Radiology Department, Stoke Mandeville Hospital, Buckinghamshire Healthcare NHS Trust, Aylesbury, HP21 8AL, UK.
Radiology Department, Royal Berkshire Hospital, Royal Berkshire NHS Foundation Trust, Reading, UK.
Skeletal Radiol. 2019 Aug;48(8):1269-1274. doi: 10.1007/s00256-018-3105-3. Epub 2018 Nov 16.
To describe and evaluate the outcome following shoulder manipulation under rotator interval block for the treatment of adhesive capsulitis.
Patients with adhesive capsulitis referred by our local orthopaedic shoulder surgeons consented to targeted ultrasound-guided injection of the glenohumeral joint via the rotator interval. Inclusion criteria included a failure to respond to conservative treatment and the absence of a full-thickness rotator cuff tear. Twelve millilitres of a mixture of local anaesthetic and steroid was injected into the rotator interval using a 21-gauge needle, with a small volume of the same solution instilled into the subacromial bursa. Following injection, under local anaesthetic block, patients were gently manipulated into abduction, external rotation and internal rotation as far as they could comfortably tolerate. Patients were assessed pre-injection with documented pain scores from 0 to 10 on a visual analogue scale (VAS) and the Oxford Shoulder Score (OSS) questionnaire. Initial follow-up comprised a VAS pain score at 1 h, 24 h and 2 weeks. Clinical review by the referring orthopaedic surgeon was performed at 2 months post-injection. Long-term follow-up involved a VAS pain score and the OSS questionnaire at 5 months.
Forty patients were suitable for inclusion in the study. Twenty-three were female (57.5%) and 17 were male. The mean age was 52 years (range, 31-73 years). Twelve patients were post-operative. The duration of symptoms ranged from 3 months to 18 months. Mean pre-procedure OSS was recorded as 23.3 (range, 4-36). The mean VAS pain score was 7.7 before the procedure (range, 4 - 10), 3.4 at 1 h (range, 0-8), 2.9 at 24 h (range, 0-8), and 1.8 at 2 weeks (range 1-4). Orthopaedic follow-up at an average of 66 days post-injection was recorded in 18 patients. All patients reported initial improvement of their shoulder pain and return to near full range of movement; however, recurrence of adhesive capsulitis symptoms was recorded in 5 patients. One case of rupture of the long head of the biceps tendon was reported, but the patient remained asymptomatic. Long-term follow-up at 5 months was obtained in 31 patients, with a mean OSS of 42 (range, 21-60) and VAS of 2.3 (range, 0-7).
Manipulation under general anaesthesia is a well-recognised treatment for adhesive capsulitis. We report that targeted ultrasound-guided injection of the rotator interval and manipulation of the shoulder under local anaesthetic blockade result in good outcomes in reducing shoulder pain and symptoms of adhesive capsulitis with low recurrence and complication rates.
描述和评估经肩袖间隙下肩关节手法松解治疗粘连性肩关节囊炎的疗效。
我们当地的骨科肩关节外科医生转诊的粘连性肩关节囊炎患者,同意接受经肩袖间隙行靶向超声引导下的关节内注射。纳入标准包括对保守治疗无反应且无全层肩袖撕裂。使用 21 号针头将 12 毫升局部麻醉剂和类固醇混合液注入肩袖间隙,同时向肩峰下囊内注入少量相同溶液。注射后,在局部麻醉阻滞下,将患者轻柔地外展、外旋和内旋至能舒适耐受的最大程度。患者在注射前用视觉模拟评分法(VAS)记录了从 0 到 10 的疼痛评分,并填写了牛津肩肘评分(OSS)问卷。初始随访包括注射后 1 小时、24 小时和 2 周的 VAS 疼痛评分。注射后 2 个月由转诊的骨科医生进行临床评估。长期随访包括 5 个月时的 VAS 疼痛评分和 OSS 问卷。
40 名患者符合研究纳入标准。23 名女性(57.5%),17 名男性。平均年龄为 52 岁(范围 31-73 岁)。12 名患者为术后。症状持续时间为 3 个月至 18 个月。术前平均 OSS 记录为 23.3(范围 4-36)。术前 VAS 疼痛评分平均为 7.7(范围 4-10),1 小时时为 3.4(范围 0-8),24 小时时为 2.9(范围 0-8),2 周时为 1.8(范围 1-4)。18 名患者平均在注射后 66 天进行了骨科随访。所有患者均报告肩部疼痛初始改善,活动范围接近完全恢复;然而,5 名患者出现粘连性肩关节囊炎症状复发。报告 1 例肱二头肌长头肌腱断裂,但患者无症状。31 名患者获得 5 个月的长期随访,平均 OSS 为 42(范围 21-60),VAS 为 2.3(范围 0-7)。
全麻下手法松解是治疗粘连性肩关节囊炎的一种公认方法。我们报告经肩袖间隙靶向超声引导下注射并在局部麻醉阻滞下手法松解肩关节可显著减轻肩关节疼痛和粘连性肩关节囊炎症状,复发率和并发症率低。