Your browser doesn't support javascript.
loading
Relation Between Ventricular Premature Complexes and Incident Heart Failure.
Agarwal, Vratika; Vittinghoff, Eric; Whitman, Isaac R; Dewland, Thomas A; Dukes, Jonathan W; Marcus, Gregory M.
Afiliación
  • Agarwal V; Department of Cardiology, Staten Island University Hospital, New York, New York.
  • Vittinghoff E; Department of Epidemiology and Biostatistics, University of California, San Francisco, California.
  • Whitman IR; Division of Cardiology, Electrophysiology Section, University of California, San Francisco, California.
  • Dewland TA; Knight Cardiovascular Institute, Oregon Health and Science University, Portland, Oregon.
  • Dukes JW; Division of Cardiology, Electrophysiology Section, University of California, San Francisco, California.
  • Marcus GM; Division of Cardiology, Electrophysiology Section, University of California, San Francisco, California. Electronic address: marcusg@medicine.ucsf.edu.
Am J Cardiol ; 119(8): 1238-1242, 2017 04 15.
Article en En | MEDLINE | ID: mdl-28214002
ABSTRACT
Ventricular premature complexes (VPCs) may represent a reversible cause of heart failure (HF); however, the type of patients most prone remains unknown. This study leverages a large population-based database to examine interactions that might prove clinically useful in risk-stratifying patients with VPCs. We used the California Healthcare Cost and Utilization Project to identify patients with VPCs and incident systolic HF from January 1, 2005, to December 31, 2009. We calculated hazard ratios for predictors of incident systolic HF using multivariable Cox proportional hazard models. Interactions with known risk factors were studied. Of the 16.8 million patients experiencing 48.1 million hospitalizations, 35,817 (0.2%) had a VPC diagnosis and 198,818 (1.2%) developed systolic HF. Incidence of systolic HF was 62.8 per 1,000 patient-years (95% confidence interval [CI] 61.2 to 64.4) in those with and 6.1 per 1,000 patient-years (95% CI 6.1 to 6.2) in those without VPCs (p <0.001). After adjusting for potential confounders, VPCs were associated with a nearly twofold risk of systolic HF (HR 1.8, 95% CI 1.8 to 1.9, p <0.001). Interaction analyses revealed a stronger relation between VPCs and HF among those with fewer cardiovascular risk factors. A VPC diagnosis in younger patients (<65 years) without coronary artery disease, hypertension, diabetes, or atrial fibrillation exhibited a sixfold increased risk of systolic HF (HR 6.5, 95% CI 5.5 to 7.7, p <0.001). In conclusion, these results suggest that a diagnosis of VPCs independently predicts incident systolic HF. This effect is most pronounced in younger patients without co-morbidities, suggesting that VPCs may be an important cause of "idiopathic" HF.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Complejos Prematuros Ventriculares / Insuficiencia Cardíaca Sistólica Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Am J Cardiol Año: 2017 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Complejos Prematuros Ventriculares / Insuficiencia Cardíaca Sistólica Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Am J Cardiol Año: 2017 Tipo del documento: Article