Evidence map›Paper›PMID 42888997›Full record

ArticleDiabetes, obesity, and cardiometabolic CARE

Trends in Diabetes Medications After Metformin in Patients at High Versus Moderate Cardiovascular Risk: The BESTMED Consortium 2014-2022.

M Cecilia Lansang, Lucia C Petito, Emma Hegermiller, Indhumathy Chelliah, Ryan M Carnahan, Marie E McDonnell, Andrea DeVries, Elisa Priest, Vincent Willey, Vinit Nair and 4 more

Abstract read
In one paragraph

Article in Diabetes, obesity, and cardiometabolic CARE. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

M Cecilia LansangDepartment of Endocrinology, Diabetes and Metabolism, Cleveland Clinic, Cleveland, OH.ORCID https://orcid.org/0000-0002-7364-5550
Lucia C PetitoFeinberg School of Medicine, Northwestern University, Chicago, IL.
Emma HegermillerIndus Consulting, Inc., Chicago, IL.
Indhumathy ChelliahIndus Consulting, Inc., Chicago, IL.
Ryan M CarnahanCollege of Public Health, University of Iowa, Iowa City, IA.
Marie E McDonnellHarvard Medical School, Boston, MA.
Andrea DeVriesHumana Healthcare Research, Pittsburgh, PA.
Elisa PriestBaylor Scott & White Research Institute, Dallas, TX.
Vincent WilleyCarelon Research, Wilmington, DE.
Vinit NairIndus Consulting, Inc., Chicago, IL.
Satyender GoelFeinberg School of Medicine, Northwestern University, Chicago, IL.
Alan F KaulMedical Outcomes Management, Inc., Boston, MA.
Alexander TurchinHarvard Medical School, Boston, MA.ORCID https://orcid.org/0000-0002-8609-564X
BESTMED Research Group*

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo compare nationwide prescription trends in medications (dipeptidyl peptidase 4 inhibitors [DPP-4i], glucagon-like peptide 1 receptor agonists [GLP-1 RAs], sodium-glucose cotransporter 2 inhibitors [SGLT2i], or sulfonylureas [SUs]) after treatment with metformin in patients with type 2 diabetes (T2D) at high versus moderate cardiovascular risk by key sociodemographic and health characteristics. RESEARCH DESIGN AND

methodsElectronic health records and insurance claims from 2014 to 2022 from 10 health systems and two insurance plans from different U.S. regions were evaluated. Risk-stratified multinomial log-linear models were used to model trends in prescribing patterns, adjusted for sociodemographic variables.

resultsA total of 104,474 patients were included (28% at high and 72% at moderate cardiovascular risk). Among those at high cardiovascular risk, DPP-4i (2014 24.0%; 2022 11.0%) and SU (66.4%; 35.7%) prescriptions declined, whereas GLP-1 RA (4.4%; 20.5%) and SGLT2i (5.2%; 32.8%) prescriptions increased. Among those at moderate cardiovascular risk, DPP-4i (23.7%; 11.7%) and SU (63.7%; 31.5%) prescriptions declined, whereas GLP-1 RA (5.7%; 30.0%) and SGLT2i (6.9%; 26.8%) prescriptions increased. Annual increases differed by high versus moderate cardiovascular risk for GLP-1 RAs (+2.5% vs. +3.6%/year;

conclusionsPrescribing patterns for second-line T2D therapies in those at moderate cardiovascular risk are approaching guideline recommendations for those at high risk. Some trends are potentially clinically explainable, whereas certain racial/ethnic differences may warrant exploration. Video 1.Video abstract3e51f820-63ec-4c76-86f4-002f78d7c5f0doc260027video1.

Identifiers

PMID42888997
PMCPMC13644838

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.