Wajon Anne, Vinycomb Toby, Carr Emma, Edmunds Ian, Ada Louise
Macquarie Hand Therapy, Macquarie University Clinic, 2 Technology Place, Macquarie University, New South Wales, Australia, 2109.
Department of Surgery (MMC), Monash University, Melbourne, Australia.
Cochrane Database Syst Rev. 2017 Apr 3;4(4):CD004631. doi: 10.1002/14651858.CD004631.pub5.
Surgery is used to treat persistent pain and dysfunction at the base of the thumb when conservative management, such as splinting, or medical management, such as oral analgesics, is no longer adequate in reducing disability and pain. This is an update of a Cochrane Review first published in 2005.
To assess the effects of different surgical techniques for trapeziometacarpal (thumb) osteoarthritis.
We searched the following sources up to 08 August 2013: CENTRAL (The Cochrane Library 2013, Issue 8), MEDLINE (1950 to August 2013), EMBASE (1974 to August 2013), CINAHL (1982 to August 2013), Clinicaltrials.gov (to August 2013) and World Health Organization (WHO) Clinical Trials Portal (to August 2013).
Randomised controlled trials (RCTs) or quasi-RCTs where the intervention was surgery for people with thumb osteoarthritis. Outcomes were pain, physical function, quality of life, patient global assessment, adverse events, treatment failure or trapeziometacarpal joint imaging.
We used standard methodological procedures expected by the Cochrane Collaboration. Two review authors independently screened and included studies according to the inclusion criteria, assessed the risk of bias and extracted data, including adverse events.
We included 11 studies with 670 participants. Seven surgical procedures were identified (trapeziectomy with ligament reconstruction and tendon interposition (LRTI), trapeziectomy, trapeziectomy with ligament reconstruction, trapeziectomy with interpositional arthroplasty (IA), Artelon joint resurfacing, arthrodesis and Swanson joint replacement). We did not find any studies that compared surgery with sham surgery or surgery with non-surgical interventions.Most included studies had an unclear risk of most biases which raises doubt about the results. No procedure demonstrated any superiority over another in terms of pain, physical function, quality of life, patient global assessment, adverse events, treatment failure (re-operation) or trapeziometacarpal joint imaging. One study demonstrated a difference in adverse events (mild-moderate swelling) between Artelon joint replacement and trapeziectomy with tendon interposition. However, the quality of evidence was very low due to a high risk of bias and imprecision of results.Low quality evidence suggests trapeziectomy with LRTI may not provide additional benefits or result in more adverse events over trapeziectomy alone. Mean pain (three studies, 162 participants) was 26 mm on a 0 to 100 mm VAS (0 is no pain) for trapeziectomy alone, trapeziectomy with LRTI reduced pain by a mean of 2.8 mm (95% confidence interval (CI) -9.8 to 4.2) or an absolute reduction of 3% (-10% to 4%). Mean physical function (three studies, 211 participants) was 31.1 points on a 0 to 100 point scale (0 is best physical function, or no disability) with trapeziectomy alone, trapeziectomy with LRTI resulted in sightly lower function scores (standardised mean difference 0.1, 95% CI -0.30 to 0.32), an equivalent to a worsening of 0.2 points (95% CI -5.8 to 6.1) on a 0 to 100 point scale (absolute decrease in function 0.03% (-0.83% to 0.88%)). Low quality evidence from four studies (328 participants) indicates that the mean number of adverse events was 10 per 100 participants for trapeziectomy alone, and 19 events per 100 participants for trapeziectomy with LRTI (RR 1.89, 95% CI 0.96 to 3.73) or an absolute risk increase of 9% (95% CI 0% to 28%). Low quality evidence from one study (42 participants) indicates that the mean scapho-metacarpal distance was 2.3 mm for the trapeziectomy alone group, trapeziectomy with LRTI resulted in a mean of 0.1 mm less distance (95% CI -0.81 to 0.61). None of the included trials reported global assessment, quality of life, and revision or re-operation rates.Low-quality evidence from two small studies (51 participants) indicated that trapeziectomy with LRTI may not improve function or slow joint degeneration, or produce additional adverse events over trapeziectomy and ligament reconstruction.We are uncertain of the benefits or harms of other surgical techniques due to the mostly low quality evidence from single studies and the low reporting rates of key outcomes. There was insufficient evidence to assess if trapeziectomy with LRTI had additional benefit over arthrodesis or trapeziectomy with IA. There was also insufficient evidence to assess if trapeziectomy with IA had any additional benefit over the Artelon joint implant, the Swanson joint replacement or trapeziectomy alone.
AUTHORS' CONCLUSIONS: We did not identify any studies that compared surgery to sham surgery or to non-operative treatments. We were unable to demonstrate that any technique confers a benefit over another technique in terms of pain and physical function. Furthermore, the included studies were not of high enough quality to provide conclusive evidence that the compared techniques provided equivalent outcomes.
当保守治疗(如夹板固定)或药物治疗(如口服镇痛药)在减轻残疾和疼痛方面不再充分有效时,手术可用于治疗拇指基部的持续性疼痛和功能障碍。这是Cochrane系统评价的更新版,首次发表于2005年。
评估不同手术技术治疗第一掌腕关节(拇指)骨关节炎的效果。
截至2013年8月8日,我们检索了以下资源:Cochrane中心对照试验注册库(CENTRAL,2013年第8期)、医学期刊数据库(MEDLINE,1950年至2013年8月)、荷兰医学文摘数据库(EMBASE,1974年至2013年8月)、护理学与健康领域数据库(CINAHL,1982年至2013年8月)、美国国立医学图书馆临床试验数据库(Clinicaltrials.gov,至2013年8月)以及世界卫生组织(WHO)临床试验平台(至2013年8月)。
随机对照试验(RCT)或半随机对照试验,干预措施为针对拇指骨关节炎患者的手术。结局指标包括疼痛、身体功能、生活质量、患者整体评估、不良事件、治疗失败或第一掌腕关节影像学检查。
我们采用了Cochrane协作网期望的标准方法程序。两名综述作者根据纳入标准独立筛选并纳入研究,评估偏倚风险并提取数据,包括不良事件。
我们纳入了11项研究,共670名参与者。确定了七种手术方法(带韧带重建和肌腱植入的大多角骨切除术(LRTI)、大多角骨切除术、带韧带重建的大多角骨切除术、带间置关节成形术(IA)的大多角骨切除术、Artelon关节表面置换术、关节融合术和Swanson关节置换术)。我们未发现任何将手术与假手术或手术与非手术干预进行比较的研究。大多数纳入研究的大多数偏倚风险不明确,这对结果产生了疑问。在疼痛、身体功能、生活质量、患者整体评估、不良事件、治疗失败(再次手术)或第一掌腕关节影像学检查方面,没有任何一种手术方法显示出优于其他方法。一项研究表明,Artelon关节置换术与带肌腱植入的大多角骨切除术在不良事件(轻至中度肿胀)方面存在差异。然而,由于偏倚风险高和结果不精确,证据质量非常低。低质量证据表明,与单纯大多角骨切除术相比,带LRTI的大多角骨切除术可能不会带来额外益处或导致更多不良事件。单纯大多角骨切除术的平均疼痛程度(三项研究,162名参与者)在0至100毫米视觉模拟量表(VAS)上为26毫米(0表示无疼痛),带LRTI的大多角骨切除术使疼痛平均减轻2.8毫米(95%置信区间(CI)-9.8至4.2),或绝对减轻3%(-10%至4%)。单纯大多角骨切除术的平均身体功能(三项研究,211名参与者)在0至100分的量表上为31.1分(0表示最佳身体功能或无残疾),带LRTI的大多角骨切除术导致功能评分略低(标准化均差0.1,95%CI -0.30至0.32),相当于在0至100分的量表上恶化0.2分(95%CI -5.8至6.1)(功能绝对下降0.03%(-0.83%至0.88%))。四项研究(328名参与者)的低质量证据表明,单纯大多角骨切除术每100名参与者的不良事件平均数量为10起,带LRTI的大多角骨切除术每100名参与者的不良事件为19起(风险比1.89,95%CI 0.96至3.73),或绝对风险增加9%(95%CI 0%至28%)。一项研究(42名参与者)的低质量证据表明,单纯大多角骨切除术组的平均舟掌距离为2.3毫米,带LRTI的大多角骨切除术导致距离平均减少0.1毫米(95%CI -0.81至0.61)。纳入的试验均未报告整体评估、生活质量以及翻修或再次手术率。两项小型研究(51名参与者)的低质量证据表明,与大多角骨切除术和韧带重建相比,带LRTI的大多角骨切除术可能不会改善功能或减缓关节退变,也不会产生额外的不良事件。由于大多数来自单项研究的证据质量较低且关键结局的报告率较低,我们不确定其他手术技术的益处或危害。没有足够的证据评估带LRTI的大多角骨切除术比关节融合术或带IA的大多角骨切除术是否具有额外益处。也没有足够的证据评估带IA的大多角骨切除术比Artelon关节植入物、Swanson关节置换术或单纯大多角骨切除术是否具有任何额外益处。
我们未发现任何将手术与假手术或非手术治疗进行比较的研究。我们无法证明在疼痛和身体功能方面,任何一种技术比另一种技术更具优势。此外,纳入的研究质量不够高,无法提供确凿证据表明所比较的技术能产生等效的结果。