Skip to main content
Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2023 May 4;32(8):107171. doi: 10.1016/j.jstrokecerebrovasdis.2023.107171

Mortality following mechanical thrombectomy for ischemic stroke in patients with COVID-19

Jonathan Dallas a,, Talia A Wenger b, Kristie Q Liu b, Li Ding c, Benjamin S Hopkins a, Frank J Attenello a, William J Mack a
PMCID: PMC10156987  PMID: 37172468

Abstract

Objectives

Multiple prior studies have shown a relationship between COVID-19 and strokes; further, COVID-19 has been shown to influence both time-to-thrombectomy and overall thrombectomy rates. Using large-scale, recently released national data, we assessed the association between COVID-19 diagnosis and patient outcomes following mechanical thrombectomy.

Materials and methods

Patients in this study were identified from the 2020 National Inpatient Sample. All patients with arterial strokes undergoing mechanical thrombectomy were identified using ICD-10 coding criteria. Patients were further stratified by COVID diagnosis (positive vs. negative). Other covariates, including patient/hospital demographics, disease severity, and comorbidities were collected. Multivariable analysis was used to determine the independent effect of COVID-19 on in-hospital mortality and unfavorable discharge.

Results

5078 patients were identified in this study; 166 (3.3%) were COVID-19 positive. COVID-19 patients had a significantly higher mortality rate (30.1% vs. 12.4%, p < 0.001). When controlling for patient/hospital characteristics, APR-DRG disease severity, and Elixhauser Comorbidity Index, COVID-19 was an independent predictor of increased mortality (OR 1.13, p = 0.002). COVID-19 was not significantly related to discharge disposition (p = 0.480). Older age and increased APR-DRG disease severity were also correlated with increase morality.

Conclusions

Overall, this study indicates that COVID-19 is a predictor of mortality among mechanical thrombectomy. This finding is likely multifactorial but may be related to multisystem inflammation, hypercoagulability, and re-occlusion seen in COVID-19 patients. Further research would be needed to clarify these relationships.

Keywords: Stroke, Thrombectomy, Mortality, COVID-19, Coronavirus

Introduction

Cerebrovascular accident (CVA), or stroke, is an extremely common pathology in the United States, affecting nearly 800,000 patients per year.1 Treatment for stroke is highly variable and depends greatly on presenting factors and time to presentation; however, if indicated, mechanical thrombectomy is often the ideal treatment modality for large-vessel occlusions.2

With the onset of the coronavirus-19 (COVID-19) global pandemic, millions of patients have been impacted by disruptions in healthcare.3 Due to its effect on hospital workflow, patient volume, and acuity of illness, COVID-19 has affected not only patients primarily hospitalized with COVID-19, but also patients with sequelae of systemic infections or patients coincidentally diagnosed with COVID-19.4, 5, 6, 7, 8 Furthermore, hospitals were required to reorganize ICU management and care processes to meet the increased demands of these patients.4, 5, 6, 7, 8 Despite these efforts, COVID-19 still led to significant delays and/or cancellations of many urgent, non-elective procedures, including stroke treatment.9, 10, 11

Among many systemic sequelae of COVID-19, it has been shown to have a significant relationship with ischemic stroke. This is likely, at least in part, due to multisystem dysfunction, inflammation, and hypercoagulability.12 , 13 Previous studies have reported up to a 9.4% incidence of ischemic stroke among COVID-19 patients, although reported incidences varied widely within the literature.12 , 14 However, prior studies have reported that severe COVID-19 infection is associated with an increase in ischemic stroke risk as well as increased stroke severity.12 , 14

With the onset of the COVID-19 pandemic, various facilities have also documented decreased rates of mechanical thrombectomy for stroke patients, and COVID-19 surges were found to be associated with increased time to mechanical thrombectomy.15 , 16 These delays in stroke treatment may play a role in adverse patient outcomes, but prior studies have only examined small patient cohorts, limiting their generalizability. Specifically, the outcomes of mechanical thrombectomy patients with and without COVID-19 have yet to be examined with a large national dataset.

In this study, the National Inpatient Sample (NIS) database from April 2020 to December 2020 was utilized to evaluate demographics, mortality rates, and unfavorable discharge for mechanical thrombectomy patients with and without COVID-19. Our hypothesis is that concurrent COVID-19 diagnosis in mechanical thrombectomy patients is associated with increased likelihood of mortality compared to mechanical thrombectomy patients without COVID-19.

Methods

Patient identification

Patients in this study were identified from the 2020 version of the National Inpatient Sample (NIS). The NIS is a large administrative databased published as part of the Healthcare Cost and Utilization Project (HCUP) by the Agency for Healthcare Research and Quality (AHRQ). The NIS is a discharge-level database the contains sociodemographic, diagnostic, and outcomes data from over 7 million United States hospitalizations per year. When weighted, this accounts for approximately 35 million annual hospitalizations. COVID-19 diagnosis was of particular interest to the investigators; as such, the 2020 year of the NIS (the most recently published edition) was chosen due to the addition of a specific ICD-10 code for proven COVID-19 diagnosis (U07.1); specifically, patients were taken from April to December of 2020 (COVID-19 coding was not available prior to April 2020).

The primary inclusion criteria selected for patients with arterial cerebral infarctions (I63.0X–163.5X, I63.81) that underwent mechanical thrombectomy (03CGXXX – 03CQXXX). Patients with cerebral infarction due to venous thrombosis and other/unspecified infarctions were excluded. Pediatric patients (less than 18 years old) or missing mortality/length of stay (LOS) data were also excluded. A flowchart detailing patient selection is provided in Fig. 1 . A full list of ICD-10 codes used for patient inclusion/exclusion is provided in the supplementary material (Table S1).

Fig. 1.

Fig 1

Flowchart detailing patient selection criteria.

Data collection

Additional patient-related information was obtained via multiple methods. Basic sociodemographic information was obtained directly from the NIS; this included age, sex, race, residence, income quartile, and insurance status. Hospital information was also collected (hospital bedsize, ownership structure, and US census division/region). Comorbidities were estimated by both (1) APR-DRG risk of mortality (obtained directly from the NIS) and (2) the Elixhauser Comorbidity Index (ECI; calculated from ICD-10 codes).

The primary outcomes in this study include (1) in-hospital mortality and (2) discharge disposition (which is a binary variable considered to be either “favorable” or “unfavorable”). For the purposes of this study, “unfavorable discharge” was defined as either (1) in-hospital mortality or (2) transfer to non-short-term care, such as skilled nursing facilities or intermediate care.

Statistical analysis

Patient demographics and clinical characteristics were reported by frequency/percentage for the entire cohort and further stratified by COVID-19 status. Differences between groups were evaluated using χ2 tests. Two types of multivariable regressions were used for assessing association between COVID-19 infection and outcomes: (1) Logistic regression for mortality, with results reported as odds ratios (OR), and (2) Log-binomial regression for discharge disposition, with results reported as relative risks (RR). Both models used generalized estimation equations to incorporate hospital clustering. Hosmer-Lemeshow goodness-of-fit test was used to check logistic model assumptions. All covariates mentioned above were included in the model for adjustment. Missing data affected less than 4% of patients, so only admissions with no missing information regarding exposures, outcomes, or covariates were used for regression models. A p-value < 0.05 was considered statistically significant. Analysis was performed using SAS, version 9.4 (SAS Institute, Cary, North Carolina, USA).

Results

Patient demographics

The overall demographics of the patient cohort are summarized in Table 1 . 5078 patients in the NIS underwent mechanical thrombectomy stroke from April to December 2020. Of those patients, 4912 were COVID-19 negative (96.7%), and 166 were COVID-19 positive (3.3%). When stratified by COVID-19 status, there were a number of differences noted for multiple demographic factors. Patients with COVID-19 were more likely to be younger (37.3% 18-59 years of age for COVID-19 positive patients, 23.4% for COVID-19 negative patients, p < 0.001). Multiple demographic differences were noted among the two populations regarding both race and insurance status. As expected, patients with COVID-19 had worse risk of mortality and illness severity (per APR-DRG); however, there was no difference in the ECI.

Table 1.

Demographic characteristics of all stroke thrombectomy patients stratified by COVID-19 status.

Total Cohort COVID (–) COVID (+) p-value
Patient Count 5078 4912 (96.7%) 166 (3.3%)
Age (years) <0.0001
 18-44 314 (6.2%) 298 (6.1%) 16 (9.6%)
 45-59 897 (17.7%) 851 (17.3%) 46 (27.7%)
 60-74 1876 (37.0%) 1814 (36.9%) 62 (37.4%)
 75+ 1991 (39.2%) 1949 (39.7%) 42 (25.3%)
Sex 0.21
 Male 2480 (48.8%) 2391 (48.7%) 89 (53.6%)
 Female 2598 (51.2%) 2521 (51.3%) 77 (46.4%)
Race <0.0001
 White 3294 (64.9%) 3223 (65.6%) 71 (42.8%)
 Black 773 (15.2%) 735 (15.0%) 38 (22.9%)
 Hispanic 426 (8.4%) 393 (8.0%) 33 (19.9%)
 Asian or Pacific Islander 170 (3.4%) 166 (3.4%) DS*
 Native American 13 (0.3%) 11 (0.2%) DS*
 Other 171 (3.4%) 160 (3.3%) 11 (6.6%)
 Missing 231 (4.6%) 224 (4.6%) DS*
Insurance 0.02
 Medicare 3087 (60.8%) 3007 (61.2%) 80 (48.2%)
 Medicaid 557 (11.0%) 529 (10.8%) 28 (16.9%)
 Private Insurance 1093 (21.5%) 1052 (21.4%) 41 (24.7%)
 Self-Pay 177 (3.5%) 169 (3.4%) DS*
 No Charge 16 (0.3%) 16 (0.3%) 0 (0.0%)
 Other 137 (2.7%) 130 (2.7%) DS*
 Missing 11 (0.2%) DS* DS*
NCHS Urban/Rural Code 0.61
 Central counties of metro areas of ≥ 1 million population 1560 (30.7%) 1500 (30.5%) 60 (36.1%)
 “Fringe” countries of metro areas of ≥ 1 million population 1238 (24.4%) 1199 (24.4%) 39 (23.5%)
 Counties in metro areas of 250,000-999,999 population 1075 (21.2%) 1042 (21.2%) 33 (19.9%)
 Counties in metro areas of 50,000-249,999 population 431 (8.5%) 417 (8.5%) 14 (8.4%)
 Micropolitan counties 410 (8.1%) 398 (8.1%) 12 (7.2%)
 Not metropolitan or micropolitan counties 341 (6.7%) 334 (6.8%) DS*
 Missing 23 (0.5%) 22 (0.5%) DS*
Median Household Income (percentile) 0.17
 0-25% 1443 (28.4%) 1387 (28.2%) 56 (33.7%)
 26-50% 1354 (26.7%) 1305 (26.6%) 49 (29.5%)
 51-75% 1181 (23.3%) 1148 (23.4%) 33 (19.9%)
 76-100% 1037 (20.4%) 1011 (20.6%) 26 (15.7%)
 Missing 63 (1.2%) 61 (1.2%) DS*
Hospital Bedsize 0.02
 Small 367 (7.2%) 363 (7.4%) DS*
 Medium 1094 (21.5%) 1050 (21.4%) 44 (26.5%)
 Large 3617 (71.2%) 3499 (71.2%) 118 (71.1%)
Hospital Ownership 0.75
 Government, nonfederal 606 (11.9%) 584 (11.9%) 22 (13.3%)
 Private, not-profit 3844 (75.7%) 3718 (75.7%) 126 (75.9%)
 Private, invest-own 628 (12.4%) 610 (12.4%) 18 (10.8%)
Hospital Division 0.14
 New England 190 (3.7%) 187 (3.8%) DS*
 Middle Atlantic 701 (13.8%) 672 (13.7%) 29 (17.5%)
 East North Central 748 (14.7%) 719 (14.6%) 29 (17.5%)
 West North Central 368 (7.3%) 352 (7.2%) 16 (9.6%)
 South Atlantic 1126 (22.2%) 1094 (22.3%) 32 (19.3%)
 East South Central 384 (7.6%) 370 (7.5%) 14 (8.4%)
 West South Central 485 (9.6%) 465 (9.5%) 20 (12.1%)
 Mountain 355 (7.0%) 346 (7.0%) DS*
 Pacific 721 (14.2%) 707 (14.4%) 14 (8.4%)
Hospital Region 0.08
 Northeast 891 (17.6%) 859 (17.5%) 32 (19.3%)
 Midwest 1116 (22.0%) 1071 (21.8%) 45 (27.1%)
 South 1995 (39.3%) 1929 (39.3%) 66 (39.8%)
 West 1076 (21.2%) 1053 (21.4%) 23 (13.9%)
APR-DRG Risk of Mortality <0.0001
 Minor 608 (12.0%) 607 (12.4%) DS*
 Moderate 843 (16.6%) 838 (17.1%) DS*
 Major 1027 (20.2%) 1006 (20.5%) 21 (12.7%)
 Extreme 2600 (51.2%) 2461 (50.1%) 139 (83.7%)
APR-DRG Illness Severity <0.0001
 Minor 49 (1.0%) 49 (1.0%) 0 (0%)
 Moderate 1117 (22.0%) 1116 (22.7%) DS*
 Major 1508 (29.7%) 1481 (30.2%) 27 (16.3%)
 Extreme 2404 (47.3%) 2266 (46.1%) 138 (83.1%)
Elixhauser Comorbidity Index 0.62
 0 49 (1.0%) 49 (1.0%) 0 (0.0%)
 1 189 (3.7%) 183 (3.7%) DS*
 2 578 (11.4%) 560 (11.4%) 18 (10.8%)
 ≥3 4262 (83.9%) 4120 (83.9%) 142 (85.5%)
Mortality <0.0001
 No 4420 (87.0%) 4304 (87.6%) 116 (69.9%)
 Yes 658 (13.0%) 608 (12.4%) 50 (30.1%)
Discharge Disposition 0.007
 Unfavorable 3260 (64.2%) 3137 (63.9%) 123 (74.1%)
 Favorable 1818 (35.8%) 1775 (36.1%) 43 (25.9%)

DS*: data suppressed - per NIS policy, specific patient counts are not provided for cells with less than 10 patients to protect patient anonymity

Patients with COVID-19 were noted to have a higher mortality rate (30.1% vs. 12.4%, p < 0.001). Additionally, patients with COVID-19 were more likely to have unfavorable discharge disposition (74.1% vs. 63.9%, p = 0.007).

Patient outcomes

Predictors of in-hospital mortality among patients undergoing thrombectomy are shown in Table 2 . Most notably, even when controlling for factors such as ECI and APR-DRG disease severity, concurrent COVID-19 diagnosis was an independent predictor of mortality (OR 1.13, p = 0.002). This means that, after adjusting for all other covariates, COVID-19 led to an independent increase in mortality by 10%. Various demographic factors were related to mortality; not unsurprisingly, there is a direct relationship between age and morality rate. None of the assessed hospital factors (bedsize, census division, or ownership) were related to mortality rates. As expected, APR-DRG disease severity was directly correlated with mortality.

Table 2.

Significant predictors of mortality among patient going mechanical thrombectomy.

OR (95% Cl) p-value*
Age
 <45 Ref
 45-59 1.02 (0.98-1.05) 0.343
 60-74 1.05 (1.01-1.09) 0.010
 ≥75 1.08 (1.04-1.12) < 0.001
Race
 White Ref
 Black 0.95 (0.93-0.98) < 0.001
 Hispanic 1.03 (0.99-1.07) 0.158
 Asian or Pacific Islander 0.96 (0.91-1.00) 0.066
 Native American 0.88 (0.82-0.95) 0.001
 Other 0.99 (0.94-1.03) 0.548
Primary Insurance
 Medicaid Ref
 Medicare 1.02 (0.99-1.06) 0.189
 Private insurance 1.00 (0.97-1.03) 0.939
 Self-pay 1.06 (1.00-1.12) 0.039
 No charge 1.00 (0.87-1.16) 0.987
 Other 1.05 (0.99-1.12) 0.121
Median household income (percentile)
 0-25 Ref
 26-50 0.99 (0.96-1.01) 0.366
 51-75 0.98 (0.96-1.01) 0.290
 76-100 0.96 (0.93-0.99) 0.016
APR-DRG Disease Severity
 Minor Ref
 Moderate 1.01 (0.99-1.02) 0.271
 Major 1.04 (1.02-1.06) < 0.001
 Extreme 1.24 (1.21-1.26) < 0.001
Elixhauser Comorbidity Score
 0 Ref
 1 0.88 (0.76-1.03) 0.103
 2 0.88 (0.75-1.02) 0.082
 ≥3 0.86 (0.74-1.00) 0.048
COVID
 No Ref
 Yes 1.13 (1.05-1.21) 0.002

Significance calculated via multivariable logistic regression

Similarly, predictors of unfavorable discharge disposition are shown in Table 3 . Unlike mortality, COVID-19 diagnosis was found to have no significant relationship with discharge disposition (p = 0.480). Like mortality, advanced age was found to have a direct relationship with unfavorable discharge. Patient were less likely to have unfavorable discharge if they had private insurance (RR 0.93, p = 0.004) or were self-pay (RR 0.66, p < 0.001). APG-DRG disease severity was again found to be directly correlated with unfavorable discharge.

Table 3.

Significant predictors of unfavorable discharge among patient going mechanical thrombectomy.

RR (95% Cl) p-value*
Age
 <45 Ref
 45-59 1.14 (1.02-1.26) 0.018
 60-74 1.24 (1.11-1.38) < 0.001
 ≥75 1.23 (1.11-1.37) < 0.001
Race
 White Ref
 Black 0.97 (0.93-1.02) 0.244
 Hispanic 0.97 (0.90-1.04) 0.354
 Asian or Pacific Islander 0.75 (0.64-0.87) < 0.001
 Native American 0.85 (0.59-1.23) 0.389
 Other 0.92 (0.82-1.03) 0.138
Primary Insurance
 Medicare Ref
 Medicaid 0.97 (0.91-1.04) 0.458
 Private insurance 0.93 (0.88-0.98) 0.004
 Self-pay 0.66 (0.56-0.78) < 0.001
 No charge 0.44 (0.17-1.19) 0.105
 Other 0.82 (0.71-0.94) 0.004
Census Division of Hospital
 New England Ref
 Middle Atlantic 0.99 (0.92-1.06) 0.775
 East North Central 1.02 (0.96-1.09) 0.535
 West North Central 0.93 (0.85-1.01) 0.077
 South Atlantic 0.98 (0.92-1.05) 0.585
 East South Central 0.98 (0.90-1.07) 0.648
 West South Central 0.97 (0.89-1.04) 0.387
 Mountain 1.00 (0.94-1.08) 0.903
 Pacific 0.82 (0.74-0.90) < 0.001
APR-DRG Disease Severity
 Minor Ref
 Moderate 2.17 (1.12-4.18) 0.021
 Major 3.15 (1.63-6.08) < 0.001
 Extreme 4.26 (2.20-8.23) < 0.001
Elixhauser Comorbidity Score
 0 Ref
 1 0.75 (0.62-0.92) 0.006
 2 0.87 (0.75-1.01) 0.074
 ≥3 0.93 (0.80-1.07) 0.279
COVID
 No Ref
 Yes 0.97 (0.89-1.06) 0.480

Significance calculated via multivariable log-binomial regression

Discussion

As hypothesized, COVID-19 infection was associated with a higher likelihood of mortality among stroke patients that received thrombectomy, even when controlling for disease severity/comorbidities. Our analysis also showed an association between post-thrombectomy mortality and (1) APR-DRG disease severity and (2) advanced age. To the best of our knowledge, this study is the first to leverage a large national dataset to compare mortality rates in stroke patients with and without COVID-19 who underwent mechanical thrombectomy.

Prior studies have demonstrated poor outcomes and high mortality rates among COVID-19 positive stroke patients despite appropriate treatment with thrombectomy.11 , 17, 18, 19 One 2020 single-center analysis found that COVID-19 was an independent predictor for in-hospital mortality in stroke patients that received mechanical thrombectomy (OR 6.67, 95% Cl 1.1-40.4).20 A retrospective study of COVID-19 positive stroke patients that received mechanical thrombectomy found high complication rates, extensive clot burden, procedures requiring multiple attempts, and a high mortality rate.13 Our study builds upon these findings by offering the perspective of a large-scale national database that can overcome many of the biases of small single-institution analyses.

In this study, we found that COVID-19 patients undergoing thrombectomy for treatment of stroke had a significantly increased likelihood of inpatient mortality than non-COVID patients (OR 1.13, 95% Cl 1.05-1.21). It's widely believed that COVID-19 may contribute to a high inflammatory state and hypoxemia, leading to cytokine-storm-triggered coagulopathies.21, 22, 23, 24 Many studies have reported high re-occlusion rates among COVID-19 patients treated with thrombectomy, potentially related to a hypercoagulable state induced by infection.25 Microvascular inflammation and endotheliitis could also contribute to higher rates of complications and re-occlusions in COVID patients receiving thrombectomy.19 , 26 , 27 Still, other explanations should also be explored; patients with underlying cardiovascular disease and risk factors are more likely to develop severe cases of COVID-19 and may also contribute to a higher probability of serious complications and poor outcomes from stroke.28 , 29 Further investigation into the pathophysiology underlying COVID-related stroke and complications leading to poor outcomes in COVID patients post-thrombectomy is necessary.

Interestingly, while COVID-19 was shown to have a significant effect on in-hospital mortality, it did not appear to effect overall disposition (i.e. favorable vs. unfavorable). While mortality is included in the definition “unfavorable discharge”, it also includes discharge to skilled nursing facilities and intermediate care (whereas “favorable discharge” includes routine home discharges, short-term care, and home health). As such, while mortality is more inherently related to both stroke severity and systemic disease burden, discharge disposition is also tied to a patient's functional status following a stroke. While the effect of COVID-19 on systemic disease burden and subsequent mortality is more straightforward, it may be that COVID-19 has little to no independent effect on a patient's functional status following a stroke.

Our study also found that several demographics significantly impacted likelihood of mortality post-thrombectomy. Patients that self-paid (did not have/use health insurance) had a higher likelihood of mortality post-thrombectomy compared to Medicare patients, while patients in the 76-100th percentile of median household income had a lower likelihood of mortality post-thrombectomy. Similar trends in disparities across insurance and income have been observed in other studies; one analysis of NIS data from 2006-2016 found that 4th quartile median household income (OR 1.10, 95% Cl 1.06-1.14) and private insurance (OR 1.36, 95% Cl 1.31-1.39) were predictors of good outcome following mechanical thrombectomy.30 , 31 These trends may be confounded by decreased access to preventative care among patients with lower income or poor insurance coverage, contributing to both the severity of stroke and response to treatment. There may also be variation in time to presentation to medical care and access to quality treatments and hospitals. Further review of these factors and others would be needed to investigate this.

Limitations

As with all NIS-based studies, this project has a set of limitations that are present in nearly all studies with data from administrative databases. Given that diagnoses are characterized by ICD-10 codes, only diagnostic data with a corresponding ICD-10 code can be utilized. Additionally, any administrative database is subject to a certain rate of coding inaccuracies, and this is impossibly to retrospectively verify. While administrative databases are useful in their ability to assess large amounts of patients, they cannot imply direct causality. Lastly, the NIS is a discharge-level database and not a patient-level database; as such, patients are not trackable across multiple hospital stays, thereby limiting assessment of long-term outcomes (such as post-discharge mortality).

Also of note, as the NIS is a large and generalized database for all tyles of hospital admissions; while this proves beneficial in obtaining large patient samples, it does not include stroke-specific information that is not readily codable via ICD-10 codes. For example, information on stroke severity (such as the NIH Stroke Scale) and the amount of time from stroke onset until presentation are not available and likely act as confounders in the data. Similarly, specifics of individual thrombectomies (such door-to-puncture time or procedural difficulty) are unable to be assessed.

Conclusions

In this study, the relationship between COVID-19, stroke, and outcomes following mechanical thrombectomy are assessed using a large, administrative database (the NIS). Specifically, it was hypothesized that patients with COVID-19-related strokes would have higher mortality rates following mechanical thrombectomy, even when controlling for disease severity and comorbidities. After a review of all patients in the NIS undergoing thrombectomy from April to December of 2020, COVID-19 was found to be an independent predictor of increased mortality rates. Although the exact causal relationship cannot be established, it is likely multifactorial and may be related to multisystem inflammation, hypercoagulability, and re-occlusion seen in COVID-19 patients. Further research would be needed to identify the pathophysiological relationship of this finding.

Declaration of Competing Interest

None.

Footnotes

Jonathan Dallas MD, (323) 409-7422, 1200 North State Street, Suite 3300, Los Angeles, CA 90033

Talia A. Wenger BA, (323) 409-7422

Kristie Q. Liu MS, (323) 409-7422

Li Ding MD MPH, (323) 409-7422

Benjamin S. Hopkins MD, (323) 409-7422

Frank J. Attenello MD MS, (323) 409-7422

William J. Mack MD, (323) 409-7422

The authors report no conflicts of interest for this study. This work was supported by grants UL1TR001855 from the National Center for Advancing Translational Science (NCATS) of the U.S. National Institutes of Health. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Supplementary material associated with this article can be found in the online version at doi:10.1016/j.jstrokecerebrovasdis.2023.107171.

Appendix. Supplementary materials

mmc1.docx (17.6KB, docx)

References

  • 1.Stroke Facts Centers for Disease Control and Prevention [updated October 14, 2022; cited 2023]. Available from: https://www.cdc.gov/stroke/facts.htm.
  • 2.Morotti A, Poli L, Costa P. Acute stroke. Semin Neurol. 2019;39(1):61–72. doi: 10.1055/s-0038-1676992. [DOI] [PubMed] [Google Scholar]
  • 3.Ciotti M, Ciccozzi M, Terrinoni A, et al. The COVID-19 pandemic. Crit Rev Clin Lab Sci. 2020;57(6):365–388. doi: 10.1080/10408363.2020.1783198. [DOI] [PubMed] [Google Scholar]
  • 4.Anesi GL, Lynch Y, Evans L. A conceptual and adaptable approach to hospital preparedness for acute surge events due to emerging infectious diseases. Crit Care Explor. 2020;2(4):e0110. doi: 10.1097/CCE.0000000000000110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Butler CR, Wong SPY, Wightman AG, et al. US clinicians' experiences and perspectives on resource limitation and patient care during the COVID-19 pandemic. JAMA Netw Open. 2020;3(11) doi: 10.1001/jamanetworkopen.2020.27315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Carenzo L, Costantini E, Greco M, et al. Hospital surge capacity in a tertiary emergency referral centre during the COVID-19 outbreak in Italy. Anaesthesia. 2020;75(7):928–934. doi: 10.1111/anae.15072. [DOI] [PubMed] [Google Scholar]
  • 7.Vranas KC, Golden SE, Mathews KS, et al. The influence of the COVID-19 pandemic on ICU organization, care processes, and frontline clinician experiences: a qualitative study. Chest. 2021;160(5):1714–1728. doi: 10.1016/j.chest.2021.05.041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Xie J, Tong Z, Guan X, et al. Critical care crisis and some recommendations during the COVID-19 epidemic in China. Intensive Care Med. 2020;46(5):837–840. doi: 10.1007/s00134-020-05979-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Gagliano A, Villani PG, Co FM, et al. COVID-19 epidemic in the middle province of Northern Italy: impact, logistics, and strategy in the First Line Hospital. Disaster Med Public Health Prep. 2020;14(3):372–376. doi: 10.1017/dmp.2020.51. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Zhao J, Rudd A, Liu R. Challenges and potential solutions of stroke care during the coronavirus disease 2019 (COVID-19) outbreak. Stroke. 2020;51(5):1356–1357. doi: 10.1161/STROKEAHA.120.029701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Zureigat H, Alhusban M, Cobia M. Mechanical thrombectomy outcomes in COVID-19 patients with acute ischemic stroke: a narrative review. Neurologist. 2021;26(6):261–267. doi: 10.1097/NRL.0000000000000360. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Sagris D, Papanikolaou A, Kvernland A, et al. COVID-19 and ischemic stroke. Eur J Neurol. 2021;28(11):3826–3836. doi: 10.1111/ene.15008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Sweid A, Hammoud B, Bekelis K, et al. Cerebral ischemic and hemorrhagic complications of coronavirus disease 2019. Int J Stroke. 2020;15(7):733–742. doi: 10.1177/1747493020937189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Narrett JA, Mallawaarachchi I, Aldridge CM, et al. Increased stroke severity and mortality in patients with SARS-CoV-2 infection: an analysis from the N3C database. J Stroke Cerebrovasc Dis. 2023;32(3) doi: 10.1016/j.jstrokecerebrovasdis.2023.106987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Gu S, Li J, Shen H, et al. The impact of COVID-19 pandemic on treatment delay and short-term neurological functional prognosis for acute ischemic stroke during the lockdown period. Front Neurol. 2022;13 doi: 10.3389/fneur.2022.998758. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Kojundzic SL, Sablic S, Budimir Mrsic D, et al. Mechanical thrombectomy in acute ischemic stroke COVID-19 and Non-COVID-19 patients: a single comprehensive stroke center study. Life (Basel) 2023;13(1) doi: 10.3390/life13010186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Al-Smadi AS, Mach JC, Abrol S, et al. Endovascular thrombectomy of COVID-19-related large vessel occlusion: a systematic review and summary of the literature. Curr Radiol Rep. 2021;9(4):4. doi: 10.1007/s40134-021-00379-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Ntaios G, Michel P, Georgiopoulos G, et al. Characteristics and outcomes in patients with COVID-19 and acute ischemic stroke: the global COVID-19 stroke registry. Stroke. 2020;51(9):e254–e2e8. doi: 10.1161/STROKEAHA.120.031208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Escalard S, Maier B, Redjem H, et al. Treatment of acute ischemic stroke due to large vessel occlusion with COVID-19: experience from Paris. Stroke. 2020;51(8):2540–2543. doi: 10.1161/STROKEAHA.120.030574. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Requena M, Olive-Gadea M, Muchada M, et al. COVID-19 and stroke: incidence and etiological description in a high-volume center. J Stroke Cerebrovasc Dis. 2020;29(11) doi: 10.1016/j.jstrokecerebrovasdis.2020.105225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Papanagiotou P, Parrilla G, Pettigrew LC. Thrombectomy for treatment of acute stroke in the COVID-19 pandemic. Cerebrovasc Dis. 2021;50(1):20–25. doi: 10.1159/000511729. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Qin C, Zhou L, Hu Z, et al. Dysregulation of immune Response in patients with coronavirus 2019 (COVID-19) in Wuhan, China. Clin Infect Dis. 2020;71(15):762–768. doi: 10.1093/cid/ciaa248. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Zhang Y, Xiao M, Zhang S, et al. Coagulopathy and antiphospholipid antibodies in patients with Covid-19. N Engl J Med. 2020;382(17):e38. doi: 10.1056/NEJMc2007575. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Oxley TJ, Mocco J, Majidi S, et al. Large-vessel stroke as a presenting feature of Covid-19 in the young. N Engl J Med. 2020;382(20):e60. doi: 10.1056/NEJMc2009787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Paganini-Hill A, Lozano E, Fischberg G, et al. Infection and risk of ischemic stroke: differences among stroke subtypes. Stroke. 2003;34(2):452–457. doi: 10.1161/01.str.0000053451.28410.98. [DOI] [PubMed] [Google Scholar]
  • 26.Varga Z, Flammer AJ, Steiger P, et al. Endothelial cell infection and endotheliitis in COVID-19. Lancet. 2020;395(10234):1417–1418. doi: 10.1016/S0140-6736(20)30937-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Barnes BJ, Adrover JM, Baxter-Stoltzfus A, et al. Targeting potential drivers of COVID-19: Neutrophil extracellular traps. J Exp Med. 2020;217(6) doi: 10.1084/jem.20200652. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Du RH, Liang LR, Yang CQ, et al. Predictors of mortality for patients with COVID-19 pneumonia caused by SARS-CoV-2: a prospective cohort study. Eur Respir J. 2020;55(5) doi: 10.1183/13993003.00524-2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Ruan Q, Yang K, Wang W, et al. Clinical predictors of mortality due to COVID-19 based on an analysis of data of 150 patients from Wuhan, China. Intensive Care Med. 2020;46(5):846–848. doi: 10.1007/s00134-020-05991-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Mehta AM, Fifi JT, Shoirah H, et al. Racial and socioeconomic disparities in the use and outcomes of endovascular thrombectomy for acute ischemic stroke. AJNR Am J Neuroradiol. 2021;42(9):1576–1583. doi: 10.3174/ajnr.A7217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Elgendy IY, Omer MA, Kennedy KF, et al. 30-Day Readmissions after endovascular thrombectomy for acute ischemic stroke. JACC Cardiovasc Interv. 2018;11(23):2414–2424. doi: 10.1016/j.jcin.2018.09.006. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

mmc1.docx (17.6KB, docx)

Articles from Journal of Stroke and Cerebrovascular Diseases are provided here courtesy of Elsevier

RESOURCES