Cargando…

Acute Effects of Aerosolized Iloprost in COPD Related Pulmonary Hypertension - A Randomized Controlled Crossover Trial

BACKGROUND: Inhaled iloprost potentially improves hemodynamics and gas exchange in patients with chronic obstructive pulmonary disease (COPD) and secondary pulmonary hypertension (PH). OBJECTIVES: To evaluate acute effects of aerosolized iloprost in patients with COPD-associated PH. METHODS: A rando...

Descripción completa

Detalles Bibliográficos
Autores principales: Boeck, Lucas, Tamm, Michael, Grendelmeier, Peter, Stolz, Daiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531427/
https://www.ncbi.nlm.nih.gov/pubmed/23300624
http://dx.doi.org/10.1371/journal.pone.0052248
_version_ 1782254176696270848
author Boeck, Lucas
Tamm, Michael
Grendelmeier, Peter
Stolz, Daiana
author_facet Boeck, Lucas
Tamm, Michael
Grendelmeier, Peter
Stolz, Daiana
author_sort Boeck, Lucas
collection PubMed
description BACKGROUND: Inhaled iloprost potentially improves hemodynamics and gas exchange in patients with chronic obstructive pulmonary disease (COPD) and secondary pulmonary hypertension (PH). OBJECTIVES: To evaluate acute effects of aerosolized iloprost in patients with COPD-associated PH. METHODS: A randomized, double blind, crossover study was conducted in 16 COPD patients with invasively confirmed PH in a single tertiary care center. Each patient received a single dose of 10 µg iloprost (low dose), 20 µg iloprost (high dose) and placebo during distinct study-visits. The primary end-point of the study was exercise capacity as assessed by the six minute walking distance. RESULTS: Both iloprost doses failed to improve six-minute walking distance (p = 0.36). Low dose iloprost (estimated difference of the means −1.0%, p = 0.035) as well as high dose iloprost (−2.2%, p<0.001) significantly impaired oxygenation at rest. Peak oxygen consumption and carbon dioxide production differed significantly over the three study days (p = 0.002 and p = 0.003, accordingly). As compared to placebo, low dose iloprost was associated with reduced peak oxygen consumption (−76 ml/min, p = 0.002), elevated partial pressure of carbon dioxide (0.27 kPa, p = 0.040) and impaired ventilation during exercise (−3.0l/min, p<0.001). CONCLUSIONS: Improvement of the exercise capacity after iloprost inhalation in patients with COPD-associated mild to moderate PH is very unlikely. TRIAL REGISTRATION: Controlled-Trials.com ISRCTN61661881
format Online
Article
Text
id pubmed-3531427
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35314272013-01-08 Acute Effects of Aerosolized Iloprost in COPD Related Pulmonary Hypertension - A Randomized Controlled Crossover Trial Boeck, Lucas Tamm, Michael Grendelmeier, Peter Stolz, Daiana PLoS One Research Article BACKGROUND: Inhaled iloprost potentially improves hemodynamics and gas exchange in patients with chronic obstructive pulmonary disease (COPD) and secondary pulmonary hypertension (PH). OBJECTIVES: To evaluate acute effects of aerosolized iloprost in patients with COPD-associated PH. METHODS: A randomized, double blind, crossover study was conducted in 16 COPD patients with invasively confirmed PH in a single tertiary care center. Each patient received a single dose of 10 µg iloprost (low dose), 20 µg iloprost (high dose) and placebo during distinct study-visits. The primary end-point of the study was exercise capacity as assessed by the six minute walking distance. RESULTS: Both iloprost doses failed to improve six-minute walking distance (p = 0.36). Low dose iloprost (estimated difference of the means −1.0%, p = 0.035) as well as high dose iloprost (−2.2%, p<0.001) significantly impaired oxygenation at rest. Peak oxygen consumption and carbon dioxide production differed significantly over the three study days (p = 0.002 and p = 0.003, accordingly). As compared to placebo, low dose iloprost was associated with reduced peak oxygen consumption (−76 ml/min, p = 0.002), elevated partial pressure of carbon dioxide (0.27 kPa, p = 0.040) and impaired ventilation during exercise (−3.0l/min, p<0.001). CONCLUSIONS: Improvement of the exercise capacity after iloprost inhalation in patients with COPD-associated mild to moderate PH is very unlikely. TRIAL REGISTRATION: Controlled-Trials.com ISRCTN61661881 Public Library of Science 2012-12-27 /pmc/articles/PMC3531427/ /pubmed/23300624 http://dx.doi.org/10.1371/journal.pone.0052248 Text en © 2012 Boeck et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Boeck, Lucas
Tamm, Michael
Grendelmeier, Peter
Stolz, Daiana
Acute Effects of Aerosolized Iloprost in COPD Related Pulmonary Hypertension - A Randomized Controlled Crossover Trial
title Acute Effects of Aerosolized Iloprost in COPD Related Pulmonary Hypertension - A Randomized Controlled Crossover Trial
title_full Acute Effects of Aerosolized Iloprost in COPD Related Pulmonary Hypertension - A Randomized Controlled Crossover Trial
title_fullStr Acute Effects of Aerosolized Iloprost in COPD Related Pulmonary Hypertension - A Randomized Controlled Crossover Trial
title_full_unstemmed Acute Effects of Aerosolized Iloprost in COPD Related Pulmonary Hypertension - A Randomized Controlled Crossover Trial
title_short Acute Effects of Aerosolized Iloprost in COPD Related Pulmonary Hypertension - A Randomized Controlled Crossover Trial
title_sort acute effects of aerosolized iloprost in copd related pulmonary hypertension - a randomized controlled crossover trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531427/
https://www.ncbi.nlm.nih.gov/pubmed/23300624
http://dx.doi.org/10.1371/journal.pone.0052248
work_keys_str_mv AT boecklucas acuteeffectsofaerosolizediloprostincopdrelatedpulmonaryhypertensionarandomizedcontrolledcrossovertrial
AT tammmichael acuteeffectsofaerosolizediloprostincopdrelatedpulmonaryhypertensionarandomizedcontrolledcrossovertrial
AT grendelmeierpeter acuteeffectsofaerosolizediloprostincopdrelatedpulmonaryhypertensionarandomizedcontrolledcrossovertrial
AT stolzdaiana acuteeffectsofaerosolizediloprostincopdrelatedpulmonaryhypertensionarandomizedcontrolledcrossovertrial