Journal Article

Risk of febrile convulsions after MMRV vaccination in comparison to MMR or MMR+V vaccination

Schink, Tania, Kowalzik, Frank, Zepp, Fred, Holstiege, Jakob, Garbe, Edeltraut

2014

Overview

•First dose vaccination with the MMRV vaccine ProQuad® showed a >2-fold risk of FC compared to MMR+V.•This is the first observational study investigating the risk of FC for MMRV vaccine Priorix-Tetra™.•An increased risk of FC similar in magnitude to that of ProQuad® was observed for Priorix-Tetra™.•1 excess FC case per 2747 immunisations with Priorix-Tetra™ compared to MMR/MMR+V.•Our results suggest a class effect for these quadrivalent vaccines. In July 2006, Priorix-Tetra™, a combined measles-mumps-rubella-varicella (MMRV) vaccine, was licensed in Germany. Since a postlicensure study had shown a more than twofold elevated risk of febrile convulsions (FC) after first dose vaccination with the combined MMRV vaccine ProQuad® compared to separately administered MMR and V vaccines (MMR+V), the Paul-Ehrlich-Institute, the German regulatory agency for vaccine licensing and safety, requested a study investigating the risk of FC for Priorix-Tetra™. We performed a matched cohort study based on claims data of more than 17 million insurees in the German Pharmacoepidemiological Research Database. All children born between 01.01.2004 and 31.12.2008 who received a 1st dose of MMRV vaccine were matched to children vaccinated with MMR, MMR+V and MMR or MMR+V (combined group), respectively, by sex, age, month of vaccination and statutory health insurance. The primary outcome was defined as hospitalization with a diagnosis of FC without any alternative plausible cause of FC, e.g. an infection or neurological condition, coded as main discharge diagnosis. The secondary outcome excluded only neurological conditions to provide a more comparable outcome definition to the one used in the ProQuad® study. Numbers needed to harm (NNH), risk ratios and confounder adjusted odds ratios (ORs) with 95% CIs were estimated to compare the exposure groups. In the main risk period 5–12 days after immunization, the adjusted ORs of the primary endpoint for immunization with MMRV vaccine relative to the comparator vaccine indicated in brackets were 4.1 [95% CI 1.3–12.7; MMR], 3.5 [0.7–19.0; MMR+V], and 4.1 [1.5–11.1; MMR and MMR+V]. The corresponding ORs for the secondary outcome were 2.3 [1.4–3.9; MMR], 1.5 [0.8–2.9; MMR+V] and 2.4 [1.5–3.9; MMR and MMR+V]. This study in children younger than 5 years, 90% of them between 11 and 23 months, shows a risk of FC similar in magnitude for Priorix-Tetra™ as has previously been reported for ProQuad® suggesting a class effect for these quadrivalent vaccines.

• Publisher: Elsevier Ltd,Elsevier,Elsevier Limited
• Subject: Allergy and Immunology / Applied microbiology / Biological and medical sciences / Chickenpox Vaccine - administration & dosage / Chickenpox Vaccine - adverse effects / Child, Preschool / children / Cohort Studies / Febrile convulsion / Female / First dose / Fundamental and applied biological sciences. Psychology / Germany / Germany - epidemiology / health insurance / Hospitalization / Hospitals / Humans / Immunization / Infant / Male / Measles / Measles-Mumps-Rubella Vaccine - administration & dosage / Measles-Mumps-Rubella Vaccine - adverse effects / Microbiology / MMR / MMRV / Mumps / odds ratio / risk / seizures / Seizures, Febrile - chemically induced / Seizures, Febrile - epidemiology / Vaccination / Vaccination - adverse effects / Vaccines / Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) / Vaccines, Combined - administration & dosage / Vaccines, Combined - adverse effects