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Prescribing trends of anti-diabetes medications near end-of-life among adults with type 2 diabetes: a cohort study

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posted on 2025-01-02, 20:19 authored by Alexander Kutz, Dae Hyun Kim, Jun Liu, Medha N Munshi, Elisabetta Patorno

Objective

To assess prescribing trends of anti-diabetes medications in the last year of life among older adults with type 2 diabetes (T2D) and explore whether frailty is associated with differential prescribing.

Research design and methods

In this observational cohort study of Medicare beneficiaries aged ≥67 years (2015-2019) with T2D, we assessed temporal trends in prescribing an anti-diabetes medication, stratified by frailty. The main outcome included anti-diabetes medication fills within 1 year of death.

Results

Among 975,407 community-dwelling Medicare beneficiaries with T2D, the use of anti-diabetes medications within 1 year of death slightly increased from 71.4% during the first 6-month period in 2015 to 72.9% (standardized mean difference [SMD], -0.03) during the second 6-month period in 2019. The most pronounced increase in use was observed for metformin (40.7% to 46.5%; SMD, -0.12), whereas the largest decrease was observed for sulfonylureas (37.0% to 31.8%; SMD, 0.11). Overall anti-diabetes medication use decreased from 66.1% in the 9 to 12 months before death to 60.8% in the last 4 months of life (p<0.01; SMD, 0.11), driven by reduced non-insulin medication use. The use of both short-acting and long-acting insulin increased near death, with frailer individuals more likely to receive insulin. Sodium-glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists, though less common, became more frequent in more recent years.

Conclusions

The use of anti-diabetes medications declined in the last year of life, mainly due to reduced non-insulin use. Insulin use increased near death, particularly among frailer individuals, highlighting the need for careful “end-of-life” management.

Funding

This study was supported by the Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA. Dr. Kutz was supported by a Postdoc.Mobility grant (P400PM_194479 / 1) from the Swiss National Science Foundation and by an educational grant from Novo Nordisk. Dr. Patorno was supported by research grants from the National Institute of Diabetes and Digestive and Kidney Diseases (R01DK138036), the Patient Centered Outcomes Research Institute (DB-2020C2-20326) and the Food and Drug Administration (5U01FD007213). Dr. Kim was supported by the grant K24AG073527 from the National Institute on Aging of the National Institutes of Health.

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