Therapy for Pulmonary Arterial Hypertension in Adults: Update of the CHEST Guideline and Expert Panel Report
Pulmonary arterial hypertension (PAH) carries a poor prognosis if not promptly diagnosed and appropriately treated. The development and approval of 14 medications over the last several decades have led to a rapidly evolving approach to therapy, and have necessitated periodic updating of evidence-bas...
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Published in: | Chest Vol. 155; no. 3; pp. 565 - 586 |
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01-03-2019
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Abstract | Pulmonary arterial hypertension (PAH) carries a poor prognosis if not promptly diagnosed and appropriately treated. The development and approval of 14 medications over the last several decades have led to a rapidly evolving approach to therapy, and have necessitated periodic updating of evidence-based treatment guidelines. This guideline statement, which now includes a visual algorithm to enhance its clinical utility, represents the fourth iteration of the American College of Chest Physicians Guideline and Expert Panel Report on Pharmacotherapy for PAH.
The guideline panel conducted an updated systematic review to identify studies published after those included in the 2014 guideline. A systematic literature search was conducted using MEDLINE via PubMed and the Cochrane Library. The quality of the body of evidence was assessed for each critical or important outcome of interest using the Grading of Recommendations Assessment, Development and Evaluation approach. Graded recommendations and ungraded consensus-based statements were developed and voted on using a modified Delphi technique to achieve consensus.
Two new recommendations on combination therapy and two ungraded consensus-based statements on palliative care were developed. An evidence-based and consensus-driven treatment algorithm was created to guide the clinician through an organized approach to management, and to direct readers to the appropriate area of the document for more detailed information.
Therapeutic options for the patient with PAH continue to expand through basic discovery, translational science, and clinical trials. Optimal use of new treatment options requires prompt evaluation at an expert center, utilization of current evidence-based guidelines, and collaborative care using sound clinical judgment. |
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AbstractList | BACKGROUNDPulmonary arterial hypertension (PAH) carries a poor prognosis if not promptly diagnosed and appropriately treated. The development and approval of 14 medications over the last several decades have led to a rapidly evolving approach to therapy, and have necessitated periodic updating of evidence-based treatment guidelines. This guideline statement, which now includes a visual algorithm to enhance its clinical utility, represents the fourth iteration of the American College of Chest Physicians Guideline and Expert Panel Report on Pharmacotherapy for PAH. METHODSThe guideline panel conducted an updated systematic review to identify studies published after those included in the 2014 guideline. A systematic literature search was conducted using MEDLINE via PubMed and the Cochrane Library. The quality of the body of evidence was assessed for each critical or important outcome of interest using the Grading of Recommendations Assessment, Development and Evaluation approach. Graded recommendations and ungraded consensus-based statements were developed and voted on using a modified Delphi technique to achieve consensus. RESULTSTwo new recommendations on combination therapy and two ungraded consensus-based statements on palliative care were developed. An evidence-based and consensus-driven treatment algorithm was created to guide the clinician through an organized approach to management, and to direct readers to the appropriate area of the document for more detailed information. CONCLUSIONSTherapeutic options for the patient with PAH continue to expand through basic discovery, translational science, and clinical trials. Optimal use of new treatment options requires prompt evaluation at an expert center, utilization of current evidence-based guidelines, and collaborative care using sound clinical judgment. Pulmonary arterial hypertension (PAH) carries a poor prognosis if not promptly diagnosed and appropriately treated. The development and approval of 14 medications over the last several decades have led to a rapidly evolving approach to therapy, and have necessitated periodic updating of evidence-based treatment guidelines. This guideline statement, which now includes a visual algorithm to enhance its clinical utility, represents the fourth iteration of the American College of Chest Physicians Guideline and Expert Panel Report on Pharmacotherapy for PAH. The guideline panel conducted an updated systematic review to identify studies published after those included in the 2014 guideline. A systematic literature search was conducted using MEDLINE via PubMed and the Cochrane Library. The quality of the body of evidence was assessed for each critical or important outcome of interest using the Grading of Recommendations Assessment, Development and Evaluation approach. Graded recommendations and ungraded consensus-based statements were developed and voted on using a modified Delphi technique to achieve consensus. Two new recommendations on combination therapy and two ungraded consensus-based statements on palliative care were developed. An evidence-based and consensus-driven treatment algorithm was created to guide the clinician through an organized approach to management, and to direct readers to the appropriate area of the document for more detailed information. Therapeutic options for the patient with PAH continue to expand through basic discovery, translational science, and clinical trials. Optimal use of new treatment options requires prompt evaluation at an expert center, utilization of current evidence-based guidelines, and collaborative care using sound clinical judgment. |
Author | Frantsve-Hawley, Julie Rosenzweig, Erika B Levine, Deborah J Badesch, David B Kawut, Steven M Fagan, Karen Steen, Virginia D Klinger, James R Ryan, John J Elliott, C Gregory Duvall, Laura Sederstrom, Nneka Bossone, Eduardo |
Author_xml | – sequence: 1 givenname: James R surname: Klinger fullname: Klinger, James R organization: Brown University, Providence, RI – sequence: 2 givenname: C Gregory surname: Elliott fullname: Elliott, C Gregory organization: Intermountain Healthcare and the University of Utah School of Medicine, Murray, UT – sequence: 3 givenname: Deborah J surname: Levine fullname: Levine, Deborah J organization: University of Texas Health Science Center at San Antonio, San Antonio, TX – sequence: 4 givenname: Eduardo surname: Bossone fullname: Bossone, Eduardo organization: A. Cardarelli Hospital, Naples, Italy – sequence: 5 givenname: Laura surname: Duvall fullname: Duvall, Laura organization: OhioHealth/The Ohio State University, Columbus, OH – sequence: 6 givenname: Karen surname: Fagan fullname: Fagan, Karen organization: University of South Alabama, Mobile, AL – sequence: 7 givenname: Julie surname: Frantsve-Hawley fullname: Frantsve-Hawley, Julie organization: CHEST, Glenview, IL – sequence: 8 givenname: Steven M surname: Kawut fullname: Kawut, Steven M organization: Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA – sequence: 9 givenname: John J surname: Ryan fullname: Ryan, John J organization: University of Utah, Salt Lake City, UT – sequence: 10 givenname: Erika B surname: Rosenzweig fullname: Rosenzweig, Erika B organization: Columbia University Medical Center, New York, NY – sequence: 11 givenname: Nneka surname: Sederstrom fullname: Sederstrom, Nneka organization: Children's Hospitals and Clinics of Minnesota, Minneapolis, MN – sequence: 12 givenname: Virginia D surname: Steen fullname: Steen, Virginia D organization: Georgetown University Medical Center, Washington, DC – sequence: 13 givenname: David B surname: Badesch fullname: Badesch, David B email: David.Badesch@ucdenver.edu organization: University of Colorado School of Medicine, Aurora, CO. Electronic address: David.Badesch@ucdenver.edu |
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Copyright | Copyright © 2019 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved. |
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References | 31279370 - Chest. 2019 Jul;156(1):187-188 33422229 - Chest. 2021 Jan;159(1):457 31279369 - Chest. 2019 Jul;156(1):187 |
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Snippet | Pulmonary arterial hypertension (PAH) carries a poor prognosis if not promptly diagnosed and appropriately treated. The development and approval of 14... BACKGROUNDPulmonary arterial hypertension (PAH) carries a poor prognosis if not promptly diagnosed and appropriately treated. The development and approval of... |
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SubjectTerms | Adult Antihypertensive Agents - classification Antihypertensive Agents - pharmacology Diagnostic Techniques, Respiratory System Drug Monitoring - methods Evidence-Based Medicine Exercise Tolerance - drug effects Humans Pulmonary Arterial Hypertension - diagnosis Pulmonary Arterial Hypertension - drug therapy Pulmonary Arterial Hypertension - etiology Pulmonary Medicine - methods Pulmonary Medicine - standards Respiratory System Agents - classification Respiratory System Agents - pharmacology |
Title | Therapy for Pulmonary Arterial Hypertension in Adults: Update of the CHEST Guideline and Expert Panel Report |
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