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Dopamine versus norepinephrine in the treatment of cardiogenic shock: A PRISMA-compliant meta-analysis
BACKGROUND: Guidelines recommend that norepinephrine (NA) should be used to reach the target mean arterial pressure (MAP) during cardiogenic shock (CS), rather than epinephrine and dopamine (DA). However, there has actually been few studies on comparing norepinephrine with dopamine and their results...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671870/ https://www.ncbi.nlm.nih.gov/pubmed/29069037 http://dx.doi.org/10.1097/MD.0000000000008402 |
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author | Rui, Qing Jiang, Yufeng Chen, Min Zhang, Nannan Yang, Huajia Zhou, Yafeng |
author_facet | Rui, Qing Jiang, Yufeng Chen, Min Zhang, Nannan Yang, Huajia Zhou, Yafeng |
author_sort | Rui, Qing |
collection | PubMed |
description | BACKGROUND: Guidelines recommend that norepinephrine (NA) should be used to reach the target mean arterial pressure (MAP) during cardiogenic shock (CS), rather than epinephrine and dopamine (DA). However, there has actually been few studies on comparing norepinephrine with dopamine and their results conflicts. These studies raise a heat discussion. This study aimed to validate the effectiveness of norepinephrine for treating CS in comparison with dopamine. METHODS: We performed a meta-analysis of randomized controlled trials (RCTs) to assess pooled estimates of risk ratio (RR) and 95% confidence interval (CI) for 28-day mortality, incidence of arrhythmic events, gastrointestinal reaction, and some indexes after treatment. RESULTS: Compared with dopamine, patients receiving norepinephrine had a lower 28-day mortality (RR 1.611 [95% CI 1.219–2.129]; P < .001; P heterogeneity = .01), a lower risk of arrhythmic events (RR 3.426 [95% CI 2.120–5.510]; P < .001; P heterogeneity = .875) and a lower risk of gastrointestinal reaction (RR 5.474 [95% CI 2.917–10.273]; P < .001; P heterogeneity = 0). In subgroup analyses on 28-day mortality by causes of CS, there were more benefits from norepinephrine than dopamine in 2 subgroups. CONCLUSIONS: Our analysis revealed that norepinephrine was associated with a lower 28-day mortality, a lower risk of arrhythmic events, and gastrointestinal reaction. No matter whether CS is caused by coronary heart disease or not, norepinephrine is superior to dopamine for correcting CS on the 28-day mortality. |
format | Online Article Text |
id | pubmed-5671870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-56718702017-11-22 Dopamine versus norepinephrine in the treatment of cardiogenic shock: A PRISMA-compliant meta-analysis Rui, Qing Jiang, Yufeng Chen, Min Zhang, Nannan Yang, Huajia Zhou, Yafeng Medicine (Baltimore) 3400 BACKGROUND: Guidelines recommend that norepinephrine (NA) should be used to reach the target mean arterial pressure (MAP) during cardiogenic shock (CS), rather than epinephrine and dopamine (DA). However, there has actually been few studies on comparing norepinephrine with dopamine and their results conflicts. These studies raise a heat discussion. This study aimed to validate the effectiveness of norepinephrine for treating CS in comparison with dopamine. METHODS: We performed a meta-analysis of randomized controlled trials (RCTs) to assess pooled estimates of risk ratio (RR) and 95% confidence interval (CI) for 28-day mortality, incidence of arrhythmic events, gastrointestinal reaction, and some indexes after treatment. RESULTS: Compared with dopamine, patients receiving norepinephrine had a lower 28-day mortality (RR 1.611 [95% CI 1.219–2.129]; P < .001; P heterogeneity = .01), a lower risk of arrhythmic events (RR 3.426 [95% CI 2.120–5.510]; P < .001; P heterogeneity = .875) and a lower risk of gastrointestinal reaction (RR 5.474 [95% CI 2.917–10.273]; P < .001; P heterogeneity = 0). In subgroup analyses on 28-day mortality by causes of CS, there were more benefits from norepinephrine than dopamine in 2 subgroups. CONCLUSIONS: Our analysis revealed that norepinephrine was associated with a lower 28-day mortality, a lower risk of arrhythmic events, and gastrointestinal reaction. No matter whether CS is caused by coronary heart disease or not, norepinephrine is superior to dopamine for correcting CS on the 28-day mortality. Wolters Kluwer Health 2017-10-27 /pmc/articles/PMC5671870/ /pubmed/29069037 http://dx.doi.org/10.1097/MD.0000000000008402 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://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), 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. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 3400 Rui, Qing Jiang, Yufeng Chen, Min Zhang, Nannan Yang, Huajia Zhou, Yafeng Dopamine versus norepinephrine in the treatment of cardiogenic shock: A PRISMA-compliant meta-analysis |
title | Dopamine versus norepinephrine in the treatment of cardiogenic shock: A PRISMA-compliant meta-analysis |
title_full | Dopamine versus norepinephrine in the treatment of cardiogenic shock: A PRISMA-compliant meta-analysis |
title_fullStr | Dopamine versus norepinephrine in the treatment of cardiogenic shock: A PRISMA-compliant meta-analysis |
title_full_unstemmed | Dopamine versus norepinephrine in the treatment of cardiogenic shock: A PRISMA-compliant meta-analysis |
title_short | Dopamine versus norepinephrine in the treatment of cardiogenic shock: A PRISMA-compliant meta-analysis |
title_sort | dopamine versus norepinephrine in the treatment of cardiogenic shock: a prisma-compliant meta-analysis |
topic | 3400 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671870/ https://www.ncbi.nlm.nih.gov/pubmed/29069037 http://dx.doi.org/10.1097/MD.0000000000008402 |
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