Human immunodeficiency virus in total hip arthroplasty
- PMID: 32296550
- PMCID: PMC7144891
- DOI: 10.1302/2058-5241.5.190030
Human immunodeficiency virus in total hip arthroplasty
Abstract
Human immunodeficiency virus (HIV) is a pandemic affecting more than 35 million people worldwide. The aim of this review is to describe the association between HIV and total hip arthroplasty (THA) and assess patient risk factors to optimize functional outcomes and decrease rates of revision.Since the advent of highly active antiretroviral treatment (HAART), HIV-infected patients are living longer, which allows them to develop degenerative joint conditions. HIV and HAART act independently to increase the demand for THA. HIV-positive patients are also more predisposed to developing avascular necrosis (AVN) of the hip and femoral neck fractures due to decreased bone mineral density (BMD).Prior to the widespread implementation of access to HAART in homogenous cohorts of HIV-infected patients undergoing THA, reports indicated increased rates of complications. However, current literature describes equivocal functional outcomes and survival rates after THA in HIV-positive patients controlled on HAART when compared to HIV-negative controls.HIV-infected patients eligible for THA should be assessed for medical co-morbidities and serum markers of disease control should be optimized.Periprosthetic joint infection (PJI) is a leading cause of revision THA, and HIV is a modifiable risk factor. Importantly, the significance is negated once patients are placed on HAART and achieve viral suppression.THA should not be withheld in HIV-infected patients injudiciously. However, HIV is a burgeoning epidemic and all patients should be identified and started on HAART to avoid preventable peri-operative complications. Cite this article: EFORT Open Rev 2020;5:164-171. DOI: 10.1302/2058-5241.5.190030.
Keywords: human immunodeficiency virus; immunocompromise; total hip arthroplasty.
© 2020 The author(s).
Conflict of interest statement
ICMJE Conflict of interest statement: LM reports consultancy for Zimmerbiomet and Implantcast; payment for lectures including service on speakers’ bureaus for Zimmerbiomet, Smith and Nephew and Advanced Orthopaedics, all outside the submitted work. The other authors declare no conflict of interest relevant to this work.
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