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Hemodynamic effects of inotropic drugs in heart failure: A network meta-analysis of clinical trials
BACKGROUND: There is currently no consensus on the appropriate selection of inotropic therapy in ventricular dysfunction. The objective of the study was to detect the effects of different inotropes on the hemodynamics of patients who developed low cardiac output. METHODS: PubMed, Embase, and the Coc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882628/ https://www.ncbi.nlm.nih.gov/pubmed/31764856 http://dx.doi.org/10.1097/MD.0000000000018144 |
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author | Long, Ling Zhao, Hao-tian Shen, Li-min He, Cong Ren, Shan Zhao, He-ling |
author_facet | Long, Ling Zhao, Hao-tian Shen, Li-min He, Cong Ren, Shan Zhao, He-ling |
author_sort | Long, Ling |
collection | PubMed |
description | BACKGROUND: There is currently no consensus on the appropriate selection of inotropic therapy in ventricular dysfunction. The objective of the study was to detect the effects of different inotropes on the hemodynamics of patients who developed low cardiac output. METHODS: PubMed, Embase, and the Cochrane Central Register of Controlled Trials (CENTRAL) were searched (all updated December 31, 2017). The inclusion criteria were as follows: low cardiac index (CI < 2.5 L/min/m(2)) or New York Heart Association class II–IV, and at least 1 group receiving an inotropic drug compared to another group receiving a different inotropic/placebo treatment. The exclusion criteria were studies published as an abstract only, crossover studies, and studies with a lack of data on the cardiac index. RESULTS: A total of 1402 patients from 37 trials were included in the study. Inotropic drugs were shown to increase the cardiac index (0.32, 95%CI:0.25, 0.38), heart rate (7.68, 95%CI:6.36, 9.01), and mean arterial pressure (3.17, 95%CI:1.96, 4.38) than the placebo. Overall, the pooled estimates showed no difference in terms of cardiac index, heart rate, mean arterial pressure, systemic vascular resistance, and mean pulmonary arterial pressure among the groups receiving different inotropes. CONCLUSIONS: Our systematic review found that inotrope therapy is not associated with the amelioration of hemodynamics. An accurate evaluation of the benefits and risks, and selection of the correct inotropic agent is required in all clinical settings. |
format | Online Article Text |
id | pubmed-6882628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-68826282020-01-22 Hemodynamic effects of inotropic drugs in heart failure: A network meta-analysis of clinical trials Long, Ling Zhao, Hao-tian Shen, Li-min He, Cong Ren, Shan Zhao, He-ling Medicine (Baltimore) 3400 BACKGROUND: There is currently no consensus on the appropriate selection of inotropic therapy in ventricular dysfunction. The objective of the study was to detect the effects of different inotropes on the hemodynamics of patients who developed low cardiac output. METHODS: PubMed, Embase, and the Cochrane Central Register of Controlled Trials (CENTRAL) were searched (all updated December 31, 2017). The inclusion criteria were as follows: low cardiac index (CI < 2.5 L/min/m(2)) or New York Heart Association class II–IV, and at least 1 group receiving an inotropic drug compared to another group receiving a different inotropic/placebo treatment. The exclusion criteria were studies published as an abstract only, crossover studies, and studies with a lack of data on the cardiac index. RESULTS: A total of 1402 patients from 37 trials were included in the study. Inotropic drugs were shown to increase the cardiac index (0.32, 95%CI:0.25, 0.38), heart rate (7.68, 95%CI:6.36, 9.01), and mean arterial pressure (3.17, 95%CI:1.96, 4.38) than the placebo. Overall, the pooled estimates showed no difference in terms of cardiac index, heart rate, mean arterial pressure, systemic vascular resistance, and mean pulmonary arterial pressure among the groups receiving different inotropes. CONCLUSIONS: Our systematic review found that inotrope therapy is not associated with the amelioration of hemodynamics. An accurate evaluation of the benefits and risks, and selection of the correct inotropic agent is required in all clinical settings. Wolters Kluwer Health 2019-11-22 /pmc/articles/PMC6882628/ /pubmed/31764856 http://dx.doi.org/10.1097/MD.0000000000018144 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 3400 Long, Ling Zhao, Hao-tian Shen, Li-min He, Cong Ren, Shan Zhao, He-ling Hemodynamic effects of inotropic drugs in heart failure: A network meta-analysis of clinical trials |
title | Hemodynamic effects of inotropic drugs in heart failure: A network meta-analysis of clinical trials |
title_full | Hemodynamic effects of inotropic drugs in heart failure: A network meta-analysis of clinical trials |
title_fullStr | Hemodynamic effects of inotropic drugs in heart failure: A network meta-analysis of clinical trials |
title_full_unstemmed | Hemodynamic effects of inotropic drugs in heart failure: A network meta-analysis of clinical trials |
title_short | Hemodynamic effects of inotropic drugs in heart failure: A network meta-analysis of clinical trials |
title_sort | hemodynamic effects of inotropic drugs in heart failure: a network meta-analysis of clinical trials |
topic | 3400 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882628/ https://www.ncbi.nlm.nih.gov/pubmed/31764856 http://dx.doi.org/10.1097/MD.0000000000018144 |
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