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Efficacy of nimodipine in the treatment of subarachnoid hemorrhage: a meta-analysis
BACKGROUND: Subarachnoid hemorrhage (SAH) is an uncommon and serious subtype of stroke, which leads to the loss of the patient’s ability to produce and live for many years. OBJECTIVE: To investigate the clinical effect of nimodipine in the treatment of SAH. Methods Electronic databases including Chi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Academia Brasileira de Neurologia - ABNEURO
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685822/ https://www.ncbi.nlm.nih.gov/pubmed/36254437 http://dx.doi.org/10.1055/s-0042-1755301 |
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author | Liu, Jianqiang Sun, Cuimei Wang, Ying Nie, Guangjun Dong, Qihao You, Jiebing Li, Qiang Li, Mingyue |
author_facet | Liu, Jianqiang Sun, Cuimei Wang, Ying Nie, Guangjun Dong, Qihao You, Jiebing Li, Qiang Li, Mingyue |
author_sort | Liu, Jianqiang |
collection | PubMed |
description | BACKGROUND: Subarachnoid hemorrhage (SAH) is an uncommon and serious subtype of stroke, which leads to the loss of the patient’s ability to produce and live for many years. OBJECTIVE: To investigate the clinical effect of nimodipine in the treatment of SAH. Methods Electronic databases including China National Knowledge Infrastructure (CNKI), VIP, SinoMed, China Master’s Theses Full-text Database (CMFD), China Doctoral Dissertations Full-text Database (CDFD), Cochrane Library, PubMed and Embase were searched from 2010 and 2021. All randomized controlled trials evaluating the efficacy of nimodipine in the treatment of SAH were included in our meta-analysis. The patients were divided into control group and treatment group. Meta-analysis was performed with Stata16.0 software. RESULTS: A total of 10 studies were included. Compared with the control group, the treatment group had higher effective rate (OR = 3.21, 95% CI: 2.25, 4.58; p < 0.001), and lower incidence of adverse reactions (OR = 0.35, 95% CI: 0.19, 0.67; p = 0.001). Before treatment, no significant differences were identified in middle cerebral artery blood flow velocity and Glasgow coma scale (GCS) score between the two groups. However, after treatment, the middle cerebral artery blood flow velocity (SMD = — 1.36, 95% CI: —2.28, —0.49; p = 0.002) and GCS score (SMD = 1.24, 95% CI: 0.58, 1.89; p < 0.001) in the treatment group were significantly better than those in the control group. CONCLUSIONS: Nimodipine is effective in the treatment of SAH, lowering incidence of adverse reactions and therefore improving the prognosis of patients. |
format | Online Article Text |
id | pubmed-9685822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Academia Brasileira de Neurologia - ABNEURO |
record_format | MEDLINE/PubMed |
spelling | pubmed-96858222022-12-08 Efficacy of nimodipine in the treatment of subarachnoid hemorrhage: a meta-analysis Liu, Jianqiang Sun, Cuimei Wang, Ying Nie, Guangjun Dong, Qihao You, Jiebing Li, Qiang Li, Mingyue Arq Neuropsiquiatr Original Article BACKGROUND: Subarachnoid hemorrhage (SAH) is an uncommon and serious subtype of stroke, which leads to the loss of the patient’s ability to produce and live for many years. OBJECTIVE: To investigate the clinical effect of nimodipine in the treatment of SAH. Methods Electronic databases including China National Knowledge Infrastructure (CNKI), VIP, SinoMed, China Master’s Theses Full-text Database (CMFD), China Doctoral Dissertations Full-text Database (CDFD), Cochrane Library, PubMed and Embase were searched from 2010 and 2021. All randomized controlled trials evaluating the efficacy of nimodipine in the treatment of SAH were included in our meta-analysis. The patients were divided into control group and treatment group. Meta-analysis was performed with Stata16.0 software. RESULTS: A total of 10 studies were included. Compared with the control group, the treatment group had higher effective rate (OR = 3.21, 95% CI: 2.25, 4.58; p < 0.001), and lower incidence of adverse reactions (OR = 0.35, 95% CI: 0.19, 0.67; p = 0.001). Before treatment, no significant differences were identified in middle cerebral artery blood flow velocity and Glasgow coma scale (GCS) score between the two groups. However, after treatment, the middle cerebral artery blood flow velocity (SMD = — 1.36, 95% CI: —2.28, —0.49; p = 0.002) and GCS score (SMD = 1.24, 95% CI: 0.58, 1.89; p < 0.001) in the treatment group were significantly better than those in the control group. CONCLUSIONS: Nimodipine is effective in the treatment of SAH, lowering incidence of adverse reactions and therefore improving the prognosis of patients. Academia Brasileira de Neurologia - ABNEURO 2022-11-21 /pmc/articles/PMC9685822/ /pubmed/36254437 http://dx.doi.org/10.1055/s-0042-1755301 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons AttributionNoncommercial No Derivative License, which permits unrestricted noncommercial use, distribution, and reproduction in any medium provided the original work is properly cited and the work is not changed in any way. |
spellingShingle | Original Article Liu, Jianqiang Sun, Cuimei Wang, Ying Nie, Guangjun Dong, Qihao You, Jiebing Li, Qiang Li, Mingyue Efficacy of nimodipine in the treatment of subarachnoid hemorrhage: a meta-analysis |
title | Efficacy of nimodipine in the treatment of subarachnoid hemorrhage: a meta-analysis |
title_full | Efficacy of nimodipine in the treatment of subarachnoid hemorrhage: a meta-analysis |
title_fullStr | Efficacy of nimodipine in the treatment of subarachnoid hemorrhage: a meta-analysis |
title_full_unstemmed | Efficacy of nimodipine in the treatment of subarachnoid hemorrhage: a meta-analysis |
title_short | Efficacy of nimodipine in the treatment of subarachnoid hemorrhage: a meta-analysis |
title_sort | efficacy of nimodipine in the treatment of subarachnoid hemorrhage: a meta-analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685822/ https://www.ncbi.nlm.nih.gov/pubmed/36254437 http://dx.doi.org/10.1055/s-0042-1755301 |
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