AHA 2018 | PIONEER-HF: Sacubitril/Valsartan in Acute Decompensated Heart Failure

Treating acute decompensated heart failure patients with an angiotensin receptor inhibitor plus a neprilysin receptor inhibitor significantly reduces N-terminal pro-B-type natriuretic peptide (NT-proBNP) concentrations and clinical events, according to the PIONEER-HF study presented at the American Heart Association (AHA) Congress Scientific Sessions and published simultaneously in the New England Journal of Medicine (NEJM).

AHA 2018 | PIONEER-HF: sacubitril/valsartan en insuficiencia cardíaca aguda descompensadaThe study showed that the clinical benefit was driven by a 44% reduction in heart failure rehospitalizations. Additionally, the sacubitril/valsartan combination was well tolerated, with comparable rates of worsening renal function, hyperkalemia, symptomatic hypotension, or angioedema when compared with enalapril alone.

 

This treatment initiated in the hospital can be continued in the long term, as proven by the PARADIGM-HF trial in 2014.

 

The PIONEER-HF study included patients with heart failure, reduced ejection fraction and elevated NT-proBNP concentrations in a setting of acute decompensation.


Read also: AHA 2018 | No Benefits with Methothrexate as Anti-Inflammatory Drug.


All patients had to be stable before randomization, i.e. with a 100 mmHg blood pressure, no increase in the use of intravenous diuretics, no use of intravenous vasodilators in the preceding 6 hours, and no use of inotropes during the preceding 24 hours.

 

There was a 29% reduction in the primary endpoint, defined as the change in NT-proBNP concentrations from baseline to weeks 4 and 8.

 

Original title: Angiotensin-Neprilysin Inhibition in Acute Decompensated Heart Failure.

Reference: Velazquez EJ et al. N Engl J Med. 2018; Epub ahead of print.

 

PIONEER-HF-presentación

PIONEER-HF-artículo-original


Subscribe to our weekly newsletter

Get the latest scientific articles on interventional cardiology

We are interested in your opinion. Please, leave your comments, thoughts, questions, etc., below. They will be most welcome.

More articles by this author

AHA 2025 | OPTIMA-AF: 1 Month vs. 12 Months of Dual Therapy (DOAC + P2Y12) After PCI in Atrial Fibrillation

Concomitant atrial fibrillation (AF) and coronary artery disease is a common occurrence in clinical practice. In these patients, current guidelines recommend 1 month of...

AHA 2025 | OCEAN Study: Anticoagulation vs. Antiplatelet Therapy After Successful Atrial Fibrillation Ablation

After a successful atrial fibrillation (AF) ablation, the need to maintain long-term anticoagulation (AC) remains uncertain, especially considering the very low residual embolic risk...

AHA 2025 | VESALIUS-CV: Evolocumab in High-Cardiovascular-Risk Patients Without Prior MI or Stroke

LDL cholesterol is a well-established factor for cardiovascular disease. Therapy with PCSK9 inhibitors, including evolocumab, has been shown to reduce the risk of cardiovascular...

AHA 2025 | DAPT-MVD: Extended DAPT vs. Aspirin Monotherapy After PCI in Multivessel Disease

In patients with multivessel coronary artery disease who remain stable 12 months after drug-eluting stent (DES) stenting, there is uncertainty as to prolonging dual...

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Related Articles

SOLACI Sessionsspot_img

Recent Articles

COILSEAL: Use of Coils in Percutaneous Coronary Intervention, Useful for Complication Management?

The use of coils as vascular closing tool has been steadily expanding beyond its traditional role in neuroradiology into coronary territory, where it remains...

Treatment of In-Stent Restenosis in Small Vessels with Paclitaxel-Coated Balloons

Coronary artery disease (CAD) in smaller epicardial vessels occurs in 30% to 67% of patients undergoing percutaneous coronary intervention and poses particular technical challenges....

Contemporary Challenges in Left Atrial Appendage Closure: Updated Approach to Device Embolization

Even though percutaneous left atrial appendage (LAA) closure is generally safe, device embolization – with 0 to 1.5% global incidence – is still a...