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Stroke Among SARS-CoV-2 Vaccine Recipients in Mexico: A Nationwide Descriptive Study

机译:中风SARS-CoV-2疫苗接受者之一墨西哥:全国性的描述性研究

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Information on stroke among severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines remains scarce. We report stroke incidence as an adverse event following immunization (AEFI) among recipients of 79,399,446 doses of 6 different SARS-CoV-2 vaccines (BNT162b2, ChAdOx1 nCov-19, Gam-COVID-Vac, CoronaVac, Ad5-nCoV, and Ad26.COV2-S) between December 24, 2020, and August 31, 2021, in Mexico. This retrospective descriptive study analyzed stroke incidence per million doses among hospitalized adult patients (≥18 years) during an 8-month interval. According to the World Health Organization, AEFIs were defined as clinical events occurring within 30 days after immunization and categorized as either nonserious or serious, depending on severity, treatment, and hospital admission requirements. Acute ischemic stroke (AIS), intracerebral hemorrhage (ICH), subarachnoid hemorrhage (SAH), and cerebral venous thrombosis (CVT) cases were collected through a passive epidemiologic surveillance system in which local health providers report potential AEFI to the Mexican General Board of Epidemiology. Data were captured with standardized case report formats by an ad hoc committee appointed by the Mexican Ministry of Health to evaluate potential neurologic AEFI against SARS-COV-2. We included 56 patients (31 female patients [55.5%]) for an overall incidence of 0.71 cases per 1,000,000 administered doses (95% CI 0.54–0.92). Median age was 65 years (interquartile range [IQR] 55–76 years); median time from vaccination to stroke (of any subtype) was 2 days (IQR 1–5 days). In 27 (48.2%) patients, the event was diagnosed within the first 24 hours after immunization. The most frequent subtype was AIS in 43 patients (75%; 0.54 per 1,000,000 doses, 95% CI 0.40–0.73), followed by ICH in 9 (16.1%; 0.11 per 1,000,000 doses, 95% CI 0.06–0.22) and SAH and CVT, each with 2 cases (3.6%; 0.03 per 1,000,000 doses, 95% CI 0.01–0.09). Overall, the most common risk factors were hypertension in 33 (58.9%) patients and diabetes in 22 (39.3%). Median hospital length of stay was 6 days (IQR 4–13 days). At discharge, functional outcome was good (modified Rankin Scale score 0–2) in 41.1% of patients; in-hospital mortality rate was 21.4%. Stroke is an exceedingly rare AEFI against SARS-CoV-2. Preexisting stroke risk factors were identified in most patients. Further research is needed to evaluate causal associations between SARS-COV-2 vaccines and stroke.
机译:信息在严重急性中风呼吸系统综合症冠状病毒2 (SARS-CoV-2)疫苗仍然稀缺。作为不良事件发生率免疫(AEFI)接受者之一79399446剂量的6 SARS-CoV-2不同疫苗(BNT162b2, ChAdOx1 nCov-19,Ad26.COV2-S) 2020年12月24日,2021年8月31日,在墨西哥。描述性研究分析中风发病率百万剂量住院成人患者(≥18年)在为期8个月的时间间隔。世界卫生组织,免疫接种后不良事件定义为临床事件发生在30几天后免疫和分为不严重或严重,根据严重程度,治疗和住院的需求。急性缺血性中风(AIS)、颅内出血(我),蛛网膜下腔出血(SAH),和脑静脉血栓形成(CVT)病例通过一个被动的收集流行病学当地的卫生监测系统供应商报告潜在的AEFI到墨西哥通用董事会的流行病学。由一个广告标准化的病例报告格式临时委员会任命的墨西哥健康评估潜在的神经免疫接种后不良事件反对SARS-COV-2。女性患者总发病率[55.5%])每1000000人0.71例服用剂量(95% CI 0.54 - -0.92)。(四分位距(差)55 - 76年);从接种到中风(任何子类型)2天(差1 - 5天)。病人,事件中被诊断第一次免疫后24小时。频繁的亚型AIS 43例(75%;每1000000剂0.54,95%可信区间0.40 - -0.73),其次是我在9 (16.1%;剂量,95%可信区间0.06 - -0.22)和长官和CVT,2例(3.6%;可信区间0.01 - -0.09)。在33例(58.9%)患者高血压的因素在22个(39.3%)和糖尿病。滞留时间是6天(IQR 42天)。放电,功能结果很好(修改Rankin量表得分0 - 2)在41.1%的患者;住院死亡率为21.4%。一个针对SARS-CoV-2极其罕见的免疫接种后不良事件。既存的中风危险因素被识别在大多数病人。评估SARS-COV-2之间的因果关联疫苗和中风。

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