Optimal Heart Failure Medical Therapy and ...
Document type :
Compte-rendu et recension critique d'ouvrage
DOI :
PMID :
Title :
Optimal Heart Failure Medical Therapy and Mortality in Survivors of Cardiogenic Shock: Insights From the FRENSHOCK Registry
Author(s) :
Matsushita, Kensuke [Auteur]
Nanomédecine Régénérative [NanoRegMed]
Delmas, Clément [Auteur correspondant]
Institut des Maladies Métaboliques et Casdiovasculaires [UPS/Inserm U1297 - I2MC]
Marchandot, Benjamin [Auteur]
Roubille, François [Auteur]
Physiologie & médecine expérimentale du Cœur et des Muscles [U 1046] [PhyMedExp]
Centre Hospitalier Régional Universitaire [Montpellier] [CHRU Montpellier]
Lamblin, Nicolas [Auteur]
Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 [RID-AGE]
Leurent, Guillaume [Auteur]
Centre Hospitalier Universitaire de Rennes [CHU Rennes] = Rennes University Hospital [Pontchaillou]
Laboratoire Traitement du Signal et de l'Image [LTSI]
Levy, Bruno [Auteur]
Elbaz, Meyer [Auteur]
Champion, Sebastien [Auteur]
Lim, Pascal [Auteur]
Institut Mondor de Recherche Biomédicale [IMRB]
Schneider, Francis [Auteur]
Khachab, Hadi [Auteur]
Carmona, Adrien [Auteur]
Trimaille, Antonin [Auteur]
Nanomédecine Régénérative [NanoRegMed]
Bourenne, Jeremy [Auteur]
Seronde, Marie‐france [Auteur]
Schurtz, Guillaume [Auteur]
Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 [RID-AGE]
Harbaoui, Brahim [Auteur]
Centre de Recherche en Acquisition et Traitement de l'Image pour la Santé [CREATIS]
Vanzetto, Gerald [Auteur]
Biendel, Caroline [Auteur]
Labbe, Vincent [Auteur]
Combaret, Nicolas [Auteur]
Mansourati, Jacques [Auteur]
Filippi, Emmanuelle [Auteur]
Maizel, Julien [Auteur]
CHU Amiens-Picardie
Mécanismes physiopathologiques et conséquences des calcifications cardiovasculaires - UR UPJV 7517 [MP3CV]
Merdji, Hamid [Auteur]
Lattuca, Benoit [Auteur]
Gerbaud, Edouard [Auteur]
Centre de recherche Cardio-Thoracique de Bordeaux [Bordeaux] [CRCTB]
Bonnefoy, Eric [Auteur]
Puymirat, Etienne [Auteur]
Bonello, Laurent [Auteur]
Assistance Publique - Hôpitaux de Marseille [APHM]
Morel, Olivier [Auteur correspondant]
Nanomédecine Régénérative [NanoRegMed]
Nanomédecine Régénérative [NanoRegMed]
Delmas, Clément [Auteur correspondant]
Institut des Maladies Métaboliques et Casdiovasculaires [UPS/Inserm U1297 - I2MC]
Marchandot, Benjamin [Auteur]
Roubille, François [Auteur]
Physiologie & médecine expérimentale du Cœur et des Muscles [U 1046] [PhyMedExp]
Centre Hospitalier Régional Universitaire [Montpellier] [CHRU Montpellier]
Lamblin, Nicolas [Auteur]
Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 [RID-AGE]
Leurent, Guillaume [Auteur]
Centre Hospitalier Universitaire de Rennes [CHU Rennes] = Rennes University Hospital [Pontchaillou]
Laboratoire Traitement du Signal et de l'Image [LTSI]
Levy, Bruno [Auteur]
Elbaz, Meyer [Auteur]
Champion, Sebastien [Auteur]
Lim, Pascal [Auteur]
Institut Mondor de Recherche Biomédicale [IMRB]
Schneider, Francis [Auteur]
Khachab, Hadi [Auteur]
Carmona, Adrien [Auteur]
Trimaille, Antonin [Auteur]
Nanomédecine Régénérative [NanoRegMed]
Bourenne, Jeremy [Auteur]
Seronde, Marie‐france [Auteur]
Schurtz, Guillaume [Auteur]
Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 [RID-AGE]
Harbaoui, Brahim [Auteur]
Centre de Recherche en Acquisition et Traitement de l'Image pour la Santé [CREATIS]
Vanzetto, Gerald [Auteur]
Biendel, Caroline [Auteur]
Labbe, Vincent [Auteur]
Combaret, Nicolas [Auteur]
Mansourati, Jacques [Auteur]
Filippi, Emmanuelle [Auteur]
Maizel, Julien [Auteur]
CHU Amiens-Picardie
Mécanismes physiopathologiques et conséquences des calcifications cardiovasculaires - UR UPJV 7517 [MP3CV]
Merdji, Hamid [Auteur]
Lattuca, Benoit [Auteur]
Gerbaud, Edouard [Auteur]
Centre de recherche Cardio-Thoracique de Bordeaux [Bordeaux] [CRCTB]
Bonnefoy, Eric [Auteur]
Puymirat, Etienne [Auteur]
Bonello, Laurent [Auteur]
Assistance Publique - Hôpitaux de Marseille [APHM]
Morel, Olivier [Auteur correspondant]
Nanomédecine Régénérative [NanoRegMed]
Journal title :
Journal of the American Heart Association
Pages :
e030975
Publisher :
Wiley-Blackwell
Publication date :
2024-02-23
ISSN :
2047-9980
English keyword(s) :
cardiogenic shock
guideline‐directed medical therapy
heart failure
left ventricular ejection fraction
guideline‐directed medical therapy
heart failure
left ventricular ejection fraction
HAL domain(s) :
Sciences du Vivant [q-bio]/Médecine humaine et pathologie/Cardiologie et système cardiovasculaire
Sciences du Vivant [q-bio]/Ingénierie biomédicale
Sciences du Vivant [q-bio]/Ingénierie biomédicale
English abstract : [en]
Background The effects of pharmacological therapy on cardiogenic shock (CS) survivors have not been extensively studied. Thus, this study investigated the association between guideline‐directed heart failure (HF) medical ...
Show more >Background The effects of pharmacological therapy on cardiogenic shock (CS) survivors have not been extensively studied. Thus, this study investigated the association between guideline‐directed heart failure (HF) medical therapy (GDMT) and one‐year survival rate in patients who are post‐CS. Methods and Results FRENSHOCK (French Observatory on the Management of Cardiogenic Shock in 2016) registry was a prospective multicenter observational survey, conducted in metropolitan French intensive care units and intensive cardiac care units. Of 772 patients, 535 patients were enrolled in the present analysis following the exclusion of 217 in‐hospital deaths and 20 patients with missing medical records. Patients with triple GDMT (beta‐blockers, renin‐angiotensin system inhibitors, and mineralocorticoid receptor antagonists) at discharge (n=112) were likely to have lower left ventricular ejection fraction on admission and at discharge compared with those without triple GDMT (n=423) (22% versus 28%, P <0.001 and 29% versus 37%, P <0.001, respectively). In the overall cohort, the one‐year mortality rate was 23%. Triple GDMT prescription was significantly associated with a lower one‐year all‐cause mortality compared with non‐triple GDMT (adjusted hazard ratio 0.44 [95% CI, 0.19–0.80]; P =0.007). Similarly, 2:1 propensity score matching and inverse probability treatment weighting based on the propensity score demonstrated a lower incidence of one‐year mortality in the triple GDMT group. As the number of HF drugs increased, a stepwise decrease in mortality was observed (log rank; P <0.001). Conclusions In survivors of CS, the one‐year mortality rate was significantly lower in those with triple GDMT. Therefore, this study suggests that intensive HF therapy should be considered in patients following CS.Show less >
Show more >Background The effects of pharmacological therapy on cardiogenic shock (CS) survivors have not been extensively studied. Thus, this study investigated the association between guideline‐directed heart failure (HF) medical therapy (GDMT) and one‐year survival rate in patients who are post‐CS. Methods and Results FRENSHOCK (French Observatory on the Management of Cardiogenic Shock in 2016) registry was a prospective multicenter observational survey, conducted in metropolitan French intensive care units and intensive cardiac care units. Of 772 patients, 535 patients were enrolled in the present analysis following the exclusion of 217 in‐hospital deaths and 20 patients with missing medical records. Patients with triple GDMT (beta‐blockers, renin‐angiotensin system inhibitors, and mineralocorticoid receptor antagonists) at discharge (n=112) were likely to have lower left ventricular ejection fraction on admission and at discharge compared with those without triple GDMT (n=423) (22% versus 28%, P <0.001 and 29% versus 37%, P <0.001, respectively). In the overall cohort, the one‐year mortality rate was 23%. Triple GDMT prescription was significantly associated with a lower one‐year all‐cause mortality compared with non‐triple GDMT (adjusted hazard ratio 0.44 [95% CI, 0.19–0.80]; P =0.007). Similarly, 2:1 propensity score matching and inverse probability treatment weighting based on the propensity score demonstrated a lower incidence of one‐year mortality in the triple GDMT group. As the number of HF drugs increased, a stepwise decrease in mortality was observed (log rank; P <0.001). Conclusions In survivors of CS, the one‐year mortality rate was significantly lower in those with triple GDMT. Therefore, this study suggests that intensive HF therapy should be considered in patients following CS.Show less >
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Anglais
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