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Use of Aerosolized Prostacyclins in Critically Ill Patients and Association With Clinical Outcomes
Aerosolized prostacyclins are frequently used in patients with severe acute respiratory distress syndrome and refractory hypoxia. Previous studies have shown improvement in oxygenation with use of pulmonary vasodilators such as iloprost and epoprostenol; however, there is no head-to-head comparison...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829278/ https://www.ncbi.nlm.nih.gov/pubmed/36699246 http://dx.doi.org/10.1097/CCE.0000000000000845 |
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author | Hussain, S. Talal Jaliawala, Huzaifa A. Zhao, Daniel Ijaz, Sardar Hassan Tsui, Janice Chasteen, Bobby Brown, Brent R. Bernardo, Roberto J. |
author_facet | Hussain, S. Talal Jaliawala, Huzaifa A. Zhao, Daniel Ijaz, Sardar Hassan Tsui, Janice Chasteen, Bobby Brown, Brent R. Bernardo, Roberto J. |
author_sort | Hussain, S. Talal |
collection | PubMed |
description | Aerosolized prostacyclins are frequently used in patients with severe acute respiratory distress syndrome and refractory hypoxia. Previous studies have shown improvement in oxygenation with use of pulmonary vasodilators such as iloprost and epoprostenol; however, there is no head-to-head comparison between these agents. OBJECTIVES: To compare the effects of inhaled epoprostenol and inhaled iloprost in critically ill patients with refractory hypoxia. DESIGN, SETTING, AND PARTICIPANTS: We performed a retrospective cohort analysis of patients admitted to the ICUs at the University of Oklahoma Health Sciences Center between 2015 and 2018. Adult patients who received aerosolized epoprostenol or iloprost for more than 4 hours were included in the analysis. MAIN OUTCOMES AND MEASURES: The primary endpoint measured was to compare the change in Pao(2)/Fio(2) ratio between patients treated with iloprost compared with epoprostenol. Secondary outcomes measured were 90-day in-hospital mortality and improvement in vasopressor requirements. RESULTS: A total of 126 patients were included in the study, 95 of whom received iloprost (75%) and 31 patients (25%) received epoprostenol. There were significant improvements in Pao(2)/Fio(2) ratio in both the iloprost and epoprostenol group. Patients in the epoprostenol group appeared to have a higher 90-day mortality compared with the iloprost group. However, our study was not powered to detect a mortality difference and this finding likely represents a sicker population in the epoprostenol group and prescription bias. The use of iloprost was associated with higher vasopressor requirements in the first 12 hours of administration, an association was not observed in the epoprostenol group. CONCLUSIONS AND RELEVANCE: In this retrospective cohort analysis, use of both pulmonary vasodilators was associated with similar improvement in gas exchange. The mortality difference observed likely represents difference in severity of illness. Further studies are needed to corroborate these findings. |
format | Online Article Text |
id | pubmed-9829278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-98292782023-01-24 Use of Aerosolized Prostacyclins in Critically Ill Patients and Association With Clinical Outcomes Hussain, S. Talal Jaliawala, Huzaifa A. Zhao, Daniel Ijaz, Sardar Hassan Tsui, Janice Chasteen, Bobby Brown, Brent R. Bernardo, Roberto J. Crit Care Explor Observational Study Aerosolized prostacyclins are frequently used in patients with severe acute respiratory distress syndrome and refractory hypoxia. Previous studies have shown improvement in oxygenation with use of pulmonary vasodilators such as iloprost and epoprostenol; however, there is no head-to-head comparison between these agents. OBJECTIVES: To compare the effects of inhaled epoprostenol and inhaled iloprost in critically ill patients with refractory hypoxia. DESIGN, SETTING, AND PARTICIPANTS: We performed a retrospective cohort analysis of patients admitted to the ICUs at the University of Oklahoma Health Sciences Center between 2015 and 2018. Adult patients who received aerosolized epoprostenol or iloprost for more than 4 hours were included in the analysis. MAIN OUTCOMES AND MEASURES: The primary endpoint measured was to compare the change in Pao(2)/Fio(2) ratio between patients treated with iloprost compared with epoprostenol. Secondary outcomes measured were 90-day in-hospital mortality and improvement in vasopressor requirements. RESULTS: A total of 126 patients were included in the study, 95 of whom received iloprost (75%) and 31 patients (25%) received epoprostenol. There were significant improvements in Pao(2)/Fio(2) ratio in both the iloprost and epoprostenol group. Patients in the epoprostenol group appeared to have a higher 90-day mortality compared with the iloprost group. However, our study was not powered to detect a mortality difference and this finding likely represents a sicker population in the epoprostenol group and prescription bias. The use of iloprost was associated with higher vasopressor requirements in the first 12 hours of administration, an association was not observed in the epoprostenol group. CONCLUSIONS AND RELEVANCE: In this retrospective cohort analysis, use of both pulmonary vasodilators was associated with similar improvement in gas exchange. The mortality difference observed likely represents difference in severity of illness. Further studies are needed to corroborate these findings. Lippincott Williams & Wilkins 2023-01-06 /pmc/articles/PMC9829278/ /pubmed/36699246 http://dx.doi.org/10.1097/CCE.0000000000000845 Text en Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Observational Study Hussain, S. Talal Jaliawala, Huzaifa A. Zhao, Daniel Ijaz, Sardar Hassan Tsui, Janice Chasteen, Bobby Brown, Brent R. Bernardo, Roberto J. Use of Aerosolized Prostacyclins in Critically Ill Patients and Association With Clinical Outcomes |
title | Use of Aerosolized Prostacyclins in Critically Ill Patients and Association With Clinical Outcomes |
title_full | Use of Aerosolized Prostacyclins in Critically Ill Patients and Association With Clinical Outcomes |
title_fullStr | Use of Aerosolized Prostacyclins in Critically Ill Patients and Association With Clinical Outcomes |
title_full_unstemmed | Use of Aerosolized Prostacyclins in Critically Ill Patients and Association With Clinical Outcomes |
title_short | Use of Aerosolized Prostacyclins in Critically Ill Patients and Association With Clinical Outcomes |
title_sort | use of aerosolized prostacyclins in critically ill patients and association with clinical outcomes |
topic | Observational Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829278/ https://www.ncbi.nlm.nih.gov/pubmed/36699246 http://dx.doi.org/10.1097/CCE.0000000000000845 |
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