Evidence map›Paper›PMID 42231258›Full record

ArticleBMC medicine2026

Prenatal and/or childhood acid-suppressive medication use and risk of serious infections in children: A retrospective analysis of Taiwanese medical claims data.

Tsung-Chieh Yao, Yu-Lung Hsu, Jing-Long Huang, Yen-Chen Chang, Sheng-Mao Chang, Jen-Jung Pan, Xiumei Hong, Jiu-Yao Wang, Hui-Ju Tsai

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Article in BMC medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Tsung-Chieh YaoDivision of Allergy, Asthma, and Rheumatology, Department of Pediatrics, Chang Gung Memorial Hospital, Taoyuan, Taiwan. yao@adm.cgmh.org.tw.ORCID 0000-0002-5457-1402
Yu-Lung HsuDepartment of Pediatric Infectious Diseases, China Medical University Children's Hospital, China Medical University, Taichung, Taiwan.
Jing-Long HuangDivision of Allergy, Asthma, and Rheumatology, Department of Pediatrics, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Yen-Chen ChangInstitute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan.
Sheng-Mao ChangDepartment of Statistics, National Taipei University, Taipei, Taiwan.
Jen-Jung PanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona; Banner - University Medical Center Phoenix, Phoenix, AZ, US.ORCID 0000-0001-5347-3387
Xiumei HongDepartment of Population, Family and Reproductive Health, Center on Early Life Origins of Disease, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.
Jiu-Yao WangCenter of Allergy, Immunology and Microbiome, China Medical University Hospital and Children's Hospital, Taichung, Taiwan.
Hui-Ju TsaiInstitute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan. tsaihj@nhri.edu.tw.ORCID 0000-0002-5338-6117

Funding

Chang Gung Medical Foundation OMRPG3Q0031National Health Research Institutes PH-114-PP-08National Science and Technology Council 111-2314-B-400-040-MY3National Science and Technology Council 112-2314-B-182-030-MY3; NSTC 114-2321-B-182-005
6 · The paper itself

Abstract

backgroundRecent studies suggest an increased risk of serious infections associated with proton pump inhibitor (PPI) use in young children, but no study simultaneously examined the impact of acid-suppressive medication (ASM) use during pregnancy and childhood on infection risk in children. This study aimed to investigate the associations between prenatal and/or childhood exposure to ASMs and serious infections in children.

methodsA national cohort study was conducted based on the entire medical claims data in Taiwan, comparing prenatal and/or childhood exposure to PPIs or histamine-2 receptor antagonists (H2RAs) with antacid exposure in an active-comparator design. We quantified the risks of hospitalization for overall serious infection and specific infections, including sepsis, acute bronchiolitis or bronchitis, pneumonia, acute gastroenteritis, pyelonephritis, cellulitis or soft-tissue infection, meningitis or encephalitis, and septic arthritis or osteoarthritis, among children with prenatal and/or childhood exposure to PPIs or H2RAs. Adjusted hazard ratios (AHRs) with 95% confidence intervals (CIs) were estimated using Cox proportional hazard models.

resultsAmong 195,377 mother-child pairs prenatally exposed to PPIs or H2RAs (13.39% of the prenatal cohort) and 1,263,741 pairs exposed to antacids, prenatal exposure to PPIs or H2RAs was associated with an increased risk of overall serious infection compared with antacid exposure (AHR: 1.09; 95% CI: 1.06-1.12), as well as specific infections, including sepsis (AHR: 1.21; 95% CI: 1.03-1.12), acute bronchiolitis or bronchitis (AHR: 1.07; 95% CI: 1.03-1.11), pneumonia (AHR: 1.10; 95% CI: 1.04-1.15), acute gastroenteritis (AHR: 1.12; 95% CI: 1.06-1.18), and pyelonephritis (AHR: 1.10; 95% CI: 1.02-1.19). Subgroup analyses demonstrated consistent results for PPI and H2RA exposure when analyzed separately. Childhood exposure to PPIs or H2RAs was also associated with increased risks of serious infections, with the highest risks generally observed among children exposed during both prenatal and childhood periods (AHR 1.12 for overall serious infection; AHR 1.62 for sepsis; AHR 1.29 for acute bronchiolitis or bronchitis; AHR 1.06 for pneumonia; AHR 1.30 for acute gastroenteritis; and AHR 1.24 for pyelonephritis).

conclusionsThis nationwide cohort study provides real-world evidence of an association between prenatal and childhood exposure to PPIs or H2RAs and an increased risk of serious infections in children.

Indexed as

AntacidsHistamine H2 AntagonistsInfectionsPrenatal Exposure Delayed EffectsProton Pump InhibitorsChildChild, PreschoolFemaleHospitalizationHumansInfantInfant, NewbornMalePregnancyRetrospective StudiesRisk FactorsAntacidsHistamine H2 AntagonistsProton Pump InhibitorsAcid-suppressive medicationChildrenHistamine-2 receptor antagonistProton pump inhibitorSerious infection

Identifiers

PMID42231258
PMCPMC13445769

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.