Selzman Institute for Kidney Health, Section of Nephrology, Department of Medicine, Baylor College of Medicine, Houston, Texas; Section of Nephrology Michael E. DeBakey Veterans Affairs Medical Center, and Michael E. DeBakey VA Medical Center Health Services Research & Development Center for Innovations in Quality, Effectiveness and Safety, Houston, TX; Michael E. DeBakey Veterans Affairs Medical Center, and Michael E. DeBakey VA Medical Center Health Services Research & Development Center for Innovations in Quality, Effectiveness and Safety, Houston, TX.
Michael E. DeBakey Veterans Affairs Medical Center, and Michael E. DeBakey VA Medical Center Health Services Research & Development Center for Innovations in Quality, Effectiveness and Safety, Houston, TX.
Am J Kidney Dis. 2023 Jul;82(1):53-62.e1. doi: 10.1053/j.ajkd.2022.11.017. Epub 2023 Jan 23.
RATIONALE & OBJECTIVE: Sodium/glucose cotransporter 2 (SGLT2) inhibitors are recommended 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.
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.
Race, sex, and individual Veterans Affairs (VA) location.
SGLT2 inhibitor prescription.
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.
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 inhibitor prescription was 1.58 (95% CI 1.48-1.67) in the total cohort, indicating an unexplained 58% variation in treatment between VA facilities, independent 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]).
Albuminuria was not assessed.
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.
钠-葡萄糖协同转运蛋白 2(SGLT2)抑制剂被推荐用于患有慢性肾脏病(CKD)或动脉粥样硬化性心血管疾病(ASCVD)的 2 型糖尿病(T2DM)患者。我们评估了与 SGLT2 抑制剂处方相关的因素、种族和性别差异以及医疗机构处方模式的差异。
回顾性队列研究。
这是一项全国性的研究,纳入了 2020 年 1 月 1 日至 12 月 31 日期间在美 VA 就诊的患有合并 T2DM、CKD 和 ASCVD 的合并症的美国退伍军人。
种族、性别和个人 VA 地点。
SGLT2 抑制剂的处方。
多变量逻辑回归评估了种族和性别与 SGLT2 抑制剂处方之间的关联。通过中位数比率比(MRR)来量化 SGLT2i 处方的医疗机构间差异,MRR 表达了在相似患者中,随机选择的 2 个医疗机构使用 SGLT2 抑制剂的可能性差异。
在 174443 名患有 CKD、T2DM 和 ASCVD 的患者中,有 20024 名(11.5%)患者开具了 SGLT2 抑制剂。与白人患者相比,黑人或非裔美国患者(OR,0.87 [95%CI,0.83-0.91])和女性患者(OR,0.59 [95%CI 0.52-0.67])开具 SGLT2 抑制剂的可能性较低。在整个队列中,SGLT2 抑制剂处方的调整后 MRR 为 1.58(95%CI 1.48-1.67),这表明 VA 医疗机构之间在治疗方面存在无法解释的 58%的差异,独立于患者和医疗机构特征。在黑人或非裔美国患者(MRR,1.55 [95%CI 1.41-1.68])、白人患者(MRR,1.57 [95%CI 1.47-1.66])、女性患者(MRR,1.40 [95%CI 1.28-1.51])和男性患者(MRR,1.57 [95%CI 1.48-1.67])中评估了医疗机构间差异。
未评估白蛋白尿。
在可能符合条件的患者中,SGLT2 抑制剂的处方率较低,且存在明显的性别和种族差异以及各个 VA 医疗机构之间的差异。需要努力研究和解决这些差异的原因,以改善这些重要药物的公平采用。