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SARS-Cov2 is responsible for COVID-19 that can cause severe respiratory illness, and which can be associated with ischaemic stroke (IS).1 The objectives of our comparative cross-sectional study were to describe the characteristics of consecutive patients with IS and COVID-19, to compare them to COVID-19-negative IS patients admitted within the same period and to attempt to identify a specific pattern of IS in COVID-19.
We conducted a comparative cross-sectional study at two tertiary stroke units, Pitié-Salpêtrière and Saint-Antoine Hospitals, between March 20 and April 20 2020. Cases and controls were all consecutive adult patients hospitalised for recent IS, confirmed on neuroimaging. Cases were diagnosed with COVID-19 if a nasopharyngeal reverse transcription (RT-PCR) test for SARS-CoV-2 (Allplex 2019-nCoV Assay, Seegene) was positive and/or if a chest CT-scan was typical for COVID-19. Exclusion criteria were diagnoses of transient ischaemic attack, haemorrhagic stroke or stroke secondary to cerebral venous thrombosis.
We collected demographic data, cardiovascular risk factors, neurological data, blood test results, in-hospital treatments and discharge outcomes. After reviewing the available workup for each patient (vascular imaging of cerebral and cervical arteries and cardiac evaluation including a 12-lead ECG, 48 hours continuous ECG monitoring and transthoracic echocardiogram), aetiology of IS was classified according to ASCODphenotyping (A: atherosclerosis; S: small-vessel disease; C: cardiac pathology; O: other causes; D: dissection).
Fisher’s exact test and Wilcoxon-Mann-Whitney test were used to compare cases and controls for categorical and continuous variables respectively. P values <0.05 defined statistical significance. All data analyses were conducted using Stata V.14.0.
Between March 20 and April 20 2020, 67 patients with IS were hospitalised (41 at Pitié-Salpêtrière and 26 at Saint-Antoine Hospital). Among them, 12 (17.9%) were infected with SARS Cov-2. Patient characteristics are detailed in table 1.
Stroke revealed COVID-19 in 41.7% of COVID-19 patients. For the other COVID-19 patients with IS, the median delay (P25;P75) between initial COVID-19 symptoms and imaging for stroke was 17 days (7;20). COVID-19 pulmonary severity was mild as only two patients required more than 6 L/min of supplemental oxygen, and none of them presented acute respiratory distress syndrome.
The proportion of patients under the age of 60 was higher among COVID-19 patients as well as the proportion of patients of Afro-Caribbean descent (p=0.008). Stroke severity at presentation tended to be higher in the case group which was consistent with a trend towards an increased frequency of proximal arterial occlusion (p=0.053), although none of the COVID-19 patients presented with multiple cerebral large vessel occlusions.
Unusual symptoms at presentation such as delirium or apathy were more frequently found in COVID-19 patients. Among the COVID-19 patients who presented with delirium, two had small infarcts of the corpus callosum (online supplemental figure 1D, F), one of these patients had mild lymphocytic meningitis (with Cerebrospinal fluid [CSF] RT-PCR negative for COVID-19) and sporadic bilateral frontotemporal delta waves at EEG recording.
Arterial causes (atherothrombosis and small cerebral vessel disease) of IS were significantly more frequent in the COVID-19 group (58.3%, n=7/12) than in controls (27.3%, n=15/55) (p=0.049). Potentially causal atherothrombosis was present in 41.7% of cases vs 20.4% of controls. Among the five COVID-19 patients with significant atheroma, four had ipsilateral carotid stenosis superior to 50% according to the North American Symptomatic Carotid Endarterectomy Trial classification. The fifth patient had a floating thrombus in the aortic arch associated with an atherosclerotic plaque <4 mm (online supplemental figure 2).
Inflammatory markers such as C reactive protein, fibrinogen, platelet count and coagulopathy parameters (D-dimer) were found at high levels in cases. Six COVID-19 patients were screened for lupus anticoagulant (LA). Among them, testing was positive in five out of these six patients, whereas it was positive in only one out of nine controls (p=0.011). AntiB2Gp1 antibody was rarely found (one patient in both groups) and none were positive for anticardiolipin antibody at a significant level.
In our study, conducted during the peak of COVID-19 outbreak, IS associated with COVID-19 accounted for nearly one-fifth of hospitalised IS patients. IS was frequently the first manifestation of SARS-CoV-2 infection. Accordingly, stroke neurologists should be aware of this neurological presentation of COVID-19 even in the absence of reported fever or cough. Although the first descriptions of stroke in COVID-19 concerned mostly critically ill patients, our series confirms that IS in COVID-19 occurs even in the absence of severe pneumonia. The mild pulmonary severity may also account for the low mortality observed among COVID-19 IS compared with previous reports,2 3 although stroke severity was higher among cases. Individuals of Afro-Caribbean descent represented half of COVID-19 IS in our series. Whether the possible association of COVID-19 IS with Afro-Caribbean origin is due to a biological vulnerability or socioeconomic or environmental factors requires further investigation.
About 40% of COVID-19 patients presented with a pronounced delirium and/or apathy at admission. One of these patients had CSF and electroencephalographic features suggestive of meningoencephalitis. In two of these patients, we found a small infarct of the corpus callosum, a rare ischaemic location, highlighted in another report in COVID-19 patients.4 We, therefore, hypothesise that both small deep infarcts and delirium might be at least partially linked to COVID-19-associated acute cerebral endotheliopathy, as described by Hernández-Fernández et al.3
We found a marked increase of coagulation activity in the majority of our cases, with the presence of LA. Whether LA is directly involved in the pathogenesis or simply associated with the inflammatory process is uncertain. Moreover, contrary to others series,2 3 5 IS aetiological analysis also highlighted a majority of underlying cervico-encephalic arterial injuries among COVID-19 IS, in particular atherothrombotic disease. In these predisposed patients, COVID-19-associated hypercoagulable state may have precipitated atherosclerotic plaque disruption, lowering the threshold for cervico-encephalic arterial disease to become clinically manifest.
In conclusion, our study highlights the characteristics of IS in COVID-19 patients admitted to stroke units during the outbreak. Several non-exclusive and synergistic mechanisms seem at work in this novel infectious disease, including atherosclerotic plaque vulnerability, coagulopathy and microvasculature impairment. Because of the small sample size of our study, further larger confirmatory studies are warranted to corroborate our findings.
We thank Cecile Delorme and Jean-Christophe Corvol on behalf of CoCo Neurosciences study group. We thank all the patients and their families.
EJ, LB, MY, CR and SA contributed equally.
Contributors EJ, LB and MY were responsible for data acquisition, analysis and interpretation and drafting of the manuscript. EJ was responsible for statistical analysis. LB was responsible for imaging draft. SA and CR were responsible for study conception, design, supervision, analysis and interpretation of data, and drafting of the manuscript. All other authors were responsible for acquisition of data and for revision of the manuscript.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests EJ reports reimbursement for conference registration fees, travel expenses and accommodation from Sanofi Genzyme, outside the submitted work. LB reports reimbursement for conference registration fees, travel expenses and accommodation from Pfizer and reimbursement for conference registration fees from Boehringer Ingelheim, outside the submitted work. MY reports reimbursement for conference registration fees from Pfizer and Boehringer Ingelheim, outside the submitted work. JC reports payment for consultancy and readings from Eisai, outside the submitted work; reimbursement for conference registration fees, travel expenses and accommodation from Pfizer SAS, noutside the submitted work. FC reports payment for readings from Medtronic, Guerbet, Balt Extrusion, Penumbra, outside the submitted work; and conflict of interest with Codman Neurovascular and Microvention (core lab; outside the submitted work). NAS reports payment for consultancy from Medtronic, Balt Extrusion, Microvention, outside the submitted work. SA reports payment for consultancy and readings from Astra Zeneca, outside the submitted work; payment for readings from Bayer and BMS-Pfizer, outside the submitted work; and is associate editor of Revue Neurologique.
Patient consent for publication Not required.
Ethics approval This study was approved by the Research Ethics Committee of Sorbonne University (CER-2020–41).
Provenance and peer review Not commissioned; externally peer reviewed.
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