Abstract
HIV reduces bone mineral density, mineralization, and turnover and may impair fracture healing. This prospective cohort study in South Africa investigated whether HIV infection was associated with impaired fracture healing after trauma. All adults with acute tibia and femur fractures who underwent intermedullary (IM) nailing for fracture fixation between September 2017 and December 2018, at 2 tertiary hospitals, were followed up for a minimum of 12 months postoperatively. The primary outcome was delayed bone union at 6 months (defined by the radiological union scoring system for the tibia score <9), and the secondary outcome was nonunion (defined as radiological union scoring system for the tibia score <9) at 9 months. Multivariable logistic regression models were constructed to investigate the associations between HIV status and impaired fracture healing. In total, 358 participants, who underwent 395 IM nailings, were enrolled in the study and followed up for 12 months. Seventy-one of the 358 (19.8%) participants were HIV-positive [83/395 (21%) IM nailings]. HIV was not associated with delayed fracture healing after IM nailing of the tibia or femur (multivariable odds ratio: 1.06; 95% confidence interval: 0.50 to 2.22). HIV-positive participants had a statistically significant lower odds ratio of nonunion compared with HIV-negative participants (multivariable odds ratio: 0.17; 95% confidence interval: 0.01 to 0.92). Fractures sustained in HIV-positive individuals can undergo surgical fixation as effectively as those in HIV-negative individuals, with no increased risk of delayed union or nonunion.
Highlights
Human immunodeficiency virus (HIV) reduces bone mineral density, mineralisation and turnover, andC may impair fracture healing
Participants with HIV had a statistically significant lower odds of non-union compared to HIV-negative participants
To the authors’ knowledge, this is the first large prospective study to assess the association between HIV infection and bone healing following a fracture
Summary
Division of Orthopaedic Surgery, Groote Schuur Hospital, Cape Town, South Africa. 4. Orthopaedic Research Unit (ORU), University of Cape Town, Cape Town, South Africa. Division of Orthopaedic Surgery, Stellenbosch University, Cape Town, South Africa. 6. Department of Orthopaedic and Trauma Surgery, Countess of Chester Hospital, Chester, UK 7. Clinical Research Department, London School of Hygiene and Tropical Medicine, London, UK 10.
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