Disparities in TKA Outcomes: Census Tract Data Show Interactions Between Race and Poverty. Issue 9 (September 2016)

• Record Type: Journal Article
• Authors: Goodman, Susan M.; Mandl, Lisa A.; Parks, Michael L.; Zhang, Meng; McHugh, Kelly R.; Lee, Yuo‐Yu; Nguyen, Joseph T.; Russell, Linda A.; Bogardus, Margaret H.; Figgie, Mark P.; Bass, Anne R.
• Is Part Of: Clinical orthopaedics and related research. Volume 474:Issue 9(2016)
• Publication Date: 2016-09
• Subjects: Orthopedic surgery -- Periodicals; Orthopedics -- Periodicals; Orthopedics -- Research -- Periodicals; Orthopedics -- Periodicals; Research -- Periodicals; Chirurgie orthopédique -- Périodiques; 616.7005
• DOI: 10.1007/s11999-016-4919-8
• Languages: English
• ISSNs: 0009-921X

Abstract

Abstract: Background: Race is an important predictor of TKA outcomes in the United States; however, analyses of race can be confounded by socioeconomic factors, which can result in difficulty determining the root cause of disparate outcomes after TKA. Questions/purposes: We asked: (1) Are race and socioeconomic factors at the individual level associated with patient‐reported pain and function 2 years after TKA? (2) What is the interaction between race and community poverty and patient‐reported pain and function 2 years after TKA? Methods: We identified all patients undergoing TKA enrolled in a hospital‐based registry between 2007 and 2011 who provided 2‐year outcomes and lived in New York, Connecticut, or New Jersey. Of patients approached to participate in the registry, more than 82% consented and provided baseline data, and of these patients, 72% provided 2‐year data. Proportions of patients with complete followup at 2 years were lower among blacks (57%) than whites (74%), among patients with Medicaid insurance (51%) compared with patients without Medicaid insurance (72%), and among patients without a college education (67%) compared with those with a college education (71%). Our final study cohort consisted of 4035 patients, 3841 (95%) of whom were white and 194 (5%) of whom were black. Using geocoding, we linked individual‐level registry data to US census tracts data through patient addresses. We constructed a multivariate linear mixed‐effect model in multilevel frameworks to assess the interaction between race and census tract poverty on WOMAC pain and function scores 2 years after TKA. We defined a clinically important effect as 10 points on the WOMAC (which is scaled from 1 to 100 points, with higher scores being better). Results: Race, education, patient expectations, and baseline WOMAC scores are all associated with 2‐year WOMAC pain and function; however, the effect sizes were small, and below the threshold of clinical importance. Whites and blacks from census tracts with less than 10% poverty have similar levels of pain and function 2 years after TKA (WOMAC pain, 1.01 ± 1.59 points lower for blacks than for whites, p = 0.53; WOMAC function, 2.32 ± 1.56 lower for blacks than for whites, p = 0.14). WOMAC pain and function scores 2 years after TKA worsen with increasing levels of community poverty, but do so to a greater extent among blacks than whites. Disparities in pain and function between blacks and whites are evident only in the poorest communities; decreasing in a linear fashion as poverty increases. In census tracts with greater than 40% poverty, blacks score 6 ± 3 points lower (worse) than whites for WOMAC pain (p = 0.03) and 7 ± 3 points lower than whites for WOMAC function (p = 0.01). Conclusions: Blacks and whites living in communities with little poverty have similar patient‐reported TKA outcomes, whereas in communities with high levels of poverty, there are important racial disparities. Efforts to improve TKA outcomes among blacks will need to address individual‐ and community‐level socioeconomic factors. Level of Evidence: Level III, therapeutic study.