Increasing incidence of late-onset neonatal invasive group B streptococcal infections in Iceland.

To access publisher full text version of this article. Please click on the hyperlink in Additional Links field. BACKGROUND: Group B streptococci (GBS) may cause life-threatening invasive infections in infants. The incidence of these infections has been increasing during the last decades. The aim of...

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Bibliographic Details
Published in:Pediatric Infectious Disease Journal
Main Authors: Óladóttir, Guđrún Lilja, Erlendsdóttir, Helga, Pálsson, Gestur, Björnsdóttir, Erla Soffía, Kristinsson, Karl G, Haraldsson, Ásgeir
Other Authors: Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Format: Article in Journal/Newspaper
Language:English
Published: Lippincott Williams & Wilkins 2012
Subjects:
Blood
Cerebrospinal Fluid
Female
Humans
Iceland
Incidence
Infant
Newborn
Male
Retrospective Studies
Serotyping
Streptococcal Infections
Streptococcus agalactiae
Online Access:http://hdl.handle.net/2336/227571
https://doi.org/10.1097/INF.0b013e3182184fe4
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Summary:To access publisher full text version of this article. Please click on the hyperlink in Additional Links field. BACKGROUND: Group B streptococci (GBS) may cause life-threatening invasive infections in infants. The incidence of these infections has been increasing during the last decades. The aim of the study was to determine the epidemiology of neonatal GBS infections to be able to implement therapeutic and preventive measures more effectively. METHODS: A retrospective case study was conducted in Iceland that included all neonates with positive GBS cultures from blood or cerebrospinal fluid during the period 1975 to 2006. Serotyping of all available GBS isolates was performed. RESULTS: A total of 87 children with 89 infections were included in the study. In all, 53 infants had early-onset (EO) GBS infections (occurring <7 days after birth) and 34 had late-onset (LO) infections (occurring on days 7-90). EO infections increased during the first 3 quartiles of the study period but decreased during the last quartile. LO infections increased throughout the entire study period. GBS was cultured from cerebrospinal fluid in 21 patients; 9 with EO and 12 with LO infections. Premature infants comprised 15 with EO and 14 with LO infections. Eight children died of GBS infection, 7 with EO and 1 with LO infections; no correlation with serotypes was found. Serotype III was most common for both EO (34%) and LO infections (62%). CONCLUSION: The number of GBS infections increased during the study period. The decrease in EO infections in recent years could be attributed to intrapartum antibiotic treatment. The increasing number of LO infections is a concern.

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