Evidence mapPaperPMID 32350793Full record

ReviewCardiovascular drugs and therapy2020

Sodium-Glucose Co-transporter 2 Inhibitors in the Failing Heart: a Growing Potential.

Dulce Brito, Paulo Bettencourt, Davide Carvalho, Jorge Ferreira, Ricardo Fontes-Carvalho, Fátima Franco, Brenda Moura, José Carlos Silva-Cardoso, Rachel Tavares de Melo, Cândida Fonseca

Open access · hybridAbstract readReview
In one paragraph

Review in Cardiovascular drugs and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Mitochondrial CaJournal of molecular and cellular cardiology · 2021
    Review
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

10 authors at 9 institutions in 1 country.

Dulce BritoDepartment of Cardiology, Centro Hospitalar Universitário Lisboa Norte, Av. Prof. Egas Moniz, 1649-035, Lisboa, Portugal. dulce.brito@chln.min-saude.pt.
Paulo BettencourtDepartment of Internal Medicine, Hospital CUF Porto, Porto, Portugal.
Davide CarvalhoFaculdade de Medicina, Universidade do Porto, Porto, Portugal.
Jorge FerreiraDepartment of Cardiology, Hospital de Santa Cruz, Centro Hospitalar de Lisboa Ocidental, Lisbon, Portugal.
Ricardo Fontes-CarvalhoDepartment of Cardiology, Centro Hospitalar Vila Nova de Gaia/Espinho, Espinho, Portugal.
Fátima FrancoDepartment of Cardiology, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Brenda MouraFaculdade de Medicina, Universidade do Porto, Porto, Portugal.
José Carlos Silva-CardosoFaculdade de Medicina, Universidade do Porto, Porto, Portugal.
Rachel Tavares de MeloMedical Department, Boehringer Ingelheim, Lisboa, Portugal.
Cândida FonsecaHeart Failure Clinic, Hospital São Francisco Xavier, Centro Hospitalar de Lisboa Ocidental, Lisboa, Portugal.
Universidade do Porto · PTBoehringer Ingelheim (Portugal) · PTCentro Hospitalar Lisboa Norte · PTCUF Porto Hospital · PTHospitais da Universidade de Coimbra · PTHospital das Forças ArmadasHospital de Santa Cruz · PTHospital de São João · PTUniversidade Nova de Lisboa · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sodium-glucose co-transporter 2 inhibitors (SGLT2i) are a new drug class designed to treat patients with type 2 diabetes (T2D). However, cardiovascular outcome trials showed that SGLT2i also offer protection against heart failure (HF)-related events and cardiovascular mortality. These benefits appear to be independent of glycaemic control and have recently been demonstrated in the HF population with reduced ejection fraction (HFrEF), with or without T2D. This comprehensive, evidence-based review focuses on the published studies concerning HF outcomes with SGLT2i, discussing issues that may underlie the different results, along with the impact of these new drugs in clinical practice. The potential translational mechanisms behind SGLT2i cardio-renal benefits and the information that ongoing studies may add to the already existing body of evidence are also reviewed. Finally, we focus on practical management issues regarding SGLT2i use in association with other T2D and HFrEF common pharmacological therapies. Safety considerations are also highlighted. Considering the paradigm shift in T2D management, from a focus on glycaemic control to a broader approach on cardiovascular protection and event reduction, including the potential for wide SGLT2i implementation in HF patients, with or without T2D, we are facing a promising time for major changes in the global management of cardiovascular disease.

Indexed as

AnimalsDiabetes Mellitus, Type 2Heart FailureHumansKidneyRecovery of FunctionRisk FactorsSodium-Glucose Transporter 2 InhibitorsStroke VolumeTreatment OutcomeVentricular Function, LeftSodium-Glucose Transporter 2 InhibitorsCardiovascular outcomes trialsCardiovascular riskDiabetesHeart failureSGLT2i

Identifiers

PMID32350793
PMCPMC7242490
OpenAlexW3022733632

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.