The use of a ceramic talar body prosthesis in patients with aseptic necrosis of the talus

A. Taniguchi, Y. Takakura, K. Sugimoto, K. Hayashi, K. Ouchi, Tsukasa Kumai, Y. Tanaka

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

The purpose of this study was to evaluate the clinical results of a newly designed prosthesis to replace the body of the talus in patients with aseptic necrosis. Between 1999 and 2006, 22 tali in 22 patients were replaced with a ceramic prosthesis. A total of eight patients were treated with the first-generation prosthesis, incorporating a peg to fix into the retained neck and head of the talus, and the remaining 14 were treated with the second-generation prosthesis, which does not have the peg. The clinical results were assessed by the American Orthopaedic Foot and Ankle Society ankle/hindfoot scale. The mean follow-up was 98 months (18 to 174). The clinical results of the first-generation prostheses were excellent in three patients, good in one, fair in three and poor in one. There were, however, radiological signs of loosening, prompting a change in design. The clinical results of the second-generation prostheses were excellent in three patients, good in five, fair in four and poor in two, with more favourable radiological appearances. Revision was required using a total talar implant in four patients, two in each group. Although the second-generation prosthesis produced better results, we cannot recommend the use of a talar body prosthesis. We now recommend the use of a total talar implant in these patients.

Original languageEnglish
Pages (from-to)1529-1533
Number of pages5
JournalJournal of Bone and Joint Surgery - Series B
Volume94 B
Issue number11
DOIs
Publication statusPublished - 2012 Nov
Externally publishedYes

    Fingerprint

ASJC Scopus subject areas

  • Surgery
  • Orthopedics and Sports Medicine

Cite this