key: cord-334814-stswaiep
authors: Vogrig, Alberto; Bagatto, Daniele; Gigli, Gian Luigi; Cobelli, Milena; D’Agostini, Serena; Bnà, Claudio; Morassi, Mauro
title: Causality in COVID-19-associated stroke: a uniform case definition for use in clinical research
date: 2020-08-01
journal: J Neurol
DOI: 10.1007/s00415-020-10103-2
sha: 
doc_id: 334814
cord_uid: stswaiep

nan

Increasing evidence supports the association between the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the etiologic agent of the coronavirus disease 2019 (COVID-19), and neurological complications, including encephalopathy, encephalitis, Guillain-Barré syndrome, and cerebrovascular disease [1, 2] . In particular, both ischemic and hemorrhagic strokes have been linked to COVID-19 [3] [4] [5] . Since a substantial proportion of these reported patients had associated vascular risk factors, it is crucial to determine whether this association is causal or coincidental [1, 3, 6] . In an effort to systematically assess this issue, Shtaya et al. proposed to classify cases of COVID-19-related stroke in three major groups:

(1) hospital acquired; (2) community acquired; (3) stroke as direct complications of COVID-19 [7] . Most of the cases of our report [3] and other series [4, 5] fulfill the criteria for the latter group as defined by the authors. Conversely, we did not encounter hospital-acquired COVID-19 infections in patients hospitalized for stroke, since protective measures were readily implemented in our institutions. Although we believe that this proposed classification is valuable in highlighting a relevant clinical problem, these definitions are based on both epidemiological data (location of infection, as for pneumonia, difficult to ascertain in real-life settings) and pathogenetic aspects (as in group 3, for which few information is available at the moment), making their use impractical. Moreover, we believe that it is possible that some patients can fit two of the proposed categories (e.g., patients with community-acquired COVID-19 can develop stroke as direct complication of SARS-CoV-2). Ellul et al. suggested an alternative classification, subdividing cases with "probable" (SARS-CoV-2 identified, lack of vascular risk factors) and "possible" (when vascular risk factors are present) association [1] . We suggest some adaptations of the latter case definition as emerging data have shown distinct stroke patterns in COVID-19 infection [3] [4] [5] 8] . These features (clinical, laboratory, and pathological characteristics, shown in the Table 1 ) can provide supporting evidence in favor of a link in doubtful cases.

We propose a revised definition of CAS, with three degrees of certainty (possible, probable, and confirmed, as illustrated in the Table 1 ). Even if the World Health Organization (WHO) has provided definition for suspected, probable, and confirmed COVID-19 cases, we believe that only patients with laboratory-confirmed SARS-CoV-2 should enter in the classification, in addition to clinic-radiological evidence of acute stroke (ischemic or hemorrhagic). These two represent the major criteria of this revised definition. Minor criteria were designed to capture additional evidence of a causal and biologically plausible association: (1) onset of stroke few days to 3 weeks after COVID-19 symptoms [3] [4] [5] ,(2) lack of cardiovascular risk factors [1, 8] ,(3) D-dimer and/or lactate dehydrogenase elevation [3] [4] [5] . The presence of at least one of these features is required for "possible CAS", and two for "probable CAS", while confirmed CAS requires pathological evidence of disappearance of endothelial cells in the affected arterioles, capillaries and venules. These findings reflect the pathogenesis of CAS, which involves a thrombotic microangiopathy caused by endotheliopathy [4, 9] . Some additional features, such as the detection of SARS-CoV-2 in the cerebrospinal fluid (CSF), can possibly provide additional evidence of a causal association, although cases with negative CSF have been described [10] . Therefore, we do not believe that this represents a necessary feature. It is important to notice that the absence of the typical clinical patterns of CAS should question the diagnosis. Typical clinical features of COVID-19-related stroke include large vessel occlusion, multi-territory involvement, and posterior circulation predisposition (Fig. 1a-g) [3] [4] [5] 8 ]. In addition, less frequent presentations were also observed: onset with seizures and/or encephalopathy [3, 4] , extra-cranial dissection [4, 11, 12] , including bilateral carotid artery dissection [12] (Fig. 1h-j) , and posterior reversible encephalopathy (PRES) [4] or laminar cortical damage [13] .

Interestingly, if we retrospectively apply the CAS criteria to the 12 patients with community-acquired COVID-19 reported by Shtaya et al. [7] , 3 of their cases do not fulfill the major criteria (neuroimaging not performed). Among the other nine patients, stroke developed few days to 3 weeks later in all cases (criteria for possible CAS fulfilled) and in two, there were no known vascular risk factors (criteria for probable CAS fulfilled). In particular, case 12 was a previously healthy 50-year-old man who developed a posterior circulation stroke 3 days after the onset of COVID-19 symptoms in the context of vertebral artery dissection [7] , consistent with our proposed definition. This example suggests that the CAS criteria can be useful in identifying stroke cases more likely to be causally linked to COVID-19, irrespective of where the infection was acquired.

Development of a standardized case definition for stroke of presumed infectious etiology related to SARS-CoV-2 is important for epidemiological surveillance, clinical research, outbreak investigations, as well as for allocation of healthcare resources. As the understanding of this novel disease is expanding rapidly, the proposed definition will likely need refining as more data emerge. Nevertheless, this proposal represents a first step into harmonization of research studies into the topic of CAS. Major criteria 1. Clinical and neuroradiological evidence of acute stroke (ischemic or hemorrhagic) 2. SARS-CoV-2 detection by PCR testing OR detection of SARS-CoV-2-specific antibody in serum indicating acute infection Minor criteria 1. Timing of onset (from few days to 3 weeks after COVID-19 symptoms) 2. Lack of cardiovascular risk factors 3. D-dimer and/or LDH elevation Possible CAS: 2 major criteria and 1 minor criterion Probable CAS: 2 major criteria and ≥ 2 minor criteria Confirmed CAS: criteria for probable CAS and consistent pathologic findings * Note: the absence of the typical clinical patterns of CAS ** should question the diagnosis Clinical supporting features ** 1. Large vessel occlusion 2. Vertebrobasilar location 3. Multi-territory involvement 4. Onset with seizures 5. Extra-cranial dissection 6. PRES or laminar cortical damage Pathologic supporting features * Evidence of endothelial disruption Fig.1 Neuroimaging features of COVID-19-associated stroke. a A 70-year-old man with critical COVID-19-related ARDS developed acute right-sided weakness. Brain CT showed a large fronto-insular ischemic lesion within the vascular territory of the left middle cerebral artery. b A 64-year-old man with COVID-19 infection developed multi-organ failure. Brain CT showed multiple recent ischemic lesions involving cortical-subcortical regions of both parietal lobes and centrum semiovale. c-e A 67-year-old man with COVID-19 and critical ARDS presented myocardial infarction 2 days after hospitalization. On day 14, he developed a tetraparesis. Brain and spine MRI were requested. As an incidental finding (given the final diagnosis of critical illness neuropathy), brain MRI showed a left parieto-occipital infarction, hyperintense on T1-weighted images (c) and bright on DWI (d) along the cortex, with subcortical white matter perilesional edema on FLAIR sequence (e). f-g A 72-year-old man diagnosed with COVID-19 presented with ataxia and vomiting. MRI showed infarction of the postero-inferior part of the left cerebellar hemisphere and the inferior part of the vermis in the territory of PICA (f, coronal FLAIR). Areas of hypointensity within the vermis, corresponding to blood degradation products, were also noted. The lesion underwent extensive hemorrhagic transformation with large parenchymal hematoma (g, axial CT). h-j A 58-year-old man with moderate COVID-19 presented with intense headache and neck pain. h CT angiography showed a long stenosis of the distal part of internal carotid artery bilaterally. MRI axial T1-weighted images obtained with fat saturation (i) and T2-weighted images (j) showed a narrowed eccentric flow void surrounded by a crescent-shaped subacute mural hematoma. This case of bilateral carotid dissection was previously reported by our group [12] . ARDS acute respiratory distress syndrome, CT computed tomography, DWI diffusion-weighted imaging, FLAIR fluidattenuated inversion recovery, MRI magnetic resonance imaging, PICA posterior inferior cerebellar artery

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