Decline in mild stroke presentations and intravenous thrombolysis during the COVID-19 pandemic: The Society of Vascular and Interventional Neurology Multicenter Collaboration.


Journal

Clinical neurology and neurosurgery
ISSN: 1872-6968
Titre abrégé: Clin Neurol Neurosurg
Pays: Netherlands
ID NLM: 7502039

Informations de publication

Date de publication:
02 2021
Historique:
received: 19 10 2020
revised: 10 12 2020
accepted: 11 12 2020
pubmed: 1 1 2021
medline: 18 2 2021
entrez: 31 12 2020
Statut: ppublish

Résumé

To evaluate overall ischemic stroke volumes and rates, specific subtypes, and clinical presentation during the COVID-19 pandemic in a multicenter observational study from eight states across US. We compared all ischemic strokes admitted between January 2019 and May 2020, grouped as; March-May 2020 (COVID-19 period) and March-May 2019 (seasonal pre-COVID-19 period). Primary outcome was stroke severity at admission measured by NIHSS stratified as mild (0-7), moderate [8-14], and severe (>14). Secondary outcomes were volume of large vessel occlusions (LVOs), stroke etiology, IV-tPA rates, and discharge disposition. Of the 7969 patients diagnosed with acute ischemic stroke during the study period, 933 (12 %) presented in the COVID-19 period while 1319 (17 %) presented in the seasonal pre-COVID-19 period. Significant decline was observed in the mean weekly volumes of newly diagnosed ischemic strokes (98 ± 3 vs 50 ± 20,p = 0.003), LVOs (16.5 ± 3.8 vs 8.3 ± 5.9,p = 0.008), and IV-tPA (10.9 ± 3.4 vs 5.3 ± 2.9,p = 0.0047), whereas the mean weekly proportion of LVOs (18 % ±5 vs 16 % ±7,p = 0.24) and IV-tPA (10.4 % ±4.5 vs. 9.9 % ±2.4,p = 0.66) remained the same, when compared to the seasonal pre-COVID-19 period. Additionally, an increased proportion of patients presented with a severe disease (NIHSS > 14) during the COVID-19 period (29.7 % vs 24.5 %,p < 0.025). The odds of being discharged to home were 26 % greater in the COVID-19 period when compared to seasonal pre-COVID-19 period (OR:1.26, 95 % CI:1.07-1.49,p = 0.016). During COVID-19 period there was a decrease in volume of newly diagnosed ischemic stroke cases and IV-tPA administration. Patients admitted to the hospital had severe neurological clinical presentation and were more likely to discharge home.

Sections du résumé

BACKGROUND
To evaluate overall ischemic stroke volumes and rates, specific subtypes, and clinical presentation during the COVID-19 pandemic in a multicenter observational study from eight states across US.
METHODS
We compared all ischemic strokes admitted between January 2019 and May 2020, grouped as; March-May 2020 (COVID-19 period) and March-May 2019 (seasonal pre-COVID-19 period). Primary outcome was stroke severity at admission measured by NIHSS stratified as mild (0-7), moderate [8-14], and severe (>14). Secondary outcomes were volume of large vessel occlusions (LVOs), stroke etiology, IV-tPA rates, and discharge disposition.
RESULTS
Of the 7969 patients diagnosed with acute ischemic stroke during the study period, 933 (12 %) presented in the COVID-19 period while 1319 (17 %) presented in the seasonal pre-COVID-19 period. Significant decline was observed in the mean weekly volumes of newly diagnosed ischemic strokes (98 ± 3 vs 50 ± 20,p = 0.003), LVOs (16.5 ± 3.8 vs 8.3 ± 5.9,p = 0.008), and IV-tPA (10.9 ± 3.4 vs 5.3 ± 2.9,p = 0.0047), whereas the mean weekly proportion of LVOs (18 % ±5 vs 16 % ±7,p = 0.24) and IV-tPA (10.4 % ±4.5 vs. 9.9 % ±2.4,p = 0.66) remained the same, when compared to the seasonal pre-COVID-19 period. Additionally, an increased proportion of patients presented with a severe disease (NIHSS > 14) during the COVID-19 period (29.7 % vs 24.5 %,p < 0.025). The odds of being discharged to home were 26 % greater in the COVID-19 period when compared to seasonal pre-COVID-19 period (OR:1.26, 95 % CI:1.07-1.49,p = 0.016).
CONCLUSIONS
During COVID-19 period there was a decrease in volume of newly diagnosed ischemic stroke cases and IV-tPA administration. Patients admitted to the hospital had severe neurological clinical presentation and were more likely to discharge home.

Identifiants

pubmed: 33383463
pii: S0303-8467(20)30779-4
doi: 10.1016/j.clineuro.2020.106436
pmc: PMC7836428
pii:
doi:

Substances chimiques

Tissue Plasminogen Activator EC 3.4.21.68

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

106436

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

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Auteurs

Santiago Ortega-Gutierrez (S)

Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242, USA. Electronic address: santy-ortega@uiowa.edu.

Mudassir Farooqui (M)

Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242, USA.

Alicia Zha (A)

Institute of Stroke and Cerebrovascular Disease, Department of Neurology, University of Texas McGovern Medical School, Houston TX, 77030, USA.

Alexandra Czap (A)

Institute of Stroke and Cerebrovascular Disease, Department of Neurology, University of Texas McGovern Medical School, Houston TX, 77030, USA.

Jacob Sebaugh (J)

Institute of Stroke and Cerebrovascular Disease, Department of Neurology, University of Texas McGovern Medical School, Houston TX, 77030, USA.

Shashvat Desai (S)

University of Pittsburgh Medical Center Mercy Hospital, Pittsburgh, PA, 15219, USA; University of Pittsburgh Medical Center Presbyterian Medical Center, Pittsburgh, PA, 15213, USA.

Ashutosh Jadhav (A)

University of Pittsburgh Medical Center Mercy Hospital, Pittsburgh, PA, 15219, USA; University of Pittsburgh Medical Center Presbyterian Medical Center, Pittsburgh, PA, 15213, USA.

Nirav Vora (N)

Ohio Health Neuroscience Center, Riverside Methodist Hospital, Columbus, OH, 43214, USA.

Vivek Rai (V)

Ohio Health Neuroscience Center, Riverside Methodist Hospital, Columbus, OH, 43214, USA.

Tudor G Jovin (TG)

Cooper Neurological Institute, Cooper University Hospital, Camden, NJ, 08103, USA.

Jesse M Thon (JM)

Cooper Neurological Institute, Cooper University Hospital, Camden, NJ, 08103, USA.

Mark Heslin (M)

Cooper Neurological Institute, Cooper University Hospital, Camden, NJ, 08103, USA.

Lauren Thau (L)

Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242, USA.

Cynthia Zevallos (C)

Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242, USA.

Darko Quispe-Orozco (D)

Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, IA, 52242, USA.

Dinesh V Jillella (DV)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, 30322, USA; Marcus Stroke & Neuroscience Center, Grady Memorial Hospital, Atlanta, GA, 30303, USA.

Fadi Nahab (F)

Department of Neurology & Pediatrics, Emory University, Atlanta, GA, 30319, USA.

Mahmoud H Mohammaden (MH)

Marcus Stroke & Neuroscience Center, Grady Memorial Hospital, Atlanta, GA, 30303, USA.

Raul G Nogueira (RG)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, 30322, USA; Marcus Stroke & Neuroscience Center, Grady Memorial Hospital, Atlanta, GA, 30303, USA.

Diogo C Haussen (DC)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, 30322, USA; Marcus Stroke & Neuroscience Center, Grady Memorial Hospital, Atlanta, GA, 30303, USA.

Thanh N Nguyen (TN)

Department of Neurology, Boston Medical Center, Boston University School of Medicine, MA, 02118, USA.

Jose Rafael Romero (JR)

Department of Neurology, Boston Medical Center, Boston University School of Medicine, MA, 02118, USA.

Hugo J Aparicio (HJ)

Department of Neurology, Boston Medical Center, Boston University School of Medicine, MA, 02118, USA.

Mohamed Osman (M)

Department of Neurology, Mercy Health St. Vincent Hospital, Toledo, OH, 43608, USA.

Israr Ul Haq (IU)

Department of Neurology, Mercy Health St. Vincent Hospital, Toledo, OH, 43608, USA.

David Liebeskind (D)

Department of Neurology, Ronald Reagan University of California at Los Angeles, Los Angeles, CA, 90095, USA.

Ameer E Hassan (AE)

Department of Neurology, University of Texas Rio Grande Valley, Valley Baptist Medical Center, Harlingen, TX, 78550, USA.

Osama Zaidat (O)

Department of Neurology, Mercy Health St. Vincent Hospital, Toledo, OH, 43608, USA.

James E Siegler (JE)

Cooper Neurological Institute, Cooper University Hospital, Camden, NJ, 08103, USA.

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