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Community versus hospital-acquired pneumonia in patients requiring extracorporeal membrane oxygenation

BACKGROUND: Bacterial pneumonia is a major cause of acute respiratory distress syndrome (ARDS) requiring extracorporeal membrane oxygenation (ECMO) support. However, it is unknown whether the type of pneumonia, community-acquired pneumonia (CAP) versus hospital-acquired pneumonia (HAP), should be co...

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Autores principales: Park, Chul, Na, Soo Jin, Chung, Chi Ryang, Cho, Yang Hyun, Suh, Gee Young, Jeon, Kyeongman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327342/
https://www.ncbi.nlm.nih.gov/pubmed/30803350
http://dx.doi.org/10.1177/1753466618821038
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author Park, Chul
Na, Soo Jin
Chung, Chi Ryang
Cho, Yang Hyun
Suh, Gee Young
Jeon, Kyeongman
author_facet Park, Chul
Na, Soo Jin
Chung, Chi Ryang
Cho, Yang Hyun
Suh, Gee Young
Jeon, Kyeongman
author_sort Park, Chul
collection PubMed
description BACKGROUND: Bacterial pneumonia is a major cause of acute respiratory distress syndrome (ARDS) requiring extracorporeal membrane oxygenation (ECMO) support. However, it is unknown whether the type of pneumonia, community-acquired pneumonia (CAP) versus hospital-acquired pneumonia (HAP), should be considered when predicting outcomes for ARDS patients treated with ECMO. METHODS: We divided a sample of adult patients receiving ECMO for acute respiratory distress syndrome caused by bacterial pneumonia between January 2012 and December 2016 into CAP (n = 21) and HAP (n = 35) groups and compared clinical and bacteriological characteristics and outcomes. RESULTS: The median acute physiology and chronic health evaluation II and sequential organ failure assessment scores were 22 and 8, respectively, in the CAP and HAP groups. The most commonly identified organism in the CAP group was Streptococcus pneumonia (n = 12, 57.1%), while Acinectobacter baumanii was the most commonly identified in the HAP group (n = 13, 37.1%). However, the incidence of multidrug resistant bacteria was not different between groups (57.1% versus 74.3%, p = 0.125). Of the 56 patients in the study, 26 were successfully weaned from ECMO, and 20 were discharged from the hospital. There were no significant differences in ECMO weaning rate (47.6% versus 45.7%, p > 0.999) or survival to discharge rate (33.3% versus 37.1%, p > 0.999) between the two groups. The 30-day and 90-day mortality rates were also similar. CONCLUSION: Patients with CAP and HAP who received ECMO for respiratory support had similar characteristics and clinical outcomes.
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spelling pubmed-63273422019-01-22 Community versus hospital-acquired pneumonia in patients requiring extracorporeal membrane oxygenation Park, Chul Na, Soo Jin Chung, Chi Ryang Cho, Yang Hyun Suh, Gee Young Jeon, Kyeongman Ther Adv Respir Dis Original Research BACKGROUND: Bacterial pneumonia is a major cause of acute respiratory distress syndrome (ARDS) requiring extracorporeal membrane oxygenation (ECMO) support. However, it is unknown whether the type of pneumonia, community-acquired pneumonia (CAP) versus hospital-acquired pneumonia (HAP), should be considered when predicting outcomes for ARDS patients treated with ECMO. METHODS: We divided a sample of adult patients receiving ECMO for acute respiratory distress syndrome caused by bacterial pneumonia between January 2012 and December 2016 into CAP (n = 21) and HAP (n = 35) groups and compared clinical and bacteriological characteristics and outcomes. RESULTS: The median acute physiology and chronic health evaluation II and sequential organ failure assessment scores were 22 and 8, respectively, in the CAP and HAP groups. The most commonly identified organism in the CAP group was Streptococcus pneumonia (n = 12, 57.1%), while Acinectobacter baumanii was the most commonly identified in the HAP group (n = 13, 37.1%). However, the incidence of multidrug resistant bacteria was not different between groups (57.1% versus 74.3%, p = 0.125). Of the 56 patients in the study, 26 were successfully weaned from ECMO, and 20 were discharged from the hospital. There were no significant differences in ECMO weaning rate (47.6% versus 45.7%, p > 0.999) or survival to discharge rate (33.3% versus 37.1%, p > 0.999) between the two groups. The 30-day and 90-day mortality rates were also similar. CONCLUSION: Patients with CAP and HAP who received ECMO for respiratory support had similar characteristics and clinical outcomes. SAGE Publications 2019-01-08 /pmc/articles/PMC6327342/ /pubmed/30803350 http://dx.doi.org/10.1177/1753466618821038 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Park, Chul
Na, Soo Jin
Chung, Chi Ryang
Cho, Yang Hyun
Suh, Gee Young
Jeon, Kyeongman
Community versus hospital-acquired pneumonia in patients requiring extracorporeal membrane oxygenation
title Community versus hospital-acquired pneumonia in patients requiring extracorporeal membrane oxygenation
title_full Community versus hospital-acquired pneumonia in patients requiring extracorporeal membrane oxygenation
title_fullStr Community versus hospital-acquired pneumonia in patients requiring extracorporeal membrane oxygenation
title_full_unstemmed Community versus hospital-acquired pneumonia in patients requiring extracorporeal membrane oxygenation
title_short Community versus hospital-acquired pneumonia in patients requiring extracorporeal membrane oxygenation
title_sort community versus hospital-acquired pneumonia in patients requiring extracorporeal membrane oxygenation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327342/
https://www.ncbi.nlm.nih.gov/pubmed/30803350
http://dx.doi.org/10.1177/1753466618821038
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