Sood Aditya, Therattil Paul J, Paik Angie M, Simpson Mary F, Lee Edward S
Division of Plastic and Reconstructive Surgery, Department of Surgery, New Jersey Medical School, Rutgers University, Newark, NJ.
Department of Veterans Affairs New Jersey Health Care System, East Orange, NJ.
Eplasty. 2014 Mar 27;14:e13. eCollection 2014.
Clinical trials seeking to establish long-term efficacy of injectable collagenase clostridium histolyticum for treatment of Dupuytren disease are ongoing. In this quality improvement study, the efficacy, recurrence rate, and complications of collagenase injection for Dupuytren disease are reviewed in a population of Veteran patients.
A retrospective chart review was performed for patients who underwent treatment with injectable collagenase for Dupuytren disease from 2010 to 2013 at our regional Department of Veterans Affairs medical center. Data points of interest included the degree of joint contracture preoperatively, immediately after treatment, and at follow-up, complications, and patient satisfaction.
Sixteen patients received 27 injections (18 metacarpophalangeal and 9 proximal interphalangeal injections). The mean time of follow-up was 12.3 months. There was a 50% or greater reduction of the original extension deficit in 74.1% (n = 27) of the joints treated. Metacarpophalangeal joint recurrence was "high" (≥50°) in 0% (n = 18) of joints, and "low" (5°-50°) in 33.3% (n = 18) of joints with a mean follow-up of 12 months. Proximal interphalangeal joint recurrence was "high" (≥40°) in 18.5% (n = 9) of joints and "low" (5°-40°) in 7.4% (n = 9) of joints with a mean follow-up of 12.9 months. Minor complications were experienced in 93.8% (n = 16) of patients who underwent collagenase injection and included ecchymosis, skin laceration, injection-site swelling, injection-site hemorrhage, tenderness, and pruritus. Seventy-five percent (n = 12) of patients in our study reported they would undergo treatment with collagenase again.
The case series presented demonstrates that injectable collagenase clostridium histolyticum produced a clinical success rate of 74.1% and is a safe method to treat Dupuytren disease.
旨在确定注射用溶组织梭状芽孢杆菌胶原酶治疗掌腱膜挛缩症长期疗效的临床试验正在进行。在这项质量改进研究中,对一组退伍军人患者注射胶原酶治疗掌腱膜挛缩症的疗效、复发率和并发症进行了回顾。
对2010年至2013年在我们地区退伍军人事务医疗中心接受注射用胶原酶治疗掌腱膜挛缩症的患者进行回顾性病历审查。感兴趣的数据点包括术前、治疗后即刻及随访时的关节挛缩程度、并发症和患者满意度。
16名患者接受了27次注射(18次掌指关节注射和9次近端指间关节注射)。平均随访时间为12.3个月。74.1%(n = 27)接受治疗的关节原始伸展缺损减少了50%或更多。掌指关节复发率在平均随访12个月的关节中,“高”(≥50°)的为0%(n = 18),“低”(5° - 50°)的为33.3%(n = 18)。近端指间关节复发率在平均随访12.9个月的关节中,“高”(≥40°)的为18.5%(n = 9),“低”(5° - 40°)的为7.4%(n = 9)。93.8%(n = 16)接受胶原酶注射的患者出现了轻微并发症,包括瘀斑、皮肤撕裂、注射部位肿胀、注射部位出血、压痛和瘙痒。我们研究中75%(n = 12)的患者表示他们会再次接受胶原酶治疗。
本病例系列表明,注射用溶组织梭状芽孢杆菌胶原酶的临床成功率为74.1%,是治疗掌腱膜挛缩症的一种安全方法。