Guidelines for Mechanical Thrombectomy in Japan, the Fourth Edition, March 2020: A Guideline from the Japan Stroke Society, the Japan Neurosurgical Society, and the Japanese Society for Neuroendovascular Therapy

[Preface from the Guidelines for Mechanical Thrombectomy in Japan, the First Edition (April 2014)] Acute cerebral artery occlusion is associated with very poor outcomes. Early recanalization of occluded arteries, however, may improve the outcome, and recanalization therapy has been attempted with a...

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Published inNeurologia medico-chirurgica Vol. 61; no. 3; pp. 163 - 192
Main Authors YAMAGAMI, Hiroshi, HAYAKAWA, Mikito, INOUE, Manabu, IIHARA, Koji, OGASAWARA, Kuniaki, TOYODA, Kazunori, HASEGAWA, Yasuhiro, OHATA, Kenji, SHIOKAWA, Yoshiaki, NOZAKI, Kazuhiko, EZURA, Masayuki, IWAMA, Toru, JSS/JNS/JSNET Joint Guideline Authoring Committee
Format Journal Article
LanguageEnglish
Published Japan The Japan Neurosurgical Society 2021
THE JAPAN NEUROSURGICAL SOCIETY
Japan Science and Technology Agency
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Summary:[Preface from the Guidelines for Mechanical Thrombectomy in Japan, the First Edition (April 2014)] Acute cerebral artery occlusion is associated with very poor outcomes. Early recanalization of occluded arteries, however, may improve the outcome, and recanalization therapy has been attempted with a variety of approaches. The most well-known approach is intravenous therapy with the recombinant tissue-plasminogen activator (IV rt-PA), alteplase. The efficacy of IV rt-PA has been established through many randomized controlled trials (RCTs). IV rt-PA is classified as a Class I therapy in the Guidelines for the Early Management of Patients with Acute Ischemic Stroke of the American Heart Association/American Stroke Association (AHA/ASA) and a Grade A recommendation in the Japanese Guidelines for the Management of Stroke. Even as cerebrovascular medical technology has progressed, IV rt-PA remains the priority therapy for patients with acute ischemic stroke. Currently, IV rt-PA is indicated for acute ischemic stroke within 4.5 hours of onset with no contraindications.
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ISSN:0470-8105
1349-8029
DOI:10.2176/nmc.nmc.st.2020-0357