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Human immunodeficiency virus in total hip arthroplasty
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 t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
British Editorial Society of Bone and Joint Surgery
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144891/ https://www.ncbi.nlm.nih.gov/pubmed/32296550 http://dx.doi.org/10.1302/2058-5241.5.190030 |
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author | Pietrzak, Jurek Rafal Tomasz Maharaj, Zia Mokete, Lipalo Sikhauli, Nkhodiseni |
author_facet | Pietrzak, Jurek Rafal Tomasz Maharaj, Zia Mokete, Lipalo Sikhauli, Nkhodiseni |
author_sort | Pietrzak, Jurek Rafal Tomasz |
collection | PubMed |
description | 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 |
format | Online Article Text |
id | pubmed-7144891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | British Editorial Society of Bone and Joint Surgery |
record_format | MEDLINE/PubMed |
spelling | pubmed-71448912020-04-15 Human immunodeficiency virus in total hip arthroplasty Pietrzak, Jurek Rafal Tomasz Maharaj, Zia Mokete, Lipalo Sikhauli, Nkhodiseni EFORT Open Rev Hip 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 British Editorial Society of Bone and Joint Surgery 2020-03-02 /pmc/articles/PMC7144891/ /pubmed/32296550 http://dx.doi.org/10.1302/2058-5241.5.190030 Text en © 2020 The author(s) https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-Non Commercial 4.0 International (CC BY-NC 4.0) licence (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed. |
spellingShingle | Hip Pietrzak, Jurek Rafal Tomasz Maharaj, Zia Mokete, Lipalo Sikhauli, Nkhodiseni Human immunodeficiency virus in total hip arthroplasty |
title | Human immunodeficiency virus in total hip arthroplasty |
title_full | Human immunodeficiency virus in total hip arthroplasty |
title_fullStr | Human immunodeficiency virus in total hip arthroplasty |
title_full_unstemmed | Human immunodeficiency virus in total hip arthroplasty |
title_short | Human immunodeficiency virus in total hip arthroplasty |
title_sort | human immunodeficiency virus in total hip arthroplasty |
topic | Hip |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144891/ https://www.ncbi.nlm.nih.gov/pubmed/32296550 http://dx.doi.org/10.1302/2058-5241.5.190030 |
work_keys_str_mv | AT pietrzakjurekrafaltomasz humanimmunodeficiencyvirusintotalhiparthroplasty AT maharajzia humanimmunodeficiencyvirusintotalhiparthroplasty AT moketelipalo humanimmunodeficiencyvirusintotalhiparthroplasty AT sikhaulinkhodiseni humanimmunodeficiencyvirusintotalhiparthroplasty |