Abstract

The issue of feasibility and effectiveness of probiotics use in newborns is still discussable. A position letter of the Committee on nutrition of the European Society for Pediatric NutritionGastroenterology, Hepatology, and(ESPGHAN) and the Working group of the ESPGHAN on probiotics and prebiotics issues was published in May 2020 in “Pediatric Gastroenterology and Nutrition” magazine as for the use of probiotics in premature newborns. The third part of the literature continues with the position paper and the results of many randomized controlled clinical trials of probiotics. The article considers the answers to 6 clinical questions posed by the working group of the Committee to assess the feasibility of use, routes of administration, dosage and duration of use, as well as the effectiveness and quality of probiotic drugs. It was proved that probiotics, in general, could decrease the level of necrotising enterocolitis, sepsis, and mortality. On the other hand, an increasing number of commercial products containing probiotics of non optimal quality are available. In addition, a large number of departments in the world regularly suggest probiotic supplements as a treatment standard despite the absence of any solid evidence. Moreover, the emphasis was placed on issues of safety of probiotic supplements for premature newborns. Guarantee of quality of probiotic product is deliverance of probiotic strains by transfer genes of resistance to antibiotics, the ability to regularly detect sepsis while using probiotics.

Highlights

  • The issue of feasibility and effectiveness of probiotics use in newborns is still discussable

  • the Working group of the ESPGHAN on probiotics and prebiotics issues was published in May 2020

  • The third part of the literature continues with the position paper

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Summary

Introduction

Після ретельного аналізу усіх досліджень [18,19,20] із залученням використання пробіотика L. rhamnosus GG (LGG) було зроблено наступні рекомендації: При дотриманні усіх умов безпеки можна умовно рекомендувати використання L. rhamnosus GG ATCC 53103 у дозі від 1 x 109 КУО до 6 x 109 КУО, оскільки це може зменшити NEC стадії 2 або 3 (низька впевненість доказів). На основі РКД, описаних вище, можна дати умовну рекомендацію щодо використання комбінації B. infantis Bb-02, B. lactis Bb-12 та Str. thermophilus TH-4 в дозі 3,0 до 3,5×108 КУО (кожного штаму) у недоношених дітей, оскільки є докази низької якості, які можуть зменшити НЕК стадії 2 або 3.

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Conclusion

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