Abstract

BackgroundTemporal trends in clinical composition and outcome in dilated cardiomyopathy (DCM) are largely unknown, despite considerable advances in heart failure management. We set out to study clinical characteristics and prognosis over time in DCM in Sweden during 2003–2015.MethodsDCM patients (n = 7873) from the Swedish Heart Failure Registry were divided into three calendar periods of inclusion, 2003–2007 (Period 1, n = 2029), 2008–2011 (Period 2, n = 3363), 2012–2015 (Period 3, n = 2481). The primary outcome was the composite of all-cause death, transplantation and hospitalization during 1 year after inclusion into the registry.ResultsOver the three calendar periods patients were older (p = 0.022), the proportion of females increased (mean 22.5%, 26.4%, 27.6%, p = 0.0001), left ventricular ejection fraction was higher (p = 0.0014), and symptoms by New York Heart Association less severe (p < 0.0001). Device (implantable cardioverter defibrillator and/or cardiac resynchronization) therapy increased by 30% over time (mean 11.6%, 12.3%, 15.1%, p < 0.0001). The event rates for mortality, and hospitalization were consistently decreasing over calendar periods (p < 0.0001 for all), whereas transplantation rate was stable. More advanced physical symptoms correlated with an increased risk of a composite outcome over time (p = 0.0043).ConclusionsFrom 2003 until 2015, we observed declining mortality and hospitalizations in DCM, paralleled by a continuous change in both demographic profile and therapy in the DCM population in Sweden, towards a less affected phenotype.

Highlights

  • Dilated cardiomyopathy (DCM) constitutes a subset of heart failure (HF) conditions, characterized by the presence of left ventricular dilatation and contractile dysfunction, which is not explained by abnormal loading conditions or coronary artery disease

  • We present a report of patients with dilated cardiomyopathy (DCM) from an unselected nationwide population of patients included in the Swedish Heart Failure Registry (SwedeHF) from 2003 to 2015 and describe their composition, and unfolding changes over time, relative to the calendar period for inclusion in the registry

  • Transplantation was stable over time (Fig. 1b), whereas HF hospitalization, CV hospitalization, hospitalization for any cause, and composite outcome decreased significantly relative risks (RR) 0.97 [0.96–0.98,], p < 0.0001 for all (Fig. 1c–f )

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Summary

Introduction

Dilated cardiomyopathy (DCM) constitutes a subset of heart failure (HF) conditions, characterized by the presence of left ventricular dilatation and contractile dysfunction, which is not explained by abnormal loading conditions (hypertension or valvular heart disease) or coronary artery disease. Sjöland et al BMC Cardiovasc Disord (2021) 21:307 increase of 27% during the last 10 years [2]. It makes up the most common indication for heart transplantation [3]. We present a report of patients with DCM from an unselected nationwide population of patients included in the Swedish Heart Failure Registry (SwedeHF) from 2003 to 2015 and describe their composition, and unfolding changes over time, relative to the calendar period for inclusion in the registry. Temporal trends in clinical composition and outcome in dilated cardiomyopathy (DCM) are largely unknown, despite considerable advances in heart failure management. We set out to study clinical characteristics and prognosis over time in DCM in Sweden during 2003–2015

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