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. 2020 Jun 24;41(8):1985–1989. doi: 10.1007/s10072-020-04521-3

COVID-19-related strokes in adults below 55 years of age: a case series

Farzad Ashrafi 1,, Alireza Zali 1, Davood Ommi 1, Mehri Salari 1, Alireza Fatemi 1, Mehran Arab-Ahmadi 2, Behdad Behnam 3, Arash Azhideh 1, Mohammad Vahidi 1, Maryam Yousefi-Asl 1, Reza Jalili khoshnood 1, Soroor Advani 1
PMCID: PMC7311861  PMID: 32583169

Abstract

Background

Coronavirus infection is a novel respiratory disease affecting people across the world. Although the majority of patients present with fever, dyspnea, cough, or myalgia, various signs and symptoms have been reported for this disease. Recently, neurological symptoms have been noticed in patients with COVID-19 with unknown etiology. However, the occurrence of strokes in young and middle aged patients with COVID-19 is not fully explained.

Methods

In this series, six patients younger than 55 years of age with diagnosis of stroke and a confirmed diagnosis of COVID-19 were evaluated for symptoms, lab data, imaging findings, and outcomes from March 2020 to the end of April 2020 from all stroke cases in a tertiary academic hospital. Patients older than 55 and all others who had evidence of cardiac abnormalities (arrhythmia/valvular) were excluded.

Results

Fever, myalgia, cough, and dyspnea were the most common clinical symptoms noted in 66.66% (4/6), 66.66% (4/6), 50% (3/6), and 50% (3/6) of the patients, respectively. The mean ± standard deviation (SD) of National Institutes of Health Stroke Scale (NIHSS) for the patient was 10.16 ± 7.13 (ranged 5–24). The most involved area was middle cerebral artery (MCA) (five in MCA versus one in basal ganglia) and the majority of our patients had a low lung involvement score (mean ± SD: 13.16 ± 6.49 out of 24). Finally, one patient was deceased and rest discharged.

Conclusion

Stroke may be unrelated to age and the extent of lung involvement. However, different factors may play roles in co-occurrence of stroke and COVID-19 and its outcome. Future studies with long-term follow-up and more cases are needed to assess prognostic factors.

Keywords: COVID-19, Coronavirus, Stroke, Neurological manifestation

Background

Coronavirus infection is a novel, highly contagious respiratory disease caused by SARS-CoV-2 affecting people across the world [1]. The most frequent symptoms are fever, dyspnea, cough, or myalgia [2]. Although various signs and symptoms have been reported for this disease, some of them are not clear yet. It may involve both the central nervous system (CNS) and peripheral nervous system (PNS). In this regard, headache, vertigo, cognitive impairment, epilepsy, acute cerebrovascular event ataxia, ageusia, anosmia, neuralgia, and Guillain-Barre syndrome are some of the reported neurological manifestations [35].

According to previous reports, viral infections including COVID-19 may play a role as a potential risk factor in developing cerebrovascular diseases such as acute ischemic stroke especially in patients with the severe form of infection [6].

The role of COVID-19 in initiating proinflammatory and hypercoagulable state has been well described [7]. Also, because of inflammation, hypoxia, immobilization, and diffuse intravascular coagulation (DIC), patients with COVID-19 are at a higher risk of both venous and arterial thromboembolic events. Recently, heparin has been associated with lower mortality in severe cases of COVID-19 or with elevated D-dimer [8]. However, the mechanism and its pathology are rarely understood.

There are currently limited data about patient’s characteristics, extent of lung involvement, and other factors in the patients with stroke and COVID-19. This series is presented to point out to physicians to keep cerebrovascular attacks in mind as an important condition in patients with COVID-19 that may need urgent interventions. In addition, the other aim of this study was to show coronavirus as a causative agent for stroke which is unrelated to age and lung involvement extension.

Cases

Our cases were patients presented to our academic tertiary hospital, stroke unit, with clinical symptoms of stroke from March 2020 to the end of April 2020. We exclude patients older than 55 and all others who had evidence of cardiac arrhythmia or cardiac valvular disease based on electrocardiogram, transthoracic and transesophageal echocardiography, and 24-h Holter monitoring findings. Although all patients primarily presented with neurological symptoms, the diagnosis of COVID-19 was made based on positive nasopharyngeal polymerase chain reaction (PCR) and lung CT scan except one of them who was a 49-year-old female with previous diagnosis of COVID-19 who was discharged from another hospital and admitted to our stroke unit 5 days later.

The mean age (±standard deviation [SD]) was 43.5 ± 7.42 (range 33–53 years) and half of them were male. COVID-19 symptoms were evaluated by history taking except one of our cases (33 years old female) who presented altered levels of consciousness and fever. The most common sign and symptom of COVID-19 were fever (four/six), myalgia (four/six), cough (three/six), and dyspnea (three/six). All patients had O2 saturation below 92% in room air while none of them were hypotensive. Half of the patients had history of hypertension and one case had diabetes mellitus.

Mean (±standard deviation) of National Institutes of Health Stroke Scale (NIHSS) for the patient was 10.16 ± 7.13 (ranged 5–24). Detailed clinical features and outcomes of the patients are noted in Table 1. In addition, the initial laboratory findings are shown in Table 2.

Table 1.

Demographic, clinical features, and outcome of the patients

Patient No. Age, year/gender Comorbidities Fever COVID-19 symptoms Stroke symptoms O2 sat on room air (%) NIHSS Hospital length of stay Outcome
1 33/F + lethargy Reduced level of consciousness, global aphasia, right side hemiplegia 85 24 5 Death
2 39/M + Cough, headache, myalgia, dyspnea Left side hemiparesis, homonymous hemianopia, sensory deficit, dysarthria 89 9 10 Discharged
3 49/F HTN Myalgia Left side hemiplagia,heminimous hemianopia, dysarthera 90 11 14 Discharged
4 40/M Myalgia, dyspnea Right side hemiparesis, dysarthera 89 6 7 Discharged
5 53/M HTN + Cough, diarrhea Left side hemiparesis, dysarthria 91 5 7 Discharged
6 47/ F DM/HTN + Myalgia, cough and dyspnea Right side hemiparesis, dysarthria 82 6 9 Discharged

F female, M male, HTN hypertension, NIHHS National Institutes of Health Stroke Scale

Table 2.

Summary of baseline laboratory findings

1 2 3 4 5 6 Summery (mean ± SD)
White blood cell count 8000 5500 8700 7400 4500 9000 7183.33 ± 1808.22
Neutrophil count 5600 4700 6960 6364 2925 7650 5699.83 ± 1705.38
Lymphocyte count 2400 800 1392 888 1575 1350 1400.83 ± 575.38
Hemoglobin (mg/dL) 9.8 10.7 11.8 16.8 15.8 12.5 12.89 ± 2.80
Platelet × 103 305 183 146 223 101 210 194.66 ± 69.98
CRP (mg/L) 24 12 27 5 12 10 15.0 ± 8.57
LDH (μ/L) 345 347 1393 356 430 460 555.16 ± 413.24
Cr (mg/dL) 0.8 0.8 1.09 1.2 1.2 1.04 1.02 ± 0.18
AST (μ/L) 16 14 94 21 17 11 28.83 ± 32.09
ALT (μ/L) 15 11 106 13 10 14 28.16 ± 38.17
ALP (μ/L) 143 134 415 209 204 162 211.16 ± 104.52
Albumin (g/dL) 5.01 4.8 3.9 4.8 4.1 4.3 4.48 ± 0.44
D-Dimer 728 810 954 682 600 1293 844.50 ± 250.63
PT (s) 13 13 13 14 13 14 13.33 ± 0.51
PTT (s) 28 40 30 40 38 30 34.33 ± 5.57
INR 1 1 1 1.1 1 1.1 1.03 ± 0.51

CRP C-reactive protein, LDH lactic acid dehydrogenase, Cr creatinine, BUN blood urea nitrogen, AST aspartate transaminase, ALT alanine transaminase, ALP alkaline phosphatase, PT prothrombin time, PTT partial thromboplastin time, INR international normalized ratio

All patients underwent imaging studies for stroke and also chest CT scan with low-dose protocol [9]. The initial chest CT scan evaluated for estimation of lung involvement score using zonal involvement percentage method with the maximum score of 24 [10]. The mean score (±SD) was 13.16 ± 6.49 (ranged 2–16) and bilateral ground glass opacities were the most predominant pattern (Fig. 2).

Fig. 2.

Fig. 2

Thirty-nine-year-old male with fever, cough, and mylgia from 6 days before presentation and sudden onset of left side hemiplegia and dysartheria. a Hypodensities in right MCA branch territorty suggestive of subacute infarct. b Diffused ground glass opacities with interalobular septal thickening in superior segment of left lung lower lobes highly suggestive for COVID-19

Brain CT scan findings revealed the stroke territories as follows: right middle cerebral artery (MCA) infarction (n = 3), left MCA (n = 2), and left basal ganglia infarction (n = 1), and the majority of the patients had large vessel stroke. Figures 1, 2, and 3 show brain CT beside lung CT scans of three patients. Our data demonstrated that the majority of our patients had low lung involvement rate while they had more severe conditions based on NIHSS score. Carotid duplex was negative for any significant findings (stenosis, atherosclerotic plaque, or dissection) and results of transcranial color-coded duplex ultrasonography (TCCS) have been summarized in Table 3.

Fig. 1.

Fig. 1

Thirty-three-year-old female with fever and reduced level of consciuosness who had a history of exposure to known case of COVID-19 in his family. a Left MCA territory hypodencities in brain CT scan (a) and increased signal of cortex, white matter, head of left caudete, lentiform nulclei, and anterior horn of internal capsule in T2 and FLAIR brain MRI sequences (c, d), in favor of subacute infarct. b Small subpleuroal consodiation in superior segment of right lung inferior lobe highly suggestive for COVID-19

Fig. 3.

Fig. 3

Forty-nine-year-old female with pervious history of moderate COVID-19 who admitted to our stroke unit with left side hemiplegia, sensory deficiet, and dysarthria. a Wedge-shaped hypodensities in right MCA territory consistent with subacute infarct in brain CT scan. b Diffused peripheral and central consoliadtion patches with crazy paving pattern in some areas consistent with late phase of COVID-19

Table 3.

Summary of baseline imaging findings

Patient No. Infarcted area based on imaging Lung CT scan findings (lung involvement score out of 24) TCCS
1 Left middle cerebral artery territory Small subpleuroal consodiation in right lower lobes (2) Flow was not detected in Left MCA.
2 Right middle cerebral artery territory Ground glass opacities in left lower lobes (3) Poor temporal window
3 Right middle cerebral artery territory Diffused consoliadtion patches (16) Normal
4 Left middle cerebral artery territory Bilateral peripheral ground glass opacities in lower zones (4) Normal
5 Right middle cerebral artery territory Bilateral peripheral ground glass opacities in middle zones (8) Normal
6 Left basal ganglia Right side lower and middle zones ground glass with sub pleural ground glass opacities in left lower zone (10) Poor temporal window

TCCS transcranial color-coded duplex ultrasonography, MCA middle cerebral artery

Regarding our national guidelines, all patients were placed on hydroxychloroquine 400 mg stat and lopinavir/ritonavir 400/100 mg twice daily and intravenous antibiotic. In addition, because all the patients were presented to the emergency room 3 h after their symptom initiation, they were not candidate for thrombolytic therapy so all of them underwent medical treatment with ASA and Plavix for secondary prevention. All patients were followed up to the study endpoint, five patients were discharged; however, one case did not survive.

Discussion

This series showed the co-occurrence of stroke and COVID-19 in adults younger than 55 years of age. To date, there is limited data on the association of COVID-19 and ischemic stroke mechanism, clinical course, prevention, management, and risk stratification.

Valderrama et al. reported a 52-year-old man with COVID-19 who presented with sudden onset hemiparesis and aphasia (NIHSS: 20) on his seventh day of treatment and brain CT scan confirmed the diagnosis of stroke in MCA territory. On further work up, they did not find any risk factor for stroke [11].

In this study, the majority of our patients (five/six) were not known cases of COVID-19 infection and all of them were admitted to our stroke unit with neurological complaints while Mao et al. reported the occurrence of stroke in approximately 2% of COVID-19 patients during their admission [12]. In a study by TJ Oxley et al., large-vessel strokes were presented in five COVID-19 cases younger than 50 years old, and unlike our patients, all of them had severe COVID-19 [13].

Avula et al., described acute stroke in four old-aged patients (range 73–88 years) with confirmed diagnosis of COVID-19, while the oldest patient in this study was 53 years old [14].

It seems that factors such as direct virus invasion, inflammatory processes, cytokine release, hypoxemia, hypotension, or vasculitis are possible mechanisms of coronavirus affecting the nervous system.

This is the first study evaluating the association of long involvement extension and stroke severity. In this regard, our cases showed that lung involvement extension may be unrelated to developing a stroke and its severity based on NIHSS. On the other hand, D-Dimer level may play a critical role as a prognostic factor as elevated D-Dimer levels were seen in all of our patients.

Poggiali et al. reported two cases of COVID-19 who complicated with DVT and PE after at least 10 days since their symptoms started [15]. Also, based on a recent study, COVID-19 could be predisposed to venous and arterial thromboembolism leading to diffuse intravascular coagulation, severe inflammation, immobilization, and hypoxia [16].

An investigation on ICU-admitted patients with COVID-19 showed that the incidence of thrombotic complications was extremely high (31%). The study revealed that pharmacological thrombosis prophylaxis is critically important to be added to the treatment regimen of all COVID-19 patients admitted to ICU [16].

Conclusion

In conclusion, COVID-19 can cause thrombotic complications, hyper-inflammation, and tissue damage, which may increase the risk of ischemic stroke in young and middle aged patients even in early stages and mild forms of COVID-19.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Ethics approval

The study protocol was approved by the ethics committee of the Shahid Beheshti University of Medical Sciences (IR.SBMU.RETECH.REC.1399.115).

Informed consent

Written informed consents were obtained from patients or their guardian.

Footnotes

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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