Chronic deltoid ligament insufficiency repair with Internal Brace™ augmentation

•Patients with chronic deltoid ligament insufficiency (CDLI) present a challenging situation.•The treatment armamentarium ranges from simple ligament repair to complex reconstructions. Direct repair augmented with an Internal Brace™ device appears to be an attractive intermediate option.•Our results...

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Veröffentlicht in:Foot and ankle surgery 2019-12, Vol.25 (6), p.812-818
Hauptverfasser: Pellegrini, M.J., Torres, N., Cuchacovich, N.R., Huertas, P., Muñoz, G., Carcuro, G.M.
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Sprache:eng
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Zusammenfassung:•Patients with chronic deltoid ligament insufficiency (CDLI) present a challenging situation.•The treatment armamentarium ranges from simple ligament repair to complex reconstructions. Direct repair augmented with an Internal Brace™ device appears to be an attractive intermediate option.•Our results suggest that deltoid ligament repair with Internal Brace™ augmentation in patients with CDLI is a reliable option with good functional outcomes and high satisfaction grade in short term follow-up. Patients with chronic deltoid ligament insufficiency (CDLI) present a challenging situation. Although numerous procedures have been described, optimal treatment is still a matter of debate. While the treatment armamentarium ranges from simple ligament repair to complex reconstructions with or without realignment osteotomies, direct repair augmented with an Internal Brace™ device appears to be an attractive intermediate option. We investigated functional outcomes and complications in patients with CDLI operated on using Internal Brace™ augmentation. A prospective study was conducted. Patients were included if they presented medial ankle pain and/or giving way, exhibited asymmetric flexible hindfoot valgus, failed conservative treatment, and had a positive MRI evaluated by an independent radiologist. Patients with stage IV flatfoot deformity, neuropathy and/or inflammatory arthritis were excluded. CDLI was confirmed intraoperatively with the arthroscopic drive-through sign. Patients were evaluated preoperatively and postoperatively using FAAM, SF-36 and grade of satisfaction. Paired t-tests were used to assess FAAM and SF-36 scores variation. Thirteen patients met inclusion criteria. No patient was lost to follow-up, with a mean follow-up time of 13.5 months (range 6-21). Preoperative FAAM and SF-36 scores improved from 58.7 to 75.3 and from 60.2 to 84.4 postoperatively, respectively (p
ISSN:1268-7731
1460-9584
DOI:10.1016/j.fas.2018.10.004