Laohathaimongkol Thongchai, Wipatasinlapin Thada, Ongkanchana Chavithorn, Srimongkolpitak Surasak, Prasathaporn Niti, Jiamton Chittawee
Queen Savang Vadhana Memorial Hospital, Chon Buri, Thailand.
Ramkhamhaeng Hospital, Bangkok, Thailand.
Eur J Orthop Surg Traumatol. 2025 Jul 11;35(1):300. doi: 10.1007/s00590-025-04428-9.
To compare postoperative range of motion (ROM), pain and functional outcomes in patients immobilized with an abduction neutral rotation brace (ANRB) versus a conventional arm sling following arthroscopic rotator cuff repair (ARCR).
Thirty patients aged 40-75 years with full-thickness supraspinatus and/or infraspinatus tear undergoing ARCR were randomized to immobilized using either an abduction neutral rotation brace (n = 16) or a conventional arm sling (n = 16). Outcomes including ROM, visual analogue scale (VAS) for pain, and Constant-Murley score (CMS) were assessed preoperatively and at 6 weeks, 3, 6, and 12 months postoperatively.
At 3 months, patients in the abduction neutral rotation brace group demonstrated significantly greater forward flexion and external rotation compared to the arm sling group (P < 0.05). VAS pain scores were significantly lower at 6 weeks and 6 months in the brace group (P < 0.05). CMS showed no significant difference between groups at final follow-up. No re-tears or complications were observed in either group.
Use of an abduction neutral rotation brace after ARCR results in improved early postoperative ROM and pain control compared to a conventional arm sling. This technique may facilitate earlier rehabilitation and higher patient satisfaction.
Level I; Randomized Controlled Trial.
比较关节镜下肩袖修复术(ARCR)后使用外展中立位旋转支具(ANRB)与传统手臂吊带固定的患者术后的活动范围(ROM)、疼痛及功能结局。
30例年龄在40 - 75岁、患有全层冈上肌和/或冈下肌撕裂并接受ARCR的患者被随机分为两组,分别使用外展中立位旋转支具固定(n = 16)或传统手臂吊带固定(n = 16)。在术前以及术后6周、3个月、6个月和12个月评估包括ROM、疼痛视觉模拟量表(VAS)和Constant-Murley评分(CMS)等结局指标。
在术后3个月时,外展中立位旋转支具组患者的前屈和外旋活动范围明显大于手臂吊带组(P < 0.05)。支具组在术后6周和6个月时的VAS疼痛评分明显更低(P < 0.05)。最终随访时两组的CMS无显著差异。两组均未观察到再撕裂或并发症。
与传统手臂吊带相比,ARCR后使用外展中立位旋转支具可改善术后早期的ROM并控制疼痛。该技术可能有助于更早进行康复治疗并提高患者满意度。
I级;随机对照试验。