Efficacy of new medical therapies in patients with heart failure, reduced ejection fraction, and chronic kidney disease already receiving neurohormonal inhibitors: a network meta-analysis

Author:

Ameri Pietro12ORCID,De Marzo Vincenzo12,Zoccai Giuseppe Biondi34,Tricarico Lucia56,Correale Michele5,Brunetti Natale Daniele56,Canepa Marco12ORCID,De Ferrari Gaetano Maria78ORCID,Castagno Davide78,Porto Italo12

Affiliation:

1. Cardiology Unit, Cardiothoracic and Vascular Department, IRCCS Ospedale Policlinico San Martino, IRCCS Italian Cardiology Network, Genova, Italy

2. Department of Internal Medicine, University of Genova, Viale Benedetto XV, 6, 16132 Genova, Italy

3. Department of Medical-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy

4. Mediterranea Cardiocentro, Napoli, Italy

5. Cardiology Unit, Ospedali Riuniti di Foggia, Foggia, Italy

6. University of Foggia, Foggia, Italy

7. Division of Cardiology, Cardiovascular and Thoracic Department, Città della Salute e della Scienza Hospital, Turin, Italy

8. Department of Medical Sciences, University of Turin, Turin, Italy

Abstract

Abstract Aims We assessed the efficacy of the drugs developed after neurohormonal inhibition (NEUi) in patients with heart failure (HF) with reduced ejection fraction (HFrEF) and concomitant chronic kidney disease (CKD). Methods and results The literature was systematically searched for phase 3 randomized controlled trials (RCTs) involving ≥90% patients with left ventricular ejection fraction <45%, of whom <30% were acutely decompensated, and with published information about the subgroup of estimated glomerular filtration rate <60 mL/min/1.73 m2. Six RCTs were included in a study-level network meta-analysis evaluating the effect of NEUi, ivabradine, angiotensin receptor–neprilysin inhibitor (ARNI), sodium–glucose cotransporter-2 inhibitors (SGLT2i), vericiguat, and omecamtiv mecarbil (OM) on a composite outcome of cardiovascular death or hospitalization for HF. In a fixed-effects model, SGLT2i [hazard ratio (HR) 0.78, 95% credible interval (CrI) 0.69–0.89], ARNI (HR 0.79, 95% CrI 0.69–0.90), and ivabradine (HR 0.82, 95% CrI 0.69–0.98) decreased the risk of the composite outcome vs. NEUi, whereas OM did not (HR 0.98, 95% CrI 0.89–1.10). A trend for improved outcome was also found for vericiguat (HR 0.90, 95% CrI 0.80–1.00). In indirect comparisons, both SLGT2i (HR 0.80, 95% CrI 0.68–0.94) and ARNI (HR 0.80, 95% CrI 0.68–0.95) reduced the risk vs. OM; furthermore, there was a trend for a greater benefit of SGLT2i vs. vericiguat (HR 0.88, 95% CrI 0.73–1.00) and ivabradine vs. OM (HR 0.84, 95% CrI 0.68–1.00). Results were comparable in a random-effects model and in sensitivity analyses. Surface under the cumulative ranking area scores were 81.8%, 80.8%, 68.9%, 44.2%, 16.6%, and 7.8% for SGLT2i, ARNI, ivabradine, vericiguat, OM, and NEUi, respectively. Conclusion Expanding pharmacotherapy beyond NEUi improves outcomes in HFrEF with CKD.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Cardiology and Cardiovascular Medicine

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