Abstract

Background. Pelvic inflammatory disease (PID) is a leading cause of both tubal factor infertility and ectopic pregnancy. Chlamydia trachomatis is an important risk factor for PID, but the proportion of PID cases caused by C. trachomatis is unclear. Estimates of this are required to evaluate control measures.Methods. We consider 5 separate methods of estimating age-group-specific population excess fractions (PEFs) of PID due to C. trachomatis, using routine data, surveys, case-control studies, and randomized controlled trials, and apply these to data from the United Kingdom before introduction of the National Chlamydia Screening Programme.Results. As they are informed by randomized comparisons and national exposure and outcome estimates, our preferred estimates of the proportion of PID cases caused by C. trachomatis are 35% (95% credible interval [CrI], 11%–69%) in women aged 16–24 years and 20% (95% CrI, 6%–38%) in women aged 16–44 years in the United Kingdom. There is a fair degree of consistency between adjusted estimates of PEF, but all have wide 95% CrIs. The PEF decreases from 53.5% (95% CrI, 15.6%–100%) in women aged 16–19 years to 11.5% (95% CrI, 3.0%–25.7%) in women aged 35–44 years.Conclusions. The PEFs of PID due to C. trachomatis decline steeply with age by a factor of around 5-fold between younger and older women. Further studies of the etiology of PID in different age groups are required.

Highlights

  • Pelvic inflammatory disease (PID) is a leading cause of both tubal factor infertility and ectopic pregnancy

  • As they are informed by randomized comparisons and national exposure and outcome estimates, our preferred estimates of the proportion of PID cases caused by C. trachomatis are 35% (95% credible interval [CrI], 11%–69%) in women aged 16–24 years and 20% (95% CrI, 6%–38%) in women aged 16–44 years in the United Kingdom

  • There are around 50–75 000 PID cases diagnosed in England annually, around one third of which are in women aged 16–24 years [4]

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Summary

Methods

We consider 5 separate methods of estimating age-group-specific population excess fractions (PEFs) of PID due to C. trachomatis, using routine data, surveys, case-control studies, and randomized controlled trials, and apply these to data from the United Kingdom before introduction of the National Chlamydia Screening Programme. We set out the relevant data sources for the United Kingdom and any statistical models used to analyze them, and we derive the joint functional relationships between the parameters they provide estimates of and the PEF. PEF Estimate 1 (PEF-1): Crude Estimate From Case-Control Studies and Age-Specific C. trachomatis Infection Prevalence Estimates. Case-control studies are commonly used to estimate PEFs. The standard formula for estimating the PEF from case-control data [9] is PEF = p:ðOR p:ðOR À À 1Þ 1Þ þ. The impact of confounding in observational studies of C. trachomatis and PID is likely to be significant as the risk factors for C. trachomatis infection are similar to the risk factors for many other causes of PID (eg, other sexually transmitted infections [STIs])

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