School of Public Health, Imperial College London, London, UK.
Sex Transm Dis. 2013 Mar;40(3):230-4. doi: 10.1097/OLQ.0b013e31827b9d75.
There is uncertainty in the risk of pelvic inflammatory disease (PID) after chlamydia infection. We analyzed a prospective cohort of sex workers recruited in London between 1985 and 1993 to estimate the risk of PID after a diagnosed case of chlamydia.
Chlamydia and gonorrhea were defined as "recent" if they occurred during the most recent 6 months of follow-up or "previous" if they were more than 6 months ago, were the second infection during follow-up, or occurred before the study. Pelvic inflammatory disease was diagnosed using clinical criteria. We used Cox proportional hazards regression to estimate the association between chlamydia and PID controlled for gonorrhea.
Three hundred seven women contributed 401.2 person-years of follow-up. The rate of PID in women with recent chlamydia was 27.4 per 100 person-years compared with 11.2 in those without recent chlamydia. Recent and previous chlamydia significantly increased the risk of PID; this association persisted but was no longer significant after controlling for age and history of gonorrhea: recent chlamydia (adjusted hazard ratio [aHR], 2.0; 95% confidence interval [CI], 0.7-5.5), previous chlamydia (aHR, 1.8; 95% CI, 1.0-3.5), previous gonorrhea (aHR, 2.3; 95% CI, 1.1-4.6), and age (HR, 0.9; 95% CI, 0.9-1.0).
Women with recent or previous chlamydia are at increased risk for PID. However, this association may be explained by previous exposure to gonorrhea, which was found to increase the risk of PID after a future chlamydia infection.
衣原体感染后发生盆腔炎(PID)的风险存在不确定性。我们分析了 1985 年至 1993 年期间在伦敦招募的性工作者前瞻性队列,以估计诊断为衣原体感染后 PID 的风险。
如果衣原体和淋病发生在随访的最近 6 个月内,则定义为“近期”,如果发生在随访 6 个月之前、是随访期间的第二次感染,或发生在研究之前,则定义为“既往”。PID 的诊断采用临床标准。我们使用 Cox 比例风险回归估计衣原体与 PID 的关联,同时控制淋病的影响。
307 名女性共提供了 401.2 人年的随访。近期衣原体感染的女性 PID 发生率为 27.4/100 人年,而无近期衣原体感染的女性 PID 发生率为 11.2/100 人年。近期和既往衣原体感染显著增加了 PID 的风险;在控制年龄和淋病史后,这种关联仍然存在,但不再具有统计学意义:近期衣原体感染(调整后的危险比 [aHR],2.0;95%置信区间 [CI],0.7-5.5)、既往衣原体感染(aHR,1.8;95% CI,1.0-3.5)、既往淋病感染(aHR,2.3;95% CI,1.1-4.6)和年龄(HR,0.9;95% CI,0.9-1.0)。
近期或既往衣原体感染的女性 PID 风险增加。然而,这种关联可能是由既往淋病暴露解释的,后者被发现增加了未来衣原体感染后的 PID 风险。