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
相关论文
共 33 条
[1]   DIFFERENCES IN THERAPEUTIC EFFICACY AMONG CELL WALL-ACTIVE ANTIBIOTICS IN A MOUSE MODEL OF GRAM-NEGATIVE SEPSIS [J].
BUCKLIN, SE ;
MORRISON, DC .
JOURNAL OF INFECTIOUS DISEASES, 1995, 172 (06) :1519-1527
[2]  
BYL B, 1998, INT C ANT AG CHEM SA, P38
[3]  
CHAOWAGUL W, 1993, J INFECT DIS, V168, P1181, DOI 10.1093/infdis/168.5.1181
[4]   MELIOIDOSIS - A MAJOR CAUSE OF COMMUNITY-ACQUIRED SEPTICEMIA IN NORTHEASTERN THAILAND [J].
CHAOWAGUL, W ;
WHITE, NJ ;
DANCE, DAB ;
WATTANAGOON, Y ;
NAIGOWIT, P ;
DAVIS, TME ;
LOOAREESUWAN, S ;
PITAKWATCHARA, N .
JOURNAL OF INFECTIOUS DISEASES, 1989, 159 (05) :890-899
[5]  
Chaowagul W, 1996, SCAND J INFECT DIS, P14
[6]   AMANTADINE PROPHYLAXIS FOR HEALTH-CARE WORKERS - UNANSWERED QUESTIONS [J].
COX, RA .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1991, 27 (01) :1-3
[7]  
Currie Bart, 1993, Southeast Asian Journal of Tropical Medicine and Public Health, V24, P436
[8]   EFFECTS OF DIFFERENT TYPES AND COMBINATIONS OF ANTIMICROBIAL AGENTS ON ENDOTOXIN RELEASE FROM GRAM-NEGATIVE BACTERIA - AN INVITRO AND INVIVO STUDY [J].
DOFFERHOFF, ASM ;
NIJLAND, JH ;
DEVRIESHOSPERS, HG ;
MULDER, POM ;
WEITS, J ;
BOM, VJJ .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 1991, 23 (06) :745-754
[9]  
DOFFERHOFF ASM, 1995, J ENDOTOXIN RES, V2, P37
[10]   CHLORAMPHENICOL IN TYPHOID FEVER [J].
GALPINE, JF .
BRITISH MEDICAL JOURNAL, 1949, 2 (4635) :1047-1048