Florida Orthopaedic Institute, 13020 North Telecom Parkway, Tampa, FL 33637, USA.
J Bone Joint Surg Am. 2010 Nov 3;92(15):2544-56. doi: 10.2106/JBJS.I.00912.
The purpose of the present study was to evaluate the indications for, and outcomes of, reverse shoulder arthroplasty in patients with massive rotator cuff tears but without glenohumeral arthritis.
From December 1998 to December 2006, sixty-nine patients (seventy-two shoulders) were managed with reverse shoulder arthroplasty for the treatment of irreparable rotator cuff dysfunction without glenohumeral arthritis. The indications for reverse shoulder arthroplasty were persistent shoulder pain and dysfunction despite a minimum of six months of nonoperative treatment, the presence of at least a two-tendon tear, and Hamada stage-1, 2, or 3 changes in a patient for whom a non-arthroplasty option did not exist. Fifty-eight patients (sixty shoulders) had a minimum of two years of follow-up. Thirty-four shoulders had had no previous surgery (Group A), and twenty-six shoulders had had at least one previous surgical procedure (Group B). Postoperatively, patients were prospectively followed both clinically and radiographically. Survival analysis was performed, with the end points being removal or revision of the implant, radiographic loosening, and declining American Shoulder and Elbow Surgeons score.
Common characteristics of patients managed with reverse shoulder arthroplasty in this study were pain and (1) <90° of arm elevation at the shoulder without anterosuperior escape (n = 40; 66.6%); (2) <90° of elevation with anterosuperior escape (n = 16; 26.7%); or (3) irreparable rotator cuff tear and pain with >90° of elevation (n = 4; 6.7%). The average duration of follow-up was fifty-two months (range, twenty-four to 101 months). All measured outcomes improved postoperatively. For all patients, the average American Shoulder and Elbow Surgeons score improved from 33.3 to 75.4 (p < 0.0001), the average Simple Shoulder Test score improved from 1.6 to 6.5 (p < 0.0001), the average visual analog score for pain improved from 6.3 to 1.9 (p < 0.0001), the average visual analog score for function improved from 3.2 to 7.1 (p < 0.0001), the average forward flexion improved from 53° to 134° (p < 0.0001), the average abduction improved from 49° to 125° (p < 0.0001), the average internal rotation improved from S1 to L2 (p < 0.0001), and the average external rotation improved from 27° to 51° (p = 0.001). There were a total of twelve complications in eleven patients (prevalence, 20%). The survivorship at a mean of fifty-two months (range, twenty-four to 101 months) was 90.7% for all patients, 91.8% for Group A, and 87% for Group B.
When non-arthroplasty options either have failed or have a low likelihood of success, reverse shoulder arthroplasty provides reliable pain relief and return of shoulder function in patients with massive rotator cuff tears without arthritis at the time of short to intermediate-term follow-up.
本研究的目的是评估在患有巨大肩袖撕裂但无肩关节炎的患者中进行反向肩关节置换的适应证和结果。
1998 年 12 月至 2006 年 12 月,69 例(72 个肩)因不可修复的肩袖功能障碍而接受反向肩关节置换术治疗,无肩关节炎。反向肩关节置换术的适应证为:尽管至少接受了 6 个月的非手术治疗,但仍持续存在肩部疼痛和功能障碍,至少存在两肌腱撕裂,且在非关节置换选择不存在的情况下,患者的 Hamada 分期为 1、2 或 3 期。58 例(60 个肩)有至少 2 年的随访。34 个肩(A 组)无既往手术史,26 个肩(B 组)至少有一次既往手术史。术后对患者进行前瞻性临床和影像学随访。采用生存分析,终点为植入物的取出或翻修、影像学松动和美国肩肘外科医生评分下降。
在这项研究中,接受反向肩关节置换术的患者的共同特征是疼痛和(1)无前上脱位时肩部上肢抬高<90°(n=40;66.6%);(2)有前上脱位时上肢抬高<90°(n=16;26.7%);或(3)不可修复的肩袖撕裂和疼痛时上肢抬高>90°(n=4;6.7%)。平均随访时间为 52 个月(范围 24 至 101 个月)。所有测量的结果均在术后得到改善。对于所有患者,美国肩肘外科医生评分平均从 33.3 分提高到 75.4 分(p<0.0001),简单肩部测试评分平均从 1.6 分提高到 6.5 分(p<0.0001),疼痛视觉模拟评分平均从 6.3 分提高到 1.9 分(p<0.0001),功能视觉模拟评分平均从 3.2 分提高到 7.1 分(p<0.0001),前屈平均从 53°提高到 134°(p<0.0001),外展平均从 49°提高到 125°(p<0.0001),内旋平均从 S1 提高到 L2(p<0.0001),外旋平均从 27°提高到 51°(p=0.001)。11 例患者(20%)共发生 12 例并发症。平均随访 52 个月(范围 24 至 101 个月)时,所有患者的生存率为 90.7%,A 组为 91.8%,B 组为 87%。
在非关节置换选择失败或成功率低的情况下,反向肩关节置换术可为患有巨大肩袖撕裂且无关节炎的患者在短至中期随访时提供可靠的疼痛缓解和肩部功能恢复。