Differential antibiotic-induced endotoxin release in severe melioidosis

被引:57
作者
Simpson, AJH
Opal, SM
Angus, BJ
Prins, JM
Palardy, JE
Parejo, NA
Chaowagul, W
White, NJ
机构
[1] Mahidol Univ, Fac Trop Med, Bangkok, Thailand
[2] Sappasitprasong Hosp, Dept Med, Ubon Ratchathani, Thailand
[3] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Med, Ctr Trop Med, Oxford OX3 9DU, England
[4] Brown Univ, Sch Med, Div Infect Dis, Providence, RI 02912 USA
[5] Brown Univ, Sch Med, Div Microbiol, Providence, RI 02912 USA
[6] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
基金
英国惠康基金;
关键词
D O I
10.1086/315306
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Severe melioidosis is a life-threatening, systemic bacterial infection caused by Burkholderia pseudomallei. A prospective, randomized treatment trial was conducted in northeast Thailand to compare ceftazidime (a penicillin-binding protein [PBP]-3-specific agent that causes release of large amounts of endotoxin in vitro) and imipenem (a PBP-2-specific agent that kills B. pseudomallei more rapidly but releases low amounts of endotoxin) in severe melioidosis over a 6-h time course after the first dose of antibiotic. Despite similar clinical, microbiological, endotoxin, and cytokine measures at study entry, ceftazidime-treated patients (n = 34) had significantly greater systemic endotoxin (P < .001) than patients treated with imipenem (n = 34) after the first dose of antibiotic. No overall difference in mortality was observed (35% in both groups [95% confidence interval, 20%-50%]). Differential antibiotic-induced endotoxin release is demonstrable in severe melioidosis, These differences in endotoxin release did not appear to have a significant impact on survival in this group of patients.
引用
收藏
页码:1014 / 1019
页数:6
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