Risk of reproductive complications following chlamydia testing: a population-based retrospective cohort study in Denmark

被引:92
作者
Davies, Bethan [1 ]
Turner, Katy M. E. [2 ]
Frolund, Maria [4 ]
Ward, Helen [1 ]
May, Margaret T. [3 ]
Rasmussen, Steen [5 ]
Benfield, Thomas [6 ,7 ]
Westh, Henrik [5 ,7 ]
机构
[1] Imperial Coll London, Sch Publ Hlth, Dept Infect Dis Epidemiol, London, England
[2] Univ Bristol, Sch Vet Sci, Bristol, Avon, England
[3] Univ Bristol, Sch Social & Community Med, Bristol, Avon, England
[4] Statens Serum Inst, Dept Microbiol & Infect Control, Copenhagen, Denmark
[5] Hvidovre Univ Hosp, Dept Clin Microbiol, Hvidovre, Denmark
[6] Hvidovre Univ Hosp, Dept Infect Dis, Hvidovre, Denmark
[7] Univ Copenhagen, Inst Clin Med, Copenhagen, Denmark
关键词
PELVIC-INFLAMMATORY-DISEASE; COST-EFFECTIVENESS; NATURAL-HISTORY; TRACHOMATIS; WOMEN; INFECTION; HETEROGENEITY; DIAGNOSIS; PROGRAM; IMPACT;
D O I
10.1016/S1473-3099(16)30092-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Uncertainty in the risk of reproductive complications (pelvic inflammatory disease, ectopic pregnancy, and tubal factor infertility) following chlamydia infection and repeat infection hampers the design of evidence-based chlamydia control programmes. We estimate the association between diagnosed chlamydia and episodes of hospital health care (inpatient, outpatient, and emergency department) for a reproductive complication. Methods We constructed and analysed a retrospective population-based cohort of women aged 15-44 years from administrative records in Denmark (1995-2012). We used a subset of the national Danish Chlamydia Study. The master dataset contains all residents of Denmark (induding Greenland) who had a positive chlamydia test recorded by a public health microbiology laboratory from Jan 1, 1992, to Nov 2, 2011. Individuals were randomly matched (by age and sex) to four individuals drawn from the population register (Danish Civil Registration System) who did not have a positive chlamydia test during this interval. The outcomes in the study were hospital episodes of health-care (inpatient, outpatient, and emergency department) with a diagnosis of pelvic inflammatory disease, ectopic pregnancy, or tubal factor infertility. Findings The 516 720 women (103344 positive, 182 879 negative, 230497 never-tested) had a mean follow-up of 7.96 years. Compared with women with only negative tests, the risk of each complication was 30% higher in women with one or more positive tests (pelvic inflammatory disease, adjusted hazard ratio [AHR] 1.50 [95% CI 1.43-1.57]; ectopic pregnancy, AHR 1.31 [1.25-1.38]; tubal factor infertility, AHR 1.37 [1.24-1.52]) and 60% lower in women who were never-tested (pelvic inflammatory disease, AHR 0.33 [0.31-0.35]; ectopic pregnancy, AHR 0.42 [0.39-0.44]; tubal factor infertility AHR 0.29 [0.25-0.33]). A positive test had a minor absolute impact on health as the difference in the lifetime incidence of complications was small between women who tested positive and those who tested negative (pelvic inflammatory disease, 0.6%; ectopic pregnancy, 0.2%; tubal factor infertility, 0.1%). Repeat infections increased the risk of pelvic inflammatory disease by a further 20% (AHR 1.20, 95% CI 1.11-1.31). Interpretation A single diagnosed chlamydia infection increased the risk of all complications and a repeat diagnosed infection further increased the risk of pelvic inflammatory disease. Therefore, control programmes must prevent first and repeat infections to improve women's reproductive health.
引用
收藏
页码:1057 / 1064
页数:8
相关论文
共 29 条
[1]   The cost effectiveness of opportunistic chlamydia screening in England - Commentary [J].
Roberts, T. E. ;
Low, N. .
SEXUALLY TRANSMITTED INFECTIONS, 2007, 83 (04) :274-275
[2]   Ectopic pregnancies and reproductive capacity after chlamydia trachomatis positive and negative test results: A historical follow-up study [J].
Andersen, B ;
Ostergaard, L ;
Puho, E ;
Skriver, MV ;
Schonheyder, HC .
SEXUALLY TRANSMITTED DISEASES, 2005, 32 (06) :377-381
[3]   Prediction of costs, effectiveness, and disease control of a population-based program using home sampling for diagnosis of urogenital Chlamydia trachomatis infections [J].
Andersen, Berit ;
Gundgaard, Jens ;
Kretzschmar, Mirjam ;
Olsen, Jens ;
Welte, Robert ;
Oster-Gaard, Lars .
SEXUALLY TRANSMITTED DISEASES, 2006, 33 (07) :407-415
[4]  
[Anonymous], 2014, CHLAM CONTR EUR LIT
[5]   Incidence of pelvic inflammatory disease in a large cohort of women tested for Chlamydia trachomatis: a historical follow-up study [J].
Bakken, Inger J. ;
Ghaderi, Sara .
BMC INFECTIOUS DISEASES, 2009, 9
[6]   Births and ectopic prelgnancies in a large cohort of women tested for Chlamydia trachomatis [J].
Bakken, Inger Johanne ;
Skjeldestad, Finn Egil ;
Lydersen, Stian ;
Nordbo, Svein Arne .
SEXUALLY TRANSMITTED DISEASES, 2007, 34 (10) :739-743
[7]   Pelvic Inflammatory Disease Among Privately Insured Women, United States, 2001-2005 [J].
Bohm, Michele K. ;
Newman, Lori ;
Satterwhite, Catherine Lindsey ;
Tao, Guoyu ;
Weinstock, Hillard S. .
SEXUALLY TRANSMITTED DISEASES, 2010, 37 (03) :131-136
[8]  
Davies B., 2014, ASS CHLAMYDIA TRACHO
[9]   Heterogeneity in Risk of Pelvic Inflammatory Diseases After Chlamydia Infection: A Population-Based Study in Manitoba, Canada [J].
Davies, Bethan ;
Ward, Helen ;
Leung, Stella ;
Turner, Katy M. E. ;
Garnett, Geoff P. ;
Blanchard, James F. ;
Yu, B. Nancy .
JOURNAL OF INFECTIOUS DISEASES, 2014, 210 :S549-S555
[10]   Systematic screening for Chlamydia trachomatis:: Estimating cost-effectiveness using dynamic modeling and Dutch data [J].
de Vries, R ;
van Bergen, JEAM ;
de Jong-van den Berg, LTW ;
Postma, MJ .
VALUE IN HEALTH, 2006, 9 (01) :1-11