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JAMA Network Open· 2026Q1

Probiyotikler Çok Erken Doğan Bebeklerde Ölüm/NEC Riskini Azalttı

Probiotics and Risk of Death, Necrotizing Enterocolitis, and Sepsis in Very Preterm Infants

Ayoub Mitha, Sofia Söderquist Kruth, Emma Sinervo, Magnus Domellöf ve diğerleri

Kısa özet

Çok erken doğan bebeklerde (28-31 hafta gebelik) probiyotik takviyesi, ölüm ve/veya nekrotizan enterokolit (NEC) riskinde %72'lik bir azalmayla ilişkiliydi; oranlar %3,4'ten %0,8'e düştü.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Ana noktalar

  • Probiyotik takviyesi, çok erken doğan bebeklerde (28-31 hafta) ölüm ve/veya NEC (Bell evre 2-3) riskinin daha düşük olmasıyla ilişkiliydi (%0,8'e karşılık %3,4).
  • Probiyotik grubunda tek başına ölüm riski %84 (%0,3'e karşılık %1,4) ve tek başına NEC riski %75 (%0,6'ya karşılık %2,5) azaldı.
  • Çok değişkenli modelleme, gözlemlenen mortalite azalmasının %42,3'ünün azalan NEC insidansı aracılığıyla gerçekleştiğini gösterdi.
  • Probiyotik kullanımı, ölüm ve/veya kültürle kanıtlanmış sepsis riskinde azalma ile ilişkili değildi (%3,4'e karşılık %4,4).

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Özet (abstract)

Importance Probiotics are reported to benefit preterm infants, but population-based clinical evidence is limited. In 2020, the Swedish Neonatal Society issued a national recommendation to supplement very preterm infants (28 weeks 0 days’ to 31 weeks 6 days’ gestation) with probiotics. Objective To investigate whether probiotic supplementation was associated with risk of death, necrotizing enterocolitis (NEC), and/or culture-proven sepsis in infants born very preterm. Design, Setting, and Participants This population-based cohort study examined data from the Swedish Neonatal Quality Register from January 1, 2017, through December 31, 2024. Live-born, very preterm infants, excluding those who died within the first 3 days of life or due to congenital or chromosomal abnormalities, were included. Exposure Daily probiotic supplementation of 1 billion colony-forming units of freeze-dried Bifidobacterium infantis , Bifidobacterium lactis , and Streptococcus thermophilus initiated following birth and discontinued at postmenstrual week 34. Main Outcomes and Measures Composites of death and/or NEC (Bell stage 2-3), death and/or surgical NEC (Bell stage 3), and death and/or culture-proven sepsis were assessed. Modified Poisson regression, propensity score–matched, and inverse probability of treatment weighting analyses were used for replication analyses. A multivariate bayesian modeling analysis accounting for the association between NEC and mortality was performed to estimate the association between probiotic exposure and mortality. Results Among 4695 infants (mean [SD] gestational age, 30.2 [1.1] weeks; 2550 male [54.3%]), probiotic exposure increased from 0% before the national recommendation in 2020 to 16.9% in 2020 and a mean (SD) of 64.8% (4.7%) in 2021 to 2024. Probiotic supplementation vs no supplementation was associated with lower risk of death and/or NEC (rate, 0.8% vs 3.4%; adjusted relative risk [ARR], 0.28 [95% CI, 0.14-0.56]). When assessed separately, risks of death (rate, 0.3% vs 1.4%; ARR, 0.16 [95% CI, 0.06-0.45]) and NEC (rate, 0.6% vs 2.5%; ARR, 0.25 [95% CI, 0.10-0.61]) were both lower in the probiotic group. Multivariate bayesian modeling suggested that a substantial proportion of the observed mortality reduction was mediated via reduced NEC incidence (42.3% [credible interval, 16.1%-100%]). Probiotic supplementation was not associated with death and/or culture-proven sepsis (rate, 3.4% vs 4.4%; ARR, 0.86 [95% CI, 0.58-1.26]). Conclusions and Relevance This cohort study of very preterm infants found that implementation of a multistrain probiotic was associated with a significant reduction in death and/or NEC, which may help inform shared decision-making between clinicians and families. These results should not be generalized to extremely preterm infants (<28 weeks’ gestation).

Yazarların özeti; kaynağından alınmıştır. JAMA Network Open, 2026 · DOI ↗

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