4.6 Article

Predictors, Disparities, and Facility-Level Variation: SGLT2 Inhibitor Prescription Among US Veterans With CKD

Journal

AMERICAN JOURNAL OF KIDNEY DISEASES
Volume 82, Issue 1, Pages 53-+

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.ajkd.2022.11.017

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This study evaluated factors associated with SGLT2 inhibitor prescription, including disparities in prescription patterns based on race and sex, and facility-level variation. The results showed lower odds of SGLT2 inhibitor prescription in Black or African American patients compared to White patients, and among women compared to men. There was also an unexplained 58% variation in treatment between VA facilities, independent of patient and facility characteristics. Efforts are needed to study and address the reasons for these disparities to improve equitable adoption of these important medications.
Rationale & Objective: Sodium/glucose cotransporter 2 (SGLT2) inhibitors are recom-mended for type 2 diabetes mellitus (T2DM) in patients with chronic kidney disease (CKD) or atherosclerotic cardiovascular disease (ASCVD). We evaluated factors associated with SGLT2 inhibitor prescription, disparities by race and sex, and facility-level variation in prescription patterns. Study Design: Retrospective cohort. Setting & Participants: A national sample of US veterans with comorbid T2DM, CKD, and ASCVD with a primary care visit between January 1 and December 31, 2020. Exposure: Race, sex, and individual Veterans Affairs (VA) location. Outcome: SGLT2 inhibitor prescription. Analytical Approach: Multivariable logistic regression assessed associations of race and sex with SGLT2 inhibitor prescription. Facility-level variation in SGLT2i prescription was quantified by median rate ratios (MRR), which express the likelihood that 2 randomly selected facilities differ in their use of SGLT2 inhibitor among similar patients. Results: Of 174,443 patients with CKD, T2DM, and ASCVD, 20,024 (11.5%) were prescribed an SGLT2 inhibitor. Lower odds of SGLT2 inhibitor prescription were seen in Black or African American patients compared with White patients (OR, 0.87 [95% CI, 0.83-0.91]) and among women compared with men (OR, 0.59 [95% CI 0.52-0.67]). The adjusted MRR for SGLT2 in-hibitor prescription was 1.58 (95% CI 1.48-1.67) in the total cohort, indicating an unexplained 58% variation in treatment between VA facilities, in-dependent of patient and facility characteristics. Facility-level variation was evaluated among Black or African American patients (MRR, 1.55 [95% CI 1.41-1.68]), White patients (MRR, 1.57 [95% CI 1.47-1.66]), women (MRR, 1.40 [95% CI 1.28-1.51]), and men (MRR, 1.57 [95% CI 1.48-1.67]). Limitations: Albuminuria was not assessed. Conclusions: Prescription for SGLT2 inhibitors was low among likely eligible patients, with evident disparities by sex and race and between individual VA facilities. Efforts are needed to study and address the reasons for these disparities to improve equitable adoption of these important medications.

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