Orthopedics and Reconstructive Foot and Ankle Surgery, Cairo, Egypt.
Ankle and Knee Section, Orthopaedics Department, Centro Artroscópico Jorge Batista, Ciudad Autónoma de Buenos Aires, Argentina.
Foot Ankle Int. 2022 Sep;43(9):1174-1184. doi: 10.1177/10711007221096674. Epub 2022 Jun 10.
Both percutaneous and endoscopically assisted methods are reported to produce good results in the surgical management of acute Achilles tendon ruptures. The aim of this retrospective study was to compare between a percutaneous method and a recently described isolated endoscopically assisted flexor hallucis longus (FHL) transfer method as surgical means of management in patients with acute Achilles tendon ruptures.
One hundred seventeen patients were included in the current study and divided into 2 groups: 59 patients who underwent percutaneous Achilles repair (PAR Group) and 58 patients who underwent isolated endoscopic FHL transfer (FHL Group) were compared. Patients were clinically evaluated using American Orthopaedic Foot & Ankle Society (AOFAS) ankle-hindfoot score, Achilles tendon Total Rupture Score (ATRS), and Achilles tendon resting angle (ATRA) measures. In addition, ankle plantarflexion power, FHL dynamometry, Tegner activity levels, and return to previous levels of activity were also documented for all patients.
Nine months after surgery, patients in the FHL transfer group were more likely to be able to return to normal activities (91% vs 73%, < .01). Thirty months after surgical treatment, we found no difference in ATRS, AOFAS, ATRA, ankle plantarflexion strength, or Tegner activity scores between study groups. Overall complications were reported in 6 patients in the FHL group (10.3%) and in 8 patients in the PAR group (13.6%). No major neurovascular or skin complications were encountered.
The current study demonstrated satisfactory and comparable results and complications when comparing isolated endoscopic FHL tendon transfer or percutaneous Achilles tendon repairs in the surgical management of acute Achilles tendon ruptures.
Level III, retrospective controlled trial.
经皮和内镜辅助方法均被报道可在急性跟腱断裂的手术治疗中取得良好效果。本回顾性研究的目的是比较经皮方法和最近描述的单独内镜辅助屈肌长肌腱(FHL)转移方法作为急性跟腱断裂患者的手术治疗手段。
本研究共纳入 117 例患者,分为两组:59 例行经皮跟腱修复(PAR 组),58 例行单独内镜 FHL 转移(FHL 组)。采用美国矫形足踝协会(AOFAS)踝后足评分、跟腱总断裂评分(ATRS)和跟腱静息角度(ATRA)对患者进行临床评估。此外,还记录了所有患者的踝关节跖屈肌力、FHL 动力测定、Tegner 活动水平以及恢复到之前活动水平的情况。
术后 9 个月,FHL 转移组患者更有可能恢复正常活动(91%比 73%,<.01)。术后 30 个月,两组间 ATRS、AOFAS、ATRA、踝关节跖屈肌力和 Tegner 活动评分无差异。FHL 组有 6 例(10.3%)和 PAR 组有 8 例(13.6%)患者报告有总体并发症。未发生重大神经血管或皮肤并发症。
本研究表明,在急性跟腱断裂的手术治疗中,单独内镜 FHL 肌腱转移或经皮跟腱修复的结果和并发症相似。
III 级,回顾性对照试验。