Practical considerations in the management of inhaled prostacyclin therapy for pulmonary hypertension associated with interstitial lung disease (WHO group 3).

Administration Adverse event management Inhaled treprostinil Interstitial lung disease Pulmonary hypertension Titration Tolerability

Journal

Respiratory medicine
ISSN: 1532-3064
Titre abrégé: Respir Med
Pays: England
ID NLM: 8908438

Informations de publication

Date de publication:
05 2022
Historique:
received: 04 11 2021
revised: 12 02 2022
accepted: 06 03 2022
pubmed: 26 3 2022
medline: 27 4 2022
entrez: 25 3 2022
Statut: ppublish

Résumé

Pulmonary hypertension (PH), as a consequence of lung disease or hypoxia, has been classified as Group 3 PH by the World Symposium on Pulmonary Hypertension. The most common lung diseases associated with Group 3 PH are chronic obstructive pulmonary disease (COPD) and interstitial lung disease (ILD). PH in ILD (PH-ILD) is associated with reduced exercise capacity, greater supplemental oxygen needs, decreased quality of life, and earlier death compared to ILD alone. Several agents have been evaluated in clinical trials for the treatment of Group 3 PH, but only one treatment has been recently approved by the FDA as conclusively demonstrating efficacy for the treatment of pulmonary hypertension in this group. In the INCREASE study, treprostinil inhalation solution (Tyvaso) demonstrated significant clinical benefit for patients with PH-ILD. The inhaled route of administration may be associated with cough, throat irritation, pharyngolaryngeal pain and risk of bronchospasm and are important considerations upon initiation of therapy. Here we provide a practical review of inhaled prostacyclin therapy and suggestions for healthcare professionals to optimize the management and outcomes for the treatment of WHO Group 3, PH-ILD patients. Recommendations include up-to-date practical considerations pertaining to the entire care team and encompass patient education and communication, monitoring, titration methods and mitigation of side effects.

Identifiants

pubmed: 35334313
pii: S0954-6111(22)00071-3
doi: 10.1016/j.rmed.2022.106806
pii:
doi:

Substances chimiques

Prostaglandins I 0
Epoprostenol DCR9Z582X0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

106806

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Charlie Lee (C)

Brigham and Women's Hospital, USA. Electronic address: clee39@bwh.harvard.edu.

Joan Hamlyn (J)

University of Louisville, USA.

Julie Porcelli (J)

New York Presbyterian Hospital, USA.

Ann Schmit (A)

Ascension St. Vincent Medical Group, Indianapolis, USA.

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Classifications MeSH