Estimates of the Burden of Group B Streptococcal Disease Worldwide for Pregnant Women, Stillbirths, and Children

被引:346
作者
Seale, Anna C. [1 ,2 ]
Bianchi-Jassir, Fiorella [1 ]
Russell, Neal J. [1 ,3 ]
Kohli-Lynch, Maya [1 ,4 ]
Tann, Cally J. [1 ,5 ]
Hall, Jenny [6 ]
Madrid, Lola [1 ,7 ]
Blencowe, Hannah [1 ]
Cousens, Simon [1 ]
Baker, Carol J. [8 ,9 ,10 ]
Bartlett, Linda [11 ]
Cutland, Clare [12 ,13 ]
Gravett, Michael G. [14 ,15 ]
Heath, Paul T. [16 ,17 ]
Ip, Margaret [18 ]
Le Doare, Kirsty [16 ,17 ,19 ]
Madhi, Shabir A. [12 ,13 ,20 ]
Rubens, Craig E. [14 ,21 ]
Saha, Samir K. [22 ]
Schrag, Stephanie J. [23 ]
Sobanjo-ter Meulen, Ajoke [24 ]
Vekemans, Johan [25 ]
Lawn, Joy E. [1 ]
机构
[1] London Sch Hyg & Trop Med, Maternal Adolescent Reprod & Child Hlth Ctr, London, England
[2] Haramaya Univ, Coll Hlth & Med Sci, Dire Dawa, Ethiopia
[3] Kings Coll London, London, England
[4] Univ Bristol, Sch Social & Community Med, Ctr Child & Adolescent Hlth, Bristol, Avon, England
[5] Univ Coll London Hosp NHS Fdn Trust, Neonatal Med, London, England
[6] UCL, Inst Womens Hlth, Dept Reprod Hlth Res, London, England
[7] Univ Barcelona, Hosp Clin, Barcelona Ctr Int Hlth Res, ISGlobal, Barcelona, Spain
[8] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[9] Baylor Coll Med, Dept Mol Virol, Houston, TX 77030 USA
[10] Baylor Coll Med, Dept Microbiol, Houston, TX 77030 USA
[11] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Int Hlth, Baltimore, MD USA
[12] Univ Witwatersrand, Fac Hlth Sci, Med Res Council, Resp & Meningeal Pathogens Res Unit, Johannesburg, South Africa
[13] Univ Witwatersrand, Fac Hlth Sci, Dept Sci & Technol, Natl Res Fdn Vaccine Preventable Dis, Johannesburg, South Africa
[14] Global Alliance Prevent Prematur & Stillbirth, Seattle, WA USA
[15] Univ Washington, Sch Med, Dept Obstet & Gynecol, Seattle, WA USA
[16] St Georges Univ London, Inst Infect & Immun, Vaccine Inst, London, England
[17] St Georges Univ Hosp NHS Fdn, London, England
[18] Chinese Univ Hong Kong, Dept Microbiol, Fac Med, Hong Kong, Hong Kong, Peoples R China
[19] Imperial Coll London, Ctr Int Child Hlth, London, England
[20] Nat Inst Communicable Dis, Natl Hlth Lab Serv, Johannesburg, South Africa
[21] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
[22] Bangladesh Inst Child Hlth, Dhaka, Bangladesh
[23] Nat Ctr Immunizat & Resp Dis, Ctr Dis Control & Prevent, Atlanta, GA USA
[24] Bill & Melinda Gates Fdn, Seattle, WA USA
[25] WHO, Geneva, Switzerland
基金
比尔及梅琳达.盖茨基金会;
关键词
group B Streptococcus; infection; newborn; stillbirth; maternal; MATERNAL COLONIZATION; NEURODEVELOPMENTAL IMPAIRMENT; NEONATAL ENCEPHALOPATHY; BACTERIAL-MENINGITIS; SYSTEMATIC ANALYSIS; CONJUGATE VACCINE; HEALTHY WOMEN; GLOBAL LEVELS; IMMUNOGENICITY; PREVENTION;
D O I
10.1093/cid/cix664
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. We aimed to provide the first comprehensive estimates of the burden of group B Streptococcus (GBS), including invasive disease in pregnant and postpartum women, fetal infection/stillbirth, and infants. Intrapartum antibiotic prophylaxis is the current mainstay of prevention, reducing early-onset infant disease in high-income contexts. Maternal GBS vaccines are in development. Methods. For 2015 live births, we used a compartmental model to estimate (1) exposure to maternal GBS colonization, (2) cases of infant invasive GBS disease, (3) deaths, and (4) disabilities. We applied incidence or prevalence data to estimate cases of maternal and fetal infection/stillbirth, and infants with invasive GBS disease presenting with neonatal encephalopathy. We applied risk ratios to estimate numbers of preterm births attributable to GBS. Uncertainty was also estimated. Results. Worldwide in 2015, we estimated 205 000 (uncertainty range [UR], 101 000-327 000) infants with early-onset disease and 114 000 (UR, 44 000-326 000) with late-onset disease, of whom a minimum of 7000 (UR, 0-19 000) presented with neonatal encephalopathy. There were 90 000 (UR, 36 000-169 000) deaths in infants < 3 months age, and, at least 10 000 (UR, 3 000-27 000) children with disability each year. There were 33 000 (UR, 13 000-52 000) cases of invasive GBS disease in pregnant or postpartum women, and 57 000 (UR, 12 000-104 000) fetal infections/stillbirths. Up to 3.5 million preterm births may be attributable to GBS. Africa accounted for 54% of estimated cases and 65% of all fetal/infant deaths. A maternal vaccine with 80% efficacy and 90% coverage could prevent 107 000 (UR, 20 000-198 000) stillbirths and infant deaths. Conclusions. Our conservative estimates suggest that GBS is a leading contributor to adverse maternal and newborn outcomes, with at least 409 000 (UR, 144 000-573 000) maternal/fetal/infant cases and 147 000 (UR, 47 000-273 000) stillbirths and infant deaths annually. An effective GBS vaccine could reduce disease in the mother, the fetus, and the infant.
引用
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页码:S200 / S219
页数:20
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