The Mortality of Congenital Syphilis.


Journal

The Journal of pediatrics
ISSN: 1097-6833
Titre abrégé: J Pediatr
Pays: United States
ID NLM: 0375410

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 19 02 2023
revised: 09 07 2023
accepted: 26 07 2023
medline: 27 11 2023
pubmed: 4 8 2023
entrez: 3 8 2023
Statut: ppublish

Résumé

To document the case-fatality rate (CFR) of congenital syphilis diagnosed by molecular tools and rabbit infectivity testing (RIT) of clinical specimens in addition to standard evaluation and to compare that with the CFR using the Centers for Disease Control and Prevention (CDC) surveillance case definition. Prospective, single site, cohort study of all cases of syphilis among mothers and their infants from 1984 to 2002. The diagnosis of congenital syphilis was determined using IgM immunoblotting, polymerase chain reaction, and RIT of fetal or infant specimens in addition to clinical, laboratory, and radiographic criteria. Data were retrospectively reviewed to ascertain fetal and neonatal mortality. During the 18-year study, there were 191 cases of congenital syphilis confirmed by abnormalities on clinical, laboratory, or radiographic evaluation and/or positive serum IgM immunoblot, blood polymerase chain reaction, or blood/cerebrospinal fluid RIT. Of the 191 cases, 59 died for a CFR of 31%. Of the 59 deaths, 53 (90%) were stillborn and 6 (10%) died in the neonatal period. The majority (74%, 39/53) of stillbirths occurred in the third trimester. The CDC surveillance case definition correctly identified all infants with congenital syphilis, but the CDC CFR was 10% which underestimated the CFR by more than 300%. Our findings corroborate the high sensitivity of the CDC surveillance definition for congenital syphilis but highlight its poor estimation of its associated mortality. The CFR among infected progeny of pregnant women with syphilis was 31%, due mostly to demise in the third trimester and as such highlights the need for detection and appropriate treatment of syphilis during pregnancy.

Identifiants

pubmed: 37536483
pii: S0022-3476(23)00513-9
doi: 10.1016/j.jpeds.2023.113650
pii:
doi:

Substances chimiques

Immunoglobulin M 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113650

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest National Institutes of Health (1 R29 AI 34932-01 to PJS) and Centers for Disease Control and Prevention (C1000 689 to PJS, GDW). The authors declare no conflicts of interest.

Auteurs

Phillip S Wozniak (PS)

University of Missouri Kansas City, Kansas City, MO; Children's Mercy Hospital, Kansas City, MO; University of Texas Southwestern Medical Center, Dallas, TX; Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, OH.

Joseph B Cantey (JB)

University of Texas Southwestern Medical Center, Dallas, TX; University of Texas Health Science Center at San Antonio, San Antonio, TX.

Fiker Zeray (F)

University of Texas Southwestern Medical Center, Dallas, TX.

Nora K Leos (NK)

University of Texas Southwestern Medical Center, Dallas, TX.

Ian C Michelow (IC)

Connecticut Children's Medical Center, University of Connecticut School of Medicine, Hartford, CT.

Jeanne S Sheffield (JS)

University of Texas Southwestern Medical Center, Dallas, TX; Johns Hopkins University School of Medicine, Baltimore, MD.

George D Wendel (GD)

University of Texas Southwestern Medical Center, Dallas, TX.

Pablo J Sánchez (PJ)

University of Texas Southwestern Medical Center, Dallas, TX; Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, OH. Electronic address: Pablo.Sanchez@NationwideChildrens.org.

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Classifications MeSH