The Risk of Immune Thrombocytopenic Purpura After Vaccination in Children and Adolescents

Author:

O'Leary Sean T.123,Glanz Jason M.3,McClure David L.3,Akhtar Aysha4,Daley Matthew F.13,Nakasato Cynthia5,Baxter Roger6,Davis Robert L.7,Izurieta Hector S.4,Lieu Tracy A.89,Ball Robert4

Affiliation:

1. Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado;

2. Children's Outcomes Research Program, Children's Hospital Colorado, Aurora, Colorado;

3. Institute for Health Research, Kaiser Permanente Colorado, Denver, Colorado;

4. Center for Biologics Evaluation and Research, Food and Drug Administration, Rockville, Maryland;

5. Center for Health Research Hawaii, Kaiser Permanente Hawaii, Honolulu, Hawaii;

6. Kaiser Permanente Vaccine Study Center, Oakland, California;

7. Center for Health Research Southeast, Kaiser Permanente of Georgia, Atlanta, Georgia;

8. Center for Child Health Care Studies, Department of Ambulatory Care and Prevention, Harvard Pilgrim Health Care Institute, Boston, Massachusetts; and

9. Division of General Pediatrics, Children’s Hospital Boston, Massachusetts

Abstract

BACKGROUND: The risk of immune thrombocytopenic purpura (ITP) after childhood vaccines other than measles-mumps-rubella vaccine (MMR) is unknown. METHODS: Using data from 5 managed care organizations for 2000 to 2009, we identified a cohort of 1.8 million children ages 6 weeks to 17 years. Potential ITP cases were identified by using diagnostic codes and platelet counts. All cases were verified by chart review. Incidence rate ratios were calculated comparing the risk of ITP in risk (1 to 42 days after vaccination) and control periods. RESULTS: There were 197 chart-confirmed ITP cases out of 1.8 million children in the cohort. There was no elevated risk of ITP after any vaccine in early childhood other than MMR in the 12- to 19-month age group. There was a significantly elevated risk of ITP after hepatitis A vaccine at 7 to 17 years of age, and for varicella vaccine and tetanus-diphtheria-acellular pertussis vaccine at 11 to 17 years of age. For hepatitis A, varicella, and tetanus-diphtheria-acellular pertussis vaccines, elevated risks were based on one to two vaccine-exposed cases. Most cases were acute and mild with no long-term sequelae. CONCLUSIONS: ITP is unlikely after early childhood vaccines other than MMR. Because of the small number of exposed cases and potential confounding, the possible association of ITP with hepatitis A, varicella, and tetanus-diphtheria-acellular pertussis vaccines in older children requires further investigation.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Reference43 articles.

1. Thrombocytopenic purpura following measles;Fisher;Arch Dis Child,1952

2. Effect of live measles vaccine on the platelet count;Oski;N Engl J Med,1966

3. Thrombocytopenic purpura after isolated or combined vaccination against measles, mumps and rubella [in French];Autret;Therapie,1996

4. Thrombocytopenia after immunization with measles vaccines: review of the vaccine adverse events reporting system (1990 to 1994);Beeler;Pediatr Infect Dis J,1996

5. MMR vaccine and idiopathic thrombocytopaenic purpura;Black;Br J Clin Pharmacol,2003

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