Overview of the current use of levosimendan in France: a prospective observational cohort study
dc.rights.license | open | en_US |
dc.contributor.author | CHOLLEY, Bernard | |
dc.contributor.author | BOJAN, Mirela | |
dc.contributor.author | GUILLON, Benoit | |
dc.contributor.author | BESNIER, Emmanuel | |
dc.contributor.author | MATTEI, Mathieu | |
dc.contributor.author | LEVY, Bruno | |
hal.structure.identifier | Biologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases | |
dc.contributor.author | OUATTARA, Alexandre | |
hal.structure.identifier | Biologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases | |
dc.contributor.author | TAFER, Nadir | |
dc.contributor.author | DELMAS, Clément | |
dc.contributor.author | TONON, David | |
dc.contributor.author | ROZEC, Bertrand | |
dc.contributor.author | FELLAHI, Jean-Luc | |
dc.contributor.author | LIM, Pascal | |
dc.contributor.author | LABASTE, François | |
hal.structure.identifier | Physiologie & médecine expérimentale du Cœur et des Muscles [U 1046] [PhyMedExp] | |
hal.structure.identifier | Centre Hospitalier Régional Universitaire [Montpellier] [CHRU Montpellier] | |
dc.contributor.author | ROUBILLE, François | |
dc.contributor.author | CARUBA, Thibaut | |
dc.contributor.author | MAURIAT, Philippe | |
dc.contributor.author | BARBOT, Olivier | |
dc.contributor.author | LAURENT, Berthomieu | |
dc.contributor.author | BESSELAT, Anne-Marie | |
dc.contributor.author | KATRIEN, Blanchart | |
dc.contributor.author | BOUGLE, Adrien | |
dc.contributor.author | BOURGOIN, Pierre | |
dc.contributor.author | ARNAUD, Causeret | |
dc.contributor.author | CHARBONNEAU, Hélène | |
dc.contributor.author | CRISTINAR, Mircea | |
dc.contributor.author | DESEBBE, Olivier | |
dc.contributor.author | ELJEZI, Veldat | |
dc.contributor.author | GENET, Thibaud | |
dc.contributor.author | GRENIER, Maxime | |
dc.contributor.author | GUINOT, Pierre Grégoire | |
dc.contributor.author | LEBEL, Stéphane | |
dc.contributor.author | LEVY, Yael | |
dc.contributor.author | LION, François | |
dc.contributor.author | MANSOURATI, Jacques | |
dc.contributor.author | MARLIÈRE, Stéphanie | |
dc.contributor.author | MARTIN, Anne-Céline | |
dc.contributor.author | MEBAZAA, Alexandre | |
dc.contributor.author | MOHAMMAD, Usman | |
dc.contributor.author | MONSEGU, Jacques | |
dc.contributor.author | NESSLER, Nicolas | |
dc.contributor.author | ORSEL, Isabelle | |
dc.contributor.author | PUYMIRAT, Etienne | |
dc.contributor.author | RECHER, Morgan | |
dc.contributor.author | SOUSSI, Sabri | |
dc.contributor.author | TROUSSARD, Vincent | |
dc.contributor.author | UHRY, Sabrina | |
dc.contributor.author | ZIRPHILE, Xavier | |
dc.date.accessioned | 2023-10-09T14:59:52Z | |
dc.date.available | 2023-10-09T14:59:52Z | |
dc.date.issued | 2023-12 | |
dc.identifier.issn | 2110-5820 | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/184368 | |
dc.description.abstractEn | Abstract Background Following the results of randomized controlled trials on levosimendan, French health authorities requested an update of the current use and side-effects of this medication on a national scale. Method The France-LEVO registry was a prospective observational cohort study reflecting the indications, dosing regimens, and side-effects of levosimendan, as well as patient outcomes over a year. Results The patients included ( n = 602) represented 29.6% of the national yearly use of levosimendan in France. They were treated for cardiogenic shock ( n = 250, 41.5%), decompensated heart failure ( n = 127, 21.1%), cardiac surgery-related low cardiac output prophylaxis and/or treatment ( n = 86, 14.3%), and weaning from veno-arterial extracorporeal membrane oxygenation ( n = 82, 13.6%). They received 0.18 ± 0.07 µg/kg/min levosimendan over 26 ± 8 h. An initial bolus was administered in 45 patients (7.5%), 103 (17.1%) received repeated infusions, and 461 (76.6%) received inotropes and or vasoactive agents concomitantly. Hypotension was reported in 218 patients (36.2%), atrial fibrillation in 85 (14.1%), and serious adverse events in 17 (2.8%). 136 patients (22.6%) died in hospital, and 26 (4.3%) during the 90-day follow-up. Conclusions We observed that levosimendan was used in accordance with recent recommendations by French physicians. Hypotension and atrial fibrillation remained the most frequent side-effects, while serious adverse event potentially attributable to levosimendan were infrequent. The results suggest that this medication was safe and potentially associated with some benefit in the population studied. | |
dc.language.iso | EN | en_US |
dc.rights | Attribution 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
dc.subject | Article clinique | |
dc.title.en | Overview of the current use of levosimendan in France: a prospective observational cohort study | |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.1186/s13613-023-01164-3 | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Médecine humaine et pathologie | en_US |
bordeaux.journal | Annals of Intensive Care | en_US |
bordeaux.page | 69 | en_US |
bordeaux.volume | 13 | en_US |
bordeaux.hal.laboratories | Biologie des maladies cardiovasculaires (BMC) - UMR 1034 | en_US |
bordeaux.issue | 1 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.institution | INSERM | en_US |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
bordeaux.import.source | hal | |
hal.identifier | hal-04179341 | |
hal.version | 1 | |
hal.popular | non | en_US |
hal.audience | Internationale | en_US |
hal.export | true | |
workflow.import.source | hal | |
dc.rights.cc | CC BY | en_US |
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