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非阿片类镇痛药作为阿片类药物在 ICU 成人患者疼痛管理中的辅助药物:系统评价和荟萃分析。

Non-opioid analgesics as adjuvants to opioid for pain management in adult patients in the ICU: A systematic review and meta-analysis.

机构信息

Department of Critical Care Medicine, Peking University People's Hospital, Beijing, China.

Department of Critical Care Medicine, Peking University People's Hospital, Beijing, China.

出版信息

J Crit Care. 2019 Dec;54:136-144. doi: 10.1016/j.jcrc.2019.08.022. Epub 2019 Aug 13.

Abstract

PURPOSE

To identify the impact of non-opioid analgesics as adjuvants to opioid on opioid consumption and its side effects, as well as the analgesic effectiveness in adult patients in the ICU.

METHODS

Only randomized clinical trials using non-opioid analgesics for analgesia in the ICU were included. Pooled analyses with 95% CI were determined.

RESULTS

Twelve studies (mainly surgical and Guillain-Barre syndrome patients) were included. Non-opioid analgesics as adjuvants to opioid were associated with a significant reduction in the consumption of opioids when compared with opioid use alone at Day 1 (MD -15.40; 95% CI -22.41 to -8.39; P < .001) and Day 2 (MD -22.93; 95% CI -27.70 to -18.16; P < .001). Non-opioid analgesics as adjuvants to opioid were associated with a significantly lower incidence of nausea and vomiting when compared with opioid use alone (RR 0.46; 95% CI 0.30 to 0.68; P < .001). Non-opioid analgesics as adjuvants to opioid significantly decreased the pain score at Day 1 (MD -0.68; 95% CI -1.28 to -0.08; P = .03) and Day 2 (MD -1.36; 95% CI -2.47 to -0.24; P = .02).

CONCLUSIONS

Non-opioid analgesics as adjuvants to opioid reduced the consumption and the side effects of opioids in adult surgical and Guillain-Barre syndrome patients in the ICU.

TRIAL REVIEW REGISTRATION

PROSPERO international prospective register of systematic reviews on January 23, 2017, registration number CRD42017055768.

摘要

目的

确定非阿片类镇痛药作为阿片类药物辅助治疗对阿片类药物消耗及其副作用的影响,以及在 ICU 成人患者中的镇痛效果。

方法

仅纳入使用非阿片类镇痛药进行 ICU 镇痛的随机临床试验。采用 95%CI 进行汇总分析。

结果

纳入 12 项研究(主要为外科和吉兰-巴雷综合征患者)。与单独使用阿片类药物相比,非阿片类镇痛药作为阿片类药物的辅助治疗,在第 1 天(MD-15.40;95%CI-22.41 至-8.39;P<0.001)和第 2 天(MD-22.93;95%CI-27.70 至-18.16;P<0.001)时,阿片类药物的消耗量显著降低。与单独使用阿片类药物相比,非阿片类镇痛药作为阿片类药物的辅助治疗,恶心和呕吐的发生率显著降低(RR 0.46;95%CI 0.30 至 0.68;P<0.001)。与单独使用阿片类药物相比,非阿片类镇痛药作为阿片类药物的辅助治疗在第 1 天(MD-0.68;95%CI-1.28 至-0.08;P=0.03)和第 2 天(MD-1.36;95%CI-2.47 至-0.24;P=0.02)时疼痛评分显著降低。

结论

非阿片类镇痛药作为阿片类药物的辅助治疗可减少 ICU 成人外科和吉兰-巴雷综合征患者阿片类药物的消耗和副作用。

试验注册

PROSPERO 国际前瞻性系统评价注册系统于 2017 年 1 月 23 日注册,注册号 CRD42017055768。

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