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FinalExamination For Clinical Efficacy of LF in Neonates
FinalExamination For Clinical Efficacy of LF in Neonates
Efficacy of Lf in Neonates
Reem Yahya Mohamed
- VLBW infants carry an enhanced risk for bacterial sepsis and
potentially devastating sequelae and are frequently unable to
tolerate feeds (thus depriving them of the protective benefits
of maternal
milk)
Duration: 4 – 6 weeks
Outcome: Significantly lower invasive infections in the treatment groups, with an effect on infection-
related mortality (0% for bLf and 0.7% for bLf plus LGG, vs. 4.8% for placebo).
A follow-up study from the same group in 2014
found that bLf supplementation alone or in
combination with LGG significantly reduced the
incidence of ≥ stage 2 NEC, and of death-and/or ≥
stage 2 NEC in VLBW neonates
In 2015, another study has also examined bovine Lf and found that treatment with bLf
led to a reduction in infection in both VLBW and 500–2500 g neonates:
- oral bLf vs placebo
- Initiation: as soon as the patient started oral or NG feeding
- Duration : 4 weeks
- Outcome : primary: decreased risk of 1st episode of LOS
secondary :- decreased frequency of culture proven sepsis
- decreased incidence of NEC
- shorter duration of hospitalization
- decreased overall mortality rate
NB : none of these investigations noted any
adverse effects or intolerance with bovine Lf.
CONCLUSION:
• Significant evidence supporting the LF direct anti microbial and
immune boosting properties and effect on gut proliferation ,
maturation & development of beneficial bacteria .
• Lactoferrin supplementation to enteral feeding with or without
probiotics decrease late onset sepsis, NEC stage II or III in P.T infants
without adverse effects .
• LF is well tolerated by most infants
• Early supplementation may mimic the higher LF in human colostrum
& may allow for early gut proliferation.
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