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dc.contributor.authorHernandez Poblete, Glenn Wilsonpt_BR
dc.contributor.authorCavalcanti, Alexandre Biasipt_BR
dc.contributor.authorOspina-Tascón, Gustavo Adolfopt_BR
dc.contributor.authorZampieri, Fernando Godinhopt_BR
dc.contributor.authorDubin, Arnaldopt_BR
dc.contributor.authorHurtado Bredda, Francisco Javierpt_BR
dc.contributor.authorFriedman, Gilbertopt_BR
dc.contributor.authorCastro Lopez, Ricardo Adolfopt_BR
dc.contributor.authorAlegria Vargas, Leyla Moreliapt_BR
dc.contributor.authorCecconi, Mauriziopt_BR
dc.contributor.authorTeboul, Jean-Louispt_BR
dc.contributor.authorBakker, Janpt_BR
dc.contributor.authorThe ANDROMEDA-SHOCK Study Investigatorspt_BR
dc.date.accessioned2018-07-04T02:27:22Zpt_BR
dc.date.issued2018pt_BR
dc.identifier.issn2110-5820pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/180083pt_BR
dc.description.abstractBackground: Septic shock is a highly lethal condition. Early recognition of tissue hypoperfusion and its reversion are key factors for limiting progression to multiple organ dysfunction and death. Lactate-targeted resuscitation is the gold-standard under current guidelines, although it has several pitfalls including that non-hypoxic sources of lactate might predominate in an unknown proportion of patients. Peripheral perfusion-targeted resuscitation might provide a real-time response to increases in flow that could lead to a more timely decision to stop resuscitation, thus avoiding fluid overload and the risks of over-resuscitation. This article reports the rationale, study design and analysis plan of the ANDROMEDA-SHOCK Study. Methods: ANDROMEDA-SHOCK is a randomized controlled trial which aims to determine if a peripheral perfusiontargeted resuscitation is associated with lower 28-day mortality compared to a lactate-targeted resuscitation in patients with septic shock with less than 4 h of diagnosis. Both groups will be treated with the same sequential approach during the 8-hour study period pursuing normalization of capillary refill time versus normalization or a decrease of more than 20% of lactate every 2 h. The common protocol starts with fluid responsiveness assessment and fluid loading in responders, followed by a vasopressor and an inodilator test if necessary. The primary outcome is 28-day mortality, and the secondary outcomes are: free days of mechanical ventilation, renal replacement therapy and vasopressor support during the first 28 days after randomization; multiple organ dysfunction during the first 72 h after randomization; intensive care unit and hospital lengths of stay; and all-cause mortality at 90-day. A sample size of 422 patients was calculated to detect a 15% absolute reduction in mortality in the peripheral perfusion group with 90% power and two-tailed type I error of 5%. All analysis will follow the intention-to-treat principle. Conclusions: If peripheral perfusion-targeted resuscitation improves 28-day mortality, this could lead to simplified algorithms, assessing almost in real-time the reperfusion process, and pursuing more physiologically sound objectives. At the end, it might prevent the risk of over-resuscitation and lead to a better utilization of intensive care unit resources.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofAnnals of intensive care. Heidelberg : Springer-Verlag, 2011-. Vol. 8 (2018), 10 f.pt_BR
dc.rightsOpen Accessen
dc.subjectSeptic shocken
dc.subjectChoque sépticopt_BR
dc.subjectRessuscitaçãopt_BR
dc.subjectResuscitationen
dc.subjectPeripheral perfusionen
dc.subjectReperfusão miocárdicapt_BR
dc.subjectDeslocamentos de líquidos corporaispt_BR
dc.subjectLactateen
dc.subjectÁcido lácticopt_BR
dc.subjectFluid responsivenessen
dc.titleEarly goal directed therapy using a physiological holistic view : the ANDROMEDA SHOCK—a randomized controlled trialpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001070298pt_BR
dc.type.originEstrangeiropt_BR


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