Randomized controlled trial of granulocyte colony-stimulating factor for the treatment of severe sepsis due to melioidosis in Thailand

被引:67
作者
Cheng, Allen C.
Limmathurotsakul, Direk
Chierakul, Wirongrong
Getchalarat, Nongluk
Wuthiekanun, Vanaporn
Stephens, Dianne P.
Day, Nicholas P. J.
White, Nicholas J.
Chaowagul, Wipada
Currie, Bart J.
Peacock, Sharon J.
机构
[1] Charles Darwin Univ, Menzies Sch Hlth Res, Darwin, NT, Australia
[2] Royal Darwin Hosp, Darwin, NT, Australia
[3] Mahidol Univ, Fac Trop Med, Bangkok 10700, Thailand
[4] Sappasithiprasong Hosp, Dept Med, Ubon Ratchathani, Thailand
[5] John Radcliffe Hosp, Ctr Trop Dis, Nuffield Dept Clin Med, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
D O I
10.1086/519261
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Melioidosis is a tropical infectious disease associated with significant mortality. Most deaths occur early and are caused by fulminant sepsis. Methods. In this randomized, placebo-controlled trial, we assessed the efficacy of lenograstim (granulocyte colony-stimulating factor [G-CSF], 263 mu g per day administered intravenously) in ceftazidime-treated patients with severe sepsis caused by suspected melioidosis in Thailand. Results. Over a 27-month period, 60 patients were enrolled to receive either G-CSF (30 patients, 18 of whom had culture-confirmed melioidosis) or placebo (30 patients, 23 of whom had culture-confirmed melioidosis). Mortality rates were similar in both groups (G-CSF group, 70%; placebo group, 87%; risk ratio, 0.81; 95% confidence interval, 0.61-1.06; P = .2), including among patients with confirmed melioidosis (83% vs. 96%; P = .3). The duration of survival was longer for patients who received G-CSF than for patients who received placebo (33 h vs. 18.6 h; hazard ratio, 0.56; 95% confidence interval, 0.31-1.00; P = .05). Conclusions. Receipt of G-CSF is associated with a longer duration of survival but is not associated with a mortality benefit in patients with severe sepsis who are suspected of having melioidosis in Thailand. We hypothesize that G-CSF may "buy time" for severely septic patients, but survival is more likely to be improved by management of associated metabolic abnormalities and organ dysfunction associated with severe sepsis.
引用
收藏
页码:308 / 314
页数:7
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