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Title: | Inborn Errors of Immunity in Children With Invasive Pneumococcal Disease: A Multicenter Prospective Study | Authors: | Phuong, Linny Kimly Cheung, Abigail Agrawal, Rishi Butters, Coen Buttery, Jim Clark, Julia Connell, Tom Curtis, Nigel Daley, Andrew J. Dobinson, Hazel C. Frith, Catherine Hameed, Nadha Shahul Hernstadt, Hayley Krieser, David M. Loke, Paxton Ojaimi, Samar McMullan, Brendan Pinzon-Charry, Alberto Sharp, Ella Grace Sinnappurajar, Praisoody Templeton, Tiarni Wen, Sophie Cole, Theresa Gwee, Amanda |
Issue Date: | 2023 | Source: | The Pediatric infectious disease journal, 2023 (42) 10 p.908-913 | Pages: | 908-913 | Journal Title: | The Pediatric infectious disease journal | Abstract: | Background: In settings with universal conjugate pneumococcal vaccination, invasive pneumococcal disease (IPD) can be a marker of an underlying inborn error of immunity. The aim of this study was to determine the prevalence and characterize the types of immunodeficiencies in children presenting with IPD.; Methods: Multicenter prospective audit following the introduction of routinely recommended immunological screening in children presenting with IPD. The minimum immunological evaluation comprised a full blood examination and film, serum immunoglobulins (IgG, IgA and IgM), complement levels and function. Included participants were children in whom Streptococcus pneumoniae was isolated from a normally sterile site (cerebrospinal fluid, pleura, peritoneum and synovium). If isolated from blood, features of sepsis needed to be present. Children with predisposing factors for IPD (nephrotic syndrome, anatomical defect or malignancy) were excluded.; Results: Overall, there were 379 episodes of IPD of which 313 (83%) were eligible for inclusion and 143/313 (46%) had an immunologic evaluation. Of these, 17/143 (12%) were diagnosed with a clinically significant abnormality: hypogammaglobulinemia (n = 4), IgA deficiency (n = 3), common variable immunodeficiency (n = 2), asplenia (n = 2), specific antibody deficiency (n = 2), incontinentia pigmenti with immunologic dysfunction (n = 1), alternative complement deficiency (n = 1), complement factor H deficiency (n = 1) and congenital disorder of glycosylation (n = 1). The number needed to investigate to identify 1 child presenting with IPD with an immunologic abnormality was 7 for children under 2 years and 9 for those 2 years old and over.; Conclusions: This study supports the routine immune evaluation of children presenting with IPD of any age, with consideration of referral to a pediatric immunologist.; Competing Interests: The authors have no funding or conflicts of interest to disclose. (Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.) | DOI: | 10.1097/INF.0000000000004004 | Resources: | https://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=mdc&AN=37463351&site=ehost-live |
Appears in Sites: | Children's Health Queensland Publications |
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