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      The Baffling Case of Ischemic Stroke Disappearance from the Casualty Department in the COVID-19 Era

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          Abstract

          Dear Editor, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is rapidly spreading worldwide, and the WHO declared the coronavirus disease 2019 (COVID-19) outbreak a pandemic on March 11, 2020 [1]. The outbreak has hit Europe and, as of March 27, 2020, Italy has the second largest number of confirmed cases, that is, a total of 86,498 cases according to the Istituto Superiore di Sanità and 9,134 deaths [2]. This health emergency issue has plunged the Italian health system into an unprecedented state of emergency, and many hospitals are now dedicated exclusively to COVID-19 assistance. We work at the Guglielmo da Saliceto Hospital in Piacenza, a city in northern Italy near Milan. Despite being a relatively small city, Piacenza and its province (about 280,000 inhabitants) are one of the epicenters of the Italian epidemic, listing 2,276 cases at the time of writing. This health emergency has revolutionized the hospital organization, and everything has changed for practicing clinicians in just a few weeks. For example, neurologists also contribute to the management and care of COVID-19 patients or have been “converted back” to operating as emergency physicians, as numerous colleagues have been infected. The question is: what can we say about the remaining non-COVID-19 pathologies? Let us take the ischemic stroke as an example: it seems to have almost disappeared from the Casualty Department! Over the past 5 years (2015-2019), the city of Piacenza has recorded an annual average of 612 new cases of ischemic stroke, with a monthly average of 51 cases, and 21% of them are large vessel occlusion (LVO). We investigated the monthly variance of ischemic stroke using the ANOVA test. Surprisingly, between February 21, 2020 (first SARS-CoV-2 patient recorded in Italy-in Codogno, a nearby city), and March 25, 2020, there were only 6 admissions from the Casualty Department for ischemic stroke (2 transient ischemic attacks, 1 cardioembolic LVO, and 3 lacunar stroke). What could we hypothesize for this observation? On March 8, 2020, the Italian government implemented extraordinary measures to limit viral transmission, including restricting the mobility of the general population. This strict measure was aimed at minimizing the likelihood that people who were already infected came into contact with noninfected ones. Moreover, the population was asked to refer to the Casualty Department only if really necessary. It is true that the significant reduction in currently registered strokes may well be attributable to fewer people going to the Casualty Department for fear of being infected. However, this can be true only for minor, non-disabling strokes. LVO strokes are always disabling (i.e., aphasia and/or hemiplegia), and it is impossible to avoid hospitalization in such a serious condition. Moreover, the point is that there may be an underestimation of the number of stroke, as when patients arrive in a Casualty Department with fever and respiratory distress, they take priority and the neurological deficit may, therefore, be overlooked. We wonder why these patients have almost disappeared. It is known that viral infections are associated with an increased risk of stroke, as described in influenza pneumonia [3], which is exactly the opposite of what we are currently observing. Could then the seasonal pattern of stroke occurrence and/or cytokine storm described in COVID-19 patients play a role in explaining these observations? It does not seem so. First, data on seasonal differences in stroke incidence are conflicting. Some studies have reported that ischemic stroke occurrence was significantly higher during spring and autumn than in summer [4, 5]. However, another study stated that there was a fairly even distribution of ischemic stroke over all 4 seasons [6] and a recent meta-analysis showed very little seasonal variation [7]. Also, our analysis of variance of the monthly number of ischemic stroke between 2015 and 2019 was not significant. Second, in COVID-19 affected patients, high levels of thrombosis and inflammation serum markers, such as D-dimer, fibrinogen, and C-reactive protein, have been reported, as well as increased levels of inflammatory cytokines (i.e., tumor necrosis factor-α, interleukin [IL]-2R, and IL-6) [8]. All these laboratory findings, including the rise of IL-6, seem to be present also in patients with mild or moderate SARS-CoV-2 clinical manifestations, with no need for hospitalization [9]. So, why do COVID-19 patients not have an increased risk of developing ischemic stroke? One hypothesis could be related to the controversial role IL-6 plays in stroke. Indeed, although high IL-6 levels have been reported to have a negative effect on brain infarct volume and long-term outcome [10], conversely, in ischemic stroke, there is also experimental evidence that IL-6 has a protective effect and helps in the improvement of poststroke angiogenesis [11]. According to these observations, should a beneficial role of IL-6 in patients without other systemic complications be considered? Another interesting possible explanation is related to the presence of thrombocytopenia in COVID-19 patients, also in patients with mild symptoms [12]. Could the decreased platelet levels be involved in the reduction of LVO strokes? Furthermore, based on previous evidence, the burden of chronic persistent infections and/or past infections, rather than one single current infectious disease, seems to be associated with stroke risk [13]. Moreover, the extraordinary measures taken by the Italian government might have reduced the spread of seasonal flu and its unfavorable effect upon stroke incidence. Indeed, what may be true for influenza pneumonia (i.e., increased stroke risk) may not be true for SARS-CoV-2. The main limit of our remark is certainly the short observation period of just 1 month. The baffling case of ischemic stroke disappearance from the Casualty Department has yet to be resolved. Disclosure Statement The authors have no conflicts of interest to declare. Funding Sources This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors. No financial support was provided for the research, authorship, and/or publication of this article. Author Contributions Study concepts: N. Morelli, E. Rota, and C. Terracciano. Study design: N. Morelli, E. Rota, and M. Spallazzi. Data analysis/interpretation: N. Morelli, D. Zaino, P. Immovilli, and D. Colombi. Manuscript preparation and definition of intellectual content: N. Morelli, E. Rota, and C. Terracciano. Manuscript editing: N. Morelli and E. Rota. Manuscript revision/review: D. Guidetti and E. Michieletti.

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          Most cited references10

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          COVID-19: consider cytokine storm syndromes and immunosuppression

          As of March 12, 2020, coronavirus disease 2019 (COVID-19) has been confirmed in 125 048 people worldwide, carrying a mortality of approximately 3·7%, 1 compared with a mortality rate of less than 1% from influenza. There is an urgent need for effective treatment. Current focus has been on the development of novel therapeutics, including antivirals and vaccines. Accumulating evidence suggests that a subgroup of patients with severe COVID-19 might have a cytokine storm syndrome. We recommend identification and treatment of hyperinflammation using existing, approved therapies with proven safety profiles to address the immediate need to reduce the rising mortality. Current management of COVID-19 is supportive, and respiratory failure from acute respiratory distress syndrome (ARDS) is the leading cause of mortality. 2 Secondary haemophagocytic lymphohistiocytosis (sHLH) is an under-recognised, hyperinflammatory syndrome characterised by a fulminant and fatal hypercytokinaemia with multiorgan failure. In adults, sHLH is most commonly triggered by viral infections 3 and occurs in 3·7–4·3% of sepsis cases. 4 Cardinal features of sHLH include unremitting fever, cytopenias, and hyperferritinaemia; pulmonary involvement (including ARDS) occurs in approximately 50% of patients. 5 A cytokine profile resembling sHLH is associated with COVID-19 disease severity, characterised by increased interleukin (IL)-2, IL-7, granulocyte-colony stimulating factor, interferon-γ inducible protein 10, monocyte chemoattractant protein 1, macrophage inflammatory protein 1-α, and tumour necrosis factor-α. 6 Predictors of fatality from a recent retrospective, multicentre study of 150 confirmed COVID-19 cases in Wuhan, China, included elevated ferritin (mean 1297·6 ng/ml in non-survivors vs 614·0 ng/ml in survivors; p 39·4°C 49 Organomegaly None 0 Hepatomegaly or splenomegaly 23 Hepatomegaly and splenomegaly 38 Number of cytopenias * One lineage 0 Two lineages 24 Three lineages 34 Triglycerides (mmol/L) 4·0 mmol/L 64 Fibrinogen (g/L) >2·5 g/L 0 ≤2·5 g/L 30 Ferritin ng/ml 6000 ng/ml 50 Serum aspartate aminotransferase <30 IU/L 0 ≥30 IU/L 19 Haemophagocytosis on bone marrow aspirate No 0 Yes 35 Known immunosuppression † No 0 Yes 18 The Hscore 11 generates a probability for the presence of secondary HLH. HScores greater than 169 are 93% sensitive and 86% specific for HLH. Note that bone marrow haemophagocytosis is not mandatory for a diagnosis of HLH. HScores can be calculated using an online HScore calculator. 11 HLH=haemophagocytic lymphohistiocytosis. * Defined as either haemoglobin concentration of 9·2 g/dL or less (≤5·71 mmol/L), a white blood cell count of 5000 white blood cells per mm3 or less, or platelet count of 110 000 platelets per mm3 or less, or all of these criteria combined. † HIV positive or receiving longterm immunosuppressive therapy (ie, glucocorticoids, cyclosporine, azathioprine).
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            Thrombocytopenia is associated with severe coronavirus disease 2019 (COVID-19) infections: A meta-analysis

            Highlights • Platelet count can discriminate between patients with severe and non-severe novel coronavirus disease 2019 (COVID-19) infections. • Patients who did not survive have a significantly lower platelet count than survivors. • Thrombocytopenia is associated with increased risk of severe disease. • A substantial decrease in platelet count should serve as clinical indicator of worsening illness in hospitalized patients with COVID-19.
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              Clinical Features of 69 Cases with Coronavirus Disease 2019 in Wuhan, China

              Abstract Background From December 2019 to February 2020, 2019 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a serious outbreak of coronavirus disease 2019 (COVID-19) in Wuhan, China. Related clinical features are needed. Methods We reviewed 69 patients who were hospitalized in Union hospital in Wuhan between January 16 to January 29, 2020. All patients were confirmed to be infected with SARS-CoV-2 and the final date of follow-up was February 4, 2020. Results The median age of 69 enrolled patients was 42.0 years (IQR 35.0-62.0), and 32 patients (46%) were men. The most common symptoms were fever (60[87%]), cough (38[55%]), and fatigue (29[42%]). Most patients received antiviral therapy (66 [98.5%] of 67 patients) and antibiotic therapy (66 [98.5%] of 67 patients). As of February 4, 2020, 18 (26.9%) of 67 patients had been discharged, and five patients had died, with a mortality rate of 7.5%. According to the lowest SpO2 during admission, cases were divided into the SpO2≥90% group (n=55) and the SpO2<90% group (n=14). All 5 deaths occurred in the SpO2<90% group. Compared with SpO2≥90% group, patients of the SpO2<90% group were older, and showed more comorbidities and higher plasma levels of IL6, IL10, lactate dehydrogenase, and c reactive protein. Arbidol treatment showed tendency to improve the discharging rate and decrease the mortality rate. Conclusions COVID-19 appears to show frequent fever, dry cough, and increase of inflammatory cytokines, and induced a mortality rate of 7.5%. Older patients or those with underlying comorbidities are at higher risk of death.
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                Author and article information

                Journal
                Eur Neurol
                Eur. Neurol
                ENE
                European Neurology
                S. Karger AG (Allschwilerstrasse 10, P.O. Box · Postfach · Case postale, CH–4009, Basel, Switzerland · Schweiz · Suisse, Phone: +41 61 306 11 11, Fax: +41 61 306 12 34, karger@karger.com )
                0014-3022
                1421-9913
                14 April 2020
                : 1-3
                Affiliations
                [1] aNeurology Unit, Guglielmo da Saliceto Hospital, Piacenza, Italy
                [2] bNeurology Unit, San Giacomo Hospital, Alessandria, Italy
                [3] cRadiology Unit, Guglielmo da Saliceto Hospital, Piacenza, Italy
                Author notes
                *Dr. Nicola Morelli, Neurology and Radiology Unit, Guglielmo da Saliceto Hospital, Via Taverna 49, IT-29121 Piacenza (Italy), nicola.morelli.md@ 123456gmail.com

                The authors contributed equally to the manuscript.

                Article
                ene-0001
                10.1159/000507666
                7179532
                32289789
                0214386f-4999-40c2-9fa7-db7104292560
                Copyright © 2020 by S. Karger AG, Basel

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                : 27 March 2020
                : 31 March 2020
                Page count
                References: 13, Pages: 3
                Categories
                Clinical Neurology: Editorial

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