Intrapartum tests for group B streptococcus: accuracy and acceptability of screening.

Jane Daniels, Joanna Gray, HM Pattison, Richard Gray, Robert Hills, Khalid Khan

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

OBJECTIVE To assess the accuracy and acceptability of polymerase chain reaction (PCR) and optical immunoassay (OIA) tests for the detection of maternal group B streptococcus (GBS) colonisation during labour, comparing their performance with the current UK policy of risk factor-based screening. DESIGN Diagnostic test accuracy study. SETTING AND POPULATION Fourteen hundred women in labour at two large UK maternity units provided vaginal and rectal swabs for testing. METHODS The PCR and OIA index tests were compared with the reference standard of selective enriched culture, assessed blind to index tests. Factors influencing neonatal GBS colonisation were assessed using multiple logistic regression, adjusting for antibiotic use. The acceptability of testing to participants was evaluated through a structured questionnaire administered after delivery. MAIN OUTCOME MEASURES The sensitivity and specificity of PCR, OIA and risk factor-based screening. RESULTS Maternal GBS colonisation was 21% (19-24%) by combined vaginal and rectal swab enriched culture. PCR test of either vaginal or rectal swabs was more sensitive (84% [79-88%] versus 72% [65-77%]) and specific (87% [85-89%] versus 57% [53-60%]) than OIA (P <0.001), and far more sensitive (84 versus 30% [25-35%]) and specific (87 versus 80% [77-82%]) than risk factor-based screening (P <0.001). Maternal antibiotics (odds ratio, 0.22 [0.07-0.62]; P = 0.004) and a positive PCR test (odds ratio, 29.4 [15.8-54.8]; P <0.001) were strongly related to neonatal GBS colonisation, whereas risk factors were not (odds ratio, 1.44 [0.80-2.62]; P = 0.2). CONCLUSION Intrapartum PCR screening is a more accurate predictor of maternal and neonatal GBS colonisation than is OIA or risk factor-based screening, and is acceptable to women.
Original languageEnglish
Pages (from-to)257-65
Number of pages9
JournalBJOG
Volume118
Issue number2
DOIs
Publication statusPublished - 1 Jan 2011

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