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Nonsurgical Treatment of De Quervain Tenosynovitis: A Prospective Randomized Trial

机译:De Quercain Tenosynovitis的非诊断治疗:预期随机试验

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摘要

Background: De Quervain tenosynovitis is commonly seen in patients who perform repetitive wrist ulnar deviation with thumb abduction and extension. Previous studies comparing nonsurgical options have contributed to a lack of consensus about ideal management. This study’s purpose was to analyze results in prospectively randomized patients treated with either corticosteroid injection (CSI) alone versus CSI with immobilization. Methods: Radial sided wrist pain, first dorsal compartment tenderness, and positive Finkelstein test were used to define De Quervain. Pain score of 4 or higher on a visual analog scale (VAS) was utilized for inclusion. Following exclusion criteria, patients underwent randomization into groups: (1) CSI alone; or (2) CSI with 3 weeks of immobilization. We followed at 3 weeks and 6 months for further evaluation, where resolution of symptoms and improvements in VAS and Disabilities of the Arm, Shoulder, and Hand (DASH) scores were assessed to evaluate treatment success. Results: Nine patients with CSI alone and 11 patients with CSI and immobilization were followed. At 6 months in both groups, patients experienced significant improvement in VAS and DASH scores, while 88% of patients with CSI alone and 73% of patients with CSI and immobilization experienced complete resolution of at least 2 out of 3 of their pretreatment symptoms. Between groups, outcomes were comparable except for resolution of radial-sided wrist pain, which was superior in patients with CSI alone (100% vs 64%). Conclusions: Immobilization following injection increases costs, may hinder activities of daily living, and did not contribute to improved patient outcomes in this study. Further prospective studies are warranted.
机译:背景:德Quervain腱鞘炎在谁执行与拇指外展和延伸重复手腕尺侧偏斜患者中常见。比较非手术方案以前的研究已经缺乏关于理想的管理共识做出了贡献。这项研究的目的是分析与任何注射糖皮质激素(CSI)与单独用CSI固定治疗的前瞻性随机患者的结果。方法:径向双面手腕疼痛,第一背鳍隔间压痛,并积极芬克尔斯坦测试被用来定义德Quervain。疼痛评分为4或更高的视觉模拟评分(VAS)被利用列入。继排除标准,患者接受了随机分组:(1)单独CSI;或(2)与CSI3周固定的。其次,我们在第3周和6个月进行进一步的评估,其中在VAS和臂,肩的残疾人,和手部症状和改进分辨率(DASH)得分进行了评估,以评估治疗成功。结果:9例CSI单独和11例CSI和固定随访。 6个月时两组患者经历了VAS和DASH得分显著改善,而患者单独CSI 88%和患者的CSI和固定73%经历了至少2完全解决了的他们的预处理症状3。组之间,结局是除了径向双面手腕疼痛的分辨率,这是优越的患者单独CSI(100%对64%)媲美。结论:固定化注射后增加的成本,可能会妨碍日常生活活动,并在此研究并未有助于改善患者的预后。有必要进一步的预期研究。

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