Arthroscopy combined with bone tunnel technique for treating Berndt and Harty stage III or IV osteochondral lesions of the talus.

IF 2 3区 医学 Q2 ORTHOPEDICS International Orthopaedics Pub Date : 2025-02-01 Epub Date: 2024-12-09 DOI:10.1007/s00264-024-06384-1
Mingliang Xu, Renlong Li, Guoliang Chen, Lin Li, Jing Chen, Rongjian Shi
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Abstract

Purpose: To explore the efficacy and feasibility of arthroscopy combined with bone tunnel technique in treating Berndt and Harty stage III or IV osteochondral lesions of the talus (OLT).

Methods: A retrospective analysis was conducted on the clinical data of 21 patients with Berndt and Harty stage III or IV OLT who underwent surgical treatment at our institution from September 2017 to September 2022. Under arthroscopy, the displaced talar osteochondral lesion was restored. A 2.0 mm Kirschner wire (K-wire) was used to create a bone tunnel from the medial (or lateral) malleolus to the realigned osteochondral lesion. A 1.5 mm K-wire was then used to drill through this tunnel into the osteochondral fragment, and a 1.5 mm absorbable bone rod was inserted for fixation. Preoperative and final follow-up visual analogue scale (VAS) for pain and American Orthopedic Foot and Ankle Society (AOFAS) ankle-hindfoot scale were recorded and compared.

Results: All 21 patients were followed up for an average of 23.95 ± 6.01 months. All wounds healed by primary intention, with no nerve, blood vessel, or tendon injuries. All osteochondral lesions healed, with an average healing time of 3.71 ± 0.62 months. The VAS score decreased from a preoperative average of 5.38 ± 0.59 to 0.48 ± 0.51 at the final follow-up. The AOFAS ankle-hindfoot scale increased from a preoperative average of 56.29 ± 5.98 to 88.43 ± 2.68 at the final follow-up (P < 0.05), showing statistically significant differences. Two cases experienced medial pain after 12 months, which was tolerable with non-steroidal anti-inflammatory drugs.

Conclusion: Arthroscopy combined with bone tunnel technique for treating Berndt and Harty stage III or IV OLT has the advantages of minimal injury, visualization of fracture reduction, and fewer complications.

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关节镜联合骨隧道技术治疗距骨Berndt和Harty III期或IV期骨软骨病变。
目的:探讨关节镜联合骨隧道技术治疗距骨骨性软骨病变(Berndt and Harty III期或IV期)的疗效和可行性。方法:回顾性分析我院2017年9月至2022年9月手术治疗的21例Berndt和Harty III期或IV期OLT患者的临床资料。关节镜下复位距骨软骨病变。使用2.0 mm克氏针(k -丝)从内踝(或外侧)到重新排列的骨软骨病变处建立骨隧道。然后使用1.5 mm的k -丝穿过该隧道钻入骨软骨碎片,并插入1.5 mm的可吸收骨棒进行固定。术前、终期随访疼痛视觉模拟量表(VAS)与美国骨科足踝学会(AOFAS)踝关节-后足量表进行比较。结果:21例患者平均随访23.95±6.01个月。所有伤口均愈合,无神经、血管或肌腱损伤。所有骨软骨病变均愈合,平均愈合时间为3.71±0.62个月。VAS评分从术前平均(5.38±0.59)下降到最终随访时的0.48±0.51。AOFAS踝后足评分从术前平均56.29±5.98上升至最终随访时的88.43±2.68。(P)结论:关节镜联合骨隧道技术治疗Berndt and Harty III期或IV期OLT损伤小,骨折复位可见,并发症少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Orthopaedics
International Orthopaedics 医学-整形外科
CiteScore
5.50
自引率
7.40%
发文量
360
审稿时长
1 months
期刊介绍: International Orthopaedics, the Official Journal of the Société Internationale de Chirurgie Orthopédique et de Traumatologie (SICOT) , publishes original papers from all over the world. The articles deal with clinical orthopaedic surgery or basic research directly connected with orthopaedic surgery. International Orthopaedics will also link all the members of SICOT by means of an insert that will be concerned with SICOT matters. Finally, it is expected that news and information regarding all aspects of orthopaedic surgery, including meetings, panels, instructional courses, etc. will be brought to the attention of the readers. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted. Reports of animal experiments must state that the "Principles of laboratory animal care" (NIH publication No. 85-23, revised 1985) were followed, as well as specific national laws (e.g. the current version of the German Law on the Protection of Animals) where applicable. The editors reserve the right to reject manuscripts that do not comply with the above-mentioned requirements. The author will be held responsible for false statements or for failure to fulfil the above-mentioned requirements.
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