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PubMed14 Apr 2026·Diabetes, obesity & metabolism● 6/10i

Discontinuation of SGLT2i After a Urogenital Infection: A Population-Based Matched Cohort Study of Patients With Type 2 Diabetes.

Ljungberg C, Nørgaard M, Vandenbroucke-Grauls C, Dalager-Pedersen M, Sørensen HT et al.

Patients with type 2 diabetes who experienced urogenital infections after starting SGLT2 inhibitors showed discontinuation rates of 39.5% for UTIs and 43.6% for genital infections at one year, versus 28.6% and 30.3% respectively in matched controls. Population-based matched cohort study of 68,277 SGLT2i initiators in Denmark, 2016-2021. This quantifies for the first time the medication adherence impact of SGLT2i-associated infections, despite guidelines recommending continuation through these episodes. The excess discontinuation represents approximately 8% additional treatment cessation for UTIs beyond baseline rates.

Strategic signal

This persistence gap creates a medical education imperative for SGLT2i manufacturers across US and EU markets. Real-world discontinuation rates of 40%+ following infections undermine the CV and renal protection that drives formulary preference and premium pricing. Companies must invest in prescriber training emphasizing infection management without drug cessation, similar to how Novo and Lilly addressed GLP-1 GI tolerability concerns. The 7.6% excess discontinuation risk after UTI particularly threatens market expansion in primary care, where infection fears already limit SGLT2i adoption versus cardiologists.

SGLT2Side effectsReal-world evidence

Original Abstract

AIMS: Sodium-glucose cotransporter 2 inhibitors (SGLT2is) improve glycaemic control and cardiorenal outcomes in Type 2 diabetes, particularly in patients at elevated cardiovascular and kidney risk, yet discontinuation following infections appears common. Guidelines do not generally recommend stopping treatment after a urinary tract infection (UTI) or genital tract infection (GTI). We investigated the impact of these infections on SGLT2i discontinuation. MATERIALS AND METHODS: We conducted a population-based matched cohort study of new SGLT2i users with Type 2 diabetes in Denmark during 2016-2021. All SGLT2i users with an incident UTI or GTI episode within the first year after treatment initiation were matched 1:3 to users without a UTI/GTI by sex, age, treatment duration and calendar year. Discontinuation was defined as not filling a new prescription within 60 days after previous medication supply ended. RESULTS: Among 68 277 SGLT2i initiators, 5892 (8.6%) experienced UTI and 1389 (2%) experienced GTI during the following year. Among users with versus without UTI, discontinuation was 21.9% versus 14.3% on the date of the first expected SGLT2i refill (excess risk among users with UTI: 7.6% [95% CI 6.4%, 8.8%]), increasing to 39.5% versus 28.6% after 1 year. Among users with versus without GTI, discontinuation was 17.9% versus 15.6% (excess risk: 2.2% [95% CI -0.1%, 4.5%]) on the date of the first expected refill, rising to 43.6% versus 30.3% after 1 year. CONCLUSIONS: Patients with Type 2 diabetes who initiate SGLT2i and experience a UTI or GTI within the following year have an elevated frequency of subsequent SGLT2i discontinuation.

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PubMed17 Apr 2026·Annals of internal medicine● 7/10i

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PubMed16 Apr 2026·European heart journal● 7/10i

PCSK9 inhibitor treatment and outcomes in patients with atherosclerotic cardiovascular disease but without prior ischaemic events: an observational study.

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PCSK9CardiovascularReal-world evidenceAmgenRegeneron
PubMed14 Apr 2026·Circulation● 7/10iPick of the week

Risk of Heart Failure Hospitalization for GLP-1 Receptor Agonists Versus DPP-4 Inhibitors or SGLT-2 Inhibitors in Patients With Type 2 Diabetes: A Target Trial Emulation.

GLP-1 receptor agonists reduced heart failure hospitalization risk by 23% versus DPP-4 inhibitors (HR 0.77) but matched SGLT-2 inhibitors (HR 1.02) in adults with type 2 diabetes. Target trial emulation of Swedish health records, 63,083 patients across two comparisons, 3-year follow-up. This provides the first direct head-to-head comparison of GLP-1RAs versus SGLT-2 inhibitors for heart failure prevention, confirming cardiovascular benefits extend beyond major adverse events to heart failure hospitalization.

GLP-1SGLT2Type 2 diabetesCardiovascularReal-world evidenceNovo NordiskEli Lilly
PubMed1 Apr 2026·The lancet. Diabetes & endocrinology● 7/10i

Combined associations of GLP-1 receptor agonists and a healthy lifestyle with cardiovascular outcomes among individuals with type 2 diabetes: a prospective cohort study.

GLP-1 receptor agonists combined with comprehensive lifestyle interventions reduced MACE risk by 43% compared to poor lifestyle habits without GLP-1 therapy in adults with type 2 diabetes. Prospective cohort study of 98,261 US veterans over 632,543 person-years of follow-up. This provides the first large-scale evidence quantifying the additive cardiovascular benefit of combining GLP-1 therapy with multiple lifestyle factors beyond diet and exercise alone.

GLP-1CardiovascularType 2 diabetesReal-world evidence

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