Bohlke Kari, Davis Robert L, Marcy S M, Braun M M, DeStefano Frank, Black Steven B, Mullooly John P, Thompson Robert S
Center for Health Studies, Group Health Cooperative, Seattle, Washington 98101-1448, USA.
Pediatrics. 2003 Oct;112(4):815-20. doi: 10.1542/peds.112.4.815.
To quantify the risk of anaphylaxis after vaccination of children and adolescents.
The study population consisted of children and adolescents who were enrolled at 4 health maintenance organizations that participated in the Vaccine Safety Datalink Project. For the period 1991-1997, we identified potential cases by searching for occurrences of International Classification of Diseases, Ninth Revision (ICD-9) code 995.0 (anaphylactic shock), E948.0 through E948.9 (adverse reaction from bacterial vaccines), and E949.0 through E949.9 (adverse reaction from other vaccines and biological substances). At 1 study site, we also included a range of other allergy codes. We restricted to diagnoses on days 0 to 2 after vaccination (ICD-9 995.0) or day 0 (all other ICD-9 codes). We then reviewed the medical record to confirm the diagnosis.
We identified 5 cases of potentially vaccine-associated anaphylaxis after administration of 7 644 049 vaccine doses, for a risk of 0.65 cases/million doses (95% confidence interval: 0.21-1.53). None of the episodes resulted in death. Vaccines that were administered before the anaphylactic episodes were generally given in combination and included measles-mumps-rubella, hepatitis B, diphtheria-tetanus, diphtheria-tetanus-pertussis, Haemophilus influenzae type b, and oral polio vaccine. One case of anaphylaxis followed measles-mumps-rubella vaccine alone. At the site at which we reviewed additional allergy codes, we identified 1 case after 653 990 vaccine doses, for a risk of 1.53 cases/million doses (95% confidence interval: 0.04-8.52).
Patients and health care providers can be reassured that vaccine-associated anaphylaxis is a rare event. Nevertheless, providers should be prepared to provide immediate medical treatment should it occur.
量化儿童和青少年接种疫苗后发生过敏反应的风险。
研究人群包括在4个参与疫苗安全数据链项目的健康维护组织登记的儿童和青少年。在1991 - 1997年期间,我们通过查找国际疾病分类第九版(ICD - 9)编码995.0(过敏性休克)、E948.0至E948.9(细菌疫苗不良反应)以及E949.0至E949.9(其他疫苗和生物制品不良反应)来确定潜在病例。在1个研究地点,我们还纳入了一系列其他过敏编码。我们将诊断限制在接种疫苗后第0至2天(ICD - 9 995.0)或第0天(所有其他ICD - 9编码)。然后我们查阅病历以确认诊断。
在接种7644049剂疫苗后,我们确定了5例可能与疫苗相关的过敏反应病例,风险为0.65例/百万剂(95%置信区间:0.21 - 1.53)。所有发作均未导致死亡。过敏反应发作前接种的疫苗通常为联合疫苗,包括麻疹 - 腮腺炎 - 风疹疫苗、乙型肝炎疫苗、白喉 - 破伤风疫苗、白喉 - 破伤风 - 百日咳疫苗、b型流感嗜血杆菌疫苗和口服脊髓灰质炎疫苗。1例过敏反应仅发生在接种麻疹 - 腮腺炎 - 风疹疫苗之后。在我们查阅了其他过敏编码的那个地点,在接种653990剂疫苗后我们确定了1例,风险为1.53例/百万剂(95%置信区间:0.04 - 8.52)。
患者和医疗服务提供者可以放心,与疫苗相关的过敏反应是罕见事件。然而,一旦发生,医疗服务提供者应准备好提供即时医疗救治。