Is intraoperative dexmedetomidine a new option for postoperative pain treatment? A meta-analysis of randomized controlled trials

被引:197
作者
Schnabel, A. [1 ]
Meyer-Friessem, C. H. [2 ]
Reichl, S. U. [3 ]
Zahn, P. K. [2 ]
Pogatzki-Zahn, E. M. [1 ]
机构
[1] Univ Hosp Muenster, Dept Anaesthesiol Intens Care & Pain Med, D-48149 Munster, Germany
[2] Ruhr Univ Bochum, Dept Anaesthesiol Intens Care Med Palliat Care Me, Berufsgenossenschaftl Univ Klinikum Bergmannsheil, Bochum, Germany
[3] Paracelsus Med Univ Salzburg, Dept Anaesthesiol Perioperat & Intens Care Med, Salzburg, Austria
关键词
Dexmedetomidine; Opioid consumption; Postoperative pain; INTRAVENOUS DEXMEDETOMIDINE; PERIOPERATIVE HEMODYNAMICS; AMBULATORY ANESTHESIA; DOSE DEXMEDETOMIDINE; NONCARDIAC SURGERY; ALPHA-2; AGONISTS; DOUBLE-BLIND; INFUSION; MANAGEMENT; REMIFENTANIL;
D O I
10.1016/j.pain.2013.03.029
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
In the present meta-analysis, we assessed the efficacy and safety of intravenous administration of dexmedetomidine (DEX) compared with placebo or opioids for acute postoperative pain treatment in adults undergoing surgery. The meta-analysis was performed according to the preferred reporting items for systematic reviews and meta-analyses (PRISMA) statement and the recommendations of the Cochrane Collaboration. Randomized controlled trials investigating perioperative administration of DEX were included. For dichotomous outcomes relative risks (RR; 95% confidence intervals [CI]) and for continuous outcomes mean differences (MD; 95% CI) were calculated. Twenty-eight randomized controlled trials including 1420 patients were finally included. Patients treated with DEX reported lower postoperative pain intensity (MD1 h postoperatively: -1.59 U (numeric rating scale: 0 to 10) 95% CI: -2.37 to -0.82; P = .000001) and showed a lower postoperative opioid consumption (MD24 h postoperatively: -17.24 mg; 95% CI: -24.38 to -10.10; P =.00001) compared with placebo. Additionally, the DEX group showed a lower RR for opioid-related adverse events (e.g. RRNausea (postanesthesia care unit): 0.66; 95% CI: 0.43 to 1.02; P=.06). The most common adverse event in patients treated with DEX was intraoperative bradycardia with a RR of 2.66 (RR: 2.66; 95% CI: 1.54 to 4.58; P=.0004) compared with placebo. There is evidence that DEX administration leads to lower postoperative pain, reduced opioid consumption, and a lower risk for opioid-related adverse events. The comparison of DEX vs opioids for postoperative pain treatment is less clear due to limited data. The most common adverse event was intraoperative bradycardia after DEX administration. Therefore cautions in patients at risk are warranted, and large trials focusing on long-term outcomes after intraoperative DEX use are needed. (C) 2013 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1140 / 1149
页数:10
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