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在大型综合医疗体系中,COVID-19 mRNA 疫苗接种后的心肌炎风险:两种方法的完整性和及时性比较。

Risk of myopericarditis following COVID-19 mRNA vaccination in a large integrated health system: A comparison of completeness and timeliness of two methods.

机构信息

Department of Infectious Diseases, Kaiser Permanente Northwest, Portland, Oregon, USA.

Department of Analytics, Kaiser Permanente Northwest, Portland, Oregon, USA.

出版信息

Pharmacoepidemiol Drug Saf. 2022 Aug;31(8):921-925. doi: 10.1002/pds.5439. Epub 2022 Apr 16.

Abstract

PURPOSE

How completely do hospital discharge diagnoses identify cases of myopericarditis after an mRNA vaccine?

METHODS

We assembled a cohort 12-39 year-old patients, insured by Kaiser Permanente Northwest, who received at least one dose of an mRNA vaccine (Pfizer-BioNTech or Moderna) between December 2020 and October 2021. We followed them for up to 30 days after their second dose of an mRNA vaccine to identify encounters for myocarditis, pericarditis or myopericarditis. We compared two identification methods: A method that searched all encounter diagnoses using a brief text description (e.g., ICD-10-CM code I40.9 is defined as 'acute myocarditis, unspecified'). We searched the text description of all inpatient or outpatient encounter diagnoses (in any position) for "myocarditis" or "pericarditis." The other method was developed by the Centers for Disease Control and Prevention's Vaccine Safety Datalink (VSD), which searched for emergency department visits or hospitalizations with a select set of discharge ICD-10-CM diagnosis codes. For both methods, two physicians independently reviewed the identified patient records and classified them as confirmed, probable or not cases using the CDC's case definition.

RESULTS

The encounter methodology identified 14 distinct patients who met the confirmed or probable CDC case definition for acute myocarditis or pericarditis with an onset within 21 days of receipt of COVID-19 vaccination. When we extended the search for relevant diagnoses to 30 days since vaccination, we identified two additional patients (for a total of 16 patients) who met the case definition for acute myocarditis or pericarditis, but those patients had been misdiagnosed at the time of their original presentation. Three of these patients had an ICD-10-CM code of I51.4 "Myocarditis, Unspecified;" that code was omitted by the VSD algorithm (in the late fall of 2021). The VSD methodology identified 11 patients who met the CDC case definition for acute myocarditis or pericarditis. Seven (64%) of the 11 patients had initial care for myopericarditis outside of a KPNW facility and their diagnosis could not be ascertained by the VSD methodology until claims were submitted (median delay of 33 days; range of 12-195 days). Among those who received a second dose of vaccine (n = 146 785), we estimated a risk as 95.4 cases of myopericarditis per million second doses administered (95% CI, 52.1-160.0).

CONCLUSION

We identified additional valid cases of myopericarditis following an mRNA vaccination that would be missed by the VSD's search algorithm, which depends on select hospital discharge diagnosis codes. The true incidence of myopericarditis is markedly higher than the incidence reported to US advisory committees in the fall of 2021. The VSD should validate its search algorithm to improve its sensitivity for myopericarditis.

摘要

目的

医院出院诊断在接受 mRNA 疫苗后对心肌炎病例的识别率有多高?

方法

我们组建了一个年龄在 12-39 岁的队列,这些患者都有 Kaiser Permanente Northwest 的保险,在 2020 年 12 月至 2021 年 10 月期间至少接种过一剂 mRNA 疫苗(辉瑞-生物技术或 Moderna)。我们在第二剂 mRNA 疫苗接种后最多 30 天对他们进行随访,以确定是否有心肌炎、心包炎或心肌炎的就诊记录。我们比较了两种识别方法:一种方法是使用简短的文本描述搜索所有就诊诊断(例如,ICD-10-CM 代码 I40.9 定义为“急性心肌炎,未特指”)。我们搜索了所有住院或门诊就诊诊断的文本描述(任何位置)中是否有“心肌炎”或“心包炎”。另一种方法是由疾病控制与预防中心的疫苗安全数据链(VSD)开发的,它通过一组选择的出院 ICD-10-CM 诊断代码搜索急诊就诊或住院记录。对于这两种方法,两位医生独立审查了识别出的患者记录,并使用疾病控制与预防中心的病例定义将其分类为确诊、可能或非病例。

结果

就诊方法识别出 14 名符合疾病控制与预防中心急性心肌炎或心包炎确诊或可能病例定义的患者,这些患者在接受 COVID-19 疫苗接种后 21 天内发病。当我们将搜索相关诊断的时间延长到接种疫苗后 30 天时,我们又发现了另外 2 名(总计 16 名)符合急性心肌炎或心包炎病例定义的患者,但这些患者在最初就诊时被误诊。其中 3 名患者的 ICD-10-CM 代码为 I51.4“心肌炎,未特指”;该代码被 VSD 算法遗漏(2021 年底)。VSD 方法识别出 11 名符合疾病控制与预防中心急性心肌炎或心包炎病例定义的患者。这 11 名患者中有 7 名(64%)最初在 KPNW 以外的医疗机构接受了心肌炎的治疗,他们的诊断直到提交索赔后才能通过 VSD 方法确定(中位延迟 33 天;范围 12-195 天)。在接受第二剂疫苗的患者中(n=146785 人),我们估计每接种 100 万剂第二剂疫苗会出现 95.4 例心肌炎(95%CI,52.1-160.0)。

结论

我们发现了更多接受 mRNA 疫苗接种后经证实的心肌炎病例,这些病例会被 VSD 的搜索算法遗漏,后者依赖于特定的出院诊断代码。心肌炎的真实发病率远高于 2021 年秋季向美国咨询委员会报告的发病率。VSD 应验证其搜索算法,以提高对心肌炎的敏感性。

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