The association between levosimendan and mortality in patients with sepsis or septic shock: a systematic review and meta-analysis

被引:1
|
作者
Ge, Zengzheng [1 ]
Gao, Yanxia [2 ]
Lu, Xin [1 ]
Yu, Shiyuan [1 ]
Qin, Mubing [1 ]
Gong, Chao [1 ]
Walline, Joseph Harold [3 ,4 ]
Zhu, Huadong [1 ]
Li, Yi [1 ,5 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Chinese Acad Med Sci Peking Union Med Coll, Emergency Dept, State Key Lab Complex Severe & Rare Dis, Beijing, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Emergency Med, Zhengzhou, Peoples R China
[3] Milton S Hershey Med Ctr, Penn State Hlth, Dept Emergency Med, Hershey, PA USA
[4] Penn State Univ, Coll Med, Hershey, PA USA
[5] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Emergency Med, State Key Lab Complex Severe & Rare Dis, Beijing 100730, Peoples R China
关键词
levosimendan; meta-analysis; sepsis; septic shock; ORGAN INJURY; DYSFUNCTION; THIAMINE;
D O I
10.1097/MEJ.0000000000001105
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BackgroundLevosimendan is increasingly being used in patients with sepsis or septic shock because of its potential to improve organ function and reduce mortality. We aimed to determine if levosimendan can reduce mortality in patients with sepsis or septic shock via meta-analysis.Evidence sources and study selectionWe comprehensively searched the PubMed, Embase, Web of Science, and Cochrane Library databases from inception through 1 October 2022. Literature evaluating the efficacy of levosimendan in patients with sepsis or septic shock was included.Data extraction and outcome measurementsTwo reviewers extracted data and assessed study quality. A meta-analysis was performed to calculate an odds ratio (OR), 95% confidence intervals (CI), and P-values for 28-day mortality (primary outcome). Secondary outcomes included changes in indexes reflecting cardiac function before and after treatment, changes in serum lactate levels in the first 24 h of treatment, and the mean SOFA score during the study period. Safety outcomes included rates of tachyarrhythmias and total adverse reactions encountered with levosimendan.ResultsEleven randomized controlled trials were identified, encompassing a total of 1044 patients. After using levosimendan, there was no statistical difference between groups for 28-day mortality (34.9% and 36.2%; OR: 0.93; 95% CI [0.72-1.2]; P = 0.57; I2 = 0%; trial sequential analysis-adjusted CI [0.6-1.42]) and sequential organ failure assessment (SOFA) score, and more adverse reactions seemed to occur in the levosimendan group, although the septic shock patient's heart function and serum lactate level improved.ConclusionThere was no association between the use of levosimendan and 28-day mortality and SOFA scores in patients with septic shock, though there was statistically significant improvement in cardiac function and serum lactate.
引用
收藏
页码:90 / 97
页数:8
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