Related Experiment Video
Updated: Feb 6, 2026

An Assessment Method and Toolkit to Evaluate Keyboard Design on Smartphones
Published on: October 5, 2020
Design, Rationale, and Methods of the INITIATE-HFrEF Trial: ARNI and SGLT2 Inhibitors Sequencing in HFrEF
João Pedro Ferreira1, Ana Cristina Oliveira2, Francisca Saraiva2
1RISE-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.
Insights
Simultaneous initiation of angiotensin receptor-neprilysin inhibitors (ARNi) and sodium glucose co-transporter 2 inhibitors (SGLT2i) is as safe and effective as sequential initiation for heart failure with reduced ejection fraction (HFrEF). This finding supports rapid guideline-directed therapy for HFrEF patients.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Angiotensin receptor-neprilysin inhibitors (ARNi) and sodium glucose co-transporter 2 inhibitors (SGLT2i) are essential therapies for heart failure with reduced ejection fraction (HFrEF).
- Guidelines recommend rapid initiation of both ARNi and SGLT2i.
- No prior studies have compared simultaneous versus sequential initiation of these agents.
Purpose of the Study:
- To evaluate the efficacy and safety of simultaneous versus sequential initiation of ARNi and SGLT2i in HFrEF patients.
- To determine if simultaneous initiation is noninferior to sequential initiation.
Main Methods:
- A randomized noninferiority trial comparing two strategies: simultaneous initiation (within 5 days) versus sequential initiation (4-12 weeks apart).
- Primary endpoint: composite of hypotension, electrolyte abnormalities, significant estimated glomerular filtration rate (eGFR) drop, HF emergency visit, HF hospitalization, or cardiovascular death.
- Follow-up duration was approximately 24 weeks.
Main Results:
- Sixty-two patients were randomized: 29 to simultaneous and 33 to sequential initiation.
- Baseline characteristics were well-balanced between groups.
- The study met its primary endpoint, demonstrating noninferiority of simultaneous initiation (specific results on the composite endpoint are not detailed in the abstract).
Conclusions:
- Simultaneous initiation of ARNi and SGLT2i is noninferior to sequential initiation in HFrEF patients.
- This approach supports rapid implementation of guideline-directed medical therapies.
- Further research may explore optimal sequencing and patient selection for simultaneous initiation.
Background:
Angiotensin 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.
Objectives:
The purpose of this study was to evaluate the efficacy and safety of simultaneous vs sequential initiation of ARNi and SGLT2i in HFrEF.
Methods:
Randomized 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.
Results:
Sixty-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 m2, and serum potassium was 4.3 ± 0.5 mmol/L. Most patients in the sequential group (n = 27) were started on SGLT2i and 6 were started on ARNi.
Conclusions:
Initiation 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.
More Related Videos
Related Concept Videos
Initiation of Translation
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
Initiation of Translation
Eukaryotic Transcription Inhibitors
Eukaryotic transcription inhibitors usually contain two distinct domains, a...
Clinical Trials: Overview
Trial and Error and Algorithm
Clinical Trials
There are four phases in a clinical trial. A phase one...

