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American Academy of Pediatrics
Commentary

Vaccines and Febrile Seizures: Quantifying the Risk

Mark H. Sawyer, Geoff Simon and Carrie Byington
Pediatrics July 2016, 138 (1) e20160976; DOI: https://doi.org/10.1542/peds.2016-0976
Mark H. Sawyer
aUniversity of California, San Diego Department of Pediatrics and Rady Children’s Hospital San Diego, San Diego, California;
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Geoff Simon
bNemours duPont Pediatrics, Wilmington, Delaware; and
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Carrie Byington
cDepartment of Pediatrics, University of Utah, Salt Lake City, Utah
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  • Abbreviations:
    DTaP —
    diphtheria-tetanus-acellular pertussis
    PCV —
    conjugated pneumococcal vaccine
    VSD —
    Vaccine Safety Datalink
  • Vaccines can cause fever, and fever in young children can lead to febrile seizures; these facts are not new. Febrile seizures are the most common seizure disorder of childhood and occur in ∼5% of all children, usually those younger than 24 months. We know that vaccines, often administered to children in this age group, can trigger febrile seizures. The article by Duffy et al1 in this edition of Pediatrics provides pediatric practitioners with a fairly precise estimate of how often influenza vaccine, conjugated pneumococcal vaccine (PCV), and diphtheria-tetanus-acellular pertussis (DTaP) vaccines given alone or in various combinations lead to febrile seizures. This study, conducted by the Vaccine Safety Datalink2 (VSD), and others like it, are important as we engage in dialogue with parents about the risks and benefits of vaccines.

    The VSD, started in 1990, is a collaborative project between the Centers for Disease Control and Prevention’s Immunization Safety Office and 9 health care organizations and was created to address the upsurge of concerns about vaccine safety that have marked the past 2 decades. By leveraging the collective patient populations enrolled in these large organizations and the ability to evaluate the electronic medical records of those patients, the VSD can tell us scientifically, rapidly, and with good precision what happens to people after they receive vaccines. It is perhaps the best tool we have to assess vaccine safety.

    Duffy et al1 used the VSD to follow up on observations made between 2010 and 2012 linking specific influenza vaccine products, sometimes given with other vaccines, to febrile seizures.3,4 In the current study, the VSD used its patient power to carefully evaluate the frequency of febrile seizures after influenza vaccine given during 5 seasons (2006–2007 through 2010–2011) either alone or in combinations with PCV and DTaP because these vaccines are recommended to be given together routinely. Each of these vaccines alone was already known to cause fever, so it was reasonable to think that the potential additive fevers caused when these vaccines are given at the same time could lead to febrile seizures. The authors found that, when given alone, only PCV vaccine, but none of the influenza vaccines or DTaP, were associated with an increased rate of febrile seizures. What about the combination of all 3? The answer is that febrile seizures happen, but not often. As reported by Duffy et al,1 influenza, DTaP, and PCV vaccines given together can lead to febrile seizures at a rate of up to 30 in 100 000 children immunized. This means for the average pediatrician, who may care for 1000 children younger than 5 including 3 to 500 between 6 and 24 months of age annually, one could expect to see at most 1 child who experiences a febrile seizure every 5 to 10 years due to administration of these vaccines together in the first 2 years of life.5 This would be in addition to the 30 to 75 patients in each birth year cohort in a practice that would experience a febrile seizure from other causes given the background rate of 2% to 5%.

    Does this mean we should stop giving these vaccines together or stop giving them at all? We say, emphatically, no. With the results of this study, we can accurately calculate the risks and benefits of this practice. The risk is 1 febrile seizure per pediatric practice every 5 to 10 years. Febrile seizures, although frightening to parents, rarely have any long-term sequelae.6,7 The benefits of giving these vaccines simultaneously include decreased office visits associated with painful vaccines, decreased episodes of vaccine-associated fussiness, and, most important, the assurance that children will be fully immunized and protected from infections that carry real morbidity and mortality. It is well established that the vaccines we miss when we fail to give all the vaccines we can (simultaneously at each health care visit) may never be administered to some children, thus leaving them at risk for the diseases the vaccines prevent.8 It goes without saying that influenza, diphtheria, tetanus, pertussis, and pneumococcal infections may result in serious illness. These infections also have the potential to cause fevers and febrile seizures. Without vaccines to prevent these illnesses, pediatricians would see many more than 1 case of most of these infections each decade. In fact, they would see children in their practices with both febrile seizures and life-threatening infections. The risk from these diseases far outweighs the risk from the vaccines. Fortunately, because of the surveillance and research of the VSD, we no longer need to wonder how often adverse events happen after vaccinations; instead, we can measure them scientifically, and studies like that by Duffy et al1 increase our confidence in vaccines.

    Footnotes

      • Accepted April 6, 2016.
    • Address correspondence to Mark H. Sawyer, MD, 3020 Children’s Way, #5124, San Diego, CA 92123. E-mail: mhsawyer{at}ucsd.edu
    • Opinions expressed in these commentaries are those of the author and not necessarily those of the American Academy of Pediatrics or its Committees.

    • FINANCIAL DISCLOSURE: Dr Byington has intellectual property in and receives royalties from BioFire Diagnostics, Inc (Salt Lake City, UT); Drs Sawyer and Simon have indicated they have no financial relationships relevant to this article to disclose.

    • FUNDING: Dr Byington is supported by the HA and Edna Benning Presidential Endowment; National Center for Advancing Translational Sciences of the National Institutes of Health under award 1ULTR001067. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Funded by the National Institutes of Health (NIH).

    • POTENTIAL CONFLICT OF INTEREST: The authors have indicated they have no potential conflicts of interest to disclose.

    • COMPANION PAPER: A companion to this article can be found online at www.pediatrics.org/cgi/doi/10.1542/peds.2016-0320.

    • Drs Sawyer and Simon are members and Dr Byington is the Chair of the American Academy of Pediatrics Committee on Infectious Disease. Dr Simon is the Chair of the American Academy of Pediatrics Committee on Practice and Ambulatory Medicine.

    References

    1. ↵
      1. Duffy J,
      2. Weintraub E,
      3. Hambidge SJ, et al
      . Risk of febrile seizure following vaccination among children age 6 through 23 months. Pediatrics. 2016;138(1):e20160320
    2. ↵
      1. Centers for Disease Control and Prevention
      . Vaccine Safety Datalink. Available at: www.cdc.gov/vaccinesafety/ensuringsafety/monitoring/vsd/. Accessed March 10, 2016
    3. ↵
      1. Broder KR,
      2. Martin DB,
      3. Vellozzi C
      . In the heat of a signal: responding to a vaccine safety signal for febrile seizures after 2010–11 influenza vaccine in young children, United States. Vaccine. 2012;30(11):2032–2034pmid:22361305
      OpenUrlCrossRefPubMed
    4. ↵
      1. Armstrong PK,
      2. Dowse GK,
      3. Effler PV, et al
      . Epidemiological study of severe febrile reactions in young children in Western Australia caused by a 2010 trivalent inactivated influenza vaccine. BMJ Open. 2011;1(1):e000016pmid:22021725
      OpenUrlAbstract/FREE Full Text
    5. ↵
      1. American Academy of Pediatrics
      . Profile of Pediatric Visits. 2010. Available at: https://www.aap.org/en-us/professional-resources/practice-support/financing-and-payment/Billing-and-Payment/pages/Profile-of-Pediatric-Office-Visits.aspx
    6. ↵
      1. Verity CM,
      2. Greenwood R,
      3. Golding J
      . Long-term intellectual and behavioral outcomes of children with febrile convulsions. N Engl J Med. 198;338(24):1723–1728
    7. ↵
      1. American Academy of Pediatrics
      2. Subcommittee on Febrile Seizures
      . Neurodiagnostic evaluation of the child with a simple febrile seizure. Pediatrics. 2011;127(2):389–394pmid:21285335
      OpenUrlAbstract/FREE Full Text
    8. ↵
      1. Hammer LD,
      2. Curry ES,
      3. Harlor AD, et al; Committee on Practice and Ambulatory Medicine; Council on Community Pediatrics
      . Increasing immunization coverage. Pediatrics. 2010;125(6):1295–1304pmid:20513736
      OpenUrlAbstract/FREE Full Text
    • Copyright © 2016 by the American Academy of Pediatrics
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    Vaccines and Febrile Seizures: Quantifying the Risk
    Mark H. Sawyer, Geoff Simon, Carrie Byington
    Pediatrics Jul 2016, 138 (1) e20160976; DOI: 10.1542/peds.2016-0976

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    Vaccines and Febrile Seizures: Quantifying the Risk
    Mark H. Sawyer, Geoff Simon, Carrie Byington
    Pediatrics Jul 2016, 138 (1) e20160976; DOI: 10.1542/peds.2016-0976
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