Epidemiology of Invasive Early-Onset and Late-Onset Group B Streptococcal Disease in the United States, 2006 to 2015: Multistate Laboratory and Population-Based Surveillance.


Journal

JAMA pediatrics
ISSN: 2168-6211
Titre abrégé: JAMA Pediatr
Pays: United States
ID NLM: 101589544

Informations de publication

Date de publication:
01 03 2019
Historique:
pubmed: 15 1 2019
medline: 26 11 2019
entrez: 15 1 2019
Statut: ppublish

Résumé

Invasive disease owing to group B Streptococcus (GBS) remains an important cause of illness and death among infants younger than 90 days in the United States, despite declines in early-onset disease (EOD; with onset at 0-6 days of life) that are attributed to intrapartum antibiotic prophylaxis (IAP). Maternal vaccines to prevent infant GBS disease are currently under development. To describe incidence rates, case characteristics, antimicrobial resistance, and serotype distribution of EOD and late-onset disease (LOD; with onset at 7-89 days of life) in the United States from 2006 to 2015 to inform IAP guidelines and vaccine development. This study used active population-based and laboratory-based surveillance for invasive GBS disease conducted through Active Bacterial Core surveillance in selected counties of 10 states across the United States. Residents of Active Bacterial Core surveillance areas who were younger than 90 days and had invasive GBS disease in 2006 to 2015 were included. Data were analyzed from December 2017 to April 2018. Group B Streptococcus isolated from a normally sterile site. Early-onset disease and LOD incidence rates and associated GBS serotypes and antimicrobial resistance. The Active Bacterial Core surveillance program identified 1277 cases of EOD and 1387 cases of LOD. From 2006 to 2015, EOD incidence declined significantly from 0.37 to 0.23 per 1000 live births (P < .001), and LOD rates remained stable (mean, 0.31 per 1000 live births). Among the mothers of 1277 infants with EOD, 617 (48.3%) had no indications for IAP and did not receive it, and 278 (21.8%) failed to receive IAP despite having indications. Serotype data were available for 1743 of 1897 patients (91.3%) from 7 sites that collect GBS isolates. Among patients with EOD, serotypes Ia (242 [27.3%]) and III (242 [27.3%]) were most common. Among patients with LOD, serotype III was most common (481 [56.2%]), and this increased from 2006 to 2015 from 0.12 to 0.20 cases per 1000 live births (P < .001). Serotype IV caused 53 cases (6.2%) of EOD and LOD combined. The 6 most common serotypes (Ia, Ib, II, III, IV, and V) caused 881 EOD cases (99.3%) and 853 LOD cases (99.7%). No β-lactam resistance was identified; 359 isolates (20.8%) tested showed constitutive clindamycin resistance. In 2015, an estimated 840 EOD cases and 1265 LOD cases occurred nationally. The rates of LOD among US infants are now higher than EOD rates. Combined with addressing IAP implementation gaps, an effective vaccine covering the most common serotypes might further reduce EOD rates and help prevent LOD, for which there is no current public health intervention.

Identifiants

pubmed: 30640366
pii: 2721003
doi: 10.1001/jamapediatrics.2018.4826
pmc: PMC6439883
mid: NIHMS1024870
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

224-233

Subventions

Organisme : Intramural CDC HHS
ID : CC999999
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : ErratumIn
Type : ErratumIn

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Auteurs

Srinivas Acharya Nanduri (SA)

Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.

Susan Petit (S)

Connecticut Department of Public Health, Hartford.

Chad Smelser (C)

New Mexico Department of Public Health, Santa Fe.

Mirasol Apostol (M)

California Emerging Infections Program, Oakland.

Nisha B Alden (NB)

Colorado Department of Public Health and Environment, Denver.

Lee H Harrison (LH)

Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.

Ruth Lynfield (R)

Minnesota Department of Health, St Paul.

Paula S Vagnone (PS)

Minnesota Department of Health, St Paul.

Kari Burzlaff (K)

New York State Department of Health, Albany.

Nancy L Spina (NL)

New York State Department of Health, Albany.

Elizabeth M Dufort (EM)

New York State Department of Health, Albany.

William Schaffner (W)

Vanderbilt University School of Medicine, Nashville, Tennessee.

Ann R Thomas (AR)

Oregon Department of Human Services, Portland.

Monica M Farley (MM)

Emory University School of Medicine, Atlanta, Georgia.
Atlanta VA Medical Center, Atlanta, Georgia.

Jennifer H Jain (JH)

Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.

Tracy Pondo (T)

Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.

Lesley McGee (L)

Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.

Bernard W Beall (BW)

Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.

Stephanie J Schrag (SJ)

Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.

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Classifications MeSH