Costa Susana Correia, Machado Ana Paula, Teixeira Cláudia, Cerqueira Luísa, Rodrigues Teresa, Ribeiro Manuela, Moucho Marina
Serviço de Obstetrícia, Unidade Autónoma de Gestão da Mulher e da Criança, Centro Hospitalar Universitário São João, Porto, Portugal.
Serviço de Patologia Clínica, Unidade Autónoma de Gestão dos Meios Complementares de Diagnóstico e Terapêutica, Centro Hospitalar Universitário São João, Porto, Portugal.
J Matern Fetal Neonatal Med. 2023 Dec;36(2):2262078. doi: 10.1080/14767058.2023.2262078. Epub 2023 Sep 27.
The aim of this study was to evaluate if screening Group B colonization by intrapartum polymerase chain reaction could improve intrapartum administration of antibiotic prophylaxis, compared with antepartum culture screening and analyze the sensitivity and specificity of polymerase chain reaction test.
198 pregnant women with Group B colonization antepartum culture screening were included. When they arrived at hospital for delivery, two rectovaginal swabs were collected: for culture and polymerase chain reaction method.
The rate of Group B colonization antepartum detected by culture was 16.7%; at delivery was 17.2% when detected by culture and 19.7% using polymerase chain reaction method. The rate of inconclusive polymerase chain reaction tests was 0.5%. Considering intrapartum culture screening as gold standard, sensitivity and specificity of polymerase chain reaction test for intrapartum Group B colonization was 97.1% and 95.7%, respectively. The global rate of discordance between antepartum and intrapartum Group B colonization was 6.6%. The rate of women not treated with intrapartum antibiotic prophylaxis in the setting of positive intrapartum culture was significantly lower using intrapartum polymerase chain reaction test (0.5%) than with antepartum culture method (3.5%, = 0.035).
The use of intrapartum antibiotic prophylaxis can be more efficient when screening Group B colonization intrapartum by polymerase chain reaction test. Polymerase chain reaction method had a good performance in our study, with high sensitivity and specificity.
本研究旨在评估与产前培养筛查相比,通过产时聚合酶链反应(PCR)筛查B族链球菌定植是否能改善产时抗生素预防性用药,并分析PCR检测的敏感性和特异性。
纳入198例产前培养筛查出B族链球菌定植的孕妇。她们入院分娩时,采集两份直肠阴道拭子:一份用于培养,另一份用于PCR检测。
产前培养检测出的B族链球菌定植率为16.7%;分娩时培养检测出的定植率为17.2%,而PCR检测的定植率为19.7%。PCR检测结果不确定的比例为0.5%。以产时培养筛查为金标准,产时B族链球菌定植的PCR检测敏感性和特异性分别为97.1%和95.7%。产前和产时B族链球菌定植不一致的总体比例为6.6%。在产时培养阳性的情况下,使用产时PCR检测未接受产时抗生素预防性用药的女性比例(0.5%)显著低于产前培养方法(3.5%,P = 0.035)。
通过PCR检测在产时筛查B族链球菌定植时,使用产时抗生素预防性用药可能更有效。PCR方法在我们的研究中表现良好,具有高敏感性和特异性。