Department of Orthopaedic Surgery, Washington University School of Medicine, St Louis, MO.
Department of Orthopaedic Surgery, Washington University School of Medicine, St Louis, MO.
J Hand Surg Am. 2024 Oct;49(10):955-965. doi: 10.1016/j.jhsa.2024.04.012. Epub 2024 Jun 26.
We performed a randomized controlled trial assessing patient-reported outcome measures following trapeziectomy with ligament reconstruction and tendon interposition (LRTI) or suture tape suspensionplasty (STS) for treatment of thumb carpometacarpal joint osteoarthritis.
Patients undergoing surgery for thumb carpometacarpal joint osteoarthritis were prospectively randomized to LRTI or STS. Outcome measures were collected at 2 weeks, 4 weeks, 3 months, and 1 year and included visual analog scale pain, Patient-Reported Outcomes Measurement Information System (PROMIS) Upper Extremity, return to work/activity, range of motion, grip/pinch strength, and complications.
Thirty-one patients (32 thumbs) were randomized from 51 patients offered participation over two years. One-year follow-up was 97%. Both groups had a decrease in visual analog scale pain scores at all postoperative time points. The trajectory of postoperative Patient-Reported Outcomes Measurement Information System Upper Extremity scores was similar, and both groups achieved the meaningful clinically important difference for improvement in PROMIS Upper Extremity by three months. Grip strength was substantially increased in both groups at one year. Return to work/activity and surgical complications favored the LRTI group.
Our study did not suggest any clinically relevant differences in the postoperative patient-reported outcome measures or objective clinical measurements between LRTI and STS, although LRTI patients had a faster return to work/activity and lower complication rates.
TYPE OF STUDY/LEVEL OF EVIDENCE: Therapeutic IIB.
我们进行了一项随机对照试验,评估了韧带重建和肌腱置入(LRTI)或缝线带悬吊成形术(STS)治疗拇指腕掌关节骨关节炎患者的患者报告结局测量。
前瞻性随机选择接受拇指腕掌关节骨关节炎手术的患者进行 LRTI 或 STS。在术后 2 周、4 周、3 个月和 1 年收集了包括视觉模拟量表疼痛、患者报告的测量信息系统(PROMIS)上肢、恢复工作/活动、活动范围、握力/捏力和并发症等在内的结局测量。
在两年内有 51 名患者被邀请参与,其中 31 名患者(32 个拇指)被随机分配。1 年随访率为 97%。两组患者在所有术后时间点的视觉模拟量表疼痛评分均下降。术后 PROMIS 上肢评分的轨迹相似,两组在 3 个月时均达到了 PROMIS 上肢改善的有意义的临床重要差异。两组患者在术后 1 年均明显增加了握力。LRTI 组患者更快地恢复工作/活动和手术并发症发生率较低。
尽管 LRTI 组患者的工作/活动恢复更快,并发症发生率更低,但我们的研究并未表明 LRTI 和 STS 之间在术后患者报告的结局测量或客观临床测量方面存在任何临床相关差异。
类型的研究/证据水平:治疗性 IIB。