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Arch Phys Med Rehabil · Jun 2012
Randomized Controlled Trial Multicenter Study Comparative StudySubacromial corticosteroid injection on poststroke hemiplegic shoulder pain: a randomized, triple-blind, placebo-controlled trial.
- Ueon Woo Rah, Seung-Hyun Yoon, Do Jun Moon, Kyu-Sung Kwack, Ji Yeon Hong, Yong Cheol Lim, and Bohyun Joen.
- Department of Physical Medicine and Rehabilitation, Ajou University School of Medicine and Ajou University Hospital, Suwon, Republic of Korea.
- Arch Phys Med Rehabil. 2012 Jun 1;93(6):949-56.
ObjectiveTo evaluate the effect of subacromial corticosteroid injection on hemiplegic shoulder pain (HSP).DesignMulticenter, randomized, triple-blind, placebo-controlled trial.SettingThree primary and 1 university-affiliated tertiary-care hospitals.ParticipantsPoststroke HSP patients (N=58) with evidence of rotator cuff disorder.InterventionsParticipants were randomly assigned to receive ultrasound-guided subacromial injection with triamcinolone 40mg (treatment group, n=29), or lidocaine (placebo group, n=29). After a single injection, participants were followed up for 8 weeks.Main Outcome MeasuresVisual analog scale (VAS) of the average shoulder pain level at day and night (VAS-day/night, the primary outcome measures), Modified Barthel Index, Shoulder Disability Questionnaire (SDQ), and angles of shoulder active range of motion (flexion, abduction, external rotation, and internal rotation) at pretreatment and weeks 2, 4, and 8 posttreatment.ResultsThere was no significant difference between the 2 groups in the main outcome measures at pretreatment. Compared with the placebo group, VAS-day/night, SDQ, flexion, external rotation, and internal rotation showed significant improvement in the treatment group.ConclusionsTo our knowledge, this is the first randomized, placebo-controlled study to assess the efficacy of subacromial injection in HSP patients with evidence of rotator cuff disorder. Subacromial corticosteroid injection showed improvement in pain, disability, and active range of motion, and the duration of its efficacy continued up to 8 weeks.Copyright © 2012 American Congress of Rehabilitation Medicine. Published by Elsevier Inc. All rights reserved.
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