Early-onset neonatal group B streptococcus sepsis following national risk-based prevention guidelines

被引:32
作者
Darlow, Brian A. [1 ]
Voss, Lesley [2 ]
Lennon, Diana R. [3 ,4 ]
Grimwood, Keith [5 ,6 ,7 ]
机构
[1] Univ Otago, Dept Paediat, Christchurch, New Zealand
[2] Starship Childrens Hosp, Dept Paediat Infect Dis, Auckland, New Zealand
[3] Univ Auckland, Auckland 1, New Zealand
[4] Kidz First & Starship Childrens Hosp, Auckland, New Zealand
[5] Childrens Hlth Queensland, Queensland Childrens Med Res Inst, South Brisbane, Qld, Australia
[6] Griffith Univ, Menzies Hlth Inst Queensland, Gold Coast Campus, Nathan, Qld 4111, Australia
[7] Gold Coast Univ Hosp, Gold Coast Campus, Southport, Qld, Australia
关键词
newborn; prevention and control; sepsis; Streptococcus agalactiae; surveillance and monitoring; ANTIBIOTIC-PROPHYLAXIS; DISEASE; INFECTIONS; 10-YEAR; INFANTS;
D O I
10.1111/ajo.12378
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BackgroundNeonatal infection with group B streptococcus (GBS) is an important cause of infant mortality. Intrapartum antibiotics reduce early-onset GBS sepsis, but recommendations vary as to whether they should be offered following antenatal screening or based on risk factors alone. We aimed to determine the incidence of early-onset GBS sepsis in NewZealand fiveyears after the publication of national risk-based GBS prevention guidelines. Materials and MethodsProspective surveillance of early-onset GBS sepsis (defined as infection in the first 48h of life) was undertaken between April 2009 and March 2011 through the auspices of the New Zealand Paediatric Surveillance Unit as part of a survey of infection presenting in the first week of life. ResultsThere were 29 cases of confirmed early-onset GBS sepsis, including one case of meningitis, giving an incidence rate of 0.23 per 1000 (95% CI 0.16-0.33) live births. Three infants (10.3%) died. In 16 cases (55%), a maternal risk factor qualifying the mother for intrapartum antibiotics was present, but only five (31%) received this intervention. A retrospective review of the major hospital laboratory databases for this period identified two additional cases. A secondary sensitivity analysis taking account of these cases provided an estimated national incidence of 0.26 (95% CI 0.18-0.37) per1000 live births. ConclusionsTen years after a similar survey and fiveyears after promoting a single, risk-based prevention protocol nationally, the incidence of early-onset GBS disease in New Zealand has more than halved, but opportunities remain to further reduce the rate.
引用
收藏
页码:69 / 74
页数:6
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