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Clinical Trial
. 1991 Jan;74(1):14-8.

Intravenous immunoglobulin prophylaxis for infection in very low birth-weight infants

Affiliations
  • PMID: 1902866
Clinical Trial

Intravenous immunoglobulin prophylaxis for infection in very low birth-weight infants

V Ratrisawadi et al. J Med Assoc Thai. 1991 Jan.

Abstract

The effectiveness of intravenous immunoglobulin for prevention of sepsis in very low birth weight infants was studied on 102 neonates at the Children Hospital, Bangkok from February 1988 to February 1990. Infants were randomly allocated into 3 groups of 35 each. Group I and group II received 250 mg/kg and 500 mg/kg of immunoglobulin intravenously respectively within four hours of life. Group III was not given immunoglobulin and served as the control group. It was found that during the early neonatal period the infection rate of group I (14.7%) and group II (14.7%) was significantly lower than that of group III (38.2%). There was no difference in the infection rate of group I and group II. The mortality rate was also higher in group III than in group I and group II. It suggested that the intravenous immunoglobulin dosage of 250 mg per kilogram body weight is effective as well as dosage of 500 mg per kilogram body weight in prevention of sepsis in very low birth weight infants during the early neonatal period.

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