TY - JOUR
T1 - Sacubitril/valsartan reduces indications for arrhythmic primary prevention in heart failure with reduced ejection fraction
T2 - insights from DISCOVER-ARNI, a multicenter Italian register
AU - Collaborators: DISCOVER-ARNI Collaborators
AU - Pastore, Maria Concetta
AU - Mandoli, Giulia Elena
AU - Giannoni, Alberto
AU - Benfari, Giovanni
AU - Dini, Frank Lloyd
AU - Pugliese, Nicola Riccardo
AU - Taddei, Claudia
AU - Correale, Michele
AU - Brunetti, Natale Daniele
AU - Carluccio, Erberto
AU - Mengoni, Anna
AU - Guaricci, Andrea Igoren
AU - Piscitelli, Laura
AU - Citro, Rodolfo
AU - Ciccarelli, Michele
AU - Novo, Giuseppina
AU - Corrado, Egle
AU - Pasquini, Annalisa
AU - Loria, Valentina
AU - Degiovanni, Anna
AU - Patti, Giuseppe
AU - Santoro, Ciro
AU - Moderato, Luca
AU - Malagoli, Alessandro
AU - Emdin, Michele
AU - Cameli, Matteo
AU - Rosa, Gianmarco
AU - Magnesa, Michele
AU - Mazzeo, Pietro
AU - De Carli, Giuseppe
AU - Bellino, Michele
AU - Iuliano, Giuseppe
AU - Casciano, Ofelia
AU - Binno, Simone
AU - Canepa, Marco
AU - Tondi, Stefano
AU - Cicoira, Mariantonietta
AU - Mega, Simona
N1 - Publisher Copyright:
© The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Aims This sub-study deriving from a multicentre Italian register [Deformation Imaging by Strain in Chronic Heart Failure Over Sacubitril-Valsartan: A Multicenter Echocardiographic Registry (DISCOVER)-ARNI] investigated whether sacubitril/valsartan in addition to optimal medical therapy (OMT) could reduce the rate of implantable cardioverter-defibrillator (ICD) indications for primary prevention in heart failure with reduced ejection fraction (HFrEF) according to European guidelines indications, and its potential predictors. Methods In this observational study, consecutive patients with HFrEF eligible for sacubitril/valsartan from 13 Italian centres and results were included. Lack of follow-up or speckle tracking data represented exclusion criteria. Demographic, clinical, biochemical, and echocardiographic data were collected at baseline and after 6 months from sacubitril/valsartan initiation. Of 351 patients, 225 (64%) were ICD carriers and 126 (36%) were not ICD carriers (of whom 13 had no indication) at baseline. After 6 months of sacubitril/valsartan, among 113 non-ICD carriers despite having baseline left ventricular (LV) ejection fraction (EF) <_ 35% and New York Heart Association (NYHA) class = II–III, 69 (60%) did not show ICD indications; 44 (40%) still fulfilled ICD criteria. Age, atrial fibrillation, mitral regurgitation > moderate, left atrial volume index (LAVi), and LV global longitudinal strain (GLS) significantly varied between the groups. With receiver operating characteristic curves, age >_ 75 years, LAVi >_ 42 mL/m2 and LV GLS >_-8.3% were associated with ICD indications persistence (area under the curve = 0.65, 0.68, 0.68, respectively). With univariate and multivariate analysis, only LV GLS emerged as significant predictor of ICD indications at follow-up in different predictive models. Conclusions Sacubitril/valsartan may provide early improvement of NYHA class and LVEF, reducing the possible number of implanted ICD for primary prevention in HFrEF. Baseline reduced LV GLS was a strong marker of ICD indication despite OMT. Early therapy with sacubitril/valsartan may save infective/haemorrhagic risks and unnecessary costs deriving from ICDs.
AB - Aims This sub-study deriving from a multicentre Italian register [Deformation Imaging by Strain in Chronic Heart Failure Over Sacubitril-Valsartan: A Multicenter Echocardiographic Registry (DISCOVER)-ARNI] investigated whether sacubitril/valsartan in addition to optimal medical therapy (OMT) could reduce the rate of implantable cardioverter-defibrillator (ICD) indications for primary prevention in heart failure with reduced ejection fraction (HFrEF) according to European guidelines indications, and its potential predictors. Methods In this observational study, consecutive patients with HFrEF eligible for sacubitril/valsartan from 13 Italian centres and results were included. Lack of follow-up or speckle tracking data represented exclusion criteria. Demographic, clinical, biochemical, and echocardiographic data were collected at baseline and after 6 months from sacubitril/valsartan initiation. Of 351 patients, 225 (64%) were ICD carriers and 126 (36%) were not ICD carriers (of whom 13 had no indication) at baseline. After 6 months of sacubitril/valsartan, among 113 non-ICD carriers despite having baseline left ventricular (LV) ejection fraction (EF) <_ 35% and New York Heart Association (NYHA) class = II–III, 69 (60%) did not show ICD indications; 44 (40%) still fulfilled ICD criteria. Age, atrial fibrillation, mitral regurgitation > moderate, left atrial volume index (LAVi), and LV global longitudinal strain (GLS) significantly varied between the groups. With receiver operating characteristic curves, age >_ 75 years, LAVi >_ 42 mL/m2 and LV GLS >_-8.3% were associated with ICD indications persistence (area under the curve = 0.65, 0.68, 0.68, respectively). With univariate and multivariate analysis, only LV GLS emerged as significant predictor of ICD indications at follow-up in different predictive models. Conclusions Sacubitril/valsartan may provide early improvement of NYHA class and LVEF, reducing the possible number of implanted ICD for primary prevention in HFrEF. Baseline reduced LV GLS was a strong marker of ICD indication despite OMT. Early therapy with sacubitril/valsartan may save infective/haemorrhagic risks and unnecessary costs deriving from ICDs.
KW - Heart failure
KW - Implantable cardioverter-defibrillator
KW - Left ventricular strain
KW - Remodelling
KW - Sacubitril/valsartan
UR - http://www.scopus.com/inward/record.url?scp=85136811858&partnerID=8YFLogxK
U2 - 10.1093/ehjopen/oeab046
DO - 10.1093/ehjopen/oeab046
M3 - Article
SN - 2752-4191
VL - 2
JO - European Heart Journal Open
JF - European Heart Journal Open
IS - 1
M1 - oeab046
ER -