- Implantable Cardioverter-Defibrillator(ICD) Therapy in a Patient with the Long QT Syndrome
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Choi KJ, Lee CW, Kim JJ, Kim YH
- KMID: 1672272
- Korean Circ J.
- 1996 Dec;26(6):1198-1203.
- doi: 10.4070/kcj.1996.26.6.1198
The long QT syndrome is believed to result from abnormalities of cardiac sympathetic innervation and of myocardial repolarization. The therapeutic modalities for patients with ventricular arrhythmias due to the long... -
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- Anesthetic Management of a Patient with Congenital Long QT Syndrome: A case report
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Koo BN, Kang OC, Kim KB, Park WK, Kil HK
- KMID: 2299086
- Korean J Anesthesiol.
- 2004 Jun;46(6):743-746.
- doi: 10.4097/kjae.2004.46.6.743
Long QT syndrome is characterized by syncope and fatal ventricular arrhythmia or fibrillation at an young age. A 25-year-old female patient with congenital Long QT syndrome (Jervell and Lange-Nielsen syndrome)... -
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- Cardiac Arrest under Anesthesia in a Child with Previously Undiagnosed Long QT Syndrome: A case report
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Gil NS, Oh AY, Kim HS, Kim CS
- KMID: 2092046
- Korean J Anesthesiol.
- 2005 Aug;49(2):274-277.
- doi: 10.4097/kjae.2005.49.2.274
Congenital long QT syndrome is a rare but potentially lethal disease, characterized by a corrected QT interval of at least 440 msec, ventricular arrhythmia, recurrent syncope, and sudden death. We... -
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- A Case of Congenital Long QT Syndrome with Reccurent Syncope
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Hwang JH, Kim HB
- KMID: 2207575
- J Korean Pediatr Soc.
- 2000 May;43(5):725-729.
Congenital long QT syndrome (LQTS) is a disease characterized by prolongation of ventricle repolarization and by the occurrence, usually during emotional or physical stress, of life-threatening arrhythmias that lead to... -
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- Fever-Induced QTc Prolongation and Ventricular Fibrillation in a Healthy Young Man
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Lim SM, Pak HN, Lee MH, Kim SS, Joung B
- KMID: 1058826
- Yonsei Med J.
- 2011 Nov;52(6):1025-1027.
- doi: 10.3349/ymj.2011.52.6.1025
Long QT syndrome is associated with lethal tachyarrhythmia that can lead to syncope, seizure, and sudden death. Congenital long QT syndrome is a genetic disorder, characterized by delayed cardiac repolarization... -
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- Marked QT prolongation and T inversion in a patient with acute pulmonary thromboembolism
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Park TI, Kim J, Hong TJ, Shin YW
- KMID: 2256160
- Korean J Med.
- 2008 Jul;75(1):37-38.
No abstract available. -
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- A Case of Congenital Long QT Syndrome Associated with Deafness and Syncope
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Lee SM, Choe CW, Kang HS, Kim KS, Song JS, Bae JH
- KMID: 1858300
- Korean Circ J.
- 1998 Nov;28(11):1882-1888.
- doi: 10.4070/kcj.1998.28.11.1882
Congenital long QT syndrome (LQTS) is an inherited disease characterized by prolonged QT intervals and polymorphic ventricular tachycardia. The clinical manifestations vary from sudden cardiac death by ventricular arrhythmia to... -
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- A Case of Idiopathic Long QT Syndrome with 2:1 Atrioventricular Block
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Lee KI, Kim CH, Lim IS, Lee DK, Yoo BH
- KMID: 1661458
- J Korean Pediatr Soc.
- 1995 Dec;38(12):1701-1705.
No abstract available. -
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- Initiation of Torsades de pointes by head-up tilt test in congenital long QT syndrome patient
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Jeon IS, Cha TJ, Kim KS, Kim DW, Kim KJ, Kim SM, Joo SJ, Lee JW
- KMID: 2298034
- Korean Circ J.
- 2000 Aug;30(8):1040-1044.
- doi: 10.4070/kcj.2000.30.8.1040
Long QT syndrome is a cardiac disorder of repolarization which is characterized by elctrocardiographic abnormalities including prolonged QT interval, T-wave abnormalities and polymorphic ventricular tachycardia known as Torsades de Pointes.... -
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- Left Stellate Ganglion Block Prior to Induction of Anesthesia for Surgical Sympathectomy in a Patient with Long QT Syndrome
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Kweon SH, Jee DL, Song SO
- KMID: 2031571
- Korean J Anesthesiol.
- 2000 Aug;39(2):265-269.
- doi: 10.4097/kjae.2000.39.2.265
Long QT Syndrome is characterized by syncope and fatal ventricular arrhythmia. Monotherapy with beta blockers is the first-line therapy. In patients with recurrent syncope despite therapy with beta blockers, combinations... -
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- Clinical Experience for a Patient with Long QT Syndrome
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Park TK, Lee JK
- KMID: 2335894
- J Korean Pain Soc.
- 2000 Jun;13(1):115-118.
Stellate ganglion block is most commonly used in pain clinic because it is an easy procedure and it has broad indications reported that Angina pectoris, tachyarrhythmia and long QT syndrome (LQTS) are... -
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- Long QT Syndrome and Torsade de Pointes Associated with Takotsubo Cardiomyopathy
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Ahn JH, Park SH, Shin WY, Lee SW, Lee SJ, Jin DK, Lee HM, Eun JY
- KMID: 1094271
- J Korean Med Sci.
- 2011 Jul;26(7):959-961.
- doi: 10.3346/jkms.2011.26.7.959
Prolongation of QTc interval associated with Takotsubo cardiomyopathy (TC) has previously been reported in published case series. We report an unusual case of a patient who presented with TC associated... -
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- A Case of Idiopathic Long QT Syndrome Presenting as Epilepsy
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Kim YJ, Ko JK, Park IS, Ko TS
- KMID: 2177103
- J Korean Child Neurol Soc.
- 1999 May;6(2):388-393.
"Idiopathic long QT syndrome" is characterized by prolongation of the QT interval due to unusual electrocardiographic repolarization abnormality and associated with variable clinical manifestations from no specific symptoms in lifetime... -
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- A Case with Excercise Induced Seizures: Long QT Syndrome Misdiagnosed as Epilepsy
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Lee EH, Jeong MH, Ko JK, Ko TS
- KMID: 2329455
- J Korean Child Neurol Soc.
- 2010 May;18(1):123-128.
Long QT syndrome(LQTS) is characterized by prolongation of the QT interval, frequent episodes of syncope, and ventricular tachycardia leading to sudden cardiac death in adolescents and young adults. Early diagnosis... -
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- Long QT syndrome provoked by induction of general anesthesia: A case report
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Kim HT, Lee JH, Park IB, Heo HE, Kim TY, Lee MJ
- KMID: 2237367
- Korean J Anesthesiol.
- 2010 Dec;59(Suppl):S114-S118.
- doi: 10.4097/kjae.2010.59.S.S114
Long QT syndrome (LQTS) is an arrhythmogenic cardiovascular disorder resulting from mutations in cardiac ion channels. LQTS is characterized by prolonged ventricular repolarization and frequently manifests itself as QT interval... -
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- Pain medication and long QT syndrome
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Klivinyi C, Bornemann-Cimenti H
- KMID: 2400902
- Korean J Pain.
- 2018 Jan;31(1):3-9.
- doi: 10.3344/kjp.2018.31.1.3
Long QT syndrome is a cardiac repolarization disorder and is associated with an increased risk of torsades de pointes. The acquired form is most often attributable to administration of specific... -
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- Anesthetic Management for Cervicothoracic Sympathectomy in a Patient with Congenital Long QT Syndrome
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Park SH, Lee SW, Kim SS, Kim DS, Ryu SJ, Kim KH, Jang TH, Kim SH
- KMID: 2237612
- Korean J Anesthesiol.
- 2000 Sep;39(3):438-443.
- doi: 10.4097/kjae.2000.39.3.438
A 23-year-old female patient was diagnosed with congenital long QT syndrome, discovered when she visited our cardiac department due to chest discomfort, because she had a prolonged QTc interval on... -
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- Management of Patients with Long QT Syndrome
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Cho Y
- KMID: 2355447
- Korean Circ J.
- 2016 Nov;46(6):747-752.
- doi: 10.4070/kcj.2016.46.6.747
Long QT syndrome (LQTS) is a rare cardiac channelopathy associated with syncope and sudden death due to torsades de pointes and ventricular fibrillation. Syncope and sudden death are frequently associated... -
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- Successful pharmacotherapy for asthma exacerbation in an asthmatic patient with long QT syndrome
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Kim HK, Cho DK, Lee WJ, Myung DS, Han ER, Choi IS, Koh YI
- KMID: 2258157
- Korean J Med.
- 2009 Aug;77(Suppl 1):S249-S253.
beta -Blockers can cause bronchospasm in asthma. beta 2-agonists prolong the QT interval and alter the clinical course of long QT syndrome (LQTS). We report a case of asthma exacerbation... -
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- Epinephrine-Induced Polymorphic Ventricular Tachycardia in a Patient With Congenital Long QT Syndrome
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Kim JH, Park SH, Kim KH, Choi WS, Kang JK, Kim NY, Cho Y
- KMID: 2225676
- Korean Circ J.
- 2009 Sep;39(9):386-388.
- doi: 10.4070/kcj.2009.39.9.386
A 24-year-old woman presented to the department of plastic surgery for surgical excision of a nevus on her nose. Although her history failed to reveal any cardiac disease, her pre-operative... -
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