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Hip

Similar range of motion and function after resurfacing large–head or standard total hip arthroplasty

2–year results from a randomized clinical trial

, , &
Pages 246-253 | Published online: 26 Mar 2013
 

Abstract

Background and purpose Large–size hip articulations may improve range of motion (ROM) and function compared to a 28–mm THA, and the low risk of dislocation allows the patients more activity postoperatively. On the other hand, the greater extent of surgery for resurfacing hip arthroplasty (RHA) could impair rehabilitation. We investigated the effect of head size and surgical procedure on postoperative rehabilitation in a randomized clinical trial (RCT).

Methods We followed randomized groups of RHAs, large–head THAs and standard THAs at 2 months, 6 months, 1 and 2 years postoperatively, recording clinical rehabilitation parameters.

Results Large articulations increased the mean total range of motion by 13° during the first 6 postoperative months. The increase was not statistically significant and was transient. The 2–year total ROM (SD) for RHA, standard THA, and large–head THA was 221° (35), 232° (36), and 225° (30) respectively, but the differences were not statistically significant. The 3 groups were similar regarding Harris hip score, UCLA activity score, step rate, and sick leave.

Interpretation Head size had no influence on range of motion. The lack of restriction allowed for large articulations did not improve the clinical and patient–perceived outcomes. The more extensive surgical procedure of RHA did not impair the rehabilitation.

This project is registered at ClinicalTrials.gov under # NCT01113762.

SO, OO, KB, and JØP designed the study. JØP obtained and analyzed the data. JØP. SO, OO, and JEV wrote the initial draft. JØP ensured the accuracy of the data and analysis.

We thank project nurse Annie Gam–Pedersen for handling all the logistics, and biostatistician Lars Korsholm for help in planning and carrying out the statistical analyses.

The project was mainly funded by a grant from the Danish Ministry of the Interior and Health, but there was also some regional and hospital funding. Biomet Denmark and Protesekompagniet/DePuy provided institutional support for the project in terms of patient transportation and special analyses not published in this paper. None of the authors are employed or otherwise financially involved with any of these companies.