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鞘内注射右美托咪定对预防脊髓麻醉的剖宫产术后寒战的作用:荟萃分析和试验序贯分析

 

Authors Miao S, Shi M, Zou L, Wang G

Received 29 June 2018

Accepted for publication 9 October 2018

Published 2 November 2018 Volume 2018:12 Pages 3775—3783

DOI https://doi.org/10.2147/DDDT.S178665

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Cristina Weinberg

Peer reviewer comments 2

Editor who approved publication: Dr Sukesh Voruganti

Objective: Intrathecal dexmedetomidine (DEX) has been used to prevent shivering in patients undergoing cesarean section. The aim of this meta-analysis was to evaluate whether intrathecal DEX could prevent shivering in cesarean section after spinal anesthesia.
Methods: We searched PubMed, Embase, Web of Science, and the Cochrane Library for randomized controlled trials (RCTs) comparing intrathecal DEX in cesarean section after spinal anesthesia with placebo and reporting on shivering, postoperative nausea and vomiting (PONV), hypotension, and bradycardia. Trial sequential analysis (TSA) was also carried out for RCTs comparing DEX with placebo. This meta-analysis has been registered on PROSPERO, and the registration number is CRD42017071640.
Results: Six randomized clinical trials comparing 360 patients were included in this study. Compared with placebo, intrathecal DEX significantly reduced the incidence of shivering (risk ratio [RR]=0.40; 95% CI [0.26, 0.62]; <0.0001). No significant difference was found in the incidence of PONV (RR=1.34; 95% CI [0.82, 2.18]; =0.24), hypotension (RR=1.09; 95% CI [0.84, 1.42]; =0.50), or bradycardia (RR=1.55; 95% CI [0.54, 4.42]; =0.42). However, no firm conclusions can be made based on the results of all outcomes according to the TSA.
Conclusion: This meta-analysis found that intrathecal DEX could prevent shivering in cesarean section after spinal anesthesia and did not induce PONV, hypotension, or bradycardia. However, firm conclusions cannot be made until more studies are conducted.
Keywords: dexmedetomidine, cesarean section, spinal anesthesia, meta-analysis, trial sequential analysis, adverse effect




Figure 2 The risk of bias of all the included trials.