Coverage is the key for effective screening of Chlamydia trachomatis in Australia

被引:93
作者
Regan, David G. [1 ]
Wilson, David P. [1 ]
Hocking, Jane S. [2 ]
机构
[1] Univ New S Wales, Natl Ctr HIV Epidemiol & Clin Res, Sydney, NSW, Australia
[2] Univ Melbourne, Sch Populat Hlth, Key Ctr Womens Hlth Soc, Melbourne, Vic, Australia
关键词
D O I
10.1086/589883
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The rate of diagnosis of Chlamydia trachomatis (chlamydia) infection has risen dramatically in Australia. In response, the Australian government is planning to implement systematic screening and testing. Several decisions must be made, including whom to screen. Methods. To inform decisions surrounding screening, a dynamic transmission model of the chlamydia epidemic was developed and parameterized with Australian sexual behavior and epidemiology data. A range of screening strategies and coverage rates were evaluated targeting various groups based on age and sex. Rigorous uncertainty and sensitivity analyses were undertaken. Results. The model predicts that even moderate screening coverage in young adults (< 25 years old) will reduce prevalence rapidly. The absolute numbers of people screened, rather than the sex targeted, is the key determinant in reducing prevalence. Sensitivity analysis determined that chlamydia transmission is strongly related to 2 biological parameters (the proportion of infections that are asymptomatic in women and the duration of infection in men) and 2 behavioral parameters (the frequency of sex acts for 20-24-year-olds and the level of condom usage). Conclusions. The model predicts that routine annual screening can significantly reduce the prevalence of chlamydia within 10 years, provided that adequate screening coverage is achieved. The most effective screening strategies will be those that target 20-24-year-olds.
引用
收藏
页码:349 / 358
页数:10
相关论文
共 42 条
[31]  
Morré SA, 1998, J CLIN PATHOL-MOL PA, V51, P149
[32]   The natural course of asymptomatic Chlamydia trachomatis infections:: 45% clearance and no development of clinical PID after one-year follow-up [J].
Morré, SA ;
van den Brule, AJC ;
Rozendaal, L ;
Boeke, AJP ;
Voorhorst, FJ ;
de Blok, S ;
Meijer, CJLM .
INTERNATIONAL JOURNAL OF STD & AIDS, 2002, 13 :12-18
[33]   An outreach programme for sexually transmitted infection screening in street sex workers using self-administered samples [J].
Morton, AN ;
Wakefield, T ;
Tabrizi, SN ;
Garland, SM ;
Fairley, CK .
INTERNATIONAL JOURNAL OF STD & AIDS, 1999, 10 (11) :741-743
[34]   Genital chlamydial infections [J].
Peipert, JF .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (25) :2424-2430
[35]   Epidemiologic and microbiologic correlates of Chlamydia trachomatis infection in sexual partnerships [J].
Quinn, TC ;
Gaydos, C ;
Shepherd, M ;
Bobo, L ;
Hook, EW ;
Viscidi, R ;
Rompalo, A .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (21) :1737-1742
[36]   PARAMETER SENSITIVITIES, MONTE-CARLO FILTERING, AND MODEL FORECASTING UNDER UNCERTAINTY [J].
ROSE, KA ;
SMITH, EP ;
GARDNER, RH ;
BRENKERT, AL ;
BARTELL, SM .
JOURNAL OF FORECASTING, 1991, 10 (1-2) :117-133
[37]   Sex in australia: A guide for readers [J].
Smith, AMA ;
Rissel, CE ;
Richters, J ;
Grulich, AE ;
de Visser, RO .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PUBLIC HEALTH, 2003, 27 (02) :103-105
[38]   Prevalence and high rate of asymptomatic infection of Chlamydia trachomatis in male college Reserve Officer Training Corps cadets [J].
Sutton, TL ;
Martinko, T ;
Hale, S ;
Fairchok, MP .
SEXUALLY TRANSMITTED DISEASES, 2003, 30 (12) :901-904
[39]   INFECTIOUS-DISEASES OF HUMANS - DYNAMICS AND CONTROL - ANDERSON,RM, MAY,RM [J].
TULJAPURKAR, S .
SCIENCE, 1991, 254 (5031) :591-592
[40]   Modelling the effectiveness of chlamydia screening in England [J].
Turner, K. M. E. ;
Adams, E. J. ;
LaMontagne, D. S. ;
Emmett, L. ;
Baster, K. ;
Edmunds, W. J. .
SEXUALLY TRANSMITTED INFECTIONS, 2006, 82 (06) :496-502