AI Article Synopsis

  • Recognizing that race doesn’t have a biological basis, healthcare groups push for the elimination of race in kidney disease diagnosis methods.
  • The National Kidney Foundation and the American Society of Nephrology formed a Task Force to assess how to adjust kidney disease diagnostic algorithms and recommend using the new CKD-EPI 2021 formulas for calculating eGFR without incorporating race.
  • The Task Force encourages labs to shift to the CKD-EPI 2021 equations to standardize testing and avoid discrepancies caused by outdated methods, ensuring eGFR results are race-neutral.

Article Abstract

Recognizing that race is a social and not a biological construct, healthcare professionals and the public have called for removal of race in clinical algorithms. In response, the National Kidney Foundation and the American Society of Nephrology created the Task Force on Reassessing the Inclusion of Race in Diagnosing Kidney Diseases to examine the issue and provide recommendations. The final report from the Task Force recommends calculating estimated glomerular filtration rate (eGFR) without a race coefficient using the recently published CKD-EPI 2021 creatinine (cr) and creatinine-cystatin C (cr-cys) equations. The Task Force recommends immediately replacing older eGFRcr equations (MDRD Study and CKD-EPI 2009) with the new CKD-EPI 2021 equation. In a 2019 survey by the College of American Pathologists, 23% of 6200 laboratories reporting eGFRcr used an incorrect equation that is not suitable for use with standardized creatinine measurements, 34% used the CKD-EPI 2009 equation and 43% used the MDRD Study 2006 equation re-expressed for standardized creatinine measurement. Rapid transition to using the CKD-EPI 2021 equation is an opportunity for laboratories to standardize to a single equation to eliminate differences in eGFRcr due to different equations used by different laboratories, and to report eGFR without use of race. We provide guidance to laboratories for implementing the CKD-EPI 2021 equations for both eGFRcr and eGFRcr-cys.

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http://dx.doi.org/10.1093/clinchem/hvab278DOI Listing

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