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Infantile Colic Treated With Bifidobacterium longum CECT7894 and Pediococcus pentosaceus CECT8330: A Randomized, Double-Blind, Placebo-Controlled Trial.
Chen, Ke; Liu, Changqi; Li, Hua; Lei, Yuehua; Zeng, Chenggui; Xu, Shuhong; Li, Jianqiu; Savino, Francesco.
Afiliación
  • Chen K; Department of Nutrition, Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
  • Liu C; Department of Child Health Care, Angel Children's Hospital, Chengdu, China.
  • Li H; School of Exercise and Nutritional Sciences, San Diego State University, San Diego, CA, United States.
  • Lei Y; Department of Child Health Care, Qingbaijiang Maternal and Child Health Hospital, Chengdu, China.
  • Zeng C; Department of Child Health Care, Qingbaijiang Maternal and Child Health Hospital, Chengdu, China.
  • Xu S; Department of Child Health Care, Chengdu Caojiaxiang Community Healthcare Center, Chengdu, China.
  • Li J; Department of Child Health Care, Huili Maternity and Child Care Center, Huili, China.
  • Savino F; Department of Child Health Care, Angel Children's Hospital, Chengdu, China.
Front Pediatr ; 9: 635176, 2021.
Article en En | MEDLINE | ID: mdl-34568236
ABSTRACT

Background:

Colic is a common condition in infants <4 months of age. Attempts to treat infantile colic with probiotics have shown variable efficacy and overall low evidence of success. In this work, we tested the hypothesis that oral administration of Bifidobacterium longum CECT7894 (KABP042) and Pediococcus pentosaceus CECT8330 (KABP041) mix (1 × 109 colony forming units) would improve the symptoms of infantile colic.

Methods:

A total of 112 exclusively breastfed or mixed fed infants aged <2 months and meeting the ROME IV criteria for infantile colic were recruited. The infants were randomized in a double-blind, placebo-controlled trial to receive orally administered probiotics (intervention group, IG, n = 48) or placebo (placebo group, PG, n = 42) daily for 21 days.

Results:

Infants in the IG had significantly shorter crying time (p < 0.001) on day 7 [IG vs. PG, median (25-75th percentile) 38 (3.5-40.5) vs. 62 (40-108) min/day], day 14 [IG vs. PG 20 (0-40) vs. 50 (30-75) min/day], and day 21 [IG vs. PG 14 (0-33) vs. 40 (28-62) min/day]. Higher responder ratio and fewer crying/fussing episodes on days 7, 14, and 21 and better stool consistency on day 21 were observed in the IG (p < 0.01) as compared to the PG. Conversely, no significant effects on stool frequency or quality of life were observed.

Conclusions:

In summary, daily oral administration of B. longum CECT7894 (KABP042) and P. pentosaceus CECT8330 (KABP041) was an effective treatment for shortening crying time due to infantile colic and for improving fecal consistency. This trial was registered retrospectively in December 2019 with a trial number of ISRCTN92431452.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Front Pediatr Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Front Pediatr Año: 2021 Tipo del documento: Article País de afiliación: China