Landiolol suppression of electrical storm of torsades de pointes in patients with congenital long-QT syndrome type 2 and myocardial ischemia

A 76-year-old man who had been diagnosed with long-QT syndrome type 2 had frequent syncopal attacks. The electrocardiogram was monitored, and frequent torsades de pointes (TdP) was detected despite administration of conventional medications: oral propranolol, verapamil, intravenous magnesium sulfate...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Ryota Kitajima, MD, Takeshi Aiba, MD, Tsukasa Kamakura, MD, Kohei Ishibashi, MD, Mitsuru Wada, MD, Yuko Inoue, MD, Koji Miyamoto, MD, Hideo Okamura, MD, Takashi Noda, MD, Satoshi Nagase, MD, Yu Kataoka, MD, Yasuhide Asaumi, MD, Teruo Noguchi, MD, Satoshi Yasuda, MD, Kengo Kusano, MD
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Wiley 2017-10-01
Cyfres:Journal of Arrhythmia
Pynciau:
Torsade de pointes
Long-QT syndrome
β-blocker
Landiolol
Mynediad Ar-lein:http://www.sciencedirect.com/science/article/pii/S1880427617301011
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