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JOA - 2026-04-06 - Journal Article

Comorbidities Affect the Racial Disparities in the Incidence of Periprosthetic Joint Infection after Total Knee Arthroplasty.

Furukawa D, Pike CW, Hui G, Coyle J, Amanatullah DF

database studyLOE IIIn = 175,205N/A if not reported.

Topics

arthroplastyoncology
PMID: 41951063DOI: 10.1016/j.arth.2026.03.090View on PubMed ->

Key Takeaway

Black patients had a 29% higher unadjusted PJI incidence after TKA versus White patients, but this disparity disappeared after propensity score matching (HR 1.11, p=0.119), implicating comorbidity burden rather than race as the independent driver.

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Summary

This study used a national ICD-10/CPT-coded database to determine whether race independently predicts PJI incidence after TKA and AKA incidence after PJI. Non-Hispanic Black patients had an unadjusted HR of 1.29 for PJI versus White patients, which became non-significant after high-dimensional propensity score matching (HR 1.11, CI 0.97–1.27, p=0.119); Hispanic and Other race groups showed no difference at baseline or after matching. Among patients who developed PJI, male sex—not race—was the independent predictor of AKA (HR 1.09, CI 1.09–3.43, p=0.023).

Key Limitation

Reliance on administrative coding for PJI diagnosis without validation against consensus diagnostic criteria (MSIS/ICM) introduces potential outcome misclassification that could systematically differ by race or institution.

Original Abstract

BACKGROUND

Racial disparity exists in arthroplasty-related outcomes. However, there is little known about racial disparity in the incidence and management of periprosthetic joint infections (PJI). This study aimed to evaluate racial differences in the incidence of PJI after total knee arthroplasty (TKA) and in the incidence of above-knee amputation (AKA) after PJI.

METHODS

Patients who had a PJI were identified using International Classification of Diseases, 10 th edition, and Current Procedural Terminology codes from a national database. The primary outcomes were incidence of PJI and incidence of AKA after PJI stratified by race. There were 175,205 patients who underwent a TKA and were included in the cohort, of which 152,270 (86.9%) were non-Hispanic White, 4,259 (2.4%) were Hispanic, 10,712 (6.1%) were non-Hispanic Black, and 7,964 (4.5%) were non-Hispanic Other. High-dimensional propensity score-matched analysis of non-Hispanic White patients was used to evaluate the effect of race on PJI and AKA incidence, controlling for confounding factors with alpha error set to 5%.

RESULTS

Compared to non-Hispanic White patients, non-Hispanic Black patients had a higher incidence of PJI after TKA (hazard ratio [HR] 1.29, 95% confidence interval [CI] 1.18 to 1.42, P < 0.001) in the unadjusted model, but there was no difference in incidence after propensity score matching (HR 1.11, CI 0.97 to 1.27, P = 0.119). There were no differences in incidence of PJI for non-Hispanic Other (HR 1.08, CI 0.92 to 1.28, P = 0.350) and Hispanic patients (HR 0.99, CI 0.80 to 1.24, P = 0.950) after propensity score matching. In the subgroup of patients who had a PJI, there was no difference in the incidence of AKA across race, but men were associated with a higher incidence of AKA (HR 1.09, CI 1.09 to 3.43, P = 0.023) after propensity score matching.

CONCLUSIONS

Racial disparity exists in the incidence of PJI. However, this observed difference was lost after propensity score matching, suggesting that comorbidities drive the observed difference, not race as an independent factor.