LONG-ACTING CHLORAMPHENICOL VERSUS INTRAVENOUS AMPICILLIN FOR TREATMENT OF BACTERIAL-MENINGITIS

被引:55
作者
PECOUL, B
VARAINE, F
KEITA, M
SOGA, G
DJIBO, A
SOULA, G
ABDOU, A
ETIENNE, J
REY, M
机构
[1] GABRIEL TOURE HOSP,BAMAKO,MALI
[2] NATL HOSP,NIAMEY,NIGER
[3] POINT G HOSP,BAMAKO,MALI
关键词
D O I
10.1016/0140-6736(91)91511-R
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In most developing countries, bacterial meningitis (BM) is associated with a high case-fatality rate. The search for a simple, convenient, and inexpensive antibiotic treatment remains a priority. In this study, a non-blinded, multicentre, randomised clinical trial of 528 cases of BM was done in two hospitals in Mali and Niger, between March, 1989, and May, 1990, to see whether a double injection of long-acting chloramphenicol (on admission to hospital and 48 h later) is as effective as a course of intravenous ampicillin (8 days, 4 times a day). The cumulative case-fatality rate on day 4 (principal end-point) among the chloramphenicol (254 patients) and ampicillin (274) groups were, respectively, 28% and 24.5% (relative risk 1.14, 95% confidence interval 0.86-1.52). No outbreak occurred during the study period. The hospital case-fatality rate was 33.1%. Main risk factors for death were associated with clinical condition on admission-ie, altered consciousness, convulsions, or dehydration. The case-fatality rates were 13% (21/161) for Neisseria meningitidis, 36.1% (48/133) for Haemophilus influenzae, and 67% (77/115) for Streptococcus pneumoniae. In a multiple logistic regression model, controlling for the differential distribution of potential risk factors (including bacterial species), there was no difference between treatment groups. Our findings suggest that long-acting chloramphenicol is a useful first-line presumptive treatment for BM in high-incidence countries.
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页码:862 / 866
页数:5
相关论文
共 17 条
[1]  
BLANCKWELDER WC, 1982, CONTROLLED CLIN TRIA, V3, P345
[2]  
Cisse M F, 1989, Med Trop (Mars), V49, P265
[3]  
ESSAN GJF, 1973, W AFRICAN J S, V22, P534
[4]  
GEDDEDAHL TW, 1990, REV INFECT DIS, V12, P359
[5]  
GLESKMAN RA, 1975, ARCH INTERN MED, V135, P1125
[6]  
GREENWOOD BM, 1984, REV INFECT DIS, V6, P374
[7]  
MAR ID, 1979, MED AFR NOIRE, V26, P599
[8]   MULTIPLE TESTING PROCEDURE FOR CLINICAL-TRIALS [J].
OBRIEN, PC ;
FLEMING, TR .
BIOMETRICS, 1979, 35 (03) :549-556
[9]  
PELTOLA H, 1989, LANCET, V1, P1282
[10]  
REY M, 1972, LYON MED, V228, P503