Nelson H D, Helfand M
Division of Medical Informatics and Outcomes Research and Evidence-based Practice Center, Oregon Health Sciences University, Portland, Oregon 97201-3098, USA.
Am J Prev Med. 2001 Apr;20(3 Suppl):95-107. doi: 10.1016/s0749-3797(01)00253-7.
To examine data on the effectiveness of screening for chlamydial infection by a physician or other health care professional. Specifically, we examine the evidence that early treatment of chlamydial infection improves health outcomes, as well as evidence of the effectiveness of screening strategies in nonpregnant women, pregnant women, and men, and the accuracy of tests used for screening. This review updates the literature since the last recommendation of the U.S. Preventive Services Task Force published in 1996.
We searched the topic of chlamydia in the MEDLINE, HealthSTAR, and Cochrane Library databases from January 1994 to July 2000, supplemented by reference lists of relevant articles and from experts in the field. Articles published prior to 1994 and research abstracts were cited if particularly important to the key questions or to the interpretation of included articles.
A single reader reviewed all English abstracts. Articles were selected for full review if they were about Chlamydia trachomatis genitourinary infections in nonpregnant women, pregnant women, or men and were relevant to key questions in the analytic framework. Investigators read the full-text version of the retrieved articles and applied additional eligibility criteria. For all topics, we excluded articles if they did not provide sufficient information to determine the methods for selecting subjects and for analyzing data.
We systematically reviewed three types of studies about screening in nonpregnant women that relate to three key questions: (1) studies about the effectiveness of screening programs in reducing prevalence rates of infection, (2) studies about risk factors for chlamydial infection in women, and (3) studies about chlamydial screening tests in women. Our search found too few studies on pregnant women to systematically review, although pertinent studies are described. We systematically reviewed two types of studies about screening in men: (1) studies about prevalence rates and risk factors for chlamydial infection in men and (2) studies about chlamydial screening tests in men.
Nonpregnant women. The results of a randomized controlled trial conducted in a large health maintenance organization indicate that screening women selected by a set of risk factors reduces the incidence of pelvic inflammatory disease (PID) over a 1-year period. Changes in population prevalence rates have not been well documented because few studies have employed a representative population sample. Age continues to be the best predictor of chlamydial infection in women, with most studies evaluating cut-offs at age younger than 25 years. Other risk factors may be useful predictors, but these are likely to be population specific. To determine the accuracy of screening tests for women, we retrieved and critically reviewed 34 articles on test performance. Results indicate that endocervical swab specimens and first-void urine specimens have similar performance when using DNA amplification tests and have better sensitivity than endocervical culture. Recurrent chlamydial infections in women have been associated with increased risks for PID and ectopic pregnancies. Pregnant women. The Second Task Force recommendations for screening pregnant women were based on two major studies demonstrating improved pregnancy outcomes following treatment of chlamydial infection. We identified no recent studies on this topic in our literature search. Very few studies describe risk factors for chlamydial infection in pregnant women. Nonculture testing techniques appear to perform well in pregnant women, although studies are limited. Men. No studies described the effectiveness of screening or early treatment for men in reducing transmission to women or in preventing acute infections or complications in men. Studies of prevalence rates and risk factors for chlamydial infection in men are limited. Age lower than 25 years is the strongest known risk factor cited so far. Results of urethral swab specimens compared to first-void urine specimens were similar for DNA amplification tests. DNA amplification techniques are more sensitive than culture.
Screening women for Chlamydia trachomatis reduces the incidence of PID, and it is associated with reductions in prevalence of infection in uncontrolled studies. No studies were found to determine whether screening asymptomatic men would reduce transmission or prevent acute infections or complications. Age is the strongest risk factor for men and women. A variety of tests can detect chlamydial infection with acceptable sensitivity and specificity, including new DNA amplification tests that use either endocervical swabs in women, urethral swabs in men, or first-void urine specimens from men and women.
研究由医生或其他医护专业人员进行衣原体感染筛查的有效性数据。具体而言,我们将审视衣原体感染早期治疗可改善健康结局的证据,以及非孕妇、孕妇和男性筛查策略有效性的证据,还有用于筛查的检测准确性。本综述更新了自1996年美国预防服务工作组上次发布建议以来的文献。
我们检索了1994年1月至2000年7月期间MEDLINE、HealthSTAR和Cochrane图书馆数据库中关于衣原体的主题,并辅以相关文章的参考文献列表以及该领域专家提供的信息。若1994年之前发表的文章及研究摘要对关键问题或纳入文章的解读特别重要,则予以引用。
由一位读者审阅所有英文摘要。若文章涉及非孕妇、孕妇或男性的沙眼衣原体泌尿生殖系统感染且与分析框架中的关键问题相关,则入选进行全文审阅。研究人员阅读检索到的文章全文,并应用其他纳入标准。对于所有主题,若文章未提供足够信息以确定选择研究对象和分析数据的方法,则予以排除。
我们系统回顾了三类关于非孕妇筛查的研究,这些研究与三个关键问题相关:(1)关于筛查项目在降低感染率方面有效性的研究;(2)关于女性衣原体感染危险因素的研究;(3)关于女性衣原体筛查检测的研究。我们的检索发现关于孕妇的研究太少,无法进行系统回顾,不过对相关研究进行了描述。我们系统回顾了两类关于男性筛查的研究:(1)关于男性衣原体感染患病率及危险因素的研究;(2)关于男性衣原体筛查检测的研究。
非孕妇。在一个大型健康维护组织中进行的一项随机对照试验结果表明,对一组有风险因素的女性进行筛查可在1年内降低盆腔炎(PID)的发病率。由于很少有研究采用具有代表性的人群样本,因此人群患病率的变化情况尚无充分记录。年龄仍然是女性衣原体感染的最佳预测指标,大多数研究评估的年龄界限为25岁以下。其他风险因素可能是有用的预测指标,但可能因人群而异。为确定女性筛查检测的准确性,我们检索并严格审阅了34篇关于检测性能的文章。结果表明,使用DNA扩增检测时,宫颈拭子标本和首次晨尿标本的性能相似,且比宫颈培养具有更高的敏感性。女性衣原体反复感染与PID和异位妊娠风险增加有关。孕妇。第二次工作组关于孕妇筛查的建议基于两项主要研究,这些研究表明衣原体感染治疗后妊娠结局得到改善。在我们的文献检索中未发现近期关于该主题的研究。很少有研究描述孕妇衣原体感染的危险因素。尽管研究有限,但非培养检测技术在孕妇中似乎表现良好。男性。没有研究描述男性筛查或早期治疗在减少向女性传播或预防男性急性感染及并发症方面的有效性。关于男性衣原体感染患病率及危险因素的研究有限。年龄低于25岁是目前已知最强的危险因素。对于DNA扩增检测,尿道拭子标本与首次晨尿标本的结果相似。DNA扩增技术比培养更敏感。
对女性进行沙眼衣原体筛查可降低PID的发病率,在非对照研究中也与感染率降低相关。未发现有研究确定对无症状男性进行筛查是否会减少传播或预防急性感染及并发症。年龄是男性和女性最强的风险因素。多种检测方法可检测衣原体感染,其敏感性和特异性均可接受,包括使用女性宫颈拭子、男性尿道拭子或男性和女性首次晨尿标本的新型DNA扩增检测方法。