Kawasaki Disease Following the 13-valent Pneumococcal Conjugate Vaccine and Rotavirus Vaccines

Author:

Kamidani Satoshi12,Panagiotakopoulos Lakshmi2,Licata Charles2,Daley Matthew F.3,Yih W. Katherine4,Zerbo Ousseny5,Tseng Hung Fu6,DeSilva Malini B.7,Nelson Jennifer C.8,Groom Holly C.9,Williams Joshua T.B.10,Hambidge Simon J.10,Donahue James G.11,Belay Ermias D.12,Weintraub Eric S.2

Affiliation:

1. aThe Center for Childhood Infections and Vaccines of Children’s Healthcare of Atlanta and the Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia

2. bImmunization Safety Office, Centers for Disease Control and Prevention, Atlanta, Georgia

3. cInstitute for Health Research, Kaiser Permanente Colorado, Denver, Colorado

4. dThe Harvard Pilgrim Health Care Institute, Boston, Massachusetts

5. eKaiser Permanente Northern California, Vaccine Study Center, Oakland, California

6. fKaiser Permanente Southern California, Pasadena, California

7. gHealthPartners Institute, Bloomington, Minnesota

8. hKaiser Permanente Washington Health Research Institute, Seattle, Washington

9. iCenter for Health Research, Kaiser Permanente Northwest, Portland, Oregon

10. jAmbulatory Care Services, Denver Health, Denver, Colorado

11. kMarshfield Clinic Research Institute, Marshfield, Wisconsin

12. lDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia

Abstract

BACKGROUND Temporal associations between Kawasaki disease (KD) and childhood vaccines have been reported. Limited data on KD following 13-valent pneumococcal conjugate (PCV13) and rotavirus vaccines are available. METHODS We conducted a self-controlled risk interval study using Vaccine Safety Datalink electronic health record data to investigate the risk of KD following PCV13 and rotavirus vaccines in children <2 years of age who were born from 2006 to 2017. All hospitalized KD cases identified by International Classification of Diseases diagnosis codes that fell within predefined risk (days 1–28 postvaccination) and control (days 29–56 for doses 1 and 2, and days 43–70 for doses 3 and 4) intervals were confirmed by manual chart review. RESULTS During the study period, 655 cases of KD were identified by International Classification of Diseases codes. Of these, 97 chart-confirmed cases were within risk or control intervals. In analyses, the age-adjusted relative risk for KD following any dose of PCV13 was 0.75 (95% confidence interval, 0.47–1.21). Similarly, the age-adjusted relative risk for KD following any dose of rotavirus vaccine was 0.66 (95% CI, 0.40–1.09). Overall, there was no evidence of an elevated risk of KD following PCV13 or rotavirus vaccines by dose. In addition, no statistically significant temporal clustering of KD cases was identified during days 1 to 70 postvaccination. CONCLUSIONS PCV13 and rotavirus vaccination were not associated with an increased risk of KD in children <2 years of age. Our findings provide additional evidence for the overall safety of PCV13 and rotavirus vaccines.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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