Validation study of medicare claims to identify older US adults with CKD using the Reasons for Geographic and Racial

Paul Muntner1, Orlando M Gutiérrez2, Hong Zhao1

  • 1Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL.

Insights

Health care claims data can identify chronic kidney disease (CKD) patients, but may overrepresent high-risk individuals. Both claims-based and lab-based CKD definitions are linked to higher mortality and end-stage renal disease (ESRD).

Area of Science:

  • Nephrology
  • Epidemiology
  • Health Services Research

Background:

  • Health care claims data offer a potentially cost-effective method for studying chronic kidney disease (CKD).
  • The accuracy of claims data in identifying CKD compared to research study definitions needs evaluation.

Purpose of the Study:

  • To compare the characteristics and outcomes of individuals with CKD identified through laboratory measurements versus health care claims data.
  • To assess the utility of Medicare claims data for identifying CKD and its association with mortality and end-stage renal disease (ESRD).

Main Methods:

  • A prospective cohort study involving 6,982 participants from the Reasons for Geographic and Racial Differences in Stroke (REGARDS) Study with Medicare fee-for-service coverage.
  • CKD was defined using both research study criteria (CKDREGARDS: eGFR < 60mL/min/1.73m² or albumin-creatinine ratio > 30mg/g) and a Medicare claims-based algorithm (CKDMedicare) applied retrospectively.
  • Comparison of participant characteristics, mortality, and ESRD incidence rates between individuals identified with CKD by each method.

Main Results:

  • Overall, 32% of participants met the CKDREGARDS definition, while only 6% met the CKDMedicare definition.
  • CKDMedicare demonstrated a sensitivity of 15.5% and specificity of 97.7% for identifying CKDREGARDS.
  • Both CKDMedicare and CKDREGARDS were associated with significantly higher rates of mortality and ESRD incidence compared to individuals without CKD. Participants identified via claims data (CKDMedicare) exhibited higher mortality and ESRD rates than those identified solely by research criteria.

Conclusions:

  • While CKD identified through either claims data or research measurements is associated with adverse outcomes, claims data may identify a higher-risk subgroup.
  • The findings suggest that CKD identified in claims data represents a select, high-risk population, necessitating careful interpretation in epidemiological studies.
  • Further research is needed to refine claims-based algorithms for CKD detection and to understand the clinical implications of discrepancies between claims and laboratory-based definitions.
Abstract

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