治疗盂肱骨关节炎的最有效皮质类固醇剂量:可行性试验和双盲随机对照试验方案

Cayce Onks , Lynn Weaver , Johan Latorre , Matthew Silvis , Arthur Berg , Shawn Phillips , Jayson Loeffert , Cristy French , April Armstrong
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引用次数: 0

摘要

目的美国有 540 多万人患有骨关节炎。常见的治疗方法是进行关节内皮质类固醇注射。然而,理想的类固醇剂量尚不清楚。本研究旨在对原发性盂肱关节 OA 的皮质类固醇注射方案进行试点。方法我们进行了一项双盲随机可行性试点研究。我们招募了原发性盂肱关节骨关节炎患者,并将其随机分为20毫克、40毫克或80毫克三苯氧胺。研究的主要结果是方案的可行性以及注射 6 个月后肩关节疼痛和残疾指数(SPADI)的变化。19名受试者完成了研究。不参加研究的最常见原因是担心注射的剂量比以前小。辍学率为 26%,其中 2 名患者接受了全肩关节置换术。虽然所有治疗组的 SPADI 在 6 个月时都比基线有所下降,但在 6 个月时,各组之间的 SPADI 没有临床显著差异(p = 0.090)。20 毫克组出现了一次不良反应,一名患者在注射后面部潮红。我们成功地制定了可行的方案。今后,将以前接受过注射的患者排除在外将有助于提高入选率。患者的这种担忧凸显了完成临床试验以指导皮质类固醇注射医疗决策的必要性。NCT03586687。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The most effective corticosteroid dose in the treatment of glenohumeral osteoarthritis: Feasibility pilot and protocol for double blinded randomized controlled trial

Objective

Osteoarthritis affects over 5.4 million people in the United States. A common treatment is to perform intra-articular corticosteroid injections. However, the ideal steroid dose is unknown. This study aimed to pilot a corticosteroid injection protocol for primary glenohumeral OA.

Methods

We conducted a double blinded randomized feasibility pilot study. Patients with primary osteoarthritis of the glenohumeral joint were recruited and randomized to receive 20 ​mg, 40 ​mg, or 80 ​mg of triamcinolone. The primary outcome was the feasibility of the protocol and change in the Shoulder Pain and Disability Index (SPADI) 6 months following injection.

Results

300 patients were screened for participation with 78 meeting inclusion criteria. 19 subjects completed the study. The most common reason for not participating was concern they would receive a smaller dose than previous injections. There was a 26% dropout rate, with 2 patients undergoing a total shoulder arthroplasty. There was no clinically significant difference (p ​= ​0.090) between the groups at 6-months for the SPADI although all treatment groups showed a reduction of SPADI from baseline at 6 months. There was one adverse event in the 20 ​mg group, with a patient experiencing facial flushing after the injection.

Conclusion

We were successful in developing a feasible protocol. In the future excluding those who have received previous injections would be helpful for a higher enrollment rate. This patient concern highlights the need to complete clinical trials to guide medical decisions surrounding corticosteroid administration. NCT03586687.

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来源期刊
Osteoarthritis and cartilage open
Osteoarthritis and cartilage open Orthopedics, Sports Medicine and Rehabilitation
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