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Orthop Traumatol Surg Res. 2012 Dec;98(8):863-7. doi: 10.1016/j.otsr.2012.09.010. Epub 2012 Nov 15.

Fibular nonunion after closed-wedge high tibial osteotomy.

Author information

1
Service de chirurgie orthopédique, université Paris-Descartes, hôpital européen Georges-Pompidou, AP-HP, Paris, France. ramanoudjame.mira@yahoo.fr

Abstract

Closed-wedge valgus high tibial osteotomy (HTO) has been reported to be an effective procedure for the treatment of medial compartment osteoarthritis of the knee. It requires shortening the fibula, for which many techniques have been described. Dislocation of the proximal tibiofibular joint limits the correction angle of the procedure and the osteotomy of the fibular head runs the rare but dramatic risk of common fibular nerve palsy, which is why many surgeons perform the osteotomy more distally at the shaft. However, the potential complications of fibula shaft osteotomy in closed-wedge proximal tibial osteotomy have been poorly reported. The purpose of this study is to accurately define the incidence and risk of fibular complications.

MATERIALS AND METHODS:

One hundred and eight patients (59 men, 49 women, 53±10years old, preoperative varus: 6.7°±4°) underwent a closed-wedge HTO with fibular shaft osteotomy between 1999 and 2004. They were followed up prospectively for clinical and radiological evaluation (2years of follow-up). The main evaluation criterion was the presence of fibular nonunion.

RESULTS:

Eighteen knees (16.6%) underwent fibular complications: 15 nonunions were indexed (13.9%); 11 of them (10.1%) required surgical revision. Three knees had nerve injury, with spontaneous recovery for two of them.

DISCUSSION:

Fibular nonunion is the most frequent complication, which often leads to revision procedures. Nonunion was correlated to the preoperative body mass index, the obliquity of the osteotomy plane, and the fragmentary contact. No nonunion was reported when the obliquity of the osteotomy plane was above 50° or the fragment contact greater than 50%.

LEVEL OF EVIDENCE:

Level IV, therapeutic study.

PMID:
23158781
DOI:
10.1016/j.otsr.2012.09.010
[Indexed for MEDLINE]
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