A reiterative method for calculating the early bactericidal activity of antituberculosis drugs

被引:41
作者
Gillespie, SH [1 ]
Gosling, RD [1 ]
Charalambous, BM [1 ]
机构
[1] UCL Royal Free & Univ Coll Med Sch, Acad Det Med Microbiol, London NW3 2PF, England
关键词
tuberculosis; pulmonary; clinical trials; therapy; bacterial count;
D O I
10.1164/rccm.2112077
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Studies of early bactericidal activity (EBA) are important in the rapid evaluation of new antituberculosis drugs. Historically, these have concentrated on the log fall in the viable count in sputum during the first 48 hours of therapy. In this paper, we provide a mathematical model that suggests that the viable count in sputum follows an exponential decay curve with the equation V = S + Me-kt (where V is the viable count, M the population of bacteria susceptible to the test drug, S the population susceptible only to sterilizing agents, t the day of sputum collection as related to start of therapy, k the rate constant for the bacteria killed each day, and e the Napierian constant). We demonstrate that data from clinical trials fits the exponential decay model. We propose that future IEBA studies should be performed by measuring daily quantitative counts for at least 5 days. We also propose that the comparison of the early bactericidal activity of antituberculosis drugs should be evaluated using the time taken to reduce the viable count by 50% (vt(50)). A further reiterative refinement following a rule set based on statistically the best fit to the exponential decay model is described that will allow investigators to identify anomalous results and thus enhance the accuracy in measuring early bactericidal activity.
引用
收藏
页码:31 / 35
页数:5
相关论文
共 22 条
[1]  
[Anonymous], 2000, INT J TUBERC LUNG D, V4, P489
[2]  
Botha FJH, 1996, S AFR MED J, V86, P155
[3]   THE EARLY BACTERICIDAL ACTIVITY OF RIFABUTIN MEASURED BY SPUTUM VIABLE COUNTS IN HONG-KONG PATIENTS WITH PULMONARY TUBERCULOSIS [J].
CHAN, SL ;
YEW, WW ;
MA, WK ;
GIRLING, DJ ;
ABER, VR ;
FELMINGHAM, D ;
ALLEN, BW ;
MITCHISON, DA .
TUBERCLE AND LUNG DISEASE, 1992, 73 (01) :33-38
[4]   USPHS TUBERCULOSIS SHORT-COURSE CHEMOTHERAPY TRIAL-21 - EFFECTIVENESS, TOXICITY, AND ACCEPTABILITY - THE REPORT OF FINAL RESULTS [J].
COMBS, DL ;
OBRIEN, RJ ;
GEITER, LJ .
ANNALS OF INTERNAL MEDICINE, 1990, 112 (06) :397-406
[5]   Early bactericidal activity of paromomycin (aminosidine) in patients with smear-positive pulmonary tuberculosis [J].
Donald, PR ;
Sirgel, FA ;
Kanyok, TP ;
Danziger, LH ;
Venter, A ;
Botha, FJ ;
Parkin, DP ;
Seifart, HI ;
Van de Wal, BW ;
Martiz, JS ;
Mitchison, DA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (12) :3285-3287
[6]  
DOSTER B, 1973, AM REV RESPIR DIS, V107, P177
[7]  
Dye C, 2000, INT J TUBERC LUNG D, V4, pS146
[8]  
Fox W, 1999, INT J TUBERC LUNG D, V3, pS231
[9]  
FOX W, 1978, Bulletin of the International Union Against Tuberculosis, V53, P268
[10]   A comparison of the bactericidal activity of quinolone antibiotics in a Mycobacterium fortuitum model [J].
Gillespie, SH ;
Morrissey, I ;
Everett, D .
JOURNAL OF MEDICAL MICROBIOLOGY, 2001, 50 (06) :565-570