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Association between proton pump inhibitor use and risk of pneumonia in children: nationwide self-controlled case series study in Sweden
Clinical Epidemiology Division, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Clinical Epidemiology Division, Department of Medicine, Karolinska Institutet, Stockholm, Sweden; Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
Clinical Epidemiology Division, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Örebro University, School of Medical Sciences. Örebro University Hospital. Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden; Department of Pediatrics, Örebro University Hospital, Örebro, Sweden; Celiac Disease Center, Department of Medicine, Columbia University College of Physicians and Surgeons, New York NY, USA.ORCID iD: 0000-0003-1024-5602
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2022 (English)In: BMJ Open, E-ISSN 2044-6055, Vol. 12, no 4, article id e060771Article in journal (Refereed) Published
Abstract [en]

Objective: To evaluate the association between use of proton pump inhibitors (PPIs) and risk of pneumonia in children.

Design: Nationwide register-based self-controlled case series study.

Setting: Sweden, July 2006 to December 2016.

Participants: Children aged <18 years who were treated with PPIs and had a hospitalisation or hospital emergency care visit for pneumonia within 1 year before and 2 years after PPI initiation.

Main outcomes and measures: The primary analysis examined the risk of pneumonia during the risk period (ongoing PPI treatment), the pre-exposure period (<= 30 days preceding PPI treatment) and the postexposure period (days 1-365 after PPI discontinuation), comparing to the unexposed period. Conditional Poisson regression was used to estimate incidence rate ratios (IRRs) and 95% CIs.

Results: A total of 2356 cases of pneumonia were included. Compared with the unexposed period, the risk of pneumonia was significantly increased during ongoing PPI treatment, with an adjusted IRR of 1.40 (95% CI 1.21 to 1.62). The risk of pneumonia was also increased in the pre-exposure period (adjusted IRR, 1.80, 95% CI 1.51 to 2.13), but not in the postexposure period (adjusted IRR 0.98, 95% CI 0.89 to 1.08). Dividing the risk period by time since treatment initiation, the increased risk of pneumonia was highest in the first 30 days (adjusted IRR 1.63, 95% CI 1.35 to 1.97), remained during days 31-90 (adjusted IRR 1.32, 95% CI 1.04 to 1.69), but waned in days >= 91 (IRR 1.06, 95% CI 0.79 to 1.41).

Conclusions and relevance: An increased risk of pneumonia was observed both immediately before and immediately after PPI initiation. This pattern of association can likely be explained by an underlying risk of pneumonia due to factors transiently present at the time around PPI initiation. Thus, our findings do not support a causal relationship between PPI use and risk of pneumonia.

Place, publisher, year, edition, pages
BMJ Publishing Group Ltd, 2022. Vol. 12, no 4, article id e060771
Keywords [en]
adverse events, epidemiology, paediatric infectious disease & immunisation
National Category
Pediatrics
Identifiers
URN: urn:nbn:se:oru:diva-98943DOI: 10.1136/bmjopen-2022-060771ISI: 000786631000006PubMedID: 35450917Scopus ID: 2-s2.0-85128657379OAI: oai:DiVA.org:oru-98943DiVA, id: diva2:1657457
Funder
Swedish Research Council, 2016-01974
Note

Funding agencies:

Frimurare Barnhuset Foundation

Consolidator investigator grant from Karolinska Institutet

Available from: 2022-05-11 Created: 2022-05-11 Last updated: 2023-08-28Bibliographically approved

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Ludvigsson, Jonas F.

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