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Winners all
Everyone who attended CHEST Annual Meeting 2018 is a winner, but we would like to call out the winners participating in CHEST’s special categories of awards and events. Congratulations to all!
ANNUAL CHEST AWARDS
Master FCCP
David Gutterman, MD, Master FCCP
Distinguished Service Award
David Gutterman, MD, Master FCCP
College Medalist Award
Ghada Bourjeily, MD, FCCP
Master Clinician Educator
Lisa Moores, MD, FCCP
Early Career Clinician Educator
Amy Morris, MD, FCCP
Alfred Soffer Award for Editorial Excellence
Jean Rice
Presidential Citation
Darcy Marciniuk, MD, FCCP
Presidential Citation
D. Robert McCaffree, MD, Master FCCP
HONOR LECTURES AND MEMORIAL AWARDS
Edward C. Rosenow III, MD, Master FCCP/Master Teacher Honor Lecture Accelerated Aging in COPD and Its Comorbidities: Novel Therapeutic Targets
Peter Barnes, MD, Master FCCP
The lecture is generously funded by the CHEST Foundation.
Distinguished Scientist Honor Lecture in Cardiopulmonary Physiology
Understanding Diaphragm Performance: The Role of Ultrasound
F. Dennis McCool, MD, FCCP
The lecture is generously funded by the CHEST Foundation.
Presidential Honor Lecture
Asthma: Past, Present, and Future
Jay Peters, MD, FCCP
Thomas L. Petty, MD, Master FCCP Memorial Lecture
Recent Developments in Pulmonary Rehabilitation and Long-Term Oxygen Therapy: Would Tom Petty be Pleased?
Richard Casaburi, MD, PhD, FCCP
The lecture is generously funded by the CHEST Foundation.
Margaret Pfrommer Memorial Lecture in Long-term Mechanical Ventilation
Saving Lives…One Ventilator at a Time - HMV in 2018 and Beyond
Douglas McKim, MD, FCCP
The Margaret Pfrommer Memorial Lecture in Long-term Mechanical Ventilation is generously supported by International Ventilator Users Network of Post-Polio Health International and the CHEST Foundation.
Pasquale Ciaglia Memorial Lecture in Interventional Medicine
Evolution of Endobronchial Ultrasound: From Diagnostics to Therapeutics
Kazuhiro Yasufuku, MD, PhD, FCCP
The lecture is generously funded by the CHEST Foundation.
Roger C. Bone Memorial Lecture in Critical Care
Methylprednisolone in ARDS: A Highly Effective Treatment. How it Works, How to Use it
G. Umberto Meduri, MD
The lecture is generously funded by the CHEST Foundation.
CHEST FOUNDATION GRANT WINNERS
Distinguished Scholar
Robert C. Hyzy, MD, FCCP
Eli Lilly and Company Distinguished Scholar in Critical Care MedicineGrant Title: The Use of Electrical Impedance Tomography to Assess Mechanical Ventilation in Acute Respiratory Distress Syndrome
This grant is made possible due to the philanthropic support from Eli Lilly and Company.
Community Service Grantees
Deborah Haisch, MD
Columbia University Medical Center – New York, NY
CHEST Foundation Community Service Grant Honoring D. Robert McCaffree, MD, Master FCCP
Grant Title: East African Training Initiative in Pulmonary and Critical Care Medicine
Pamela Garrett, CCRN, MN
Gwinnett Medical Center – Lawrenceville, GA
CHEST Foundation Community Service Grant Honoring D. Robert McCaffree, MD, Master FCCP
Grant Title: Breathe Better Gwinnett
Phillip Sheridan
Mobile Care Chicago – Chicago, IL
CHEST Foundation Community Service Grant Honoring D. Robert McCaffree, MD, Master FCCP
Grant Title: Home Environment Education for Children with Asthma
These grants are supported in full by the CHEST Foundation.
Research Grant Winners
Ayodeji Adegunsoye, MD, MS
Research Grant in Pulmonary Fibrosis
Grant Title: Impact of Telomere Length on Pulmonary Fibrosis Clusters Across Diverse Racial Cohorts
Justin Oldham, MD, MS
Research Grant in Pulmonary Fibrosis
Grant Title: Plasma Biomarkers to Predict Outcomes and Treatment Response in Patients with Pulmonary Fibrosis
These grants above are supported by Boehringer Ingelheim Pharmaceuticals, Inc and Genentech.
Jacob Brenner, MD, PhD
Research Grant in Chronic Obstructive Pulmonary Disease
Grant Title: Ambulatory Cuirass Ventilation for Relief of Exertional Dyspnea in Severe COPD Patients
William Zhang, MD
Research Grant in Chronic Obstructive Pulmonary Disease
Grant Title: Pulmonary Iron Overload as a Novel COPD Endotype
These grants above are supported by AstraZeneca LP and Sunovion Pharmaceuticals Inc.
Margaret Bublitz, PhD
CHEST Foundation Research Grant in Women’s Lung Health
Grant Title: Sex as a Predictor of Sleep-Disordered Breathing and Its Consequences in Pregnancy
This grant is supported in full by the CHEST Foundation.
Tim Morris, MD, FCCP
CHEST Foundation Research Grant in Venous Thromboembolism
Grant Title: Long-term Follow-up of Acute Pulmonary Embolism
This grant is supported in full by the CHEST Foundation.
Monica Mukherjee, MD, MPH
CHEST Foundation Research Grant in Pulmonary Arterial Hypertension
Grant Title: Exercise Provocation in the Noninvasive Detection of Occult Right Ventricular Dysfunction and Emerging Pulmonary Hypertension in Systemic Sclerosis
This grant is supported in full by the CHEST Foundation.
Don Sanders, MD, MS
CHEST Foundation Research Grant in Cystic Fibrosis
Grant Title: Whole-genome Shotgun Sequencing of Oropharyngeal Swabs in Infants With CF
This grant is supported by Vertex Pharmaceuticals.
Imran Sulaiman, MD, PhD
CHEST Foundation Research Grant in Nontuberculosis Mycobacteria Diseases
Grant Title: Lower Airway Microbiota Signatures Associated W ith Impaired Immune Response in Non-Tuberculous Mycobacterium
This grant is supported by Insmed.
Samira Shojaee, MD, MPH, FCCP
CHEST Foundation Research Grant in Lung Cancer
Grant Title: Extracellular Vesicle miRNA as a Biomarker in Malignant Pleural Effusion
This grant is supported in full by the CHEST Foundation.
Anna Volerman, MD
CHEST Foundation Research Grant in Severe Asthma
Grant Title: A Randomized Clinical Trial Evaluating the Effectiveness of Virtual Teach-to-Goal(TM) Education versus Brief Intervention for Children with Severe Asthma
This grant is supported by AstraZeneca LP.
ABSTRACT AND CASE REPORT WINNERS
Alfred Soffer Research Award Winners
Clauden Louis, MD: Left ventricular assist devices in Intermacs 1 acute cardiogenic shock patients
Babith J. Mankidy, MBBS, FCCP: Reduction in in-hospital cardiac arrest with early interventions in the emergency department and non-ICU units by a novel approach of rapid response teams and mobile ICU management
Young Investigator Award Winners
Fayez Kheir, MD, MSc: Intrapleural tissue plasminogen activator and deoxyribonuclease therapy vs early medical thoracoscopy for treatment of pleural infection: a randomized clinical trial
Michael Rosman, MD: The utility of end tidal CO2 (ETCO2) monitoring during in-hospital cardiac arrest to predict return of spontaneous circulation
Top 5 Abstract Poster Winners
Neha Agarwal, MD: The 3 wishes project: a feasible intervention to improve end of life care in the ICU at UCLA
Hiroaki Harada, MD: Usefulness of comprehensive preoperative pulmonary rehabilitation program including intensive nutritional support concomitant with physical exercise through an interdisciplinary team approach
Joseph M. Carrington, DO, MHA: Targeting the trans-IL-6 signaling pathway to reduce agriculture organic dust exposure-induced airway inflammation in mice
Yu Kuang Lai, MBBCh: The utility of parametric response mapping in pulmonary graft vs host disease following hematopoietic stem cell transplant
Top Abstract Poster Finalists
Ligia M. Puiu, MD, PhD, FCCP: Association between echocardiographic and lipid parameters to workers in the metalliferous mines
Kush R. Dholakia, MD: Colloids vs crystalloids for postoperative resuscitation in patients undergoing off-pump coronary artery bypass surgery
Kulothungan Gunasekaran, MD, MBBS: Risk of VTE in idiopathic pulmonary fibrosis: a systematic review
Laura B. Sutton, PharmD: Ease and correct use of Ellipta by age in patients with asthma and COPD
Ankur Mogla, MD: To assess the utilization of pulmonary function testing for perioperative respiratory complications in bariatric surgery patients
Ali Ammar: Tracheostomy and admission diagnosis as predictors for an extended length of stay (ELOS)
Charlene Kalani, PharmD: Efficacy and safety of direct oral anticoagulants (DOACS) in morbidly obese patients
Jonghoo Lee, MD: Performances of modified CRB-65 score compared to SIRS and QSOFA as a rapid screening tool for sepsis among infected patients in initial emergency department: a propensity score matching study
Frank J. Trudo, MD, FCCP: Clinical burden of eosinophilic COPD
Elise L. Stephenson, MD: Vitamin C and point of care glucose measurements: a retrospective, observational study
Faisal Siddiqi, MD: Implementation of an early mobility program in the medical ICU
Eileen Harder, MD: Connective tissue disease-associated pulmonary arterial hypertension hospitalizations from 2001-2014
Sophie Korzan, MD: Exhaled nitric oxide and asthma-COPD overlap in patients hospitalized with exacerbations of airway disease: preliminary observations
Andreas Grove, MD: MicroRNA (MIRNA) and biological markers discriminate between normotensive and prehypertensive young men in hypobaric hypoxic environments
Snigdha Nutalapati, MBBS: Large cell neuroendocrine cancer of the lung: SEER 2004-2014 analysis
Anubhav Jain, MBBS: Survival benefit of beta-blockers in patients hospitalized for acute exacerbation of COPD
Case Report Slide Winners
Ze Ying Tan: All that wheezes is not asthma
Jason Lam: Pulmonary mucor mycetoma
Adam Young: Nonresolving pneumonia and cyclic fevers in an immunocompetent patient
Ritu Modi: Histopathological misdiagnosis of pulmonary coccidiodes
Argun Can: A rare inborn error of fatty acid oxidation presenting with severe hyperammonemia in the ICU
Morgan Gilani: A colorful cause of cardiovascular collapse
Katie Jeans: A sweet surprise
Anthony Mattox: Unusual case of interstitial lung disease
Andrew Berglund: Pulmonary light chain deposition disease in a 29-year-old army soldier
Cristia Maysol Morales: A case report of a primary malignant melanoma of anterior mediastinum
Anthony McClafferty: Fibrosing mediastinitis and rheumatoid arthritis: an autoimmune inflammatory connection
Ahmed Munir: HIV with disseminated tularemia: a rare presentation Benjamin Garren: Mycobacterium avium complex mediastinal lymphadenitis in an immunocompetent adolescent with erosion into the airway
Robert Hilton: Obtunded with a chest mass: a case of a rare neurologic paraneoplastic syndrome,
Audra Schwalk: Mucoepidermoid carcinoma: a rare malignancy treated endobronchially
Jessica Riggs: Successful transplantation defies genetics: a case of rapidly-progressive pulmonary fibrosis due to Hermansky-Pudlak syndrome
Meghan Cirulis: Acute vasodilator testing: an opportunity to refine study design and provide precision care in pulmonary hypertension
Patrick Chan: VATS lobectomy for bronchial atresia in an adult
Andrew Mehlman: Multivessel coronary artery aneurysms presenting as myocardial ischemia
Scott Maughan: Diagnosing milliary Mycobacterium bovis from the prostate of an immunocompetent host
Adam Austin: Survived ECMO, death by BLASTO: the first reported fatal case of disseminated blastomycosis in pregnancy
Tie: Donnie Carter: Subclinical polycythemia vera presenting as extensive thrombosis due to massive transfusion, and
Lindsay Hammons: Rare case of Serratia pneumonia causing transient aplastic anemia
Paola Baskin: Novel observations during point-of-care ultrasound (POCUS) in cardiopulmonary resuscitation: a case of ultrasound-guided probe pressure to reduce esophageal insufflation during bag-valve-mask ventilator
David Dennis: Pulmonary alveolar proteinosis presenting as intracerebral nocardiosis
Rakin Choudhury: Severe asthma caused by therapy-resistant asthmatic granulomatosis
Andrew Lytle: Lung adenocarcinoma in a patient with Turcot syndrome
Chelsea Leipold: Case of a granulomatous-lymphocytic interstitial lung disease in a patient with common variable immunodeficiency disorder
Galyna Ivashchuk: Double trouble: ANCA vasculitis with concomitant IGA nephropathy presenting as massive diffuse alveolar hemorrhage and fulminant renal failure
Case Report Poster Winners
Christine Zhou: Role of transbronchial lung cryobiopsy in the diagnosis of adenocarcinoma in situ
Parin Shah: A rare case of Erdheim-Chester disease masquerading as metastatic lung cancer
Avanthika Wynn : A rare asthma mimic
Muhammad S. Ali: Severe pancolitis: a rare adverse effect of nintedanib
Brian Foster: Don’t forget to breathe: a case of hypoxemia after carotid body resection
Kelly Pennington: Intra-cardiac embolization of an inferior vena cava filter resulting in cardiac arrest
George Elkomos-Botros: Acute generalized exanthematous pustulosis presenting as distributive shock with multi-organ failure
Ashley M. Scott: Avian occupational hypersensitivity pneumonitis in a restaurant employee
Andrew Polito: Pulmonary amyloidosis: an unusual presentation of a rare disease
CHEST B-I-N-G-O WINNERS
Stella Ogake, MD
Erin E. Peterson, APRN, CNP
Megan J. Castillo, PA-C
Gretchen R. Winter, MD
Jeanette P. Brown, MD, PhD
Yu Hong Chan, MBBS
Anita Naik, DO
Gary A. Aaronson, DO, FCCP
Allison S. Cowl, MD
Kyle Halligan, MD
Palaniappan Muthappan, MD
Faizullah S. Lokhandwala, MBBS, FCCP
Jamie R. Chua, MD
Francis L. Ervin, MD, FCCP
Robyn Luper
CHEST CHALLENGE WINNER (AND RUNNER’S-UP)
Emory University (First Place)
Mirza Haider Ali, MD
Mohleen Kang, MD
Matthew Schimmel, MD
University of Michigan (Second Place)
Patrick Bradley, MD
Matthew Hensley, MD
Bonnie Wang, MD
Cleveland Clinic (Third Place)
Jorge Mirales-Estrella, MD
Apostolos Perelas, MD
Gretchen Winter, MD
2018 DISTINGUISHED CHEST EDUCATORS
Michael H Ackerman, DNSc
Sandra G Adams, MD, MS, FCCP
Doreen J Addrizzo-Harris, MD, FCCP
Cara Lyn Agerstrand, MD, BS
Jason A Akulian, MD, FCCP
Raed H Alalawi, MD, FCCP
A. Christine Argento, MD, FCCP
Robert Arntfield, MD, FCCP
Alex A Balekian, MD
Meyer S Balter, MD, FCCP
Gisela I Banauch, MD, MS, FCCP
Robert P Baughman, MD, FCCP
David G Bell, MD, FCCP
Michel A Boivin, MD, FCCP
Gabriel T Bosslet, MD, FCCP
Jean Bourbeau, MD, MS, FCCP
Ghada R Bourjeily, MD, FCCP
David L Bowton, MD, FCCM
Jack D Buckley, MD, MPH, FCCP
Marie M Budev, DO, MPH, FCCP
Kristin M Burkart, MD, MS, FCCP
Brian Carlin, MD, FCCP
Christopher L Carroll, MD, FCCP
Roberto F Casal, MD
Kevin M Chan, MD, FCCP
Subani Chandra, MD, FCCP
Ching-Fei Chang, MD
Alexander C Chen, MD
Nancy A Collop, MD, FCCP
Clayton T Cowl, MD, MS, FCCP
Angel O Coz Yataco, MD, FCCP
Gerard J Criner, MD, FCCP
Carolyn M D’Ambrosio, MD, FCCP
Mauricio Danckers, MD, FCCP
Aneesa M Das, MD, FCCP
John Davies, RRT, MA, FCCP
Zachary S DePew, MD, FCCP
Frank C Detterbeck, MD, FCCP
Naresh A. Dewan, MBBS, FCCP
Kevin C Doerschug, MD, MS, FCCP
Meagan Dubosky, RRT-ACCS
Kevin M Dushay, MD, FCCP
Eric S Edell, MD, FCCP
Jean M Elwing, MD, FCCP
William Enfinger
Michael E Ezzie, MD, FCCP
Kevin J Felner, MD, FCCP
Mark E Fenton, MD, MSc, FCCP
Jason Filopei, MD
Neil S Freedman, MD, FCCP
Laura Kathleen Frye, MD
Thomas M Fuhrman, MD, MS, FCCP
John P Gaillard, MD, FCCP
Colin T Gillespie, MD
Yonatan Y Greenstein, MD
Maritza L Groth, MD, FCCP
Keith P Guevarra, DO, FCCP
Jesse B Hall, MD, FCCP
Nicola A Hanania, MD, MBBS, FCCP
D Kyle Hogarth, MD, FCCP
Steven M Hollenberg, MD, FCCP
David W Hsia, MD, FCCP
Candace A Huebert, MD, FCCP
Robert C Hyzy, MD, FCCP
Octavian C Ioachimescu, MD, PhD, FCCP
Richard S Irwin, MD, Master FCCP
Kirk D Jones, MD
Nader Kamangar, MD, MS, FCCP
Carl A Kaplan, MD, FCCP
Brian S Kaufman, MD, FCCP
William F Kelly, MD, FCCP
Marcus P Kennedy, MD, FCCP
Sandhya Khurana, MD, FCCP
James R Klinger, MD, FCCP
Seth J Koenig, MD, FCCP
Lindsey Kreisher, RRT
Karol Kremens, MD, FCCP
Patricia A Kritek, MD, FCCP
Sunita Kumar, MD, MBBS, FCCP
Rudy P Lackner, MD, FCCP
Viera Lakticova, MD
Carla R Lamb, MD, FCCP
Hans J Lee, MD, FCCP
Peter H Lenz, MD, MEd, FCCP
Stephanie M Levine, MD, FCCP
Deborah Jo Levine, MD, MS, FCCP
Andrea Loiselle, MD
Kenneth E Lyn-Kew, MD
Michael S Machuzak, MD, FCCP
Neil R MacIntyre, MD, FCCP
Donald A Mahler, MD, FCCP
Fabien Maldonado, MD, FCCP
Atul Malhotra, MD, FCCP
Darcy D Marciniuk, MD, FCCP
Diego J Maselli Caceres, MD, FCCP
Paul H Mayo, MD, FCCP
Peter J Mazzone, MD, MPH, FCCP
John K McIlwaine, DO, MBA, FCCP
Matthew C Miles, MD, FCCP
Scott Millington, MD
Taro Minami, MD, FCCP
Lisa K Moores, MD, FCCP
Amy E Morris, MD, FCCP
John J Mullon, MD, FCCP
Septimiu D Murgu, MD, FCCP
Mangala Narasimhan, DO, FCCP
Michael S Niederman, MD, FCCP
Alexander S Niven, MD, FCCP
Anne E O’Donnell, MD, FCCP
Erik C Osborn, MD
David E Ost, MD, MPH, FCCP
Ronald J Oudiz, MD, FCCP
Daniel R Ouellette, MD, MS, FCCP
Amit D Parulekar, MD, MS, FCCP
Nicholas J Pastis, MD, FCCP
Nina M Patel, MD, FCCP
Paru S Patrawalla, MD, FCCP
Jay I Peters, MD, FCCP
Barbara A Phillips, MD, MSPH, FCCP
Margaret A Pisani, MD, MS, FCCP
Janos Porszasz, MD, PhD
Whitney S Prince, MD, FCCP
Suhail Raoof, MBBS, Master FCCP
Ruben D Restrepo, RRT, FCCP
Marcos I Restrepo, MD, PhD, FCCP
Otis B Rickman, DO, FCCP
Roy D Ridgeway
Mary Ried, RN, CCRN
Linda Rogers, MD, FCCP
Mark J Rosen, MD, Master FCCP
Bernard J Roth, MD, FCCP
Ashutosh Sachdeva, MBBS, FCCP
Anthony G Saleh, MD, FCCP
Juan F Sanchez, MD, FCCP
Pralay K Sarkar, MBBS, FCCP
Lewis G Satterwhite, MD, BA, FCCP
Gregory A Schmidt, MD, FCCP
Mary Beth Scholand, MD, FCCP
David A Schulman, MD, MPH, FCCP
Brady Scott, RRT, MS, FCCP
Bernardo Selim, MD, FCCP
Curtis N Sessler, MD, FCCP
Rakesh D Shah, MD, FCCP
Ray Wes Shepherd, MD, FCCP
John H Sherner, MD, FCCP
Ariel L Shiloh, MD
Samira Shojaee, MD, FCCP
Marcos Silva Restrepo
Gerard A Silvestri, MD, MS, FCCP
Steven Q Simpson, MD, FCCP
James K Stoller, MD, MS, FCCP
Charlie Strange, MD, FCCP
Mary E Strek, MD, FCCP
William W Stringer, MD, FCCP
Eleanor M Summerhill, MD, FCCP
Maximiliano A Tamae Kakazu, MD, FCCP
Nichole T Tanner, MD, MS, FCCP
Lynn T Tanoue, MD, FCCP
Victor J Test, MD, FCCP
Arthur J Tokarczyk, MD, FCCP
Alain Tremblay, MD, FCCP
Adey Tsegaye, MD, FCCP
Anil Vachani, MD, FCCP
Momen M Wahidi, MD, MBA, FCCP
Keith M Wille, MD, FCCP
Lisa F Wolfe, MD
Richard G Wunderink, MD, FCCP
Lonny B Yarmus, DO, FCCP
Kazuhiro Yasufuku, MD, PhD, FCCP
Gulrukh Zaidi, MD, FCCP
David Zielinski, MD, FCCP
Everyone who attended CHEST Annual Meeting 2018 is a winner, but we would like to call out the winners participating in CHEST’s special categories of awards and events. Congratulations to all!
ANNUAL CHEST AWARDS
Master FCCP
David Gutterman, MD, Master FCCP
Distinguished Service Award
David Gutterman, MD, Master FCCP
College Medalist Award
Ghada Bourjeily, MD, FCCP
Master Clinician Educator
Lisa Moores, MD, FCCP
Early Career Clinician Educator
Amy Morris, MD, FCCP
Alfred Soffer Award for Editorial Excellence
Jean Rice
Presidential Citation
Darcy Marciniuk, MD, FCCP
Presidential Citation
D. Robert McCaffree, MD, Master FCCP
HONOR LECTURES AND MEMORIAL AWARDS
Edward C. Rosenow III, MD, Master FCCP/Master Teacher Honor Lecture Accelerated Aging in COPD and Its Comorbidities: Novel Therapeutic Targets
Peter Barnes, MD, Master FCCP
The lecture is generously funded by the CHEST Foundation.
Distinguished Scientist Honor Lecture in Cardiopulmonary Physiology
Understanding Diaphragm Performance: The Role of Ultrasound
F. Dennis McCool, MD, FCCP
The lecture is generously funded by the CHEST Foundation.
Presidential Honor Lecture
Asthma: Past, Present, and Future
Jay Peters, MD, FCCP
Thomas L. Petty, MD, Master FCCP Memorial Lecture
Recent Developments in Pulmonary Rehabilitation and Long-Term Oxygen Therapy: Would Tom Petty be Pleased?
Richard Casaburi, MD, PhD, FCCP
The lecture is generously funded by the CHEST Foundation.
Margaret Pfrommer Memorial Lecture in Long-term Mechanical Ventilation
Saving Lives…One Ventilator at a Time - HMV in 2018 and Beyond
Douglas McKim, MD, FCCP
The Margaret Pfrommer Memorial Lecture in Long-term Mechanical Ventilation is generously supported by International Ventilator Users Network of Post-Polio Health International and the CHEST Foundation.
Pasquale Ciaglia Memorial Lecture in Interventional Medicine
Evolution of Endobronchial Ultrasound: From Diagnostics to Therapeutics
Kazuhiro Yasufuku, MD, PhD, FCCP
The lecture is generously funded by the CHEST Foundation.
Roger C. Bone Memorial Lecture in Critical Care
Methylprednisolone in ARDS: A Highly Effective Treatment. How it Works, How to Use it
G. Umberto Meduri, MD
The lecture is generously funded by the CHEST Foundation.
CHEST FOUNDATION GRANT WINNERS
Distinguished Scholar
Robert C. Hyzy, MD, FCCP
Eli Lilly and Company Distinguished Scholar in Critical Care MedicineGrant Title: The Use of Electrical Impedance Tomography to Assess Mechanical Ventilation in Acute Respiratory Distress Syndrome
This grant is made possible due to the philanthropic support from Eli Lilly and Company.
Community Service Grantees
Deborah Haisch, MD
Columbia University Medical Center – New York, NY
CHEST Foundation Community Service Grant Honoring D. Robert McCaffree, MD, Master FCCP
Grant Title: East African Training Initiative in Pulmonary and Critical Care Medicine
Pamela Garrett, CCRN, MN
Gwinnett Medical Center – Lawrenceville, GA
CHEST Foundation Community Service Grant Honoring D. Robert McCaffree, MD, Master FCCP
Grant Title: Breathe Better Gwinnett
Phillip Sheridan
Mobile Care Chicago – Chicago, IL
CHEST Foundation Community Service Grant Honoring D. Robert McCaffree, MD, Master FCCP
Grant Title: Home Environment Education for Children with Asthma
These grants are supported in full by the CHEST Foundation.
Research Grant Winners
Ayodeji Adegunsoye, MD, MS
Research Grant in Pulmonary Fibrosis
Grant Title: Impact of Telomere Length on Pulmonary Fibrosis Clusters Across Diverse Racial Cohorts
Justin Oldham, MD, MS
Research Grant in Pulmonary Fibrosis
Grant Title: Plasma Biomarkers to Predict Outcomes and Treatment Response in Patients with Pulmonary Fibrosis
These grants above are supported by Boehringer Ingelheim Pharmaceuticals, Inc and Genentech.
Jacob Brenner, MD, PhD
Research Grant in Chronic Obstructive Pulmonary Disease
Grant Title: Ambulatory Cuirass Ventilation for Relief of Exertional Dyspnea in Severe COPD Patients
William Zhang, MD
Research Grant in Chronic Obstructive Pulmonary Disease
Grant Title: Pulmonary Iron Overload as a Novel COPD Endotype
These grants above are supported by AstraZeneca LP and Sunovion Pharmaceuticals Inc.
Margaret Bublitz, PhD
CHEST Foundation Research Grant in Women’s Lung Health
Grant Title: Sex as a Predictor of Sleep-Disordered Breathing and Its Consequences in Pregnancy
This grant is supported in full by the CHEST Foundation.
Tim Morris, MD, FCCP
CHEST Foundation Research Grant in Venous Thromboembolism
Grant Title: Long-term Follow-up of Acute Pulmonary Embolism
This grant is supported in full by the CHEST Foundation.
Monica Mukherjee, MD, MPH
CHEST Foundation Research Grant in Pulmonary Arterial Hypertension
Grant Title: Exercise Provocation in the Noninvasive Detection of Occult Right Ventricular Dysfunction and Emerging Pulmonary Hypertension in Systemic Sclerosis
This grant is supported in full by the CHEST Foundation.
Don Sanders, MD, MS
CHEST Foundation Research Grant in Cystic Fibrosis
Grant Title: Whole-genome Shotgun Sequencing of Oropharyngeal Swabs in Infants With CF
This grant is supported by Vertex Pharmaceuticals.
Imran Sulaiman, MD, PhD
CHEST Foundation Research Grant in Nontuberculosis Mycobacteria Diseases
Grant Title: Lower Airway Microbiota Signatures Associated W ith Impaired Immune Response in Non-Tuberculous Mycobacterium
This grant is supported by Insmed.
Samira Shojaee, MD, MPH, FCCP
CHEST Foundation Research Grant in Lung Cancer
Grant Title: Extracellular Vesicle miRNA as a Biomarker in Malignant Pleural Effusion
This grant is supported in full by the CHEST Foundation.
Anna Volerman, MD
CHEST Foundation Research Grant in Severe Asthma
Grant Title: A Randomized Clinical Trial Evaluating the Effectiveness of Virtual Teach-to-Goal(TM) Education versus Brief Intervention for Children with Severe Asthma
This grant is supported by AstraZeneca LP.
ABSTRACT AND CASE REPORT WINNERS
Alfred Soffer Research Award Winners
Clauden Louis, MD: Left ventricular assist devices in Intermacs 1 acute cardiogenic shock patients
Babith J. Mankidy, MBBS, FCCP: Reduction in in-hospital cardiac arrest with early interventions in the emergency department and non-ICU units by a novel approach of rapid response teams and mobile ICU management
Young Investigator Award Winners
Fayez Kheir, MD, MSc: Intrapleural tissue plasminogen activator and deoxyribonuclease therapy vs early medical thoracoscopy for treatment of pleural infection: a randomized clinical trial
Michael Rosman, MD: The utility of end tidal CO2 (ETCO2) monitoring during in-hospital cardiac arrest to predict return of spontaneous circulation
Top 5 Abstract Poster Winners
Neha Agarwal, MD: The 3 wishes project: a feasible intervention to improve end of life care in the ICU at UCLA
Hiroaki Harada, MD: Usefulness of comprehensive preoperative pulmonary rehabilitation program including intensive nutritional support concomitant with physical exercise through an interdisciplinary team approach
Joseph M. Carrington, DO, MHA: Targeting the trans-IL-6 signaling pathway to reduce agriculture organic dust exposure-induced airway inflammation in mice
Yu Kuang Lai, MBBCh: The utility of parametric response mapping in pulmonary graft vs host disease following hematopoietic stem cell transplant
Top Abstract Poster Finalists
Ligia M. Puiu, MD, PhD, FCCP: Association between echocardiographic and lipid parameters to workers in the metalliferous mines
Kush R. Dholakia, MD: Colloids vs crystalloids for postoperative resuscitation in patients undergoing off-pump coronary artery bypass surgery
Kulothungan Gunasekaran, MD, MBBS: Risk of VTE in idiopathic pulmonary fibrosis: a systematic review
Laura B. Sutton, PharmD: Ease and correct use of Ellipta by age in patients with asthma and COPD
Ankur Mogla, MD: To assess the utilization of pulmonary function testing for perioperative respiratory complications in bariatric surgery patients
Ali Ammar: Tracheostomy and admission diagnosis as predictors for an extended length of stay (ELOS)
Charlene Kalani, PharmD: Efficacy and safety of direct oral anticoagulants (DOACS) in morbidly obese patients
Jonghoo Lee, MD: Performances of modified CRB-65 score compared to SIRS and QSOFA as a rapid screening tool for sepsis among infected patients in initial emergency department: a propensity score matching study
Frank J. Trudo, MD, FCCP: Clinical burden of eosinophilic COPD
Elise L. Stephenson, MD: Vitamin C and point of care glucose measurements: a retrospective, observational study
Faisal Siddiqi, MD: Implementation of an early mobility program in the medical ICU
Eileen Harder, MD: Connective tissue disease-associated pulmonary arterial hypertension hospitalizations from 2001-2014
Sophie Korzan, MD: Exhaled nitric oxide and asthma-COPD overlap in patients hospitalized with exacerbations of airway disease: preliminary observations
Andreas Grove, MD: MicroRNA (MIRNA) and biological markers discriminate between normotensive and prehypertensive young men in hypobaric hypoxic environments
Snigdha Nutalapati, MBBS: Large cell neuroendocrine cancer of the lung: SEER 2004-2014 analysis
Anubhav Jain, MBBS: Survival benefit of beta-blockers in patients hospitalized for acute exacerbation of COPD
Case Report Slide Winners
Ze Ying Tan: All that wheezes is not asthma
Jason Lam: Pulmonary mucor mycetoma
Adam Young: Nonresolving pneumonia and cyclic fevers in an immunocompetent patient
Ritu Modi: Histopathological misdiagnosis of pulmonary coccidiodes
Argun Can: A rare inborn error of fatty acid oxidation presenting with severe hyperammonemia in the ICU
Morgan Gilani: A colorful cause of cardiovascular collapse
Katie Jeans: A sweet surprise
Anthony Mattox: Unusual case of interstitial lung disease
Andrew Berglund: Pulmonary light chain deposition disease in a 29-year-old army soldier
Cristia Maysol Morales: A case report of a primary malignant melanoma of anterior mediastinum
Anthony McClafferty: Fibrosing mediastinitis and rheumatoid arthritis: an autoimmune inflammatory connection
Ahmed Munir: HIV with disseminated tularemia: a rare presentation Benjamin Garren: Mycobacterium avium complex mediastinal lymphadenitis in an immunocompetent adolescent with erosion into the airway
Robert Hilton: Obtunded with a chest mass: a case of a rare neurologic paraneoplastic syndrome,
Audra Schwalk: Mucoepidermoid carcinoma: a rare malignancy treated endobronchially
Jessica Riggs: Successful transplantation defies genetics: a case of rapidly-progressive pulmonary fibrosis due to Hermansky-Pudlak syndrome
Meghan Cirulis: Acute vasodilator testing: an opportunity to refine study design and provide precision care in pulmonary hypertension
Patrick Chan: VATS lobectomy for bronchial atresia in an adult
Andrew Mehlman: Multivessel coronary artery aneurysms presenting as myocardial ischemia
Scott Maughan: Diagnosing milliary Mycobacterium bovis from the prostate of an immunocompetent host
Adam Austin: Survived ECMO, death by BLASTO: the first reported fatal case of disseminated blastomycosis in pregnancy
Tie: Donnie Carter: Subclinical polycythemia vera presenting as extensive thrombosis due to massive transfusion, and
Lindsay Hammons: Rare case of Serratia pneumonia causing transient aplastic anemia
Paola Baskin: Novel observations during point-of-care ultrasound (POCUS) in cardiopulmonary resuscitation: a case of ultrasound-guided probe pressure to reduce esophageal insufflation during bag-valve-mask ventilator
David Dennis: Pulmonary alveolar proteinosis presenting as intracerebral nocardiosis
Rakin Choudhury: Severe asthma caused by therapy-resistant asthmatic granulomatosis
Andrew Lytle: Lung adenocarcinoma in a patient with Turcot syndrome
Chelsea Leipold: Case of a granulomatous-lymphocytic interstitial lung disease in a patient with common variable immunodeficiency disorder
Galyna Ivashchuk: Double trouble: ANCA vasculitis with concomitant IGA nephropathy presenting as massive diffuse alveolar hemorrhage and fulminant renal failure
Case Report Poster Winners
Christine Zhou: Role of transbronchial lung cryobiopsy in the diagnosis of adenocarcinoma in situ
Parin Shah: A rare case of Erdheim-Chester disease masquerading as metastatic lung cancer
Avanthika Wynn : A rare asthma mimic
Muhammad S. Ali: Severe pancolitis: a rare adverse effect of nintedanib
Brian Foster: Don’t forget to breathe: a case of hypoxemia after carotid body resection
Kelly Pennington: Intra-cardiac embolization of an inferior vena cava filter resulting in cardiac arrest
George Elkomos-Botros: Acute generalized exanthematous pustulosis presenting as distributive shock with multi-organ failure
Ashley M. Scott: Avian occupational hypersensitivity pneumonitis in a restaurant employee
Andrew Polito: Pulmonary amyloidosis: an unusual presentation of a rare disease
CHEST B-I-N-G-O WINNERS
Stella Ogake, MD
Erin E. Peterson, APRN, CNP
Megan J. Castillo, PA-C
Gretchen R. Winter, MD
Jeanette P. Brown, MD, PhD
Yu Hong Chan, MBBS
Anita Naik, DO
Gary A. Aaronson, DO, FCCP
Allison S. Cowl, MD
Kyle Halligan, MD
Palaniappan Muthappan, MD
Faizullah S. Lokhandwala, MBBS, FCCP
Jamie R. Chua, MD
Francis L. Ervin, MD, FCCP
Robyn Luper
CHEST CHALLENGE WINNER (AND RUNNER’S-UP)
Emory University (First Place)
Mirza Haider Ali, MD
Mohleen Kang, MD
Matthew Schimmel, MD
University of Michigan (Second Place)
Patrick Bradley, MD
Matthew Hensley, MD
Bonnie Wang, MD
Cleveland Clinic (Third Place)
Jorge Mirales-Estrella, MD
Apostolos Perelas, MD
Gretchen Winter, MD
2018 DISTINGUISHED CHEST EDUCATORS
Michael H Ackerman, DNSc
Sandra G Adams, MD, MS, FCCP
Doreen J Addrizzo-Harris, MD, FCCP
Cara Lyn Agerstrand, MD, BS
Jason A Akulian, MD, FCCP
Raed H Alalawi, MD, FCCP
A. Christine Argento, MD, FCCP
Robert Arntfield, MD, FCCP
Alex A Balekian, MD
Meyer S Balter, MD, FCCP
Gisela I Banauch, MD, MS, FCCP
Robert P Baughman, MD, FCCP
David G Bell, MD, FCCP
Michel A Boivin, MD, FCCP
Gabriel T Bosslet, MD, FCCP
Jean Bourbeau, MD, MS, FCCP
Ghada R Bourjeily, MD, FCCP
David L Bowton, MD, FCCM
Jack D Buckley, MD, MPH, FCCP
Marie M Budev, DO, MPH, FCCP
Kristin M Burkart, MD, MS, FCCP
Brian Carlin, MD, FCCP
Christopher L Carroll, MD, FCCP
Roberto F Casal, MD
Kevin M Chan, MD, FCCP
Subani Chandra, MD, FCCP
Ching-Fei Chang, MD
Alexander C Chen, MD
Nancy A Collop, MD, FCCP
Clayton T Cowl, MD, MS, FCCP
Angel O Coz Yataco, MD, FCCP
Gerard J Criner, MD, FCCP
Carolyn M D’Ambrosio, MD, FCCP
Mauricio Danckers, MD, FCCP
Aneesa M Das, MD, FCCP
John Davies, RRT, MA, FCCP
Zachary S DePew, MD, FCCP
Frank C Detterbeck, MD, FCCP
Naresh A. Dewan, MBBS, FCCP
Kevin C Doerschug, MD, MS, FCCP
Meagan Dubosky, RRT-ACCS
Kevin M Dushay, MD, FCCP
Eric S Edell, MD, FCCP
Jean M Elwing, MD, FCCP
William Enfinger
Michael E Ezzie, MD, FCCP
Kevin J Felner, MD, FCCP
Mark E Fenton, MD, MSc, FCCP
Jason Filopei, MD
Neil S Freedman, MD, FCCP
Laura Kathleen Frye, MD
Thomas M Fuhrman, MD, MS, FCCP
John P Gaillard, MD, FCCP
Colin T Gillespie, MD
Yonatan Y Greenstein, MD
Maritza L Groth, MD, FCCP
Keith P Guevarra, DO, FCCP
Jesse B Hall, MD, FCCP
Nicola A Hanania, MD, MBBS, FCCP
D Kyle Hogarth, MD, FCCP
Steven M Hollenberg, MD, FCCP
David W Hsia, MD, FCCP
Candace A Huebert, MD, FCCP
Robert C Hyzy, MD, FCCP
Octavian C Ioachimescu, MD, PhD, FCCP
Richard S Irwin, MD, Master FCCP
Kirk D Jones, MD
Nader Kamangar, MD, MS, FCCP
Carl A Kaplan, MD, FCCP
Brian S Kaufman, MD, FCCP
William F Kelly, MD, FCCP
Marcus P Kennedy, MD, FCCP
Sandhya Khurana, MD, FCCP
James R Klinger, MD, FCCP
Seth J Koenig, MD, FCCP
Lindsey Kreisher, RRT
Karol Kremens, MD, FCCP
Patricia A Kritek, MD, FCCP
Sunita Kumar, MD, MBBS, FCCP
Rudy P Lackner, MD, FCCP
Viera Lakticova, MD
Carla R Lamb, MD, FCCP
Hans J Lee, MD, FCCP
Peter H Lenz, MD, MEd, FCCP
Stephanie M Levine, MD, FCCP
Deborah Jo Levine, MD, MS, FCCP
Andrea Loiselle, MD
Kenneth E Lyn-Kew, MD
Michael S Machuzak, MD, FCCP
Neil R MacIntyre, MD, FCCP
Donald A Mahler, MD, FCCP
Fabien Maldonado, MD, FCCP
Atul Malhotra, MD, FCCP
Darcy D Marciniuk, MD, FCCP
Diego J Maselli Caceres, MD, FCCP
Paul H Mayo, MD, FCCP
Peter J Mazzone, MD, MPH, FCCP
John K McIlwaine, DO, MBA, FCCP
Matthew C Miles, MD, FCCP
Scott Millington, MD
Taro Minami, MD, FCCP
Lisa K Moores, MD, FCCP
Amy E Morris, MD, FCCP
John J Mullon, MD, FCCP
Septimiu D Murgu, MD, FCCP
Mangala Narasimhan, DO, FCCP
Michael S Niederman, MD, FCCP
Alexander S Niven, MD, FCCP
Anne E O’Donnell, MD, FCCP
Erik C Osborn, MD
David E Ost, MD, MPH, FCCP
Ronald J Oudiz, MD, FCCP
Daniel R Ouellette, MD, MS, FCCP
Amit D Parulekar, MD, MS, FCCP
Nicholas J Pastis, MD, FCCP
Nina M Patel, MD, FCCP
Paru S Patrawalla, MD, FCCP
Jay I Peters, MD, FCCP
Barbara A Phillips, MD, MSPH, FCCP
Margaret A Pisani, MD, MS, FCCP
Janos Porszasz, MD, PhD
Whitney S Prince, MD, FCCP
Suhail Raoof, MBBS, Master FCCP
Ruben D Restrepo, RRT, FCCP
Marcos I Restrepo, MD, PhD, FCCP
Otis B Rickman, DO, FCCP
Roy D Ridgeway
Mary Ried, RN, CCRN
Linda Rogers, MD, FCCP
Mark J Rosen, MD, Master FCCP
Bernard J Roth, MD, FCCP
Ashutosh Sachdeva, MBBS, FCCP
Anthony G Saleh, MD, FCCP
Juan F Sanchez, MD, FCCP
Pralay K Sarkar, MBBS, FCCP
Lewis G Satterwhite, MD, BA, FCCP
Gregory A Schmidt, MD, FCCP
Mary Beth Scholand, MD, FCCP
David A Schulman, MD, MPH, FCCP
Brady Scott, RRT, MS, FCCP
Bernardo Selim, MD, FCCP
Curtis N Sessler, MD, FCCP
Rakesh D Shah, MD, FCCP
Ray Wes Shepherd, MD, FCCP
John H Sherner, MD, FCCP
Ariel L Shiloh, MD
Samira Shojaee, MD, FCCP
Marcos Silva Restrepo
Gerard A Silvestri, MD, MS, FCCP
Steven Q Simpson, MD, FCCP
James K Stoller, MD, MS, FCCP
Charlie Strange, MD, FCCP
Mary E Strek, MD, FCCP
William W Stringer, MD, FCCP
Eleanor M Summerhill, MD, FCCP
Maximiliano A Tamae Kakazu, MD, FCCP
Nichole T Tanner, MD, MS, FCCP
Lynn T Tanoue, MD, FCCP
Victor J Test, MD, FCCP
Arthur J Tokarczyk, MD, FCCP
Alain Tremblay, MD, FCCP
Adey Tsegaye, MD, FCCP
Anil Vachani, MD, FCCP
Momen M Wahidi, MD, MBA, FCCP
Keith M Wille, MD, FCCP
Lisa F Wolfe, MD
Richard G Wunderink, MD, FCCP
Lonny B Yarmus, DO, FCCP
Kazuhiro Yasufuku, MD, PhD, FCCP
Gulrukh Zaidi, MD, FCCP
David Zielinski, MD, FCCP
Everyone who attended CHEST Annual Meeting 2018 is a winner, but we would like to call out the winners participating in CHEST’s special categories of awards and events. Congratulations to all!
ANNUAL CHEST AWARDS
Master FCCP
David Gutterman, MD, Master FCCP
Distinguished Service Award
David Gutterman, MD, Master FCCP
College Medalist Award
Ghada Bourjeily, MD, FCCP
Master Clinician Educator
Lisa Moores, MD, FCCP
Early Career Clinician Educator
Amy Morris, MD, FCCP
Alfred Soffer Award for Editorial Excellence
Jean Rice
Presidential Citation
Darcy Marciniuk, MD, FCCP
Presidential Citation
D. Robert McCaffree, MD, Master FCCP
HONOR LECTURES AND MEMORIAL AWARDS
Edward C. Rosenow III, MD, Master FCCP/Master Teacher Honor Lecture Accelerated Aging in COPD and Its Comorbidities: Novel Therapeutic Targets
Peter Barnes, MD, Master FCCP
The lecture is generously funded by the CHEST Foundation.
Distinguished Scientist Honor Lecture in Cardiopulmonary Physiology
Understanding Diaphragm Performance: The Role of Ultrasound
F. Dennis McCool, MD, FCCP
The lecture is generously funded by the CHEST Foundation.
Presidential Honor Lecture
Asthma: Past, Present, and Future
Jay Peters, MD, FCCP
Thomas L. Petty, MD, Master FCCP Memorial Lecture
Recent Developments in Pulmonary Rehabilitation and Long-Term Oxygen Therapy: Would Tom Petty be Pleased?
Richard Casaburi, MD, PhD, FCCP
The lecture is generously funded by the CHEST Foundation.
Margaret Pfrommer Memorial Lecture in Long-term Mechanical Ventilation
Saving Lives…One Ventilator at a Time - HMV in 2018 and Beyond
Douglas McKim, MD, FCCP
The Margaret Pfrommer Memorial Lecture in Long-term Mechanical Ventilation is generously supported by International Ventilator Users Network of Post-Polio Health International and the CHEST Foundation.
Pasquale Ciaglia Memorial Lecture in Interventional Medicine
Evolution of Endobronchial Ultrasound: From Diagnostics to Therapeutics
Kazuhiro Yasufuku, MD, PhD, FCCP
The lecture is generously funded by the CHEST Foundation.
Roger C. Bone Memorial Lecture in Critical Care
Methylprednisolone in ARDS: A Highly Effective Treatment. How it Works, How to Use it
G. Umberto Meduri, MD
The lecture is generously funded by the CHEST Foundation.
CHEST FOUNDATION GRANT WINNERS
Distinguished Scholar
Robert C. Hyzy, MD, FCCP
Eli Lilly and Company Distinguished Scholar in Critical Care MedicineGrant Title: The Use of Electrical Impedance Tomography to Assess Mechanical Ventilation in Acute Respiratory Distress Syndrome
This grant is made possible due to the philanthropic support from Eli Lilly and Company.
Community Service Grantees
Deborah Haisch, MD
Columbia University Medical Center – New York, NY
CHEST Foundation Community Service Grant Honoring D. Robert McCaffree, MD, Master FCCP
Grant Title: East African Training Initiative in Pulmonary and Critical Care Medicine
Pamela Garrett, CCRN, MN
Gwinnett Medical Center – Lawrenceville, GA
CHEST Foundation Community Service Grant Honoring D. Robert McCaffree, MD, Master FCCP
Grant Title: Breathe Better Gwinnett
Phillip Sheridan
Mobile Care Chicago – Chicago, IL
CHEST Foundation Community Service Grant Honoring D. Robert McCaffree, MD, Master FCCP
Grant Title: Home Environment Education for Children with Asthma
These grants are supported in full by the CHEST Foundation.
Research Grant Winners
Ayodeji Adegunsoye, MD, MS
Research Grant in Pulmonary Fibrosis
Grant Title: Impact of Telomere Length on Pulmonary Fibrosis Clusters Across Diverse Racial Cohorts
Justin Oldham, MD, MS
Research Grant in Pulmonary Fibrosis
Grant Title: Plasma Biomarkers to Predict Outcomes and Treatment Response in Patients with Pulmonary Fibrosis
These grants above are supported by Boehringer Ingelheim Pharmaceuticals, Inc and Genentech.
Jacob Brenner, MD, PhD
Research Grant in Chronic Obstructive Pulmonary Disease
Grant Title: Ambulatory Cuirass Ventilation for Relief of Exertional Dyspnea in Severe COPD Patients
William Zhang, MD
Research Grant in Chronic Obstructive Pulmonary Disease
Grant Title: Pulmonary Iron Overload as a Novel COPD Endotype
These grants above are supported by AstraZeneca LP and Sunovion Pharmaceuticals Inc.
Margaret Bublitz, PhD
CHEST Foundation Research Grant in Women’s Lung Health
Grant Title: Sex as a Predictor of Sleep-Disordered Breathing and Its Consequences in Pregnancy
This grant is supported in full by the CHEST Foundation.
Tim Morris, MD, FCCP
CHEST Foundation Research Grant in Venous Thromboembolism
Grant Title: Long-term Follow-up of Acute Pulmonary Embolism
This grant is supported in full by the CHEST Foundation.
Monica Mukherjee, MD, MPH
CHEST Foundation Research Grant in Pulmonary Arterial Hypertension
Grant Title: Exercise Provocation in the Noninvasive Detection of Occult Right Ventricular Dysfunction and Emerging Pulmonary Hypertension in Systemic Sclerosis
This grant is supported in full by the CHEST Foundation.
Don Sanders, MD, MS
CHEST Foundation Research Grant in Cystic Fibrosis
Grant Title: Whole-genome Shotgun Sequencing of Oropharyngeal Swabs in Infants With CF
This grant is supported by Vertex Pharmaceuticals.
Imran Sulaiman, MD, PhD
CHEST Foundation Research Grant in Nontuberculosis Mycobacteria Diseases
Grant Title: Lower Airway Microbiota Signatures Associated W ith Impaired Immune Response in Non-Tuberculous Mycobacterium
This grant is supported by Insmed.
Samira Shojaee, MD, MPH, FCCP
CHEST Foundation Research Grant in Lung Cancer
Grant Title: Extracellular Vesicle miRNA as a Biomarker in Malignant Pleural Effusion
This grant is supported in full by the CHEST Foundation.
Anna Volerman, MD
CHEST Foundation Research Grant in Severe Asthma
Grant Title: A Randomized Clinical Trial Evaluating the Effectiveness of Virtual Teach-to-Goal(TM) Education versus Brief Intervention for Children with Severe Asthma
This grant is supported by AstraZeneca LP.
ABSTRACT AND CASE REPORT WINNERS
Alfred Soffer Research Award Winners
Clauden Louis, MD: Left ventricular assist devices in Intermacs 1 acute cardiogenic shock patients
Babith J. Mankidy, MBBS, FCCP: Reduction in in-hospital cardiac arrest with early interventions in the emergency department and non-ICU units by a novel approach of rapid response teams and mobile ICU management
Young Investigator Award Winners
Fayez Kheir, MD, MSc: Intrapleural tissue plasminogen activator and deoxyribonuclease therapy vs early medical thoracoscopy for treatment of pleural infection: a randomized clinical trial
Michael Rosman, MD: The utility of end tidal CO2 (ETCO2) monitoring during in-hospital cardiac arrest to predict return of spontaneous circulation
Top 5 Abstract Poster Winners
Neha Agarwal, MD: The 3 wishes project: a feasible intervention to improve end of life care in the ICU at UCLA
Hiroaki Harada, MD: Usefulness of comprehensive preoperative pulmonary rehabilitation program including intensive nutritional support concomitant with physical exercise through an interdisciplinary team approach
Joseph M. Carrington, DO, MHA: Targeting the trans-IL-6 signaling pathway to reduce agriculture organic dust exposure-induced airway inflammation in mice
Yu Kuang Lai, MBBCh: The utility of parametric response mapping in pulmonary graft vs host disease following hematopoietic stem cell transplant
Top Abstract Poster Finalists
Ligia M. Puiu, MD, PhD, FCCP: Association between echocardiographic and lipid parameters to workers in the metalliferous mines
Kush R. Dholakia, MD: Colloids vs crystalloids for postoperative resuscitation in patients undergoing off-pump coronary artery bypass surgery
Kulothungan Gunasekaran, MD, MBBS: Risk of VTE in idiopathic pulmonary fibrosis: a systematic review
Laura B. Sutton, PharmD: Ease and correct use of Ellipta by age in patients with asthma and COPD
Ankur Mogla, MD: To assess the utilization of pulmonary function testing for perioperative respiratory complications in bariatric surgery patients
Ali Ammar: Tracheostomy and admission diagnosis as predictors for an extended length of stay (ELOS)
Charlene Kalani, PharmD: Efficacy and safety of direct oral anticoagulants (DOACS) in morbidly obese patients
Jonghoo Lee, MD: Performances of modified CRB-65 score compared to SIRS and QSOFA as a rapid screening tool for sepsis among infected patients in initial emergency department: a propensity score matching study
Frank J. Trudo, MD, FCCP: Clinical burden of eosinophilic COPD
Elise L. Stephenson, MD: Vitamin C and point of care glucose measurements: a retrospective, observational study
Faisal Siddiqi, MD: Implementation of an early mobility program in the medical ICU
Eileen Harder, MD: Connective tissue disease-associated pulmonary arterial hypertension hospitalizations from 2001-2014
Sophie Korzan, MD: Exhaled nitric oxide and asthma-COPD overlap in patients hospitalized with exacerbations of airway disease: preliminary observations
Andreas Grove, MD: MicroRNA (MIRNA) and biological markers discriminate between normotensive and prehypertensive young men in hypobaric hypoxic environments
Snigdha Nutalapati, MBBS: Large cell neuroendocrine cancer of the lung: SEER 2004-2014 analysis
Anubhav Jain, MBBS: Survival benefit of beta-blockers in patients hospitalized for acute exacerbation of COPD
Case Report Slide Winners
Ze Ying Tan: All that wheezes is not asthma
Jason Lam: Pulmonary mucor mycetoma
Adam Young: Nonresolving pneumonia and cyclic fevers in an immunocompetent patient
Ritu Modi: Histopathological misdiagnosis of pulmonary coccidiodes
Argun Can: A rare inborn error of fatty acid oxidation presenting with severe hyperammonemia in the ICU
Morgan Gilani: A colorful cause of cardiovascular collapse
Katie Jeans: A sweet surprise
Anthony Mattox: Unusual case of interstitial lung disease
Andrew Berglund: Pulmonary light chain deposition disease in a 29-year-old army soldier
Cristia Maysol Morales: A case report of a primary malignant melanoma of anterior mediastinum
Anthony McClafferty: Fibrosing mediastinitis and rheumatoid arthritis: an autoimmune inflammatory connection
Ahmed Munir: HIV with disseminated tularemia: a rare presentation Benjamin Garren: Mycobacterium avium complex mediastinal lymphadenitis in an immunocompetent adolescent with erosion into the airway
Robert Hilton: Obtunded with a chest mass: a case of a rare neurologic paraneoplastic syndrome,
Audra Schwalk: Mucoepidermoid carcinoma: a rare malignancy treated endobronchially
Jessica Riggs: Successful transplantation defies genetics: a case of rapidly-progressive pulmonary fibrosis due to Hermansky-Pudlak syndrome
Meghan Cirulis: Acute vasodilator testing: an opportunity to refine study design and provide precision care in pulmonary hypertension
Patrick Chan: VATS lobectomy for bronchial atresia in an adult
Andrew Mehlman: Multivessel coronary artery aneurysms presenting as myocardial ischemia
Scott Maughan: Diagnosing milliary Mycobacterium bovis from the prostate of an immunocompetent host
Adam Austin: Survived ECMO, death by BLASTO: the first reported fatal case of disseminated blastomycosis in pregnancy
Tie: Donnie Carter: Subclinical polycythemia vera presenting as extensive thrombosis due to massive transfusion, and
Lindsay Hammons: Rare case of Serratia pneumonia causing transient aplastic anemia
Paola Baskin: Novel observations during point-of-care ultrasound (POCUS) in cardiopulmonary resuscitation: a case of ultrasound-guided probe pressure to reduce esophageal insufflation during bag-valve-mask ventilator
David Dennis: Pulmonary alveolar proteinosis presenting as intracerebral nocardiosis
Rakin Choudhury: Severe asthma caused by therapy-resistant asthmatic granulomatosis
Andrew Lytle: Lung adenocarcinoma in a patient with Turcot syndrome
Chelsea Leipold: Case of a granulomatous-lymphocytic interstitial lung disease in a patient with common variable immunodeficiency disorder
Galyna Ivashchuk: Double trouble: ANCA vasculitis with concomitant IGA nephropathy presenting as massive diffuse alveolar hemorrhage and fulminant renal failure
Case Report Poster Winners
Christine Zhou: Role of transbronchial lung cryobiopsy in the diagnosis of adenocarcinoma in situ
Parin Shah: A rare case of Erdheim-Chester disease masquerading as metastatic lung cancer
Avanthika Wynn : A rare asthma mimic
Muhammad S. Ali: Severe pancolitis: a rare adverse effect of nintedanib
Brian Foster: Don’t forget to breathe: a case of hypoxemia after carotid body resection
Kelly Pennington: Intra-cardiac embolization of an inferior vena cava filter resulting in cardiac arrest
George Elkomos-Botros: Acute generalized exanthematous pustulosis presenting as distributive shock with multi-organ failure
Ashley M. Scott: Avian occupational hypersensitivity pneumonitis in a restaurant employee
Andrew Polito: Pulmonary amyloidosis: an unusual presentation of a rare disease
CHEST B-I-N-G-O WINNERS
Stella Ogake, MD
Erin E. Peterson, APRN, CNP
Megan J. Castillo, PA-C
Gretchen R. Winter, MD
Jeanette P. Brown, MD, PhD
Yu Hong Chan, MBBS
Anita Naik, DO
Gary A. Aaronson, DO, FCCP
Allison S. Cowl, MD
Kyle Halligan, MD
Palaniappan Muthappan, MD
Faizullah S. Lokhandwala, MBBS, FCCP
Jamie R. Chua, MD
Francis L. Ervin, MD, FCCP
Robyn Luper
CHEST CHALLENGE WINNER (AND RUNNER’S-UP)
Emory University (First Place)
Mirza Haider Ali, MD
Mohleen Kang, MD
Matthew Schimmel, MD
University of Michigan (Second Place)
Patrick Bradley, MD
Matthew Hensley, MD
Bonnie Wang, MD
Cleveland Clinic (Third Place)
Jorge Mirales-Estrella, MD
Apostolos Perelas, MD
Gretchen Winter, MD
2018 DISTINGUISHED CHEST EDUCATORS
Michael H Ackerman, DNSc
Sandra G Adams, MD, MS, FCCP
Doreen J Addrizzo-Harris, MD, FCCP
Cara Lyn Agerstrand, MD, BS
Jason A Akulian, MD, FCCP
Raed H Alalawi, MD, FCCP
A. Christine Argento, MD, FCCP
Robert Arntfield, MD, FCCP
Alex A Balekian, MD
Meyer S Balter, MD, FCCP
Gisela I Banauch, MD, MS, FCCP
Robert P Baughman, MD, FCCP
David G Bell, MD, FCCP
Michel A Boivin, MD, FCCP
Gabriel T Bosslet, MD, FCCP
Jean Bourbeau, MD, MS, FCCP
Ghada R Bourjeily, MD, FCCP
David L Bowton, MD, FCCM
Jack D Buckley, MD, MPH, FCCP
Marie M Budev, DO, MPH, FCCP
Kristin M Burkart, MD, MS, FCCP
Brian Carlin, MD, FCCP
Christopher L Carroll, MD, FCCP
Roberto F Casal, MD
Kevin M Chan, MD, FCCP
Subani Chandra, MD, FCCP
Ching-Fei Chang, MD
Alexander C Chen, MD
Nancy A Collop, MD, FCCP
Clayton T Cowl, MD, MS, FCCP
Angel O Coz Yataco, MD, FCCP
Gerard J Criner, MD, FCCP
Carolyn M D’Ambrosio, MD, FCCP
Mauricio Danckers, MD, FCCP
Aneesa M Das, MD, FCCP
John Davies, RRT, MA, FCCP
Zachary S DePew, MD, FCCP
Frank C Detterbeck, MD, FCCP
Naresh A. Dewan, MBBS, FCCP
Kevin C Doerschug, MD, MS, FCCP
Meagan Dubosky, RRT-ACCS
Kevin M Dushay, MD, FCCP
Eric S Edell, MD, FCCP
Jean M Elwing, MD, FCCP
William Enfinger
Michael E Ezzie, MD, FCCP
Kevin J Felner, MD, FCCP
Mark E Fenton, MD, MSc, FCCP
Jason Filopei, MD
Neil S Freedman, MD, FCCP
Laura Kathleen Frye, MD
Thomas M Fuhrman, MD, MS, FCCP
John P Gaillard, MD, FCCP
Colin T Gillespie, MD
Yonatan Y Greenstein, MD
Maritza L Groth, MD, FCCP
Keith P Guevarra, DO, FCCP
Jesse B Hall, MD, FCCP
Nicola A Hanania, MD, MBBS, FCCP
D Kyle Hogarth, MD, FCCP
Steven M Hollenberg, MD, FCCP
David W Hsia, MD, FCCP
Candace A Huebert, MD, FCCP
Robert C Hyzy, MD, FCCP
Octavian C Ioachimescu, MD, PhD, FCCP
Richard S Irwin, MD, Master FCCP
Kirk D Jones, MD
Nader Kamangar, MD, MS, FCCP
Carl A Kaplan, MD, FCCP
Brian S Kaufman, MD, FCCP
William F Kelly, MD, FCCP
Marcus P Kennedy, MD, FCCP
Sandhya Khurana, MD, FCCP
James R Klinger, MD, FCCP
Seth J Koenig, MD, FCCP
Lindsey Kreisher, RRT
Karol Kremens, MD, FCCP
Patricia A Kritek, MD, FCCP
Sunita Kumar, MD, MBBS, FCCP
Rudy P Lackner, MD, FCCP
Viera Lakticova, MD
Carla R Lamb, MD, FCCP
Hans J Lee, MD, FCCP
Peter H Lenz, MD, MEd, FCCP
Stephanie M Levine, MD, FCCP
Deborah Jo Levine, MD, MS, FCCP
Andrea Loiselle, MD
Kenneth E Lyn-Kew, MD
Michael S Machuzak, MD, FCCP
Neil R MacIntyre, MD, FCCP
Donald A Mahler, MD, FCCP
Fabien Maldonado, MD, FCCP
Atul Malhotra, MD, FCCP
Darcy D Marciniuk, MD, FCCP
Diego J Maselli Caceres, MD, FCCP
Paul H Mayo, MD, FCCP
Peter J Mazzone, MD, MPH, FCCP
John K McIlwaine, DO, MBA, FCCP
Matthew C Miles, MD, FCCP
Scott Millington, MD
Taro Minami, MD, FCCP
Lisa K Moores, MD, FCCP
Amy E Morris, MD, FCCP
John J Mullon, MD, FCCP
Septimiu D Murgu, MD, FCCP
Mangala Narasimhan, DO, FCCP
Michael S Niederman, MD, FCCP
Alexander S Niven, MD, FCCP
Anne E O’Donnell, MD, FCCP
Erik C Osborn, MD
David E Ost, MD, MPH, FCCP
Ronald J Oudiz, MD, FCCP
Daniel R Ouellette, MD, MS, FCCP
Amit D Parulekar, MD, MS, FCCP
Nicholas J Pastis, MD, FCCP
Nina M Patel, MD, FCCP
Paru S Patrawalla, MD, FCCP
Jay I Peters, MD, FCCP
Barbara A Phillips, MD, MSPH, FCCP
Margaret A Pisani, MD, MS, FCCP
Janos Porszasz, MD, PhD
Whitney S Prince, MD, FCCP
Suhail Raoof, MBBS, Master FCCP
Ruben D Restrepo, RRT, FCCP
Marcos I Restrepo, MD, PhD, FCCP
Otis B Rickman, DO, FCCP
Roy D Ridgeway
Mary Ried, RN, CCRN
Linda Rogers, MD, FCCP
Mark J Rosen, MD, Master FCCP
Bernard J Roth, MD, FCCP
Ashutosh Sachdeva, MBBS, FCCP
Anthony G Saleh, MD, FCCP
Juan F Sanchez, MD, FCCP
Pralay K Sarkar, MBBS, FCCP
Lewis G Satterwhite, MD, BA, FCCP
Gregory A Schmidt, MD, FCCP
Mary Beth Scholand, MD, FCCP
David A Schulman, MD, MPH, FCCP
Brady Scott, RRT, MS, FCCP
Bernardo Selim, MD, FCCP
Curtis N Sessler, MD, FCCP
Rakesh D Shah, MD, FCCP
Ray Wes Shepherd, MD, FCCP
John H Sherner, MD, FCCP
Ariel L Shiloh, MD
Samira Shojaee, MD, FCCP
Marcos Silva Restrepo
Gerard A Silvestri, MD, MS, FCCP
Steven Q Simpson, MD, FCCP
James K Stoller, MD, MS, FCCP
Charlie Strange, MD, FCCP
Mary E Strek, MD, FCCP
William W Stringer, MD, FCCP
Eleanor M Summerhill, MD, FCCP
Maximiliano A Tamae Kakazu, MD, FCCP
Nichole T Tanner, MD, MS, FCCP
Lynn T Tanoue, MD, FCCP
Victor J Test, MD, FCCP
Arthur J Tokarczyk, MD, FCCP
Alain Tremblay, MD, FCCP
Adey Tsegaye, MD, FCCP
Anil Vachani, MD, FCCP
Momen M Wahidi, MD, MBA, FCCP
Keith M Wille, MD, FCCP
Lisa F Wolfe, MD
Richard G Wunderink, MD, FCCP
Lonny B Yarmus, DO, FCCP
Kazuhiro Yasufuku, MD, PhD, FCCP
Gulrukh Zaidi, MD, FCCP
David Zielinski, MD, FCCP
Introducing CHEST’s new CEO/EVP
Greetings! My name is Robert Musacchio; I am proud to introduce myself as the new Chief Executive Officer and Executive Vice President of CHEST. I am honored to join this team of distinguished clinicians as we spearhead progress in the fight against lung disease.
I have had the pleasure of working at CHEST for the last 4 years, first joining CHEST Enterprises as Senior Vice President of Business Development. In that role, I focused on revenue growth and product diversification before becoming COO of CHEST. As COO, I dedicated myself to strengthening our team by mentoring staff and collaborating with senior leadership, a challenge that I have deeply enjoyed.
Before joining CHEST, I worked at the American Medical Association for 35 years in roles encompassing research, advocacy, membership, and publishing. I also worked with boards and membership groups as a member of the AMA’s CPT® Editorial Panel and as a publisher for JAMA.
As CEO, I hope to leverage those experiences to support CHEST in its mission, which is to improve lung health not just for 1 year but for the next 25 years. For that reason, our leadership team has outlined an organizational culture that fosters short-term success and long-term innovation, focusing on four key areas:
People: How do we attract and retain the right people?
Strategy: How do we create a truly differentiated strategy?
Execution: How do we improve our process to drive flawless execution?
Resources: How do we ensure that we have sufficient resources to invest in our mission?
Those questions in mind, we have established several standards that guide the way we work. We are focusing on leading with integrity, cultivating passion and innovation, honoring our team, and having fun while we deliver cutting-edge education and create community for our members. With these norms, we can continue to foster an environment that generates results. This, in turn, will enable CHEST to fulfill its core purpose of crushing lung disease.
We can crush lung disease by arming our members with industry-leading education offerings—including simulation experiences and live lab courses—and expanding them worldwide to Thailand and Greece in 2019. We can crush lung disease by using cutting-edge technologies—including interactive gaming platforms—to glean further insights. We can crush lung disease by connecting our membership of nearly 20,000 pulmonary, critical care, and sleep medicine professionals to innovative education tools, along with a network of prestigious colleagues to deliver the highest quality patient care.
Most importantly, we can crush lung disease by empowering our members in their work—if you care about lung disease, we care about you!
And, if you care about lung disease, I am excited to partner with you in this cause. I am thankful for this opportunity to lead CHEST and the CHEST Foundation into the future and look forward to working with you.
Greetings! My name is Robert Musacchio; I am proud to introduce myself as the new Chief Executive Officer and Executive Vice President of CHEST. I am honored to join this team of distinguished clinicians as we spearhead progress in the fight against lung disease.
I have had the pleasure of working at CHEST for the last 4 years, first joining CHEST Enterprises as Senior Vice President of Business Development. In that role, I focused on revenue growth and product diversification before becoming COO of CHEST. As COO, I dedicated myself to strengthening our team by mentoring staff and collaborating with senior leadership, a challenge that I have deeply enjoyed.
Before joining CHEST, I worked at the American Medical Association for 35 years in roles encompassing research, advocacy, membership, and publishing. I also worked with boards and membership groups as a member of the AMA’s CPT® Editorial Panel and as a publisher for JAMA.
As CEO, I hope to leverage those experiences to support CHEST in its mission, which is to improve lung health not just for 1 year but for the next 25 years. For that reason, our leadership team has outlined an organizational culture that fosters short-term success and long-term innovation, focusing on four key areas:
People: How do we attract and retain the right people?
Strategy: How do we create a truly differentiated strategy?
Execution: How do we improve our process to drive flawless execution?
Resources: How do we ensure that we have sufficient resources to invest in our mission?
Those questions in mind, we have established several standards that guide the way we work. We are focusing on leading with integrity, cultivating passion and innovation, honoring our team, and having fun while we deliver cutting-edge education and create community for our members. With these norms, we can continue to foster an environment that generates results. This, in turn, will enable CHEST to fulfill its core purpose of crushing lung disease.
We can crush lung disease by arming our members with industry-leading education offerings—including simulation experiences and live lab courses—and expanding them worldwide to Thailand and Greece in 2019. We can crush lung disease by using cutting-edge technologies—including interactive gaming platforms—to glean further insights. We can crush lung disease by connecting our membership of nearly 20,000 pulmonary, critical care, and sleep medicine professionals to innovative education tools, along with a network of prestigious colleagues to deliver the highest quality patient care.
Most importantly, we can crush lung disease by empowering our members in their work—if you care about lung disease, we care about you!
And, if you care about lung disease, I am excited to partner with you in this cause. I am thankful for this opportunity to lead CHEST and the CHEST Foundation into the future and look forward to working with you.
Greetings! My name is Robert Musacchio; I am proud to introduce myself as the new Chief Executive Officer and Executive Vice President of CHEST. I am honored to join this team of distinguished clinicians as we spearhead progress in the fight against lung disease.
I have had the pleasure of working at CHEST for the last 4 years, first joining CHEST Enterprises as Senior Vice President of Business Development. In that role, I focused on revenue growth and product diversification before becoming COO of CHEST. As COO, I dedicated myself to strengthening our team by mentoring staff and collaborating with senior leadership, a challenge that I have deeply enjoyed.
Before joining CHEST, I worked at the American Medical Association for 35 years in roles encompassing research, advocacy, membership, and publishing. I also worked with boards and membership groups as a member of the AMA’s CPT® Editorial Panel and as a publisher for JAMA.
As CEO, I hope to leverage those experiences to support CHEST in its mission, which is to improve lung health not just for 1 year but for the next 25 years. For that reason, our leadership team has outlined an organizational culture that fosters short-term success and long-term innovation, focusing on four key areas:
People: How do we attract and retain the right people?
Strategy: How do we create a truly differentiated strategy?
Execution: How do we improve our process to drive flawless execution?
Resources: How do we ensure that we have sufficient resources to invest in our mission?
Those questions in mind, we have established several standards that guide the way we work. We are focusing on leading with integrity, cultivating passion and innovation, honoring our team, and having fun while we deliver cutting-edge education and create community for our members. With these norms, we can continue to foster an environment that generates results. This, in turn, will enable CHEST to fulfill its core purpose of crushing lung disease.
We can crush lung disease by arming our members with industry-leading education offerings—including simulation experiences and live lab courses—and expanding them worldwide to Thailand and Greece in 2019. We can crush lung disease by using cutting-edge technologies—including interactive gaming platforms—to glean further insights. We can crush lung disease by connecting our membership of nearly 20,000 pulmonary, critical care, and sleep medicine professionals to innovative education tools, along with a network of prestigious colleagues to deliver the highest quality patient care.
Most importantly, we can crush lung disease by empowering our members in their work—if you care about lung disease, we care about you!
And, if you care about lung disease, I am excited to partner with you in this cause. I am thankful for this opportunity to lead CHEST and the CHEST Foundation into the future and look forward to working with you.
ASTHMA-COPD Overlap resource
https://www.medscape.com/viewarticle/902668?src=par_chest_stm_mscpedt&faf=1
https://www.medscape.com/viewarticle/902668?src=par_chest_stm_mscpedt&faf=1
https://www.medscape.com/viewarticle/902668?src=par_chest_stm_mscpedt&faf=1
New Updates to Afib Guidelines from CHEST
The American College of Chest Physicians® announced updates to the evidence-based guidelines on antithrombotic therapy for atrial fibrillation. The guideline panel submitted the manuscript, Antithrombotic Therapy for Atrial Fibrillation: CHEST Guideline and Expert Panel Report, for publication in the journal CHEST®.
Key recommendations and shifts from previous guidelines include:
• For patients with atrial fibrillation without valvular heart disease, including those with paroxysmal atrial fibrillation who are at low risk of stroke (eg, CHA2DS2VASc score of 0 in males or 1 in females), we suggest no antithrombotic therapy.
• For patients with a single non-sex CHA2DS2VASc stroke risk factor, we suggest oral anticoagulation rather than no therapy, aspirin or combination therapy with aspirin and clopidogrel.
• For those at high risk of stroke, we recommend oral anticoagulation rather than no therapy, aspirin or combination therapy with aspirin and clopidogrel.
• Where we recommend or suggest in favor of oral anticoagulation, we suggest using a novel oral anticoagulant (NOAC) rather than adjusted-dose vitamin K antagonist therapy. With the latter, it is important to aim for good quality anticoagulation control with a time in therapeutic range (TTR) >70%.
• Attention to modifiable bleeding risk factors should be made at each patient contact, and HAS-BLED score should be used to assess the risk of bleeding where high-risk patients (>=3) can be identified for earlier review and follow-up visits.
The complete guideline article is free to view in the Online First section of the journal CHEST.
The American College of Chest Physicians® announced updates to the evidence-based guidelines on antithrombotic therapy for atrial fibrillation. The guideline panel submitted the manuscript, Antithrombotic Therapy for Atrial Fibrillation: CHEST Guideline and Expert Panel Report, for publication in the journal CHEST®.
Key recommendations and shifts from previous guidelines include:
• For patients with atrial fibrillation without valvular heart disease, including those with paroxysmal atrial fibrillation who are at low risk of stroke (eg, CHA2DS2VASc score of 0 in males or 1 in females), we suggest no antithrombotic therapy.
• For patients with a single non-sex CHA2DS2VASc stroke risk factor, we suggest oral anticoagulation rather than no therapy, aspirin or combination therapy with aspirin and clopidogrel.
• For those at high risk of stroke, we recommend oral anticoagulation rather than no therapy, aspirin or combination therapy with aspirin and clopidogrel.
• Where we recommend or suggest in favor of oral anticoagulation, we suggest using a novel oral anticoagulant (NOAC) rather than adjusted-dose vitamin K antagonist therapy. With the latter, it is important to aim for good quality anticoagulation control with a time in therapeutic range (TTR) >70%.
• Attention to modifiable bleeding risk factors should be made at each patient contact, and HAS-BLED score should be used to assess the risk of bleeding where high-risk patients (>=3) can be identified for earlier review and follow-up visits.
The complete guideline article is free to view in the Online First section of the journal CHEST.
The American College of Chest Physicians® announced updates to the evidence-based guidelines on antithrombotic therapy for atrial fibrillation. The guideline panel submitted the manuscript, Antithrombotic Therapy for Atrial Fibrillation: CHEST Guideline and Expert Panel Report, for publication in the journal CHEST®.
Key recommendations and shifts from previous guidelines include:
• For patients with atrial fibrillation without valvular heart disease, including those with paroxysmal atrial fibrillation who are at low risk of stroke (eg, CHA2DS2VASc score of 0 in males or 1 in females), we suggest no antithrombotic therapy.
• For patients with a single non-sex CHA2DS2VASc stroke risk factor, we suggest oral anticoagulation rather than no therapy, aspirin or combination therapy with aspirin and clopidogrel.
• For those at high risk of stroke, we recommend oral anticoagulation rather than no therapy, aspirin or combination therapy with aspirin and clopidogrel.
• Where we recommend or suggest in favor of oral anticoagulation, we suggest using a novel oral anticoagulant (NOAC) rather than adjusted-dose vitamin K antagonist therapy. With the latter, it is important to aim for good quality anticoagulation control with a time in therapeutic range (TTR) >70%.
• Attention to modifiable bleeding risk factors should be made at each patient contact, and HAS-BLED score should be used to assess the risk of bleeding where high-risk patients (>=3) can be identified for earlier review and follow-up visits.
The complete guideline article is free to view in the Online First section of the journal CHEST.
National Board of Echocardiography offering board exam
Due to significant interest in the pulmonary/critical care community, the National Board of Echocardiography (NBE) has opened registration for a board examination as a requirement for national level certification in advanced critical care echocardiography (ACCE). The examination has been developed by the National Board of Medical Examiners; CHEST and the other professional societies are well represented on the writing committee. The first examination is scheduled to be given on January 15, 2019.
The board of the NBE will be the final arbiter for other requirements for certification. We anticipate that these will be available in 2019.
A few essential questions about the certification:
1. Who will be eligible for certification in ACCE?
The policy of the NBE is that any licensed physician may take the examination. Passing the examination confers testamur status, which is only one of several requirements for certification. The board of the NBE will make the final decision as to how to define the clinical background of the candidate that will be required for certification.
2. What will be the requirements for demonstration of competence at image acquisition for ACCE?
Competence at ACCE requires that the intensivist be expert at image acquisition of a comprehensive image set. The board of the NBE will make the final decision as to what constitutes a full ACCE image set, how many studies must be performed by the candidate, and how the studies will be documented. Regarding the latter question, it is likely that there will be a need for identification of qualified mentors to guide the candidate through the process of demonstrating competence in image acquisition.
3. What resources exist to learn more about the examination?
For some suggestions regarding mastery of the cognitive base, Dr. Yonatan Greenstein has set up an independent website that has recommendations about study material and an example of the full ACCE image set (advancedcriticalcareecho.org). The NBE website has a list of subjects that will be covered in the examination. In addition to passing the examination, there will be other elements required for ACCE certification. The NBE has not yet made final decision on the additional requirements. As soon as they are available, they will be posted on the NBE website (echoboards.org).
There is keen interest amongst fellows and junior attendings in the NBE certification who are already competent in whole body ultrasonography. They see ACCE as a natural and necessary extension of their scope of practice, as a means of better helping their critically ill patients, and as a means of acquiring a unique skill that defines them as having a special skill compared with other intensivists. A smaller group of senior attending intensivists are primarily motivated by a well-defined practice-related need of skill at ACCE and/or a strong perception that knowledge of ACCE may directly improve their ability to care for the critically ill patient. Interest in certification extends across the various specialties that provide critical care services. The NBE has indicated that there has been a strong showing of registrations for the examination thus far.
We recommend that candidates for certification consider that passing the examination should be the priority. Collection of the image set may occur in parallel, as the two will complement each other. Preparation for the examination requires intensive study of the cognitive base of ACCE and mastery of image interpretation.
To aid in preparation for the ACCE examination, CHEST is offering a comprehensive review course, Advanced Critical Care Echocardiography Board Review Exam Course, being held at the CHEST Innovation, Simulation, and Training Center, December 7-8, 2018, in Glenview, Illinois.
Due to significant interest in the pulmonary/critical care community, the National Board of Echocardiography (NBE) has opened registration for a board examination as a requirement for national level certification in advanced critical care echocardiography (ACCE). The examination has been developed by the National Board of Medical Examiners; CHEST and the other professional societies are well represented on the writing committee. The first examination is scheduled to be given on January 15, 2019.
The board of the NBE will be the final arbiter for other requirements for certification. We anticipate that these will be available in 2019.
A few essential questions about the certification:
1. Who will be eligible for certification in ACCE?
The policy of the NBE is that any licensed physician may take the examination. Passing the examination confers testamur status, which is only one of several requirements for certification. The board of the NBE will make the final decision as to how to define the clinical background of the candidate that will be required for certification.
2. What will be the requirements for demonstration of competence at image acquisition for ACCE?
Competence at ACCE requires that the intensivist be expert at image acquisition of a comprehensive image set. The board of the NBE will make the final decision as to what constitutes a full ACCE image set, how many studies must be performed by the candidate, and how the studies will be documented. Regarding the latter question, it is likely that there will be a need for identification of qualified mentors to guide the candidate through the process of demonstrating competence in image acquisition.
3. What resources exist to learn more about the examination?
For some suggestions regarding mastery of the cognitive base, Dr. Yonatan Greenstein has set up an independent website that has recommendations about study material and an example of the full ACCE image set (advancedcriticalcareecho.org). The NBE website has a list of subjects that will be covered in the examination. In addition to passing the examination, there will be other elements required for ACCE certification. The NBE has not yet made final decision on the additional requirements. As soon as they are available, they will be posted on the NBE website (echoboards.org).
There is keen interest amongst fellows and junior attendings in the NBE certification who are already competent in whole body ultrasonography. They see ACCE as a natural and necessary extension of their scope of practice, as a means of better helping their critically ill patients, and as a means of acquiring a unique skill that defines them as having a special skill compared with other intensivists. A smaller group of senior attending intensivists are primarily motivated by a well-defined practice-related need of skill at ACCE and/or a strong perception that knowledge of ACCE may directly improve their ability to care for the critically ill patient. Interest in certification extends across the various specialties that provide critical care services. The NBE has indicated that there has been a strong showing of registrations for the examination thus far.
We recommend that candidates for certification consider that passing the examination should be the priority. Collection of the image set may occur in parallel, as the two will complement each other. Preparation for the examination requires intensive study of the cognitive base of ACCE and mastery of image interpretation.
To aid in preparation for the ACCE examination, CHEST is offering a comprehensive review course, Advanced Critical Care Echocardiography Board Review Exam Course, being held at the CHEST Innovation, Simulation, and Training Center, December 7-8, 2018, in Glenview, Illinois.
Due to significant interest in the pulmonary/critical care community, the National Board of Echocardiography (NBE) has opened registration for a board examination as a requirement for national level certification in advanced critical care echocardiography (ACCE). The examination has been developed by the National Board of Medical Examiners; CHEST and the other professional societies are well represented on the writing committee. The first examination is scheduled to be given on January 15, 2019.
The board of the NBE will be the final arbiter for other requirements for certification. We anticipate that these will be available in 2019.
A few essential questions about the certification:
1. Who will be eligible for certification in ACCE?
The policy of the NBE is that any licensed physician may take the examination. Passing the examination confers testamur status, which is only one of several requirements for certification. The board of the NBE will make the final decision as to how to define the clinical background of the candidate that will be required for certification.
2. What will be the requirements for demonstration of competence at image acquisition for ACCE?
Competence at ACCE requires that the intensivist be expert at image acquisition of a comprehensive image set. The board of the NBE will make the final decision as to what constitutes a full ACCE image set, how many studies must be performed by the candidate, and how the studies will be documented. Regarding the latter question, it is likely that there will be a need for identification of qualified mentors to guide the candidate through the process of demonstrating competence in image acquisition.
3. What resources exist to learn more about the examination?
For some suggestions regarding mastery of the cognitive base, Dr. Yonatan Greenstein has set up an independent website that has recommendations about study material and an example of the full ACCE image set (advancedcriticalcareecho.org). The NBE website has a list of subjects that will be covered in the examination. In addition to passing the examination, there will be other elements required for ACCE certification. The NBE has not yet made final decision on the additional requirements. As soon as they are available, they will be posted on the NBE website (echoboards.org).
There is keen interest amongst fellows and junior attendings in the NBE certification who are already competent in whole body ultrasonography. They see ACCE as a natural and necessary extension of their scope of practice, as a means of better helping their critically ill patients, and as a means of acquiring a unique skill that defines them as having a special skill compared with other intensivists. A smaller group of senior attending intensivists are primarily motivated by a well-defined practice-related need of skill at ACCE and/or a strong perception that knowledge of ACCE may directly improve their ability to care for the critically ill patient. Interest in certification extends across the various specialties that provide critical care services. The NBE has indicated that there has been a strong showing of registrations for the examination thus far.
We recommend that candidates for certification consider that passing the examination should be the priority. Collection of the image set may occur in parallel, as the two will complement each other. Preparation for the examination requires intensive study of the cognitive base of ACCE and mastery of image interpretation.
To aid in preparation for the ACCE examination, CHEST is offering a comprehensive review course, Advanced Critical Care Echocardiography Board Review Exam Course, being held at the CHEST Innovation, Simulation, and Training Center, December 7-8, 2018, in Glenview, Illinois.
Interventional Chest/Diagnostic Procedures
Interventional Chest/Diagnostic Procedures
Endobronchial valve therapy receives FDA approval for bronchoscopic LVR
Lung volume reduction surgery (LVRS) is an established approach to improve exercise capacity and lung function in patients with heterogeneous emphysema and may confer survival benefit in patients with apical-predominant disease (Fishman, et al. N Engl J Med. 2003;348[21]:2059). Despite this, LVRS case numbers remain low due to patient and procedural morbidity. Bronchoscopic alternatives for LVRS have advanced considerably over the last decade with endobronchial valve (EBV) therapy emerging as a viable option for select subsets of patients with heterogeneous emphysema. Endobronchial valves are removable devices placed in segmental/subsegmental airways, which allow efflux of air during exhalation but close during inspiration, resulting in distal atelectasis in the absence of collateral ventilation.
The LIBERATE study, a multicenter randomized controlled trial demonstrated improvement in FEV1 ≥15% in 48% of patients after EBV placement compared with 17% of patients receiving standard medical therapy has resulted in FDA approval (Criner G, et al. Am J Respir Crit Care Med. 2018 May 22. doi: 10.1164/rccm.201803-0590OC. [Epub ahead of print]). Patients with EBV had improved subjective dyspnea scores, residual volume, and 6-minute walk distance; however, the pneumothorax rate was 27%.
All study patients with EBV underwent bronchoscopic evaluation for collateral ventilation using a proprietary digital system, which measures expiratory airflow in target airways to establish the presence of collateral ventilation. Previous data have demonstrated improved transplant-free survival when implanted EBVs result in atelectasis of the target lobe, which requires intact interlobar fissures (Garner, et al. Am J Respir Crit Care Med. 2016;194[4]:519). Ongoing clinical trials are attempting to clarify the role of EBV therapy in different phenotypes of COPD, including patients with homogenous emphysema. Long-term follow-up data will be important in determining the broader implementation of bronchoscopic lung volume reduction moving forward.
Vivek Murthy, MD
Jason A. Akulian, MD, FCCP
Steering Committee Members
Pediatric Chest Medicine
CFTR modulators
Cystic fibrosis (CF) is a progressive genetic disorder resulting in multiorgan disease with progressive respiratory decline. CF is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This codes for the CFTR anion channel and contributes to the movement of salt in and out of the cell. CFTR dysfunction leads to thickened secretions in the lungs and other organs, such as the gut and pancreas. This leads to more lung infections and other organ dysfunction that ultimately leads to premature death.
Established CF treatments include pulmonary and nutritional interventions. CFTR modulators are recent novel therapies that improve the function of CFTR and target the basic defect. Two types of modulator drugs (potentiators and correctors) have been developed with effectiveness depending upon the kind of CF mutation the person has.
CFTR potentiators, such as Kalydeco® (ivacaftor monotherapy), increase the likelihood that the CFTR channel will transport ions through the cell membrane, ie, they increase the channel’s “open probability.” Kalydeco has been approved for patients 12 months or older with mutations that result in partial CFTR protein function in the cell membrane. CFTR correctors, such as lumacaftor and tezacaftor, increase the amount of normal or mutated CFTR protein that gets transported, increasing the amount of CFTR protein on the cell surface. Combination drugs such as Orkambi® (lumacaftor/ivacaftor) for patients 2 years and older, and Symdeko™ (tezacaftor/ivacaftor) for patients 12 years and older, are considered in patients homozygous for the F508del mutation.
Sumit Bhargava, MBBS, FCCP
Steering Committee Member
Pulmonary Physiology, Function, and Rehabilitation
Wildfires, particulate matter, and lung function
In the last 3 decades, human-caused climate change contributed to wildfires in an additional 4.2 million hectares of land across the western US alone. Human impact on climate is responsible for nearly doubling the expected wildfire area (Abatzoglou, et al. PNAS. 2016;113:11770). Year 2017 saw the most destructive wildfires in California recorded to date, and over $2 billion dollars was spent by the US Forest Service, the most-expensive on record. Besides the devastating effects on the forestry and nearby communities, wildfires also generate a large amount of particulate matter (PM). In western US, wildfires contributed to 71.3% of total PM2.5 on days exceeding regulatory PM2.5 standards during 2004-2009 (Liu et al. Clim Change. 2016;138:655). Acute PM exposure is associated with respiratory health effects, such as exacerbation of asthma and COPD, increased ED visits and hospitalization for pneumonia, and increased mortality. Chronic PM2.5 exposure may also affect lung function. Cross-shift and cross-season FEV1 declined by 0.150 L and 0.104 L, respectively in forest firefighters (Betchley, et al. Am. J Ind Med. 1997;31:503). The Children’s Health Study conducted in California found that subjects who were exposed to the highest level of exposure to PM2.5 were five times more likely to have an FEV1 less than 80% of expected FEV1 when they reached 18 years of age than subjects exposed to the lowest level of PM2.5 (Gauderman et al. N Engl J Med. 2004;351:1057). Clinicians should educate patients and the public how to protect our environment and, when wildfires occur, how to protect themselves from exposure to PM.
Thomas W. DeCato, MD
Fellow-in-Training Committee Member
Yuh-Chin T. Huang, MD, FCCP
Steering Committee Member
Pulmonary Vascular Disease
Small increases in pulmonary pressures—big impact
Pulmonary hypertension (PH) is a progressive, life-limiting pulmonary vascular disease that is diagnosed hemodynamically by right-sided heart catheterization (RHC) and defined by a mean pulmonary artery pressure (mPAP) >25 mm Hg (Hoeper MM, et al. JACC. 2013;62(25 Suppl):D42).
The impact of PH on survival both in its “pure” form, pulmonary arterial hypertension, and in the setting of underlying cardiopulmonary disease, is well established. However, the clinical relevance of mildly elevated mPAP, defined as mPAP between 18 and 24 mm Hg, has been unclear until recently. Two large cohort studies have suggested that mild increases in mPAP are clinically relevant. A large retrospective analysis of hemodynamic data from 21,727 US veterans found mildly increased mPAP (19-24 mm Hg) was associated with increased hospitalization and decreased survival (Maron, et al. Circulation. 2016;133:1240).
While this population was skewed toward elderly men, a study from Vanderbilt University that included equal numbers of men and women showed similar results. Patients with mPAP 19-24 mm Hg experienced incrementally increased mortality (HR:1.31, P=.001). Importantly, in the subset of patients who underwent a repeat RHC in follow-up, 61% developed progressive increases of pulmonary pressures (>25 mm Hg) on follow-up RHC suggesting that the disease process may progress in a substantial proportion of patients (Assad, et al. JAMA Cardiol. 2017;2[1]):1361). Combined with prior data from smaller cohorts, these studies highlight the impact of mildly increased pulmonary pressures on outcomes. Given the dearth of available data regarding interventions for these patients, there is an urgent need to study to role of specific therapy for mildly elevated pulmonary pressures.
Vijay Balasubramanian, MD, FCCP
Steering Committee Member
Jean Elwing, MD, FCCP
Steering Committee Vice-Chair
Thoracic Oncology
Multiple tumor nodules in lung cancer diagnosis
Low dose CT (LDCT) scan screening for lung cancer is a recommended preventative modality for adults with a significant smoking history (Mayer et al. Ann Int Med. 2014;160(5):330). The screening approach aims to identify adults at significant risk for lung cancer. The goal is to discover lung cancers at low stage with benign mediastinal nodes for optimal treatment and potential for cure. In a minority, but significant number of cases, the LDCT demonstrates multiple lung nodules or masses confounding the attempt to adequately stage the tumor. Two tumors representing a primary cancer and separate malignant spread, namely, intra-pulmonary metastases, in the same lobe, different ipsilateral lobe, or contralateral lobe would be staged, respectively, as T3, T4, or M1a (Detterbeck et al. Chest. 2013;143(5):e191S). Clearly, if the two tumors are separate unique primary cancers, independent of one another, then at best they would be considered as multiple T1 tumors. The treatment modalities of and clinical survival outcomes for these multiple conditions would be markedly different.
The identification of additional tumors may be synchronous (at the same time of the primary discovery) or metachronous (at a later time than the primary discovery). The approach is basically the same. Two tumors with different histologic types, or having separate in-situ squamous cell carcinoma patterns, or disparate immunohistochemical or molecular expressions, or different genomic profiles or driver mutations may be considered as separate distinct primary malignancies (Detterbeck et al. J Thorac Oncol. 2016;11:639; Nicholson et al. J Thorac Oncol. 2017;13:205). Separate foci of ground-glass opacities with small solid central component indicative of minimally invasive adenocarcinoma may be designated as the highest T-stage. These cited and more challenging cases should be presented to a lung cancer tumor board with multiple specialties represented for analysis and judgment. The approach to diagnostic decision-making and clinical management should involve the expertise of all specialties in the lung cancer patient care team.
Arnold M. Schwartz, MD, PhD, FCCP
Steering Committee Member
Interventional Chest/Diagnostic Procedures
Endobronchial valve therapy receives FDA approval for bronchoscopic LVR
Lung volume reduction surgery (LVRS) is an established approach to improve exercise capacity and lung function in patients with heterogeneous emphysema and may confer survival benefit in patients with apical-predominant disease (Fishman, et al. N Engl J Med. 2003;348[21]:2059). Despite this, LVRS case numbers remain low due to patient and procedural morbidity. Bronchoscopic alternatives for LVRS have advanced considerably over the last decade with endobronchial valve (EBV) therapy emerging as a viable option for select subsets of patients with heterogeneous emphysema. Endobronchial valves are removable devices placed in segmental/subsegmental airways, which allow efflux of air during exhalation but close during inspiration, resulting in distal atelectasis in the absence of collateral ventilation.
The LIBERATE study, a multicenter randomized controlled trial demonstrated improvement in FEV1 ≥15% in 48% of patients after EBV placement compared with 17% of patients receiving standard medical therapy has resulted in FDA approval (Criner G, et al. Am J Respir Crit Care Med. 2018 May 22. doi: 10.1164/rccm.201803-0590OC. [Epub ahead of print]). Patients with EBV had improved subjective dyspnea scores, residual volume, and 6-minute walk distance; however, the pneumothorax rate was 27%.
All study patients with EBV underwent bronchoscopic evaluation for collateral ventilation using a proprietary digital system, which measures expiratory airflow in target airways to establish the presence of collateral ventilation. Previous data have demonstrated improved transplant-free survival when implanted EBVs result in atelectasis of the target lobe, which requires intact interlobar fissures (Garner, et al. Am J Respir Crit Care Med. 2016;194[4]:519). Ongoing clinical trials are attempting to clarify the role of EBV therapy in different phenotypes of COPD, including patients with homogenous emphysema. Long-term follow-up data will be important in determining the broader implementation of bronchoscopic lung volume reduction moving forward.
Vivek Murthy, MD
Jason A. Akulian, MD, FCCP
Steering Committee Members
Pediatric Chest Medicine
CFTR modulators
Cystic fibrosis (CF) is a progressive genetic disorder resulting in multiorgan disease with progressive respiratory decline. CF is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This codes for the CFTR anion channel and contributes to the movement of salt in and out of the cell. CFTR dysfunction leads to thickened secretions in the lungs and other organs, such as the gut and pancreas. This leads to more lung infections and other organ dysfunction that ultimately leads to premature death.
Established CF treatments include pulmonary and nutritional interventions. CFTR modulators are recent novel therapies that improve the function of CFTR and target the basic defect. Two types of modulator drugs (potentiators and correctors) have been developed with effectiveness depending upon the kind of CF mutation the person has.
CFTR potentiators, such as Kalydeco® (ivacaftor monotherapy), increase the likelihood that the CFTR channel will transport ions through the cell membrane, ie, they increase the channel’s “open probability.” Kalydeco has been approved for patients 12 months or older with mutations that result in partial CFTR protein function in the cell membrane. CFTR correctors, such as lumacaftor and tezacaftor, increase the amount of normal or mutated CFTR protein that gets transported, increasing the amount of CFTR protein on the cell surface. Combination drugs such as Orkambi® (lumacaftor/ivacaftor) for patients 2 years and older, and Symdeko™ (tezacaftor/ivacaftor) for patients 12 years and older, are considered in patients homozygous for the F508del mutation.
Sumit Bhargava, MBBS, FCCP
Steering Committee Member
Pulmonary Physiology, Function, and Rehabilitation
Wildfires, particulate matter, and lung function
In the last 3 decades, human-caused climate change contributed to wildfires in an additional 4.2 million hectares of land across the western US alone. Human impact on climate is responsible for nearly doubling the expected wildfire area (Abatzoglou, et al. PNAS. 2016;113:11770). Year 2017 saw the most destructive wildfires in California recorded to date, and over $2 billion dollars was spent by the US Forest Service, the most-expensive on record. Besides the devastating effects on the forestry and nearby communities, wildfires also generate a large amount of particulate matter (PM). In western US, wildfires contributed to 71.3% of total PM2.5 on days exceeding regulatory PM2.5 standards during 2004-2009 (Liu et al. Clim Change. 2016;138:655). Acute PM exposure is associated with respiratory health effects, such as exacerbation of asthma and COPD, increased ED visits and hospitalization for pneumonia, and increased mortality. Chronic PM2.5 exposure may also affect lung function. Cross-shift and cross-season FEV1 declined by 0.150 L and 0.104 L, respectively in forest firefighters (Betchley, et al. Am. J Ind Med. 1997;31:503). The Children’s Health Study conducted in California found that subjects who were exposed to the highest level of exposure to PM2.5 were five times more likely to have an FEV1 less than 80% of expected FEV1 when they reached 18 years of age than subjects exposed to the lowest level of PM2.5 (Gauderman et al. N Engl J Med. 2004;351:1057). Clinicians should educate patients and the public how to protect our environment and, when wildfires occur, how to protect themselves from exposure to PM.
Thomas W. DeCato, MD
Fellow-in-Training Committee Member
Yuh-Chin T. Huang, MD, FCCP
Steering Committee Member
Pulmonary Vascular Disease
Small increases in pulmonary pressures—big impact
Pulmonary hypertension (PH) is a progressive, life-limiting pulmonary vascular disease that is diagnosed hemodynamically by right-sided heart catheterization (RHC) and defined by a mean pulmonary artery pressure (mPAP) >25 mm Hg (Hoeper MM, et al. JACC. 2013;62(25 Suppl):D42).
The impact of PH on survival both in its “pure” form, pulmonary arterial hypertension, and in the setting of underlying cardiopulmonary disease, is well established. However, the clinical relevance of mildly elevated mPAP, defined as mPAP between 18 and 24 mm Hg, has been unclear until recently. Two large cohort studies have suggested that mild increases in mPAP are clinically relevant. A large retrospective analysis of hemodynamic data from 21,727 US veterans found mildly increased mPAP (19-24 mm Hg) was associated with increased hospitalization and decreased survival (Maron, et al. Circulation. 2016;133:1240).
While this population was skewed toward elderly men, a study from Vanderbilt University that included equal numbers of men and women showed similar results. Patients with mPAP 19-24 mm Hg experienced incrementally increased mortality (HR:1.31, P=.001). Importantly, in the subset of patients who underwent a repeat RHC in follow-up, 61% developed progressive increases of pulmonary pressures (>25 mm Hg) on follow-up RHC suggesting that the disease process may progress in a substantial proportion of patients (Assad, et al. JAMA Cardiol. 2017;2[1]):1361). Combined with prior data from smaller cohorts, these studies highlight the impact of mildly increased pulmonary pressures on outcomes. Given the dearth of available data regarding interventions for these patients, there is an urgent need to study to role of specific therapy for mildly elevated pulmonary pressures.
Vijay Balasubramanian, MD, FCCP
Steering Committee Member
Jean Elwing, MD, FCCP
Steering Committee Vice-Chair
Thoracic Oncology
Multiple tumor nodules in lung cancer diagnosis
Low dose CT (LDCT) scan screening for lung cancer is a recommended preventative modality for adults with a significant smoking history (Mayer et al. Ann Int Med. 2014;160(5):330). The screening approach aims to identify adults at significant risk for lung cancer. The goal is to discover lung cancers at low stage with benign mediastinal nodes for optimal treatment and potential for cure. In a minority, but significant number of cases, the LDCT demonstrates multiple lung nodules or masses confounding the attempt to adequately stage the tumor. Two tumors representing a primary cancer and separate malignant spread, namely, intra-pulmonary metastases, in the same lobe, different ipsilateral lobe, or contralateral lobe would be staged, respectively, as T3, T4, or M1a (Detterbeck et al. Chest. 2013;143(5):e191S). Clearly, if the two tumors are separate unique primary cancers, independent of one another, then at best they would be considered as multiple T1 tumors. The treatment modalities of and clinical survival outcomes for these multiple conditions would be markedly different.
The identification of additional tumors may be synchronous (at the same time of the primary discovery) or metachronous (at a later time than the primary discovery). The approach is basically the same. Two tumors with different histologic types, or having separate in-situ squamous cell carcinoma patterns, or disparate immunohistochemical or molecular expressions, or different genomic profiles or driver mutations may be considered as separate distinct primary malignancies (Detterbeck et al. J Thorac Oncol. 2016;11:639; Nicholson et al. J Thorac Oncol. 2017;13:205). Separate foci of ground-glass opacities with small solid central component indicative of minimally invasive adenocarcinoma may be designated as the highest T-stage. These cited and more challenging cases should be presented to a lung cancer tumor board with multiple specialties represented for analysis and judgment. The approach to diagnostic decision-making and clinical management should involve the expertise of all specialties in the lung cancer patient care team.
Arnold M. Schwartz, MD, PhD, FCCP
Steering Committee Member
Interventional Chest/Diagnostic Procedures
Endobronchial valve therapy receives FDA approval for bronchoscopic LVR
Lung volume reduction surgery (LVRS) is an established approach to improve exercise capacity and lung function in patients with heterogeneous emphysema and may confer survival benefit in patients with apical-predominant disease (Fishman, et al. N Engl J Med. 2003;348[21]:2059). Despite this, LVRS case numbers remain low due to patient and procedural morbidity. Bronchoscopic alternatives for LVRS have advanced considerably over the last decade with endobronchial valve (EBV) therapy emerging as a viable option for select subsets of patients with heterogeneous emphysema. Endobronchial valves are removable devices placed in segmental/subsegmental airways, which allow efflux of air during exhalation but close during inspiration, resulting in distal atelectasis in the absence of collateral ventilation.
The LIBERATE study, a multicenter randomized controlled trial demonstrated improvement in FEV1 ≥15% in 48% of patients after EBV placement compared with 17% of patients receiving standard medical therapy has resulted in FDA approval (Criner G, et al. Am J Respir Crit Care Med. 2018 May 22. doi: 10.1164/rccm.201803-0590OC. [Epub ahead of print]). Patients with EBV had improved subjective dyspnea scores, residual volume, and 6-minute walk distance; however, the pneumothorax rate was 27%.
All study patients with EBV underwent bronchoscopic evaluation for collateral ventilation using a proprietary digital system, which measures expiratory airflow in target airways to establish the presence of collateral ventilation. Previous data have demonstrated improved transplant-free survival when implanted EBVs result in atelectasis of the target lobe, which requires intact interlobar fissures (Garner, et al. Am J Respir Crit Care Med. 2016;194[4]:519). Ongoing clinical trials are attempting to clarify the role of EBV therapy in different phenotypes of COPD, including patients with homogenous emphysema. Long-term follow-up data will be important in determining the broader implementation of bronchoscopic lung volume reduction moving forward.
Vivek Murthy, MD
Jason A. Akulian, MD, FCCP
Steering Committee Members
Pediatric Chest Medicine
CFTR modulators
Cystic fibrosis (CF) is a progressive genetic disorder resulting in multiorgan disease with progressive respiratory decline. CF is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This codes for the CFTR anion channel and contributes to the movement of salt in and out of the cell. CFTR dysfunction leads to thickened secretions in the lungs and other organs, such as the gut and pancreas. This leads to more lung infections and other organ dysfunction that ultimately leads to premature death.
Established CF treatments include pulmonary and nutritional interventions. CFTR modulators are recent novel therapies that improve the function of CFTR and target the basic defect. Two types of modulator drugs (potentiators and correctors) have been developed with effectiveness depending upon the kind of CF mutation the person has.
CFTR potentiators, such as Kalydeco® (ivacaftor monotherapy), increase the likelihood that the CFTR channel will transport ions through the cell membrane, ie, they increase the channel’s “open probability.” Kalydeco has been approved for patients 12 months or older with mutations that result in partial CFTR protein function in the cell membrane. CFTR correctors, such as lumacaftor and tezacaftor, increase the amount of normal or mutated CFTR protein that gets transported, increasing the amount of CFTR protein on the cell surface. Combination drugs such as Orkambi® (lumacaftor/ivacaftor) for patients 2 years and older, and Symdeko™ (tezacaftor/ivacaftor) for patients 12 years and older, are considered in patients homozygous for the F508del mutation.
Sumit Bhargava, MBBS, FCCP
Steering Committee Member
Pulmonary Physiology, Function, and Rehabilitation
Wildfires, particulate matter, and lung function
In the last 3 decades, human-caused climate change contributed to wildfires in an additional 4.2 million hectares of land across the western US alone. Human impact on climate is responsible for nearly doubling the expected wildfire area (Abatzoglou, et al. PNAS. 2016;113:11770). Year 2017 saw the most destructive wildfires in California recorded to date, and over $2 billion dollars was spent by the US Forest Service, the most-expensive on record. Besides the devastating effects on the forestry and nearby communities, wildfires also generate a large amount of particulate matter (PM). In western US, wildfires contributed to 71.3% of total PM2.5 on days exceeding regulatory PM2.5 standards during 2004-2009 (Liu et al. Clim Change. 2016;138:655). Acute PM exposure is associated with respiratory health effects, such as exacerbation of asthma and COPD, increased ED visits and hospitalization for pneumonia, and increased mortality. Chronic PM2.5 exposure may also affect lung function. Cross-shift and cross-season FEV1 declined by 0.150 L and 0.104 L, respectively in forest firefighters (Betchley, et al. Am. J Ind Med. 1997;31:503). The Children’s Health Study conducted in California found that subjects who were exposed to the highest level of exposure to PM2.5 were five times more likely to have an FEV1 less than 80% of expected FEV1 when they reached 18 years of age than subjects exposed to the lowest level of PM2.5 (Gauderman et al. N Engl J Med. 2004;351:1057). Clinicians should educate patients and the public how to protect our environment and, when wildfires occur, how to protect themselves from exposure to PM.
Thomas W. DeCato, MD
Fellow-in-Training Committee Member
Yuh-Chin T. Huang, MD, FCCP
Steering Committee Member
Pulmonary Vascular Disease
Small increases in pulmonary pressures—big impact
Pulmonary hypertension (PH) is a progressive, life-limiting pulmonary vascular disease that is diagnosed hemodynamically by right-sided heart catheterization (RHC) and defined by a mean pulmonary artery pressure (mPAP) >25 mm Hg (Hoeper MM, et al. JACC. 2013;62(25 Suppl):D42).
The impact of PH on survival both in its “pure” form, pulmonary arterial hypertension, and in the setting of underlying cardiopulmonary disease, is well established. However, the clinical relevance of mildly elevated mPAP, defined as mPAP between 18 and 24 mm Hg, has been unclear until recently. Two large cohort studies have suggested that mild increases in mPAP are clinically relevant. A large retrospective analysis of hemodynamic data from 21,727 US veterans found mildly increased mPAP (19-24 mm Hg) was associated with increased hospitalization and decreased survival (Maron, et al. Circulation. 2016;133:1240).
While this population was skewed toward elderly men, a study from Vanderbilt University that included equal numbers of men and women showed similar results. Patients with mPAP 19-24 mm Hg experienced incrementally increased mortality (HR:1.31, P=.001). Importantly, in the subset of patients who underwent a repeat RHC in follow-up, 61% developed progressive increases of pulmonary pressures (>25 mm Hg) on follow-up RHC suggesting that the disease process may progress in a substantial proportion of patients (Assad, et al. JAMA Cardiol. 2017;2[1]):1361). Combined with prior data from smaller cohorts, these studies highlight the impact of mildly increased pulmonary pressures on outcomes. Given the dearth of available data regarding interventions for these patients, there is an urgent need to study to role of specific therapy for mildly elevated pulmonary pressures.
Vijay Balasubramanian, MD, FCCP
Steering Committee Member
Jean Elwing, MD, FCCP
Steering Committee Vice-Chair
Thoracic Oncology
Multiple tumor nodules in lung cancer diagnosis
Low dose CT (LDCT) scan screening for lung cancer is a recommended preventative modality for adults with a significant smoking history (Mayer et al. Ann Int Med. 2014;160(5):330). The screening approach aims to identify adults at significant risk for lung cancer. The goal is to discover lung cancers at low stage with benign mediastinal nodes for optimal treatment and potential for cure. In a minority, but significant number of cases, the LDCT demonstrates multiple lung nodules or masses confounding the attempt to adequately stage the tumor. Two tumors representing a primary cancer and separate malignant spread, namely, intra-pulmonary metastases, in the same lobe, different ipsilateral lobe, or contralateral lobe would be staged, respectively, as T3, T4, or M1a (Detterbeck et al. Chest. 2013;143(5):e191S). Clearly, if the two tumors are separate unique primary cancers, independent of one another, then at best they would be considered as multiple T1 tumors. The treatment modalities of and clinical survival outcomes for these multiple conditions would be markedly different.
The identification of additional tumors may be synchronous (at the same time of the primary discovery) or metachronous (at a later time than the primary discovery). The approach is basically the same. Two tumors with different histologic types, or having separate in-situ squamous cell carcinoma patterns, or disparate immunohistochemical or molecular expressions, or different genomic profiles or driver mutations may be considered as separate distinct primary malignancies (Detterbeck et al. J Thorac Oncol. 2016;11:639; Nicholson et al. J Thorac Oncol. 2017;13:205). Separate foci of ground-glass opacities with small solid central component indicative of minimally invasive adenocarcinoma may be designated as the highest T-stage. These cited and more challenging cases should be presented to a lung cancer tumor board with multiple specialties represented for analysis and judgment. The approach to diagnostic decision-making and clinical management should involve the expertise of all specialties in the lung cancer patient care team.
Arnold M. Schwartz, MD, PhD, FCCP
Steering Committee Member
This month in the journal CHEST®
Editor’s picks
Original Research
Pilot Feasibility Study in Establishing the Role of Ultrasound-Guided Pleural Biopsies in Pleural Infection (The AUDIO Study). By Dr. I. Psallidas, et al.
Commentary
Sleep Apnea Morbidity: A Consequence of Microbial-Immune Cross-Talk? By Dr. N. Farre, et al.
Evidence-Based Medicine
Treatment of Interstitial Lung Disease-Associated Cough: CHEST guideline and expert panel report. By Dr. S. S. Birring, et al.
Editor’s picks
Original Research
Pilot Feasibility Study in Establishing the Role of Ultrasound-Guided Pleural Biopsies in Pleural Infection (The AUDIO Study). By Dr. I. Psallidas, et al.
Commentary
Sleep Apnea Morbidity: A Consequence of Microbial-Immune Cross-Talk? By Dr. N. Farre, et al.
Evidence-Based Medicine
Treatment of Interstitial Lung Disease-Associated Cough: CHEST guideline and expert panel report. By Dr. S. S. Birring, et al.
Editor’s picks
Original Research
Pilot Feasibility Study in Establishing the Role of Ultrasound-Guided Pleural Biopsies in Pleural Infection (The AUDIO Study). By Dr. I. Psallidas, et al.
Commentary
Sleep Apnea Morbidity: A Consequence of Microbial-Immune Cross-Talk? By Dr. N. Farre, et al.
Evidence-Based Medicine
Treatment of Interstitial Lung Disease-Associated Cough: CHEST guideline and expert panel report. By Dr. S. S. Birring, et al.
Upcoming CPT® Changes
Pulmonary, critical care, and sleep physicians often provide services to patients, as well as consultative services to other health-care professionals, without a patient being present. This can be done via telephone or electronic (internet or electronic health record) communications. Many are not aware that Current Procedural Terminology (CPT®) codes were published to describe and define the work involved in these services. In 2019, there will be additional CPT codes available for health-care workers to use for these non-face-to-face services.
Telephone services are reported using CPT codes 99441-99443 and may be used for evaluation and management (E/M) services provided by telephone for an established patient that do not result in a patient visit within the next 24 hours or are associated with an E/M visit from the last 7 days.
99441 Telephone evaluation and management service by a physician or other qualified health-care professional who may report evaluation and management services provided to an established patient, parent, or guardian not originating from a related E/M serv ice provided within the previous 7 days nor leading to an E/M service or procedure within the next 24 hours or soonest available appointment; 5-10 minutes of medical discussion
99442 11-20 minutes of medical discussion
99443 21-30 minutes of medical discussion
These codes may not be reported by a provider more frequently than every 7 days. The details of the service should be documented in the medical record.
If the E/M service is prompted by an online patient request, then CPT code 99444 can be used.
99444 Online evaluation and management service provided by a physician or other qualified health care professional who may report evaluation and management services provided to an established patient or guardian, not originating from a related E/M service provided within the previous 7 days, using the internet or similar electronic communications network.
This code may be reported only every 7 days and can not be related to a previous E/M evaluation in the last 7 days or to a previous surgical procedure. The service includes all of the communication (eg, related telephone calls, prescription provision, laboratory orders) pertaining to the online patient encounter.
There are also CPT codes for Interprofessional Telephone/Internet/Electronic Health Record Consultations. These codes are used when one health-care provider requests the opinion and/or treatment advice of another provider (consultant) for either a new or established patient without face-to-face contact between the patient and the consultant.
99446 Interprofessional telephone/Internet/electronic health record assessment and management service provided by a consultative physician, including a verbal and written report to the patient’s treating/requesting physician or other qualified health care professional; 5-10 minutes of medical consultative discussion and review.
99447 11-20 minutes of medical consultative discussion and review
99448 21-30 minutes of medical consultative discussion and review
99449 31 minutes or more of medical consultative discussion and review
These codes are not used if the consultant has seen the patient in a face-to-face encounter within the last 14 days or the consultation results in a transfer of care or other face-to-face service with the consultant within the next 14 days. In addition, greater than 50% of the service time reported must be devoted to the medical consultative verbal or internet discussion. The request and reason for telephone/internet/electronic health record consultation by the requesting health-care professional should be documented in the patient’s medical record. After an oral report from the consultant is provided to the treating/requesting physician, a written report should be documented in the medical record. Consultations of less than 5 minutes should not be reported.
As noted, CPT codes 99446-49 require an oral and written report. A new code is added for 2019.
99451 Interprofessional telephone/Internet/electronic health record assessment and management service provided by a consultative physician, including a written report to the patient’s treating/requesting physician or other qualified health care professional, 5 minutes or more of medical consultative time.
CPT code 99451 describes a consultative service lasting more than 5 minutes and requires only a written report to the requesting physician. This was added recognizing that oral communications do not always occur between healthcare professionals and may facilitate consultative services in geographic areas with no specialists available.
99452 Interprofessional telephone/Internet/electronic health record referral service(s) provided by a treating/requesting physician or other qualified health care professional, 30 minutes.
CPT code 99452 is reported for 16-30 minutes preparing for the referral and/or communicating with a consultant. If more than 30 minutes is spent by the treating/requesting healthcare provider, then one would use a prolonged services code (99358-59).
As with all coding and billing issues, review the CPT manual for parentheticals that describe coding rules not included in the code description. In addition, not all CPT codes are paid by all providers. Knowledge of payer policies is, therefore, important for appropriate reimbursement.
Pulmonary, critical care, and sleep physicians often provide services to patients, as well as consultative services to other health-care professionals, without a patient being present. This can be done via telephone or electronic (internet or electronic health record) communications. Many are not aware that Current Procedural Terminology (CPT®) codes were published to describe and define the work involved in these services. In 2019, there will be additional CPT codes available for health-care workers to use for these non-face-to-face services.
Telephone services are reported using CPT codes 99441-99443 and may be used for evaluation and management (E/M) services provided by telephone for an established patient that do not result in a patient visit within the next 24 hours or are associated with an E/M visit from the last 7 days.
99441 Telephone evaluation and management service by a physician or other qualified health-care professional who may report evaluation and management services provided to an established patient, parent, or guardian not originating from a related E/M serv ice provided within the previous 7 days nor leading to an E/M service or procedure within the next 24 hours or soonest available appointment; 5-10 minutes of medical discussion
99442 11-20 minutes of medical discussion
99443 21-30 minutes of medical discussion
These codes may not be reported by a provider more frequently than every 7 days. The details of the service should be documented in the medical record.
If the E/M service is prompted by an online patient request, then CPT code 99444 can be used.
99444 Online evaluation and management service provided by a physician or other qualified health care professional who may report evaluation and management services provided to an established patient or guardian, not originating from a related E/M service provided within the previous 7 days, using the internet or similar electronic communications network.
This code may be reported only every 7 days and can not be related to a previous E/M evaluation in the last 7 days or to a previous surgical procedure. The service includes all of the communication (eg, related telephone calls, prescription provision, laboratory orders) pertaining to the online patient encounter.
There are also CPT codes for Interprofessional Telephone/Internet/Electronic Health Record Consultations. These codes are used when one health-care provider requests the opinion and/or treatment advice of another provider (consultant) for either a new or established patient without face-to-face contact between the patient and the consultant.
99446 Interprofessional telephone/Internet/electronic health record assessment and management service provided by a consultative physician, including a verbal and written report to the patient’s treating/requesting physician or other qualified health care professional; 5-10 minutes of medical consultative discussion and review.
99447 11-20 minutes of medical consultative discussion and review
99448 21-30 minutes of medical consultative discussion and review
99449 31 minutes or more of medical consultative discussion and review
These codes are not used if the consultant has seen the patient in a face-to-face encounter within the last 14 days or the consultation results in a transfer of care or other face-to-face service with the consultant within the next 14 days. In addition, greater than 50% of the service time reported must be devoted to the medical consultative verbal or internet discussion. The request and reason for telephone/internet/electronic health record consultation by the requesting health-care professional should be documented in the patient’s medical record. After an oral report from the consultant is provided to the treating/requesting physician, a written report should be documented in the medical record. Consultations of less than 5 minutes should not be reported.
As noted, CPT codes 99446-49 require an oral and written report. A new code is added for 2019.
99451 Interprofessional telephone/Internet/electronic health record assessment and management service provided by a consultative physician, including a written report to the patient’s treating/requesting physician or other qualified health care professional, 5 minutes or more of medical consultative time.
CPT code 99451 describes a consultative service lasting more than 5 minutes and requires only a written report to the requesting physician. This was added recognizing that oral communications do not always occur between healthcare professionals and may facilitate consultative services in geographic areas with no specialists available.
99452 Interprofessional telephone/Internet/electronic health record referral service(s) provided by a treating/requesting physician or other qualified health care professional, 30 minutes.
CPT code 99452 is reported for 16-30 minutes preparing for the referral and/or communicating with a consultant. If more than 30 minutes is spent by the treating/requesting healthcare provider, then one would use a prolonged services code (99358-59).
As with all coding and billing issues, review the CPT manual for parentheticals that describe coding rules not included in the code description. In addition, not all CPT codes are paid by all providers. Knowledge of payer policies is, therefore, important for appropriate reimbursement.
Pulmonary, critical care, and sleep physicians often provide services to patients, as well as consultative services to other health-care professionals, without a patient being present. This can be done via telephone or electronic (internet or electronic health record) communications. Many are not aware that Current Procedural Terminology (CPT®) codes were published to describe and define the work involved in these services. In 2019, there will be additional CPT codes available for health-care workers to use for these non-face-to-face services.
Telephone services are reported using CPT codes 99441-99443 and may be used for evaluation and management (E/M) services provided by telephone for an established patient that do not result in a patient visit within the next 24 hours or are associated with an E/M visit from the last 7 days.
99441 Telephone evaluation and management service by a physician or other qualified health-care professional who may report evaluation and management services provided to an established patient, parent, or guardian not originating from a related E/M serv ice provided within the previous 7 days nor leading to an E/M service or procedure within the next 24 hours or soonest available appointment; 5-10 minutes of medical discussion
99442 11-20 minutes of medical discussion
99443 21-30 minutes of medical discussion
These codes may not be reported by a provider more frequently than every 7 days. The details of the service should be documented in the medical record.
If the E/M service is prompted by an online patient request, then CPT code 99444 can be used.
99444 Online evaluation and management service provided by a physician or other qualified health care professional who may report evaluation and management services provided to an established patient or guardian, not originating from a related E/M service provided within the previous 7 days, using the internet or similar electronic communications network.
This code may be reported only every 7 days and can not be related to a previous E/M evaluation in the last 7 days or to a previous surgical procedure. The service includes all of the communication (eg, related telephone calls, prescription provision, laboratory orders) pertaining to the online patient encounter.
There are also CPT codes for Interprofessional Telephone/Internet/Electronic Health Record Consultations. These codes are used when one health-care provider requests the opinion and/or treatment advice of another provider (consultant) for either a new or established patient without face-to-face contact between the patient and the consultant.
99446 Interprofessional telephone/Internet/electronic health record assessment and management service provided by a consultative physician, including a verbal and written report to the patient’s treating/requesting physician or other qualified health care professional; 5-10 minutes of medical consultative discussion and review.
99447 11-20 minutes of medical consultative discussion and review
99448 21-30 minutes of medical consultative discussion and review
99449 31 minutes or more of medical consultative discussion and review
These codes are not used if the consultant has seen the patient in a face-to-face encounter within the last 14 days or the consultation results in a transfer of care or other face-to-face service with the consultant within the next 14 days. In addition, greater than 50% of the service time reported must be devoted to the medical consultative verbal or internet discussion. The request and reason for telephone/internet/electronic health record consultation by the requesting health-care professional should be documented in the patient’s medical record. After an oral report from the consultant is provided to the treating/requesting physician, a written report should be documented in the medical record. Consultations of less than 5 minutes should not be reported.
As noted, CPT codes 99446-49 require an oral and written report. A new code is added for 2019.
99451 Interprofessional telephone/Internet/electronic health record assessment and management service provided by a consultative physician, including a written report to the patient’s treating/requesting physician or other qualified health care professional, 5 minutes or more of medical consultative time.
CPT code 99451 describes a consultative service lasting more than 5 minutes and requires only a written report to the requesting physician. This was added recognizing that oral communications do not always occur between healthcare professionals and may facilitate consultative services in geographic areas with no specialists available.
99452 Interprofessional telephone/Internet/electronic health record referral service(s) provided by a treating/requesting physician or other qualified health care professional, 30 minutes.
CPT code 99452 is reported for 16-30 minutes preparing for the referral and/or communicating with a consultant. If more than 30 minutes is spent by the treating/requesting healthcare provider, then one would use a prolonged services code (99358-59).
As with all coding and billing issues, review the CPT manual for parentheticals that describe coding rules not included in the code description. In addition, not all CPT codes are paid by all providers. Knowledge of payer policies is, therefore, important for appropriate reimbursement.
Welcome Dr. Cowl!
As we greet our new CHEST President, Clayton T. Cowl, MD, MS, FCCP, we asked him for a few thoughts about his upcoming presidential year. He kindly offered these responses:
What would be one of the many things you would like to accomplish as President of CHEST?
We plan to increase the engagement of our membership, and, in do so, allow for more opportunities to serve in leadership roles, educate as faculty, or to participate in more of the wide array of educational opportunities within CHEST – whether the member is a long-tenured physician, a trainee, an earlier career researcher or educator, or a colleague in the care team, such as a respiratory therapist, advanced practice provider, or a pharmacist. CHEST has been and will continue to be a leader in delivery of education, and will further advance opportunities to present breaking research. Ultimately, the reason we are in medicine is to improve the care that we deliver to our patients, so it is incumbent upon us to keep the mission aimed toward “patient-centric” goals.
What do you consider to be the greatest strength of CHEST, and how will you build upon this during your Presidency?
Our greatest strength is our members, who bring a diversity of experience, expertise, and passion for what they do at the forefront. Together, with our incredibly talented and dedicated support staff at CHEST, as well as our industry and publishing partners, our organization is poised to bring medical education in pulmonary, critical care, and sleep medicine globally to the next level. The CHEST Foundation has stimulated important opportunities for research, increased the ability for younger members to attend meetings and actively engage in CHEST activities, and provided valuable information to patients in a language they can understand. Thanks to advances in technology, there are improved platforms for communicating with our membership and for delivering education in novel and more effective ways than ever before. We plan to double down on our strategic focus of utilizing innovation and new technologies to lead trends in education, influence health-care improvements for our patients and their families, and to deliver the latest in medical education to clinicians and investigators worldwide.
What are some challenges facing CHEST, and how will you address these challenges?
Many of our members are facing challenges in their practices – both domestically and internationally. Industry and employer-based sponsorship to attend meetings has declined, travel remains expensive, and time away from the practice has become more and more difficult for a variety of reasons. Our members are being challenged with greater regulatory and administrative burdens and are bombarded with the demands of work overload. In addition to working with other organizations to identify workplace burnout and, more importantly, to offer better solutions, we are focused on leveraging a variety of new technologies to bring our CHEST brand of quality education to all of our members, regardless of location, and to do so in a way that best suits individual needs. The traditional model of attending a large meeting comprised solely of didactic presentations is, frankly, becoming outdated. CHEST will continue to “tip the apple cart” of worn out educational delivery methods and look toward innovating courses that are more accessible, more effective and relevant, more affordable, and more fun.
And finally, what is your charge to the members and new Fellows of CHEST?
We have each been blessed with the opportunity to serve patients and their families in their times of need. Let’s not forget that privilege as we deliver care each and every day. The word “doctor” comes from an agentive noun of the Latin verb docēre (“to teach”). Regardless of where you practice, what your role is in the health-care paradigm, or whether your contribution is directly with patients or indirectly through research, education, or administration, we are all teachers in various ways to various people. That’s why the American College of Chest Physicians (CHEST) needs to listen to your needs, cultivate your collective wisdom, and continue to be the leading organization within our specialties for delivering medical education and, ultimately, for providing outstanding care and compassion to our patients.
As we greet our new CHEST President, Clayton T. Cowl, MD, MS, FCCP, we asked him for a few thoughts about his upcoming presidential year. He kindly offered these responses:
What would be one of the many things you would like to accomplish as President of CHEST?
We plan to increase the engagement of our membership, and, in do so, allow for more opportunities to serve in leadership roles, educate as faculty, or to participate in more of the wide array of educational opportunities within CHEST – whether the member is a long-tenured physician, a trainee, an earlier career researcher or educator, or a colleague in the care team, such as a respiratory therapist, advanced practice provider, or a pharmacist. CHEST has been and will continue to be a leader in delivery of education, and will further advance opportunities to present breaking research. Ultimately, the reason we are in medicine is to improve the care that we deliver to our patients, so it is incumbent upon us to keep the mission aimed toward “patient-centric” goals.
What do you consider to be the greatest strength of CHEST, and how will you build upon this during your Presidency?
Our greatest strength is our members, who bring a diversity of experience, expertise, and passion for what they do at the forefront. Together, with our incredibly talented and dedicated support staff at CHEST, as well as our industry and publishing partners, our organization is poised to bring medical education in pulmonary, critical care, and sleep medicine globally to the next level. The CHEST Foundation has stimulated important opportunities for research, increased the ability for younger members to attend meetings and actively engage in CHEST activities, and provided valuable information to patients in a language they can understand. Thanks to advances in technology, there are improved platforms for communicating with our membership and for delivering education in novel and more effective ways than ever before. We plan to double down on our strategic focus of utilizing innovation and new technologies to lead trends in education, influence health-care improvements for our patients and their families, and to deliver the latest in medical education to clinicians and investigators worldwide.
What are some challenges facing CHEST, and how will you address these challenges?
Many of our members are facing challenges in their practices – both domestically and internationally. Industry and employer-based sponsorship to attend meetings has declined, travel remains expensive, and time away from the practice has become more and more difficult for a variety of reasons. Our members are being challenged with greater regulatory and administrative burdens and are bombarded with the demands of work overload. In addition to working with other organizations to identify workplace burnout and, more importantly, to offer better solutions, we are focused on leveraging a variety of new technologies to bring our CHEST brand of quality education to all of our members, regardless of location, and to do so in a way that best suits individual needs. The traditional model of attending a large meeting comprised solely of didactic presentations is, frankly, becoming outdated. CHEST will continue to “tip the apple cart” of worn out educational delivery methods and look toward innovating courses that are more accessible, more effective and relevant, more affordable, and more fun.
And finally, what is your charge to the members and new Fellows of CHEST?
We have each been blessed with the opportunity to serve patients and their families in their times of need. Let’s not forget that privilege as we deliver care each and every day. The word “doctor” comes from an agentive noun of the Latin verb docēre (“to teach”). Regardless of where you practice, what your role is in the health-care paradigm, or whether your contribution is directly with patients or indirectly through research, education, or administration, we are all teachers in various ways to various people. That’s why the American College of Chest Physicians (CHEST) needs to listen to your needs, cultivate your collective wisdom, and continue to be the leading organization within our specialties for delivering medical education and, ultimately, for providing outstanding care and compassion to our patients.
As we greet our new CHEST President, Clayton T. Cowl, MD, MS, FCCP, we asked him for a few thoughts about his upcoming presidential year. He kindly offered these responses:
What would be one of the many things you would like to accomplish as President of CHEST?
We plan to increase the engagement of our membership, and, in do so, allow for more opportunities to serve in leadership roles, educate as faculty, or to participate in more of the wide array of educational opportunities within CHEST – whether the member is a long-tenured physician, a trainee, an earlier career researcher or educator, or a colleague in the care team, such as a respiratory therapist, advanced practice provider, or a pharmacist. CHEST has been and will continue to be a leader in delivery of education, and will further advance opportunities to present breaking research. Ultimately, the reason we are in medicine is to improve the care that we deliver to our patients, so it is incumbent upon us to keep the mission aimed toward “patient-centric” goals.
What do you consider to be the greatest strength of CHEST, and how will you build upon this during your Presidency?
Our greatest strength is our members, who bring a diversity of experience, expertise, and passion for what they do at the forefront. Together, with our incredibly talented and dedicated support staff at CHEST, as well as our industry and publishing partners, our organization is poised to bring medical education in pulmonary, critical care, and sleep medicine globally to the next level. The CHEST Foundation has stimulated important opportunities for research, increased the ability for younger members to attend meetings and actively engage in CHEST activities, and provided valuable information to patients in a language they can understand. Thanks to advances in technology, there are improved platforms for communicating with our membership and for delivering education in novel and more effective ways than ever before. We plan to double down on our strategic focus of utilizing innovation and new technologies to lead trends in education, influence health-care improvements for our patients and their families, and to deliver the latest in medical education to clinicians and investigators worldwide.
What are some challenges facing CHEST, and how will you address these challenges?
Many of our members are facing challenges in their practices – both domestically and internationally. Industry and employer-based sponsorship to attend meetings has declined, travel remains expensive, and time away from the practice has become more and more difficult for a variety of reasons. Our members are being challenged with greater regulatory and administrative burdens and are bombarded with the demands of work overload. In addition to working with other organizations to identify workplace burnout and, more importantly, to offer better solutions, we are focused on leveraging a variety of new technologies to bring our CHEST brand of quality education to all of our members, regardless of location, and to do so in a way that best suits individual needs. The traditional model of attending a large meeting comprised solely of didactic presentations is, frankly, becoming outdated. CHEST will continue to “tip the apple cart” of worn out educational delivery methods and look toward innovating courses that are more accessible, more effective and relevant, more affordable, and more fun.
And finally, what is your charge to the members and new Fellows of CHEST?
We have each been blessed with the opportunity to serve patients and their families in their times of need. Let’s not forget that privilege as we deliver care each and every day. The word “doctor” comes from an agentive noun of the Latin verb docēre (“to teach”). Regardless of where you practice, what your role is in the health-care paradigm, or whether your contribution is directly with patients or indirectly through research, education, or administration, we are all teachers in various ways to various people. That’s why the American College of Chest Physicians (CHEST) needs to listen to your needs, cultivate your collective wisdom, and continue to be the leading organization within our specialties for delivering medical education and, ultimately, for providing outstanding care and compassion to our patients.
CHEST Foundation – designated as a Combined Federal Campaign-approved charity
The CHEST Foundation was recently designated as a Combined Federal Campaign-approved charity! The federal campaign started on September 10 and runs through January 11, 2019. If you are a federal employee organizing your workplace giving, you can easily choose the CHEST Foundation as your designated charity! Simply list our CFC number when designating your selected charity! CFC Number: 24565
To set up your CFC account, follow these easy steps outlined below:
1. Visit https://cfcgiving.opm.gov/welcome
2. From the welcome page, select “sign up now,” and fill out the required information if you do not have an account. If you do have an account, simply log in using the email address tied to your CFC account and your password, and skip to step 6.
3. After your account is set up, the CFC will send you an email to the address you provided along with a verification pin number. Select the “CLICK HERE to enter your PIN” option from the verification email, and enter the provided pin on the page provided by the link.
4. On the next page, you will create your security questions to log back into your account, should you lose your password. Select “Save Changes” at the bottom of the page when you are ready to move on.
5. Next, you’ll be asked to fill out some personal information about yourself as a donor, such as your full name, and which department of the federal government you work for. Choose “Save Changes” at the bottom of the page when you are done.
6. Upon completing the profile page (or logging into your account), you will be directed to the welcome page. Select the “Pledge Now” button, located in the center of the page.
7. The next page will ask you questions about the charity you would like to support. Enter the CHEST Foundation’s CFC number: 24565, and click “Search for Charities” to be directed to the next page.
8. Select the “add” button next to the CHEST Foundation’s listing. Then click the “checkout” button that appears in the pop-up window.
9. Fill out the requested information regarding your pledge amount, your pledge frequency, and your annual pledge amount, then select the “Continue with your pledge” option at the bottom of the page.
10. On this final page, you can review your pledge amount and review a brief attestation agreement. After reviewing, check the “I confirm” checkbox, then click “submit pledge.”
That’s it!
Thank you for supporting the CHEST Foundation’s mission-based programming supporting patient education materials, clinical research grants, and community service initiatives.
The CHEST Foundation was recently designated as a Combined Federal Campaign-approved charity! The federal campaign started on September 10 and runs through January 11, 2019. If you are a federal employee organizing your workplace giving, you can easily choose the CHEST Foundation as your designated charity! Simply list our CFC number when designating your selected charity! CFC Number: 24565
To set up your CFC account, follow these easy steps outlined below:
1. Visit https://cfcgiving.opm.gov/welcome
2. From the welcome page, select “sign up now,” and fill out the required information if you do not have an account. If you do have an account, simply log in using the email address tied to your CFC account and your password, and skip to step 6.
3. After your account is set up, the CFC will send you an email to the address you provided along with a verification pin number. Select the “CLICK HERE to enter your PIN” option from the verification email, and enter the provided pin on the page provided by the link.
4. On the next page, you will create your security questions to log back into your account, should you lose your password. Select “Save Changes” at the bottom of the page when you are ready to move on.
5. Next, you’ll be asked to fill out some personal information about yourself as a donor, such as your full name, and which department of the federal government you work for. Choose “Save Changes” at the bottom of the page when you are done.
6. Upon completing the profile page (or logging into your account), you will be directed to the welcome page. Select the “Pledge Now” button, located in the center of the page.
7. The next page will ask you questions about the charity you would like to support. Enter the CHEST Foundation’s CFC number: 24565, and click “Search for Charities” to be directed to the next page.
8. Select the “add” button next to the CHEST Foundation’s listing. Then click the “checkout” button that appears in the pop-up window.
9. Fill out the requested information regarding your pledge amount, your pledge frequency, and your annual pledge amount, then select the “Continue with your pledge” option at the bottom of the page.
10. On this final page, you can review your pledge amount and review a brief attestation agreement. After reviewing, check the “I confirm” checkbox, then click “submit pledge.”
That’s it!
Thank you for supporting the CHEST Foundation’s mission-based programming supporting patient education materials, clinical research grants, and community service initiatives.
The CHEST Foundation was recently designated as a Combined Federal Campaign-approved charity! The federal campaign started on September 10 and runs through January 11, 2019. If you are a federal employee organizing your workplace giving, you can easily choose the CHEST Foundation as your designated charity! Simply list our CFC number when designating your selected charity! CFC Number: 24565
To set up your CFC account, follow these easy steps outlined below:
1. Visit https://cfcgiving.opm.gov/welcome
2. From the welcome page, select “sign up now,” and fill out the required information if you do not have an account. If you do have an account, simply log in using the email address tied to your CFC account and your password, and skip to step 6.
3. After your account is set up, the CFC will send you an email to the address you provided along with a verification pin number. Select the “CLICK HERE to enter your PIN” option from the verification email, and enter the provided pin on the page provided by the link.
4. On the next page, you will create your security questions to log back into your account, should you lose your password. Select “Save Changes” at the bottom of the page when you are ready to move on.
5. Next, you’ll be asked to fill out some personal information about yourself as a donor, such as your full name, and which department of the federal government you work for. Choose “Save Changes” at the bottom of the page when you are done.
6. Upon completing the profile page (or logging into your account), you will be directed to the welcome page. Select the “Pledge Now” button, located in the center of the page.
7. The next page will ask you questions about the charity you would like to support. Enter the CHEST Foundation’s CFC number: 24565, and click “Search for Charities” to be directed to the next page.
8. Select the “add” button next to the CHEST Foundation’s listing. Then click the “checkout” button that appears in the pop-up window.
9. Fill out the requested information regarding your pledge amount, your pledge frequency, and your annual pledge amount, then select the “Continue with your pledge” option at the bottom of the page.
10. On this final page, you can review your pledge amount and review a brief attestation agreement. After reviewing, check the “I confirm” checkbox, then click “submit pledge.”
That’s it!
Thank you for supporting the CHEST Foundation’s mission-based programming supporting patient education materials, clinical research grants, and community service initiatives.