key: cord-0870597-yi2vjbr0
authors: Cecchetti, Giordano; Vabanesi, Marco; Chieffo, Raffaella; Fanelli, Giovanna; Minicucci, Fabio; Agosta, Federica; Tresoldi, Moreno; Zangrillo, Alberto; Filippi, Massimo
title: Cerebral involvement in COVID-19 is associated with metabolic and coagulation derangements: an EEG study
date: 2020-06-15
journal: J Neurol
DOI: 10.1007/s00415-020-09958-2
sha: 850dbba91047c052c3b42199a1f72b300b6ea813
doc_id: 870597
cord_uid: yi2vjbr0

nan

In previous reports, clinical characteristics of SARS-CoV-2 infection have been described, and risk factors for the development of acute respiratory distress syndrome (ARDS) and death have been proposed: among them, older age, comorbidities such as hypertension and diabetes mellitus, neutrophilia and markers of end-organ and coagulation impairment [1] .

Although mortality due to COVID-19 is mainly linked to visceral multi-organ failure, cerebral involvement might worsen the clinical picture. Up to 36% of patients with COVID-19 appear to have neurological manifestations, ranging from headache and dizziness to impaired consciousness and cerebrovascular events [2] . The EEG correlates of such manifestations are still not clear.

We report a series of 18 consecutive COVID-19 patients, admitted to our Institution between March and April 2020, evaluated with basal electroencephalogram (EEG) to investigate infection-related neurologic manifestations. All patients had their COVID-19 diagnosis confirmed by means of duplo SARS-CoV-2 real-time polymerase chain reaction (RT-PCR) on nasopharyngeal swabs, and compatible chest X-ray and/ or CT scan.

Patients were divided in three groups, according to the level of EEG background activity alteration on a threegrade scale [normal/mild (N = 5), moderate (N = 9) or severe (N = 4)] derived with modifications from Amodio et al. [3] . Neurological manifestations prompting EEG examination were transient loss of consciousness, seizures/spasms, delirium and coma, with different distribution in the patient groups; no subjects reported history of anosmia/ageusia. Demographic and clinical features of patients are reported in Table 1 . The frequency of focal central nervous system (CNS) lesions at neuroimaging (CT and/or MRI scan) did not differ among groups. We observed generalized EEG slowing in 16/18 (88.9%) patients; an anterior (bifrontal) prevalence of slow waves was noted in 10/18 (55.6%) cases (Fig. S1 ), a finding observed also in metabolic encephalopathies [4] . Its presence and severity correlated with the degree of EEG alteration (p = 0.02, linear regression model). This kind of abnormalities has been recently observed also by Helms [5] . Only two patients presented with epileptiform discharges (one with operated high-grade glioma, one with coma and severe hypernatremia); no seizures were detected.

According to clinical protocols, only one subject in our cohort underwent lumbar puncture to rule out acute encephalitis, with normal results (cells, protein and glucose) and negative RT-PCR test for SARS-CoV-2; in addition, bacterial and virologic assays were negative. In the remaining 17 subjects, lumbar puncture was not performed, since not indicated on the basis of clinical judgement. Giordano Cecchetti and Marco Vabanesi contributed equally to the article and should be both considered first authors.

The online version of this article (https ://doi.org/10.1007/s0041 5-020-09958 -2) contains supplementary material, which is available to authorized users. We visually screened vital and laboratory parameters for association with the degree of EEG alteration. Univariate linear regression models were built to evaluate the relationship between patient groups and selected parameters. Among vital parameters (including heart rate and body temperature), only oxygen saturation on room air (SpO 2 ), measured at hospital admission appeared to be associated to the EEG abnormalities (Table 1, Fig. 1 ). As to laboratory parameters, a linear relationship with the severity of EEG alteration was observed for white blood cell (WBC) count, the presence of plasma sodium alterations, serum creatinine, and coagulation parameters (prothrombin time, activated partial thromboplastin time, and d-dimer) (Table 1, Fig. 1 ).

We recorded for all but three patients the antibiotic and/ or antiviral drugs administered at the time of EEG. We did not observe significant effects of drug-related toxicity in our cohort. Moreover, laboratory parameters most commonly associated to drug therapies did not appear to influence EEG alteration; association with creatinine may be correlated to aggressive diuretic therapy salvage protocols.

Our findings suggest variable degrees of CNS involvement in COVID-19 patients. The presence of focal brain lesions did not appear to impact significantly on EEG background activity. Subjects with laboratory findings which have been associated to poor prognosis [1] showed more frequent CNS impairment, as reflected by EEG alterations. Moreover, lower values of oxygen saturation at admission were associated with more severe EEG abnormalities, suggesting that higher levels of hypoxemia, and possibly longer periods before access to cures, may contribute to brain dysfunction.

Electroencephalogram (EEG) may therefore represent a useful tool to evaluate early cerebral involvement in COVID-19, especially in severe cases; a frequent finding in our cohort was an anterior prevalence of slow waves. We hypothesize that the main drivers of EEG alterations in these patients are metabolic and/or hypoxic encephalopathy, even if our data cannot exclude the contribution of cerebral microangiopathy, yet to be demonstrated. We believe that our data raise a warning against a delayed access to specialized cures in SARS-CoV-2 infection, in order to reduce the incidence of brain suffering.

Values are mean ± SD or N (%) CKD chronic kidney disease, COPD chronic obstructive pulmonary disease, IHD ischemic heart disease, SDH subdural hematoma, d days, LOC loss of consciousness, WBC white blood cells, Ly lymphocyte, CRP C-reactive protein, LDH lactate dehydrogenase, CK creatine kinase, PRES posterior reversible encephalopathy syndrome, PT prothrombin time, APTT activated partial prothrombin time a Kruskal-Wallis rank sum test b Univariate linear regression model of the specified parameter on the level of EEG alteration (normal, mild, moderate, severe); the estimate of effect (± SE), when significant, is shown on the right column. For CK, log transformation was used. Author contributions GC and MV equally contributed to study conception, data collection, analysis and interpretation and paper drafting. GF contributed to data collection, analysis and interpretation. RC, FA, MT, and AZ contributed to data analysis and interpretation. FM supervised data collection, analysis and interpretation. MF contributed to study conception, data analysis and interpretation. All authors critically reviewed the paper.

Funding Not applicable. oxygen saturation on room air, WBC white blood cells, PT prothrombin time, APTT activated partial prothrombin time

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