A New Surgical Technique for Achilles Tendon Rupture: A Retrospective Study of 18 Cases.

IF 1.1 4区 医学 Q3 ORTHOPEDICS
Indian Journal of Orthopaedics Pub Date : 2025-06-29 eCollection Date: 2025-08-01 DOI:10.1007/s43465-025-01459-6
Dawei Xin, Zhuosong Mu, Linru Zeng, Gan Luo, Yafeng Mo
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引用次数: 0

Abstract

Background: The optimal treatment for acute closed Achilles tendon rupture (ATR) is still controversial. Many grassroots hospitals lack advanced equipment to perform effective minimally invasive surgeries, and open surgeries increase the incidence of complications. Therefore, we have developed a new technique specifically for grassroots hospitals. It involves using oval forceps-assisted minimally invasive suture bridge technology to treat acute closed Achilles tendon ruptures. This technique is easy to perform and has shown good clinical outcomes.

Methods: We reviewed the therapeutic effectiveness of using oval forceps-assisted minimally invasive suture bridge technique in the treatment of 18 patients with ATR. All patients were followed up for a minimum of 12 months. Preoperative and postoperative follow-up data were reviewed to analyze the results and evaluate the surgical outcomes.

Results: The patients were followed up for 12-16 months [( 13.9 ± 1.6 ) months]. There was no statistically significant difference in the ankle joint visual analog scale (VAS) scores at 3, 6, and 12 months postoperatively ( P > 0.05). However, there was a statistically significant increase in ankle joint active range of motion(AROM) at 3, 6, and 12 months postoperatively ( P < 0.05). At the same time, there was no statistically significant difference in AROM between the healthy side and the affected side at 12 months postoperatively. The American Orthopaedic Foot & Ankle Society(AOFAS) scores and Achilles Tendon Total Rupture Score (ATRS) showed a gradual improvement at 3, 6, and 12 months postoperatively, with statistical significance ( P < 0.05). All surgical incisions healed well without complications such as injury to the sural nerve or incision infection. Three patients experienced pain at the site of ATR at 3 months postoperatively, which resolved after a 2-week course of oral nonsteroidal anti-inflammatory drugs (NSAIDs). One patient experienced transient pain at the Achilles tendon insertion point after 6 months of activity, which disappeared after a 2-week course of oral NSAIDs.

Conclusion: The use of oval forceps-assisted suture bridge technique for the treatment of acute closed ATR is characterized by its small incision, simple operation, and minimal complications, meeting the requirements for early functional rehabilitation of patients. For grassroots hospitals that receive a large number of patients, the oval forceps-assisted suture bridge technique is a surgical method worth popularizing.

一种治疗跟腱断裂的新手术技术:18例回顾性分析。
背景:急性闭合性跟腱断裂(ATR)的最佳治疗方法仍存在争议。许多基层医院缺乏先进的设备,无法开展有效的微创手术,开放性手术增加了并发症的发生率。因此,我们开发了一种专门针对基层医院的新技术。它包括使用椭圆钳辅助微创缝合桥技术治疗急性闭合性跟腱断裂。该技术操作简单,临床效果良好。方法:回顾应用椭圆钳辅助微创缝合桥技术治疗18例ATR患者的疗效。所有患者至少随访12个月。回顾术前和术后随访资料,分析结果并评价手术效果。结果:患者随访12 ~ 16个月[(13.9±1.6)个月]。两组术后3、6、12个月踝关节视觉模拟评分(VAS)比较,差异均无统计学意义(P < 0.05)。然而,术后3、6、12个月踝关节活动范围(AROM)增加有统计学意义(P < 0.05)。同时,术后12个月健康侧与患侧的AROM比较,差异无统计学意义。美国骨科足踝学会(AOFAS)评分和跟腱总断裂评分(ATRS)在术后3、6、12个月逐渐改善,差异均有统计学意义(P < 0.05)。手术切口愈合良好,无腓肠神经损伤、切口感染等并发症。3例患者术后3个月出现ATR部位疼痛,经2周口服非甾体抗炎药(NSAIDs)治疗后疼痛缓解。一名患者在活动6个月后出现跟腱插入点的短暂疼痛,在口服非甾体抗炎药2周后消失。结论:椭圆钳辅助缝合桥技术治疗急性闭合性ATR切口小,操作简单,并发症少,满足患者早期功能康复的要求。对于收治患者较多的基层医院,椭圆钳辅助缝合桥技术是一种值得推广的手术方法。
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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
185
审稿时长
9 months
期刊介绍: IJO welcomes articles that contribute to Orthopaedic knowledge from India and overseas. We publish articles dealing with clinical orthopaedics and basic research in orthopaedic surgery. Articles are accepted only for exclusive publication in the Indian Journal of Orthopaedics. Previously published articles, articles which are in peer-reviewed electronic publications in other journals, are not accepted by the Journal. Published articles and illustrations become the property of the Journal. The copyright remains with the journal. Studies must be carried out in accordance with World Medical Association Declaration of Helsinki.
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