Oral supplementation of vitamins A and E, zinc, selenite for neonate with infection pneumonia: a randomized placebo-controlled clinical trial of 150 cases
JIANG Wei,FANG Chun-xiao,QU Ping,LIU Xing,CHEN Ke,HUANG Hong-mei,LI Ting-yu.Oral supplementation of vitamins A and E, zinc, selenite for neonate with infection pneumonia: a randomized placebo-controlled clinical trial of 150 cases[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(05):450-453.
JIANG Wei,FANG Chun-xiao,QU Ping,LIU Xing,CHEN Ke,HUANG Hong-mei,LI Ting-yu.Oral supplementation of vitamins A and E, zinc, selenite for neonate with infection pneumonia: a randomized placebo-controlled clinical trial of 150 cases[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(05):450-453.DOI:
Objective To assess the clinical efficacy of supplemental administration of vitamin A and E
zinc
and selenite for neonatal pneumonia by evaluating their effects on biochemical and immune indexes. Methods A total of 150 matched child (age30 d) with neonatal pneumonia were recruited in this randomized
double-blind
placebo-controlled
7-day clinical trial. The cases were randomly and equally divided into 3 groups
that is
VA group (4 500 IU vitamin A once per day)
multinutrient group (daily 4 500 IU vitamin A
20 mg vitamin E
9 mg zinc
and 20 g selenite) and placebo group (daily 1 ml normal sodium). Routine treatment for pneumonia were given to all patients. Before and 7 d after supplementation
their serum contents of vitamin A
retinol binding protein (RBP)
IgM and malondialdehyde (MOD) were tested by HPLC
ELISA
immunoturbidimetry
and spectrophotometry with thiobarbituric acid respectively. Vitamin A deficiency (VAD) was evaluated according to WHO standard. Results Only 111 neonates had all clinical data with VA group 37 children
multinutrient group 39
and placebo group 35
and 65 patients had clinical data and laboratory indexes
including 23 in VA group
24 in multinutrient group and 18 in placebo group. VA group and multinutrient group had a shorter recovery time in signs and symptoms than placebo group (P0.01)
but no difference was seen in these 2 supplementation groups. Among the 65 patients
the prevalence rates of serious VAD
VAD
marginal form VAD were 13.8%
26.2% and 36.9% respectively before supplementation
and the serum VA content in 2 supplementation groups were significantly higher after supplementation than before (P0.01)
but no such difference was seen in placebo group. After supplementation
there was no significant difference in serum RBP concentration in VA and multinutrient groups
but that of placebo group was obviously increased (P0.01). The serum IgM and MDA were significantly declined in VA group and multinutrient group (P0.05)
no change was seen in placebo group. No toxic symptom was observed in period of hospitalization. Conclusion Daily low-dose oral nutrient supplementation significantly promotes the release of clinical symptoms
enhances the immune function and antioxidation capacity for neonatal pneumonia
but no difference is seen between single oral administration of vitamin A and of vitamin A
E
zinc and selenite
which may be due to our short observation time. The oral multinutrient administration is safe and feasible for neonate on clinical treatment.