Department of Orthopaedics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Occupational Therapy and Physiotherapy, Sahlgrenska University Hospital, Mölndalsvägen 31, SE-431 80, Mölndal, Sweden.
Int Orthop. 2020 Jul;44(7):1353-1365. doi: 10.1007/s00264-020-04605-x. Epub 2020 May 29.
The purpose of this randomised, controlled, double-blind trial was to evaluate functional outcome during the first year after corrective osteotomy for malunited distal radius fractures, with or without filling the osteotomy void.
Patients were randomised to receive a HydroSet bone substitute or no graft. Cortical contact was maintained and stabilisation of the osteotomy was carried out with a DiPhos R- or RM Plate. To evaluate subjective functional outcome, the Patient-Rated Wrist Evaluation (PRWE), the Quick Disabilities of the Arm, Shoulder and Hand Questionnaire (Q-DASH), the Canadian Occupational Performance Measure (COPM) and the RAND-36 were used. Moreover, range of motion and grip strength were measured by blinded evaluators. Evaluations were made pre-operatively and three, six and 12 months post-operatively.
There were no significant differences between the groups at any time point post-operatively with respect to any of the PROMs that were used or range of motion or grip strength (p > 0.05). In both groups, there was a significant improvement at the 12-month follow-up compared with pre-operatively for the PRWE, the Q-DASH and the COPM satisfaction scores. The RAND-36 revealed no significant differences except for two domains, in which there was an improvement in the treatment group (p < 0.05). For grip strength and for range of motion in all movement directions, except dorsal extension, there was a significant improvement in both groups (p < 0.05).
There is no significant difference in functional outcome during the first year after corrective open-wedge distal radius osteotomy, where cortical contact is maintained, regardless of whether or not bone substitute to fill the void is used.
本随机对照双盲试验旨在评估治疗愈合不良桡骨远端骨折的矫形截骨术后 1 年内的功能结果,包括是否填充截骨间隙。
患者随机分为接受 HydroSet 骨替代物或不接受植骨的两组。维持皮质接触,并使用 DiPhos R- 或 RM 板稳定截骨。为评估主观功能结果,使用患者腕关节评分(PRWE)、手臂、肩部和手功能残疾问卷(Q-DASH)、加拿大职业表现测量(COPM)和 RAND-36 进行评估。此外,通过盲法评估者测量关节活动度和握力。在术前和术后 3、6 和 12 个月进行评估。
术后任何时间点,两组在使用的任何 PROM 或关节活动度或握力方面均无显著差异(p>0.05)。两组在 12 个月随访时与术前相比,PRWE、Q-DASH 和 COPM 满意度评分均有显著改善。RAND-36 除两个领域外,无显著差异,治疗组有改善(p<0.05)。对于握力和所有运动方向的关节活动度,除背伸外,两组均有显著改善(p<0.05)。
在维持皮质接触的情况下,进行开放性楔形桡骨远端截骨术后 1 年内,无论是否使用骨替代物填充骨缺损,功能结果均无显著差异。