Implant extrusion in subtalar arthroereisis is a common complication for pediatric flexible flatfoot. However, there were a limited number of articles addressing the body weight effects on implant extrusion after the procedure. We conducted a 24-month follow-up assessment after subtalar arthroereisis. Surgical patients who underwent the Vulpius procedure were retrospectively collected from May 2010 to January 2017, including 59 cases of both feet having implants in situ and 43 cases of both feet having implant extrusion. The average age of 102 patients was 9 years old. The mean body mass index (BMI) of the implant in situ group was 19.5, whilst the extrusion group was 21.2 (p = 0.035). The inter-observer correlation was excellent. There were 11 cases (39.3%) of bilateral extrusion in the overweight group (BMI ≥ 24) and 13 cases (23.2%) in the low body weight group (BMI ≤ 18.5) (p < 0.0004). Postoperative radiographic angles were corrected in both the implant in situ group and the extrusion group. Nonetheless, the implant in situ group revealed better postoperative outcomes of Meary’s angle and the talonavicular angle from an anterior-posterior view, and the talar inclination angle from a lateral view. We conclude that a higher BMI is related to implant extrusion and worse results after subtalar arthroereisis. Further prospective study to investigate whether preoperative weight loss results in improved surgical outcomes is warranted in the future.
reviewed for relevant reference. Literature not written in English, not available in full text, adult patients, focus on gait analysis, review articles, patients with neuromuscular diseases, case reports, or techniques except exosinotarsal subtalar screw in calcaneus or endosinotarsal cone-shaped implant were excluded. We investigated studies using endosinotarsal tunnel subtalar arthroereisis for pediatric flexible flatfoot treatment. The search strategy comprised the following keywords combined with subtalar arthroereisis: flexible flatfoot and pes planus. Regarding the types of included studies, we enrolled randomized controlled trials (RCTs), comparative experimental trials, or single-armed follow up studies. We excluded case series and case reports. The target population comprised pediatric patients who suffered from painful flexible flatfoot.
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