBSC combined with HA resulted in improved quality of articular cartilage repair over the same treatment without PBSC.

The other human studies analyzed had a low level of evidence (grade IV, case series) but found that intra-articular injections of MSCs reduced pain and improved function in patients with KOA over the short term, 1 year (Appendix 3).^19-25

 

Discussion

This review aimed to define the role of MSC therapy in the treatment of KOA. MSC therapy has yielded encouraging outcomes in experimental models of KOA.^4-15 These experimental studies have suggested that MSCs can halt cartilage degeneration in KOA. So far, however, only 3 human studies with grade II evidence (randomized prospective trials) have been reported on the role of MSCs in KOA, but results of these studies have suggested that MSCs can reduce pain and improve function.^16-18

Previous reviews of the literature^1,2 have analyzed the role of MSC therapy in KOA. Barry and Murphy¹ reported that several early-stage clinical trials, initiated or under way in 2013, were testing MSC delivery as an intra-articular injection into the knee, but optimal dose and vehicle were yet to be established. Filardo and colleagues² reported that, despite growing interest in this biological approach to cartilage regeneration, knowledge on the topic is still preliminary, as shown by the prevalence of preclinical studies and the presence of low-quality clinical studies.

Study design weakness prevents effective comparison of the efficacy of MSC therapy with that of other treatments for relief of pain and other outcomes in KOA. The consistency of evidence of the clinical studies is low because of many uncontrolled variables.^1-3

Conclusion

The results of MSC therapy in KOA are encouraging. However, optimal dose and vehicle are yet to be established.¹ Knowledge on this topic is still preliminary. Many aspects have to be optimized, and further randomized controlled trials are needed to support the potential of this biological treatment for cartilage repair and to evaluate advantages and disadvantages with respect to the available treatments. The relative short duration of these studies is also a limitation for the technique at present.

VIENNA – Transcatheter aortic valve replacement has benefited enormously from the recent introduction of CT and three-dimensional echocardiography imaging into routine preprocedural planning and periprocedural guidance.

These two imaging methods have allowed clinicians to better select the right valve size for each patient, and 3D echo performed during transcatheter aortic valve replacement (TAVR) has also refined valve placement. The result has been TAVR procedures that go faster and have more accurate results while producing fewer complications, Dr. Rebecca Hahn said during an interview at the annual meeting of the European Association of Cardiovascular Imaging.

Perhaps the biggest impact of better valve-size selection and more detailed procedural guidance has been a reduced incidence and severity of paravalvular regurgitation once TAVR is complete and the replacement valve deployed. In recent months, Dr. Hahn and her associates at Columbia University Medical Center in New York have had no patients develop moderate or severe paravalvular regurgitation following TAVR, and the incidence of mild paravalvular leaks has dropped by about half, compared with when the procedure was first performed about 5 years ago, said Dr. Hahn, director of invasive and valvular echocardiography at Columbia.

[email protected]

On Twitter@mitchelzoler

VIENNA – Transcatheter aortic valve replacement has benefited enormously from the recent introduction of CT and three-dimensional echocardiography imaging into routine preprocedural planning and periprocedural guidance.

These two imaging methods have allowed clinicians to better select the right valve size for each patient, and 3D echo performed during transcatheter aortic valve replacement (TAVR) has also refined valve placement. The result has been TAVR procedures that go faster and have more accurate results while producing fewer complications, Dr. Rebecca Hahn said during an interview at the annual meeting of the European Association of Cardiovascular Imaging.

Perhaps the biggest impact of better valve-size selection and more detailed procedural guidance has been a reduced incidence and severity of paravalvular regurgitation once TAVR is complete and the replacement valve deployed. In recent months, Dr. Hahn and her associates at Columbia University Medical Center in New York have had no patients develop moderate or severe paravalvular regurgitation following TAVR, and the incidence of mild paravalvular leaks has dropped by about half, compared with when the procedure was first performed about 5 years ago, said Dr. Hahn, director of invasive and valvular echocardiography at Columbia.

[email protected]

On Twitter@mitchelzoler

VIENNA – Transcatheter aortic valve replacement has benefited enormously from the recent introduction of CT and three-dimensional echocardiography imaging into routine preprocedural planning and periprocedural guidance.

These two imaging methods have allowed clinicians to better select the right valve size for each patient, and 3D echo performed during transcatheter aortic valve replacement (TAVR) has also refined valve placement. The result has been TAVR procedures that go faster and have more accurate results while producing fewer complications, Dr. Rebecca Hahn said during an interview at the annual meeting of the European Association of Cardiovascular Imaging.

Perhaps the biggest impact of better valve-size selection and more detailed procedural guidance has been a reduced incidence and severity of paravalvular regurgitation once TAVR is complete and the replacement valve deployed. In recent months, Dr. Hahn and her associates at Columbia University Medical Center in New York have had no patients develop moderate or severe paravalvular regurgitation following TAVR, and the incidence of mild paravalvular leaks has dropped by about half, compared with when the procedure was first performed about 5 years ago, said Dr. Hahn, director of invasive and valvular echocardiography at Columbia.

[email protected]

On Twitter@mitchelzoler

A 48-year-old man presented to the ED via emergency medical services after experiencing two episodes of syncope following the acute onset of right lower quadrant pain. He was unresponsive at the time of presentation. His vital signs were notable for tachycardia with a heart rate of 130 beats/minute. Although normotensive at initial presentation, the patient’s blood pressure began to fall rapidly. Laboratory values revealed a decreased hemoglobin and hematocrit of 5 g/dL and 18.1%, respectively.

Following his stabilization, a computed tomography (CT) scan of the abdomen and pelvis was performed. Figures 1a and 1b represent selected noncontrast and postcontrast axial images obtained through the lower abdomen/upper pelvis.

What is the diagnosis?

 

Answer

The precontrast image (Figure 1c) demonstrates a large and irregular high-density collection within the right upper pelvis (white arrows) and high density free fluid along the left lateral abdominal wall (black arrows). The right psoas muscle is obscured (white asterisk, Figure 1c) when compared to the normal psoas muscle on the contralateral side (black asterisk, Figure 1c). The postcontrast image (Figure 1d) shows the same findings and also reveals an enlarged right common iliac artery (red asterisk) and contrast actively extravasating from the artery (red arrow). These findings indicate the presence of a ruptured common iliac artery aneurysm. Both the enlarged common iliac artery aneurysm (red arrow, Figure 1d) and the extravasated contrast (red asterisk, Figure 1d) were confirmed on the three-dimensional reformats of the CT scan (Figure 1e).

An isolated aneurysm of the common iliac artery is uncommon, occurring in only 1% to 2% of the population—the same frequency as aortic aneurysm.¹ However, the risk of rupture of this type of aneurysm is high.² Patients with common iliac artery aneurysm are typically asymptomatic prior to rupture. However, some patients have reportedly presented with claudication, tenesmus/constipation, sciatica, and lower extremity paresis due to nerve compression, as well as urinary obstruction caused by ureteral obstruction.^1,3 Once the iliac artery aneurysm has ruptured, patients typically present with acute abdominal, groin, and/or thigh pain, although isolated testicular pain has been described in the literature.^1,4

Treatment for iliac artery aneurysm includes open and endovascular repair, depending on patient presentation and the adjacent structures involved. While mortality is low for patients with a nonruptured common iliac aneurysm, acute rupture is present in approximately one out of three cases, and the surgical mortality rate is as high as 55%.³

The patient presented in this case was taken to the operating room where an angiogram of the right common iliac artery (red arrow, Figure 1f) revealed continued acute extravasation of contrast (red asterisk, Figure 1f). Surgical repair was attempted but the patient did not survive due to complications of hypotension and cardiac arrest.

A 48-year-old man presented to the ED via emergency medical services after experiencing two episodes of syncope following the acute onset of right lower quadrant pain. He was unresponsive at the time of presentation. His vital signs were notable for tachycardia with a heart rate of 130 beats/minute. Although normotensive at initial presentation, the patient’s blood pressure began to fall rapidly. Laboratory values revealed a decreased hemoglobin and hematocrit of 5 g/dL and 18.1%, respectively.

Following his stabilization, a computed tomography (CT) scan of the abdomen and pelvis was performed. Figures 1a and 1b represent selected noncontrast and postcontrast axial images obtained through the lower abdomen/upper pelvis.

What is the diagnosis?

 

Answer

The precontrast image (Figure 1c) demonstrates a large and irregular high-density collection within the right upper pelvis (white arrows) and high density free fluid along the left lateral abdominal wall (black arrows). The right psoas muscle is obscured (white asterisk, Figure 1c) when compared to the normal psoas muscle on the contralateral side (black asterisk, Figure 1c). The postcontrast image (Figure 1d) shows the same findings and also reveals an enlarged right common iliac artery (red asterisk) and contrast actively extravasating from the artery (red arrow). These findings indicate the presence of a ruptured common iliac artery aneurysm. Both the enlarged common iliac artery aneurysm (red arrow, Figure 1d) and the extravasated contrast (red asterisk, Figure 1d) were confirmed on the three-dimensional reformats of the CT scan (Figure 1e).

An isolated aneurysm of the common iliac artery is uncommon, occurring in only 1% to 2% of the population—the same frequency as aortic aneurysm.¹ However, the risk of rupture of this type of aneurysm is high.² Patients with common iliac artery aneurysm are typically asymptomatic prior to rupture. However, some patients have reportedly presented with claudication, tenesmus/constipation, sciatica, and lower extremity paresis due to nerve compression, as well as urinary obstruction caused by ureteral obstruction.^1,3 Once the iliac artery aneurysm has ruptured, patients typically present with acute abdominal, groin, and/or thigh pain, although isolated testicular pain has been described in the literature.^1,4

Treatment for iliac artery aneurysm includes open and endovascular repair, depending on patient presentation and the adjacent structures involved. While mortality is low for patients with a nonruptured common iliac aneurysm, acute rupture is present in approximately one out of three cases, and the surgical mortality rate is as high as 55%.³

The patient presented in this case was taken to the operating room where an angiogram of the right common iliac artery (red arrow, Figure 1f) revealed continued acute extravasation of contrast (red asterisk, Figure 1f). Surgical repair was attempted but the patient did not survive due to complications of hypotension and cardiac arrest.

A 48-year-old man presented to the ED via emergency medical services after experiencing two episodes of syncope following the acute onset of right lower quadrant pain. He was unresponsive at the time of presentation. His vital signs were notable for tachycardia with a heart rate of 130 beats/minute. Although normotensive at initial presentation, the patient’s blood pressure began to fall rapidly. Laboratory values revealed a decreased hemoglobin and hematocrit of 5 g/dL and 18.1%, respectively.

Following his stabilization, a computed tomography (CT) scan of the abdomen and pelvis was performed. Figures 1a and 1b represent selected noncontrast and postcontrast axial images obtained through the lower abdomen/upper pelvis.

What is the diagnosis?

 

Answer

The precontrast image (Figure 1c) demonstrates a large and irregular high-density collection within the right upper pelvis (white arrows) and high density free fluid along the left lateral abdominal wall (black arrows). The right psoas muscle is obscured (white asterisk, Figure 1c) when compared to the normal psoas muscle on the contralateral side (black asterisk, Figure 1c). The postcontrast image (Figure 1d) shows the same findings and also reveals an enlarged right common iliac artery (red asterisk) and contrast actively extravasating from the artery (red arrow). These findings indicate the presence of a ruptured common iliac artery aneurysm. Both the enlarged common iliac artery aneurysm (red arrow, Figure 1d) and the extravasated contrast (red asterisk, Figure 1d) were confirmed on the three-dimensional reformats of the CT scan (Figure 1e).

An isolated aneurysm of the common iliac artery is uncommon, occurring in only 1% to 2% of the population—the same frequency as aortic aneurysm.¹ However, the risk of rupture of this type of aneurysm is high.² Patients with common iliac artery aneurysm are typically asymptomatic prior to rupture. However, some patients have reportedly presented with claudication, tenesmus/constipation, sciatica, and lower extremity paresis due to nerve compression, as well as urinary obstruction caused by ureteral obstruction.^1,3 Once the iliac artery aneurysm has ruptured, patients typically present with acute abdominal, groin, and/or thigh pain, although isolated testicular pain has been described in the literature.^1,4

Treatment for iliac artery aneurysm includes open and endovascular repair, depending on patient presentation and the adjacent structures involved. While mortality is low for patients with a nonruptured common iliac aneurysm, acute rupture is present in approximately one out of three cases, and the surgical mortality rate is as high as 55%.³

The patient presented in this case was taken to the operating room where an angiogram of the right common iliac artery (red arrow, Figure 1f) revealed continued acute extravasation of contrast (red asterisk, Figure 1f). Surgical repair was attempted but the patient did not survive due to complications of hypotension and cardiac arrest.

Case

A 62-year-old man with known adenocarcinoma of the lung with metastasis to the liver and bones presented to the ED complaining of nonproductive cough and progressively worsening shortness of breath for 2 weeks. He was started on crizotinib a week prior to presentation, and had also received multiple courses of oral antibiotics and steroids for presumed exacerbation of chronic obstructive pulmonary disease (COPD). In addition to COPD, the patient had a history of degenerative joint disease, and was previously a chronic smoker. His current medications included tiotropium, inhaled daily; albuterol, two inhalations as needed; and hydrocodone/acetaminophen as needed for pain.

His vital signs on physical examination were: heart rate, 98 beats/minute; blood pressure 138/89 mm Hg; respiratory rate, 20 breaths/minute; temperature, 99.3°F. Oxygen saturation was 84% on room air, which improved to 92% with 2 L of oxygen. He had mild rhonchi on chest auscultation, but normal heart sounds and normal neurological, gastrointestinal, and extremity examination. Laboratory data revealed persistent elevation of leukocytes ranging between 12 and 15 x 10⁹/L; hemoglobin, 9.2 g/dL; and platelet count, 220 x 10⁹/L. A basic metabolic panel was within the normal range. The chest radiograph showed no evidence of pulmonary or cardiac abnormalities.

The patient was given nebulizer therapy with albuterol, along with oral prednisone. He improved with treatment and was discharged with oral prednisone daily for 4 days and oral doxycycline daily for 7 days. A week later, however, the patient had a cardiorespiratory arrest at home and could not be revived. A postmortem examination confirmed bilateral massive pulmonary embolism (PE). 

Cancer Prevalence

According to the Cancer Facts & Figures 2014 published by the American Cancer Society, approximately 13.7 million Americans with a history of cancer were alive on January 1, 2012.¹ In 2014, there will be an estimated 1,665,540 new cancer diagnoses and 585,720 cancer deaths in the United States.¹ Cancer remains the second most common cause of death in the United States, accounting for nearly one out of every four deaths.

As seen in the above case presentation, cancer patients are at an increased risk for developing venous thromboembolism (VTE), the symptoms of which may not always be overt. Thus, with the increasing incidence and prevalence of cancer, enhanced vision and emphasis on education of emergency physicians—especially in relation to comorbidities associated with the disease—will improve care for this unique population. (See Figure 1 for an algorithm outlining the appropriate emergency management of VTE in cancer patients.)

Venous Thromboembolism

Symptoms
Classic clinical symptoms of acute VTE may not be seen in all patients. Therefore, a high level of clinical suspicion should be made on cancer patients presenting with any clinically overt signs or symptoms that could represent acute VTE. Symptoms of DVT include pain or tenderness and swelling of one or more extremities. On physical examination, increased warmth, edema, and erythema are often found. The most common signs and symptoms of PE include dyspnea, tachypnea, and pleuritic chest pain. Tachycardia, hypoxia, cough, and syncope are not present in all cases of acute PE.²

Deep Vein Thrombosis and Pulmonary Embolism
Deep vein thrombosis and PE are manifestations of a single disease entity, namely, VTE. The association between VTE and cancer has been well established since it was first recognized by the French internist Armand Trousseau more than 150 years ago.

Deep vein thrombosis is characterized by a thrombus, usually in one of the deep venous conduits that return blood to the heart from the lower extremities, proximal to and including the popliteal veins. However, emboli can also originate from the pelvic veins, the inferior vena cava, and the upper extremities. Pulmonary embolism is characterized by a fully or partially occluding thrombus in one or more arteries of the lungs. Patients with cancer carry an increased risk of developing VTE because of tumor- and treatment-mediated hypercoagulability.^6-8 Table 1 provides a summary of the risk factors associated with cancer-related VTE. 

Venous thromboembolism is the second leading noncancer-related cause of death in oncology patients, with infection being the first.^9-11 Mortality from an acute thrombotic event is four to eight times greater in patients with cancer than in those without cancer.^12-14 Based on its high prevalence (in part due to prothrombotic effects of oncologic therapies) and high mortality rate, awareness of VTE diagnostic approaches and treatment is particularly important in the ED patient with cancer.

 

Epidemiology
Patients with advanced metastatic disease of the brain, lung, stomach, pancreas, kidneys, uterus, and bladder have the highest 1-year VTE incidence rate, and are at a four to 13 times higher risk of developing VTE compared to those with localized disease.¹⁵ Approximately 15% of patients with a malignancy present with VTE at some point during the course of their illness¹⁶ compared to 2.5% of the general population.¹⁷ Furthermore, an increasing frequency of VTE among cancer patients has been observed over the years due to improved survival.¹⁸ The strongest predictor for recurrent VTE is a previous diagnosis of the condition.¹⁹ The prognosis of VTE depends on the aggressiveness of the underlying malignancy and the presence of other cancer-associated complications.²⁰

In the postoperative setting, the risk of lower extremity DVT is about twice that of noncancer patients.²¹ While commonly noted, there is limited evidence to support the relationship between DVT location and cancer. It is reasonable, however, to propose that localized anatomical compression by the tumor of nearby veins causes stasis and subsequent DVT. Bilateral DVT of the lower extremities may be seen with pelvic malignancies, and DVT of the upper extremities is associated with central venous catheters, axillary lymphomas, mediastinal tumor masses, and intravenous (IV) chemotherapy. Idiopathic DVT is a significant risk factor for underlying malignancy, found in approximately 10% of cases.²² In a prospective study of patients with newly diagnosed DVT, Hettiarachchi, et al²³ report routine clinical evaluations are sufficient to find underlying malignancies and that extensive screening is unwarranted.

Risk Assessment
The common risk factors of VTE in the general population are older age, female gender, race, prolonged immobilization, hospitalization, previous history of VTE, obesity, heart disease (ie, cardiomyopathy, atrial fibrillation), smoking, poor performance status, familial or acquired hypercoagulability (eg, pregnancy, hormone therapy, indwelling venous catheters). The cancer population, however, is unique and has other risk factors placing patients at risk for developing a VTE. Such risk factors can be grouped into four different categories: patient-related, cancer-related, treatment-related, and biochemical-related.

Patient-Related Risk Factors.  These include age, obesity, smoking, decreased mobility, history of previous VTE, comorbidities, and the presence of prothrombotic mutations.

Cancer-Related Risk Factors. Risk factors for VTE depend on the site, stage, and histological type and time from diagnosis of the cancer. Brain tumors and stomach and pancreatic cancers are associated with a high risk of VTE.^9,24 Timp, et al²⁴ also studied a strong association between the 1-year relative mortality of a cancer type and its associated thrombogenic potential. In hematologic malignancies, patients with high-grade lymphoma and acute promyelocytic leukemia are at higher risk than other forms of lymphoma or leukemia.²⁵

Treatment-Related Risk Factors. These include anticancer drugs (chemotherapy and hormonal therapy), radiation therapy, recent major surgery, and the presence of a central venous access device (CVAD).

Patients who received chemotherapy with thalidomide, lenalidomide, cisplatin, and platinum were found to be at high risk of developing VTE.⁹ Hormonal therapies including tamoxifen, raloxifene, oral contraceptives, and diethylstilbestrol phosphate (used in combination with doxorubicin) also increase the risk of VTE in cancer patients.^26-28

The incidence of symptomatic catheter-associated thrombosis is shown to be as high as 28.3%.²⁹ A recent meta-analysis of 11 studies showed that peripherally inserted central catheters are associated with a higher risk of DVT than are central venous catheters.³⁰ Mural thrombus extending from the catheter into the lumen of a vessel and leading to partial or total occlusion with or without clinical symptoms is defined as CVAD-associated thrombosis.

Biochemical-Related Risk Factors. The patient’s hemoglobin level, leukocyte, and platelet counts are associated with an increased VTE risk. Patients with a hemoglobin level <10 g/dL and a leukocyte count >11 x 10⁹/L had an almost 2-fold increased risk of developing a VTE in a study conducted by Khorana, et al.³¹ The Awareness of Neutropenia in Chemotherapy Group Registry Study reported that a platelet count ≥350 x 10⁹/L prior to chemotherapy is associated with an increased risk of VTE.³²

 

Risk Assessment Tools
The modified Korana score is a well-validated risk-assessment model incorporating clinical parameters and laboratory biomarkers to stratify cancer patients according to their propensity to develop VTE, and represents a practical approach for clinical practice.³¹ The multivariate model identified the five most predictive variables: cancer site, pretreatment platelet count and leukocyte count, hemoglobin level, and body mass index (Table 2). For example, in the case presented, considering this patient’s age, primary site of the cancer, and his laboratory results, he was at a high-risk (up to 40%) for developing VTE.

Diagnosis
In patients with a high clinical suspicion of VTE and without contraindications to anticoagulation (Table 3), early initiation of anticoagulants should be considered while awaiting results from laboratory and imaging studies.⁵ The diagnostic accuracy for VTE improves with the following tests and scores: complete blood count, platelet count, D-dimer, Wells criteria, Modified Khorana Score, duplex ultrasonography, computed tomography angiography (CTA); and ventilation perfusion (V/Q) scan.

Complete Blood Count and Platelet Count. As previously discussed, a prechemotherapy platelet count ≥350 x 10⁹/L, hemoglobin level <10g/dL, or prechemotherapy leukocyte count >11 x 10⁹/L are good predictive biomarkers to consider VTE in a cancer patient.

D-Dimer. In view of the lack of specificity of D-dimer testing (most cancer patients have elevated D-dimer levels) and the high prevalence of VTE in cancer patients, D-dimer testing is less useful in this setting. The number of false positive D-dimer assays was 3-fold higher in cancer patients compared with noncancer patients.³³ Hence, D-dimer testing is not recommended for the diagnosis of VTE in cancer patients.

Wells Criteria. Clinical prediction models such as the Wells criteria for VTE have proven useful in predicting the diagnosis of VTE: 62.5% of the 40 patients who were categorized as high-risk had positive studies; 16.1% of the 492 patients who were classified as moderate-risk and 10.2% of the 219 patients who were classified as low-risk had positive results.³⁴ However, since cancer patients comprised a minority of the subjects in this study, it is unclear whether Wells criteria is as predictive for VTE in this patient population.

Duplex Venous Ultrasonography. The most recommended and preferred choice of investigation for initial diagnosis of DVT is duplex venous ultrasonography. This test is noninvasive, inexpensive, may be performed at bedside, and does not require IV contrast. It has excellent sensitivity and specificity for proximal vein DVT, but only 50% sensitivity for calf vein DVT. Duplex ultrasonography can analyze venous compressibility (which is considered to be more definitive) and Doppler imaging of venous blood flow.³⁵ Limitations with Doppler ultrasonography include its inability to access more central veins (eg, large pelvic and iliac veins, proximal subclavian veins, inferior and superior venae cavae), and may not be used in bandaged or casted areas. Its effectiveness is operator dependent.

Computed Tomography/Computed Tomography Angiography. Computed tomography angiography is the preferred imaging technique for the initial diagnosis of PE in most patients.⁵ Along with accurate imaging of mediastinal and parenchymal structures and visualization of emboli in the pulmonary vasculature, CTA is also useful to detect signs of right heart enlargement, which can be used in assessing the patient’s risk for adverse clinical outcomes.³⁶ (See Figures 2 and 3 for examples of CT and CTA, demonstrating venous thrombosis and pulmonary thromboembolism.)

Computed Tomography Venography. The Prospective Investigation of Pulmonary Embolism Diagnosis (PIOPED) II investigators recommend stratification of all patients with suspected PE according to an objective probability assessment. A negative D-dimer rapid enzyme-linked immunosorbent assay with a low or moderate probability clinical assessment can safely exclude PE. If PE is not excluded, CTA/CT venography (CTV) is recommended by most PIOPED II investigators, though CTA alone is an option. Since there is currently a lack of evidence to support CTV and since this study was comprised only a noncancer patient population, the authors do not recommend its use in the cancer patients.³⁷

Ventilation Perfusion Scan. As it is associated with less fetal radiation exposure than CTA, the V/Q scan is useful for assessing pregnant patients and those with renal insufficiency or untreatable contrast allergies in whom IV contrast is not feasible. A normal V/Q scan essentially rules out PE.³⁸

Chest X-Ray and Electrocardiogram. Both a chest X-ray and electrocardiogram (ECG) facilitate the diagnosis of comorbidities and conditions with clinically similar presentations and can also assist in evaluating existing cardiac conditions. Findings on chest X-ray suspicious for PE include pleural effusion, localized infiltrate, Hamptons hump, and Westermark sign. In ECG, the most common finding in PE is nonspecific ST-T wave changes; a new right heart strain or an S1Q3T3 pattern is suspicious for PE.

Transthoracic Echocardiogram. More than 80% of patients with a documented PE will have some type of right heart abnormality, most commonly direct visualization of the thrombus, right ventricular dilatation, right ventricular hypokinesia with apical sparing, tricuspid regurgitation, abnormal interventricular septal motion, and pulmonary artery dilatation.³⁹

 

Miniati et al⁴⁰ have shown that using PE pretest probabilities of 10%, 50%, and 90%, the posttest probabilities with a positive echocardiogram (echo) were 38%, 85%, and 98%. With a negative echo, posttest probabilities were 5%, 33%, and 81%, respectively. The value of transthoracic echo in the diagnosis of PE results were taken from this prospective study in unselected patients.⁴⁰ Because of the poor sensitivity, echocardiography should not be used as a routine test to screen patients for suspected PE.

Magnetic Resonance Imaging. In pregnant women and in patients with kidney disease, MRI has been used to detect PE. However, the PIOPED III study found that many of the participating centers had difficulty obtaining adequate quality MR angiography (MRA) for suspected PE. The study therefore determined that this modality should be ordered only when there is appropriate expertise in both performing and reading the images, and in patients who have contraindications to standard tests.⁴

Considering the high risk of developing VTE in the cancer population, there should be a low threshold for diagnostic imaging (ie, CTA and duplex ultrasonography). The patient in this case would have benefited from a CTA to rule-out PE before he was discharged.

Treatment
The National Comprehensive Cancer Network² (NCCN), American Society of Clinical Oncology³ (ASCO), European Society for Medical Oncology⁴ (ESMO), International Society on Thrombosis and Haemostasis⁴² and American College of Chest Physicians⁵ all have recently published evidence-based clinical practice guidelines for the treatment of established VTE in cancer patients. Once a diagnosis of VTE has been established, immediate treatment with a parenteral anticoagulant should be initiated. For the purpose of this article we shall discuss only the initial treatment of VTE in the emergency setting. The available treatment options are low molecular weight heparin (LMWH), unfractionated heparin (UFH), fondaparinux, warfarin, apixaban and rivaroxaban, and thrombolytic agents.

Low Molecular Weight Heparin. As recommended by the ASCO, NCCN, and ESMO guidelines, the preferred initial treatment for VTE in cancer patients is LMWH. This recommendation stems from the Comparison of Low-Molecular-Weight Heparin versus Oral Anticoagulant Therapy for the Prevention of Recurrent Venous Thromboembolism in Patients with Cancer (CLOT) trial,⁴³ which showed a decreased incidence of recurrent VTE in patients treated with a LMWH versus a coumarin derivative. Recurrent VTE occurred in 17% of patients who received warfarin versus 9% of patients who received dalteparin after 6 months. Numerous other studies evaluating LMWH versus warfarin have shown superior efficacy with LMWH for the treatment of VTE in cancer patients.

Options for LMWH currently available include enoxaparin, dalteparin, and tinzaparin. Enoxaparin is dosed at 1 mg/kg subcutaneously every 12 hours or 1.5 mg/kg subcutaneously every 24 hours. A subgroup analysis of cancer patients with PE showed a higher VTE recurrence rate in those who received once-daily versus twice-daily dosing of enoxaparin in a trial conducted by Merli and colleagues.⁴⁴ Therefore, it is the authors’ recommendation to utilize the twice-daily regimen of enoxaparin for the treatment of PE in cancer patients during the acute phase of treatment.

Dalteparin is dosed at 200 IU/kg subcutaneously every 24 hours for the first month, and then 150 IU/kg subcutaneously every 24 hours thereafter. Tinzaparin is dosed at 175 IU/kg subcutaneously every 24 hours.

Since the LMWH drugs are renally eliminated, they can accumulate in patients with renal impairment. Patients with renal impairment should be considered for dose reductions if applicable, anti-Xa monitoring, and carefully observed for bleeding. Limited data with both dalteparin and tinzaparin, though, suggest less accumulation in patients with severe renal impairment compared to enoxaparin.

Unfractionated Heparin. The UFH drugs are administered via an IV bolus dose of 80 units/kg, followed by a continuous infusion of 18 units/kg/h, titrated to a goal activated partial thromboplastin time. Although LMWHs are preferred, UFH should be considered in certain settings, such as in patients with renal failure, patients with questionable absorption via the subcutaneous route, or patients who are under consideration for systemic thrombolytic therapy.⁵ Hospitalized patients who are at high risk for bleeding or patients who may undergo invasive procedures are good candidates for UFH over LMWHs. This is due to the fact that UFH can be promptly discontinued and is reversible with protamine sulfate (versus the partial reversibility and longer half-life of LMWH).

 

Fondaparinux. Fondaparinux is an indirect factor Xa (FXa) inhibitor given subcutaneously. Advantages of fondaparinux include the lack of monitoring required and the ability to use it in patients with a history of heparin-induced thrombocytopenia. Fondaparinux is contraindicated in patients with a creatinine clearance <30 mL/minute. Van Doormaal et al⁴² found the rate of VTE recurrence was lower with fondaparinux than UFH in the treatment of PE. In another study conducted by Akl et al,⁴⁶ the rate of VTE recurrence was higher with fondaparinux than LMWH in the treatment of DVT.

Warfarin. Warfarin is very problematic in cancer patients due to the need for frequent laboratory monitoring, numerous drug-drug and drug-nutrient interactions, slow onset of action, and long duration of action. Although it has shown inferiority in cancer patients when compared to LMWH, it may still be an option for long-term treatment, especially for patients with financial barriers, adversity to injections, or renal failure. Due to the slow onset of action of warfarin (steady state is not achieved for 5-7 days), it is important to bridge with a parenteral anticoagulant until therapeutic International normalized ratio is achieved. 

Apixaban and Rivaroxaban. Both of these agents are direct FXa inhibitors and can be classified as new oral anticoagulants. Although initial evidence is promising and these agents may be attractive due to feasibility of oral administration without required monitoring, they are currently not recommended for initial therapy in cancer patients. Current published trials have included very few cancer patients, thus limiting the authors’ ability to extrapolate results to the cancer population. Also, these anticoagulants lack reliable agents for reversal in cases of life-threatening bleeding complications.

Thrombolytics. These agents promote rapid clot lysis, reduce venous outflow obstruction, and prevent venous valvular dysfunction, which may help to limit long-term complications such as postthrombotic syndrome. No significant differences in reduction of recurrent PE, death, or major bleeding were found in a recent meta-analysis comparing heparin and thrombolytic agents in patients with acute PE.⁴⁷ However, thrombolytic therapy is recommended for massive PE (ie, defined as PE with a systolic blood pressure <90 mm Hg).⁴⁸ There is also growing evidence to support the use of thrombolytics in certain populations for submassive or moderate PE.^2,5,48 Alteplase 100 mg via IV infusion over 2 hours can be given for thrombolysis in these settings. Absolute contraindications to thrombolysis include, but are not limited to severe, uncontrolled hypertension; known intracranial (IC) neoplasm or aneurysm; internal bleeding; or recent IC surgery or trauma (Table 3).  

Nonpharmacological Treatment
Inferior Vena Cava Filters. In patients with contraindication to therapeutic anticoagulation, an inferior vena cava (IVC) filter can be inserted for prevention of PE.⁴⁹ Insertion of an IVC filter should be assessed on a case-by-case basis after evaluation of the risk-benefit ratio. If contraindications to anticoagulant therapy are no longer present, anticoagulant therapy should be initiated.

Other treatment strategies such as catheter-directed thrombolysis and surgical thrombectomy can be considered, especially in patients presenting with severe, gangrenous limbs due to obstructive VTE. Until recently, thrombolytics were delivered systemically through an IV catheter, the main disadvantage of which was increased likelihood of bleeding and reduced efficacy of the therapy. Catheter-directed delivery of thrombolytic agents directly into the clot has allowed more localized targeting of therapy and, in combination with mechanical thrombectomy, results in a significant higher rate of complete clot dissolution than systemic anticoagulation.⁵⁰

Treatment Recommendation
Per the guidelines outlined above, the preferred therapy in cancer patients with VTE is LMWH. Depending on other factors such as risk of bleeding, renal function, anticipated procedures, and financial barriers, other anticoagulant options are available but treatment should be assessed on a case-by-case basis.

Challenging Cases
Incidental VTE. Several studies have suggested that approximately half of cancer-associated VTE events are detected incidentally on routine CT scans performed for diagnosis, staging, or follow-up.⁵¹ A meta-analysis of 12 studies including more than 10,000 patients, had a weighted mean incidental PE prevalence of 3.1% (95% CI, 2.2-4.1%).⁵² Incidental VTE found on routine CT scans should be treated similarly to patients with symptomatic VTE, as many have subtle clinical symptoms of active disease on further evaluation.

 

Patients With Thrombocytopenia. The subcommittee on hemostasis and malignancy for the Scientific and Standardization Committee of the International Society on Thrombosis and haemostasis has recently recommended that anticoagulation be administered if the platelet count can be maintained above 50 x 10⁹/L.⁵³ For platelet counts between 20 and 50 x 10⁹/L, half-dose LMWH can be administered with close monitoring for possible bleeding. If the platelet count is less than 20 x 10⁹/L therapeutic doses of anticoagulation should be held. In these cases, the placement of an IVC filter is recommended to prevent PE. Once thrombocytopenia has resolved, it is recommended to initiate or resume therapeutic anticoagulation.^2-4,42

Patients With Bleeding. In view of life-threatening bleeding complications, all patients should be assessed on a case-by-case basis and careful monitoring of additional bleeding risk is recommended. In patients with minor bleeding, anticoagulation may be continued as long as close follow-up is available; whereas, in patients with absolute contraindications to anticoagulation, the risk of bleeding likely outweighs the benefit of treatment, and anticoagulants should be withheld.³ The use of IVC filters are also recommended in this population—at least until the bleeding risk subsides and anticoagulation can be initiated.^2-4,42

Patients With Brain Tumors. As per the national and international guidelines,^3,42 a brain tumor per se is not a contraindication for anticoagulation. Anticoagulation is more effective and safer than filters when maintained in the therapeutic range in patients with brain metastases and VTE.⁵⁴ Although LMWH is the preferred drug of choice in this group of patients, a decision should be made based on individual clinical assessment. Consideration should also be made for the primary tumor type since brain metastases from certain malignancies, such as melanoma, have higher tendencies to bleed.⁵⁵

Patients With Renal Failure. Since LMWHs and fondaparinux are dependent on significant renal clearance, these agents should be avoided in patients with a creatinine clearance ≤30 mL/minute. Unfractionated heparin is the drug of choice in this setting and vitamin K antagonists can be started as early as on day 1.⁴² Fixed-dose or adjusted-dose subcutaneous UFH is also an option of outpatient management of VTE in patients with renal failure.⁵

Patients With Recurrent VTE on Anticoagulants. Extension of or a new DVT or PE despite being on anticoagulation therapy is defined as anticoagulation failure. Recurrent VTE is common in cancer patients, as seen in 9% of patients from the CLOT trial. Management strategies for recurrent VTE include optimizing or increasing the dose, switching agents, or placing an IVC filter. If patients are currently on once-daily enoxaparin regimens, this should be switched to the twice-daily regimen. Patients on agents other than LMWH should be switched to LMWH if possible, and dosed accurately based on the most recent total body weight and renal function. Although not useful in the emergency setting, an anti-Xa level should be drawn for patients who present with recurrent VTE on LMWH to assess whether patients are in therapeutic range. Peak anti-Xa levels should be checked 4 to 6 hours after the last dose. Lastly, dosing of LMWH could be increased by 20% to 25%, based on safety and efficacy data from a retrospective cohort study.⁵⁶

Patients With Symptomatic Catheter-Related Thrombosis. For the treatment of symptomatic catheter-related thrombosis in cancer patients, the international clinical practice guidelines recommend use of anticoagulants for a minimum of 3 months.⁴² The CHEST guidelines suggest that the catheter not be removed if it is functional, not infected, and there is an ongoing need for the catheter.⁵ Little data exist in this subgroup of patients, but LMWHs are suggested.

Factors one should consider before commencing anticoagulation treatment include patient refusal, lack of therapeutic benefit, quality of life and life expectancy, bleeding risk, and whether anticoagulation is associated with an unreasonable burden.

Outpatient Treatment Criteria. In the absence of renal impairment, high risk of bleeding, or poor social circumstances, patients with DVT can be treated as an outpatient.⁵⁷ Although recent studies support the safety and efficacy of outpatient PE management in noncancer patients,^58,59 there is no study to support this in cancer patients. Several prognostic tools exist to aid the clinician in deciding whether cancer patients with PE can be treated as outpatients or require hospitalization. These prediction tools identify patients at a low in-hospital mortality in which outpatient management is reasonable. A few examples include the Geneva Pulmonary Embolism Prognostic Index, Pulmonary Embolism Severity Index, and the Aujesky and Murugappan prediction tools.⁵⁷

The Decision Not to Treat
Acute intervention is not the only option in this unique population. Factors one should consider before commencing anticoagulation treatment include patient refusal, lack of therapeutic benefit, quality of life and life expectancy, bleeding risk, and whether anticoagulation is associated with an unreasonable burden. 

Conclusion
In view of an increased risk of VTE in cancer patients, an increased level of clinical suspicion should be maintained. Risk factors related to patient, cancer type, treatment, and biochemical markers should be assessed, and the clinician should also consider using the modified Khorana score. Diagnostic imaging studies should also be performed in cases in which there is a high clinical suspicion of VTE.

Regarding treatment, the preferred drug of choice in the acute phase of treatment is LMWH—unless contraindications exist. In cancer patients with VTE who have severe renal failure, thrombocytopenia, brain tumors, or catheter related thrombosis, recommendations are based on best clinical practice, and the clinician should balance the desirable and undesirable effects depending on the bleeding risk versus VTE risk.

 

Dr Banala is a clinical fellow in the department of emergency medicine, University of Texas MD Anderson Cancer Center, Houston. Dr Wattana is an instructor in the department of emergency medicine, University of Texas MD Anderson Cancer Center, Houston. Ms Ma is a clinical pharmacy specialist in the division of pharmacy, University of Texas MD Anderson Cancer Center, Houston. Dr Todd is professor and chair of the department of emergency medicine, University of Texas MD Anderson Cancer Center. He is also a member of the EMERGENCY MEDICINE editorial board.

Case

A 62-year-old man with known adenocarcinoma of the lung with metastasis to the liver and bones presented to the ED complaining of nonproductive cough and progressively worsening shortness of breath for 2 weeks. He was started on crizotinib a week prior to presentation, and had also received multiple courses of oral antibiotics and steroids for presumed exacerbation of chronic obstructive pulmonary disease (COPD). In addition to COPD, the patient had a history of degenerative joint disease, and was previously a chronic smoker. His current medications included tiotropium, inhaled daily; albuterol, two inhalations as needed; and hydrocodone/acetaminophen as needed for pain.

His vital signs on physical examination were: heart rate, 98 beats/minute; blood pressure 138/89 mm Hg; respiratory rate, 20 breaths/minute; temperature, 99.3°F. Oxygen saturation was 84% on room air, which improved to 92% with 2 L of oxygen. He had mild rhonchi on chest auscultation, but normal heart sounds and normal neurological, gastrointestinal, and extremity examination. Laboratory data revealed persistent elevation of leukocytes ranging between 12 and 15 x 10⁹/L; hemoglobin, 9.2 g/dL; and platelet count, 220 x 10⁹/L. A basic metabolic panel was within the normal range. The chest radiograph showed no evidence of pulmonary or cardiac abnormalities.

The patient was given nebulizer therapy with albuterol, along with oral prednisone. He improved with treatment and was discharged with oral prednisone daily for 4 days and oral doxycycline daily for 7 days. A week later, however, the patient had a cardiorespiratory arrest at home and could not be revived. A postmortem examination confirmed bilateral massive pulmonary embolism (PE). 

Cancer Prevalence

According to the Cancer Facts & Figures 2014 published by the American Cancer Society, approximately 13.7 million Americans with a history of cancer were alive on January 1, 2012.¹ In 2014, there will be an estimated 1,665,540 new cancer diagnoses and 585,720 cancer deaths in the United States.¹ Cancer remains the second most common cause of death in the United States, accounting for nearly one out of every four deaths.

As seen in the above case presentation, cancer patients are at an increased risk for developing venous thromboembolism (VTE), the symptoms of which may not always be overt. Thus, with the increasing incidence and prevalence of cancer, enhanced vision and emphasis on education of emergency physicians—especially in relation to comorbidities associated with the disease—will improve care for this unique population. (See Figure 1 for an algorithm outlining the appropriate emergency management of VTE in cancer patients.)

Venous Thromboembolism

Symptoms
Classic clinical symptoms of acute VTE may not be seen in all patients. Therefore, a high level of clinical suspicion should be made on cancer patients presenting with any clinically overt signs or symptoms that could represent acute VTE. Symptoms of DVT include pain or tenderness and swelling of one or more extremities. On physical examination, increased warmth, edema, and erythema are often found. The most common signs and symptoms of PE include dyspnea, tachypnea, and pleuritic chest pain. Tachycardia, hypoxia, cough, and syncope are not present in all cases of acute PE.²

Deep Vein Thrombosis and Pulmonary Embolism
Deep vein thrombosis and PE are manifestations of a single disease entity, namely, VTE. The association between VTE and cancer has been well established since it was first recognized by the French internist Armand Trousseau more than 150 years ago.

Deep vein thrombosis is characterized by a thrombus, usually in one of the deep venous conduits that return blood to the heart from the lower extremities, proximal to and including the popliteal veins. However, emboli can also originate from the pelvic veins, the inferior vena cava, and the upper extremities. Pulmonary embolism is characterized by a fully or partially occluding thrombus in one or more arteries of the lungs. Patients with cancer carry an increased risk of developing VTE because of tumor- and treatment-mediated hypercoagulability.^6-8 Table 1 provides a summary of the risk factors associated with cancer-related VTE. 

Venous thromboembolism is the second leading noncancer-related cause of death in oncology patients, with infection being the first.^9-11 Mortality from an acute thrombotic event is four to eight times greater in patients with cancer than in those without cancer.^12-14 Based on its high prevalence (in part due to prothrombotic effects of oncologic therapies) and high mortality rate, awareness of VTE diagnostic approaches and treatment is particularly important in the ED patient with cancer.

 

Epidemiology
Patients with advanced metastatic disease of the brain, lung, stomach, pancreas, kidneys, uterus, and bladder have the highest 1-year VTE incidence rate, and are at a four to 13 times higher risk of developing VTE compared to those with localized disease.¹⁵ Approximately 15% of patients with a malignancy present with VTE at some point during the course of their illness¹⁶ compared to 2.5% of the general population.¹⁷ Furthermore, an increasing frequency of VTE among cancer patients has been observed over the years due to improved survival.¹⁸ The strongest predictor for recurrent VTE is a previous diagnosis of the condition.¹⁹ The prognosis of VTE depends on the aggressiveness of the underlying malignancy and the presence of other cancer-associated complications.²⁰

In the postoperative setting, the risk of lower extremity DVT is about twice that of noncancer patients.²¹ While commonly noted, there is limited evidence to support the relationship between DVT location and cancer. It is reasonable, however, to propose that localized anatomical compression by the tumor of nearby veins causes stasis and subsequent DVT. Bilateral DVT of the lower extremities may be seen with pelvic malignancies, and DVT of the upper extremities is associated with central venous catheters, axillary lymphomas, mediastinal tumor masses, and intravenous (IV) chemotherapy. Idiopathic DVT is a significant risk factor for underlying malignancy, found in approximately 10% of cases.²² In a prospective study of patients with newly diagnosed DVT, Hettiarachchi, et al²³ report routine clinical evaluations are sufficient to find underlying malignancies and that extensive screening is unwarranted.

Risk Assessment
The common risk factors of VTE in the general population are older age, female gender, race, prolonged immobilization, hospitalization, previous history of VTE, obesity, heart disease (ie, cardiomyopathy, atrial fibrillation), smoking, poor performance status, familial or acquired hypercoagulability (eg, pregnancy, hormone therapy, indwelling venous catheters). The cancer population, however, is unique and has other risk factors placing patients at risk for developing a VTE. Such risk factors can be grouped into four different categories: patient-related, cancer-related, treatment-related, and biochemical-related.

Patient-Related Risk Factors.  These include age, obesity, smoking, decreased mobility, history of previous VTE, comorbidities, and the presence of prothrombotic mutations.

Cancer-Related Risk Factors. Risk factors for VTE depend on the site, stage, and histological type and time from diagnosis of the cancer. Brain tumors and stomach and pancreatic cancers are associated with a high risk of VTE.^9,24 Timp, et al²⁴ also studied a strong association between the 1-year relative mortality of a cancer type and its associated thrombogenic potential. In hematologic malignancies, patients with high-grade lymphoma and acute promyelocytic leukemia are at higher risk than other forms of lymphoma or leukemia.²⁵

Treatment-Related Risk Factors. These include anticancer drugs (chemotherapy and hormonal therapy), radiation therapy, recent major surgery, and the presence of a central venous access device (CVAD).

Patients who received chemotherapy with thalidomide, lenalidomide, cisplatin, and platinum were found to be at high risk of developing VTE.⁹ Hormonal therapies including tamoxifen, raloxifene, oral contraceptives, and diethylstilbestrol phosphate (used in combination with doxorubicin) also increase the risk of VTE in cancer patients.^26-28

The incidence of symptomatic catheter-associated thrombosis is shown to be as high as 28.3%.²⁹ A recent meta-analysis of 11 studies showed that peripherally inserted central catheters are associated with a higher risk of DVT than are central venous catheters.³⁰ Mural thrombus extending from the catheter into the lumen of a vessel and leading to partial or total occlusion with or without clinical symptoms is defined as CVAD-associated thrombosis.

Biochemical-Related Risk Factors. The patient’s hemoglobin level, leukocyte, and platelet counts are associated with an increased VTE risk. Patients with a hemoglobin level <10 g/dL and a leukocyte count >11 x 10⁹/L had an almost 2-fold increased risk of developing a VTE in a study conducted by Khorana, et al.³¹ The Awareness of Neutropenia in Chemotherapy Group Registry Study reported that a platelet count ≥350 x 10⁹/L prior to chemotherapy is associated with an increased risk of VTE.³²

 

Risk Assessment Tools
The modified Korana score is a well-validated risk-assessment model incorporating clinical parameters and laboratory biomarkers to stratify cancer patients according to their propensity to develop VTE, and represents a practical approach for clinical practice.³¹ The multivariate model identified the five most predictive variables: cancer site, pretreatment platelet count and leukocyte count, hemoglobin level, and body mass index (Table 2). For example, in the case presented, considering this patient’s age, primary site of the cancer, and his laboratory results, he was at a high-risk (up to 40%) for developing VTE.

Diagnosis
In patients with a high clinical suspicion of VTE and without contraindications to anticoagulation (Table 3), early initiation of anticoagulants should be considered while awaiting results from laboratory and imaging studies.⁵ The diagnostic accuracy for VTE improves with the following tests and scores: complete blood count, platelet count, D-dimer, Wells criteria, Modified Khorana Score, duplex ultrasonography, computed tomography angiography (CTA); and ventilation perfusion (V/Q) scan.

Complete Blood Count and Platelet Count. As previously discussed, a prechemotherapy platelet count ≥350 x 10⁹/L, hemoglobin level <10g/dL, or prechemotherapy leukocyte count >11 x 10⁹/L are good predictive biomarkers to consider VTE in a cancer patient.

D-Dimer. In view of the lack of specificity of D-dimer testing (most cancer patients have elevated D-dimer levels) and the high prevalence of VTE in cancer patients, D-dimer testing is less useful in this setting. The number of false positive D-dimer assays was 3-fold higher in cancer patients compared with noncancer patients.³³ Hence, D-dimer testing is not recommended for the diagnosis of VTE in cancer patients.

Wells Criteria. Clinical prediction models such as the Wells criteria for VTE have proven useful in predicting the diagnosis of VTE: 62.5% of the 40 patients who were categorized as high-risk had positive studies; 16.1% of the 492 patients who were classified as moderate-risk and 10.2% of the 219 patients who were classified as low-risk had positive results.³⁴ However, since cancer patients comprised a minority of the subjects in this study, it is unclear whether Wells criteria is as predictive for VTE in this patient population.

Duplex Venous Ultrasonography. The most recommended and preferred choice of investigation for initial diagnosis of DVT is duplex venous ultrasonography. This test is noninvasive, inexpensive, may be performed at bedside, and does not require IV contrast. It has excellent sensitivity and specificity for proximal vein DVT, but only 50% sensitivity for calf vein DVT. Duplex ultrasonography can analyze venous compressibility (which is considered to be more definitive) and Doppler imaging of venous blood flow.³⁵ Limitations with Doppler ultrasonography include its inability to access more central veins (eg, large pelvic and iliac veins, proximal subclavian veins, inferior and superior venae cavae), and may not be used in bandaged or casted areas. Its effectiveness is operator dependent.

Computed Tomography/Computed Tomography Angiography. Computed tomography angiography is the preferred imaging technique for the initial diagnosis of PE in most patients.⁵ Along with accurate imaging of mediastinal and parenchymal structures and visualization of emboli in the pulmonary vasculature, CTA is also useful to detect signs of right heart enlargement, which can be used in assessing the patient’s risk for adverse clinical outcomes.³⁶ (See Figures 2 and 3 for examples of CT and CTA, demonstrating venous thrombosis and pulmonary thromboembolism.)

Computed Tomography Venography. The Prospective Investigation of Pulmonary Embolism Diagnosis (PIOPED) II investigators recommend stratification of all patients with suspected PE according to an objective probability assessment. A negative D-dimer rapid enzyme-linked immunosorbent assay with a low or moderate probability clinical assessment can safely exclude PE. If PE is not excluded, CTA/CT venography (CTV) is recommended by most PIOPED II investigators, though CTA alone is an option. Since there is currently a lack of evidence to support CTV and since this study was comprised only a noncancer patient population, the authors do not recommend its use in the cancer patients.³⁷

Ventilation Perfusion Scan. As it is associated with less fetal radiation exposure than CTA, the V/Q scan is useful for assessing pregnant patients and those with renal insufficiency or untreatable contrast allergies in whom IV contrast is not feasible. A normal V/Q scan essentially rules out PE.³⁸

Chest X-Ray and Electrocardiogram. Both a chest X-ray and electrocardiogram (ECG) facilitate the diagnosis of comorbidities and conditions with clinically similar presentations and can also assist in evaluating existing cardiac conditions. Findings on chest X-ray suspicious for PE include pleural effusion, localized infiltrate, Hamptons hump, and Westermark sign. In ECG, the most common finding in PE is nonspecific ST-T wave changes; a new right heart strain or an S1Q3T3 pattern is suspicious for PE.

Transthoracic Echocardiogram. More than 80% of patients with a documented PE will have some type of right heart abnormality, most commonly direct visualization of the thrombus, right ventricular dilatation, right ventricular hypokinesia with apical sparing, tricuspid regurgitation, abnormal interventricular septal motion, and pulmonary artery dilatation.³⁹

 

Miniati et al⁴⁰ have shown that using PE pretest probabilities of 10%, 50%, and 90%, the posttest probabilities with a positive echocardiogram (echo) were 38%, 85%, and 98%. With a negative echo, posttest probabilities were 5%, 33%, and 81%, respectively. The value of transthoracic echo in the diagnosis of PE results were taken from this prospective study in unselected patients.⁴⁰ Because of the poor sensitivity, echocardiography should not be used as a routine test to screen patients for suspected PE.

Magnetic Resonance Imaging. In pregnant women and in patients with kidney disease, MRI has been used to detect PE. However, the PIOPED III study found that many of the participating centers had difficulty obtaining adequate quality MR angiography (MRA) for suspected PE. The study therefore determined that this modality should be ordered only when there is appropriate expertise in both performing and reading the images, and in patients who have contraindications to standard tests.⁴

Considering the high risk of developing VTE in the cancer population, there should be a low threshold for diagnostic imaging (ie, CTA and duplex ultrasonography). The patient in this case would have benefited from a CTA to rule-out PE before he was discharged.

Treatment
The National Comprehensive Cancer Network² (NCCN), American Society of Clinical Oncology³ (ASCO), European Society for Medical Oncology⁴ (ESMO), International Society on Thrombosis and Haemostasis⁴² and American College of Chest Physicians⁵ all have recently published evidence-based clinical practice guidelines for the treatment of established VTE in cancer patients. Once a diagnosis of VTE has been established, immediate treatment with a parenteral anticoagulant should be initiated. For the purpose of this article we shall discuss only the initial treatment of VTE in the emergency setting. The available treatment options are low molecular weight heparin (LMWH), unfractionated heparin (UFH), fondaparinux, warfarin, apixaban and rivaroxaban, and thrombolytic agents.

Low Molecular Weight Heparin. As recommended by the ASCO, NCCN, and ESMO guidelines, the preferred initial treatment for VTE in cancer patients is LMWH. This recommendation stems from the Comparison of Low-Molecular-Weight Heparin versus Oral Anticoagulant Therapy for the Prevention of Recurrent Venous Thromboembolism in Patients with Cancer (CLOT) trial,⁴³ which showed a decreased incidence of recurrent VTE in patients treated with a LMWH versus a coumarin derivative. Recurrent VTE occurred in 17% of patients who received warfarin versus 9% of patients who received dalteparin after 6 months. Numerous other studies evaluating LMWH versus warfarin have shown superior efficacy with LMWH for the treatment of VTE in cancer patients.

Options for LMWH currently available include enoxaparin, dalteparin, and tinzaparin. Enoxaparin is dosed at 1 mg/kg subcutaneously every 12 hours or 1.5 mg/kg subcutaneously every 24 hours. A subgroup analysis of cancer patients with PE showed a higher VTE recurrence rate in those who received once-daily versus twice-daily dosing of enoxaparin in a trial conducted by Merli and colleagues.⁴⁴ Therefore, it is the authors’ recommendation to utilize the twice-daily regimen of enoxaparin for the treatment of PE in cancer patients during the acute phase of treatment.

Dalteparin is dosed at 200 IU/kg subcutaneously every 24 hours for the first month, and then 150 IU/kg subcutaneously every 24 hours thereafter. Tinzaparin is dosed at 175 IU/kg subcutaneously every 24 hours.

Since the LMWH drugs are renally eliminated, they can accumulate in patients with renal impairment. Patients with renal impairment should be considered for dose reductions if applicable, anti-Xa monitoring, and carefully observed for bleeding. Limited data with both dalteparin and tinzaparin, though, suggest less accumulation in patients with severe renal impairment compared to enoxaparin.

Unfractionated Heparin. The UFH drugs are administered via an IV bolus dose of 80 units/kg, followed by a continuous infusion of 18 units/kg/h, titrated to a goal activated partial thromboplastin time. Although LMWHs are preferred, UFH should be considered in certain settings, such as in patients with renal failure, patients with questionable absorption via the subcutaneous route, or patients who are under consideration for systemic thrombolytic therapy.⁵ Hospitalized patients who are at high risk for bleeding or patients who may undergo invasive procedures are good candidates for UFH over LMWHs. This is due to the fact that UFH can be promptly discontinued and is reversible with protamine sulfate (versus the partial reversibility and longer half-life of LMWH).

 

Fondaparinux. Fondaparinux is an indirect factor Xa (FXa) inhibitor given subcutaneously. Advantages of fondaparinux include the lack of monitoring required and the ability to use it in patients with a history of heparin-induced thrombocytopenia. Fondaparinux is contraindicated in patients with a creatinine clearance <30 mL/minute. Van Doormaal et al⁴² found the rate of VTE recurrence was lower with fondaparinux than UFH in the treatment of PE. In another study conducted by Akl et al,⁴⁶ the rate of VTE recurrence was higher with fondaparinux than LMWH in the treatment of DVT.

Warfarin. Warfarin is very problematic in cancer patients due to the need for frequent laboratory monitoring, numerous drug-drug and drug-nutrient interactions, slow onset of action, and long duration of action. Although it has shown inferiority in cancer patients when compared to LMWH, it may still be an option for long-term treatment, especially for patients with financial barriers, adversity to injections, or renal failure. Due to the slow onset of action of warfarin (steady state is not achieved for 5-7 days), it is important to bridge with a parenteral anticoagulant until therapeutic International normalized ratio is achieved. 

Apixaban and Rivaroxaban. Both of these agents are direct FXa inhibitors and can be classified as new oral anticoagulants. Although initial evidence is promising and these agents may be attractive due to feasibility of oral administration without required monitoring, they are currently not recommended for initial therapy in cancer patients. Current published trials have included very few cancer patients, thus limiting the authors’ ability to extrapolate results to the cancer population. Also, these anticoagulants lack reliable agents for reversal in cases of life-threatening bleeding complications.

Thrombolytics. These agents promote rapid clot lysis, reduce venous outflow obstruction, and prevent venous valvular dysfunction, which may help to limit long-term complications such as postthrombotic syndrome. No significant differences in reduction of recurrent PE, death, or major bleeding were found in a recent meta-analysis comparing heparin and thrombolytic agents in patients with acute PE.⁴⁷ However, thrombolytic therapy is recommended for massive PE (ie, defined as PE with a systolic blood pressure <90 mm Hg).⁴⁸ There is also growing evidence to support the use of thrombolytics in certain populations for submassive or moderate PE.^2,5,48 Alteplase 100 mg via IV infusion over 2 hours can be given for thrombolysis in these settings. Absolute contraindications to thrombolysis include, but are not limited to severe, uncontrolled hypertension; known intracranial (IC) neoplasm or aneurysm; internal bleeding; or recent IC surgery or trauma (Table 3).  

Nonpharmacological Treatment
Inferior Vena Cava Filters. In patients with contraindication to therapeutic anticoagulation, an inferior vena cava (IVC) filter can be inserted for prevention of PE.⁴⁹ Insertion of an IVC filter should be assessed on a case-by-case basis after evaluation of the risk-benefit ratio. If contraindications to anticoagulant therapy are no longer present, anticoagulant therapy should be initiated.

Other treatment strategies such as catheter-directed thrombolysis and surgical thrombectomy can be considered, especially in patients presenting with severe, gangrenous limbs due to obstructive VTE. Until recently, thrombolytics were delivered systemically through an IV catheter, the main disadvantage of which was increased likelihood of bleeding and reduced efficacy of the therapy. Catheter-directed delivery of thrombolytic agents directly into the clot has allowed more localized targeting of therapy and, in combination with mechanical thrombectomy, results in a significant higher rate of complete clot dissolution than systemic anticoagulation.⁵⁰

Treatment Recommendation
Per the guidelines outlined above, the preferred therapy in cancer patients with VTE is LMWH. Depending on other factors such as risk of bleeding, renal function, anticipated procedures, and financial barriers, other anticoagulant options are available but treatment should be assessed on a case-by-case basis.

Challenging Cases
Incidental VTE. Several studies have suggested that approximately half of cancer-associated VTE events are detected incidentally on routine CT scans performed for diagnosis, staging, or follow-up.⁵¹ A meta-analysis of 12 studies including more than 10,000 patients, had a weighted mean incidental PE prevalence of 3.1% (95% CI, 2.2-4.1%).⁵² Incidental VTE found on routine CT scans should be treated similarly to patients with symptomatic VTE, as many have subtle clinical symptoms of active disease on further evaluation.

 

Patients With Thrombocytopenia. The subcommittee on hemostasis and malignancy for the Scientific and Standardization Committee of the International Society on Thrombosis and haemostasis has recently recommended that anticoagulation be administered if the platelet count can be maintained above 50 x 10⁹/L.⁵³ For platelet counts between 20 and 50 x 10⁹/L, half-dose LMWH can be administered with close monitoring for possible bleeding. If the platelet count is less than 20 x 10⁹/L therapeutic doses of anticoagulation should be held. In these cases, the placement of an IVC filter is recommended to prevent PE. Once thrombocytopenia has resolved, it is recommended to initiate or resume therapeutic anticoagulation.^2-4,42

Patients With Bleeding. In view of life-threatening bleeding complications, all patients should be assessed on a case-by-case basis and careful monitoring of additional bleeding risk is recommended. In patients with minor bleeding, anticoagulation may be continued as long as close follow-up is available; whereas, in patients with absolute contraindications to anticoagulation, the risk of bleeding likely outweighs the benefit of treatment, and anticoagulants should be withheld.³ The use of IVC filters are also recommended in this population—at least until the bleeding risk subsides and anticoagulation can be initiated.^2-4,42

Patients With Brain Tumors. As per the national and international guidelines,^3,42 a brain tumor per se is not a contraindication for anticoagulation. Anticoagulation is more effective and safer than filters when maintained in the therapeutic range in patients with brain metastases and VTE.⁵⁴ Although LMWH is the preferred drug of choice in this group of patients, a decision should be made based on individual clinical assessment. Consideration should also be made for the primary tumor type since brain metastases from certain malignancies, such as melanoma, have higher tendencies to bleed.⁵⁵

Patients With Renal Failure. Since LMWHs and fondaparinux are dependent on significant renal clearance, these agents should be avoided in patients with a creatinine clearance ≤30 mL/minute. Unfractionated heparin is the drug of choice in this setting and vitamin K antagonists can be started as early as on day 1.⁴² Fixed-dose or adjusted-dose subcutaneous UFH is also an option of outpatient management of VTE in patients with renal failure.⁵

Patients With Recurrent VTE on Anticoagulants. Extension of or a new DVT or PE despite being on anticoagulation therapy is defined as anticoagulation failure. Recurrent VTE is common in cancer patients, as seen in 9% of patients from the CLOT trial. Management strategies for recurrent VTE include optimizing or increasing the dose, switching agents, or placing an IVC filter. If patients are currently on once-daily enoxaparin regimens, this should be switched to the twice-daily regimen. Patients on agents other than LMWH should be switched to LMWH if possible, and dosed accurately based on the most recent total body weight and renal function. Although not useful in the emergency setting, an anti-Xa level should be drawn for patients who present with recurrent VTE on LMWH to assess whether patients are in therapeutic range. Peak anti-Xa levels should be checked 4 to 6 hours after the last dose. Lastly, dosing of LMWH could be increased by 20% to 25%, based on safety and efficacy data from a retrospective cohort study.⁵⁶

Patients With Symptomatic Catheter-Related Thrombosis. For the treatment of symptomatic catheter-related thrombosis in cancer patients, the international clinical practice guidelines recommend use of anticoagulants for a minimum of 3 months.⁴² The CHEST guidelines suggest that the catheter not be removed if it is functional, not infected, and there is an ongoing need for the catheter.⁵ Little data exist in this subgroup of patients, but LMWHs are suggested.

Factors one should consider before commencing anticoagulation treatment include patient refusal, lack of therapeutic benefit, quality of life and life expectancy, bleeding risk, and whether anticoagulation is associated with an unreasonable burden.

Outpatient Treatment Criteria. In the absence of renal impairment, high risk of bleeding, or poor social circumstances, patients with DVT can be treated as an outpatient.⁵⁷ Although recent studies support the safety and efficacy of outpatient PE management in noncancer patients,^58,59 there is no study to support this in cancer patients. Several prognostic tools exist to aid the clinician in deciding whether cancer patients with PE can be treated as outpatients or require hospitalization. These prediction tools identify patients at a low in-hospital mortality in which outpatient management is reasonable. A few examples include the Geneva Pulmonary Embolism Prognostic Index, Pulmonary Embolism Severity Index, and the Aujesky and Murugappan prediction tools.⁵⁷

The Decision Not to Treat
Acute intervention is not the only option in this unique population. Factors one should consider before commencing anticoagulation treatment include patient refusal, lack of therapeutic benefit, quality of life and life expectancy, bleeding risk, and whether anticoagulation is associated with an unreasonable burden. 

Conclusion
In view of an increased risk of VTE in cancer patients, an increased level of clinical suspicion should be maintained. Risk factors related to patient, cancer type, treatment, and biochemical markers should be assessed, and the clinician should also consider using the modified Khorana score. Diagnostic imaging studies should also be performed in cases in which there is a high clinical suspicion of VTE.

Regarding treatment, the preferred drug of choice in the acute phase of treatment is LMWH—unless contraindications exist. In cancer patients with VTE who have severe renal failure, thrombocytopenia, brain tumors, or catheter related thrombosis, recommendations are based on best clinical practice, and the clinician should balance the desirable and undesirable effects depending on the bleeding risk versus VTE risk.

 

Dr Banala is a clinical fellow in the department of emergency medicine, University of Texas MD Anderson Cancer Center, Houston. Dr Wattana is an instructor in the department of emergency medicine, University of Texas MD Anderson Cancer Center, Houston. Ms Ma is a clinical pharmacy specialist in the division of pharmacy, University of Texas MD Anderson Cancer Center, Houston. Dr Todd is professor and chair of the department of emergency medicine, University of Texas MD Anderson Cancer Center. He is also a member of the EMERGENCY MEDICINE editorial board.

Case

A 62-year-old man with known adenocarcinoma of the lung with metastasis to the liver and bones presented to the ED complaining of nonproductive cough and progressively worsening shortness of breath for 2 weeks. He was started on crizotinib a week prior to presentation, and had also received multiple courses of oral antibiotics and steroids for presumed exacerbation of chronic obstructive pulmonary disease (COPD). In addition to COPD, the patient had a history of degenerative joint disease, and was previously a chronic smoker. His current medications included tiotropium, inhaled daily; albuterol, two inhalations as needed; and hydrocodone/acetaminophen as needed for pain.

His vital signs on physical examination were: heart rate, 98 beats/minute; blood pressure 138/89 mm Hg; respiratory rate, 20 breaths/minute; temperature, 99.3°F. Oxygen saturation was 84% on room air, which improved to 92% with 2 L of oxygen. He had mild rhonchi on chest auscultation, but normal heart sounds and normal neurological, gastrointestinal, and extremity examination. Laboratory data revealed persistent elevation of leukocytes ranging between 12 and 15 x 10⁹/L; hemoglobin, 9.2 g/dL; and platelet count, 220 x 10⁹/L. A basic metabolic panel was within the normal range. The chest radiograph showed no evidence of pulmonary or cardiac abnormalities.

The patient was given nebulizer therapy with albuterol, along with oral prednisone. He improved with treatment and was discharged with oral prednisone daily for 4 days and oral doxycycline daily for 7 days. A week later, however, the patient had a cardiorespiratory arrest at home and could not be revived. A postmortem examination confirmed bilateral massive pulmonary embolism (PE). 

Cancer Prevalence

According to the Cancer Facts & Figures 2014 published by the American Cancer Society, approximately 13.7 million Americans with a history of cancer were alive on January 1, 2012.¹ In 2014, there will be an estimated 1,665,540 new cancer diagnoses and 585,720 cancer deaths in the United States.¹ Cancer remains the second most common cause of death in the United States, accounting for nearly one out of every four deaths.

As seen in the above case presentation, cancer patients are at an increased risk for developing venous thromboembolism (VTE), the symptoms of which may not always be overt. Thus, with the increasing incidence and prevalence of cancer, enhanced vision and emphasis on education of emergency physicians—especially in relation to comorbidities associated with the disease—will improve care for this unique population. (See Figure 1 for an algorithm outlining the appropriate emergency management of VTE in cancer patients.)

Venous Thromboembolism

Symptoms
Classic clinical symptoms of acute VTE may not be seen in all patients. Therefore, a high level of clinical suspicion should be made on cancer patients presenting with any clinically overt signs or symptoms that could represent acute VTE. Symptoms of DVT include pain or tenderness and swelling of one or more extremities. On physical examination, increased warmth, edema, and erythema are often found. The most common signs and symptoms of PE include dyspnea, tachypnea, and pleuritic chest pain. Tachycardia, hypoxia, cough, and syncope are not present in all cases of acute PE.²

Deep Vein Thrombosis and Pulmonary Embolism
Deep vein thrombosis and PE are manifestations of a single disease entity, namely, VTE. The association between VTE and cancer has been well established since it was first recognized by the French internist Armand Trousseau more than 150 years ago.

Deep vein thrombosis is characterized by a thrombus, usually in one of the deep venous conduits that return blood to the heart from the lower extremities, proximal to and including the popliteal veins. However, emboli can also originate from the pelvic veins, the inferior vena cava, and the upper extremities. Pulmonary embolism is characterized by a fully or partially occluding thrombus in one or more arteries of the lungs. Patients with cancer carry an increased risk of developing VTE because of tumor- and treatment-mediated hypercoagulability.^6-8 Table 1 provides a summary of the risk factors associated with cancer-related VTE. 

Venous thromboembolism is the second leading noncancer-related cause of death in oncology patients, with infection being the first.^9-11 Mortality from an acute thrombotic event is four to eight times greater in patients with cancer than in those without cancer.^12-14 Based on its high prevalence (in part due to prothrombotic effects of oncologic therapies) and high mortality rate, awareness of VTE diagnostic approaches and treatment is particularly important in the ED patient with cancer.

 

Epidemiology
Patients with advanced metastatic disease of the brain, lung, stomach, pancreas, kidneys, uterus, and bladder have the highest 1-year VTE incidence rate, and are at a four to 13 times higher risk of developing VTE compared to those with localized disease.¹⁵ Approximately 15% of patients with a malignancy present with VTE at some point during the course of their illness¹⁶ compared to 2.5% of the general population.¹⁷ Furthermore, an increasing frequency of VTE among cancer patients has been observed over the years due to improved survival.¹⁸ The strongest predictor for recurrent VTE is a previous diagnosis of the condition.¹⁹ The prognosis of VTE depends on the aggressiveness of the underlying malignancy and the presence of other cancer-associated complications.²⁰

In the postoperative setting, the risk of lower extremity DVT is about twice that of noncancer patients.²¹ While commonly noted, there is limited evidence to support the relationship between DVT location and cancer. It is reasonable, however, to propose that localized anatomical compression by the tumor of nearby veins causes stasis and subsequent DVT. Bilateral DVT of the lower extremities may be seen with pelvic malignancies, and DVT of the upper extremities is associated with central venous catheters, axillary lymphomas, mediastinal tumor masses, and intravenous (IV) chemotherapy. Idiopathic DVT is a significant risk factor for underlying malignancy, found in approximately 10% of cases.²² In a prospective study of patients with newly diagnosed DVT, Hettiarachchi, et al²³ report routine clinical evaluations are sufficient to find underlying malignancies and that extensive screening is unwarranted.

Risk Assessment
The common risk factors of VTE in the general population are older age, female gender, race, prolonged immobilization, hospitalization, previous history of VTE, obesity, heart disease (ie, cardiomyopathy, atrial fibrillation), smoking, poor performance status, familial or acquired hypercoagulability (eg, pregnancy, hormone therapy, indwelling venous catheters). The cancer population, however, is unique and has other risk factors placing patients at risk for developing a VTE. Such risk factors can be grouped into four different categories: patient-related, cancer-related, treatment-related, and biochemical-related.

Patient-Related Risk Factors.  These include age, obesity, smoking, decreased mobility, history of previous VTE, comorbidities, and the presence of prothrombotic mutations.

Cancer-Related Risk Factors. Risk factors for VTE depend on the site, stage, and histological type and time from diagnosis of the cancer. Brain tumors and stomach and pancreatic cancers are associated with a high risk of VTE.^9,24 Timp, et al²⁴ also studied a strong association between the 1-year relative mortality of a cancer type and its associated thrombogenic potential. In hematologic malignancies, patients with high-grade lymphoma and acute promyelocytic leukemia are at higher risk than other forms of lymphoma or leukemia.²⁵

Treatment-Related Risk Factors. These include anticancer drugs (chemotherapy and hormonal therapy), radiation therapy, recent major surgery, and the presence of a central venous access device (CVAD).

Patients who received chemotherapy with thalidomide, lenalidomide, cisplatin, and platinum were found to be at high risk of developing VTE.⁹ Hormonal therapies including tamoxifen, raloxifene, oral contraceptives, and diethylstilbestrol phosphate (used in combination with doxorubicin) also increase the risk of VTE in cancer patients.^26-28

The incidence of symptomatic catheter-associated thrombosis is shown to be as high as 28.3%.²⁹ A recent meta-analysis of 11 studies showed that peripherally inserted central catheters are associated with a higher risk of DVT than are central venous catheters.³⁰ Mural thrombus extending from the catheter into the lumen of a vessel and leading to partial or total occlusion with or without clinical symptoms is defined as CVAD-associated thrombosis.

Biochemical-Related Risk Factors. The patient’s hemoglobin level, leukocyte, and platelet counts are associated with an increased VTE risk. Patients with a hemoglobin level <10 g/dL and a leukocyte count >11 x 10⁹/L had an almost 2-fold increased risk of developing a VTE in a study conducted by Khorana, et al.³¹ The Awareness of Neutropenia in Chemotherapy Group Registry Study reported that a platelet count ≥350 x 10⁹/L prior to chemotherapy is associated with an increased risk of VTE.³²

 

Risk Assessment Tools
The modified Korana score is a well-validated risk-assessment model incorporating clinical parameters and laboratory biomarkers to stratify cancer patients according to their propensity to develop VTE, and represents a practical approach for clinical practice.³¹ The multivariate model identified the five most predictive variables: cancer site, pretreatment platelet count and leukocyte count, hemoglobin level, and body mass index (Table 2). For example, in the case presented, considering this patient’s age, primary site of the cancer, and his laboratory results, he was at a high-risk (up to 40%) for developing VTE.

Diagnosis
In patients with a high clinical suspicion of VTE and without contraindications to anticoagulation (Table 3), early initiation of anticoagulants should be considered while awaiting results from laboratory and imaging studies.⁵ The diagnostic accuracy for VTE improves with the following tests and scores: complete blood count, platelet count, D-dimer, Wells criteria, Modified Khorana Score, duplex ultrasonography, computed tomography angiography (CTA); and ventilation perfusion (V/Q) scan.

Complete Blood Count and Platelet Count. As previously discussed, a prechemotherapy platelet count ≥350 x 10⁹/L, hemoglobin level <10g/dL, or prechemotherapy leukocyte count >11 x 10⁹/L are good predictive biomarkers to consider VTE in a cancer patient.

D-Dimer. In view of the lack of specificity of D-dimer testing (most cancer patients have elevated D-dimer levels) and the high prevalence of VTE in cancer patients, D-dimer testing is less useful in this setting. The number of false positive D-dimer assays was 3-fold higher in cancer patients compared with noncancer patients.³³ Hence, D-dimer testing is not recommended for the diagnosis of VTE in cancer patients.

Wells Criteria. Clinical prediction models such as the Wells criteria for VTE have proven useful in predicting the diagnosis of VTE: 62.5% of the 40 patients who were categorized as high-risk had positive studies; 16.1% of the 492 patients who were classified as moderate-risk and 10.2% of the 219 patients who were classified as low-risk had positive results.³⁴ However, since cancer patients comprised a minority of the subjects in this study, it is unclear whether Wells criteria is as predictive for VTE in this patient population.

Duplex Venous Ultrasonography. The most recommended and preferred choice of investigation for initial diagnosis of DVT is duplex venous ultrasonography. This test is noninvasive, inexpensive, may be performed at bedside, and does not require IV contrast. It has excellent sensitivity and specificity for proximal vein DVT, but only 50% sensitivity for calf vein DVT. Duplex ultrasonography can analyze venous compressibility (which is considered to be more definitive) and Doppler imaging of venous blood flow.³⁵ Limitations with Doppler ultrasonography include its inability to access more central veins (eg, large pelvic and iliac veins, proximal subclavian veins, inferior and superior venae cavae), and may not be used in bandaged or casted areas. Its effectiveness is operator dependent.

Computed Tomography/Computed Tomography Angiography. Computed tomography angiography is the preferred imaging technique for the initial diagnosis of PE in most patients.⁵ Along with accurate imaging of mediastinal and parenchymal structures and visualization of emboli in the pulmonary vasculature, CTA is also useful to detect signs of right heart enlargement, which can be used in assessing the patient’s risk for adverse clinical outcomes.³⁶ (See Figures 2 and 3 for examples of CT and CTA, demonstrating venous thrombosis and pulmonary thromboembolism.)

Computed Tomography Venography. The Prospective Investigation of Pulmonary Embolism Diagnosis (PIOPED) II investigators recommend stratification of all patients with suspected PE according to an objective probability assessment. A negative D-dimer rapid enzyme-linked immunosorbent assay with a low or moderate probability clinical assessment can safely exclude PE. If PE is not excluded, CTA/CT venography (CTV) is recommended by most PIOPED II investigators, though CTA alone is an option. Since there is currently a lack of evidence to support CTV and since this study was comprised only a noncancer patient population, the authors do not recommend its use in the cancer patients.³⁷

Ventilation Perfusion Scan. As it is associated with less fetal radiation exposure than CTA, the V/Q scan is useful for assessing pregnant patients and those with renal insufficiency or untreatable contrast allergies in whom IV contrast is not feasible. A normal V/Q scan essentially rules out PE.³⁸

Chest X-Ray and Electrocardiogram. Both a chest X-ray and electrocardiogram (ECG) facilitate the diagnosis of comorbidities and conditions with clinically similar presentations and can also assist in evaluating existing cardiac conditions. Findings on chest X-ray suspicious for PE include pleural effusion, localized infiltrate, Hamptons hump, and Westermark sign. In ECG, the most common finding in PE is nonspecific ST-T wave changes; a new right heart strain or an S1Q3T3 pattern is suspicious for PE.

Transthoracic Echocardiogram. More than 80% of patients with a documented PE will have some type of right heart abnormality, most commonly direct visualization of the thrombus, right ventricular dilatation, right ventricular hypokinesia with apical sparing, tricuspid regurgitation, abnormal interventricular septal motion, and pulmonary artery dilatation.³⁹

 

Miniati et al⁴⁰ have shown that using PE pretest probabilities of 10%, 50%, and 90%, the posttest probabilities with a positive echocardiogram (echo) were 38%, 85%, and 98%. With a negative echo, posttest probabilities were 5%, 33%, and 81%, respectively. The value of transthoracic echo in the diagnosis of PE results were taken from this prospective study in unselected patients.⁴⁰ Because of the poor sensitivity, echocardiography should not be used as a routine test to screen patients for suspected PE.

Magnetic Resonance Imaging. In pregnant women and in patients with kidney disease, MRI has been used to detect PE. However, the PIOPED III study found that many of the participating centers had difficulty obtaining adequate quality MR angiography (MRA) for suspected PE. The study therefore determined that this modality should be ordered only when there is appropriate expertise in both performing and reading the images, and in patients who have contraindications to standard tests.⁴

Considering the high risk of developing VTE in the cancer population, there should be a low threshold for diagnostic imaging (ie, CTA and duplex ultrasonography). The patient in this case would have benefited from a CTA to rule-out PE before he was discharged.

Treatment
The National Comprehensive Cancer Network² (NCCN), American Society of Clinical Oncology³ (ASCO), European Society for Medical Oncology⁴ (ESMO), International Society on Thrombosis and Haemostasis⁴² and American College of Chest Physicians⁵ all have recently published evidence-based clinical practice guidelines for the treatment of established VTE in cancer patients. Once a diagnosis of VTE has been established, immediate treatment with a parenteral anticoagulant should be initiated. For the purpose of this article we shall discuss only the initial treatment of VTE in the emergency setting. The available treatment options are low molecular weight heparin (LMWH), unfractionated heparin (UFH), fondaparinux, warfarin, apixaban and rivaroxaban, and thrombolytic agents.

Low Molecular Weight Heparin. As recommended by the ASCO, NCCN, and ESMO guidelines, the preferred initial treatment for VTE in cancer patients is LMWH. This recommendation stems from the Comparison of Low-Molecular-Weight Heparin versus Oral Anticoagulant Therapy for the Prevention of Recurrent Venous Thromboembolism in Patients with Cancer (CLOT) trial,⁴³ which showed a decreased incidence of recurrent VTE in patients treated with a LMWH versus a coumarin derivative. Recurrent VTE occurred in 17% of patients who received warfarin versus 9% of patients who received dalteparin after 6 months. Numerous other studies evaluating LMWH versus warfarin have shown superior efficacy with LMWH for the treatment of VTE in cancer patients.

Options for LMWH currently available include enoxaparin, dalteparin, and tinzaparin. Enoxaparin is dosed at 1 mg/kg subcutaneously every 12 hours or 1.5 mg/kg subcutaneously every 24 hours. A subgroup analysis of cancer patients with PE showed a higher VTE recurrence rate in those who received once-daily versus twice-daily dosing of enoxaparin in a trial conducted by Merli and colleagues.⁴⁴ Therefore, it is the authors’ recommendation to utilize the twice-daily regimen of enoxaparin for the treatment of PE in cancer patients during the acute phase of treatment.

Dalteparin is dosed at 200 IU/kg subcutaneously every 24 hours for the first month, and then 150 IU/kg subcutaneously every 24 hours thereafter. Tinzaparin is dosed at 175 IU/kg subcutaneously every 24 hours.

Since the LMWH drugs are renally eliminated, they can accumulate in patients with renal impairment. Patients with renal impairment should be considered for dose reductions if applicable, anti-Xa monitoring, and carefully observed for bleeding. Limited data with both dalteparin and tinzaparin, though, suggest less accumulation in patients with severe renal impairment compared to enoxaparin.

Unfractionated Heparin. The UFH drugs are administered via an IV bolus dose of 80 units/kg, followed by a continuous infusion of 18 units/kg/h, titrated to a goal activated partial thromboplastin time. Although LMWHs are preferred, UFH should be considered in certain settings, such as in patients with renal failure, patients with questionable absorption via the subcutaneous route, or patients who are under consideration for systemic thrombolytic therapy.⁵ Hospitalized patients who are at high risk for bleeding or patients who may undergo invasive procedures are good candidates for UFH over LMWHs. This is due to the fact that UFH can be promptly discontinued and is reversible with protamine sulfate (versus the partial reversibility and longer half-life of LMWH).

 

Fondaparinux. Fondaparinux is an indirect factor Xa (FXa) inhibitor given subcutaneously. Advantages of fondaparinux include the lack of monitoring required and the ability to use it in patients with a history of heparin-induced thrombocytopenia. Fondaparinux is contraindicated in patients with a creatinine clearance <30 mL/minute. Van Doormaal et al⁴² found the rate of VTE recurrence was lower with fondaparinux than UFH in the treatment of PE. In another study conducted by Akl et al,⁴⁶ the rate of VTE recurrence was higher with fondaparinux than LMWH in the treatment of DVT.

Warfarin. Warfarin is very problematic in cancer patients due to the need for frequent laboratory monitoring, numerous drug-drug and drug-nutrient interactions, slow onset of action, and long duration of action. Although it has shown inferiority in cancer patients when compared to LMWH, it may still be an option for long-term treatment, especially for patients with financial barriers, adversity to injections, or renal failure. Due to the slow onset of action of warfarin (steady state is not achieved for 5-7 days), it is important to bridge with a parenteral anticoagulant until therapeutic International normalized ratio is achieved. 

Apixaban and Rivaroxaban. Both of these agents are direct FXa inhibitors and can be classified as new oral anticoagulants. Although initial evidence is promising and these agents may be attractive due to feasibility of oral administration without required monitoring, they are currently not recommended for initial therapy in cancer patients. Current published trials have included very few cancer patients, thus limiting the authors’ ability to extrapolate results to the cancer population. Also, these anticoagulants lack reliable agents for reversal in cases of life-threatening bleeding complications.

Thrombolytics. These agents promote rapid clot lysis, reduce venous outflow obstruction, and prevent venous valvular dysfunction, which may help to limit long-term complications such as postthrombotic syndrome. No significant differences in reduction of recurrent PE, death, or major bleeding were found in a recent meta-analysis comparing heparin and thrombolytic agents in patients with acute PE.⁴⁷ However, thrombolytic therapy is recommended for massive PE (ie, defined as PE with a systolic blood pressure <90 mm Hg).⁴⁸ There is also growing evidence to support the use of thrombolytics in certain populations for submassive or moderate PE.^2,5,48 Alteplase 100 mg via IV infusion over 2 hours can be given for thrombolysis in these settings. Absolute contraindications to thrombolysis include, but are not limited to severe, uncontrolled hypertension; known intracranial (IC) neoplasm or aneurysm; internal bleeding; or recent IC surgery or trauma (Table 3).  

Nonpharmacological Treatment
Inferior Vena Cava Filters. In patients with contraindication to therapeutic anticoagulation, an inferior vena cava (IVC) filter can be inserted for prevention of PE.⁴⁹ Insertion of an IVC filter should be assessed on a case-by-case basis after evaluation of the risk-benefit ratio. If contraindications to anticoagulant therapy are no longer present, anticoagulant therapy should be initiated.

Other treatment strategies such as catheter-directed thrombolysis and surgical thrombectomy can be considered, especially in patients presenting with severe, gangrenous limbs due to obstructive VTE. Until recently, thrombolytics were delivered systemically through an IV catheter, the main disadvantage of which was increased likelihood of bleeding and reduced efficacy of the therapy. Catheter-directed delivery of thrombolytic agents directly into the clot has allowed more localized targeting of therapy and, in combination with mechanical thrombectomy, results in a significant higher rate of complete clot dissolution than systemic anticoagulation.⁵⁰

Treatment Recommendation
Per the guidelines outlined above, the preferred therapy in cancer patients with VTE is LMWH. Depending on other factors such as risk of bleeding, renal function, anticipated procedures, and financial barriers, other anticoagulant options are available but treatment should be assessed on a case-by-case basis.

Challenging Cases
Incidental VTE. Several studies have suggested that approximately half of cancer-associated VTE events are detected incidentally on routine CT scans performed for diagnosis, staging, or follow-up.⁵¹ A meta-analysis of 12 studies including more than 10,000 patients, had a weighted mean incidental PE prevalence of 3.1% (95% CI, 2.2-4.1%).⁵² Incidental VTE found on routine CT scans should be treated similarly to patients with symptomatic VTE, as many have subtle clinical symptoms of active disease on further evaluation.

 

Patients With Thrombocytopenia. The subcommittee on hemostasis and malignancy for the Scientific and Standardization Committee of the International Society on Thrombosis and haemostasis has recently recommended that anticoagulation be administered if the platelet count can be maintained above 50 x 10⁹/L.⁵³ For platelet counts between 20 and 50 x 10⁹/L, half-dose LMWH can be administered with close monitoring for possible bleeding. If the platelet count is less than 20 x 10⁹/L therapeutic doses of anticoagulation should be held. In these cases, the placement of an IVC filter is recommended to prevent PE. Once thrombocytopenia has resolved, it is recommended to initiate or resume therapeutic anticoagulation.^2-4,42

Patients With Bleeding. In view of life-threatening bleeding complications, all patients should be assessed on a case-by-case basis and careful monitoring of additional bleeding risk is recommended. In patients with minor bleeding, anticoagulation may be continued as long as close follow-up is available; whereas, in patients with absolute contraindications to anticoagulation, the risk of bleeding likely outweighs the benefit of treatment, and anticoagulants should be withheld.³ The use of IVC filters are also recommended in this population—at least until the bleeding risk subsides and anticoagulation can be initiated.^2-4,42

Patients With Brain Tumors. As per the national and international guidelines,^3,42 a brain tumor per se is not a contraindication for anticoagulation. Anticoagulation is more effective and safer than filters when maintained in the therapeutic range in patients with brain metastases and VTE.⁵⁴ Although LMWH is the preferred drug of choice in this group of patients, a decision should be made based on individual clinical assessment. Consideration should also be made for the primary tumor type since brain metastases from certain malignancies, such as melanoma, have higher tendencies to bleed.⁵⁵

Patients With Renal Failure. Since LMWHs and fondaparinux are dependent on significant renal clearance, these agents should be avoided in patients with a creatinine clearance ≤30 mL/minute. Unfractionated heparin is the drug of choice in this setting and vitamin K antagonists can be started as early as on day 1.⁴² Fixed-dose or adjusted-dose subcutaneous UFH is also an option of outpatient management of VTE in patients with renal failure.⁵

Patients With Recurrent VTE on Anticoagulants. Extension of or a new DVT or PE despite being on anticoagulation therapy is defined as anticoagulation failure. Recurrent VTE is common in cancer patients, as seen in 9% of patients from the CLOT trial. Management strategies for recurrent VTE include optimizing or increasing the dose, switching agents, or placing an IVC filter. If patients are currently on once-daily enoxaparin regimens, this should be switched to the twice-daily regimen. Patients on agents other than LMWH should be switched to LMWH if possible, and dosed accurately based on the most recent total body weight and renal function. Although not useful in the emergency setting, an anti-Xa level should be drawn for patients who present with recurrent VTE on LMWH to assess whether patients are in therapeutic range. Peak anti-Xa levels should be checked 4 to 6 hours after the last dose. Lastly, dosing of LMWH could be increased by 20% to 25%, based on safety and efficacy data from a retrospective cohort study.⁵⁶

Patients With Symptomatic Catheter-Related Thrombosis. For the treatment of symptomatic catheter-related thrombosis in cancer patients, the international clinical practice guidelines recommend use of anticoagulants for a minimum of 3 months.⁴² The CHEST guidelines suggest that the catheter not be removed if it is functional, not infected, and there is an ongoing need for the catheter.⁵ Little data exist in this subgroup of patients, but LMWHs are suggested.

Factors one should consider before commencing anticoagulation treatment include patient refusal, lack of therapeutic benefit, quality of life and life expectancy, bleeding risk, and whether anticoagulation is associated with an unreasonable burden.

Outpatient Treatment Criteria. In the absence of renal impairment, high risk of bleeding, or poor social circumstances, patients with DVT can be treated as an outpatient.⁵⁷ Although recent studies support the safety and efficacy of outpatient PE management in noncancer patients,^58,59 there is no study to support this in cancer patients. Several prognostic tools exist to aid the clinician in deciding whether cancer patients with PE can be treated as outpatients or require hospitalization. These prediction tools identify patients at a low in-hospital mortality in which outpatient management is reasonable. A few examples include the Geneva Pulmonary Embolism Prognostic Index, Pulmonary Embolism Severity Index, and the Aujesky and Murugappan prediction tools.⁵⁷

The Decision Not to Treat
Acute intervention is not the only option in this unique population. Factors one should consider before commencing anticoagulation treatment include patient refusal, lack of therapeutic benefit, quality of life and life expectancy, bleeding risk, and whether anticoagulation is associated with an unreasonable burden. 

Conclusion
In view of an increased risk of VTE in cancer patients, an increased level of clinical suspicion should be maintained. Risk factors related to patient, cancer type, treatment, and biochemical markers should be assessed, and the clinician should also consider using the modified Khorana score. Diagnostic imaging studies should also be performed in cases in which there is a high clinical suspicion of VTE.

Regarding treatment, the preferred drug of choice in the acute phase of treatment is LMWH—unless contraindications exist. In cancer patients with VTE who have severe renal failure, thrombocytopenia, brain tumors, or catheter related thrombosis, recommendations are based on best clinical practice, and the clinician should balance the desirable and undesirable effects depending on the bleeding risk versus VTE risk.

 

Dr Banala is a clinical fellow in the department of emergency medicine, University of Texas MD Anderson Cancer Center, Houston. Dr Wattana is an instructor in the department of emergency medicine, University of Texas MD Anderson Cancer Center, Houston. Ms Ma is a clinical pharmacy specialist in the division of pharmacy, University of Texas MD Anderson Cancer Center, Houston. Dr Todd is professor and chair of the department of emergency medicine, University of Texas MD Anderson Cancer Center. He is also a member of the EMERGENCY MEDICINE editorial board.

Software that provides an estimate of a patient’s fractional flow reserve using data from a coronary CT scan has been cleared for marketing, the Food and Drug Administration announced Nov. 26.

The software, HeartFlow FFR_CT, “is a computer modeling program that provides a functional assessment of blood flow in the coronary arteries from detailed anatomical data,” Dr. William Maisel, deputy director for science and chief scientist in the FDA’s Center for Devices and Radiological Health, said in the FDA statement. He described it as a noninvasive method that “is an additional tool for clinicians who are considering the risks and benefits of invasive coronary procedures.”

The healthcare professional transmits a patient’s coronary CT scan data to the headquarters of the manufacturer, HeartFlow, where an analyst creates 3-D models of the patient’s heart and runs a blood flow simulator program on the models. The clinician is then sent a report with the estimated fractional flow reserve (FFR)-CT values “displayed as color images of the patient’s heart,” according to the FDA statement.

The FDA cleared the device based on data that compared FFR-CT measurements to those obtained with cardiac catheterization in patients with suspected coronary artery disease. The FFR-CT measurements correctly identified 84% of the significant blockages that FFR identified as requiring intervention, and 86% of blockages that FFR identified as not requiring intervention, according to the FDA.

[email protected]

Software that provides an estimate of a patient’s fractional flow reserve using data from a coronary CT scan has been cleared for marketing, the Food and Drug Administration announced Nov. 26.

The software, HeartFlow FFR_CT, “is a computer modeling program that provides a functional assessment of blood flow in the coronary arteries from detailed anatomical data,” Dr. William Maisel, deputy director for science and chief scientist in the FDA’s Center for Devices and Radiological Health, said in the FDA statement. He described it as a noninvasive method that “is an additional tool for clinicians who are considering the risks and benefits of invasive coronary procedures.”

The healthcare professional transmits a patient’s coronary CT scan data to the headquarters of the manufacturer, HeartFlow, where an analyst creates 3-D models of the patient’s heart and runs a blood flow simulator program on the models. The clinician is then sent a report with the estimated fractional flow reserve (FFR)-CT values “displayed as color images of the patient’s heart,” according to the FDA statement.

The FDA cleared the device based on data that compared FFR-CT measurements to those obtained with cardiac catheterization in patients with suspected coronary artery disease. The FFR-CT measurements correctly identified 84% of the significant blockages that FFR identified as requiring intervention, and 86% of blockages that FFR identified as not requiring intervention, according to the FDA.

[email protected]

Software that provides an estimate of a patient’s fractional flow reserve using data from a coronary CT scan has been cleared for marketing, the Food and Drug Administration announced Nov. 26.

The software, HeartFlow FFR_CT, “is a computer modeling program that provides a functional assessment of blood flow in the coronary arteries from detailed anatomical data,” Dr. William Maisel, deputy director for science and chief scientist in the FDA’s Center for Devices and Radiological Health, said in the FDA statement. He described it as a noninvasive method that “is an additional tool for clinicians who are considering the risks and benefits of invasive coronary procedures.”

The healthcare professional transmits a patient’s coronary CT scan data to the headquarters of the manufacturer, HeartFlow, where an analyst creates 3-D models of the patient’s heart and runs a blood flow simulator program on the models. The clinician is then sent a report with the estimated fractional flow reserve (FFR)-CT values “displayed as color images of the patient’s heart,” according to the FDA statement.

The FDA cleared the device based on data that compared FFR-CT measurements to those obtained with cardiac catheterization in patients with suspected coronary artery disease. The FFR-CT measurements correctly identified 84% of the significant blockages that FFR identified as requiring intervention, and 86% of blockages that FFR identified as not requiring intervention, according to the FDA.

[email protected]

SAN FRANCISCO – At least 25% of CT scans to diagnose appendicitis were unnecessary, potentially resulting in $1.8 million in costs at one institution and up to four new cancers from the radiation exposure, a retrospective study suggests.

The review of 1,054 patients who underwent appendectomy at the University of California, Davis, in 2005-2010 focused on costs for the patients who had high Alvarado scores, a clinical scoring system used to diagnose appendicitis, before they underwent appendectomy. CT scans to help diagnose appendicitis were performed on 77% of all patients.

Records showed that 26% of patients had an Alvarado score of 8-10, meaning that appendicitis was highly likely. CT was performed on 70% of patients with an Alvarado score of 8 and 77% of patients with a score of 9-10, comprising nearly 25% of all CT scans. That resulted in an estimated $1,813,399 in unnecessary costs for imaging, Dr. Adam Dougherty and his associates reported at the annual clinical congress of the American College of Surgeons.

This “overutilization” of CT scans delivered more than 4,009 mSv in unnecessary radiation exposure, averaging 19.75 mSV per scan, which is 20 times the annual limit suggested for safety, said Dr. Dougherty of the university. That excess radiation could be expected to produce up to four new cancers down the line, resulting in additional costs, he said.

The investigators also looked at the 9% of patients with low Alvarado scores, meaning that appendicitis was unlikely. CT scans were performed in 75% of patients with a score of 0-3 and 80% of patients with an Alvarado score of 4. In this subgroup, 24% showed normal/early pathology on appendectomy, which “argues against imaging and surgical treatment,” Dr. Dougherty said. The 44 CT scans in this subgroup resulted in an estimated $393,052 in unnecessary costs, he said.

That doesn’t include additional costs that could be expected from imaging, such as wait time, appendectomy and its sequelae, and potential workups of incidentalomas in the low-risk group, he added.

Previous studies have shown that a comprehensive clinical exam is as accurate as CT in diagnosing appendicitis, and that clinical assessment unaided by CT can reliably diagnose acute appendicitis, Dr. Dougherty said.

With a 72% increase in abdominal CT scans documented in other U.S. data from 2000 to 2005, he called for a “necessary, fundamental culture change” to restrain resource utilization “in order to maximize the value of the health care dollar while doing what is best for the patient.”

The investigators proposed a clinical pathway for the workup of suspected appendicitis that places greater emphasis on ultrasound imaging and conservative pathways, such as 23-hour admission for observation and next-day follow-up.

In the study, ultrasonography was underutilized across all subgroups as a viable alternative to CT scans, he said.

Dr. Dougherty reported having no financial disclosures.

[email protected]

On Twitter @sherryboschert

SAN FRANCISCO – At least 25% of CT scans to diagnose appendicitis were unnecessary, potentially resulting in $1.8 million in costs at one institution and up to four new cancers from the radiation exposure, a retrospective study suggests.

The review of 1,054 patients who underwent appendectomy at the University of California, Davis, in 2005-2010 focused on costs for the patients who had high Alvarado scores, a clinical scoring system used to diagnose appendicitis, before they underwent appendectomy. CT scans to help diagnose appendicitis were performed on 77% of all patients.

Records showed that 26% of patients had an Alvarado score of 8-10, meaning that appendicitis was highly likely. CT was performed on 70% of patients with an Alvarado score of 8 and 77% of patients with a score of 9-10, comprising nearly 25% of all CT scans. That resulted in an estimated $1,813,399 in unnecessary costs for imaging, Dr. Adam Dougherty and his associates reported at the annual clinical congress of the American College of Surgeons.

This “overutilization” of CT scans delivered more than 4,009 mSv in unnecessary radiation exposure, averaging 19.75 mSV per scan, which is 20 times the annual limit suggested for safety, said Dr. Dougherty of the university. That excess radiation could be expected to produce up to four new cancers down the line, resulting in additional costs, he said.

The investigators also looked at the 9% of patients with low Alvarado scores, meaning that appendicitis was unlikely. CT scans were performed in 75% of patients with a score of 0-3 and 80% of patients with an Alvarado score of 4. In this subgroup, 24% showed normal/early pathology on appendectomy, which “argues against imaging and surgical treatment,” Dr. Dougherty said. The 44 CT scans in this subgroup resulted in an estimated $393,052 in unnecessary costs, he said.

That doesn’t include additional costs that could be expected from imaging, such as wait time, appendectomy and its sequelae, and potential workups of incidentalomas in the low-risk group, he added.

Previous studies have shown that a comprehensive clinical exam is as accurate as CT in diagnosing appendicitis, and that clinical assessment unaided by CT can reliably diagnose acute appendicitis, Dr. Dougherty said.

With a 72% increase in abdominal CT scans documented in other U.S. data from 2000 to 2005, he called for a “necessary, fundamental culture change” to restrain resource utilization “in order to maximize the value of the health care dollar while doing what is best for the patient.”

The investigators proposed a clinical pathway for the workup of suspected appendicitis that places greater emphasis on ultrasound imaging and conservative pathways, such as 23-hour admission for observation and next-day follow-up.

In the study, ultrasonography was underutilized across all subgroups as a viable alternative to CT scans, he said.

Dr. Dougherty reported having no financial disclosures.

[email protected]

On Twitter @sherryboschert

SAN FRANCISCO – At least 25% of CT scans to diagnose appendicitis were unnecessary, potentially resulting in $1.8 million in costs at one institution and up to four new cancers from the radiation exposure, a retrospective study suggests.

The review of 1,054 patients who underwent appendectomy at the University of California, Davis, in 2005-2010 focused on costs for the patients who had high Alvarado scores, a clinical scoring system used to diagnose appendicitis, before they underwent appendectomy. CT scans to help diagnose appendicitis were performed on 77% of all patients.

Records showed that 26% of patients had an Alvarado score of 8-10, meaning that appendicitis was highly likely. CT was performed on 70% of patients with an Alvarado score of 8 and 77% of patients with a score of 9-10, comprising nearly 25% of all CT scans. That resulted in an estimated $1,813,399 in unnecessary costs for imaging, Dr. Adam Dougherty and his associates reported at the annual clinical congress of the American College of Surgeons.

This “overutilization” of CT scans delivered more than 4,009 mSv in unnecessary radiation exposure, averaging 19.75 mSV per scan, which is 20 times the annual limit suggested for safety, said Dr. Dougherty of the university. That excess radiation could be expected to produce up to four new cancers down the line, resulting in additional costs, he said.

The investigators also looked at the 9% of patients with low Alvarado scores, meaning that appendicitis was unlikely. CT scans were performed in 75% of patients with a score of 0-3 and 80% of patients with an Alvarado score of 4. In this subgroup, 24% showed normal/early pathology on appendectomy, which “argues against imaging and surgical treatment,” Dr. Dougherty said. The 44 CT scans in this subgroup resulted in an estimated $393,052 in unnecessary costs, he said.

That doesn’t include additional costs that could be expected from imaging, such as wait time, appendectomy and its sequelae, and potential workups of incidentalomas in the low-risk group, he added.

Previous studies have shown that a comprehensive clinical exam is as accurate as CT in diagnosing appendicitis, and that clinical assessment unaided by CT can reliably diagnose acute appendicitis, Dr. Dougherty said.

With a 72% increase in abdominal CT scans documented in other U.S. data from 2000 to 2005, he called for a “necessary, fundamental culture change” to restrain resource utilization “in order to maximize the value of the health care dollar while doing what is best for the patient.”

The investigators proposed a clinical pathway for the workup of suspected appendicitis that places greater emphasis on ultrasound imaging and conservative pathways, such as 23-hour admission for observation and next-day follow-up.

In the study, ultrasonography was underutilized across all subgroups as a viable alternative to CT scans, he said.

Dr. Dougherty reported having no financial disclosures.

[email protected]

On Twitter @sherryboschert