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. Author manuscript; available in PMC: 2022 Dec 7.
Published in final edited form as: Am J Nephrol. 2021 Dec 7;52(12):958–960. doi: 10.1159/000519759

Can Understanding Outcomes for Medicare Advantage Enrollees Reduce Racial and Ethnic Disparities in Kidney Disease?

Keith Norris 1
PMCID: PMC8758522  NIHMSID: NIHMS1746628  PMID: 34875651

It is well established that the burden of chronic kidney disease (CKD) falls disproportionately upon members of racial and ethnic minority communities driven mainly by higher rates of major CKD risk factors such as diabetes, hypertension, lower socioeconomic status, and limited access to care.1 A recent Kidney Disease: Improving Global Outcomes (KDIGO) controversies conference on “Early Identification and Intervention in CKD” found many available guidelines on evaluating and managing early CKD have not been universally adopted leading them to recommend immediate implementation of CKD screening coupled with risk stratification and treatment for high-risk persons, preferably in primary or community care settings.1 Identification of traditional as well as novel CKD progression factors that may enable providers to better provide high value clinical care, a major goal for the nephrology and primary care communities.

While several strategies such as KDIGO guidelines are critical to our present approaches to CKD care, the use of different large data sets can provide additional insights into CKD risk and protective factors that can help refine and possible promote the harmonization of prediction models for CKD progression and/or complications, and help to identify, validate and refine stratification of high-risk populations in different settings.2,3 For instance an observational analysis of data from nearly 700,000 veterans with a mean age of 73 years with stage 3 or 4 CKD followed over a nearly 6 year period found both Black and Hispanic veterans experienced faster progression to CKD stage 5 than White veterans despite having higher rates of nephrology referral and visits suggesting other factors are at play.3 Given the veteran’s population is 90% male and other factors that may lead to military service-level selection bias it is important to examine CKD progression in other large diverse cohorts that may yield even more generalizable information.

One such large population at high risk for CKD that is highly representative of a large portion of older Americans are persons covered by Medicare, a form of federal government health insurance for persons over 65 years of age or disabled (including persons with end-stage kidney disease). Traditionally Medicare patients have received treatment in fee-for-service (FFS) health care models. However, over the last 15 years there has been a progressive increase in the percent of Medicare recipients receiving their benefits through Medicare Advantage plans, a form of health insurance that provides Medicare benefits through a private-sector health insurer.4 As of 2020 there were more than 24 million Medicare beneficiaries enrolled in Medicare Advantage plans, representing nearly 40% of the Medicare population (and 50% of the Black and Hispanic Medicare population) making it an important population to understand.4,5

Reports of outcomes for patients in traditional FFS compared to Medicare Advantage have shown variable results. Frean et al. found no difference in 8 previously established domains of patient-perceived integrated care between patients enrolled in Medicare Advantage or traditional Medicare FFS plans.6 By contrast, Welch and co-workers reported greater physician concentration of services across Medicare advantage insurers compared to FFS was associated with a higher quality of care overall and especially among vulnerable enrollees.7 Medicare Advantage enrollees also appear to have more preventive services and less out of pocket costs.5 Thus, Medicare Advantage participants are a rapidly increasing group of insured Americans that while similar, may also have some unique characteristics in comparison to their Medicare FFS peers.

To this end, in this issue of AJN Clarissa Diamantidis and colleagues present the first study to examine CKD progression in a large longitudinal cohort of Medicare Advantage enrollees followed over 3 years with over 96% having stage 2 or 3 CKD. They found that Black and Hispanic Medicare Advantage enrollees had faster kidney function decline over time than their White peers, even after adjusting for comorbidities and despite having greater kidney function at study entry, consistent with the work of Suarez and colleagues.3,8

This is particularly important for patients with stage 2 or 3 CKD where primary care providers are most likely to start paying closer attention to CKD specific guidelines and are likely early enough to be able to have the greatest impact on preventing disease progression and complications.1,8 They also found Medicare Advantage enrollees with clinically recognized CKD had both lower eGFR levels and slower decline in kidney function than patients without clinically recognized CKD.8 This could be due to patients with clinical recognition of CKD having received closer monitoring and increased receipt of nephrology consultation, which may have led to more aggressive care or other. Diamantidis et al. also found removal of the estimated glomerular filtration rate (eGFR) race coefficient in Black enrollees led to a nearly 10ml/min/1.73m2 reduction in baseline eGFR, suggesting the use of a race modifier could mask timely identification and clinical management of CKD among Black enrollees.8 It is important to note the higher initial eGFR estimates that are associated with an accelerated decline in kidney function over time may be reflective of hyperfiltration which may be a reflection of increased dietary protein intake, elevated blood pressure, hyperglycemia, medications and more which may conspire to mask the risk for future decline of kidney function.9,10 Their findings reinforce the importance of assessing a profile of predicted risk, rather than the too often used single eGFR alone.

Important study limitations include the high number of missing serum creatinine, or urinary albumin-to-creatinine lab values (>3.4M) and lack of two serum creatinine values at least 90 days apart indicating actual CKD, although sensitivity analyses suggested these patient cohorts had a somewhat similar demographic clinical profile. Also, the lack of data on medications, especially angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) use and their relation with eGFR progression, as well as if medication use differed between groups could account, in part, for the finding. Another important consideration from the perspective of identifying high populations is the method of ascertainment of race and ethnicity, which were derived from a national supplier of consumer marketing data using a proprietary methodology and then imputed. Whether this imputation approximates individual level identity or residence in neighborhoods using addresses to estimate prevalence rates of different racial groups at a zip code or census track level is not clear and can have important implications on the interpretation of the role of race and ethnicity. As such, it will be important to carefully use race and ethnicity data for prediction models. It is also important to recognize that in research race and ethnicity should be clearly defined and even then used carefully, possibly as a contextual variable in a regression and but not as a biologic outcome variable to generate an individual level race or ethnicity modifier.11 Race and ethnicity are conceptual social terms that can provide group level estimates but neither can be consistently measured nor can they inform us what their indirect association with a health condition or outcome means at an individual level.11,12 Race and ethnicity capture a gross estimate of how a group is treated, its social class and culture in a race stratified society, gene polymorphism prevalence and more that vary tremendously across each individual within and across racial and ethnic groups.11,12 Thus, a prediction models are limited to only being able to estimate associations with race and ethnicity at a group level, but this can be valuable to inform population level actions such as targeted population level education, outreach, and messaging and designing group level interventions and monitoring outcomes. With a thoughtful approach to identifying groups at higher risk for CKD progression and complications we can advance health equity and improve outcomes for all of the patients who trust us to provide the highest quality of care and excellence and compassion.

Funding:

KN is supported in part by NIH grants UL1TR000124 and P30AG021684.

Footnotes

Conflict of Interest: There is no conflict of interest

References

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