Department of Anesthesia, Wexner Medical Center, The Ohio State University, Columbus, OH, United States.
Department of Anesthesia, Vanderbilt University Medical Centre, Nashville, TN, United States.
Pain. 2018 Oct;159(10):1955-1971. doi: 10.1097/j.pain.0000000000001292.
The role of thoracic paravertebral block (PVB) in preventing chronic postsurgical pain (CPSP) after breast cancer surgery (BCS) has gained interest, but existing evidence is conflicting, and its methodological quality is unclear. This meta-analysis evaluates efficacy of PVB, compared with Control group, in preventing CPSP after BCS, in light of the Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials (IMMPACT) recommendations. Electronic databases were searched for randomized trials comparing PVB with Control group for CPSP prevention after BCS. Eligible trials were assessed for adherence to IMMPACT recommendations. The primary outcomes were CPSP at 3 and 6 months, whereas secondary outcomes were PVB-related complications. Data were pooled and analyzed using random-effects modelling. Trial sequential analysis was used to evaluate evidence conclusiveness. Data from 9 studies (604 patients) were analyzed. The median (range) of IMMPACT recommendations met in these trials was 9 (5, 15) of 21. Paravertebral block was not different from Control group in preventing CPSP at 3 months, but was protective at 6 months, with relative risk reduction (95% confidence interval) of 54% (0.24-0.88) (P = 0.02). Meta-regression suggested that the relative risk of CPSP was lower when single-injection (R = 1.00, P < 0.001) and multilevel (R = 0.71, P = 0.01) PVB were used. Trial sequential analysis revealed that 6-month analysis was underpowered by at least 312 patients. Evidence quality was moderate according to the GRADE system. Evidence suggests that multilevel single-injection PVB may be protective against CPSP at 6 months after BCS, but methodological limitations are present. Larger trials observing IMMPACT recommendations are needed to confirm this treatment effect and its magnitude.
胸段椎旁阻滞(PVB)在预防乳腺癌手术后慢性术后疼痛(CPSP)中的作用引起了关注,但现有证据存在冲突,其方法学质量尚不清楚。本荟萃分析根据发起的方法、测量和临床试验中的疼痛评估(IMMPACT)建议,评估了 PVB 与对照组相比预防乳腺癌手术后 CPSP 的疗效。电子数据库中搜索了比较 PVB 与对照组预防乳腺癌手术后 CPSP 的随机试验。评估符合 IMMPACT 建议的合格试验。主要结局是 3 个月和 6 个月时的 CPSP,次要结局是 PVB 相关并发症。使用随机效应模型对数据进行汇总和分析。试验序贯分析用于评估证据的结论性。对 9 项研究(604 名患者)的数据进行了分析。这些试验中符合 IMMPACT 建议的中位数(范围)为 21 项中的 9 项(5、15)。与对照组相比,椎旁阻滞在 3 个月时预防 CPSP 无差异,但在 6 个月时具有保护作用,相对风险降低(95%置信区间)为 54%(0.24-0.88)(P = 0.02)。Meta 回归表明,当使用单次注射(R = 1.00,P < 0.001)和多水平(R = 0.71,P = 0.01)PVB 时,CPSP 的相对风险较低。试验序贯分析表明,6 个月分析至少需要 312 名患者才能具有足够的效力。根据 GRADE 系统,证据质量为中等。证据表明,多水平单次注射 PVB 可能对乳腺癌手术后 6 个月的 CPSP 具有保护作用,但存在方法学局限性。需要更大规模的试验来观察 IMMPACT 建议,以确认这种治疗效果及其程度。