Screening Strategies for Pulmonary Hypertension in Patients With Interstitial Lung Disease: A Multidisciplinary Delphi Study.

echocardiography idiopathic pulmonary fibrosis interstitial lung disease pulmonary hypertension right heart catheterization screening

Journal

Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335

Informations de publication

Date de publication:
07 2022
Historique:
received: 08 11 2021
revised: 20 01 2022
accepted: 07 02 2022
pubmed: 18 2 2022
medline: 14 7 2022
entrez: 17 2 2022
Statut: ppublish

Résumé

Pulmonary hypertension (PH) is a common complication of interstitial lung disease (ILD) and is associated with worse outcomes and increased mortality. Evaluation of PH is recommended in lung transplant candidates, but there are currently no standardized screening approaches. Trials have identified therapies that are effective in this setting, providing another rationale to routinely screen patients with ILD for PH. What screening strategies for identifying PH in patients with ILD are supported by expert consensus? The study convened a panel of 16 pulmonologists with expertise in PH and ILD, and used a modified Delphi consensus process with three surveys to identify PH screening strategies. Survey 1 consisted primarily of open-ended questions. Surveys 2 and 3 were developed from responses to survey 1 and contained statements about PH screening that panelists rated from -5 (strongly disagree) to 5 (strongly agree). Panelists reached consensus on several triggers for suspicion of PH including the following: symptoms, clinical signs, findings on chest CT scan or other imaging, abnormalities in pulse oximetry, elevations in brain natriuretic peptide (BNP) or N-terminal pro-brain natriuretic peptide (NT-proBNP), and unexplained worsening in pulmonary function tests or 6-min walk distance. Echocardiography and BNP/NT-proBNP were identified as screening tools for PH. Right heart catheterization was deemed essential for confirming PH. Many patients with ILD may benefit from early evaluation of PH now that an approved therapy is available. Protocols to evaluate patients with ILD often overlap with evaluations for pulmonary hypertension-interstitial lung disease and can be used to assess the risk of PH. Because standardized approaches are lacking, this consensus statement is intended to aid physicians in the identification of patients with ILD and possible PH, and provide guidance for timely right heart catheterization.

Sections du résumé

BACKGROUND
Pulmonary hypertension (PH) is a common complication of interstitial lung disease (ILD) and is associated with worse outcomes and increased mortality. Evaluation of PH is recommended in lung transplant candidates, but there are currently no standardized screening approaches. Trials have identified therapies that are effective in this setting, providing another rationale to routinely screen patients with ILD for PH.
RESEARCH QUESTION
What screening strategies for identifying PH in patients with ILD are supported by expert consensus?
STUDY DESIGN AND METHODS
The study convened a panel of 16 pulmonologists with expertise in PH and ILD, and used a modified Delphi consensus process with three surveys to identify PH screening strategies. Survey 1 consisted primarily of open-ended questions. Surveys 2 and 3 were developed from responses to survey 1 and contained statements about PH screening that panelists rated from -5 (strongly disagree) to 5 (strongly agree).
RESULTS
Panelists reached consensus on several triggers for suspicion of PH including the following: symptoms, clinical signs, findings on chest CT scan or other imaging, abnormalities in pulse oximetry, elevations in brain natriuretic peptide (BNP) or N-terminal pro-brain natriuretic peptide (NT-proBNP), and unexplained worsening in pulmonary function tests or 6-min walk distance. Echocardiography and BNP/NT-proBNP were identified as screening tools for PH. Right heart catheterization was deemed essential for confirming PH.
INTERPRETATION
Many patients with ILD may benefit from early evaluation of PH now that an approved therapy is available. Protocols to evaluate patients with ILD often overlap with evaluations for pulmonary hypertension-interstitial lung disease and can be used to assess the risk of PH. Because standardized approaches are lacking, this consensus statement is intended to aid physicians in the identification of patients with ILD and possible PH, and provide guidance for timely right heart catheterization.

Identifiants

pubmed: 35176276
pii: S0012-3692(22)00262-8
doi: 10.1016/j.chest.2022.02.012
pmc: PMC9993339
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

145-155

Subventions

Organisme : NHLBI NIH HHS
ID : K23 HL146942
Pays : United States

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.

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Auteurs

Franck F Rahaghi (FF)

Advanced Lung Disease Clinic, Cleveland Clinic Florida, Weston, FL.

Nicholas A Kolaitis (NA)

UCSF Pulmonary and Critical Care, San Francisco, CA.

Ayodeji Adegunsoye (A)

Section of Pulmonary & Critical Care, The University of Chicago School of Medicine, Chicago, IL.

Joao A de Andrade (JA)

Vanderbilt Lung Institute, Vanderbilt University Medical Center, Nashville, TN.

Kevin R Flaherty (KR)

Michigan Medicine Interstitial Lung Disease Program, University of Michigan, Ann Arbor, MI.

Lisa H Lancaster (LH)

Vanderbilt University Medical Center, Nashville, TN.

Joyce S Lee (JS)

Pulmonary Sciences & Critical Care, University of Colorado School of Medicine, Aurora, CO.

Deborah J Levine (DJ)

Pulmonary Hypertension Center, UT Health San Antonio, San Antonio, TX.

Ioana R Preston (IR)

Pulmonary Hypertension Center, Tufts Medical Center, Boston, MA.

Zeenat Safdar (Z)

Houston Methodist, Houston, TX.

Rajan Saggar (R)

Pulmonary and Critical Care Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA.

Sandeep Sahay (S)

Houston Methodist Lung Center, Houston, TX.

Mary Beth Scholand (MB)

Pulmonary Medicine, University of Utah Health, Farmington, UT.

Oksana A Shlobin (OA)

Inova Fairfax Heart & Lung Transplant Program, Inova Medical Group, Falls Church, VA.

David A Zisman (DA)

Sansum Clinic Santa Barbara, Santa Barbara, CA.

Steven D Nathan (SD)

Advanced Lung Disease Program, Lung Transplant Program, Inova Fairfax Hospital, Falls Church, VA. Electronic address: steven.nathan@inova.org.

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