Evidence map›Paper›PMID 41636670›Full record

ArticleJACC. Advances2026

Design, Rationale, and Methods of the INITIATE-HFrEF Trial: ARNI and SGLT2 Inhibitors Sequencing in HFrEF.

João Pedro Ferreira, Ana Cristina Oliveira, Francisca Saraiva, Inês Pereira-Sousa, Rita Azevedo, António Angélico-Gonçalves, Carlos Grijó, Mariana Pereira Santos, Cristina Gavina, Mário Santos and 5 more

Abstract read
In one paragraph

Article in JACC. Advances, 2026. 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
–field-weighted citation impact
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

15 authors.

João Pedro FerreiraRISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal; Université de Lorraine, INSERM, Centre d'Investigations Cliniques 1433, CHRU de Nancy, Inserm, 1116 and INI-CRCT (Cardiovascular and Renal Clinical Trialists) F-CRIN Network, Nancy, France; Serviço de Medicina Interna, Unidade Local de Saúde Gaia/Espinho, Gaia, Portugal. Electronic address: jpferreira@med.up.pt.
Ana Cristina OliveiraRISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal.
Francisca SaraivaRISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal.
Inês Pereira-SousaRISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal; Escola Superior de Saúde do Porto, Instituto Politécnico do Porto, Porto, Portugal.
Rita AzevedoServiço de Medicina Interna, Unidade Local de Saúde Gaia/Espinho, Gaia, Portugal.
António Angélico-GonçalvesRISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal; Serviço de Cardiologia, Unidade Local de Saúde Gaia/Espinho, Gaia, Portugal.
Carlos GrijóServiço de Medicina Interna, Unidade Local de Saúde São João, Porto, Portugal.
Mariana Pereira SantosServiço de Cardiologia, Unidade de Doença Vascular Pulmonar, Unidade Local de Saúde Santo António, Porto, Portugal.
Cristina GavinaServiço de Cardiologia, Unidade Local de Matosinhos, Matosinhos, Portugal.
Mário SantosServiço de Cardiologia, Unidade de Doença Vascular Pulmonar, Unidade Local de Saúde Santo António, Porto, Portugal; Department of Immuno-Physiology and Pharmacology, Unidade Multidisciplinar de Investigação Biomédica (UMIB), Instituto de Ciências Biomédicas Abel Salazar (ICBAS), Universidade do Porto, Porto, Portugal; Laboratory for Integrative and Translational Research in Population Health (ITR), Porto, Portugal.
Ricardo Fontes-CarvalhoRISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal; Serviço de Cardiologia, Unidade Local de Saúde Gaia/Espinho, Gaia, Portugal.
Joana PimentaRISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal; Serviço de Medicina Interna, Unidade Local de Saúde Gaia/Espinho, Gaia, Portugal.
Adelino Leite-MoreiraRISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal; Serviço de Cirurgia Cardio-Torácica, Unidade Local de Saúde São João, Porto, Portugal.
Francisco Vasques-NóvoaRISE-Health, Departamento de Cirurgia e Fisiologia, Faculdade de Medicina, Universidade do Porto, Porto, Portugal; Serviço de Medicina Interna, Unidade Local de Saúde São João, Porto, Portugal.
INITIATE-HFrEF Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAngiotensin receptor-neprilysin inhibitors (ARNi) and sodium glucose co-transporter 2 inhibitors (SGLT2i) are backbone guideline-directed medical therapies for patients with heart failure with reduced ejection fraction (HFrEF). Expert documents suggest that ARNi and SGLT2i should both be started rapidly. However, to date, no studies have assessed the efficacy and safety of these therapies when started simultaneously or sequentially.

objectivesThe purpose of this study was to evaluate the efficacy and safety of simultaneous vs sequential initiation of ARNi and SGLT2i in HFrEF.

methodsRandomized noninferiority trial comparing 2 treatment strategies: 1) simultaneous ARNi/SGLT2i initiation (up to 5 days apart); vs 2) sequential initiation of one agent followed by the other (4-12 weeks later). The primary endpoint is a composite of hypotension, hyperkalemia, hypokalemia, estimated glomerular filtration rate drop ≥50% from baseline, emergency visit for HF, HF hospitalization, or cardiovascular death. The prespecified noninferiority margin for the absolute between-group difference is 20% with a two-sided 95% CI. Follow-up time was approximately 24 weeks.

resultsSixty-two patients were randomized: 29 simultaneous vs 33 sequential. Baseline characteristics were overall well balanced between groups. The mean age was 68.1 ± 10.4 years, 65% were men, 48% were inpatients, 79% had a "de novo" HF diagnosis, 39% of patients had a prior treatment with angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, 61% with beta-blockers, and 27% with mineralocorticoid receptor antagonists. The mean left ventricular ejection fraction was 33% ± 9%, systolic blood pressure was 125.3 ± 17.4 mm Hg, estimated glomerular filtration rate was 78.1 ± 23.8 mL/min/1.73 m

conclusionsInitiation of ARNi and SGLT2i in Patients With HFrEF is a randomized trial to test whether a simultaneous initiation of ARNi and SGLT2i is noninferior to a sequential initiation of one agent followed by the other 4 to 12 weeks apart.

Indexed as

angiotensin-receptor neprilysin inhibitorheart failure with reduced ejection fractionsodium glucose co-transporter 2 inhibitortreatment sequencing

Identifiers

PMID41636670
PMCPMC13100719

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