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Prescription Patterns for Sodium-Glucose Cotransporter 2 Inhibitors in U.S. Health Systems
Jung-Im Shin1, Yunwen Xu1, Alexander R Chang2
1Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Insights
Sodium-glucose cotransporter 2 (SGLT2) inhibitors are recommended for many patients, but prescription rates remain low. This study highlights the need for interventions to increase the uptake of these guideline-recommended therapies.
Area of Science:
- Cardiology
- Nephrology
- Endocrinology
Background:
- Sodium-glucose cotransporter 2 (SGLT2) inhibitors are recommended for patients with diabetes, heart failure (HF), and chronic kidney disease (CKD).
- These drugs reduce HF hospitalizations, cardiovascular events, and CKD progression.
- They have a Class 1a recommendation for specific patient groups, including those with severe albuminuria or HF, irrespective of diabetes status.
Purpose of the Study:
- To assess the prescription rates of SGLT2 inhibitors in patients with a Class 1a recommendation.
- To characterize SGLT2 inhibitor prescribing patterns based on diabetes status and recommendation criteria.
Main Methods:
- Analysis of 3,189,827 adults from 28 U.S. health systems (April 2022–March 2023).
- Stratified assessment of SGLT2 inhibitor prescription rates by diabetes presence and Class 1a recommendation status.
- Examined prescribing patterns by physician specialty and health system characteristics.
Main Results:
- Among 716,387 adults with diabetes and a Class 1a recommendation, only 11.9% received an SGLT2 inhibitor prescription.
- Among 2,473,440 adults without diabetes but with a Class 1a recommendation, 3.1% received a prescription.
- No health system exceeded a 25% prescription rate for eligible patients; internists/family practitioners were more common prescribers for those with diabetes, while specialists led for those without.
Conclusions:
- SGLT2 inhibitor prescription rates among patients with a Class 1a recommendation are low in the U.S.
- Interventions are necessary to improve the adoption of guideline-recommended SGLT2 inhibitor therapy.
- Prescribing patterns vary by patient diabetes status and physician specialty.
Background:
Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce heart failure (HF) hospitalizations, recurrent cardiovascular events, and chronic kidney disease (CKD) progression, and thus constitute a Class 1a recommendation in people with diabetes and atherosclerotic cardiovascular disease, HF, or CKD and in people with severe albuminuria or HF, regardless of diabetes status.
Objectives:
The purpose of this study was to comprehensibly characterize the rate of SGLT2 inhibitor prescriptions among people with a Class 1a recommendation for SGLT2 inhibitor use.
Methods:
Among 3,189,827 adults from 28 U.S. health systems within Optum Labs Data Warehouse between April 1, 2022, and March 31, 2023, we assessed SGLT2 inhibitor prescription rates, stratified by presence of diabetes and Class 1a recommendation.
Results:
Among 716,387 adults with diabetes, 63.4% had a Class 1a recommendation for SGLT2 inhibitor therapy. There was little difference by Class 1a recommendation status (present: 11.9%; 95% CI: 11.9%-12.0% vs absent: 11.4%; 95% CI: 11.3%-11.6%; standardized mean difference: 1.3%). Among 2,473,440 adults without diabetes, 6.2% had a Class 1a recommendation for SGLT2 inhibitor therapy, and 3.1% (3.0%-3.2%) of those received a prescription. Internists/family practitioners initiated SGLT2 inhibitor prescriptions most commonly among people with diabetes, whereas specialists initiated SGLT2 inhibitor prescriptions most commonly among people without diabetes. No health system had >25% SGLT2 inhibitor prescription rate among people with a Class 1a recommendation. Health systems with higher proportions of patients with commercial insurance and lower proportions with Medicare had higher SGLT2 inhibitor prescription rates.
Conclusions:
In this analysis of U.S. data from 2022 to 2023, SGLT2 inhibitor prescription among people with a Class 1a recommendation is low. Interventions are needed to increase uptake of guideline-recommended SGLT2 inhibitor use.
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