Postoperative pain treatment after total hip arthroplasty: a systematic review

被引:146
作者
Karlsen, Anders Peder Hojer [1 ]
Geisler, Anja [2 ]
Petersen, Pernille Lykke [2 ]
Mathiesen, Ole [2 ]
Dahl, Jorgen B. [1 ]
机构
[1] Copenhagen Univ Hosp, Rigshosp, Ctr Head & Orthopaed, Dept Anaesthesia 4231, Copenhagen, Denmark
[2] Copenhagen Univ Hosp, Rigshosp, Ctr Head & Orthopaed, Sect Acute Pain Management,Dept Anaesthesia 4231, Copenhagen, Denmark
关键词
Postoperative pain management; Systematic review; Total hip arthroplasty; Non-steroidal anti-inflammatory drugs; local infiltration analgesia; Lumbar plexus block; Intrathecal morphine; LUMBAR PLEXUS BLOCK; LOCAL INFILTRATION ANALGESIA; DOUBLE-BLIND; SPINAL-ANESTHESIA; CLINICAL-TRIALS; INTRATHECAL MORPHINE; EPIDURAL-ANESTHESIA; OPIOID CONSUMPTION; NATIONAL-SURVEY; BLOOD-LOSS;
D O I
10.1016/j.pain.0000000000000003
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Treatment of postoperative pain should rely on results from randomized controlled trials and meta-analyses of high scientific quality. The efficacy of a particular intervention may depend on the type of surgical procedure, which supports the reporting of "procedure-specific" interventions. The aim of this systematic review was to document the procedure-specific evidence for analgesic interventions after total hip arthroplasty (THA). This PRISMA-compliant and PROSPERO-registered review includes randomized placebo-controlled trials (RCTs) of medication-based analgesic interventions after THA. Endpoints were postoperative opioid consumption, pain scores (rest and during mobilization), adverse events, and length of hospital stay. Fifty-eight trials with 19 different interventions were retrieved. High risk of bias, substantial differences in assessment-tools and criteria for pain, irregular reporting of adverse events, considerable differences in supplemental analgesic consumption,. and basic analgesic regimens generally characterized trials. Meta-analyses of non-steroidal anti-inflammatory drugs, local infiltration analgesia, intrathecal opioids, and lumbar plexus block provided a 24-hour intravenous morphine-sparing effect of 14.1 (95% confidence interval: 8.0-20.2) mg, 7.5 (3.7-11.3) mg, 19.8 (14.9-24.7) mg, and 11.9 (6.4-17.3) mg, respectively. Non-steroidal anti-inflammatory drugs and lumbar plexus block were demonstrated to provide reductions in postoperative pain scores. Intrathecal opioids increased pruritus, and lumbar plexus block reduced nausea and pruritus. The GRADE-rated quality of evidence ranged from low to very low throughout the analyses. This review demonstrated, that some analgesic interventions may have the capacity to reduce mean opioid requirements and/or Mean pain intensity compared with controls, but the available randomized placebo-controlled trials does not allow a designation of a "best proven intervention" for THA.
引用
收藏
页码:8 / 30
页数:23
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