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Ejection fraction improvement and reverse remodeling achieved with Sacubitril/Valsartan in heart failure with reduced ejection fraction patients.
Almufleh, Aws; Marbach, Jeffrey; Chih, Sharon; Stadnick, Ellamae; Davies, Ross; Liu, Peter; Mielniczuk, Lisa.
Afiliación
  • Almufleh A; Division of Cardiology, University of Ottawa Heart InstituteOttawa, Ontario, Canada.
  • Marbach J; Department of Cardiac Sciences, King Saud UniversityRiyadh, Saudi Arabia.
  • Chih S; Division of Cardiology, University of Ottawa Heart InstituteOttawa, Ontario, Canada.
  • Stadnick E; Division of Cardiology, University of Ottawa Heart InstituteOttawa, Ontario, Canada.
  • Davies R; Division of Cardiology, University of Ottawa Heart InstituteOttawa, Ontario, Canada.
  • Liu P; Division of Cardiology, University of Ottawa Heart InstituteOttawa, Ontario, Canada.
  • Mielniczuk L; Division of Cardiology, University of Ottawa Heart InstituteOttawa, Ontario, Canada.
Am J Cardiovasc Dis ; 7(6): 108-113, 2017.
Article en En | MEDLINE | ID: mdl-29348971
BACKGROUND: Sacubitril/Valsartan has been shown to improve mortality and reduce hospitalizations in patients with heart failure with reduced ejection fraction (HFrEF). The effect of Sacubitril/Valsartan on ejection fraction (EF) and reverse remodeling parameters have not been previously described. METHODS: We performed a single-center, retrospective, cohort study of HFrEF patients (n=48) who were treated with Sacubitril/Valsartan for a median duration of 3 months (Interquartile range 2-6 months). Clinical and echocardiographic parameters were reviewed at three time points (pre-baseline which was median of 18 months before starting Sacubitril/Valsartan, baseline before treatment started, and post-Sacubitril/Valsartan). Paired sample t-test and one-way repeated measures ANOVA were used for normally distributed data, while Wilcoxon Signed Rank test for non-normally distributed data. RESULTS: Sacubitril/Valsartan use was associated with an average 5% (±1.2) increase in EF, from a mean baseline of 25.33% to 30.14% (p<0.001) with a median duration of treatment 3 months. There was no significant change in mean LVEF over a median duration of 11 months (IQR 5.5-15.5) between pre-baseline and baseline time points prior to treatment (p=1.0). The mean increase in ejection fraction tended to be marginally greater in the medium/high dose cohort as compared to the low dose cohort, with a mean increase of 5.09% (±1.36) and 4.03% (±3.17), respectively (p=0.184). There was a 3.36 mm reduction in left ventricular end-systolic diameter (p=0.04), a 2.64 mm reduction in left ventricular end-diastolic diameter (p=0.02), and a 14.4 g/m2 reduction in left ventricular mass index (p<0.01). CONCLUSION: Sacubitril/Valsartan was found to improve EF and multiple measures of reverse remodeling beyond the effects of concomitant optimal medical therapy. Though these results are encouraging, our small sample, observational study requires confirmation in larger cohorts with longer follow-up periods.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Am J Cardiovasc Dis Año: 2017 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Am J Cardiovasc Dis Año: 2017 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos