The Assessment of Endovascular Therapies in Ischemic Stroke: Management, Problems and Future Approaches.

clots endovascular therapies ischemic stroke mechanical thrombectomy mitochondria rt-PA thrombolysis

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
28 Mar 2022
Historique:
received: 28 02 2022
revised: 18 03 2022
accepted: 25 03 2022
entrez: 12 4 2022
pubmed: 13 4 2022
medline: 13 4 2022
Statut: epublish

Résumé

Ischemic stroke accounts for over 80% of all strokes and is one of the leading causes of mortality and permanent disability worldwide. Intravenous administration of recombinant tissue plasminogen activator (rt-PA) is an approved treatment strategy for acute ischemic stroke of large arteries within 4.5 h of onset, and mechanical thrombectomy can be used for large arteries occlusion up to 24 h after onset. Improving diagnostic work up for acute treatment, reducing onset-to-needle time and urgent radiological access angiographic CT images (angioCT) and Magnetic Resonance Imaging (MRI) are real problems for many healthcare systems, which limits the number of patients with good prognosis in real world compared to the results of randomized controlled trials. The applied endovascular procedures demonstrated high efficacy, but some cellular mechanisms, following reperfusion, are still unknown. Changes in the morphology and function of mitochondria associated with reperfusion and ischemia-reperfusion neuronal death are still understudied research fields. Moreover, future research is needed to elucidate the relationship between continuously refined imaging techniques and the variable structure or physical properties of the clot along with vascular permeability and the pleiotropism of ischemic reperfusion lesions in the penumbra, in order to define targeted preventive procedures promoting long-term health benefits.

Identifiants

pubmed: 35407472
pii: jcm11071864
doi: 10.3390/jcm11071864
pmc: PMC8999747
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Jagiellonian University
ID : N42/DBS/000199

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Auteurs

Tadeusz J Popiela (TJ)

Department of Radiology, Medical College, Jagiellonian University, 31-501 Kraków, Poland.

Wirginia Krzyściak (W)

Department of Medical Diagnostics, Medical College, Jagiellonian University, 31-688 Kraków, Poland.

Fabio Pilato (F)

Neurology, Neurophysiology and Neurobiology Unit, Department of Medicine, Università Campus Bio-Medico di Roma, 00128 Rome, Italy.

Anna Ligęzka (A)

Department of Medical Diagnostics, Medical College, Jagiellonian University, 31-688 Kraków, Poland.
Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55902, USA.
Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55902, USA.

Beata Bystrowska (B)

Department of Toxicology, Medical College, Jagiellonian University, Medyczna 9, 30-688 Kraków, Poland.

Karolina Bukowska-Strakova (K)

Department of Clinical Immunology and Transplantology, Institute of Pediatrics, Medical College, Jagiellonian University, 30-663 Kraków, Poland.

Paweł Brzegowy (P)

Department of Radiology, Medical College, Jagiellonian University, 31-501 Kraków, Poland.

Karthik Muthusamy (K)

Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55902, USA.

Tamas Kozicz (T)

Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55902, USA.
Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55902, USA.

Classifications MeSH