Hay P E, Thomas B J, Horner P J, MacLeod E, Renton A M, Taylor-Robinson D
Division of Sexually Transmitted Diseases, Clinical Research Centre, Harrow, Middlesex, UK.
Genitourin Med. 1994 Apr;70(2):97-100. doi: 10.1136/sti.70.2.97.
To determine the extent to which testing of multiple sites and samples is required to define whether a woman is Chlamydia trachomatis-positive.
One-hundred and fifty women attending the Genitourinary Medicine clinic at St Mary's Hospital were enrolled; they had not received antichlamydial antibiotics in the previous three months, were not in a high-risk group for HIV infection, or pregnant, or using an intrauterine contraceptive device. Thirty-two women were re-examined three months after recruitment.
An urethral specimen was Gram stained (smear) and cultured for gonococci. Another urethral specimen was taken to detect C trachomatis elementary bodies (EBs) by the MicroTrak direct fluorescent antibody (DFA) test (Syva). An endocervical swab specimen was Gram stained (smear) and cultured for gonococci. One of two other endocervical swabs was used for the DFA test and was then placed in medium which was centrifuged in a MicroCentaur at 13,000 rpm for 10 min; the deposit was examined by using the DFA test. The first 15-20 ml of voided urine (first pass urine; FPU) was also centrifuged and the deposit tested similarly.
Of 182 cervical smears and/or deposits tested for C trachomatis, 38 were positive; more cervical deposits (37) than smears (26) were positive and, of these, one-fifth of the deposits and one-third of the smears contained fewer than 10 elementary bodies. Of 162 paired urethral smears and FPU deposits available, one or other specimen of 36 pairs was chlamydia-positive, that is 31 smears and 32 deposits; of these, two-fifths of the smears and half of the deposits contained fewer than 10 EBs. Of 150 sets of cervical and urinary tract samples tested, 31 were chlamydia-positive at both sites, six in the cervix alone and four in the urinary tract alone. Of 139 women for whom there were valid first visit sample results, 36 (26%) were chlamydia-positive in the cervix, 34 (25%) in the urinary tract and 41 (29%) had at least one sample from either site positive. Overall, DFA tests of deposits from centrifuged cervical specimens achieved the highest sensitivity (88%) and those of cervical smears the lowest (70%).
Deposits from centrifuged cervical specimens were C trachomatis-positive more often than were cervical smears. Testing deposits from centrifuged urines was as successful as testing urethral smears. One-fifth (cervical deposits) to one-half (urine deposits) of specimens contained fewer than 10 EBs. The urinary tract was chlamydia-positive almost as frequently as the cervix but both sites needed to be tested to define whether a woman was chlamydia-positive.
确定需要检测多少个部位和样本才能明确女性是否沙眼衣原体呈阳性。
招募了150名到圣玛丽医院泌尿生殖医学门诊就诊的女性;她们在过去三个月内未接受过抗衣原体抗生素治疗,不属于HIV感染高危人群,未怀孕,也未使用宫内节育器。32名女性在招募三个月后接受了复查。
采集一份尿道标本进行革兰氏染色(涂片)并培养淋球菌。采集另一份尿道标本,通过MicroTrak直接荧光抗体(DFA)检测(Syva公司)检测沙眼衣原体原体(EBs)。采集一份宫颈拭子标本进行革兰氏染色(涂片)并培养淋球菌。另外两份宫颈拭子中的一份用于DFA检测,然后放入培养基中,在微量离心机中以13000转/分钟离心10分钟;沉淀物通过DFA检测进行检查。最初排出的15 - 20毫升尿液(初段尿;FPU)也进行离心,沉淀物进行类似检测。
在检测沙眼衣原体的182份宫颈涂片和/或沉淀物中,38份呈阳性;宫颈沉淀物阳性的有37份,多于涂片阳性的26份,其中,五分之一的沉淀物和三分之一的涂片所含原体少于10个。在162对可用的尿道涂片和FPU沉淀物中,36对中的一份或另一份标本衣原体呈阳性,即31份涂片和32份沉淀物;其中,五分之二的涂片和一半的沉淀物所含EBs少于10个。在检测的150组宫颈和泌尿道样本中,两个部位均衣原体呈阳性的有31组,仅宫颈阳性的有6组,仅泌尿道阳性的有4组。在有首次就诊有效样本结果的139名女性中,36名(26%)宫颈衣原体呈阳性,34名(25%)泌尿道阳性,41名(29%)至少有一个部位的样本呈阳性。总体而言,离心宫颈标本沉淀物的DFA检测灵敏度最高(88%),宫颈涂片的最低(70%)。
离心宫颈标本的沉淀物沙眼衣原体呈阳性的情况比宫颈涂片更常见。检测离心尿液的沉淀物与检测尿道涂片同样有效。五分之一(宫颈沉淀物)到二分之一(尿液沉淀物)的标本所含EBs少于10个。泌尿道衣原体呈阳性的频率几乎与宫颈相同,但两个部位都需要检测才能确定女性是否衣原体呈阳性。