Page last updated: 2024-10-27

flecainide and Electrocardiogram QT Prolonged

flecainide has been researched along with Electrocardiogram QT Prolonged in 37 studies

Flecainide: A potent anti-arrhythmia agent, effective in a wide range of ventricular and atrial ARRHYTHMIAS and TACHYCARDIAS.
flecainide : A monocarboxylic acid amide obtained by formal condensation of the carboxy group of 2,5-bis(2,2,2-trifluoroethoxy)benzoic acid with the primary amino group of piperidin-2-ylmethylamine. An antiarrhythmic agent used (in the form of its acetate salt) to prevent and treat tachyarrhythmia (abnormal fast rhythm of the heart).

Research Excerpts

ExcerptRelevanceReference
"We have linked 2 inactivation gating defects ("closed-state" fast inactivation and intermediate inactivation) to flecainide sensitivity in patients carrying LQT3 and Brugada syndrome mutations."7.71Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes. ( Balser, JR; Bezzina, CR; George, AL; Roden, DM; Viswanathan, PC; Wilde, AA, 2001)
"Flecainide is a potent blocker of the open sodium channel."6.70Normalization of ventricular repolarization with flecainide in long QT syndrome patients with SCN5A:DeltaKPQ mutation. ( Atkins, DL; Geletka, RC; Moss, AJ; Windle, JR; Zareba, W, 2001)
" Previous reports on the long-term use of sodium channel blockers in LQT3 are sparse."5.48Long-term flecainide therapy in type 3 long QT syndrome. ( Benhorin, J; Chorin, E; Flint, N; Medina, A; Taub, R; Viskin, S, 2018)
"Flecainide treatment revealed coved ST elevation in all mutation carriers."5.40Flecainide provocation reveals concealed brugada syndrome in a long QT syndrome family with a novel L1786Q mutation in SCN5A. ( Bloch Thomsen, PE; Christiansen, M; Grunnet, M; Hedley, PL; Jespersen, T; Jons, C; Kanters, JK; Stoevring, B; Yuan, L, 2014)
"Flecainide is recommended as a first-line antiarrhythmic drug to maintain normal sinus rhythm in patients with atrial fibrillation (AF) who have structurally normal hearts or hypertension without left ventricular hypertrophy."3.80An unusual case of flecainide-induced QT prolongation leading to cardiac arrest. ( Costa, SM; Mixon, TA; Oguayo, KN; Oyetayo, OO, 2014)
"We have linked 2 inactivation gating defects ("closed-state" fast inactivation and intermediate inactivation) to flecainide sensitivity in patients carrying LQT3 and Brugada syndrome mutations."3.71Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes. ( Balser, JR; Bezzina, CR; George, AL; Roden, DM; Viswanathan, PC; Wilde, AA, 2001)
"Flecainide block of Na(+) current (I(Na)) was investigated in wild-type (WT) or the long QT syndrome 3 (LQT3) sodium channel alpha subunit mutation with three amino acids deleted (DeltaKPQ) stably transfected into human embryonic kidney 293 cells using whole-cell, patch-clamp recordings."3.70Preferential block of late sodium current in the LQT3 DeltaKPQ mutant by the class I(C) antiarrhythmic flecainide. ( January, CT; Makielski, JC; Nagatomo, T, 2000)
" Despite careful precautions, serious proarrhythmias, the major limiting side effect of dofetilide, still occurred during long-term follow-up."2.73Observations on the safety and effectiveness of dofetilide in patients with paroxysmal atrial fibrillation and normal left ventricular function. ( Bauman, JL; Kehoe, RF; Leal, S; Mykytsey, A; Razminia, M; Saleem, M; Wang, T; Zheutlin, T, 2007)
"5 ms), and there were no major adverse cardiac effects."2.71Safety and efficacy of flecainide in subjects with Long QT-3 syndrome (DeltaKPQ mutation): a randomized, double-blind, placebo-controlled clinical trial. ( Cieciorka, M; Daubert, JP; Hall, WJ; Manalan, AS; McNitt, S; Moss, AJ; Qi, M; Robinson, JL; Rosero, S; Severski, P; Windle, JR; Zareba, W, 2005)
"Flecainide is a potent blocker of the open sodium channel."2.70Normalization of ventricular repolarization with flecainide in long QT syndrome patients with SCN5A:DeltaKPQ mutation. ( Atkins, DL; Geletka, RC; Moss, AJ; Windle, JR; Zareba, W, 2001)
"Long QT syndrome was identified postnatally on the electrocardiogram, and was confirmed by genetic testing which showed a mutation in the KCNH2 gene (p."2.45Fetal ventricular tachycardia secondary to long QT syndrome treated with maternal intravenous magnesium: case report and review of the literature. ( Gill, H; Maxwell, D; Rosenthal, E; Simpson, JM, 2009)
" Previous reports on the long-term use of sodium channel blockers in LQT3 are sparse."1.48Long-term flecainide therapy in type 3 long QT syndrome. ( Benhorin, J; Chorin, E; Flint, N; Medina, A; Taub, R; Viskin, S, 2018)
"Unexplained cardiac arrest (UCA) can be caused by low-penetrance genetic disorders."1.42Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study). ( Álvarez, M; Cózar, R; Domingo, D; Fernández Pastor, J; Gimeno, JR; Grima, EZ; Heras, RP; Jiménez-Jáimez, J; Mazuelos, F; Monserrat, L; Moriña, P; Ortiz-Genga, M; Peinado, R; Sánchez Muñoz, JJ; Segura, F; Tercedor, L, 2015)
"Flecainide treatment revealed coved ST elevation in all mutation carriers."1.40Flecainide provocation reveals concealed brugada syndrome in a long QT syndrome family with a novel L1786Q mutation in SCN5A. ( Bloch Thomsen, PE; Christiansen, M; Grunnet, M; Hedley, PL; Jespersen, T; Jons, C; Kanters, JK; Stoevring, B; Yuan, L, 2014)
"Flecainide is an antiarrhythmic drug that blocks sodium channels during phase 0 of cardiac action potential, delaying conduction and reducing contractility."1.36[Flecainide poisoning]. ( Bobillo, B; Diz Gómez, JC; Doniz Campos, M; Filgueira, P; Illodo Miramontes, G; Otero Amoedo, T; Rey López, F, 2010)
"Flecainide was used in two patients for LQT-3 diagnosis and therapeutic treatment of AF."1.35A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation. ( Benito, B; Berruezo, A; Brugada, J; Brugada, P; Brugada, R; Cinca, J; Freixa, X; Lizotte, E; Mont, L; Perich, RM; Tolosana, JM, 2008)

Research

Studies (37)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's19 (51.35)29.6817
2010's14 (37.84)24.3611
2020's4 (10.81)2.80

Authors

AuthorsStudies
Nogawa, H1
Muraki, Y1
Kawai, T1
Kuninishi, Y1
Ryan, K1
Benz, P1
Zosel, A1
Farkas, A1
Theobald, J1
Shimizu, T1
Kawai, S1
Kawada, A1
Wakamiya, T1
Nakano, Y1
Watanabe, S1
Iwamoto, M1
Yang, Y1
Lv, TT1
Li, SY1
Zhang, P1
Chorin, E1
Taub, R2
Medina, A2
Flint, N1
Viskin, S1
Benhorin, J3
Bergenholm, L1
Parkinson, J1
Mettetal, J1
Evans, ND1
Chappell, MJ1
Collins, T1
Blich, M1
Khoury, A1
Suleiman, M1
Lorber, A1
Gepstein, L1
Boulous, M1
Oguayo, KN1
Oyetayo, OO1
Costa, SM1
Mixon, TA1
Kanters, JK1
Yuan, L1
Hedley, PL1
Stoevring, B1
Jons, C1
Bloch Thomsen, PE1
Grunnet, M1
Christiansen, M2
Jespersen, T1
Nakaya, H1
Jiménez-Jáimez, J1
Peinado, R1
Grima, EZ1
Segura, F1
Moriña, P1
Sánchez Muñoz, JJ1
Mazuelos, F1
Cózar, R1
Gimeno, JR1
Heras, RP1
Monserrat, L1
Domingo, D1
Ortiz-Genga, M1
Fernández Pastor, J1
Álvarez, M1
Tercedor, L1
Robyns, T1
Lu, HR1
Gallacher, DJ1
Garweg, C1
Ector, J1
Willems, R1
Janssens, S1
Nuyens, D1
Benito, B1
Brugada, R1
Perich, RM1
Lizotte, E1
Cinca, J1
Mont, L1
Berruezo, A1
Tolosana, JM1
Freixa, X1
Brugada, P1
Brugada, J1
Beinart, R1
Michailidis, A1
Gurevitz, OT1
Glikson, M1
Dautova, Y1
Zhang, Y1
Sabir, I1
Grace, AA3
Huang, CL3
Simpson, JM1
Maxwell, D1
Rosenthal, E1
Gill, H1
Aziz, PF1
Tanel, RE1
Zelster, IJ1
Pass, RH2
Wieand, TS1
Vetter, VL1
Vogel, RL1
Shah, MJ1
Blana, A1
Kaese, S1
Fortmüller, L1
Laakmann, S1
Damke, D1
van Bragt, K1
Eckstein, J1
Piccini, I1
Kirchhefer, U1
Nattel, S1
Breithardt, G1
Carmeliet, P2
Carmeliet, E1
Schotten, U1
Verheule, S1
Kirchhof, P1
Fabritz, L1
Doniz Campos, M1
Illodo Miramontes, G1
Bobillo, B1
Otero Amoedo, T1
Filgueira, P1
Rey López, F1
Diz Gómez, JC1
Carrasco, JI1
Izquierdo, I1
Medina, P1
Arnau, MÁ1
Salvador, A1
Zorio, E1
Belardinelli, L1
Liu, G1
Smith-Maxwell, C1
Wang, WQ1
El-Bizri, N1
Hirakawa, R1
Karpinski, S1
Li, CH1
Hu, L1
Li, XJ1
Crumb, W1
Wu, L1
Koltun, D1
Zablocki, J1
Yao, L1
Dhalla, AK1
Rajamani, S1
Shryock, JC1
Terrenoire, C1
Wang, K1
Tung, KW1
Chung, WK1
Lu, JT1
Jean, JC1
Omari, A1
Sampson, KJ2
Kotton, DN1
Keller, G1
Kass, RS5
Moss, AJ2
Windle, JR2
Hall, WJ1
Zareba, W2
Robinson, JL1
McNitt, S1
Severski, P1
Rosero, S1
Daubert, JP1
Qi, M1
Cieciorka, M1
Manalan, AS1
Zhu, Y1
Kyle, JW1
Lee, PJ1
Stokoe, KS1
Thomas, G1
Goddard, CA2
Colledge, WH1
Fredj, S1
Lindegger, N1
Lehtonen, A1
Fodstad, H1
Laitinen-Forsblom, P1
Toivonen, L1
Kontula, K1
Swan, H1
Mykytsey, A1
Bauman, JL1
Razminia, M1
Zheutlin, T1
Wang, T1
Saleem, M1
Leal, S1
Kehoe, RF1
Sabir, IN1
Li, LM1
Jones, VJ1
Makita, N1
Behr, E1
Shimizu, W1
Horie, M1
Sunami, A1
Crotti, L2
Schulze-Bahr, E1
Fukuhara, S1
Mochizuki, N1
Makiyama, T1
Itoh, H1
McKeown, P1
Miyamoto, K1
Kamakura, S1
Tsutsui, H1
Schwartz, PJ2
George, AL2
Roden, DM2
Nagatomo, T1
January, CT1
Makielski, JC1
Goldmit, M1
Kerem, B2
Windman, I1
Abriel, H2
Wehrens, XH1
Priori, SG1
Napolitano, C1
Bloise, R1
Ronchetti, E1
Geletka, RC1
Atkins, DL1
Viswanathan, PC1
Bezzina, CR1
Wilde, AA1
Balser, JR1
Liu, H1
Tateyama, M1
Clancy, CE1

Clinical Trials (3)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Determining the Effects of Two Different Anesthesia Induction Techniques on QT Distance in Cardiac Surgery Patients With Two Different QT Measurement Techniques[NCT04706104]60 participants (Actual)Observational2020-10-10Completed
Long QT Syndrome-Population Genetics and Cardiac Studies[NCT00005176]2,125 participants (Actual)Observational1985-08-31Completed
Efficacy of Ranolazine in LQT3 Patients[NCT01648205]Phase 225 participants (Actual)Interventional2012-09-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Change in QTc at 6 Months

Change in QTc at 6 months on ranolazine vs. at 1 month on placebo. This was prespecified outcome. (NCT01648205)
Timeframe: 1 month to 6 months

Interventionmiliseconds (Mean)
Placebo504
Ranolazine at 6 Months501

Change in QTc Duration at 2 Months

Change in QTc at 2 months on ranolazine vs. at 1 month on placebo. This was prespecified outcome. (NCT01648205)
Timeframe: 1 month to 2 months

Interventionmiliseconds (Mean)
Placebo503
Ranolazine at 2 Months497

Reviews

2 reviews available for flecainide and Electrocardiogram QT Prolonged

ArticleYear
Sodium channel blockers in the management of long QT syndrome types 3 and 2: A system review and meta-analysis.
    Journal of cardiovascular electrophysiology, 2021, Volume: 32, Issue:11

    Topics: Adrenergic beta-Antagonists; Electrocardiography; Flecainide; Humans; Long QT Syndrome; Mexiletine;

2021
Fetal ventricular tachycardia secondary to long QT syndrome treated with maternal intravenous magnesium: case report and review of the literature.
    Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 2009, Volume: 34, Issue:4

    Topics: Adult; Anti-Arrhythmia Agents; Female; Fetal Diseases; Flecainide; Humans; Injections, Intravenous;

2009

Trials

5 trials available for flecainide and Electrocardiogram QT Prolonged

ArticleYear
Predicting QRS and PR interval prolongations in humans using nonclinical data.
    British journal of pharmacology, 2017, Volume: 174, Issue:19

    Topics: Animals; Anti-Arrhythmia Agents; Azabicyclo Compounds; Carbamates; Dogs; Drug Evaluation, Preclinica

2017
Safety and efficacy of flecainide in subjects with Long QT-3 syndrome (DeltaKPQ mutation): a randomized, double-blind, placebo-controlled clinical trial.
    Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc, 2005, Volume: 10, Issue:4 Suppl

    Topics: Adolescent; Adult; Double-Blind Method; Flecainide; Humans; Long QT Syndrome; Male; Middle Aged; Neb

2005
Observations on the safety and effectiveness of dofetilide in patients with paroxysmal atrial fibrillation and normal left ventricular function.
    Journal of cardiovascular pharmacology and therapeutics, 2007, Volume: 12, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Amiodarone; Anti-Arrhythmia Agents; Atrial Fibrillation; Atrial Flut

2007
The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge.
    Circulation, 2000, Aug-29, Volume: 102, Issue:9

    Topics: Administration, Oral; Adolescent; Adult; Anti-Arrhythmia Agents; Contraindications; Diagnosis, Diffe

2000
Normalization of ventricular repolarization with flecainide in long QT syndrome patients with SCN5A:DeltaKPQ mutation.
    Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc, 2001, Volume: 6, Issue:2

    Topics: Administration, Oral; Adolescent; Adult; Anti-Arrhythmia Agents; Child; Child, Preschool; Drug Monit

2001

Other Studies

30 other studies available for flecainide and Electrocardiogram QT Prolonged

ArticleYear
Pharmacological characterisation of electrocardiogram J-T
    European journal of pharmacology, 2022, Jul-15, Volume: 927

    Topics: Animals; DNA-Binding Proteins; Electrocardiography; Flecainide; Guinea Pigs; Long QT Syndrome; Nifed

2022
QTc Prolongation in Poison Center Exposures to CredibleMeds List of Substances with "Known Risk of Torsades de Pointes".
    Cardiovascular toxicology, 2022, Volume: 22, Issue:9

    Topics: Amitriptyline; Arrhythmias, Cardiac; Diphenhydramine; Electrocardiography; Flecainide; Humans; Long

2022
Combined mexiletine and flecainide for severe long QT syndrome type 3.
    Pediatrics international : official journal of the Japan Pediatric Society, 2023, Volume: 65, Issue:1

    Topics: Anti-Arrhythmia Agents; Cardiac Conduction System Disease; Electrocardiography; Flecainide; Humans;

2023
Long-term flecainide therapy in type 3 long QT syndrome.
    Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 2018, 02-01, Volume: 20, Issue:2

    Topics: Adolescent; Adult; Anti-Arrhythmia Agents; Brugada Syndrome; Cardiac Conduction System Disease; Chil

2018
Specific Therapy Based on the Genotype in a Malignant Form of Long QT3, Carrying the V411M Mutation.
    International heart journal, 2019, Jul-27, Volume: 60, Issue:4

    Topics: Child; DNA; DNA Mutational Analysis; Electrocardiography; Female; Flecainide; Humans; Long QT Syndro

2019
An unusual case of flecainide-induced QT prolongation leading to cardiac arrest.
    Pharmacotherapy, 2014, Volume: 34, Issue:5

    Topics: Adult; Anti-Arrhythmia Agents; Atrial Fibrillation; Defibrillators; Flecainide; Heart Arrest; Humans

2014
Flecainide provocation reveals concealed brugada syndrome in a long QT syndrome family with a novel L1786Q mutation in SCN5A.
    Circulation journal : official journal of the Japanese Circulation Society, 2014, Volume: 78, Issue:5

    Topics: Amino Acid Substitution; Animals; Anti-Arrhythmia Agents; Brugada Syndrome; Family; Female; Flecaini

2014
SCN5A mutations associated with overlap phenotype of long QT syndrome type 3 and Brugada syndrome.
    Circulation journal : official journal of the Japanese Circulation Society, 2014, Volume: 78, Issue:5

    Topics: Animals; Anti-Arrhythmia Agents; Brugada Syndrome; Family; Female; Flecainide; Humans; Long QT Syndr

2014
Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study).
    The American journal of cardiology, 2015, Sep-15, Volume: 116, Issue:6

    Topics: Adolescent; Adult; Anti-Arrhythmia Agents; Arrhythmias, Cardiac; Brugada Syndrome; Cardiac Catheteri

2015
Evaluation of Index of Cardio-Electrophysiological Balance (iCEB) as a New Biomarker for the Identification of Patients at Increased Arrhythmic Risk.
    Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc, 2016, Volume: 21, Issue:3

    Topics: Adult; Anti-Arrhythmia Agents; Arrhythmias, Cardiac; Biomarkers, Pharmacological; Brugada Syndrome;

2016
A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation.
    Heart rhythm, 2008, Volume: 5, Issue:10

    Topics: Adult; Aged; Anti-Arrhythmia Agents; Atrial Fibrillation; Child; Child, Preschool; Female; Flecainid

2008
Is flecainide dangerous in long QT-3 patients?
    Pacing and clinical electrophysiology : PACE, 2009, Volume: 32, Issue:1

    Topics: Anti-Arrhythmia Agents; Brugada Syndrome; Electrocardiography; Female; Flecainide; Humans; Long QT S

2009
Atrial arrhythmogenesis in wild-type and Scn5a+/delta murine hearts modelling LQT3 syndrome.
    Pflugers Archiv : European journal of physiology, 2009, Volume: 458, Issue:3

    Topics: Animals; Anti-Arrhythmia Agents; Atrial Fibrillation; Disease Models, Animal; Flecainide; Heart Rate

2009
Congenital long QT syndrome and 2:1 atrioventricular block: an optimistic outcome in the current era.
    Heart rhythm, 2010, Volume: 7, Issue:6

    Topics: Adrenergic beta-Antagonists; Anti-Arrhythmia Agents; Atrioventricular Block; Child; Child, Preschool

2010
Knock-in gain-of-function sodium channel mutation prolongs atrial action potentials and alters atrial vulnerability.
    Heart rhythm, 2010, Volume: 7, Issue:12

    Topics: Action Potentials; Animals; Anti-Arrhythmia Agents; Atrial Fibrillation; Echocardiography, Doppler;

2010
[Flecainide poisoning].
    Revista espanola de anestesiologia y reanimacion, 2010, Volume: 57, Issue:9

    Topics: Aged; Amiodarone; Atrial Fibrillation; Cholecystectomy; Cholecystitis; Electrocardiography; Emergenc

2010
Flecainide, a therapeutic option in a patient with long QT syndrome type 3 caused by the heterozygous V411M mutation in the SCN5A gene.
    Revista espanola de cardiologia (English ed.), 2012, Volume: 65, Issue:11

    Topics: Anti-Arrhythmia Agents; Cardiac Conduction System Disease; Electrocardiography; Female; Flecainide;

2012
A novel, potent, and selective inhibitor of cardiac late sodium current suppresses experimental arrhythmias.
    The Journal of pharmacology and experimental therapeutics, 2013, Volume: 344, Issue:1

    Topics: Acetanilides; Action Potentials; Animals; Anti-Arrhythmia Agents; Arrhythmias, Cardiac; Cardiotonic

2013
Induced pluripotent stem cells used to reveal drug actions in a long QT syndrome family with complex genetics.
    The Journal of general physiology, 2013, Volume: 141, Issue:1

    Topics: Anti-Arrhythmia Agents; Biophysical Phenomena; Cell Communication; Cells, Cultured; ERG1 Potassium C

2013
Flecainide sensitivity of a Na channel long QT mutation shows an open-channel blocking mechanism for use-dependent block.
    American journal of physiology. Heart and circulatory physiology, 2006, Volume: 291, Issue:1

    Topics: Anti-Arrhythmia Agents; Cell Line; Computer Simulation; Dose-Response Relationship, Drug; Flecainide

2006
Effects of flecainide and quinidine on arrhythmogenic properties of Scn5a+/Delta murine hearts modelling long QT syndrome 3.
    The Journal of physiology, 2007, Jan-01, Volume: 578, Issue:Pt 1

    Topics: Action Potentials; Animals; Anti-Arrhythmia Agents; Disease Models, Animal; Electric Stimulation; El

2007
Altered Na+ channels promote pause-induced spontaneous diastolic activity in long QT syndrome type 3 myocytes.
    Circulation research, 2006, Nov-24, Volume: 99, Issue:11

    Topics: Animals; Anti-Arrhythmia Agents; Diastole; Electrophysiology; Flecainide; Gene Deletion; Genetic Var

2006
Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointes.
    Heart rhythm, 2007, Volume: 4, Issue:5

    Topics: Aged; Aged, 80 and over; Amiodarone; Anti-Arrhythmia Agents; DNA Mutational Analysis; Electrocardiog

2007
Criteria for arrhythmogenicity in genetically-modified Langendorff-perfused murine hearts modelling the congenital long QT syndrome type 3 and the Brugada syndrome.
    Pflugers Archiv : European journal of physiology, 2008, Volume: 455, Issue:4

    Topics: Action Potentials; Animals; Anti-Arrhythmia Agents; Brugada Syndrome; Cardiac Pacing, Artificial; Di

2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.
    The Journal of clinical investigation, 2008, Volume: 118, Issue:6

    Topics: Adolescent; Adult; Anti-Arrhythmia Agents; Biophysics; Child; DNA Mutational Analysis; Electrocardio

2008
Preferential block of late sodium current in the LQT3 DeltaKPQ mutant by the class I(C) antiarrhythmic flecainide.
    Molecular pharmacology, 2000, Volume: 57, Issue:1

    Topics: Anti-Arrhythmia Agents; Binding Sites; Cells, Cultured; Electrocardiography; Electrophysiology; Flec

2000
Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?
    Circulation, 2000, Apr-11, Volume: 101, Issue:14

    Topics: Anti-Arrhythmia Agents; Case-Control Studies; Electrocardiography; Female; Flecainide; Heart; Hetero

2000
Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?
    Circulation, 2000, Apr-11, Volume: 101, Issue:14

    Topics: Anti-Arrhythmia Agents; Case-Control Studies; Electrocardiography; Female; Flecainide; Heart; Hetero

2000
Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?
    Circulation, 2000, Apr-11, Volume: 101, Issue:14

    Topics: Anti-Arrhythmia Agents; Case-Control Studies; Electrocardiography; Female; Flecainide; Heart; Hetero

2000
Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?
    Circulation, 2000, Apr-11, Volume: 101, Issue:14

    Topics: Anti-Arrhythmia Agents; Case-Control Studies; Electrocardiography; Female; Flecainide; Heart; Hetero

2000
Molecular pharmacology of the sodium channel mutation D1790G linked to the long-QT syndrome.
    Circulation, 2000, Aug-22, Volume: 102, Issue:8

    Topics: Anti-Arrhythmia Agents; Cell Line; Dose-Response Relationship, Drug; Flecainide; Genetic Linkage; Hu

2000
Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes.
    Circulation, 2001, Sep-04, Volume: 104, Issue:10

    Topics: Anti-Arrhythmia Agents; Arrhythmias, Cardiac; Cell Line; Electrocardiography; Flecainide; Green Fluo

2001
Channel openings are necessary but not sufficient for use-dependent block of cardiac Na(+) channels by flecainide: evidence from the analysis of disease-linked mutations.
    The Journal of general physiology, 2002, Volume: 120, Issue:1

    Topics: Anti-Arrhythmia Agents; Arrhythmias, Cardiac; Cell Line; Flecainide; Humans; Long QT Syndrome; Mutat

2002