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dc.rights.licenseopenen_US
dc.contributor.authorCHOLLEY, Bernard
dc.contributor.authorLEVY, Bruno
dc.contributor.authorFELLAHI, Jean-Luc
dc.contributor.authorLONGROIS, Dan
dc.contributor.authorAMOUR, Julien
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorOUATTARA, Alexandre
dc.contributor.authorMEBAZAA, Alexandre
dc.date.accessioned2023-01-16T14:45:25Z
dc.date.available2023-01-16T14:45:25Z
dc.date.issued2019-11-29
dc.identifier.issn1466-609Xen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/171688
dc.description.abstractEnDespite interesting and unique pharmacological properties, levosimendan has not proven a clear superiority to placebo in the patient populations that have been enrolled in the various recent multicenter randomized controlled trials. However, the pharmacodynamic effects of levosimendan are still considered potentially very useful in a number of specific situations.Patients with decompensated heart failure requiring inotropic support and receiving beta-blockers represent the most widely accepted indication. Repeated infusions of levosimendan are increasingly used to facilitate weaning from dobutamine and avoid prolonged hospitalizations in patients with end-stage heart failure, awaiting heart transplantation or left ventricular assist device implantation. New trials are under way to confirm or refute the potential usefulness of levosimendan to facilitate weaning from veno-arterial ECMO, to treat cardiogenic shock due to left or right ventricular failure because the current evidence is mostly retrospective and requires confirmation with better-designed studies. Takotsubo syndrome may represent an ideal target for this non-adrenergic inotrope, but this statement also relies on expert opinion. There is no benefit from levosimendan in patients with septic shock. The two large trials evaluating the prophylactic administration of levosimendan (pharmacological preconditioning) in cardiac surgical patients with poor left ventricular ejection fraction could not show a significant reduction in their composite endpoints reflecting low cardiac output syndrome with respect to placebo. However, the subgroup of those who underwent isolated CABG appeared to have a reduction in mortality. A new study will be required to confirm this exploratory finding.Levosimendan remains a potentially useful inodilator agent in a number of specific situations due to its unique pharmacological properties. More studies are needed to provide a higher level of proof regarding these indications.
dc.language.isoENen_US
dc.subject.enCardiotonic Agents
dc.subject.enExpert Testimony
dc.subject.enHeart Failure
dc.subject.enHumans
dc.subject.enPerioperative Medicine
dc.subject.enRandomized Controlled Trials as Topic
dc.subject.enSimendan
dc.title.enLevosimendan in the light of the results of the recent randomized controlled trials: an expert opinion paper.
dc.title.alternativeCrit Careen_US
dc.typeArticle de revueen_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed31783891en_US
bordeaux.journalCritical Careen_US
bordeaux.page385en_US
bordeaux.volume23en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.exportfalse
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Critical%20Care&rft.date=2019-11-29&rft.volume=23&rft.issue=1&rft.spage=385&rft.epage=385&rft.eissn=1466-609X&rft.issn=1466-609X&rft.au=CHOLLEY,%20Bernard&LEVY,%20Bruno&FELLAHI,%20Jean-Luc&LONGROIS,%20Dan&AMOUR,%20Julien&rft.genre=article


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