デュテプラーゼ
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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/03/29 13:40:56」(JST)
[Wiki en表示]
Duteplase is a plasminogen activator.[1]
References
- ^ Malcolm AD, Keltai M, Walsh MJ (October 1996). "ESPRIT: a European study of the prevention of reocclusion after initial thrombolysis with duteplase in acute myocardial infarction". Eur. Heart J. 17 (10): 1522–31. PMID 8909909.
Antithrombotics (thrombolytics, anticoagulants and antiplatelet drugs) (B01)
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Antiplatelet drugs |
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- Abciximab
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ADP receptor/P2Y12 inhibitors
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(inhibit II, VII, IX, X)
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Factor Xa inhibitors
(with some II inhibition)
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Heparin group/
glycosaminoglycans/
(bind antithrombin)
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- low molecular weight heparin
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- bivalent: Hirudin
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Other
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- Antithrombin III
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Thrombolytic drugs/
fibrinolytics |
- plasminogen activators: r-tPA
- Alteplase
- Reteplase
- Tenecteplase
- UPA
- Anistreplase
- Monteplase
- Streptokinase#
- other serine endopeptidases: Ancrod
- Brinase
- Fibrinolysin
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Non-medicinal |
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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cell/phys (coag, heme, immu, gran), csfs
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rbmg/mogr/tumr/hist, sysi/epon, btst
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drug (B1/2/3+5+6), btst, trns
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English Journal
- Safety and efficacy of 0.6 mg/kg rt-PA: optimum rt-PA dose revisited.
- Mori E.SourceDepartment of Behavioral Neurology and Cognitive Neuroscience, Tohoku University Graduate School of Medicine, Sendai, Japan. morie@med.tohoku.ac.jp
- Annals of the New York Academy of Sciences.Ann N Y Acad Sci.2012 Sep;1268:108-12. doi: 10.1111/j.1749-6632.2012.06689.x.
- Although the internationally recommended dosage of alteplase, a single-chain rt-PA, is 0.9 mg/kg, 0.6 mg/kg is the only approved dosage in Japan, and it is widely used there. Duteplase is a two-chain rt-PA, and based on findings of the duteplase trials in the early 1990s, the smaller dosage of 0.6 m
- PMID 22994228
- [Prospects of thrombolytic therapy for acute ischemic stroke].
- Nakashima T, Minematsu K.SourceCerebrovascular Division, Department of Medicine, National Cardiovascular Center, 5 7-1 Fujishirodai, Suita-shi, Osaka 565 8565, Japan.
- Brain and nerve = Shinkei kenkyū no shinpo.Brain Nerve.2009 Sep;61(9):1003-12.
- The US Food and Drug Administration (FDA) approved the use of intravenous (IV) recombinant tissue plasminogen activator (rt-PA) in 1996, on the basis of the results of the National Institute of Neurological Disorders and Stroke (NINDS) rt-PA Stroke Study. IV rt-PA therapy at a dose of 0.9 mg/kg has
- PMID 19803399
- Percutaneous coronary intervention-related time delay, patient's risk profile, and survival benefits of primary angioplasty vs lytic therapy in ST-segment elevation myocardial infarction.
- De Luca G, Cassetti E, Marino P.SourceDivision of Cardiology, Ospedale Maggiore della Carità, Eastern Piedmont University, 28100 Novara, Italy. giuseppe.deluca@maggioreosp.novara.it
- The American journal of emergency medicine.Am J Emerg Med.2009 Jul;27(6):712-9. doi: 10.1016/j.ajem.2008.04.026.
- BACKGROUND: Previous reports have suggested an impact of patient's risk profile and percutaneous coronary intervention (PCI)-related time delay on the benefits of primary angioplasty as compared with fibrinolysis. However, several factors, such as inappropriate interpretation and definition of delay
- PMID 19751630
Japanese Journal
- 脳塞栓症に対するSM-9527 (duteplase ; rt-PA)の早期線溶療法
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