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10.1097/CCM.0000000000000718

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suck abstract from ncbi


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pmid25474535      Crit+Care+Med 2015 ; 43 (3): 534-41
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  • Randomized, Placebo-controlled Trial of Acetaminophen for the Reduction of Oxidative Injury in Severe Sepsis: The ACROSS Trial #MMPMID25474535
  • Janz DR; Bastarache JA; Rice TW; Bernard GR; Warren MA; Wickersham N; Sills G; Oates JA; Roberts LJ; Ware LB
  • Crit Care Med 2015[Mar]; 43 (3): 534-41 PMID25474535show ga
  • Objective: This trial evaluated the efficacy of acetaminophen in reducing oxidative injury, as measured by plasma F2-Isoprostanes, in adult patients with severe sepsis and detectable plasma cell-free hemoglobin. Design: Single center, randomized, double-blind, placebo controlled phase II trial. Setting: Medical ICU in a tertiary, academic medical center. Patients: Critically ill patients ?18 years old with severe sepsis and detectable plasma cell-free hemoglobin. Interventions: Patients were randomized 1:1 to enteral acetaminophen 1 gram every 6 hours for three days (n = 18) or placebo (n = 22) with the same dosing schedule and duration. Measurements and Main Results: F2-Isoprostanes on study day 3, the primary outcome, did not differ between acetaminophen (30 pg/mL, IQR 24?41) and placebo (36 pg/mL, IQR 25?80, p = 0.35). However, F2-Isoprostanes were significantly reduced on study day 2 in the acetaminophen group (24 pg/mL, IQR 19 ? 36) compared with placebo (36 pg/mL, IQR 23?55, p = 0.047). Creatinine on study day 3, a secondary outcome, was significantly lower in the acetaminophen group (1.0 mg/dL, IQR 0.6?1.4) compared with placebo (1.3 mg/dL, IQR 0.83 ? 2.0, p = 0.039). There was no statistically significant difference in hospital mortality (acetaminophen 5.6% vs. placebo 18.2%, p = 0.355) or adverse events (AST or ALT >400)(acetaminophen 9.5% vs. placebo 4.3%, p = 0.599). Conclusions: In adults with severe sepsis and detectable plasma cell-free hemoglobin, treatment with acetaminophen within 24 hours of ICU admission may reduce oxidative injury and improve renal function. Further study is needed to confirm these findings and determine the effect of acetaminophen on patient-centered outcomes.
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