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高剂量与低剂量皮质类固醇注射治疗重度疼痛性粘连性囊炎的随机对照双盲研究。

High- vs Low-Dose Corticosteroid Injection in the Treatment of Adhesive Capsulitis with Severe Pain: A Randomized Controlled Double-Blind Study.

机构信息

Department of Physical and Rehabilitation Medicine, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.

出版信息

Pain Med. 2018 Apr 1;19(4):735-741. doi: 10.1093/pm/pnx227.

DOI:10.1093/pm/pnx227
PMID:29117299
Abstract

OBJECTIVE

To compare the degree of pain relief between high-dose (40 mg of triamcinolone acetonide) and low-dose (20 mg of triamcinolone acetonide) corticosteroid injections in patients with severe pain due to adhesive capsulitis.

DESIGN

A prospective, randomized, double-blind, dose-comparative study.

SUBJECTS

A total of 32 patients who were diagnosed with adhesive capsulitis and who expressed severe pain intensity, 8 or more points on a numeric rating scale (NRS).

METHODS

Patients received injections of high- or low-dose triamcinolone acetonide under ultrasound guidance. NRS, Shoulder Pain and Disability Index (SPADI), and the passive range of motion (PROM) in four directions were evaluated before and three weeks after the injection.

RESULTS

NRS scores showed significant improvement three weeks after the injection in both groups (P = 0.01 in both the low-dose group and high-dose group), but there was no statistically significant difference between the two groups (P = 0.63). SPADI score significantly improved at three weeks after the injection in both groups (P = 0.02 in the low-dose group and P < 0.01 in the high-dose group), but group difference was not observed (P = 0.06). The change of PROM in four directions after the injection did not show any significant difference between the low- and high-dose groups.

CONCLUSIONS

Injection of 20 mg of triamcinolone acetonide is sufficient to elicit symptom relief in patients with severe adhesive capsulitis; hence, 20 mg of triamcinolone acetonide can be recommended in patients with adhesive capsulitis with severe pain.

摘要

目的

比较重度粘连性肩关节囊炎患者接受大剂量(40 毫克曲安奈德)和小剂量(20 毫克曲安奈德)皮质类固醇注射后的止痛效果。

设计

前瞻性、随机、双盲、剂量比较研究。

受试者

共 32 名被诊断为粘连性肩关节囊炎且疼痛强度为 8 分或以上(数字评分量表[NRS])的患者。

方法

患者在超声引导下接受高或低剂量曲安奈德注射。在注射前和注射后 3 周,使用 NRS、肩关节疼痛和功能障碍指数(SPADI)和四个方向的被动活动度(PROM)进行评估。

结果

两组患者的 NRS 评分在注射后 3 周均显著改善(低剂量组和高剂量组 P 值均为 0.01),但两组间无统计学差异(P 值为 0.63)。两组患者的 SPADI 评分在注射后 3 周均显著改善(低剂量组 P 值为 0.02,高剂量组 P 值 < 0.01),但组间差异无统计学意义(P 值为 0.06)。注射后四个方向的 PROM 变化在低剂量组和高剂量组之间均无显著差异。

结论

注射 20 毫克曲安奈德足以缓解重度粘连性肩关节囊炎患者的症状;因此,对于疼痛剧烈的粘连性肩关节囊炎患者,可以推荐使用 20 毫克曲安奈德。

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