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acetazolamide and Long QT Syndrome

acetazolamide has been researched along with Long QT Syndrome in 1 studies

Acetazolamide: One of the CARBONIC ANHYDRASE INHIBITORS that is sometimes effective against absence seizures. It is sometimes useful also as an adjunct in the treatment of tonic-clonic, myoclonic, and atonic seizures, particularly in women whose seizures occur or are exacerbated at specific times in the menstrual cycle. However, its usefulness is transient often because of rapid development of tolerance. Its antiepileptic effect may be due to its inhibitory effect on brain carbonic anhydrase, which leads to an increased transneuronal chloride gradient, increased chloride current, and increased inhibition. (From Smith and Reynard, Textbook of Pharmacology, 1991, p337)

Long QT Syndrome: A condition that is characterized by episodes of fainting (SYNCOPE) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Junker, J1
Haverkamp, W1
Schulze-Bahr, E1
Eckardt, L1
Paulus, W1
Kiefer, R1

Other Studies

1 other study available for acetazolamide and Long QT Syndrome

ArticleYear
Amiodarone and acetazolamide for the treatment of genetically confirmed severe Andersen syndrome.
    Neurology, 2002, Aug-13, Volume: 59, Issue:3

    Topics: Acetazolamide; Adolescent; Amiodarone; Anti-Arrhythmia Agents; Anticonvulsants; Child; Drug Therapy,

2002