TY - JOUR
T1 - Neonatal Encephalopathy with Group B Streptococcal Disease Worldwide
T2 - Systematic Review, Investigator Group Datasets, and Meta-analysis
AU - Tann, Cally J.
AU - Martinello, Kathryn A.
AU - Sadoo, Samantha
AU - Lawn, Joy E.
AU - Seale, Anna C.
AU - Vega-Poblete, Maira
AU - Russell, Neal J.
AU - Baker, Carol J.
AU - Bartlett, Linda
AU - Cutland, Clare
AU - Gravett, Michael G.
AU - Ip, Margaret
AU - Le Doare, Kirsty
AU - Madhi, Shabir A.
AU - Rubens, Craig E.
AU - Saha, Samir K.
AU - Schrag, Stephanie
AU - Sobanjo-Ter Meulen, Ajoke
AU - Vekemans, Johan
AU - Heath, Paul T.
AU - Ellis, Matthew E
AU - for the GBS Neonatal Encephalopathy Investigator Group
PY - 2017/11/15
Y1 - 2017/11/15
N2 - Neonatal encephalopathy (NE) is a leading cause of child mortality and longer-term impairment. Infection can sensitize the newborn brain to injury; however, the role of group B streptococcal (GBS) disease has not been reviewed. This paper is the ninth in an 11-article series estimating the burden of GBS disease; here we aim to assess the proportion of GBS in NE cases. We conducted systematic literature reviews (PubMed/Medline, Embase, Latin American and Caribbean Health Sciences Literature [LILACS], World Health Organization Library Information System [WHOLIS], and Scopus) and sought unpublished data from investigator groups reporting GBS-associated NE. Meta-analyses estimated the proportion of GBS disease in NE and mortality risk. UK population-level data estimated the incidence of GBS-associated NE. Four published and 25 unpublished datasets were identified from 13 countries (N = 10436). The proportion of NE associated with GBS was 0.58% (95% confidence interval [CI], 0.18%-.98%). Mortality was significantly increased in GBS-associated NE vs NE alone (risk ratio, 2.07 [95% CI, 1.47-2.91]). This equates to a UK incidence of GBS-associated NE of 0.019 per 1000 live births. The consistent increased proportion of GBS disease in NE and significant increased risk of mortality provides evidence that GBS infection contributes to NE. Increased information regarding this and other organisms is important to inform interventions, especially in low- and middle-resource contexts.
AB - Neonatal encephalopathy (NE) is a leading cause of child mortality and longer-term impairment. Infection can sensitize the newborn brain to injury; however, the role of group B streptococcal (GBS) disease has not been reviewed. This paper is the ninth in an 11-article series estimating the burden of GBS disease; here we aim to assess the proportion of GBS in NE cases. We conducted systematic literature reviews (PubMed/Medline, Embase, Latin American and Caribbean Health Sciences Literature [LILACS], World Health Organization Library Information System [WHOLIS], and Scopus) and sought unpublished data from investigator groups reporting GBS-associated NE. Meta-analyses estimated the proportion of GBS disease in NE and mortality risk. UK population-level data estimated the incidence of GBS-associated NE. Four published and 25 unpublished datasets were identified from 13 countries (N = 10436). The proportion of NE associated with GBS was 0.58% (95% confidence interval [CI], 0.18%-.98%). Mortality was significantly increased in GBS-associated NE vs NE alone (risk ratio, 2.07 [95% CI, 1.47-2.91]). This equates to a UK incidence of GBS-associated NE of 0.019 per 1000 live births. The consistent increased proportion of GBS disease in NE and significant increased risk of mortality provides evidence that GBS infection contributes to NE. Increased information regarding this and other organisms is important to inform interventions, especially in low- and middle-resource contexts.
KW - Group B Streptococcus
KW - hypoxic-ischemic encephalopathy
KW - neonatal encephalopathy
KW - newborn
KW - therapeutic hypothermia.
UR - http://www.scopus.com/inward/record.url?scp=85034247530&partnerID=8YFLogxK
U2 - 10.1093/cid/cix662
DO - 10.1093/cid/cix662
M3 - Review article (Academic Journal)
C2 - 29117330
AN - SCOPUS:85034247530
SN - 1058-4838
VL - 65
SP - S173-S189
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - suppl 2
M1 - cix662
ER -