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Bovine lactoferrin supplementation for prevention of late-onset sepsis in very low-birth-weight neonates: a randomized trial

Authors :
Paolo, Manzoni
Matteo, Rinaldi
Silvia, Cattani
Lorenza, Pugni
Mario Giovanni, Romeo
Hubert, Messner
Ilaria, Stolfi
Lidia, Decembrino
Nicola, Laforgia
Federica, Vagnarelli
Luigi, Memo
Linda, Bordignon
Onofrio Sergio, Saia
Milena, Maule
Elena, Gallo
Michael, Mostert
Cristiana, Magnani
Michele, Quercia
Lina, Bollani
Roberto, Pedicino
Livia, Renzullo
Pasqua, Betta
Fabio, Mosca
Fabrizio, Ferrari
Rosario, Magaldi
Mauro, Stronati
Daniele, Farina
Elio, Caliendo
Source :
JAMA. 302(13)
Publication Year :
2009

Abstract

Sepsis is a common and severe complication in premature neonates, particularly those with very low birth weight (VLBW) (1500 g). Whether lactoferrin, a mammalian milk glycoprotein involved in innate immune host defenses, can reduce the incidence of sepsis is unknown. In animal models, the probiotic Lactobacillus rhamnosus GG (LGG) enhances the activity of lactoferrin but has not been studied in human infants.To establish whether bovine lactoferrin (BLF), alone or in combination with LGG, reduces the incidence of late-onset sepsis in VLBW neonates.Prospective, multicenter, double-blind, placebo-controlled, randomized trial conducted in 11 Italian tertiary neonatal intensive care units. Patients were 472 VLBW infants enrolled from October 1, 2007, through July 31, 2008, and assessed until discharge for development of sepsis.Infants were randomly assigned to receive orally administered BLF (100 mg/d) alone (n = 153), BLF plus LGG (6 x 10(9) colony-forming units/d) (n = 151), or placebo (n = 168) from birth until day 30 of life (day 45 for neonates1000 g at birth).First episode of late-onset sepsis, ie, sepsis occurring more than 72 hours after birth with isolation of any pathogen from blood or from peritoneal or cerebrospinal fluid.Demographic, clinical, and management characteristics of the 3 groups were similar, including type of feeding and intake of maternal milk. Incidence of late-onset sepsis was significantly lower in the BLF and BLF plus LGG groups (9/153 [5.9%] and 7/151 [4.6%], respectively) than in the control group receiving placebo (29/168 [17.3%]) (risk ratio, 0.34; 95% confidence interval, 0.17-0.70; P = .002 for BLF vs control and risk ratio, 0.27; 95% confidence interval, 0.12-0.60; P.001 for BLF plus LGG vs control). The decrease occurred for both bacterial and fungal sepsis. No adverse effects or intolerances to treatment occurred.Compared with placebo, BLF supplementation alone or in combination with LGG reduced the incidence of a first episode of late-onset sepsis in VLBW neonates.isrctn.org Identifier: ISRCTN53107700.

Details

ISSN :
15383598
Volume :
302
Issue :
13
Database :
OpenAIRE
Journal :
JAMA
Accession number :
edsair.pmid..........f3e07386dd3a14ad76e1c8f4dcc18f39