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Diarrhea events in offspring exposed to tumour necrosis factor inhibitors and rotavirus vaccine: a population-based cohort study

Rheumatology (Oxford). 2026 Apr 3:keag161. doi: 10.1093/rheumatology/keag161. Online ahead of print.

ABSTRACT

OBJECTIVES: Previously, tumour necrosis factor inhibitors (TNFi)-exposed infants were recommended to withhold rotavirus vaccination until 6 months due to infection risk. Guidelines have recently supported earlier vaccination, although safety data remain limited. We aimed to compare diarrhea risk (during early [1.5-6 months] and later [6-24 months] infancy) in TNFi-exposed infants who received rotavirus vaccination before 6 months vs those unvaccinated by 6 months.

METHODS: We identified 3,167 TNFi-exposed offspring in MarketScan commercial claims born to mothers with chronic inflammatory diseases between 2011-2021. Early vaccination was defined as ≥ 1 rotavirus dose between 1.5-6 months and modelled as time-varying. Diarrhea events were identified using ICD-9/10 codes from hospitalizations, outpatient visits, or emergency department visits. Cox proportional hazards models estimated hazard ratios (HR) and 95% confidence intervals (CI) for diarrhea events in vaccinated vs unvaccinated infants.

RESULTS: Among TNFi-exposed offspring, no statistically significant association was found between early vaccination and diarrhea risk during early (101 events; HR 1.04; 95% CI 0.65, 1.68) or later infancy (283 events; HR 1.16; 95% CI 0.87, 1.55). Patterns remained consistent among infants exposed to TNFi in the third trimester (1.5-6 months: HR 1.07; 95% CI 0.62, 1.85; 6-24 months: HR 1.10; 95% CI 0.79, 1.52) and those exposed to high-placental transfer TNFi in the third trimester (1.5-6 months: HR 0.93; 95% CI 0.51, 1.70; 6-24 months: HR 1.09; 95% CI 0.77, 1.56).

CONCLUSION: Eaxsrly rotavirus vaccination in TNFi-exposed infants did not increase diarrhea risk, even for those exposed late in pregnancy. Findings support early vaccination and reinforce updated recommendations.

PMID:41934107 | DOI:10.1093/rheumatology/keag161

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