Allergy Department, Kaiser Permanente Southern California, San Diego, Calif.
Allergy Department, Kaiser Permanente Southern California, Los Angeles, Calif.
J Allergy Clin Immunol Pract. 2022 Mar;10(3):827-836. doi: 10.1016/j.jaip.2021.12.021. Epub 2021 Dec 29.
BACKGROUND: COVID-19 mRNA vaccination-associated acute-onset hypersensitivity reactions have caused anxiety and may be contributing to vaccine hesitancy. OBJECTIVE: To determine the incidence, severity, and risk factors for treated acute-onset COVID-19 mRNA vaccination-associated hypersensitivity reactions in a well-characterized population. METHODS: All Kaiser Permanente Southern California (KPSC) members who received COVID-19 mRNA vaccinations between December 15, 2020, and March 11, 2021, at a KPSC facility were identified and characterized, along with all treated acute-onset vaccination-associated hypersensitivity events. RESULTS: We identified 391,123 unique vaccine recipients (59.18% female, age 64.19 ± 17.86 years); 215,156 received 2 doses (53.54% Moderna), 157,615 only a first dose (50.13% Moderna) (1961 [1.46%] >2 weeks late getting a second dose), and 18,352 (74.43% Moderna) only a second dose. Only 104 (0.028%) (85.58% female, age 53.18 ± 15.96 years) had treated first dose events, 68 (0.030%) Moderna. Only 32 (0.014%) (93.75% female, age 57.28 ± 17.09 years) had treated second dose events, 21 (0.016%) Moderna. Only 2 (0.00033%) vaccinations resulted in anaphylaxis. Only 27 (20.77%) of those with treated first dose reactions failed to get a second dose. Only 6 of 77 (7.8%) with first dose reactions also had second dose reactions. Individuals with treated events were more likely to be female (P < .0001), younger (P < .0001), and had more pre-existing drug "allergies" (2.11 ± 2.12 vs 1.02 ± 1.41 [P < .0001] for average recipients). CONCLUSIONS: Treated acute-onset hypersensitivity events were mostly benign, more common with first COVID-19 mRNA vaccine doses, more likely to occur in younger females with typical risk factors associated with multiple drug intolerance syndrome, and very unlikely to be primarily immunologically mediated.
背景:COVID-19 mRNA 疫苗接种后出现的急性过敏反应引起了焦虑,并可能导致疫苗犹豫。
目的:在一个特征明确的人群中,确定经过治疗的 COVID-19 mRNA 疫苗接种后急性过敏反应的发生率、严重程度和危险因素。
方法:确定 2020 年 12 月 15 日至 2021 年 3 月 11 日期间在凯撒永久南加州(KPSC)设施接种 COVID-19 mRNA 疫苗的所有 KPSC 成员,并对其进行特征描述,以及所有经治疗的急性疫苗接种相关过敏事件。
结果:我们确定了 391123 名独特的疫苗接种者(59.18%为女性,年龄 64.19±17.86 岁);215156 人接种了 2 剂(53.54%为 Moderna),157615 人仅接种了 1 剂(50.13%为 Moderna)(1961[1.46%]晚于第 2 剂接种时间超过 2 周),18352 人(74.43%为 Moderna)仅接种了第 2 剂。仅有 104 人(0.028%)(85.58%为女性,年龄 53.18±15.96 岁)出现经治疗的第 1 剂反应,68 人(0.030%)为 Moderna。仅有 32 人(0.014%)(93.75%为女性,年龄 57.28±17.09 岁)出现经治疗的第 2 剂反应,21 人(0.016%)为 Moderna。仅有 2 人(0.00033%)接种疫苗后出现过敏反应。只有 27 人(20.77%)接受第 1 剂治疗的反应者未能接种第 2 剂。仅有 6 人(7.8%)接受第 1 剂治疗的反应者同时出现第 2 剂反应。出现治疗后反应的个体更可能为女性(P<0.0001),年龄更小(P<0.0001),并且更可能存在多种药物不耐受综合征相关的预先存在的药物“过敏”(2.11±2.12 比平均接受者的 1.02±1.41[P<0.0001])。
结论:经治疗的急性过敏反应大多为良性,与首次 COVID-19 mRNA 疫苗接种更为常见,更可能发生在有典型危险因素的年轻女性中,这些危险因素与多种药物不耐受综合征有关,而不太可能主要由免疫介导。
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