Beck-Sague C M, Cordts J R, Brown K, Larsen S A, Black C M, Knapp J S, Ridderhof J C, Barnes F G, Morse S A
Division of STD Laboratory Research, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Sex Transm Dis. 1996 Jul-Aug;23(4):342-9. doi: 10.1097/00007435-199607000-00014.
The diagnosis of many sexually transmitted diseases (STD) requires laboratory testing. The authors assessed the effects of the introduction of new tests and regulations on STD testing.
A questionnaire survey was mailed to a random sample of facilities listed in the STD Referral Database inquiring about tests offered, changes in testing, and reasons for changes.
Responses from 405 facilities were analyzed. Most responding facilities collected specimens for nontreponemal tests for syphilis (352 of 405 [86.9%]). Since each facility's information was last updated, the number reporting testing for Chlamydia trachomatis rose from 160 of 405 (39.5%) to 288 of 405 (71.1%), but testing for gonorrhea and chancroid decreased (365 of 405 [90.1%] to 328 of 405 [81%], and 182 of 405 [44.9%] to 32 of 405 [7.9%], respectively). Of 364 responses to a question on changes in tests performed in the last 2 years, 249 (68.4%) reported no change, 81 (22.3%) reported an increase, and 37 (10.2%) reported a decrease. The most frequently added tests were nonculture tests for C. trachomatis (34 of 81 [42%]) and the most frequent reason for adding tests was targeted funding (25 of 81 [30.9%]). The most frequently discontinued tests were cultures and gram stains for gonorrhea (15 of 37 [40.5%]) and other in-house tests (9 of 37 [24.3%]). Most facilities that discontinued testing cited the Clinical Laboratory Improvement Act as the reason (34 of 37 [91.9%]; 95% confidence interval = 78.1%, 98.3%).
The number of facilities testing for C. trachomatis has increased with funding and with the availability of nonculture tests, but the number of those testing for chancroid and gonorrhea has decreased. Implementation of the Clinical Laboratory Improvement Act may be associated with a decrease in the number of facilities performing tests for STD.
许多性传播疾病(STD)的诊断需要实验室检测。作者评估了新检测方法和规定的引入对性传播疾病检测的影响。
向性传播疾病转诊数据库中列出的设施随机样本邮寄问卷调查,询问所提供的检测、检测变化及变化原因。
分析了来自405个设施的回复。大多数回复设施采集梅毒非梅毒螺旋体检测标本(405个中的352个[86.9%])。自每个设施的信息上次更新以来,报告沙眼衣原体检测的数量从405个中的160个(39.5%)增至405个中的288个(71.1%),但淋病和软下疳检测减少(分别从405个中的365个[90.1%]降至405个中的328个[81%],以及从405个中的182个[44.9%]降至405个中的32个[7.9%])。在对过去2年检测变化问题的364份回复中,249份(68.4%)报告无变化,81份(22.3%)报告增加,37份(10.2%)报告减少。最常增加的检测是沙眼衣原体非培养检测(81个中的34个[42%]),增加检测的最常见原因是定向资金(81个中的25个[30.9%])。最常停止的检测是淋病培养和革兰氏染色(37个中的15个[40.5%])以及其他内部检测(37个中的9个[24.3%])。大多数停止检测的设施将《临床实验室改进法案》作为原因(37个中的34个[91.9%];95%置信区间 = 78.1%,98.3%)。
随着资金投入和非培养检测方法的出现,进行沙眼衣原体检测的设施数量增加,但进行软下疳和淋病检测的设施数量减少。《临床实验室改进法案》的实施可能与进行性传播疾病检测的设施数量减少有关。