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多模式镇痛对初次前交叉韧带重建术后即刻疼痛结局的影响:一级随机临床试验的系统评价和荟萃分析。

Contribution of Multimodal Analgesia to Postoperative Pain Outcomes Immediately After Primary Anterior Cruciate Ligament Reconstruction: A Systematic Review and Meta-analysis of Level 1 Randomized Clinical Trials.

机构信息

Midwest Orthopaedics at Rush University, Chicago, Illinois, USA.

Twin Cities Othopaedics, Eagan, Minnesota, USA.

出版信息

Am J Sports Med. 2021 Sep;49(11):3132-3144. doi: 10.1177/0363546520980429. Epub 2021 Jan 7.

Abstract

BACKGROUND

Anterior cruciate ligament reconstruction (ACLR) is associated with moderate to severe pain in the immediate postoperative period. The optimal individual preemptive or intraoperative anesthetic modality on postoperative pain control is not well-known.

PURPOSE

To systematically review and perform a meta-analysis comparing postoperative pain scores (visual analog scale [VAS]), opioid consumption, and incidence of complications during the first 24 hours after primary ACLR in patients receiving spinal anesthetic, adjunct regional nerve blocks, or local analgesics.

STUDY DESIGN

Systematic review and meta-analysis.

METHODS

PubMed, Embase, MEDLINE, Biosis Previews, SPORTDiscus, Ovid, PEDRO, and the Cochrane Library databases were systematically searched from inception to March 2020 for human studies, using a PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) checklist. Inclusion criteria consisted of (1) level 1 studies reporting on the use of spinal anesthesia, adjunct regional anesthesia (femoral nerve block [FNB] or adductor canal block [ACB]), or local analgesia in patients undergoing primary ACLR and (2) studies reporting on patient-reported VAS, opioid consumption, and incidence of complications related to anesthesia within the first 24 hours after surgery. Non-level 1 studies, studies utilizing a combination of anesthetic modalities, and those not reporting outcomes during the first 24 hours were excluded. Data were synthesized, and a random effects meta-analysis was performed to determine postoperative pain, opioid use, and complications based on anesthetic modality at multiple time points (0-4, 4-8, 8-12, 12-24 hours).

RESULTS

A total of 263 studies were screened, of which 27 level 1 studies (n = 16 regional blocks; n = 12 local; n = 4 spinal) met the inclusion criteria and were included in the meta-analysis. VAS scores were significantly lower in patients receiving a regional block as compared with spinal anesthesia 8 to 12 hours after surgery ( < .01), patients receiving an FNB versus ACB at 12 to 24 hours ( < .01), and those treated with a continuous FNB rather than single-shot regional blocks (FNB, ACB) at 12 to 24 hours ( < .01). No significant difference in VAS was appreciated when spinal, regional, and local anesthesia groups were compared.

CONCLUSION

Based on evidence from level 1 studies, pain control after primary ACLR based on VAS was significantly improved at 8 to 12 hours in patients receiving regional anesthesia as compared with spinal anesthesia. Pain scores were significantly lower at 12 to 24 hours in patients receiving FNB versus ACB and those treated with continuous FNB rather than single-shot regional anesthetic.

摘要

背景

前交叉韧带重建(ACLR)术后即刻会出现中度至重度疼痛。对于术后疼痛控制,最佳的个体预防性或术中麻醉方式尚不清楚。

目的

系统回顾和进行荟萃分析,比较接受脊髓麻醉、辅助区域神经阻滞或局部镇痛的患者在初次 ACLR 后 24 小时内的术后疼痛评分(视觉模拟评分[VAS])、阿片类药物消耗和并发症发生率。

研究设计

系统回顾和荟萃分析。

方法

从建库到 2020 年 3 月,使用 PRISMA(系统评价和荟萃分析的首选报告项目)清单,对 PubMed、Embase、MEDLINE、Biosis Previews、SPORTDiscus、Ovid、PEDRO 和 Cochrane Library 数据库进行了系统搜索,纳入了研究使用脊髓麻醉、辅助区域麻醉(股神经阻滞[FNB]或收肌管阻滞[ACB])或局部镇痛的人类研究。纳入标准包括:(1)报道初次 ACLR 后患者使用脊髓麻醉、辅助区域麻醉(股神经阻滞[FNB]或收肌管阻滞[ACB])或局部镇痛的水平 1 研究;(2)报道与麻醉相关的患者报告的 VAS、阿片类药物消耗和术后 24 小时内并发症的研究。排除非 1 级研究、使用多种麻醉方式的研究以及未报告术后 24 小时内结果的研究。对数据进行综合,并根据多种麻醉方式进行随机效应荟萃分析,以确定术后疼痛、阿片类药物使用和并发症(0-4、4-8、8-12、12-24 小时)。

结果

共筛选了 263 项研究,其中 27 项 1 级研究(n=16 个区域阻滞;n=12 个局部阻滞;n=4 个脊髓麻醉)符合纳入标准并纳入荟萃分析。与脊髓麻醉相比,术后 8 至 12 小时接受区域阻滞的患者 VAS 评分显著降低(<0.01),术后 12 至 24 小时接受 FNB 与 ACB 的患者(<0.01)以及术后 12 至 24 小时接受连续 FNB 而非单次区域阻滞(FNB、ACB)的患者(<0.01)。脊髓、区域和局部麻醉组之间的 VAS 无显著差异。

结论

基于 1 级研究证据,与脊髓麻醉相比,接受区域麻醉的患者在初次 ACLR 后 8 至 12 小时根据 VAS 评估的疼痛控制显著改善。与 ACB 相比,接受 FNB 的患者和接受连续 FNB 而非单次区域麻醉的患者在术后 12 至 24 小时的疼痛评分显著降低。

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