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PATIENT PERCEPTION OF THE EFFECTIVENESS OF SHOE RAISES IN THE MANAGEMENT OF SYMPTOMATIC LEG LENGTH DISCREPANCY FOLLOWING TOTAL HIP REPLACEMENT



Abstract

Objectives: We aimed to assess the incidence of requirement for shoe raises for a leg length discrepancy (LLD) after total hip replacement (THR). We also assessed the patient satisfaction with, and continued use of shoe raises for symptomatic LLD after THR.

Methods: We searched the orthotics records at our institution to identify all patients who had required a shoe raise for symptomatic LLD after primary unilateral total hip replacement between January 2003 and October 2008. 75 patients were identified. 72 were still alive. In the same period 4270 primary hip replacements were carried out at the institution. A questionnaire was sent out to all living patients. Patient details (including satisfaction) and operative details were recorded. Pre-operative and post-operative radiological measurements of leg length discrepancy (LLD) were performed.

Results: The incidence of requirement of a shoe raise for LLD after THR at our institution was 1.8%. 68% were women. 84% of questionnaires were returned. 31% had stopped using their shoe raise completely. Two-thirds of patients found the raise improved their symptoms of a LLD. Symptoms causing dissatisfaction with the shoe raise included new or worsening back pain, limp, uneven walking, self awareness, need to adjust trouser length, pain in other hip, discomfort while walking, and difficulty buying shoes. Patient overall satisfaction with their THR was poor in the patients who were dissatisfied with the shoe raise, but was good in those who found the raise useful.

Conclusion: About 2% of patients may require a shoe raise for symptomatic LLD after THR. Of these 65% will find the shoe raise helpful. Patient with a LLD after a THR that is not helped by a shoe raise are very dissatisfied. It is important that surgeons should take great care to avoid causing a LLD after THR as it can be a cause of very low patient satisfaction.

Correspondence should be addressed to: EFORT Central Office, Technoparkstrasse 1, CH – 8005 Zürich, Switzerland. Tel: +41 44 448 44 00; Email: office@efort.org

Author: Bolarinwa Akinola, United Kingdom

E-mail: bolaakinola@gmail.com