Time-Dose-Response Models for Microbial Risk Assessment

被引:34
作者
Huang, Yin [1 ]
Haas, Charles N. [1 ]
机构
[1] Drexel Univ, Dept Civil Architectural & Environm Engn, Philadelphia, PA 19104 USA
关键词
Infection; maximum likelihood estimation; microbial risk assessment; survival analysis; time-dose response; SUSCEPTIBILITY; TUBERCULOSIS; TULARENSIS; INFECTION; ANTHRAX; PLAGUE;
D O I
10.1111/j.1539-6924.2008.01195.x
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
While microbial risk assessment (MRA) has been used for over 25 years, traditional dose-response analysis has only predicted the overall risk of adverse consequences from exposure to a given dose. An important issue for consequence assessment from bioterrorist and other microbiological exposure is the distribution of cases over time due to the initial exposure. In this study, the classical exponential and beta-Poisson dose-response models were modified to include exponential-power dependency of time post inoculation (TPI) or its simplified form, exponential-reciprocal dependency of TPI, to quantify the time of onset of an effect presumably associated with the kinetics of in vivo bacterial growth. Using the maximum likelihood estimation approach, the resulting time-dose-response models were found capable of providing statistically acceptable fits to all tested pooled animal survival dose-response data. These new models can consequently describe the development of animal infectious response over time and represent observed responses fairly accurately. This is the first study showing that a time-dose-response model can be developed for describing infections initiated by various pathogens. It provides an advanced approach for future MRA frameworks.
引用
收藏
页码:648 / 661
页数:14
相关论文
共 21 条
[1]   Postexposure prophylaxis against anthrax: Evaluation of various treatment regimens in intranasally infected guinea pigs [J].
Altboum, Z ;
Gozes, Y ;
Barnea, A ;
Pass, A ;
White, M ;
Kobiler, D .
INFECTION AND IMMUNITY, 2002, 70 (11) :6231-6241
[2]  
CHEN TH, 1974, J INFECT DIS, V129, pS46, DOI 10.1093/infdis/129.Supplement_1.S46
[3]  
COX LA, 2006, ENVIRON INT, V25, P841
[4]  
DANZHOU C, 2006, ENDEMIC DIS B, V21, P47
[5]   EXPERIMENTAL TULAREMIA IN MACACA-MULATTA - RELATIONSHIP OF AEROSOL PARTICLE SIZE TO INFECTIVITY OF AIRBORNE PASTEURELLA-TULARENSIS [J].
DAY, WC ;
BERENDT, RF .
INFECTION AND IMMUNITY, 1972, 5 (01) :77-+
[6]   Global burden of tuberculosis - Estimated incidence, prevalence, and mortality by country [J].
Dye, C ;
Scheele, S ;
Dolin, P ;
Pathania, V ;
Raviglione, RC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (07) :677-686
[7]  
EMELYANOVA OS, 1961, EPIDEMIOLOGY IMMUNOB, V32, P853
[8]  
GUILLEMIN J, 2001, INVESTIGATION DEADLY
[9]  
Haas C.N., 1999, Quantitative Microbial Risk Assessment
[10]   ESTIMATION OF SAFE DOSES IN CARCINOGENIC EXPERIMENTS [J].
HARTLEY, HO ;
SIELKEN, RL .
BIOMETRICS, 1977, 33 (01) :1-30