Revised: August 8, 2026
Accepted: August 31, 2026
Published online: October 18, 2026
Processing time: 113 Days and 1.6 Hours
The populations undergoing total joint arthroplasty (TJA) and those receiving hormone replacement therapy (HRT) overlap considerably, as both predominantly comprise older adults. HRT includes estrogen RT (ERT) and testosterone RT (TRT). Whether these hormonal interventions influence postoperative medical complications (e.g., thromboembolism, acute kidney injury, cardiac events) or implant-related outcomes (e.g., infection, loosening, revision) remains uncertain. Existing studies provide conflicting results, and a direct comparison between ERT and TRT is lacking.
To systematically compare the associations of ERT and TRT with complications following TJA.
PubMed, EMBASE, Web of Science, and Cochrane Library were searched through April 2026. Two reviewers independently screened studies, extracted data, and assessed bias. We examined medical complications, including venous throm
A total of 15 studies met the inclusion criteria; 11 reported medical complications and 13 reported implant-related outcomes. ERT yielded mixed, procedure-specific results: Certain total knee arthroplasty (TKA) cohorts had reduced risks of deep vein thrombosis and blood transfusion, while others demonstrated elevated risks of TKA cardiac complications, total hip arthroplasty (THA) mechanical loosening, and total shoulder arthroplasty revision. By contrast, TRT showed a more consistent association with increased risks of PJI, AKI, and revision surgery, although several cohorts found no significant association with VTE after THA, periprosthetic fracture, or blood transfusion.
Evidence suggests inconsistent perioperative associations for ERT in TJA, whereas TRT may be linked to higher odds of PJI and AKI. However, heterogeneity and observational design limitations preclude causal inference, thus requiring prospective studies.
Core Tip: This study compared the associations of estrogen replacement therapy (ERT) and testosterone RT (TRT) with both medical and implant-related complications after total joint arthroplasty. The results indicated that existing clinical evidence on perioperative ERT remains contradictory, while TRT may be associated with elevated odds of periprosthetic joint infection and acute kidney injury. Nevertheless, these findings are inconsistent. Given substantial heterogeneity and the observational design of the included studies, no definitive conclusions can be drawn; prospective research is urgently needed to optimize perioperative hormone management.