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Henry Hin Kui Ma

Researcher at Monash University

Publications -  25
Citations -  480

Henry Hin Kui Ma is an academic researcher from Monash University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 8, co-authored 11 publications receiving 331 citations. Previous affiliations of Henry Hin Kui Ma include Monash Medical Centre & Florey Institute of Neuroscience and Mental Health.

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A multicenter, randomized, controlled study to investigate EXtending the time for Thrombolysis in Emergency Neurological Deficits with Intra-Arterial therapy (EXTEND-IA).

TL;DR: This study hypothesized that anterior circulation ischemic stroke patients, selected with ‘dual target’ vessel occlusion and evidence of salvageable brain using computed tomography or magnetic resonance imaging ‘mismatch’ within 4.5 h of onset, would have improved reperfusion and early neurological improvement when treated with intra-arterial clot retrieval after intravenous tissue plasminogen activator.
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Endovascular thrombectomy versus standard bridging thrombolytic with endovascular thrombectomy within 4·5 h of stroke onset: an open-label, blinded-endpoint, randomised non-inferiority trial

TL;DR: The clinical outcomes of patients with stroke with large vessel occlusion treated with direct endovascular thrombectomy within 4·5 h would be non-inferior compared with the outcomes of those treated with standard bridging therapy, as well as the intention-to-treat population, were hypothesized.
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Googling Service Boundaries for Endovascular Clot Retrieval Hub Hospitals in a Metropolitan Setting: Proof-of-Concept Study

TL;DR: In this article, the authors applied a computational method to objectively generate service boundaries for such endovascular clot retrieval hubs, defined by traveling time to hub, using Google Map application program interface.
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Salvage of the PWI/DWI mismatch up to 48 h from stroke onset leads to favorable clinical outcome.

TL;DR: Using coregistered perfusion/diffusion-weighted image criteria, mismatch persists up to 48 h post stroke and, although the effect is small, its salvage is independently associated with improved clinical outcomes at three-months.