Post-licensure safety surveillance study of routine use of quadrivalent meningococcal diphtheria toxoid conjugate vaccine (MenACWY-D) in infants and children

被引:13
|
作者
Hansen, J. [1 ]
Zhang, L. [1 ]
Eaton, A. [1 ]
Baxter, R. [1 ]
Robertson, C. A. [2 ]
Decker, M. D. [2 ,3 ]
Greenberg, D. P. [2 ,4 ]
Bassily, E. [2 ]
Klein, N. P. [1 ]
机构
[1] Kaiser Permanente Vaccine Study Ctr, 1 Kaiser Plaza 16B, Oakland, CA 94612 USA
[2] Sanofi Pasteur, 1 Discovery Dr, Swiftwater, PA 18370 USA
[3] Vanderbilt Univ, Sch Med, Dept Hlth Policy, Nashville, TN 37212 USA
[4] Univ Pittsburgh, Sch Med, Dept Pediat, 3550 Terrace St, Pittsburgh, PA 15261 USA
关键词
Meningitis; Meningococcal infections; Meningococcal vaccines; ATTENUATED INFLUENZA VACCINE; GUILLAIN-BARRE-SYNDROME; ADVERSE EVENTS; IMMUNOGENICITY; RISK;
D O I
10.1016/j.vaccine.2018.02.107
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Menactre (R) vaccine (MenACWY-D) was licensed in the United States in 2005 for persons 1155 years of age, in 2007 for children 2-10 years of age, and in 2011 for infants/toddlers 9-23 months of age. We conducted two studies at Kaiser Permanente Northern California (KPNC), an integrated health care organization, to assess the safety of MenACWY-D in 2-10-year-olds and 9-23-month-olds receiving the vaccine during routine clinical care. Methods: We conducted observational, retrospective studies of MenACWY-D in 2-10-year-olds (October 2007-October 2010) and in 9-23-month-olds (June 2011-june 2014). We monitored all subjects for non elective hospitalizations, emergency department visits, and selected outpatient outcomes (specified neurological conditions, hypersensitivity reactions and new-onset autoimmune diseases) up to 6 months after vaccination, depending on the study. Using a self-control risk-interval design, we calculated incidence rate ratios (IRRs) comparing outcomes during the post-vaccination risk interval (0-30 days) with those during more remote post-vaccination comparison intervals (31-60 and 31-180 days [children] or 31-75 days [infants/toddlers]). Results: There were 1421 children aged 2-10 years and 116 infants/toddlers aged 9-23 months who received MenACWY-D. Approximately 30% of the 2-10-year-olds and 67% of the 9-23-month-olds were considered at increased risk of meningococcal disease. Among 2-10-year-olds, there was 1 hospitalization on post-vaccination day 5 for fever, which was considered possibly related to vaccination. The only significantly elevated outcome among 2-10-year-olds was cellulitis/abscess (2 cases occurred during the risk interval versus 0 during comparison interval; IRR not evaluable [NE], 95% CI: 1.42, NE). After medical record review, the 2 cases were considered unrelated to vaccination. Among 9-23-month-olds, no outcomes were significantly elevated after vaccination and there were no hospitalizations. There were no deaths observed during the three-year accrual and subsequent six-month surveillance period for either study. Conclusions: Immunization of infants and young children with MenACWY-D vaccine was not associated with any new safety concerns; however, these small studies had limited power to detect rare or uncommon safety events. (C) 2018 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:2133 / 2138
页数:6
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