Abstract
Fifty preterm babies were randomly assigned to a group given oral bucolome (30 mg/kg per day for 5 days) and a control group. Serum bilirubin levels of the treated infants from day 4 onwards were consistently lower than those of the control infants. 3 of the 25 control infants (but none of the 25 treated infants) had bilirubin levels greater than 18 mg/100 ml (308 mumol/l) and required exchange transfusion. No sedation or drowsiness was observed in the infants given bucolome, and though the drug caused some vomiting, weight gains were unaffected.
Lingua originale | English |
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pagine (da-a) | 549-550 |
Numero di pagine | 2 |
Rivista | Archives of Disease in Childhood |
Volume | 52 |
DOI | |
Stato di pubblicazione | Pubblicato - 1977 |
Pubblicato esternamente | Sì |
Keywords
- Barbiturates
- Clinical Trials as Topic
- Female
- Humans
- Infant, Newborn
- Infant, Premature, Diseases
- Jaundice, Neonatal
- Male