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1.
Journal of Stroke ; : 272-281, 2023.
Article in English | WPRIM (Western Pacific) | ID: wpr-1001574

ABSTRACT

Background@#and Purpose This study aimed to investigate the effect of endovascular treatment (EVT, with or without intravenous thrombolysis [IVT]) versus IVT alone on outcomes in patients with acute ischemic stroke (AIS) and intracranial large vessel occlusion (LVO) attributable to cervical artery dissection (CeAD). @*Methods@#This multinational cohort study was conducted based on prospectively collected data from the EVA-TRISP (EndoVAscular treatment and ThRombolysis for Ischemic Stroke Patients) collaboration. Consecutive patients (2015–2019) with AIS-LVO attributable to CeAD treated with EVT and/or IVT were included. Primary outcome measures were (1) favorable 3-month outcome (modified Rankin Scale score 0–2) and (2) complete recanalization (thrombolysis in cerebral infarction scale 2b/3). Odds ratios with 95% confidence intervals (OR [95% CI]) from logistic regression models were calculated (unadjusted, adjusted). Secondary analyses were performed in the patients with LVO in the anterior circulation (LVOant) including propensity score matching. @*Results@#Among 290 patients, 222 (76.6%) had EVT and 68 (23.4%) IVT alone. EVT-treated patients had more severe strokes (National Institutes of Health Stroke Scale score, median [interquartile range]: 14 [10–19] vs. 4 [2–7], P<0.001). The frequency of favorable 3-month outcome did not differ significantly between both groups (EVT: 64.0% vs. IVT: 86.8%; ORadjusted 0.56 [0.24–1.32]). EVT was associated with higher rates of recanalization (80.5% vs. 40.7%; ORadjusted 8.85 [4.28–18.29]) compared to IVT. All secondary analyses showed higher recanalization rates in the EVT-group, which however never translated into better functional outcome rates compared to the IVT-group. @*Conclusion@#We observed no signal of superiority of EVT over IVT regarding functional outcome in CeAD-patients with AIS and LVO despite higher rates of complete recanalization with EVT. Whether pathophysiological CeAD-characteristics or their younger age might explain this observation deserves further research.

2.
Journal of Stroke ; : 179-188, 2022.
Article in English | WPRIM (Western Pacific) | ID: wpr-938179

ABSTRACT

As of May 2022, there have been more than 400 million cases (including re-infections) of the systemic acute respiratory syndrome-coronavirus 2 (SARS-CoV-2), and nearly 5 million deaths worldwide. Not only has the coronavirus disease 2019 (COVID-19) pandemic been responsible for diagnosis and treatment delays of a wide variety of conditions, and overwhelmed the allocation of healthcare resources, it has impacted the epidemiology and management of cerebrovascular disease. In this narrative review, we summarize the changing paradigms and latest data regarding the complex relationship between COVID-19 and cerebrovascular disease. Paradoxically, although SARS-CoV-2 has been associated with many thrombotic complications—including ischemic stroke—there have been global declines in ischemic stroke and other cerebrovascular diseases. These epidemiologic shifts may be attributed to patient avoidance of healthcare institutions due to fear of contracting the novel human coronavirus, and also related to declines in other transmissible infectious illnesses which may trigger ischemic stroke. Despite the association between SARS-CoV-2 and thrombotic events, there are inconsistent data regarding targeted antithrombotics to prevent venous and arterial events. In addition, we provide recommendations for the conduct of stroke research and clinical trial planning during the ongoing COVID-19 pandemic, and for future healthcare crises.

3.
Thanh-N. NGUYEN; Muhammad-M. QURESHI; Piers KLEIN; Hiroshi YAMAGAMI; Mohamad ABDALKADER; Robert MIKULIK; Anvitha SATHYA; Ossama-Yassin MANSOUR; Anna CZLONKOWSKA; Hannah LO; Thalia-S. FIELD; Andreas CHARIDIMOU; Soma BANERJEE; Shadi YAGHI; James-E. SIEGLER; Petra SEDOVA; Joseph KWAN; Diana-Aguiar DE-SOUSA; Jelle DEMEESTERE; Violiza INOA; Setareh-Salehi OMRAN; Liqun ZHANG; Patrik MICHEL; Davide STRAMBO; João-Pedro MARTO; Raul-G. NOGUEIRA; Espen-Saxhaug KRISTOFFERSEN; Georgios TSIVGOULIS; Virginia-Pujol LEREIS; Alice MA; Christian ENZINGER; Thomas GATTRINGER; Aminur RAHMAN; Thomas BONNET; Noémie LIGOT; Sylvie DE-RAEDT; Robin LEMMENS; Peter VANACKER; Fenne VANDERVORST; Adriana-Bastos CONFORTO; Raquel-C.T. HIDALGO; Daissy-Liliana MORA-CUERVO; Luciana DE-OLIVEIRA-NEVES; Isabelle LAMEIRINHAS-DA-SILVA; Rodrigo-Targa MARTÍNS; Letícia-C. REBELLO; Igor-Bessa SANTIAGO; Teodora SADELAROVA; Rosen KALPACHKI; Filip ALEXIEV; Elena-Adela CORA; Michael-E. KELLY; Lissa PEELING; Aleksandra PIKULA; Hui-Sheng CHEN; Yimin CHEN; Shuiquan YANG; Marina ROJE-BEDEKOVIC; Martin ČABAL; Dusan TENORA; Petr FIBRICH; Pavel DUŠEK; Helena HLAVÁČOVÁ; Emanuela HRABANOVSKA; Lubomír JURÁK; Jana KADLČÍKOVÁ; Igor KARPOWICZ; Lukáš KLEČKA; Martin KOVÁŘ; Jiří NEUMANN; Hana PALOUŠKOVÁ; Martin REISER; Vladimir ROHAN; Libor ŠIMŮNEK; Ondreij SKODA; Miroslav ŠKORŇA; Martin ŠRÁMEK; Nicolas DRENCK; Khalid SOBH; Emilie LESAINE; Candice SABBEN; Peggy REINER; Francois ROUANET; Daniel STRBIAN; Stefan BOSKAMP; Joshua MBROH; Simon NAGEL; Michael ROSENKRANZ; Sven POLI; Götz THOMALLA; Theodoros KARAPANAYIOTIDES; Ioanna KOUTROULOU; Odysseas KARGIOTIS; Lina PALAIODIMOU; José-Dominguo BARRIENTOS-GUERRA; Vikram HUDED; Shashank NAGENDRA; Chintan PRAJAPATI; P.N. SYLAJA; Achmad-Firdaus SANI; Abdoreza GHOREISHI; Mehdi FARHOUDI; Elyar SADEGHI-HOKMABADI; Mazyar HASHEMILAR; Sergiu-Ionut SABETAY; Fadi RAHAL; Maurizio ACAMPA; Alessandro ADAMI; Marco LONGONI; Raffaele ORNELLO; Leonardo RENIERI; Michele ROMOLI; Simona SACCO; Andrea SALMAGGI; Davide SANGALLI; Andrea ZINI; Kenichiro SAKAI; Hiroki FUKUDA; Kyohei FUJITA; Hirotoshi IMAMURA; Miyake KOSUKE; Manabu SAKAGUCHI; Kazutaka SONODA; Yuji MATSUMARU; Nobuyuki OHARA; Seigo SHINDO; Yohei TAKENOBU; Takeshi YOSHIMOTO; Kazunori TOYODA; Takeshi UWATOKO; Nobuyuki SAKAI; Nobuaki YAMAMOTO; Ryoo YAMAMOTO; Yukako YAZAWA; Yuri SUGIURA; Jang-Hyun BAEK; Si-Baek LEE; Kwon-Duk SEO; Sung-Il SOHN; Jin-Soo LEE; Anita-Ante ARSOVSKA; Chan-Yong CHIEH; Wan-Asyraf WAN-ZAIDI; Wan-Nur-Nafisah WAN-YAHYA; Fernando GONGORA-RIVERA; Manuel MARTINEZ-MARINO; Adrian INFANTE-VALENZUELA; Diederik DIPPEL; Dianne-H.K. VAN-DAM-NOLEN; Teddy-Y. WU; Martin PUNTER; Tajudeen-Temitayo ADEBAYO; Abiodun-H. BELLO; Taofiki-Ajao SUNMONU; Kolawole-Wasiu WAHAB; Antje SUNDSETH; Amal-M. AL-HASHMI; Saima AHMAD; Umair RASHID; Liliana RODRIGUEZ-KADOTA; Miguel-Ángel VENCES; Patrick-Matic YALUNG; Jon-Stewart-Hao DY; Waldemar BROLA; Aleksander DĘBIEC; Malgorzata DOROBEK; Michal-Adam KARLINSKI; Beata-M. LABUZ-ROSZAK; Anetta LASEK-BAL; Halina SIENKIEWICZ-JAROSZ; Jacek STASZEWSKI; Piotr SOBOLEWSKI; Marcin WIĄCEK; Justyna ZIELINSKA-TUREK; André-Pinho ARAÚJO; Mariana ROCHA; Pedro CASTRO; Patricia FERREIRA; Ana-Paiva NUNES; Luísa FONSECA; Teresa PINHO-E-MELO; Miguel RODRIGUES; M-Luis SILVA; Bogdan CIOPLEIAS; Adela DIMITRIADE; Cristian FALUP-PECURARIU; May-Adel HAMID; Narayanaswamy VENKETASUBRAMANIAN; Georgi KRASTEV; Jozef HARING; Oscar AYO-MARTIN; Francisco HERNANDEZ-FERNANDEZ; Jordi BLASCO; Alejandro RODRÍGUEZ-VÁZQUEZ; Antonio CRUZ-CULEBRAS; Francisco MONICHE; Joan MONTANER; Soledad PEREZ-SANCHEZ; María-Jesús GARCÍA-SÁNCHEZ; Marta GUILLÁN-RODRÍGUEZ; Gianmarco BERNAVA; Manuel BOLOGNESE; Emmanuel CARRERA; Anchalee CHUROJANA; Ozlem AYKAC; Atilla-Özcan ÖZDEMIR; Arsida BAJRAMI; Songul SENADIM; Syed-I. HUSSAIN; Seby JOHN; Kailash KRISHNAN; Robert LENTHALL; Kaiz-S. ASIF; Kristine BELOW; Jose BILLER; Michael CHEN; Alex CHEBL; Marco COLASURDO; Alexandra CZAP; Adam-H. DE-HAVENON; Sushrut DHARMADHIKARI; Clifford-J. ESKEY; Mudassir FAROOQUI; Steven-K. FESKE; Nitin GOYAL; Kasey-B. GRIMMETT; Amy-K. GUZIK; Diogo-C. HAUSSEN; Majesta HOVINGH; Dinesh JILLELA; Peter-T. KAN; Rakesh KHATRI; Naim-N. KHOURY; Nicole-L. KILEY; Murali-K. KOLIKONDA; Stephanie LARA; Grace LI; Italo LINFANTE; Aaron-I. LOOCHTAN; Carlos-D. LOPEZ; Sarah LYCAN; Shailesh-S. MALE; Fadi NAHAB; Laith MAALI; Hesham-E. MASOUD; Jiangyong MIN; Santiago ORGETA-GUTIERREZ; Ghada-A. MOHAMED; Mahmoud MOHAMMADEN; Krishna NALLEBALLE; Yazan RADAIDEH; Pankajavalli RAMAKRISHNAN; Bliss RAYO-TARANTO; Diana-M. ROJAS-SOTO; Sean RULAND; Alexis-N. SIMPKINS; Sunil-A. SHETH; Amy-K. STAROSCIAK; Nicholas-E. TARLOV; Robert-A. TAYLOR; Barbara VOETSCH; Linda ZHANG; Hai-Quang DUONG; Viet-Phuong DAO; Huynh-Vu LE; Thong-Nhu PHAM; Mai-Duy TON; Anh-Duc TRAN; Osama-O. ZAIDAT; Paolo MACHI; Elisabeth DIRREN; Claudio RODRÍGUEZ-FERNÁNDEZ; Jorge ESCARTÍN-LÓPEZ; Jose-Carlos FERNÁNDEZ-FERRO; Niloofar MOHAMMADZADEH; Neil-C. SURYADEVARA,-MD; Beatriz DE-LA-CRUZ-FERNÁNDEZ; Filipe BESSA; Nina JANCAR; Megan BRADY; Dawn SCOZZARI.
Journal of Stroke ; : 256-265, 2022.
Article in English | WPRIM (Western Pacific) | ID: wpr-938173

ABSTRACT

Background@#and Purpose Recent studies suggested an increased incidence of cerebral venous thrombosis (CVT) during the coronavirus disease 2019 (COVID-19) pandemic. We evaluated the volume of CVT hospitalization and in-hospital mortality during the 1st year of the COVID-19 pandemic compared to the preceding year. @*Methods@#We conducted a cross-sectional retrospective study of 171 stroke centers from 49 countries. We recorded COVID-19 admission volumes, CVT hospitalization, and CVT in-hospital mortality from January 1, 2019, to May 31, 2021. CVT diagnoses were identified by International Classification of Disease-10 (ICD-10) codes or stroke databases. We additionally sought to compare the same metrics in the first 5 months of 2021 compared to the corresponding months in 2019 and 2020 (ClinicalTrials.gov Identifier: NCT04934020). @*Results@#There were 2,313 CVT admissions across the 1-year pre-pandemic (2019) and pandemic year (2020); no differences in CVT volume or CVT mortality were observed. During the first 5 months of 2021, there was an increase in CVT volumes compared to 2019 (27.5%; 95% confidence interval [CI], 24.2 to 32.0; P<0.0001) and 2020 (41.4%; 95% CI, 37.0 to 46.0; P<0.0001). A COVID-19 diagnosis was present in 7.6% (132/1,738) of CVT hospitalizations. CVT was present in 0.04% (103/292,080) of COVID-19 hospitalizations. During the first pandemic year, CVT mortality was higher in patients who were COVID positive compared to COVID negative patients (8/53 [15.0%] vs. 41/910 [4.5%], P=0.004). There was an increase in CVT mortality during the first 5 months of pandemic years 2020 and 2021 compared to the first 5 months of the pre-pandemic year 2019 (2019 vs. 2020: 2.26% vs. 4.74%, P=0.05; 2019 vs. 2021: 2.26% vs. 4.99%, P=0.03). In the first 5 months of 2021, there were 26 cases of vaccine-induced immune thrombotic thrombocytopenia (VITT), resulting in six deaths. @*Conclusions@#During the 1st year of the COVID-19 pandemic, CVT hospitalization volume and CVT in-hospital mortality did not change compared to the prior year. COVID-19 diagnosis was associated with higher CVT in-hospital mortality. During the first 5 months of 2021, there was an increase in CVT hospitalization volume and increase in CVT-related mortality, partially attributable to VITT.

4.
Journal of Stroke ; : 266-277, 2022.
Article in English | WPRIM (Western Pacific) | ID: wpr-938172

ABSTRACT

Background@#and Purpose Knowledge about different etiologies of non-traumatic intracerebral hemorrhage (ICH) and their outcomes is scarce. @*Methods@#We assessed prevalence of pre-specified ICH etiologies and their association with outcomes in consecutive ICH patients enrolled in the prospective Swiss Stroke Registry (2014 to 2019). Results We included 2,650 patients (mean±standard deviation age 72±14 years, 46.5% female, median National Institutes of Health Stroke Scale 8 [interquartile range, 3 to 15]). Etiology was as follows: hypertension, 1,238 (46.7%); unknown, 566 (21.4%); antithrombotic therapy, 227 (8.6%); cerebral amyloid angiopathy (CAA), 217 (8.2%); macrovascular cause, 128 (4.8%); other determined etiology, 274 patients (10.3%). At 3 months, 880 patients (33.2%) were functionally independent and 664 had died (25.1%). ICH due to hypertension had a higher odds of functional independence (adjusted odds ratio [aOR], 1.33; 95% confidence interval [CI], 1.00 to 1.77; P=0.05) and lower mortality (aOR, 0.64; 95% CI, 0.47 to 0.86; P=0.003). ICH due to antithrombotic therapy had higher mortality (aOR, 1.62; 95% CI, 1.01 to 2.61; P=0.045). Within 3 months, 4.2% of patients had cerebrovascular events. The rate of ischemic stroke was higher than that of recurrent ICH in all etiologies but CAA and unknown etiology. CAA had high odds of recurrent ICH (aOR, 3.38; 95% CI, 1.48 to 7.69; P=0.004) while the odds was lower in ICH due to hypertension (aOR, 0.42; 95% CI, 0.19 to 0.93; P=0.031). @*Conclusions@#Although hypertension is the leading etiology of ICH, other etiologies are frequent. One-third of ICH patients are functionally independent at 3 months. Except for patients with presumed CAA, the risk of ischemic stroke within 3 months of ICH was higher than the risk of recurrent hemorrhage.

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