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Acute Demyelinating Events Following Vaccines: A Case-Centered Analysis.
Baxter, Roger; Lewis, Edwin; Goddard, Kristin; Fireman, Bruce; Bakshi, Nandini; DeStefano, Frank; Gee, Julianne; Tseng, Hung Fu; Naleway, Allison L; Klein, Nicola P.
Afiliação
  • Baxter R; Northern California Kaiser Permanente Vaccine Study Center, Oakland.
  • Lewis E; Northern California Kaiser Permanente Vaccine Study Center, Oakland.
  • Goddard K; Northern California Kaiser Permanente Vaccine Study Center, Oakland.
  • Fireman B; Northern California Kaiser Permanente Vaccine Study Center, Oakland.
  • Bakshi N; Permanente Medical Group, Antioch, California.
  • DeStefano F; Immunization Safety Office, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Gee J; Immunization Safety Office, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Tseng HF; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena.
  • Naleway AL; Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon.
  • Klein NP; Northern California Kaiser Permanente Vaccine Study Center, Oakland.
Clin Infect Dis ; 63(11): 1456-1462, 2016 Dec 01.
Article em En | MEDLINE | ID: mdl-27585798
BACKGROUND: Case reports have suggested that vaccines may trigger transverse myelitis (TM) or acute disseminated encephalomyelitis (ADEM), but the evidence for a causal association is inconclusive. We analyzed the association of immunization and subsequent development of TM or ADEM. METHODS: We identified all cases of TM and ADEM in the Vaccine Safety Datalink population. Using a case-centered method, we compared vaccination of each case to vaccination of all matched persons in the study population, who received the same type of vaccine, with respect to whether or not their vaccination occurred during a predetermined exposure interval. We calculated a risk difference (excess risk) of TM and ADEM for each vaccine. RESULTS: Following nearly 64 million vaccine doses, only 7 cases of TM and 8 cases of ADEM were vaccinated during the primary exposure window 5-28 days prior to onset. For TM, there was no statistically significant increased risk of immunization. For ADEM, there was no statistically significant increased risk following any vaccine except for Tdap (adolescent and adult tetanus, reduced diphtheria, acellular pertussis) vaccine. Based on 2 exposed cases, the odds ratio for Tdap exposure 5-28 days prior to ADEM onset was 15.8 (95% confidence interval [CI], 1.2-471.6; P = .04), and the estimated excess risk was 0.385 (95% CI, -.04 to 1.16) cases per million doses. CONCLUSIONS: We found no association between TM and prior immunization. There was a possible association of ADEM with Tdap vaccine, but the excess risk is not likely to be more than 1.16 cases of ADEM per million vaccines administered.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas / Encefalomielite Aguda Disseminada / Mielite Transversa Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas / Encefalomielite Aguda Disseminada / Mielite Transversa Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article