Abstract

BackgroundThe objective of our study was to assess the cost-effectiveness of ivabradine plus standard care (SoC) in chronic heart failure (CHF) patients with sinus rhythm and a baseline heart rate ≥ 75 b.p.m. in Greece, in comparison with current SoC alone.MethodsAn existing cost-effectiveness model consisting of two health states, was adapted to the Greek health care setting. All clinical inputs of the model (i.e. mortality rates, hospitalization rates, NYHA class distribution and utility values) were estimated from SHIFT trial data. All costing data used in the model reflects the year 2013 (in €). An incremental cost effectiveness ratio (ICER) per quality-adjusted life year (QALY) gained was calculated. Deterministic and probabilistic sensitivity analyses (PSA) were conducted. The horizon of analysis was over patient life time and both cost and outcomes were discounted at 3.5% per year. The analysis was conducted from a Greek third party-payer perspective.ResultsThe Markov analysis revealed that the discounted quality-adjusted survival was 4.27 and 3.99 QALYs in the ivabradine plus SoC and SoC alone treatment arms, respectively. The cumulative lifetime total cost per patient was €8,665 and €5,873, for ivabradine plus SoC and SoC alone, respectively. The ICER for ivabradine plus SoC versus SoC alone was estimated as €9,986 per QALY gained. The PSA showed that the likelihood of ivabradine plus SoC being cost-effective at a threshold of €36,000/QALY was found to be 95%.ConclusionsIvabradine plus SoC may be regarded as a cost-effective option for the treatment in CHF patients in Greece.Electronic supplementary materialThe online version of this article (doi:10.1186/s12913-014-0631-0) contains supplementary material, which is available to authorized users.

Highlights

  • The objective of our study was to assess the cost-effectiveness of ivabradine plus standard care (SoC) in chronic heart failure (CHF) patients with sinus rhythm and a baseline heart rate ≥ 75 b.p.m. in Greece, in comparison with current Standard care (SoC) alone

  • This study showed that ivabradine plus SoC was associated with fewer hospital admissions for worsening Heart failure (HF) (first event hazard ratio (HR): 0.74; 95% Confidence Interval (CI): 0.66-0.83, p < 0.0001) and lower mortality rates due to HF (HR: 0.74; 95% CI: 0.58-0.94, p = 0.014)

  • Deterministic results In the base case analysis, the Markov model revealed that the discounted survival was higher in ivabradine plus SoC arm compared to the SoC alone by 0.25 Life year (LY), while the corresponding discounted quality-adjusted life year (QALY) were increased by 0.28 QALYs

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Summary

Introduction

The objective of our study was to assess the cost-effectiveness of ivabradine plus standard care (SoC) in chronic heart failure (CHF) patients with sinus rhythm and a baseline heart rate ≥ 75 b.p.m. in Greece, in comparison with current SoC alone. Prognosis and patient management are correlated to the severity of heart disease. The main tool used to estimate the heart disease severity is the New York Heart Association (NYHA) classification [4]. Ivabradine (Procoralan®) is a new therapeutic option for patients with chronic heart failure (CHF) in sinus rhythm. Ivabradine is a pure heart rate lowering agent, and represents the first in a new class of agents acting by selective and specific inhibition of the cardiac pacemaker If current that controls the spontaneous diastolic depolarisation in the sinus node and regulates heart rate. The cardiac effects are specific to the sinus node with no effect on intra-atrial, atrioventricular or intraventricular conduction times, nor on myocardial contractility or ventricular repolarization [8]

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