Department of Diagnostic Radiology, Singapore General Hospital, Singapore.
BMC Musculoskelet Disord. 2011 Jun 25;12:137. doi: 10.1186/1471-2474-12-137.
Corticosteroid injections can be performed blind (landmark-guided) or with image guidance, and this may account for variable clinical outcomes. The objective of this study was to assess the effectiveness and safety of image-guided versus blind corticosteroid injections in improving pain and function among adults with shoulder pain.
MEDLINE, the Cochrane Controlled Trials Register and EMBASE were searched to May 2010. Additional studies were identified by searching bibliographies of shortlisted articles. Search items included blind, landmark, anatomical, clinical exam, image-guided, ultrasound, fluoroscopy, steroid injection, frozen shoulder, random allocation, randomized controlled trial (RCT) and clinical trial.Randomized controlled studies comparing image-guided versus blind (landmark-guided) corticosteroid shoulder injections that examined pain, function and/or adverse events were included. Independent extraction was done by two authors using a form with pre-specified data fields, including risk of bias appraisal. Conflicts were resolved by discussion. The decision to pool data was based on assessment of clinical design homogeneity. When warranted, studies were pooled under a random-effects model.
Two RCTs for pain, function and adverse events (n = 101) met eligibility criteria. No serious threats to validity were found. Both trials compared ultrasound-guided versus landmark-guided injections and were judged similar in clinical design. Low to moderate heterogeneity was observed: shoulder pain I2 = 60%, function I2 = 22%. A meta-analysis demonstrated greater improvement with ultrasound-guided injections at 6 weeks after injection in both pain (mean difference = 2.23 [95% CI: 1.27, 3.18]), as assessed with a 0 to 10 visual analogue scale, and shoulder function (standardised mean difference = 1.09 [95% CI: 0.61, 1.57]) as assessed with shoulder function scores. Although more adverse events (all mild) were reported with landmark-guided injections, the difference was not statistically significant (risk ratio = 0.20 [95% CI: 0.04, 1.13]).This review was only based on two moderate-sized trials. Blinding of patients was not performed in both trials, causing some risk of bias in outcome assessment since primary endpoints were wholly or partially patient-reported.
There is a paucity of RCTs on image-guided versus landmark-guided corticosteroid shoulder injections examining pain, function and adverse events. In this review, patients who underwent image-guided (ultrasound) injections had statistically significant greater improvement in shoulder pain and function at 6 weeks after injection. Image-guided (ultrasound) corticosteroid injections potentially offer a significantly greater clinical improvement over blind (landmark-guided) injections in adults with shoulder pain. However, this apparent benefit requires confirmation from further studies (adequately-powered and well-executed RCTs).
皮质类固醇注射可以在盲视(地标引导)或图像引导下进行,这可能是导致临床结果不同的原因。本研究的目的是评估在改善肩部疼痛的成年人中,图像引导与盲视(地标引导)皮质类固醇注射的有效性和安全性。
检索 MEDLINE、Cochrane 对照试验注册库和 EMBASE 至 2010 年 5 月。通过搜索入选文章的参考文献,确定了其他研究。检索项包括盲视、地标、解剖、临床检查、图像引导、超声、透视、类固醇注射、冻结肩、随机分配、随机对照试验(RCT)和临床试验。纳入了比较图像引导与盲视(地标引导)皮质类固醇肩部注射以检查疼痛、功能和/或不良事件的随机对照研究。两位作者使用预定义数据字段的表格进行独立提取,包括偏倚风险评估。通过讨论解决了冲突。是否进行数据合并取决于临床设计同质性的评估。如果有必要,将根据随机效应模型对研究进行合并。
有 2 项 RCT 符合疼痛、功能和不良事件的纳入标准(n = 101)。未发现严重的有效性威胁。这两项试验均比较了超声引导与地标引导注射,并且在临床设计上被认为是相似的。观察到低至中度的异质性:肩部疼痛 I2 = 60%,功能 I2 = 22%。荟萃分析显示,在注射后 6 周时,超声引导注射在疼痛(0 到 10 视觉模拟量表的平均差值 = 2.23 [95%CI:1.27,3.18])和肩部功能(肩部功能评分的标准化均数差值 = 1.09 [95%CI:0.61,1.57])方面的改善更大。尽管地标引导注射报告的不良事件更多(均为轻度),但差异无统计学意义(风险比 = 0.20 [95%CI:0.04,1.13])。本综述仅基于两项中等规模的试验。在这两项试验中,均未对患者进行盲法,因为主要终点完全或部分由患者报告,因此存在一定的偏倚风险。
目前关于比较图像引导与地标引导皮质类固醇肩部注射以检查疼痛、功能和不良事件的 RCT 较少。在本综述中,接受图像引导(超声)注射的患者在注射后 6 周时肩部疼痛和功能的改善具有统计学意义。与盲视(地标引导)注射相比,图像引导(超声)皮质类固醇注射可能为肩部疼痛的成年人提供显著更大的临床改善。然而,这种明显的益处需要进一步研究(充分有力和执行良好的 RCT)来证实。