Evidence map›Paper›PMID 32719080›Full record

ArticleBMJ open diabetes research & care2020

The DIVE/DPV registries: evolution of empagliflozin use in clinical practice in Germany.

Peter Bramlage, Sascha R Tittel, Christian Wagner, Kerstin König, Dirk Raddatz, Rosmarie Weber-Lauffer, Diether Erath, Jost Hilgenberg, Carsten Spies, Thomas Danne and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open diabetes research & care, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
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 at 9 institutions in 1 country.

Peter BramlageInstitute for Pharmacology and Preventive Medicine, Cloppenburg, Germany peter.bramlage@ippmed.de.ORCID 0000-0003-4970-2110
Sascha R TittelInstitut für Epidemiologie und medizinische Biometrie, University of Ulm, Ulm, Germany.
Christian WagnerPraxis Wagner, Saaldorf-Surheim, Germany.
Kerstin KönigMedizinische Kompetenzkollegium, Kamen, Germany.
Dirk RaddatzDepartment of Gastroenterology and Endocrinology, University of Göttingen, Gottingen, Germany.
Rosmarie Weber-LaufferSchwerpunktpraxis Diabetologie, Karlsruhe, Germany.
Diether ErathPraxis für Innere Medizin, Rottweil, Germany.
Jost HilgenbergGemeinschaftspraxis, Nienburg - Locum - Landsbergen, Germany.
Carsten SpiesSt Vincenz Krankenhaus, Limburg, Germany.
Thomas DanneDiabeteszentrum für Kinder und Jugendliche, Kinderkrankenhaus auf der Bult, Hannover, Germany.
Maximilian GablerBoehringer Ingelheim Pharma GmbH und Co KG, Ingelheim, Germany.
Johannes FoerschBoehringer Ingelheim Pharma GmbH und Co KG, Ingelheim, Germany.
Ludwin LeyBoehringer Ingelheim Pharma GmbH und Co KG, Ingelheim, Germany.
Jochen SeufertFreiburg University Hospital, Freiburg, Germany.
Boehringer Ingelheim (Germany) · DEIPPMed (Germany) · DEKinderkrankenhaus auf der Bult · DEOrthopädische Praxis · DEPraxis für Humangenetik · DESt. Vincenz-Krankenhaus Limburg · DEUniversität Ulm · DEUniversity Medical Center Freiburg · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEmpagliflozin reduced morbidity and mortality in patients with type 2 diabetes mellitus (T2DM) in clinical trials. A registry study was undertaken to describe evolution of patient characteristics and assess the real-world effectiveness/safety of empagliflozin. RESEARCH DESIGN AND

methodsData from the Diabetes Patienten Verlaufsdokumentation (DPV)/Diabetes Versorgungsevaluation (DIVE) registries on 9571 adults with T2DM (registered in 2014-2019) receiving empagliflozin were used. Patients were grouped according to the following: early users (group 1; n=505) received empagliflozin before the EMPA-REG OUTCOME study publication (mid-September 2015); intermediate users (group 2; n=2961) started empagliflozin after the EMPA-REG OUTCOME publication but before the European Medicines Agency label change (from mid-September 2015 to mid-January 2017); and late users (group 3; n=6105) started empagliflozin after mid-January 2017. Data on clinical and treatment characteristics were collected.

resultsOver time, the proportion of recipients aged <65 years decreased (71.1% vs 54.4% among early and late adopters), male patients increased (from 50.9% to 66.5%), body mass index (mean±SD) decreased (from 35.5±6.7 to 32.7±6.6 kg/m

conclusionsOver time, empagliflozin is being prescribed to a broader patient range in routine practice, is usually added to existing antidiabetic regimens, and is increasingly used in combination with metformin, GLP-1 agonists and/or insulin. Empagliflozin had a beneficial effect on glycemic control, with no increase in hypoglycemia.

Indexed as

Diabetes Mellitus, Type 2AdultBenzhydryl CompoundsGermanyGlucosidesHumansMaleRegistriesBenzhydryl CompoundsempagliflozinGlucosidesempagliflozinregistryroutine clinical practicesodium-glucose cotransporter-2 inhibitortype 2 diabetes mellitus

Identifiers

PMID32719080
PMCPMC7388887
OpenAlexW3045943921

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.