Strep and the city: Unexpected persistence of early-onset GBS sepsis despite increased intra-partum antibiotic prophylaxis in an urban university hospital

摘要

Strategies to reduce early-onset sepsis (EOS) with group B streptococcus (GBS) have relied on the administration of maternal intra-partum antibiotics (IPA) to mothers with identified risk factors. We studied the relationship between IPA, risk factors, and EOS for 14 years in our hospital, an inner-city, tertiary center serving primarily poor, high-risk, African-American mothers. Methods: For each birth from 1989 to 2002, we identified presence or absence of maternal risk factors (prolonged rupture of membranes [PROM], chorioamnionitis, prematurity [<37 weeks]) and IPA use. In addition, for identified cases of EOS (+blood culture <72 h for a recognized pathogen), we identified bacterial organism and prior maternal GBS culture status. During these years, our obstetricians used a combination of risk-factor-based and culture-based GBS prophylaxis strategies. Results: Data from --44,000 pregnancies were collected. The most common risk factor was prematurity (21% of deliveries). The percentage of mothers with any identified risk factor did not change significantly over the study period (-33% of deliveries). From 1989 to 2002, IPA rose from 13% to 44% of all deliveries (p<0.001). For premature delivery, IPA rose from 27% to 69% (p<0.001); for PROM, IPA rose from 43% to 88% (p<0.001); for mothers with no identified risk factors of any kind, IPA rose from 7% to 27% (p<0.001). For babies with EOS, the frequency of known GBS culture results rose from approx 15% to approx 80% (p<0.001). Nonetheless, incidence of GBS EOS was unchanged (average of 2.0/1000 births); the incidence of non-GBS EOS was also unchanged (average of 2.1/1000 births). No maternal social demographic distinguished GBS from non-GBS EOS cases. Of the 57 infants with GBS EOS and risk factors, 35 (62%) received IPA; ofthe 85 infants with non-GBS EOS and risk factors, 62 (73%) received IPA (p<0.05). Conclusions: 1) IPA tripled between 1989 and 2002. 2) Yet EOS was unaffected-both GBS and non-GBS EOS persisted at approx 2/1000 live births. 3) We suggest that vaccination will eventually be needed to reduce GBS EOS in our institution. We have no good idea how to reduce non-GBS EOS cases.