Incidence of Guillain-Barre Syndrome After COVID-19 Vaccination in the Vaccine Safety Datalink

被引:85
|
作者
Hanson, Kayla E. [1 ]
Goddard, Kristin [2 ]
Lewis, Ned [2 ]
Fireman, Bruce [2 ]
Myers, Tanya R. [3 ]
Bakshi, Nandini [4 ]
Weintraub, Eric [3 ]
Donahue, James G. [1 ]
Nelson, Jennifer C. [5 ]
Xu, Stan [6 ]
Glanz, Jason M. [7 ]
Williams, Joshua T. B. [8 ]
Alpern, Jonathan D. [9 ]
Klein, Nicola P. [2 ]
机构
[1] Marshfield Clin Res Inst, Marshfield, WI USA
[2] Kaiser Permanente Northern Calif, Kaiser Permanente Vaccine Study Ctr, One Kaiser Plaza,16th Flr, Oakland, CA 94612 USA
[3] Ctr Dis Control & Prevent, Immunizat Safety Off, Atlanta, GA USA
[4] Permanente Med Grp Inc, Oakland, CA USA
[5] Kaiser Permanente Washington Hlth Res Inst, Washington, DC USA
[6] Kaiser Permanente Southern Calif, Res & Evaluat, Pasadena, CA USA
[7] Kaiser Permanente Colorado Inst Hlth Res, Denver, CO USA
[8] Denver Hlth & Hosp Author, Ambulatory Care Serv, Denver, CO USA
[9] HealthPartners Inst, Minneapolis, MN USA
关键词
PRACTICES INTERIM RECOMMENDATION; UNITED-STATES; IMMUNIZATION PRACTICES; ADVISORY-COMMITTEE; JANSSEN JOHNSON; GUIDELINES;
D O I
10.1001/jamanetworkopen.2022.8879
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE Postauthorization monitoring of vaccines in a large population may detect rare adverse events not identified in clinical trials such as Guillain-Barre syndrome (GBS), which has a background rate of 1 to 2 per 100 000 person-years. OBJECTIVE To describe cases and incidence of GBS following COVID-19 vaccination and assess the risk of GBS after vaccination for Ad.26.COV25 (Janssen) and mRNA vaccines. DESIGN, SETTING, AND PARTICIPANTS This cohort study used surveillance data from the Vaccine Safety Datalink at 8 participating integrated health care systems in the United States. There were 10 158 003 participants aged at least 12 years. Data analysis was performed from November 2021 to February 2022. EXPOSURES Ad.26.COV2.S, BNT162b2 (Pfizer-BioNTech), or mRNA-1273 (Moderna) COVI D-19 vaccine, including mRNA vaccine doses land 2, December 13, 2020, to November 13, 2021. MAIN OUTCOMES AND MEASURES G BS with symptom onset in the 1 to 84 days after vaccination, confirmed by medical record review and adjudication. Descriptive characteristics of confirmed cases, GBS incidence rates during postvaccination risk intervals after each type of vaccine compared with the background rate, rate ratios (RRs) comparing GBS incidence in the 1 to 21 vs 22 to 42 days postvaccination, and RRs directly comparing risk of GBS after Ad.26.COV2.S vs mRNA vaccination, using Poisson regression adjusted for age, sex, race and ethnicity, site, and calendar day. RESULTS From December 13, 2020, through November 13, 2021, 15 120 073 doses of COVID-19 vaccines were administered to 7 894 989 individuals (mean [SE] age, 46.5 [0.02] years; 8 138 318 doses received [53.8%] by female individuals; 3 671 199 doses received [24.3%] by Hispanic or Latino individuals, 2 215 064 doses received [14.7%] by Asian individuals, 6 266 424 doses received [41.4%] by White individuals), including 483 053 Ad.26.COV2.S doses, 8 806 595 BNT162b2 doses, and 5 830 425 mRNA-1273 doses. Eleven cases of GBS after Ad.26.COV2.S were confirmed. The unadjusted incidence rate of GBS per 100 000 person-years in the Ito 21 days after Ad.26.COV25 was 32.4 (95% CI, 14.8-61.5), significantly higher than the background rate, and the adjusted RR in the 1 to 21 vs 22 to 42 days following Ad.26.COV2.S was 6.03 (95% CI, 0.79-147.79). Thirty-six cases of GBS after mRNA vaccines were confirmed. The unadjusted incidence rate per 100 000 person-years in the 1 to 21 days after mRNA vaccines was 1.3 (95% CI, 0.7-2.4) and the adjusted RR in the 1 to 21 vs 22 to 42 days following mRNA vaccines was 0.56 (95% CI, 0.21-1.48). In a head-to-head comparison of Ad.26.COV2.S vs mRNA vaccines, the adjusted RR was 20.56 (95% CI, 6.94-64.66). CONCLUSIONS AND RELEVANCE In this cohort study of COVID-19 vaccines, the incidence of G BS was elevated after receiving the Ad.26.COV2.S vaccine. Surveillance is ongoing.
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页数:13
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