Randomization and baseline transmission in vaccine field trials

被引:21
作者
Struchiner, C. J. [1 ]
Halloran, M. E.
机构
[1] UERJ, IMS, BR-21041 Riode Janeiro, RJ, Brazil
[2] Escola Natl Saude Publ, Fundacao Oswaldo Cruz, BR-21041 Riode Janeiro, RJ, Brazil
[3] Univ Washington, Seattle, WA 98195 USA
[4] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
关键词
D O I
10.1017/S0950268806006716
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
In randomized trials, the treatment assignment mechanism is independent of the outcome of interest and other covariates thought to be relevant in determining this outcome. It also allows, on average, for a balanced distribution of these covariates in the vaccine and placebo groups. Randomization, however, does not guarantee that the estimated effect is an unbiased estimate of the biological effect of interest. We show how exposure to infection can be a confounder even in randomized vaccine field trials. Based on a simple model of the biological efficacy of interest, we extend the arguments on comparability and collapsibility to examine the limits of randomization to control for unmeasured covariates. Estimates from randomized, placebo-controlled Phase III vaccine field trials that differ in baseline transmission are not comparable unless explicit control for baseline transmission is taken into account.
引用
收藏
页码:181 / 194
页数:14
相关论文
共 37 条
[1]  
[Anonymous], 1962, FDN STAT INFERENCE
[2]   GENERAL RELATIVE RISK FUNCTIONS FOR CASE-CONTROL STUDIES [J].
BRESLOW, NE ;
STORER, BE .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1985, 122 (01) :149-162
[3]   A non-parametric method for the reconstruction of age- and time-dependent incidence from the prevalence data of irreversible diseases with differential mortality [J].
Brunet, RC ;
Struchiner, CJ .
THEORETICAL POPULATION BIOLOGY, 1999, 56 (01) :76-90
[4]   Rate estimation from prevalence information on a simple epidemiologic model for health interventions [J].
Brunet, RC ;
Struchiner, CJ .
THEORETICAL POPULATION BIOLOGY, 1996, 50 (03) :209-226
[5]   ON THE DISTRIBUTION OF VACCINE PROTECTION UNDER HETEROGENEOUS RESPONSE [J].
BRUNET, RC ;
STRUCHINER, CJ ;
HALLORAN, ME .
MATHEMATICAL BIOSCIENCES, 1993, 116 (01) :111-125
[6]   A method for estimating time dependent intervention benefits under arbitrarily varying age and exogenous components of hazard [J].
Brunet, RC ;
Struchiner, CJ ;
Loinaz, A .
LIFETIME DATA ANALYSIS, 2001, 7 (04) :377-392
[7]   EFFICACY TRIAL OF MALARIA VACCINE SPF66 IN GAMBIAN INFANTS [J].
DALESSANDRO, U ;
LEACH, A ;
DRAKELEY, CJ ;
BENNETT, S ;
OLALEYE, BO ;
FEGAN, GW ;
JAWARA, M ;
LANGEROCK, P ;
GEORGE, MO ;
TARGETT, GAT ;
GREENWOOD, BM .
LANCET, 1995, 346 (8973) :462-467
[8]  
Durham LK, 1998, AM J EPIDEMIOL, V147, P948, DOI 10.1093/oxfordjournals.aje.a009385
[9]   FORCING A SEQUENTIAL EXPERIMENT TO BE BALANCED [J].
EFRON, B .
BIOMETRIKA, 1971, 58 (03) :403-&
[10]   THE EFFICACY OF PERTUSSIS VACCINES UNDER CONDITIONS OF HOUSEHOLD EXPOSURE - FURTHER ANALYSIS OF THE 1978-80 PHLS-ERL STUDY IN 21 AREA HEALTH AUTHORITIES IN ENGLAND [J].
FINE, PEM ;
CLARKSON, JA ;
MILLER, E .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1988, 17 (03) :635-642