Arch. Dis. Child

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
[Advanced]

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this link to a friend
Right arrow Similar articles in ADC Online
Right arrow Similar articles in PubMed
Right arrow Add article to my folders
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Huang, F.-Y.
Right arrow Articles by Liu, S.-C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Huang, F.-Y.
Right arrow Articles by Liu, S.-C.
Arch Dis Child Fetal Neonatal Ed 1997;77:F135-F138 ( September )

Hepatitis B vaccination in preterm infants

Fu-Yuan Huang, Ping-Ing Lee, Chin-Yun Lee, Li-Min Huang, Luan-Yin Chang, Su-Chin Liu

Department of Paediatrics, Mackay Memorial Hospital, Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan

Correspondence to: Dr Chin-Yun Lee, Department of Paediatrics, National Taiwan University Hospital, 7 Chung-Shan South Road, Taipei, Taiwan.

Accepted 18 April 1997

AIM---To investigate the immunogenicity and safety of existing recommendations for hepatitis B vaccination in preterm infants.
METHODS---Recombinant hepatitis B vaccine (H-B-VAX II, 5 µg per dose) was given to 85 preterm infants divided into two groups, using two different schedules. Forty four group A infants with birthweights of < 2000 g received three doses at 1, 2, and 7 months of age. Forty one group B infants with birthweights of >= 2000 g received three doses at 0, 1, and 6 months of age.
RESULTS---After vaccination, 42 infants from group A (95%) and 37 infants from group B (90%) developed protective levels of antibody. The final seropositive rate and the geometric mean concentration of hepatitis B surface antibody between the two groups were not significantly different. The immune response of preterm infants to hepatitis B vaccines was similar to that of term infants in a previous study.
CONCLUSIONS---Preterm infants can be given hepatitis B vaccines using one of the above two different schedules, at a cutoff birthweight of 2000 g.

Keywords: hepatitis B vaccine, prematurity, antibodies


© 1997 by Archives of Disease in Childhood






HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
ARCH DIS CHILD FETAL NEONATAL ED ED PRACTICE
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 1997 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health