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
Main Authors: Klinger, James R, Elliott, C Gregory, Levine, Deborah J, Bossone, Eduardo, Duvall, Laura, Fagan, Karen, Frantsve-Hawley, Julie, Kawut, Steven M, Ryan, John J, Rosenzweig, Erika B, Sederstrom, Nneka, Steen, Virginia D, Badesch, David B
Format: Journal Article
Language:English
Published: United States 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.
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
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  organization: Intermountain Healthcare and the University of Utah School of Medicine, Murray, UT
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  organization: Columbia University Medical Center, New York, NY
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  organization: Children's Hospitals and Clinics of Minnesota, Minneapolis, MN
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  givenname: David B
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  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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evidence-based medicine
pulmonary arterial hypertension (PAH)
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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
URI https://www.ncbi.nlm.nih.gov/pubmed/30660783
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