Effect of treatment delay on disease severity and need for resuscitation in porcine fecal peritonitis
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/09/2013
19/09/2013
01/10/2012
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Resumo |
Objective: Early treatment in sepsis may improve outcome. The aim of this study was to evaluate how the delay in starting resuscitation influences the severity of sepsis and the treatment needed to achieve hemodynamic stability. Design: Prospective, randomized, controlled experimental study. Setting: Experimental laboratory in a university hospital. Subjects: Thirty-two anesthetized and mechanically ventilated pigs. Interventions: Pigs were randomly assigned (n = 8 per group) to a nonseptic control group or one of three groups in which fecal peritonitis (peritoneal instillation of 2 g/kg autologous feces) was induced, and a 48-hr period of protocolized resuscitation started 6 (Delta T-6 hrs), 12 (Delta T-12 hrs), or 24 (Delta T-24 hrs) hrs later. The aim of this study was to evaluate the impact of delays in resuscitation on disease severity, need for resuscitation, and the development of sepsis-associated organ and mitochondrial dysfunction. Measurements and Main Results: Any delay in starting resuscitation was associated with progressive signs of hypovolemia and increased plasma levels of interleukin-6 and tumor necrosis factor-alpha prior to resuscitation. Delaying resuscitation increased cumulative net fluid balances (2.1 +/- 0.5 mL/kg/hr, 2.8 +/- 0.7 mL/kg/hr, and 3.2 +/- 1.5 mL/kg/hr, respectively, for groups.T-6 hrs, Delta T-12 hrs, and.T-24 hrs; p < .01) and norepinephrine requirements during the 48-hr resuscitation protocol (0.02 +/- 0.04 mu g/kg/min, 0.06 +/- 0.09 mu g/kg/min, and 0.13 +/- 0.15 mu g/kg/min; p = .059), decreased maximal brain mitochondrial complex II respiration (p = .048), and tended to increase mortality (p = .08). Muscle tissue adenosine triphosphate decreased in all groups (p < .01), with lowest values at the end in groups Delta T-12 hrs and.T-24 hrs. Conclusions: Increasing the delay between sepsis initiation and resuscitation increases disease severity, need for resuscitation, and sepsis-associated brain mitochondrial dysfunction. Our results support the concept of a critical window of opportunity in sepsis resuscitation. (Crit Care Med 2012; 40:2841-2849) Swiss National Science Foundation Swiss National Science Foundation [32003B-127619] Stiftung fur die Forschung in Anasthesioiogie und Intensivmedizin, Bern Stiftung fur die Forschung in Anasthesioiogie und Intensivmedizin, Bern |
Identificador |
CRITICAL CARE MEDICINE, PHILADELPHIA, v. 40, n. 10, pp. 2841-2849, OCT, 2012 0090-3493 http://www.producao.usp.br/handle/BDPI/33516 10.1097/CCM.0b013e31825b916b |
Idioma(s) |
eng |
Publicador |
LIPPINCOTT WILLIAMS & WILKINS PHILADELPHIA |
Relação |
Critical Care Medicine |
Direitos |
closedAccess Copyright LIPPINCOTT WILLIAMS & WILKINS |
Palavras-Chave | #CYTOKINES #FLUID THERAPY #MITOCHONDRIAL RESPIRATION #MULTIPLE ORGAN FAILURE #RESUSCITATION #SEPTIC SHOCK #SEVERE SEPSIS #SURVIVING SEPSIS CAMPAIGN #MICROCIRCULATORY BLOOD-FLOW #RANDOMIZED CONTROLLED-TRIAL #MULTIPLE ORGAN FAILURE #INTENSIVE-CARE UNITS #INDUCED SEPTIC SHOCK #ACUTE LUNG INJURY #SEVERE SEPSIS #MITOCHONDRIAL DYSFUNCTION #CRITICAL DETERMINANT #SPLANCHNIC ORGANS #CRITICAL CARE MEDICINE |
Tipo |
article original article publishedVersion |