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沙眼衣原体和淋病奈瑟菌实验室检测推荐——2014 年。

Recommendations for the laboratory-based detection of Chlamydia trachomatis and Neisseria gonorrhoeae--2014.

出版信息

MMWR Recomm Rep. 2014 Mar 14;63(RR-02):1-19.

Abstract

This report updates CDC's 2002 recommendations regarding screening tests to detect Chlamydia trachomatis and Neisseria gonorrhoeae infections (CDC. Screening tests to detect Chlamydia trachomatis and Neisseria gonorrhoeae infections-2002. MMWR 2002;51[No. RR-15]) and provides new recommendations regarding optimal specimen types, the use of tests to detect rectal and oropharyngeal C. trachomatis and N. gonorrhoeae infections, and circumstances when supplemental testing is indicated. The recommendations in this report are intended for use by clinical laboratory directors, laboratory staff, clinicians, and disease control personnel who must choose among the multiple available tests, establish standard operating procedures for collecting and processing specimens, interpret test results for laboratory reporting, and counsel and treat patients. The performance of nucleic acid amplification tests (NAATs) with respect to overall sensitivity, specificity, and ease of specimen transport is better than that of any of the other tests available for the diagnosis of chlamydial and gonococcal infections. Laboratories should use NAATs to detect chlamydia and gonorrhea except in cases of child sexual assault involving boys and rectal and oropharyngeal infections in prepubescent girls and when evaluating a potential gonorrhea treatment failure, in which case culture and susceptibility testing might be required. NAATs that have been cleared by the Food and Drug Administration (FDA) for the detection of C. trachomatis and N. gonorrhoeae infections are recommended as screening or diagnostic tests because they have been evaluated in patients with and without symptoms. Maintaining the capability to culture for both N. gonorrhoeae and C. trachomatis in laboratories throughout the country is important because data are insufficient to recommend nonculture tests in cases of sexual assault in prepubescent boys and extragenital anatomic site exposure in prepubescent girls. N. gonorrhoeae culture is required to evaluate suspected cases of gonorrhea treatment failure and to monitor developing resistance to current treatment regimens. Chlamydia culture also should be maintained in some laboratories to monitor future changes in antibiotic susceptibility and to support surveillance and research activities such as detection of lymphogranuloma venereum or rare infections caused by variant or mutated C. trachomatis.

摘要

本报告更新了疾病预防控制中心(CDC) 2002 年关于筛查试验以检测沙眼衣原体和淋病奈瑟菌感染的建议(CDC. 筛查试验以检测沙眼衣原体和淋病奈瑟菌感染-2002. MMWR 2002;51[No. RR-15]),并提供了有关最佳标本类型、检测直肠和口咽沙眼衣原体和淋病奈瑟菌感染的试验使用、以及需要补充检测的情况的新建议。本报告中的建议供临床实验室主任、实验室工作人员、临床医生和疾病控制人员使用,他们必须在多种可用的检测方法中进行选择,为标本的采集和处理制定标准操作程序,解释实验室报告中的检测结果,并为患者提供咨询和治疗。核酸扩增试验(NAATs)在总体敏感性、特异性和标本运输便利性方面的性能优于其他任何用于诊断衣原体和淋病感染的检测方法。实验室应使用 NAAT 检测衣原体和淋病,除非涉及男孩的儿童性侵犯、未成熟女孩的直肠和口咽感染,或者在评估潜在的淋病治疗失败时,此时可能需要培养和药敏试验。已经获得食品和药物管理局(FDA)批准用于检测沙眼衣原体和淋病奈瑟菌感染的 NAAT 被推荐为筛查或诊断检测,因为它们已经在有症状和无症状的患者中进行了评估。在全国范围内的实验室中保持培养淋病奈瑟菌和沙眼衣原体的能力非常重要,因为数据不足以推荐在未成熟男孩的性侵犯和未成熟女孩的外阴解剖部位暴露的情况下进行非培养检测。需要进行淋病奈瑟菌培养以评估疑似淋病治疗失败的病例,并监测当前治疗方案耐药性的发展。在一些实验室中也应保持衣原体培养,以监测未来抗生素敏感性的变化,并支持监测和研究活动,如检测性病淋巴肉芽肿或由变异或突变沙眼衣原体引起的罕见感染。

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