Literature DB >> 17035735

Fever as a marker of reactogenicity of an acellular pertussis-containing hexavalent vaccine (HEXAVAC) in a large-scale, open, randomized safety study in healthy French infants.

Philippe Reinert1, Anne Fiquet, Stéphane Thomas, Anne Schuyleman, Michael Watson.   

Abstract

OBJECTIVE: New multivalent vaccines simplify childhood immunisation schedules and can increase vaccination coverage. However, they must have a reactogenicity profile which is acceptable and comparable with that of previously available vaccines. The objective of this trial was to assess the incidence of fever of 40.0 degrees C or higher following vaccination with HEXAVAC or concomitant PENTACOQ and HBVAXPRO. STUDY
DESIGN: This was an open, randomized, pragmatic, post-licensure multicenter trial performed in France. Infants were randomly assigned to receive either a single injection of a hexavalent, aP-containing vaccine (HEXAVAC) or separate injections of a pentavalent, wP-containing vaccine (PENTACOQ) and Hepatitis B vaccine (HBVAXPRO) at 2, 3 and 4 months of age. Both groups received a HEXAVAC booster at 12-18 months of age. RESULTS AND DISCUSSION: 7151 infants were enrolled in 389 centers. During the combined three-day periods following the primary series injections, the incidence of fever of 40.0 degrees C or higher with HEXAVAC was not greater than with [PENTACOQ and HBVAXPRO]. The incidence of fever at thresholds of 38.0 degrees C, 38.5 degrees C, 39.0 degrees C and 39.5 degrees C was significantly lower in the HEXAVAC group. The vaccine attributable risk for fever of 40.0 degrees C following the booster injection with HEXAVAC was statistically acceptable.
CONCLUSION: The incidence of fever of 40.0 degrees C or higher in this study was very low and similar in both groups (HEXAVAC or [PENTACOQ + HBVAXPRO] as a three-dose primary series). Fever > or =38.0 degrees C and < or =39.5 degrees C was significantly less frequent following administration of HEXAVAC. The incidence of fever of 40.0 degrees C or higher following a HEXAVAC booster dose was low in all infants studied.

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Year:  2006        PMID: 17035735     DOI: 10.4161/hv.2.5.3220

Source DB:  PubMed          Journal:  Hum Vaccin        ISSN: 1554-8600


  3 in total

Review 1.  Is the large simple trial design used for comparative, post-approval safety research? A review of a clinical trials registry and the published literature.

Authors:  Robert F Reynolds; Joanna A Lem; Nicolle M Gatto; Sybil M Eng
Journal:  Drug Saf       Date:  2011-10-01       Impact factor: 5.606

Review 2.  Whole-cell pertussis vaccine in early infancy for the prevention of allergy in children.

Authors:  Gladymar Perez Chacon; Jessica Ramsay; Christopher G Brennan-Jones; Marie J Estcourt; Peter Richmond; Patrick Holt; Tom Snelling
Journal:  Cochrane Database Syst Rev       Date:  2021-09-06

Review 3.  Vaccination in elite athletes.

Authors:  Barbara C Gärtner; Tim Meyer
Journal:  Sports Med       Date:  2014-10       Impact factor: 11.136

  3 in total

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