key: cord-0835589-si4gcweo
authors: Liuhong Liu, Jay; Shah, Keval; Marji, Amin; Sareini, Ricky; Bhasin, Amman; Rao, Shishir; Mohamed, Wazim; Rajamani, Kumar; Chamiraju, Parthasarathi; Khawaja, Ayaz
title: Descriptive Analysis of Acute Ischemic Stroke in COVID-19 Patients Through The Course Of The COVID-19 Pandemic
date: 2021-10-29
journal: J Clin Neurosci
DOI: 10.1016/j.jocn.2021.10.023
sha: a55f36e335effcc73d75ebc0407c9fd9cb7b9d04
doc_id: 835589
cord_uid: si4gcweo

Coronavirus disease 2019 (COVID-19) has been associated with Acute Ischemic Stroke (AIS). Here, we characterize our institutional experience with management of COVID-19 and AIS. Baseline demographics, clinical, imaging, and outcomes data were determined in patients with COVID-19 and AIS presenting within March 2020 thru October 2020, and November 2020 thru August 2021, based on institutional COVID-19 hospitalization volume. Of 2512 COVID-19 patients, 35 (1.39%, mean age 63.3 years, 54% women) had AIS. AIS recognition was frequently delayed after COVID-19 symptoms (median 19.5 days). Four patients (31%) were on therapeutic anticoagulation at AIS recognition. AIS mechanism was undetermined or due to multiple etiologies in most cases (n=20, 57%). Three patients underwent IV TPA, and three underwent mechanical thrombectomy, of which two suffered re-occlusion. Three patients had incomplete mRNA vaccination course. Fourteen (40%) died with 26 (74%) having poor outcomes. Critical COVID-19 severity was associated with worsened mortality (p=0.02). More patients (12/16; 75%) had either worsening or similar 3-month functional outcomes, than those with improvement, indicating the devastating impact of co-existing AIS and COVID-19. Comparative analysis showed that patients in the later cohort had earlier AIS presentation, less stroke risk factors, more comprehensive workup, more defined stroke mechanisms, less instance of critical COVID-19 severity, more utilization of IV TPA, and a trend towards worse outcomes for the sub-group of mild-to-moderate COVID-19 severity. AIS incidence, NIHSS, and overall outcomes were similar. Further studies should investigate outcomes beyond 3 months and their predictive factors, impact of completed vaccination course, and access to neurologic care.

Coronavirus disease 2019 (COVID-19) has been associated with Acute Ischemic Stroke (AIS). Here, we characterize our institutional experience with management of COVID-19 and AIS. Baseline demographics, clinical, imaging, and outcomes data were determined in patients with and AIS presenting within March 2020 thru October 2020, and November 2020 thru August 2021, based on institutional COVID-19 hospitalization volume. Of 2512 COVID-19 patients, 35 (1.39%, mean age 63.3 years, 54% women) had AIS. AIS recognition was frequently delayed after COVID-19 symptoms (median 19.5 days). Four patients (31%) were on therapeutic anticoagulation at AIS recognition. AIS mechanism was undetermined or due to multiple etiologies in most cases (n=20, 57%). Three patients underwent IV TPA, and three underwent mechanical thrombectomy, of which two suffered re-occlusion. Three patients had incomplete mRNA vaccination course.

Fourteen (40%) died with 26 (74%) having poor outcomes. Critical COVID-19 severity was associated with worsened mortality (p=0.02). More patients (12/16; 75%) had either worsening or similar 3-month functional outcomes, than those with improvement, indicating the devastating impact of co-existing AIS and COVID-19. Comparative analysis showed that patients in the later cohort had earlier AIS presentation, less stroke risk factors, more comprehensive workup, more defined stroke mechanisms, less instance of critical COVID-19 severity, more utilization of IV TPA, and a trend towards worse outcomes for the sub-group of mild-to-moderate COVID-19 severity. AIS incidence, NIHSS, and overall outcomes were similar. Further studies should investigate outcomes beyond 3 months and their predictive factors, impact of completed vaccination course, and access to neurologic care.

Stroke (AIS), whose pathophysiology is thought to be hypercoagulability from COVID-19 [1] .

Stroke care during the pandemic has been complicated due to delayed presentation and recognition, especially during the early surge of COVID-19 cases in Michigan. Here, we describe our institutional experience in the treatment of patients with COVID-19 presenting with AIS during the initial and subsequent COVID-19 infection surges, including reporting long-term outcomes. We highlight challenges encountered in identification and investigative workup of these patients, treatment concerns, how AIS characteristics and management evolved from 2020 to 2021, the effect of COVID-19 vaccination, and considerations for future investigations.

All consecutive patients with COVID-19 and AIS treated at our institution during the various COVID-19 outbreaks, between March 1 and August 31 st , 2021, were included. All patients had either positive nasal swab samples for SARS-CoV-2 using Reverse-Transcriptase Polymerase Chain Reaction or chest radiography findings consistent with COVID-19. Due to consideration for differences in patient management early and later in the COVID-19 pandemic, patients were categorized into two separate cohorts: 1) patients diagnosed with AIS during the initial peak of COVID-19 (March thru October 2020) and 2) subsequent surges in infection (November 2020 to August 2021). These cut-offs are based on changes in COVID-19 hospitalization volumes at our institution. Baseline demographic and clinical characteristics were retrospectively determined.

COVID-19 severity was categorized into asymptomatic or mild, moderate, and severe or critical as per published criteria [2] . We defined large vascular territory strokes as stroke involving at least 1/3 rd of the vascular territory of a large intracranial artery. Stroke mechanisms were defined by the Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria and recent review and clinical update of embolic stroke of undetermined source [3, 4] . Modified-Rankin Scale (mRS) was recorded at discharge, and then at 3 months. Poor functional outcome was defined as mRS of 4-6. Cohort comparisons amongst various variables were made using Student's t-test or Mann-Whitney U-test for continuous variables, and chi-squared tests for categorical variables. The study was approved by local Institutional Review Board. A total of 19 AIS cases were identified from the first cohort of 1400 COVID-19 patients (1.36%), and 16 from the second cohort of 1112 patients (1.44%). Thirty patients (86%) presented from home, whereas the remaining presented from a nursing facility. Twenty-nine (83%) had ≥2 vascular risk factors, most commonly hypertension, prior AIS, and diabetes. Cardioembolic risk factors including atrial fibrillation, mitral prosthetic valve, patent foramen ovale, EF<45% or hypokinetic/akinetic left ventricular segments were noted in nine patients (26%). Other factors included underlying hypercoagulable states in four (11%), and Moyamoya vasculopathy in only one (3%). The most common nonvascular risk factor was chronic kidney disease (6/35; 17%).

Prior to identification of stroke, most patients (21/35; 60%) had respiratory symptoms. COVID-19 severity was severe or critical in 12 (34%), moderate in 11 (31%), and mild or asymptomatic in the remaining patients, prior to or concomitant with identification of stroke. Within 48 hours prior to stroke onset, only five patients (14%) were treated with vasopressors. Clinical symptoms of stroke included either focal neurologic signs (24/35; 69%) or persistent/worsening encephalopathy (11/35; 31%). Three patients (9%) from the second cohort each received one dose of a mRNA COVID-19 vaccine.

Mechanism of stroke (Tables 1 and 2) was cardioembolic in five patients (14%), large artery atherosclerosis in five (14%), small vessel disease in two (6%), other determined etiology in three (9%), and undetermined or more than one etiology in 20 (57%). Of the latter, 12 (60%) were due to incomplete evaluation, seven (35%) were cryptogenic with complete evaluation, of which one Positive cardiolipin antibody was observed in three patients. Eight patients (23%) received antiplatelet therapy, four (11%) received therapeutic anticoagulation, and 11 (31%) received prophylactic anticoagulation prior to stroke onset.

Patients in the later cohort had a lower proportion of multiple stroke risk factors (p = 0.04) and delayed stroke presentation of >30 days from initial COVID-19 diagnosis (p = 0.04) compared to the cohort prior to November 2020 (Table 1) . Three patients in the later cohort received IV TPA compared to none in the earlier cohort, and there was a higher proportion of patients with completed stroke work up with identified stroke mechanisms. Patients in the later cohort had a lower instance of undetermined mechanisms (p=0.004), and a higher completion rate of neurovascular imaging (0.032). More patients had critical COVID-19 severity in the earlier cohort (p=0.01). Three patients (19%) had an incomplete course of a COVID-19 mRNA vaccine in the second cohort. AIS incidence, NIHSS, and outcomes between the cohorts were similar. Despite a higher instance of mild-to-moderate COVID-19 severity in the later cohort, there was a trend towards higher mortality and poor outcomes within the mild-to-moderate COVID-19 severity subgroup (mRS of 4-6). However, the findings were statistically non-significant (Table 3A) .

Five patients (14%) developed venous thromboembolism during hospitalization, including limb ischemia, pulmonary emboli, lower extremity venous thrombosis, and splenic infarct. One out of 18 (66%) patients with blood cultures obtained developed MRSA bacteremia following stroke.

Five patients (14%) required vasopressor support 48 hours prior to stroke onset. Overall, the outcome of the patients was poor with 14 (40%) expiring and 17 (49%) discharged to nursing facility or hospice. Only nine patients (26%) had a 3-month mRS of 0-3. Of the 26 (74%) patients who survived, 3-month mRS was available in 16. On 3-month follow-up, mRS was improved in only four patients (25%), worsened in six (38%) of which five had died, and remained the same in the rest ( Table 2) . COVID-19 severity significantly impacted outcomes. There was higher mortality in patients with critical COVID-19 severity compared to mild-to-moderate (p=0.02) (Table 3B) .

We present our experience with managing AIS patients with concomitant COVID-19 infection.

Our region was particularly affected at the early stages of the pandemic and harbors a population with multiple stroke risk factors. We noticed that the overall incidence of AIS in COVID-19 has not significant changed during the course of pandemic. There were selected differences in stroke characteristics, treatments and outcomes within the later cohort, including more utilization of IV TPA, lower incidence of critical COVID-19 severity, more acute AIS presentation, and a tendency for more complete workup and identification of the stroke mechanism. Although vaccines became available in the later cohort, majority of patients were still unvaccinated, potentially due to slow vaccine roll-out and lower-than-average vaccination rates of 37% in the city of Detroit, as of September 2021 [5] . Three patients each received a single dose of an mRNA COVID-19 vaccine prior to stroke onset, but no fully vaccinated patient presented with AIS. Large scale observational studies investigating the effect of vaccination on stroke incidence in COVID-19 would be of particular interest, as although stroke incidence in COVID-19 is low, outcomes are devastating. This was particularly highlighted in our data where a non-significant trend was discovered for mortality and poor outcomes even with mild-to-moderate COVID-19 severity in the later cohort.

Due to critical limitations in medical personnel and testing availability at the start of the pandemic, stroke workups were often incomplete for patients diagnosed early in the pandemic (11/19 patients had limited evaluation in the early cohort), but most patients had full evaluations in the later period (15/16). Thus, identified stroke mechanisms became evident in patients presenting later in the pandemic with fewer undetermined mechanisms, with one factor being a higher completion rate of neurovascular imaging. Due to this, large artery atherosclerosis was identified in five patients in the later cohort and small-vessel occlusion in two, compared to none in the earlier cohort. It is likely that the mechanisms have not necessarily changed, since other stroke features such as the NIHSS, and large, multiple and bilateral vascular territorial involvement remained the same. Overall, strokes were severe, evidenced by an abundance of large vascular territory involvement and poor outcomes.

It is likely that with time, access to neurologic care has improved with greater utilization of TPA and earlier presentation, as we noted in our institution. Other studies also show similarly poor access to neurologic care within the time-frame of our early cohort, with significant decreases in the number of patients with critical neurologic conditions such as AIS presenting to the emergency room and subsequent admission, and reduced treatment utilization such as IV TPA and thrombectomy [6, 7] . Another factor determining this compromise was a time-lag between onset of COVID-19 infection and stroke recognition, potentially due to a delayed stroke inducing mechanism, and an inability to conduct neurologic exams due to sedation required for mechanical ventilation. This lag significantly shrank in the later cohort, likely from earlier recognition of and familiarity with stroke in COVID-19, full availability of neuroimaging, and more patients seeking care for neurologic conditions in the emergency departments. Despite these factors, outcomes have not improved with more patients experiencing worsening or static functional 3-month outcomes compared to those with improvement. There is a need for further studies investigating whether measures taken to improve access to neurologic care has had a meaningful benefit on earlier patient presentation, more treatment utilization, and better outcomes.

The severity of COVID-19-related symptoms evolved with early patients experiencing more instance of critical respiratory severity. There was a trend noted for patients with even mild-to-moderate COVID-19 severity in the later cohort suffering poor outcomes indicating a potential independent impact of strokes on poor outcomes, with co-existing COVID-19. However, critical COVID-19 severity for the whole cohort was significantly associated with higher mortality, indicating the major driving force of poor outcomes was critical COVID-19 rather than severe stroke. Other published reports also echo similar findings [8] [9] [10] [11] [12] .

The exact mechanism of stroke in COVID-19 remains unknown, but is likely secondary to the neurotropic potential of COVID-19. Autopsy findings suggest that stroke could be related to underlying prothrombotic state secondary to endothelial invasion via ACE-2 leading to platelet deposition and microthrombi formation within vasculature [13] . However, presence of traditional vascular risk factors, systemic inflammation and sepsis might increase predisposition to thrombotic events. We noticed this phenemon in two of three patients who underwent successful thrombectomy, but later developed re-occlusion of the same vessel within 24 hours.

Older patients with multiple risk factors are particularly vulnerable, although severe strokes from large vessel occlusions have been reported in young patients also [8] [9] [10] [11] [12] . Additional thrombotic risk may be imparted by D-dimer and fibrinogen levels, which are elevated in patients of COVID-19 with stroke, with positive correlation to disease severity and prognosis. These factors have been used as rationale for therapeutic anticoagulation in COVID-19 [1] , however it is not known if it would prevent stroke. Three patients (9%) suffered severe multi-vascular territory strokes despite being on adequate anticoagulation. Current evidence lacks sufficient evidence to necessitate the use of therapeutic anticoagulation in COVID-19 [14, 15] .

Our study is a retrospective review with a small sample size, and the weaknesses are inherent to any retrospective single-institutional studies. Nevertheless, it does lay a foundation to generate further hypotheses to investigate in AIS and COVID-19 using large multi-center observational cohorts. These include a comprehensive investigation of the effect of a completed COVID-19 vaccination course on AIS incidence and outcomes with either co-existing COVID-19, or a history of COVID-19. Effect of both the vaccination and measures taken to improve access to neurologic care should also be diligently investigated for effectiveness and the impact on outcomes.

Improved utilization of IV TPA and thrombectomy, as well as reduction in delay to these treatments as experienced during the COVID-19 pandemic, are also of research interest. There is a paucity of data regarding long-term outcomes in patients with coexisting AIS and COVID-19, and it is imperative that access to both acute rehabilitation services and ongoing neurologic care are not compromised. These items should also be investigated. Finally, the exact role of therapeutic anticoagulation in AIS that is strongly attributed to the hypercoagulability of a severe COVID-19 infection remains to be elucidated further.

Although AIS in COVID-19 is a rare phenomenon, we recommend vigilance in anticipating this issue, particularly in patients with prolonged unexplained encephalopathy, abnormal prothrombotic markers, and history of prior stroke. Although AIS characteristics and incidence in COVID-19 have not changed over the course of pandemic, there has been earlier presentation, more comprehensive evaluation including neurovascular imaging, increased utilization of IV TPA, and lower instance of concomitant critical COVID-19 severity in the later cohort. Outcomes are particularly worse with AIS and COVID-19 and worsen further with critical COVID-19 severity.

Long-term outcomes also tend to worsen more often in survivors of AIS and COVID-19. Despite similar overall outcomes between the two cohorts, there was a possible trend towards worse outcomes within the mild-to-moderate COVID-19 severity subgroup in the later cohort, indicating the devastating impact of co-existing AIS and COVID-19. Future studies should investigate outcomes longer than 3 months and factors leading to worsening long-term outcomes, the effect of a completed vaccination course, access to neurologic care, and the role of therapeutic anticoagulation in AIS with COVID-19.

Funding: No funding sources.

The authors declare that they have no conflicts of interest.

Ethical approval: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study was approved with a waiver from consent by the DMC Institutional Review Board without the need for informed consent due to the use solely of retrospective, existing data from medical records. The research involved no more than minimal risk to the participants. The research could not practicably be carried out without the requested waiver or alteration. The waiver or alteration did not adversely affect the rights and welfare of the participants. Whenever appropriate, the participants or legally authorized representative were provided with additional pertinent information after participation. 

-19 AIS COVID-19 patients presented from Mar-Oct 2020; 16 were from Nov-Aug 2021 -Late cohort patients presented earlier and had more complete stroke workup -Late cohort patients had less critical COVID-19 severity and more IV TPA treatment -AIS incidence, NIHSS and overall outcomes were similar between the cohorts -For all patients, critical COVID-19 had significant association with poor outcomes

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This article does not contain any studies with animals performed by any of the authors.