Ultrasound versus palpation-guided corticosteroid injection for de Quervain disease: A randomized controlled trial

被引:0
作者
Kuo, Ying-Chen [1 ,2 ]
Hsieh, Lin-Fen [1 ,2 ]
Liu, Ya-Fang [3 ]
Chang, Chia-Sung [1 ]
机构
[1] Shin Kong Wu Ho Su Mem Hosp, Dept Phys Med & Rehabil, Taipei 111, Taiwan
[2] Fu Jen Catholic Univ, Sch Med, New Taipei City, Taiwan
[3] Shin Kong Wu Ho Su Mem Hosp, Res Dept, Adm Div, Taipei, Taiwan
关键词
1ST EXTENSOR COMPARTMENT; ULTRASONOGRAPHIC EVALUATION; INTRACOMPARTMENTAL SEPTUM; STENOSING TENOSYNOVITIS; STEROID INJECTION; INTRA-SHEATH; ACCURACY; PREVALENCE; MANAGEMENT; WRIST;
D O I
10.1002/pmrj.13144
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Introduction: Corticosteroid injection effectively treats de Quervain disease, and due to the high prevalence of the intracompartmental septum in the first extensor compartment, ultrasound guidance improves injection accuracy. Objective: To compare the effectiveness, adverse events, and the recurrence rate between ultrasound-guided and palpation-guided injection in patients with de Quervain disease. Design: Prospective, single-blind, randomized controlled trial. Setting: Rehabilitation department of a private teaching hospital. Participants: We enrolled 49 patients, >= 20 years of age, clinically diagnosed with de Quervain disease based on their medical history and physical examination. Interventions: Patients were randomized into two groups: ultrasound-guided and palpation-guided injection. Both groups received a mixture of 10 mg triamcinolone acetonide (10 mg/1 mL) and 0.3 mL 1% lidocaine. Main Outcome Measures: The primary outcome measure was the Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) score at 1 week. The secondary outcome measures were visual analog scale for pain (pain VAS) score, patient satisfaction, and adverse events or complications from the interventions at 1 week, 3 months, and 6 months. Results: Both groups showed improvement over time in QuickDASH scores and pain VAS (p < .001); however, no statistically significant differences were noted between the groups for either QuickDASH scores (p = .22) or pain VAS (p = .30). In addition, no statistically significant differences were found between the groups in terms of patient satisfaction (p = .76) and adverse events (p = .47, .33, .58) at the 1-week, 3-month, and 6-month follow-ups. Conclusions: Both ultrasound-guided and palpation-guided injections effectively treated de Quervain disease. During a 6-month follow-up, there were no statistically significant differences between the groups in pain relief, upper limb function, or patient satisfaction. However, the palpation-guided group showed a tendency for more recurrence and skin side effects.
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收藏
页码:948 / 958
页数:11
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