Luo Jing, Hur Kwan, Salone Cedric, Huang Nina, Burk Muriel, Pandey Lucy, Thakkar Bharat, Donahue Mark, Cunningham Francesca
Division of General Internal Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, United States, United Statesw.
Pharmacy Benefits Management Services, VA Center for Medication Safety, Hines, Illinois, United States, United Statesw.
Open Forum Infect Dis. 2023 May 17;10(7):ofad268. doi: 10.1093/ofid/ofad268. eCollection 2023 Jul.
Although the benefits outweigh the risks, COVID-19 vaccines have been associated with an increased risk of myocarditis and pericarditis. This report is based on a national US veteran population with confirmed myocarditis/pericarditis following mRNA COVID-19 vaccines according to the near real-time active surveillance program of Veterans Affairs.
This study is based on a cohort evaluation of all adults administered ≥1 mRNA COVID-19 vaccine, including boosters, in the Veterans Health Administration between 14 December 2020 and 9 October 2022. diagnosis codes were used to identify potential safety signals in near real time through a database analysis. All potential cases of myocarditis/pericarditis identified in the database analysis underwent in-depth chart review and case validation by a team of pharmacists and expert clinicians. Our main outcome was the incidence rate of confirmed myocarditis/pericarditis among vaccine recipients (overall and those aged 18-39 years) within 21 days of a first, second, or booster dose of a mRNA COVID-19 vaccine. We calculated the ratio of observed events among COVID-19 vaccine recipients over expected events from historical vaccine recipient controls (2015-2020) in the Veterans Health Administration. We used confirmed cases to calculate incidence rates and 95% CIs.
Through 9 October 2022, 3 877 453 doses of BNT162b2 (Pfizer-BioNTech) and 4 221 397 doses of mRNA-1273 (Moderna) were administered as first or second dose across Veterans Affairs, and 1 012 561 BNT162b2 and 1 156 160 mRNA-1273 booster doses were administered. Among all doses, the rapid cycle analysis identified 178 potential cases of myocarditis/pericarditis among vaccinees of any age and 22 potential cases among those aged 18-39 years. Of these, 33 cases, including 6 among those 18-39 years old, were confirmed after in-depth chart review and validation, corresponding with an overall incidence rate per million ranging from 0.46 (95% CI, .01-2.55) for Moderna dose 1 to 6.91 (95% CI, 2.78-14.24) for Pfizer booster. Among those aged 18-39, incidence rates ranged from 7.1 (95% CI, .18-39.56) for Moderna dose 2 to 19.76 (95% CI, 5.38-50.58) for Pfizer dose 2. Patients with confirmed cases were hospitalized for a mean 4.1 days (range, 1-15). The final disposition for 32 (97%) of 33 cases was discharge to home.
This report is a real-world demonstration of the Veterans Affairs' active surveillance system for vaccines. Although the rapid cycle analysis initially identified 178 potential cases of myocarditis/pericarditis, only 1 of 5 cases was confirmed to be related to a COVID-19 vaccine after chart review. These findings highlight the paramount importance of active surveillance and chart validation for rare but serious adverse events related to COVID-19 vaccines.
尽管新冠病毒疾病(COVID-19)疫苗的益处大于风险,但一直以来都被认为与心肌炎和心包炎风险增加有关。本报告基于美国退伍军人事务部近乎实时的主动监测计划,针对接种mRNA新冠疫苗后确诊心肌炎/心包炎的美国退伍军人全国性人群展开。
本研究基于对2020年12月14日至2022年10月9日期间在退伍军人健康管理局接受≥1剂mRNA新冠疫苗(包括加强针)的所有成年人进行的队列评估。通过数据库分析,利用诊断编码近乎实时地识别潜在的安全信号。数据库分析中识别出的所有心肌炎/心包炎潜在病例均由一组药剂师和专家临床医生进行深入的病历审查和病例验证。我们的主要结局是在首次、第二次或加强剂量的mRNA新冠疫苗接种后21天内,疫苗接种者(总体以及18至39岁人群)中确诊心肌炎/心包炎的发病率。我们计算了新冠疫苗接种者中观察到的事件与退伍军人健康管理局历史疫苗接种对照(2015 - 2020年)预期事件的比率。我们使用确诊病例计算发病率和95%置信区间。
截至2022年10月9日,在退伍军人事务部,共接种了3877453剂BNT162b2(辉瑞 - 生物科技公司)和4221397剂mRNA - 1273(莫德纳公司)作为第一剂或第二剂,以及1012561剂BNT162b2和1156160剂mRNA - 1273加强针。在所有剂量中,快速循环分析在任何年龄的疫苗接种者中识别出178例心肌炎/心包炎潜在病例,在18至39岁人群中识别出22例潜在病例。其中,经过深入的病历审查和验证后,确认了33例,包括18至39岁人群中的6例,总体发病率每百万例从莫德纳第一剂的0.46(95%置信区间,0.01 - 2.55)到辉瑞加强针的6.91(95%置信区间,2.78 - 14.24)不等。在18至39岁人群中,发病率从莫德纳第二剂的7.1(95%置信区间,0.18 - 39.56)到辉瑞第二剂的19.76(95%置信区间,5.38 - 50.58)不等。确诊病例患者平均住院4.1天(范围为1 - 15天)。33例病例中的32例(97%)最终出院回家。
本报告是退伍军人事务部疫苗主动监测系统的真实案例展示。尽管快速循环分析最初识别出178例心肌炎/心包炎潜在病例,但经病历审查后,每5例中只有1例被确认为与新冠疫苗有关。这些发现凸显了针对与新冠疫苗相关的罕见但严重不良事件进行主动监测和病历验证的至关重要性。