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Sacubitril-valsartan initiation in chronic heart failure patients impacts sleep apnea: the ENTRESTO-SAS study.
Jaffuel, Dany; Nogue, Erika; Berdague, Philippe; Galinier, Michel; Fournier, Pauline; Dupuis, Marion; Georger, Frédéric; Cadars, Marie-Pierre; Ricci, Jean-Etienne; Plouvier, Nathalie; Picard, François; Puel, Vincent; Mallet, Jean-Pierre; Suehs, Carey M; Molinari, Nicolas; Bourdin, Arnaud; Roubille, François.
Afiliação
  • Jaffuel D; Department of Pneumology, Arnaud de Villeneuve, Regional University Hospital of Montpellier, Montpellier, France.
  • Nogue E; PhyMedExp, University of Montpellier, INSERM U1046, CNRS UMR 9214, Montpellier, France.
  • Berdague P; Department of Medical Information, Montpellier University Hospital, IMAG UMR 5149, Montpellier University, Montpellier, France.
  • Galinier M; Department of Cardiology, Béziers Hospital, Béziers, France.
  • Fournier P; MSP de Béziers, Pôle médical spécialisé, Béziers, France.
  • Dupuis M; Department of Cardiology, University Hospital of Rangueil, Toulouse, France.
  • Georger F; Department of Cardiology, University Hospital of Rangueil, Toulouse, France.
  • Cadars MP; Department of Pneumology, Respiratory Tracts Center, Hôpital Larrey, Toulouse, France.
  • Ricci JE; Department of Cardiology, Béziers Hospital, Béziers, France.
  • Plouvier N; Centre Médecine du Sommeil et Assistance respiratoire, Béziers Hospital, Béziers, France.
  • Picard F; Department of Cardiology, University Hospital Caremeau, Nîmes, France.
  • Puel V; Department of Pneumology, University Hospital Caremeau, Nîmes, France.
  • Mallet JP; Heart Failure Unit, Haut-Lévêque Hospital, Pessac, France.
  • Suehs CM; PEAS, Nouvelle Clinique Bel-Air, Bordeaux, France.
  • Molinari N; Department of Pneumology, Arnaud de Villeneuve, Regional University Hospital of Montpellier, Montpellier, France.
  • Bourdin A; PhyMedExp, University of Montpellier, INSERM U1046, CNRS UMR 9214, Montpellier, France.
  • Roubille F; Department of Pneumology, Arnaud de Villeneuve, Regional University Hospital of Montpellier, Montpellier, France.
ESC Heart Fail ; 8(4): 2513-2526, 2021 08.
Article em En | MEDLINE | ID: mdl-34102018
ABSTRACT

AIMS:

Optimizing medical cardiac treatment for sleep apnoea (SA) in patients with chronic heart failure and reduced ejection fraction (HFrEF) is an expert Grade C recommendation based on six studies encompassing a total of 67 patients only. Whether sacubitril-valsartan (SV), a cornerstone of HFrEF medical treatment, impacts SA is unknown and requires evaluation. METHODS AND

RESULTS:

The ENTRESTO-SAS trial is a six-centre, prospective, open-label real-life cohort study (NCT02916160). Ambulatory patients eligible for SV (i.e. HFrEF adults who remain symptomatic despite optimal treatment) were evaluated before and after 3 months of SV (including nocturnal ventilatory polygraphy); 118 patients were final analysed [median age was 66 (IQ25-75 56-73) years, 81.4% male, 36.5% New York Heart Association III-IV, N-terminal pro-B-type natriuretic peptide level of 1564 (701-3376) ng/L, left ventricular ejection fraction of 30 (25-34)%, 60.7% ischaemic HFrEF, 97.5% initially treated with angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers, 83.9% with beta-blockers, 64.4% with mineralocorticoid receptor antagonists, and 74.6% with diuretics]. Three groups were defined according to initial central/obstructive apnoea-hypopnoea indices (AHIs) G1 (n = 49, AHIcentral  ≥ 5/h and AHIobstructive  < 15/h); G2 (n = 27, AHIobstructive  ≥ 15/h); and G3 (n = 42, AHIcentral  < 5/h and AHIobstructive  < 15/h). At 3 months, the AHI (main predefined outcome) decreased significantly by -7.10/h (IQ25-75 -16.10 to 0.40; P < 0.001) in G1 + G2 without positive airway pressure treatment (45 patients, median initial AHI of 24.20 (IQ25-75 16.40-43.50)/h). Of these, 24.4% presented an AHI decrease ≥50% and 37.78% had a final AHI < 15/h (tendency for improvement from an initial value of 20% P = 0.0574). For G1 patients (n = 37), AHI significantly decreased from a median of 22.90 (16.00-43.50)/h to 19.20 (12.70-31.10)/h (P = 0.002). For G2 patients (n = 8), AHI decreased from a median of 30.10 (26.40-47.60)/h to 22.75 (14.60-36.90)/h (statistically non-significant, P = 0.059).

CONCLUSIONS:

In this real-life population, SV treatment for 3 months in SA patients is associated with a significant decrease in AHI. These results support the current guidelines that recommend first an optimization of the HFrEF treatment in patients with HFrEF and central SA. A potential positive airway pressure sparing effect merits further investigation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes da Apneia do Sono / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: ESC Heart Fail Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes da Apneia do Sono / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: ESC Heart Fail Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França