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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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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:De quervain tenosynovitis在用拇指绑架和延伸的重复腕骨偏差偏差的患者中常见。以前的研究比较非技术选择对理想管理缺乏共识。本研究的目的是分析患有皮质类固醇注射(CSI)治疗的前瞻性随机患者与CSI进行固定化。方法:径向双侧腕部疼痛,第一个背部室压痛和阳性Finkelstein试验用于定义de quervain。视觉模拟量表(VAS)上的疼痛评分为4或更高用于包容。在排除标准之后,患者接受随机分组的组:(1)仅限CSI;或(2)CSI,固定3周。我们随后在3周和6个月内进行进一步评估,评估症状和改善手臂,肩部和手(仪表手(DASH)评分的症状和改进,以评估治疗成功。结果:单独患有CSI和11例CSI患者和固定患者。在这两组的6个月内,患者的VAS和DASH分数均有显着改善,而88%的CSI患者患者和73%的CSI患者的患者经历了至少2个预处理症状的完全分辨率。在群体之间,除了分辨径向腕疼痛之外,结果是可比的,其单独患有CSI的患者(100%vs 64%)。结论:注射后的固定性增加成本,可能会妨碍日常生活的活动,并没有有助于改善本研究的患者结果。进一步的预期研究是有保证的。

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