Degrees of Distinction

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Thank you for stating that ARNPs “do not need physician endorsement for the advanced component” of their practice. ARNPs need to be responsible for themselves. In California, NPs are given a certificate, not a license, and operate under the rules of the state board of nursing and the board of business and professional codes. We must act in a prudent and competent manner. I think this has been demonstrated where full practice authority is in force.

The American Medical Association (AMA) and American Academy of Family Physicians (AAFP), which still want “supervision, collaboration, or participating” designations for PAs and NPs, have tripped on their own stethoscopes on this issue. In trying to suppress advanced practice providers, they have helped create a provider shortage. Many NPs will not work in a state that has practice limitations.

In Humboldt County, California, family practice doctors are so overworked due to provider shortages that they are leaving the area. Enter locum tenens to fill the gap. But at a point, there is no benefit to being in such demand. The cost of health care has risen, and patients are unhappy with the care they receive. New patients cannot see doctors in a timely manner; when they are finally seen, they have a few minutes to share their concerns with the provider, who rarely sits down or looks away from the computer screen to make eye contact with them.

We are already seeing the push for advanced education for our NPs and PAs. We have witnessed the changeover to NP programs that culminate in a doctorate (not a master’s) degree. By 2021, PA programs will be required to be master’s level; although the process has started, there are still a few holdouts. But I consider Washington State to be a front-runner in this area.

This, for me, is the area we need to address: degree designation and equivalency. Rather than give “diplomat” or similar status to someone whose base degree is an associate’s, a better idea—and one more palatable to AMA and AAFP—might be to bring everyone to at least a master’s level. For example, the Academy of Integrative Pain Management (AIPM) gives “Fellow” designation to those with master’s preparation who successfully pass AIPM’s examination, and “Diplomat” status to doctorate-prepared practitioners who have also passed the exam.

At the end of the day, many patients prefer to see a PA or NP rather than a medical doctor. Yes, patients care about credentials—but they care more about their provider being respectful, listening, remembering their history, connecting the history from their previous provider, and offering the proper treatment for the correct diagnosis.

Jan Morgan, MS, ARNP
Fellow, Academy of Integrative Pain Management
Eureka, California

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Thank you for stating that ARNPs “do not need physician endorsement for the advanced component” of their practice. ARNPs need to be responsible for themselves. In California, NPs are given a certificate, not a license, and operate under the rules of the state board of nursing and the board of business and professional codes. We must act in a prudent and competent manner. I think this has been demonstrated where full practice authority is in force.

The American Medical Association (AMA) and American Academy of Family Physicians (AAFP), which still want “supervision, collaboration, or participating” designations for PAs and NPs, have tripped on their own stethoscopes on this issue. In trying to suppress advanced practice providers, they have helped create a provider shortage. Many NPs will not work in a state that has practice limitations.

In Humboldt County, California, family practice doctors are so overworked due to provider shortages that they are leaving the area. Enter locum tenens to fill the gap. But at a point, there is no benefit to being in such demand. The cost of health care has risen, and patients are unhappy with the care they receive. New patients cannot see doctors in a timely manner; when they are finally seen, they have a few minutes to share their concerns with the provider, who rarely sits down or looks away from the computer screen to make eye contact with them.

We are already seeing the push for advanced education for our NPs and PAs. We have witnessed the changeover to NP programs that culminate in a doctorate (not a master’s) degree. By 2021, PA programs will be required to be master’s level; although the process has started, there are still a few holdouts. But I consider Washington State to be a front-runner in this area.

This, for me, is the area we need to address: degree designation and equivalency. Rather than give “diplomat” or similar status to someone whose base degree is an associate’s, a better idea—and one more palatable to AMA and AAFP—might be to bring everyone to at least a master’s level. For example, the Academy of Integrative Pain Management (AIPM) gives “Fellow” designation to those with master’s preparation who successfully pass AIPM’s examination, and “Diplomat” status to doctorate-prepared practitioners who have also passed the exam.

At the end of the day, many patients prefer to see a PA or NP rather than a medical doctor. Yes, patients care about credentials—but they care more about their provider being respectful, listening, remembering their history, connecting the history from their previous provider, and offering the proper treatment for the correct diagnosis.

Jan Morgan, MS, ARNP
Fellow, Academy of Integrative Pain Management
Eureka, California


 

Thank you for stating that ARNPs “do not need physician endorsement for the advanced component” of their practice. ARNPs need to be responsible for themselves. In California, NPs are given a certificate, not a license, and operate under the rules of the state board of nursing and the board of business and professional codes. We must act in a prudent and competent manner. I think this has been demonstrated where full practice authority is in force.

The American Medical Association (AMA) and American Academy of Family Physicians (AAFP), which still want “supervision, collaboration, or participating” designations for PAs and NPs, have tripped on their own stethoscopes on this issue. In trying to suppress advanced practice providers, they have helped create a provider shortage. Many NPs will not work in a state that has practice limitations.

In Humboldt County, California, family practice doctors are so overworked due to provider shortages that they are leaving the area. Enter locum tenens to fill the gap. But at a point, there is no benefit to being in such demand. The cost of health care has risen, and patients are unhappy with the care they receive. New patients cannot see doctors in a timely manner; when they are finally seen, they have a few minutes to share their concerns with the provider, who rarely sits down or looks away from the computer screen to make eye contact with them.

We are already seeing the push for advanced education for our NPs and PAs. We have witnessed the changeover to NP programs that culminate in a doctorate (not a master’s) degree. By 2021, PA programs will be required to be master’s level; although the process has started, there are still a few holdouts. But I consider Washington State to be a front-runner in this area.

This, for me, is the area we need to address: degree designation and equivalency. Rather than give “diplomat” or similar status to someone whose base degree is an associate’s, a better idea—and one more palatable to AMA and AAFP—might be to bring everyone to at least a master’s level. For example, the Academy of Integrative Pain Management (AIPM) gives “Fellow” designation to those with master’s preparation who successfully pass AIPM’s examination, and “Diplomat” status to doctorate-prepared practitioners who have also passed the exam.

At the end of the day, many patients prefer to see a PA or NP rather than a medical doctor. Yes, patients care about credentials—but they care more about their provider being respectful, listening, remembering their history, connecting the history from their previous provider, and offering the proper treatment for the correct diagnosis.

Jan Morgan, MS, ARNP
Fellow, Academy of Integrative Pain Management
Eureka, California

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You’re a PA? Sorry, Not Eligible for This Job

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Thank you for your thoughtful commentary on the pertinent topic of full practice authority for PAs (2017;27[2]:12-14). In more than 30 years as a PA, I have rarely regretted my career choice. In 1982, when I was planning my career path, I chose to become a PA instead of an NP because I didn’t want to further my nursing training (I was already an LPN) to advance my practice, and my impression was that PAs and NPs were equivalent in the workforce. This perception held true until the past few years; I have lost job opportunities specifically because the employer didn’t want to deal with the administrative details of PA supervisory requirements here in Colorado. I find this frustrating, as well as perplexing.

Although I’ve become more comfortable with autonomy throughout my years of practice, I’ve always reserved the right to consult when necessary and appropriate, based on my own judgment and comfort level. I certainly wouldn’t mind more relaxed supervision, but I wouldn’t want to be cut entirely loose, either. On the other hand, I resent being ineligible for job opportunities simply for administrative reasons. While this is surely misguided on the part of the employers, it is a reality that practition­ers encounter.

I learned recently—to my astonishment—that my NP colleagues pay about a tenth of what I do for malpractice insurance. Apparently the underwriters (and/or the plaintiffs) haven’t caught up with the nuances of responsibility and autonomy! From my perspective, PAs and NPs have more in common in the practice setting than NPs and RNs do. The fact that NPs are governed by nursing boards and insured as nurses is more an antiquated accident than a reflection of function in the workforce.

Ideally, there should be a governing body dedicated to the entire spectrum of nonphysician providers who are qualified to diagnose, treat, and prescribe. Since that is not likely to happen, it is our responsibility as PAs to match NPs in the marketplace while maintaining our integrity as providers.

Elizabeth Upper, PA-C
Denver, Colorado

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Thank you for your thoughtful commentary on the pertinent topic of full practice authority for PAs (2017;27[2]:12-14). In more than 30 years as a PA, I have rarely regretted my career choice. In 1982, when I was planning my career path, I chose to become a PA instead of an NP because I didn’t want to further my nursing training (I was already an LPN) to advance my practice, and my impression was that PAs and NPs were equivalent in the workforce. This perception held true until the past few years; I have lost job opportunities specifically because the employer didn’t want to deal with the administrative details of PA supervisory requirements here in Colorado. I find this frustrating, as well as perplexing.

Although I’ve become more comfortable with autonomy throughout my years of practice, I’ve always reserved the right to consult when necessary and appropriate, based on my own judgment and comfort level. I certainly wouldn’t mind more relaxed supervision, but I wouldn’t want to be cut entirely loose, either. On the other hand, I resent being ineligible for job opportunities simply for administrative reasons. While this is surely misguided on the part of the employers, it is a reality that practition­ers encounter.

I learned recently—to my astonishment—that my NP colleagues pay about a tenth of what I do for malpractice insurance. Apparently the underwriters (and/or the plaintiffs) haven’t caught up with the nuances of responsibility and autonomy! From my perspective, PAs and NPs have more in common in the practice setting than NPs and RNs do. The fact that NPs are governed by nursing boards and insured as nurses is more an antiquated accident than a reflection of function in the workforce.

Ideally, there should be a governing body dedicated to the entire spectrum of nonphysician providers who are qualified to diagnose, treat, and prescribe. Since that is not likely to happen, it is our responsibility as PAs to match NPs in the marketplace while maintaining our integrity as providers.

Elizabeth Upper, PA-C
Denver, Colorado

 

Thank you for your thoughtful commentary on the pertinent topic of full practice authority for PAs (2017;27[2]:12-14). In more than 30 years as a PA, I have rarely regretted my career choice. In 1982, when I was planning my career path, I chose to become a PA instead of an NP because I didn’t want to further my nursing training (I was already an LPN) to advance my practice, and my impression was that PAs and NPs were equivalent in the workforce. This perception held true until the past few years; I have lost job opportunities specifically because the employer didn’t want to deal with the administrative details of PA supervisory requirements here in Colorado. I find this frustrating, as well as perplexing.

Although I’ve become more comfortable with autonomy throughout my years of practice, I’ve always reserved the right to consult when necessary and appropriate, based on my own judgment and comfort level. I certainly wouldn’t mind more relaxed supervision, but I wouldn’t want to be cut entirely loose, either. On the other hand, I resent being ineligible for job opportunities simply for administrative reasons. While this is surely misguided on the part of the employers, it is a reality that practition­ers encounter.

I learned recently—to my astonishment—that my NP colleagues pay about a tenth of what I do for malpractice insurance. Apparently the underwriters (and/or the plaintiffs) haven’t caught up with the nuances of responsibility and autonomy! From my perspective, PAs and NPs have more in common in the practice setting than NPs and RNs do. The fact that NPs are governed by nursing boards and insured as nurses is more an antiquated accident than a reflection of function in the workforce.

Ideally, there should be a governing body dedicated to the entire spectrum of nonphysician providers who are qualified to diagnose, treat, and prescribe. Since that is not likely to happen, it is our responsibility as PAs to match NPs in the marketplace while maintaining our integrity as providers.

Elizabeth Upper, PA-C
Denver, Colorado

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Milk interferes with levothyroxine absorption

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– Consuming milk and levothyroxine at the same time reduced the absorption of the thyroid hormone replacement, according to Deborah Chon, MD, speaking at a press briefing at the annual meeting of the Endocrine Society.

This finding comes from a small study of 10 healthy adults with normal TSH concentration at baseline. The study participants had a mean age of 34 years and 6 were men.

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Following an overnight fast, researchers measured the subjects’ serum total thyroxine T4 (TT4) to serve as the baseline. TT4 was remeasured 1, 2, 4, and 6 hours after ingestion of 1,000 mcg of oral levothyroxine alone or given together with 12 ounces of 2% milk, a common breakfast drink. After a 4 week washout, participants crossed over to the other protocol.

The total serum T4 absorption over 6 hours, calculated as area under the curve, was significantly lower when participants took levothyroxine and milk concurrently, compared with taking it alone (67.26 vs. 73.48; P equals .02).

The best interval between taking levothyroxine and drinking milk has yet to be established, according to Dr. Chon, who is on the faculty of the University of California, Los Angeles. Findings from earlier research showed that use of elemental calcium supplements interfere with absorption of levothyroxine.

In 2014, levothyroxine became the most commonly prescribed drug in the United States, according to a survey by the IMS Institute for Healthcare Informatics, now QuintilesIMS. Patients who need to take it because of Hashimoto’s thyroiditis or after thyroidectomy are often unhappy with how they feel. Dose adjustments are common as endocrinologists struggle to improve patients’ quality of life. It may be that a simple strategy of not taking the thyroid replacement at the same time as milk might leave patients feeling better.

Dr. Chon reported having no relevant financial conflicts of interest.

This article was updated 4/10/17.

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– Consuming milk and levothyroxine at the same time reduced the absorption of the thyroid hormone replacement, according to Deborah Chon, MD, speaking at a press briefing at the annual meeting of the Endocrine Society.

This finding comes from a small study of 10 healthy adults with normal TSH concentration at baseline. The study participants had a mean age of 34 years and 6 were men.

Wikimedia Commons
Following an overnight fast, researchers measured the subjects’ serum total thyroxine T4 (TT4) to serve as the baseline. TT4 was remeasured 1, 2, 4, and 6 hours after ingestion of 1,000 mcg of oral levothyroxine alone or given together with 12 ounces of 2% milk, a common breakfast drink. After a 4 week washout, participants crossed over to the other protocol.

The total serum T4 absorption over 6 hours, calculated as area under the curve, was significantly lower when participants took levothyroxine and milk concurrently, compared with taking it alone (67.26 vs. 73.48; P equals .02).

The best interval between taking levothyroxine and drinking milk has yet to be established, according to Dr. Chon, who is on the faculty of the University of California, Los Angeles. Findings from earlier research showed that use of elemental calcium supplements interfere with absorption of levothyroxine.

In 2014, levothyroxine became the most commonly prescribed drug in the United States, according to a survey by the IMS Institute for Healthcare Informatics, now QuintilesIMS. Patients who need to take it because of Hashimoto’s thyroiditis or after thyroidectomy are often unhappy with how they feel. Dose adjustments are common as endocrinologists struggle to improve patients’ quality of life. It may be that a simple strategy of not taking the thyroid replacement at the same time as milk might leave patients feeling better.

Dr. Chon reported having no relevant financial conflicts of interest.

This article was updated 4/10/17.

– Consuming milk and levothyroxine at the same time reduced the absorption of the thyroid hormone replacement, according to Deborah Chon, MD, speaking at a press briefing at the annual meeting of the Endocrine Society.

This finding comes from a small study of 10 healthy adults with normal TSH concentration at baseline. The study participants had a mean age of 34 years and 6 were men.

Wikimedia Commons
Following an overnight fast, researchers measured the subjects’ serum total thyroxine T4 (TT4) to serve as the baseline. TT4 was remeasured 1, 2, 4, and 6 hours after ingestion of 1,000 mcg of oral levothyroxine alone or given together with 12 ounces of 2% milk, a common breakfast drink. After a 4 week washout, participants crossed over to the other protocol.

The total serum T4 absorption over 6 hours, calculated as area under the curve, was significantly lower when participants took levothyroxine and milk concurrently, compared with taking it alone (67.26 vs. 73.48; P equals .02).

The best interval between taking levothyroxine and drinking milk has yet to be established, according to Dr. Chon, who is on the faculty of the University of California, Los Angeles. Findings from earlier research showed that use of elemental calcium supplements interfere with absorption of levothyroxine.

In 2014, levothyroxine became the most commonly prescribed drug in the United States, according to a survey by the IMS Institute for Healthcare Informatics, now QuintilesIMS. Patients who need to take it because of Hashimoto’s thyroiditis or after thyroidectomy are often unhappy with how they feel. Dose adjustments are common as endocrinologists struggle to improve patients’ quality of life. It may be that a simple strategy of not taking the thyroid replacement at the same time as milk might leave patients feeling better.

Dr. Chon reported having no relevant financial conflicts of interest.

This article was updated 4/10/17.

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Key clinical point: When consumed together, cows’ milk reduces absorption of levothyroxine to an extent that might be clinically significant.

Major finding: Calculated as an area under the curve, simultaneous consumption of levothyroxine and milk reduced absorption of the supplement by a mean of 67.26 vs. 73.48 when taken without milk.

Data source: A pharmacokinetic study of 10 healthy subjects.

Disclosures: Dr. Chon reported having no relevant conflicts of interest.

From the Vascular Community

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In memoriam: Edward B. Diethrich

Edward B. Diethrich, MD, the world-renowned cardiovascular/endovascular surgeon, inventor, and philanthropist, succumbed after a brave fight with a brain tumor on February 23, 2017, at the age of 81.

Dr. Diethrich was a pioneer in noninvasive cardiovascular and vascular disease diagnosis and innovative in surgical and endovascular therapy. He obtained his undergraduate and medical degrees at the University of Michigan and completed his surgical residency at St. Joseph’s Mercy Hospital in Ann Arbor and the Henry Ford Hospital in Detroit. He went on to complete his cardiovascular surgery training under Michael DeBakey at the Baylor College of Medicine in Houston, where he played an important role in the development of human heart transplantation.

Dr. Edward B. Diethrich
Dr. Diethrich founded the Arizona Heart Institute (AHI) in Phoenix, Arizona, in 1971, which was the first freestanding outpatient clinic in the United States exclusively devoted to the diagnosis, prevention, and treatment of cardiovascular diseases. He served as the Medical Director and Chief of Cardiovascular Surgery for AHI and founded the institute’s nonprofit Arizona Heart Foundation. Later, he served as Medical Director and Chief of Cardiovascular and Endovascular Surgery at the Arizona Heart Hospital where he performed open-heart surgery and cutting-edge endovascular procedures, many of which he designed and analyzed in several clinical trials.

One of his first accomplishments was the invention of the sternal saw in 1962, which is still used today for open-chest surgery. He also contributed to the development of a preservation chamber for heart transplantation and established one of the first ultrasound companies. Dr. Diethrich spent a lifetime developing new technologies, from a bubble oxygenator for open-heart surgery to developing and manufacturing stent grafts for aortic aneurysms. He remained actively involved in advancing the practice of vascular surgery and keeping it up-to-date with the changing times: He founded a company that develops and manufactures endoluminal grafts, established a Translational Research Center that is dedicated to clinical research and developing new technologies, and started a company devoted to the prevention and management of cardiovascular disease. His contributions to surgical education are also legendary. He organized an annual meeting that attracted physicians from all over the world and show-cased state-of-the-art techniques and innovations. He authored over 400 scientific articles, several textbooks, and lay publications and produced hundreds of educational videos and films. In fact, he organized the first live international telecast of open-heart surgery. Above all, Dr. Diethrich trained several hundred surgeons and other specialists in cardiovascular surgery and endovascular techniques, and traveled the world to demonstrate his techniques and teach local physicians. He recently endowed the Edward B. Diethrich Research Professorship in Biomedical Engineering and Vascular Surgery at the University of Michigan to recognize the collaboration that is required between surgeons and engineers.

Dr. Diethrich has received several honors, such as the Frederick A. Coller Award; Presidency of the Denton A. Cooley Cardiovascular Surgical Society; the Medal for Innovation in Vascular Surgery from the Society for Vascular Surgery; the Medal of Independence from King Hussein of Jordan; and an honorary fellowship from the Royal College of Surgeons, Glasgow. The Edward B. Diethrich Vascular Surgical Society was established by several hundred of his trainees. I was honored to serve as the first President of that society.

It’s ironic that Dr. Diethrich was an early supporter of ceiling-mounted radiographic equipment, which is essential to endovascular interventions. Even with the most advanced radiation protection, Dr. Diethrich paid the ultimate price for his nearly daily exposure to radiation, which led to his 4-year battle with glioma, and, ultimately, his death. But true to form, he even used this unfortunate illness to educate others by working with the Organization for Occupational Radiation Safety in Interventional Fluoroscopy to produce a documentary on the ill effects of radiation.

Dr. Diethrich recently completed his memoirs (SLED: The Serendipitous Life of Edward Diethrich), which recounts his extraordinary 50-year career, from his early days of working and training with the world’s most renowned surgeons to his legendary international success as a cardiovascular surgeon and innovator.

In summary, Dr. Diethrich was a multifaceted, passionate, and charismatic man: a sportsman, musician, scientist, inventor, author, film producer, media personality, along with many others. His confidence, dexterity, and technical expertise were evident in both the operating room and the endovascular suite. Dr. Diethrich was a world-renowned leader and pioneer in Vascular Surgery. He was an eloquent speaker, prolific innovative scholar, and dedicated teacher. His energy was endless, and his manners were impeccable. He will be sorely missed, but his legendary contributions to medicine/vascular surgery, his trainees, and the many people he influenced will live on.

Dr. Diethrich is survived by his wife of 61 years, Gloria; daughter Lynne; son Tad; son-in-law Joe Jackson; daughter-in-law Terri Diethrich, and grandchildren Danielle Diethrich-Vargas, Courtney, Reese, and Trey Diethrich; Mackenzie, Tatum, Peyton, and Zack Jackson.

A celebration of his life will be planned in the near future. Details will be posted at drteddiethrich.com.

 

 

Ali F. AbuRahma, MD

Charleston, WV 25304

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In memoriam: Edward B. Diethrich

Edward B. Diethrich, MD, the world-renowned cardiovascular/endovascular surgeon, inventor, and philanthropist, succumbed after a brave fight with a brain tumor on February 23, 2017, at the age of 81.

Dr. Diethrich was a pioneer in noninvasive cardiovascular and vascular disease diagnosis and innovative in surgical and endovascular therapy. He obtained his undergraduate and medical degrees at the University of Michigan and completed his surgical residency at St. Joseph’s Mercy Hospital in Ann Arbor and the Henry Ford Hospital in Detroit. He went on to complete his cardiovascular surgery training under Michael DeBakey at the Baylor College of Medicine in Houston, where he played an important role in the development of human heart transplantation.

Dr. Edward B. Diethrich
Dr. Diethrich founded the Arizona Heart Institute (AHI) in Phoenix, Arizona, in 1971, which was the first freestanding outpatient clinic in the United States exclusively devoted to the diagnosis, prevention, and treatment of cardiovascular diseases. He served as the Medical Director and Chief of Cardiovascular Surgery for AHI and founded the institute’s nonprofit Arizona Heart Foundation. Later, he served as Medical Director and Chief of Cardiovascular and Endovascular Surgery at the Arizona Heart Hospital where he performed open-heart surgery and cutting-edge endovascular procedures, many of which he designed and analyzed in several clinical trials.

One of his first accomplishments was the invention of the sternal saw in 1962, which is still used today for open-chest surgery. He also contributed to the development of a preservation chamber for heart transplantation and established one of the first ultrasound companies. Dr. Diethrich spent a lifetime developing new technologies, from a bubble oxygenator for open-heart surgery to developing and manufacturing stent grafts for aortic aneurysms. He remained actively involved in advancing the practice of vascular surgery and keeping it up-to-date with the changing times: He founded a company that develops and manufactures endoluminal grafts, established a Translational Research Center that is dedicated to clinical research and developing new technologies, and started a company devoted to the prevention and management of cardiovascular disease. His contributions to surgical education are also legendary. He organized an annual meeting that attracted physicians from all over the world and show-cased state-of-the-art techniques and innovations. He authored over 400 scientific articles, several textbooks, and lay publications and produced hundreds of educational videos and films. In fact, he organized the first live international telecast of open-heart surgery. Above all, Dr. Diethrich trained several hundred surgeons and other specialists in cardiovascular surgery and endovascular techniques, and traveled the world to demonstrate his techniques and teach local physicians. He recently endowed the Edward B. Diethrich Research Professorship in Biomedical Engineering and Vascular Surgery at the University of Michigan to recognize the collaboration that is required between surgeons and engineers.

Dr. Diethrich has received several honors, such as the Frederick A. Coller Award; Presidency of the Denton A. Cooley Cardiovascular Surgical Society; the Medal for Innovation in Vascular Surgery from the Society for Vascular Surgery; the Medal of Independence from King Hussein of Jordan; and an honorary fellowship from the Royal College of Surgeons, Glasgow. The Edward B. Diethrich Vascular Surgical Society was established by several hundred of his trainees. I was honored to serve as the first President of that society.

It’s ironic that Dr. Diethrich was an early supporter of ceiling-mounted radiographic equipment, which is essential to endovascular interventions. Even with the most advanced radiation protection, Dr. Diethrich paid the ultimate price for his nearly daily exposure to radiation, which led to his 4-year battle with glioma, and, ultimately, his death. But true to form, he even used this unfortunate illness to educate others by working with the Organization for Occupational Radiation Safety in Interventional Fluoroscopy to produce a documentary on the ill effects of radiation.

Dr. Diethrich recently completed his memoirs (SLED: The Serendipitous Life of Edward Diethrich), which recounts his extraordinary 50-year career, from his early days of working and training with the world’s most renowned surgeons to his legendary international success as a cardiovascular surgeon and innovator.

In summary, Dr. Diethrich was a multifaceted, passionate, and charismatic man: a sportsman, musician, scientist, inventor, author, film producer, media personality, along with many others. His confidence, dexterity, and technical expertise were evident in both the operating room and the endovascular suite. Dr. Diethrich was a world-renowned leader and pioneer in Vascular Surgery. He was an eloquent speaker, prolific innovative scholar, and dedicated teacher. His energy was endless, and his manners were impeccable. He will be sorely missed, but his legendary contributions to medicine/vascular surgery, his trainees, and the many people he influenced will live on.

Dr. Diethrich is survived by his wife of 61 years, Gloria; daughter Lynne; son Tad; son-in-law Joe Jackson; daughter-in-law Terri Diethrich, and grandchildren Danielle Diethrich-Vargas, Courtney, Reese, and Trey Diethrich; Mackenzie, Tatum, Peyton, and Zack Jackson.

A celebration of his life will be planned in the near future. Details will be posted at drteddiethrich.com.

 

 

Ali F. AbuRahma, MD

Charleston, WV 25304

 

In memoriam: Edward B. Diethrich

Edward B. Diethrich, MD, the world-renowned cardiovascular/endovascular surgeon, inventor, and philanthropist, succumbed after a brave fight with a brain tumor on February 23, 2017, at the age of 81.

Dr. Diethrich was a pioneer in noninvasive cardiovascular and vascular disease diagnosis and innovative in surgical and endovascular therapy. He obtained his undergraduate and medical degrees at the University of Michigan and completed his surgical residency at St. Joseph’s Mercy Hospital in Ann Arbor and the Henry Ford Hospital in Detroit. He went on to complete his cardiovascular surgery training under Michael DeBakey at the Baylor College of Medicine in Houston, where he played an important role in the development of human heart transplantation.

Dr. Edward B. Diethrich
Dr. Diethrich founded the Arizona Heart Institute (AHI) in Phoenix, Arizona, in 1971, which was the first freestanding outpatient clinic in the United States exclusively devoted to the diagnosis, prevention, and treatment of cardiovascular diseases. He served as the Medical Director and Chief of Cardiovascular Surgery for AHI and founded the institute’s nonprofit Arizona Heart Foundation. Later, he served as Medical Director and Chief of Cardiovascular and Endovascular Surgery at the Arizona Heart Hospital where he performed open-heart surgery and cutting-edge endovascular procedures, many of which he designed and analyzed in several clinical trials.

One of his first accomplishments was the invention of the sternal saw in 1962, which is still used today for open-chest surgery. He also contributed to the development of a preservation chamber for heart transplantation and established one of the first ultrasound companies. Dr. Diethrich spent a lifetime developing new technologies, from a bubble oxygenator for open-heart surgery to developing and manufacturing stent grafts for aortic aneurysms. He remained actively involved in advancing the practice of vascular surgery and keeping it up-to-date with the changing times: He founded a company that develops and manufactures endoluminal grafts, established a Translational Research Center that is dedicated to clinical research and developing new technologies, and started a company devoted to the prevention and management of cardiovascular disease. His contributions to surgical education are also legendary. He organized an annual meeting that attracted physicians from all over the world and show-cased state-of-the-art techniques and innovations. He authored over 400 scientific articles, several textbooks, and lay publications and produced hundreds of educational videos and films. In fact, he organized the first live international telecast of open-heart surgery. Above all, Dr. Diethrich trained several hundred surgeons and other specialists in cardiovascular surgery and endovascular techniques, and traveled the world to demonstrate his techniques and teach local physicians. He recently endowed the Edward B. Diethrich Research Professorship in Biomedical Engineering and Vascular Surgery at the University of Michigan to recognize the collaboration that is required between surgeons and engineers.

Dr. Diethrich has received several honors, such as the Frederick A. Coller Award; Presidency of the Denton A. Cooley Cardiovascular Surgical Society; the Medal for Innovation in Vascular Surgery from the Society for Vascular Surgery; the Medal of Independence from King Hussein of Jordan; and an honorary fellowship from the Royal College of Surgeons, Glasgow. The Edward B. Diethrich Vascular Surgical Society was established by several hundred of his trainees. I was honored to serve as the first President of that society.

It’s ironic that Dr. Diethrich was an early supporter of ceiling-mounted radiographic equipment, which is essential to endovascular interventions. Even with the most advanced radiation protection, Dr. Diethrich paid the ultimate price for his nearly daily exposure to radiation, which led to his 4-year battle with glioma, and, ultimately, his death. But true to form, he even used this unfortunate illness to educate others by working with the Organization for Occupational Radiation Safety in Interventional Fluoroscopy to produce a documentary on the ill effects of radiation.

Dr. Diethrich recently completed his memoirs (SLED: The Serendipitous Life of Edward Diethrich), which recounts his extraordinary 50-year career, from his early days of working and training with the world’s most renowned surgeons to his legendary international success as a cardiovascular surgeon and innovator.

In summary, Dr. Diethrich was a multifaceted, passionate, and charismatic man: a sportsman, musician, scientist, inventor, author, film producer, media personality, along with many others. His confidence, dexterity, and technical expertise were evident in both the operating room and the endovascular suite. Dr. Diethrich was a world-renowned leader and pioneer in Vascular Surgery. He was an eloquent speaker, prolific innovative scholar, and dedicated teacher. His energy was endless, and his manners were impeccable. He will be sorely missed, but his legendary contributions to medicine/vascular surgery, his trainees, and the many people he influenced will live on.

Dr. Diethrich is survived by his wife of 61 years, Gloria; daughter Lynne; son Tad; son-in-law Joe Jackson; daughter-in-law Terri Diethrich, and grandchildren Danielle Diethrich-Vargas, Courtney, Reese, and Trey Diethrich; Mackenzie, Tatum, Peyton, and Zack Jackson.

A celebration of his life will be planned in the near future. Details will be posted at drteddiethrich.com.

 

 

Ali F. AbuRahma, MD

Charleston, WV 25304

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Shelving of AHCA a win for patients, experts say

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SAN DIEGO – The decision by House Republicans to withdraw the American Health Care Act on March 24, 2017 was a victory for the health care of all Americans, especially older, sicker, and poorer patients, according to Nitin S. Damle, MD.

“It was a terrible bill,” Dr. Damle, president of the American College of Physicians, said during a press briefing at the annual meeting of the ACP. “Fortunately it will not become law at this point, but the story doesn’t really end here. The Trump Administration needs to decide whether it’s going to help faithfully implement the Affordable Care Act or sabotage it, either by action or inaction. It’s also important that we turn the page and begin the hard work of engaging with the administration and Congress on a bipartisan agenda to improve American health care.”

Doug Brunk/Frontline Medical News
Dr. Nitin S. Damle, right, and Robert B. Doherty
According to the Congressional Budget Office (CBO), had the AHCA become law the number of uninsured would have skyrocketed to 24 million, and 14 million would have been uncovered as of 2018. Dr. Damle, who practices in Wakefield, R.I., said that without health insurance, people are less likely to have access to a physician, less likely to get cancer screening, less likely to get vaccinated, less likely to keep up with their medications, and more likely to receive care in an expensive setting like the emergency room. “They’re also more likely to wait to be treated until their disease has reached a more advanced stage and is less treatable – very serious consequences,” he said.

The ACHA would have eliminated the federal requirement that insurers cover 10 categories of essential benefits including emergency care, maternity services, and hospitalization, leaving it to states to decide. It also eliminated the requirement that Medicaid cover the same essential benefits. According to Dr. Damle, the AHCA’s age-based tax credits “were too low and the deductibles were going to be too high for older people and poorer patients, because insurers would have been allowed to charge older patients up to five times more than younger patients for their coverage.” For example, the CBO found that under the bill a 64-year-old male who makes $26,500 a year would have to pay $14,600 out of pocket for insurance in the non-group market, compared to $1,700 under the existing ACA, a 750% increase.

“In my practice, I have many older and sicker patients who would have been left behind had this become law, patients with diseases like congestive heart failure, diabetes, chronic obstructive pulmonary disease from smoking who require frequent and ongoing monitoring of their medications, development of any complications from their disease, and sometimes even need home-based support,” Dr. Damle said.

Robert B. Doherty, senior vice president of governmental affairs and public policy for the ACP, described efforts to roll back the ACA as “unchartered” territory. “I have never in the past seen an administration trying to roll back coverage on millions of people,” he said. “This history of the US has been incremental expansion of coverage since the creation of Medicare and Medicaid in 1965.” He acknowledged certain shortcomings of the ACA, including uneven participation by insurers from state to state, and “deductibles may be too high, and premiums too high for some people. On the other hand, the ACA has achieved an historic reduction in the uninsured rate in the United States. More than 20 million people have gained coverage, and according to the CDC, only 8.2% of Americans are without health insurance, an historic low. It’s still too high, but we’re basically 92% of the way to universal coverage in the U.S.”

Mr. Doherty expressed concern that legislative efforts to roll back the ACA could re-emerge. “The Republicans are still talking about bringing it back,” he said. “You can’t take it for granted because Republicans have been promising repeal and replace [legislation] for seven years now, and I think they want to move forward. I think we have to remain vigilant. We have to put pressure on the [Trump] administration to make sure they faithfully execute the law, which they swore to do when they took office. Then we have to reach out and say there are problems that need to be addressed, bipartisan solutions to stabilize the [health insurance] markets and to address other issues like the crushing administrative burden on physicians. You have to start by accepting that the ACA is the law of the land. We need to build upon it and improve it, not repeal it.”

 

 

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SAN DIEGO – The decision by House Republicans to withdraw the American Health Care Act on March 24, 2017 was a victory for the health care of all Americans, especially older, sicker, and poorer patients, according to Nitin S. Damle, MD.

“It was a terrible bill,” Dr. Damle, president of the American College of Physicians, said during a press briefing at the annual meeting of the ACP. “Fortunately it will not become law at this point, but the story doesn’t really end here. The Trump Administration needs to decide whether it’s going to help faithfully implement the Affordable Care Act or sabotage it, either by action or inaction. It’s also important that we turn the page and begin the hard work of engaging with the administration and Congress on a bipartisan agenda to improve American health care.”

Doug Brunk/Frontline Medical News
Dr. Nitin S. Damle, right, and Robert B. Doherty
According to the Congressional Budget Office (CBO), had the AHCA become law the number of uninsured would have skyrocketed to 24 million, and 14 million would have been uncovered as of 2018. Dr. Damle, who practices in Wakefield, R.I., said that without health insurance, people are less likely to have access to a physician, less likely to get cancer screening, less likely to get vaccinated, less likely to keep up with their medications, and more likely to receive care in an expensive setting like the emergency room. “They’re also more likely to wait to be treated until their disease has reached a more advanced stage and is less treatable – very serious consequences,” he said.

The ACHA would have eliminated the federal requirement that insurers cover 10 categories of essential benefits including emergency care, maternity services, and hospitalization, leaving it to states to decide. It also eliminated the requirement that Medicaid cover the same essential benefits. According to Dr. Damle, the AHCA’s age-based tax credits “were too low and the deductibles were going to be too high for older people and poorer patients, because insurers would have been allowed to charge older patients up to five times more than younger patients for their coverage.” For example, the CBO found that under the bill a 64-year-old male who makes $26,500 a year would have to pay $14,600 out of pocket for insurance in the non-group market, compared to $1,700 under the existing ACA, a 750% increase.

“In my practice, I have many older and sicker patients who would have been left behind had this become law, patients with diseases like congestive heart failure, diabetes, chronic obstructive pulmonary disease from smoking who require frequent and ongoing monitoring of their medications, development of any complications from their disease, and sometimes even need home-based support,” Dr. Damle said.

Robert B. Doherty, senior vice president of governmental affairs and public policy for the ACP, described efforts to roll back the ACA as “unchartered” territory. “I have never in the past seen an administration trying to roll back coverage on millions of people,” he said. “This history of the US has been incremental expansion of coverage since the creation of Medicare and Medicaid in 1965.” He acknowledged certain shortcomings of the ACA, including uneven participation by insurers from state to state, and “deductibles may be too high, and premiums too high for some people. On the other hand, the ACA has achieved an historic reduction in the uninsured rate in the United States. More than 20 million people have gained coverage, and according to the CDC, only 8.2% of Americans are without health insurance, an historic low. It’s still too high, but we’re basically 92% of the way to universal coverage in the U.S.”

Mr. Doherty expressed concern that legislative efforts to roll back the ACA could re-emerge. “The Republicans are still talking about bringing it back,” he said. “You can’t take it for granted because Republicans have been promising repeal and replace [legislation] for seven years now, and I think they want to move forward. I think we have to remain vigilant. We have to put pressure on the [Trump] administration to make sure they faithfully execute the law, which they swore to do when they took office. Then we have to reach out and say there are problems that need to be addressed, bipartisan solutions to stabilize the [health insurance] markets and to address other issues like the crushing administrative burden on physicians. You have to start by accepting that the ACA is the law of the land. We need to build upon it and improve it, not repeal it.”

 

 

 

SAN DIEGO – The decision by House Republicans to withdraw the American Health Care Act on March 24, 2017 was a victory for the health care of all Americans, especially older, sicker, and poorer patients, according to Nitin S. Damle, MD.

“It was a terrible bill,” Dr. Damle, president of the American College of Physicians, said during a press briefing at the annual meeting of the ACP. “Fortunately it will not become law at this point, but the story doesn’t really end here. The Trump Administration needs to decide whether it’s going to help faithfully implement the Affordable Care Act or sabotage it, either by action or inaction. It’s also important that we turn the page and begin the hard work of engaging with the administration and Congress on a bipartisan agenda to improve American health care.”

Doug Brunk/Frontline Medical News
Dr. Nitin S. Damle, right, and Robert B. Doherty
According to the Congressional Budget Office (CBO), had the AHCA become law the number of uninsured would have skyrocketed to 24 million, and 14 million would have been uncovered as of 2018. Dr. Damle, who practices in Wakefield, R.I., said that without health insurance, people are less likely to have access to a physician, less likely to get cancer screening, less likely to get vaccinated, less likely to keep up with their medications, and more likely to receive care in an expensive setting like the emergency room. “They’re also more likely to wait to be treated until their disease has reached a more advanced stage and is less treatable – very serious consequences,” he said.

The ACHA would have eliminated the federal requirement that insurers cover 10 categories of essential benefits including emergency care, maternity services, and hospitalization, leaving it to states to decide. It also eliminated the requirement that Medicaid cover the same essential benefits. According to Dr. Damle, the AHCA’s age-based tax credits “were too low and the deductibles were going to be too high for older people and poorer patients, because insurers would have been allowed to charge older patients up to five times more than younger patients for their coverage.” For example, the CBO found that under the bill a 64-year-old male who makes $26,500 a year would have to pay $14,600 out of pocket for insurance in the non-group market, compared to $1,700 under the existing ACA, a 750% increase.

“In my practice, I have many older and sicker patients who would have been left behind had this become law, patients with diseases like congestive heart failure, diabetes, chronic obstructive pulmonary disease from smoking who require frequent and ongoing monitoring of their medications, development of any complications from their disease, and sometimes even need home-based support,” Dr. Damle said.

Robert B. Doherty, senior vice president of governmental affairs and public policy for the ACP, described efforts to roll back the ACA as “unchartered” territory. “I have never in the past seen an administration trying to roll back coverage on millions of people,” he said. “This history of the US has been incremental expansion of coverage since the creation of Medicare and Medicaid in 1965.” He acknowledged certain shortcomings of the ACA, including uneven participation by insurers from state to state, and “deductibles may be too high, and premiums too high for some people. On the other hand, the ACA has achieved an historic reduction in the uninsured rate in the United States. More than 20 million people have gained coverage, and according to the CDC, only 8.2% of Americans are without health insurance, an historic low. It’s still too high, but we’re basically 92% of the way to universal coverage in the U.S.”

Mr. Doherty expressed concern that legislative efforts to roll back the ACA could re-emerge. “The Republicans are still talking about bringing it back,” he said. “You can’t take it for granted because Republicans have been promising repeal and replace [legislation] for seven years now, and I think they want to move forward. I think we have to remain vigilant. We have to put pressure on the [Trump] administration to make sure they faithfully execute the law, which they swore to do when they took office. Then we have to reach out and say there are problems that need to be addressed, bipartisan solutions to stabilize the [health insurance] markets and to address other issues like the crushing administrative burden on physicians. You have to start by accepting that the ACA is the law of the land. We need to build upon it and improve it, not repeal it.”

 

 

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Clinical Challenges - April 2017 What's Your Diagnosis?

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What's Your Diagnosis?

Answer to “What’s your diagnosis?” on page X: Pseudoachalasia in paraneoplastic syndrome, with radiographic documentation of onset and evolution

A barium esophagogram revealed an esophagus with characteristic features of achalasia: dilatation, retention of air and fluid, and a “bird’s beak” configuration distally (Figure E). Botulinum injection into the distal esophagus provided the patient with partial relief of her swallowing symptoms.

Evidence supporting the diagnosis of pseudoachalasia associated with paraneoplastic syndrome in this patient is 1) the development of characteristic features of achalasia in association with SCLC, the cancer that is most often associated with paraneoplastic achalasia;1 2) a serum antibody characteristic of SCLC-associated paraneoplastic syndrome; 3) peripheral neuropathy attributed to paraneoplastic syndrome; and 4) absence of an obstructive neoplasm at the gastroesophageal junction.

Pseudoachalasia associated with malignancy may occur by one of three mechanisms1-3: 1) Primary or secondary carcinoma located at or near the gastroesophageal junction, 2) neural invasion of the esophagus, or 3) as a component of the paraneoplastic syndrome. Pseudoachalasia associated with a paraneoplastic syndrome is rare (an estimated 1 in 750,000), although it may be becoming more common.1 The relatively rapid onset of dysphagia is a reported feature of pseudoachalasia, in contrast with the more gradual onset in primary achalasia. Our report documents radiographically the progression within a few months from a normal-diameter esophagus to a very dilated, poorly functioning esophagus. We know of no similar report. Botulinum toxin injection has been reported effective in a few cases.1

 

References

1. Katzka, D.A., Farrugia, G., Arora, A.S., et al. Achalasia secondary to neoplasia: a disease with a changing differential diagnosis. Dis Esophagus. 2012;25:331-6.

2. Liu, W., Fackler, W., Rice, T.W., et al. The pathogenesis of pseudoachalasia (A clinicopathological study of 13 cases of a rare entity). Am J Surg Pathol. 2002;26:784-8.

3. Gockel, J., Eckardt, V.F., Scmitt, T., et al. Pseudoachalasia: a case series and analysis of the literature. Scand J Gastroenterol. 2005;40:378-85.

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Answer to “What’s your diagnosis?” on page X: Pseudoachalasia in paraneoplastic syndrome, with radiographic documentation of onset and evolution

A barium esophagogram revealed an esophagus with characteristic features of achalasia: dilatation, retention of air and fluid, and a “bird’s beak” configuration distally (Figure E). Botulinum injection into the distal esophagus provided the patient with partial relief of her swallowing symptoms.

Evidence supporting the diagnosis of pseudoachalasia associated with paraneoplastic syndrome in this patient is 1) the development of characteristic features of achalasia in association with SCLC, the cancer that is most often associated with paraneoplastic achalasia;1 2) a serum antibody characteristic of SCLC-associated paraneoplastic syndrome; 3) peripheral neuropathy attributed to paraneoplastic syndrome; and 4) absence of an obstructive neoplasm at the gastroesophageal junction.

Pseudoachalasia associated with malignancy may occur by one of three mechanisms1-3: 1) Primary or secondary carcinoma located at or near the gastroesophageal junction, 2) neural invasion of the esophagus, or 3) as a component of the paraneoplastic syndrome. Pseudoachalasia associated with a paraneoplastic syndrome is rare (an estimated 1 in 750,000), although it may be becoming more common.1 The relatively rapid onset of dysphagia is a reported feature of pseudoachalasia, in contrast with the more gradual onset in primary achalasia. Our report documents radiographically the progression within a few months from a normal-diameter esophagus to a very dilated, poorly functioning esophagus. We know of no similar report. Botulinum toxin injection has been reported effective in a few cases.1

 

References

1. Katzka, D.A., Farrugia, G., Arora, A.S., et al. Achalasia secondary to neoplasia: a disease with a changing differential diagnosis. Dis Esophagus. 2012;25:331-6.

2. Liu, W., Fackler, W., Rice, T.W., et al. The pathogenesis of pseudoachalasia (A clinicopathological study of 13 cases of a rare entity). Am J Surg Pathol. 2002;26:784-8.

3. Gockel, J., Eckardt, V.F., Scmitt, T., et al. Pseudoachalasia: a case series and analysis of the literature. Scand J Gastroenterol. 2005;40:378-85.

Answer to “What’s your diagnosis?” on page X: Pseudoachalasia in paraneoplastic syndrome, with radiographic documentation of onset and evolution

A barium esophagogram revealed an esophagus with characteristic features of achalasia: dilatation, retention of air and fluid, and a “bird’s beak” configuration distally (Figure E). Botulinum injection into the distal esophagus provided the patient with partial relief of her swallowing symptoms.

Evidence supporting the diagnosis of pseudoachalasia associated with paraneoplastic syndrome in this patient is 1) the development of characteristic features of achalasia in association with SCLC, the cancer that is most often associated with paraneoplastic achalasia;1 2) a serum antibody characteristic of SCLC-associated paraneoplastic syndrome; 3) peripheral neuropathy attributed to paraneoplastic syndrome; and 4) absence of an obstructive neoplasm at the gastroesophageal junction.

Pseudoachalasia associated with malignancy may occur by one of three mechanisms1-3: 1) Primary or secondary carcinoma located at or near the gastroesophageal junction, 2) neural invasion of the esophagus, or 3) as a component of the paraneoplastic syndrome. Pseudoachalasia associated with a paraneoplastic syndrome is rare (an estimated 1 in 750,000), although it may be becoming more common.1 The relatively rapid onset of dysphagia is a reported feature of pseudoachalasia, in contrast with the more gradual onset in primary achalasia. Our report documents radiographically the progression within a few months from a normal-diameter esophagus to a very dilated, poorly functioning esophagus. We know of no similar report. Botulinum toxin injection has been reported effective in a few cases.1

 

References

1. Katzka, D.A., Farrugia, G., Arora, A.S., et al. Achalasia secondary to neoplasia: a disease with a changing differential diagnosis. Dis Esophagus. 2012;25:331-6.

2. Liu, W., Fackler, W., Rice, T.W., et al. The pathogenesis of pseudoachalasia (A clinicopathological study of 13 cases of a rare entity). Am J Surg Pathol. 2002;26:784-8.

3. Gockel, J., Eckardt, V.F., Scmitt, T., et al. Pseudoachalasia: a case series and analysis of the literature. Scand J Gastroenterol. 2005;40:378-85.

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Clinical Challenges - April 2017
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By William R. Brown, MD, and Elizabeth K. Dee, MD.

Published previously in Gastroenterology (2013;144:34, 252).

A 67-year-old woman with neuroendocrine small-cell lung cancer (SCLC), recurrent after chemotherapy and radiation therapy, complained of recent-onset dysphagia. She noticed regurgitation of liquids and some solid-food dysphagia. She had lost 20 pounds in the past 2 months. She had no past history of gastroesophageal reflux symptoms or esophagitis. Physical examination reveals no significant abnormalities, but she had had a peripheral sensory neuropathy that improved with treatment of her SCLC. Laboratory tests are unremarkable except for a positive Hu immunoglobulin (Ig)G serum anti-neuronal nuclear antibody test – an antibody that is associated with SCLC.

On serial computed tomography chest examinations, the esophagus had appeared normal (Figure A, arrow). Two months later, the esophagus was slightly dilated and contained contrast (Figure B; computed tomography).
On examinations 5 and 7 months later, the esophagus had become even more dilated and was fluid or gas filled (Figure C, D). At esophagogastroduodenoscopy, the esophagus was diffusely dilated, without contraction, and with retained food and secretions.
The endoscope passed into the stomach without much resistance, and no lesion was seen on forward view or retroflexion at the gastroesophageal junction.

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April 2017 Quiz 2

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Q2. Answer: C

Rationale: MALT lymphomas are associated with H. pylori infection in 80%-90% of cases. H. pylori triggers a B-cell clonal expansion leading to lymphoma. Detection of chronic H. pylori using histology is directly dependent on the number of mucosal biopsies. Negative H. pylori testing should prompt an alternative test for H. pylori (either breath or stool antigen test). Treatment of H. pylori is successful in achieving complete remission in up to 80% of cases. Surveillance after treatment of MALT lymphoma is indicated, though the exact protocol has not been established.

 

References

1. ASGE Standards of Practice Committee. The role of endoscopy in management of premalignant and malignant conditions of the stomach. Gastrointest Endosc. 2015 82(1):1-8.

2. Gisbert J.P., Calvet X. Review article: common misconceptions in the management of Helicobacter pylori-associated gastric MALT-lymphoma. Aliment Pharmacol Ther. 2011 Nov;34(9):1047-62.

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Q2. Answer: C

Rationale: MALT lymphomas are associated with H. pylori infection in 80%-90% of cases. H. pylori triggers a B-cell clonal expansion leading to lymphoma. Detection of chronic H. pylori using histology is directly dependent on the number of mucosal biopsies. Negative H. pylori testing should prompt an alternative test for H. pylori (either breath or stool antigen test). Treatment of H. pylori is successful in achieving complete remission in up to 80% of cases. Surveillance after treatment of MALT lymphoma is indicated, though the exact protocol has not been established.

 

References

1. ASGE Standards of Practice Committee. The role of endoscopy in management of premalignant and malignant conditions of the stomach. Gastrointest Endosc. 2015 82(1):1-8.

2. Gisbert J.P., Calvet X. Review article: common misconceptions in the management of Helicobacter pylori-associated gastric MALT-lymphoma. Aliment Pharmacol Ther. 2011 Nov;34(9):1047-62.

Q2. Answer: C

Rationale: MALT lymphomas are associated with H. pylori infection in 80%-90% of cases. H. pylori triggers a B-cell clonal expansion leading to lymphoma. Detection of chronic H. pylori using histology is directly dependent on the number of mucosal biopsies. Negative H. pylori testing should prompt an alternative test for H. pylori (either breath or stool antigen test). Treatment of H. pylori is successful in achieving complete remission in up to 80% of cases. Surveillance after treatment of MALT lymphoma is indicated, though the exact protocol has not been established.

 

References

1. ASGE Standards of Practice Committee. The role of endoscopy in management of premalignant and malignant conditions of the stomach. Gastrointest Endosc. 2015 82(1):1-8.

2. Gisbert J.P., Calvet X. Review article: common misconceptions in the management of Helicobacter pylori-associated gastric MALT-lymphoma. Aliment Pharmacol Ther. 2011 Nov;34(9):1047-62.

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Q2. A 56-year-old woman presents with epigastric pain and is found to have a 3-cm submucosal mass with thickened rugal folds in the gastric body. Biopsies of the mass show mucosa-associated lymphoid tissue (MALT lymphoma). There is no evidence of Helicobacter pylori infection in the biopsies.

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April 2017 Quiz 1

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Q1. Answer: A

While heartburn responds well to acid suppression with a proton pump inhibitor, regurgitation does not necessarily improve. It is well known that reflux persists despite acid suppression; in some patients, this manifests as troublesome postprandial regurgitation.  Transient LES relaxations (TLESRs) are the prime mechanism for persisting reflex, in patients both with and without hiatal hernias. 

Baclofen, a gamma amino butyric acid B (GABA-B) agonist, inhibits TLESRs and has potential to improve persisting regurgitation.  Metoclopramide has been demonstrated to have no adjunctive value in treating reflux disease. Hyoscyamine and sucralfate are similarly not of particular benefit in this setting. Cholesytramine is a bile salt binding resin that has value in the management of postcholecystectomy diarrhea.

 

References 

1. Kahrilas P.J., Jonsson A., Denison H., et al. Regurgitation is less responsive to acid suppression than heartburn in patients with gastroesophageal reflux disease. Clin Gastroenterol Hepatol. 2012;10(6):612-9. 

2. Vela M.F., Camacho-Lobato L., Srinivasan R., et al. Simultaneous intraesophageal impedance and pH measurement of acid and nonacid gastroesophageal reflux: effect of omeprazole. Gastroenterology. 2001 Jun;120(7):1599-606.

3. Vela M.F., Tutuian R, Katz PO, et al. Baclofen decreases acid and non-acid post-prandial gastro-oesophageal reflux measured by combined multichannel intraluminal impedance and pH. Aliment Pharmacol Ther. 2003 Jan;17(2):243-51.

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Q1. Answer: A

While heartburn responds well to acid suppression with a proton pump inhibitor, regurgitation does not necessarily improve. It is well known that reflux persists despite acid suppression; in some patients, this manifests as troublesome postprandial regurgitation.  Transient LES relaxations (TLESRs) are the prime mechanism for persisting reflex, in patients both with and without hiatal hernias. 

Baclofen, a gamma amino butyric acid B (GABA-B) agonist, inhibits TLESRs and has potential to improve persisting regurgitation.  Metoclopramide has been demonstrated to have no adjunctive value in treating reflux disease. Hyoscyamine and sucralfate are similarly not of particular benefit in this setting. Cholesytramine is a bile salt binding resin that has value in the management of postcholecystectomy diarrhea.

 

References 

1. Kahrilas P.J., Jonsson A., Denison H., et al. Regurgitation is less responsive to acid suppression than heartburn in patients with gastroesophageal reflux disease. Clin Gastroenterol Hepatol. 2012;10(6):612-9. 

2. Vela M.F., Camacho-Lobato L., Srinivasan R., et al. Simultaneous intraesophageal impedance and pH measurement of acid and nonacid gastroesophageal reflux: effect of omeprazole. Gastroenterology. 2001 Jun;120(7):1599-606.

3. Vela M.F., Tutuian R, Katz PO, et al. Baclofen decreases acid and non-acid post-prandial gastro-oesophageal reflux measured by combined multichannel intraluminal impedance and pH. Aliment Pharmacol Ther. 2003 Jan;17(2):243-51.

Q1. Answer: A

While heartburn responds well to acid suppression with a proton pump inhibitor, regurgitation does not necessarily improve. It is well known that reflux persists despite acid suppression; in some patients, this manifests as troublesome postprandial regurgitation.  Transient LES relaxations (TLESRs) are the prime mechanism for persisting reflex, in patients both with and without hiatal hernias. 

Baclofen, a gamma amino butyric acid B (GABA-B) agonist, inhibits TLESRs and has potential to improve persisting regurgitation.  Metoclopramide has been demonstrated to have no adjunctive value in treating reflux disease. Hyoscyamine and sucralfate are similarly not of particular benefit in this setting. Cholesytramine is a bile salt binding resin that has value in the management of postcholecystectomy diarrhea.

 

References 

1. Kahrilas P.J., Jonsson A., Denison H., et al. Regurgitation is less responsive to acid suppression than heartburn in patients with gastroesophageal reflux disease. Clin Gastroenterol Hepatol. 2012;10(6):612-9. 

2. Vela M.F., Camacho-Lobato L., Srinivasan R., et al. Simultaneous intraesophageal impedance and pH measurement of acid and nonacid gastroesophageal reflux: effect of omeprazole. Gastroenterology. 2001 Jun;120(7):1599-606.

3. Vela M.F., Tutuian R, Katz PO, et al. Baclofen decreases acid and non-acid post-prandial gastro-oesophageal reflux measured by combined multichannel intraluminal impedance and pH. Aliment Pharmacol Ther. 2003 Jan;17(2):243-51.

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Q1. A 25-year-old woman presents with postprandial regurgitation, typically after dinner. She initially had both heartburn and regurgitation. After she started esomeprazole 40 mg once a day 8 weeks ago, her heartburn completely resolved. An upper endoscopy, performed due to ongoing regurgitation symptoms, reveals a normal esophagus, and a 2-cm sliding hiatal hernia. 

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Don’t shy away from vaginal salpingectomy

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– Surgeons at Houston Methodist Hospital reported a 75% success rate in removing both fallopian tubes during vaginal hysterectomy in a study presented at the annual scientific meeting of the Society of Gynecologic Surgeons.

Serous ovarian carcinoma is now thought to arise from the distal fallopian tube, and it’s estimated that salpingectomy prevents diagnosis of ovarian cancer in 1 in 225 women and death from ovarian cancer in 1 in 450 women. The American Congress of Obstetricians and Gynecologists recommends that surgeons and patients “discuss the potential benefits of the removal of the fallopian tubes” during hysterectomy in women not having an oophorectomy.

Dr. Danielle Antosh
The advice has led to an increase in salpingectomies during laparoscopic and open hysterectomies, but removal is uncommon in vaginal hysterectomy, perhaps because of the perceived difficulty of removing the fallopian tubes vaginally.

The findings from the Houston team show that “it’s feasible in most cases, with very little risk,” said Danielle Antosh, MD, lead investigator and director of the Center for Restorative Pelvic Medicine at Houston Methodist Urogynecology Associates.

“People are doing laparoscopic hysterectomies or robotic hysterectomies” to get at the fallopian tubes, “but they shouldn’t be deterred from trying to remove the fallopian tubes vaginally,” Dr. Antosh said at the SGS 2017 meeting. When women are having a vaginal hysterectomy, “why not try to remove the fallopian tubes? It’s something I would definitely consider counseling your patients about.”

Dr. Antosh said that residents should be taught how to perform salpingectomy during vaginal hysterectomy. “I think it is definitely feasible for residents to do.” Technically, “it’s a lot easier than removing the ovaries” vaginally, she said.

The 70 women in the study were undergoing vaginal hysterectomies by attending physicians for benign reasons, mostly uterine prolapse, followed by heavy menstrual flow and fibroids. In total, 52 (75%) had successful concomitant bilateral vaginal salpingectomies, and 7 additional women had one tube removed. Success was more likely with increasing parity and a history of prolapse. Most of the failures were because the tubes were too high in the pelvis or there were adhesions from prior adnexal surgery. Even with prior adnexal surgery, however, the success rate was 50%.

Vaginal salpingectomy added a mean of 11 minutes to surgery and a mean of 5 mL blood loss. There were no complications reported from including salpingectomy with vaginal hysterectomy. The study wasn’t powered to detect an impact on menopause symptoms, but there was a decrease in menopause symptoms at 16 week follow-up in the salpingectomy group, perhaps related to less sexual dysfunction and urinary incontinence.

The mean age in the study was 51 years, and mean body mass index was 27 kg/m2. There were no malignancies found on tubal pathology.

Five women were transferred to an abdominal approach because of a large uterus or discovery of ovarian pathology. None were transferred for the purpose of salpingectomy.

There was no external funding for the study, and the investigators reported no relevant financial disclosures.

* The meeting sponsor information was updated 6/9/2017.

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– Surgeons at Houston Methodist Hospital reported a 75% success rate in removing both fallopian tubes during vaginal hysterectomy in a study presented at the annual scientific meeting of the Society of Gynecologic Surgeons.

Serous ovarian carcinoma is now thought to arise from the distal fallopian tube, and it’s estimated that salpingectomy prevents diagnosis of ovarian cancer in 1 in 225 women and death from ovarian cancer in 1 in 450 women. The American Congress of Obstetricians and Gynecologists recommends that surgeons and patients “discuss the potential benefits of the removal of the fallopian tubes” during hysterectomy in women not having an oophorectomy.

Dr. Danielle Antosh
The advice has led to an increase in salpingectomies during laparoscopic and open hysterectomies, but removal is uncommon in vaginal hysterectomy, perhaps because of the perceived difficulty of removing the fallopian tubes vaginally.

The findings from the Houston team show that “it’s feasible in most cases, with very little risk,” said Danielle Antosh, MD, lead investigator and director of the Center for Restorative Pelvic Medicine at Houston Methodist Urogynecology Associates.

“People are doing laparoscopic hysterectomies or robotic hysterectomies” to get at the fallopian tubes, “but they shouldn’t be deterred from trying to remove the fallopian tubes vaginally,” Dr. Antosh said at the SGS 2017 meeting. When women are having a vaginal hysterectomy, “why not try to remove the fallopian tubes? It’s something I would definitely consider counseling your patients about.”

Dr. Antosh said that residents should be taught how to perform salpingectomy during vaginal hysterectomy. “I think it is definitely feasible for residents to do.” Technically, “it’s a lot easier than removing the ovaries” vaginally, she said.

The 70 women in the study were undergoing vaginal hysterectomies by attending physicians for benign reasons, mostly uterine prolapse, followed by heavy menstrual flow and fibroids. In total, 52 (75%) had successful concomitant bilateral vaginal salpingectomies, and 7 additional women had one tube removed. Success was more likely with increasing parity and a history of prolapse. Most of the failures were because the tubes were too high in the pelvis or there were adhesions from prior adnexal surgery. Even with prior adnexal surgery, however, the success rate was 50%.

Vaginal salpingectomy added a mean of 11 minutes to surgery and a mean of 5 mL blood loss. There were no complications reported from including salpingectomy with vaginal hysterectomy. The study wasn’t powered to detect an impact on menopause symptoms, but there was a decrease in menopause symptoms at 16 week follow-up in the salpingectomy group, perhaps related to less sexual dysfunction and urinary incontinence.

The mean age in the study was 51 years, and mean body mass index was 27 kg/m2. There were no malignancies found on tubal pathology.

Five women were transferred to an abdominal approach because of a large uterus or discovery of ovarian pathology. None were transferred for the purpose of salpingectomy.

There was no external funding for the study, and the investigators reported no relevant financial disclosures.

* The meeting sponsor information was updated 6/9/2017.

 

– Surgeons at Houston Methodist Hospital reported a 75% success rate in removing both fallopian tubes during vaginal hysterectomy in a study presented at the annual scientific meeting of the Society of Gynecologic Surgeons.

Serous ovarian carcinoma is now thought to arise from the distal fallopian tube, and it’s estimated that salpingectomy prevents diagnosis of ovarian cancer in 1 in 225 women and death from ovarian cancer in 1 in 450 women. The American Congress of Obstetricians and Gynecologists recommends that surgeons and patients “discuss the potential benefits of the removal of the fallopian tubes” during hysterectomy in women not having an oophorectomy.

Dr. Danielle Antosh
The advice has led to an increase in salpingectomies during laparoscopic and open hysterectomies, but removal is uncommon in vaginal hysterectomy, perhaps because of the perceived difficulty of removing the fallopian tubes vaginally.

The findings from the Houston team show that “it’s feasible in most cases, with very little risk,” said Danielle Antosh, MD, lead investigator and director of the Center for Restorative Pelvic Medicine at Houston Methodist Urogynecology Associates.

“People are doing laparoscopic hysterectomies or robotic hysterectomies” to get at the fallopian tubes, “but they shouldn’t be deterred from trying to remove the fallopian tubes vaginally,” Dr. Antosh said at the SGS 2017 meeting. When women are having a vaginal hysterectomy, “why not try to remove the fallopian tubes? It’s something I would definitely consider counseling your patients about.”

Dr. Antosh said that residents should be taught how to perform salpingectomy during vaginal hysterectomy. “I think it is definitely feasible for residents to do.” Technically, “it’s a lot easier than removing the ovaries” vaginally, she said.

The 70 women in the study were undergoing vaginal hysterectomies by attending physicians for benign reasons, mostly uterine prolapse, followed by heavy menstrual flow and fibroids. In total, 52 (75%) had successful concomitant bilateral vaginal salpingectomies, and 7 additional women had one tube removed. Success was more likely with increasing parity and a history of prolapse. Most of the failures were because the tubes were too high in the pelvis or there were adhesions from prior adnexal surgery. Even with prior adnexal surgery, however, the success rate was 50%.

Vaginal salpingectomy added a mean of 11 minutes to surgery and a mean of 5 mL blood loss. There were no complications reported from including salpingectomy with vaginal hysterectomy. The study wasn’t powered to detect an impact on menopause symptoms, but there was a decrease in menopause symptoms at 16 week follow-up in the salpingectomy group, perhaps related to less sexual dysfunction and urinary incontinence.

The mean age in the study was 51 years, and mean body mass index was 27 kg/m2. There were no malignancies found on tubal pathology.

Five women were transferred to an abdominal approach because of a large uterus or discovery of ovarian pathology. None were transferred for the purpose of salpingectomy.

There was no external funding for the study, and the investigators reported no relevant financial disclosures.

* The meeting sponsor information was updated 6/9/2017.

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Key clinical point: Abdominal procedures are unnecessary to remove the fallopian tubes.

Major finding: Three-quarters of women undergoing vaginal hysterectomy for benign reasons had successful concomitant bilateral vaginal salpingectomy.

Data source: A single-center, observational study among 70 women undergoing vaginal hysterectomy for benign reasons.

Disclosures: There was no external funding and the investigators reported no relevant financial disclosures.

FDA: Recall of select EpiPen products

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Meridian Medical Technologies has issued a voluntary recall for 13 lots of EpiPen products, according to a press release from the U.S. Food and Drug Administration.

The voluntary recall includes EpiPen and EpiPen Jr. Auto-Injector distributed between Dec. 17, 2015, and July 1, 2016 by Mylan Specialty. Products included in the recall may contain a defective part which would prevent the device from activating.

“While the number of reported failures is small, EpiPen products that potentially contain a defective part are being recalled because of the potential for life-threatening risk if a severe allergic reaction goes untreated,” the FDA said in the press release.

Consumers who need their EpiPens should keep them until a they obtain a replacement, the FDA recommended.

Find the full press release on the FDA website.
 

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Meridian Medical Technologies has issued a voluntary recall for 13 lots of EpiPen products, according to a press release from the U.S. Food and Drug Administration.

The voluntary recall includes EpiPen and EpiPen Jr. Auto-Injector distributed between Dec. 17, 2015, and July 1, 2016 by Mylan Specialty. Products included in the recall may contain a defective part which would prevent the device from activating.

“While the number of reported failures is small, EpiPen products that potentially contain a defective part are being recalled because of the potential for life-threatening risk if a severe allergic reaction goes untreated,” the FDA said in the press release.

Consumers who need their EpiPens should keep them until a they obtain a replacement, the FDA recommended.

Find the full press release on the FDA website.
 

 

Meridian Medical Technologies has issued a voluntary recall for 13 lots of EpiPen products, according to a press release from the U.S. Food and Drug Administration.

The voluntary recall includes EpiPen and EpiPen Jr. Auto-Injector distributed between Dec. 17, 2015, and July 1, 2016 by Mylan Specialty. Products included in the recall may contain a defective part which would prevent the device from activating.

“While the number of reported failures is small, EpiPen products that potentially contain a defective part are being recalled because of the potential for life-threatening risk if a severe allergic reaction goes untreated,” the FDA said in the press release.

Consumers who need their EpiPens should keep them until a they obtain a replacement, the FDA recommended.

Find the full press release on the FDA website.
 

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