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外科研究与新技术(中英文) ›› 2026, Vol. 15 ›› Issue (3): 201-206.doi: 10.3969/j.issn.2095-378X.2026.03.002

• 论著 • 上一篇    下一篇

接骨木康方联合富血小板血浆局部注射治疗胫骨远端骨不连的临床研究

李学飞, 王庚启   

  1. 上海中医药大学附属岳阳中西医结合医院创伤骨科,上海 200437
  • 收稿日期:2026-07-30 出版日期:2026-09-28 发布日期:2026-09-30
  • 通讯作者: 王庚启,电子信箱:wanggengqi@126.com
  • 作者简介:李学飞(1993—),男,博士,主治医师,从事临床创伤骨科工作
  • 基金资助:
    上海中医药大学附属岳阳中西医结合医院揭榜挂帅项目(2024YJJB05); 岳阳医院育苗计划(yyym07)

Clinical study on treatment of distal tibial nonunion with Jiegumukang Decoction combined with local injection of platelet-rich plasma

LI Xuefei, WANG Gengqi   

  1. Department of Orthopaedic Trauma, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 200437, China
  • Received:2026-07-30 Online:2026-09-28 Published:2026-09-30

摘要: 目的 观察接骨木康方联合富血小板血浆(PRP)局部注射治疗胫骨远端骨不连的临床疗效与安全性。方法 选取2025年1月—2026年1月收治的80例胫骨远端骨不连患者,采用随机数字表分为对照组与观察组(各40例)。对照组单纯予以PRP骨折断端局部注射,每4周1次,共治疗12周;观察组在对照组PRP治疗基础上加服接骨木康方辨证加减,每日1剂,连续口服12周。对比两组治疗前,治疗4、8、12周疼痛视觉模拟评分法(VAS)评分,治疗前后Lane-Sandhu骨愈合影像学评分,美国足踝外科协会(AOFAS)踝关节功能评分,治疗12周后临床总有效率及不良反应发生率。结果 治疗前两组VAS、Lane-Sandhu、AOFAS评分基线水平无统计学差异(P>0.05);治疗4、8、12周两组VAS评分均较本组治疗前显著降低,且同时间点观察组低于对照组(P<0.05);治疗12周后两组Lane-Sandhu、AOFAS评分均较治疗前升高,且观察组高于对照组(P<0.05)。对照组总有效率80.00%,观察组95.00%,组间差异有统计学意义(χ²=4.114,P=0.043)。对照组不良反应发生率5.00%,观察组5.00%,两组间差异无统计学意义(P>0.05)。结论 接骨木康方联合PRP局部注射方案可有效减轻胫骨远端骨不连患者疼痛程度,促进骨痂生成、加速骨折愈合,改善踝关节活动功能,整体疗效优于单纯PRP局部注射,且用药安全,值得临床推广。

关键词: 胫骨远端骨不连, 接骨木康方, 富血小板血浆, 中西医结合, 骨折愈合

Abstract: Objective To observe the clinical efficacy and safety of local injection of platelet-rich plasma (PRP) combined with Jiegumukang decoction in the treatment of distal tibial nonunion. Methods Eighty patients diagnosed with distal tibial nonunion admitted between January 2025 and January 2026 were enrolled and randomly assigned into a control group and an observation group, with 40 cases in each group. The control group received local PRP injection alone at the fractured bone ends once every four weeks for a 12-week treatment course. On the basis of identical PRP intervention administered to the control group, the observation group additionally took the syndrome-differentiated and modified Jiegumukang decoction orally, one dose per day for 12 consecutive weeks. The visual analogue scale (VAS) scores for pain recorded at baseline as well as week 4, week 8, and week 12 after treatment, the Lane-Sandhu radiographic bone-healing scores and American Orthopaedic Foot and Ankle Society (AOFAS) ankle-function scores before and after intervention, the overall effective rate at week 12 and the incidence of adverse reactions were compared between the two groups. Results Baseline VAS, Lane-Sandhu, and AOFAS scores exhibited no statistically significant inter-group differences before treatment (P>0.05). VAS scores dropped markedly in both groups at 4, 8, and 12 weeks follow-ups relative to their respective baseline values, and scores in the observation group were significantly lower than those in the control group at all matched time-points (P<0.05). After the 12-week therapy, Lane-Sandhu and AOFAS scores rose in both groups, with greater improvements detected within the observation group (P<0.05). The overall effective rate reached 80.00% for the control group versus 95.00% for the observation group; the difference was significant (χ²=4.114, P=0.043). The adverse reaction incidence stood at 5.00% in both groups (P>0.05). Conclusion The combined regimen of orally administered syndrome-adapted Jiegumukang decoction and local PRP injection can effectively alleviate pain, stimulate callus formation, accelerate fracture repair, and restore ankle mobility among patients suffering from distal tibial nonunion. This combined therapy yields superior clinical outcomes to local PRP injection alone while maintaining favourable medication safety, and therefore merits widespread clinical promotion.

Key words: Distal tibial nonunion, Jiegumukang decoction, Platelet-rich plasma, Integrated traditional Chinese and Western medicine, Fracture healing

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