Literature DB >> 33830046

Clinical and genetic characteristics and course of congenital long QT syndrome in children: A nine-year single-center experience.

Yakup Ergül1, Gülhan Tunca Şahin1, Hasan Candaş Kafalı1, Erkut Öztürk1, Senem Özgür1, Sertaç Haydin2, Alper Güzeltaş1.   

Abstract

OBJECTIVE: Long QT syndrome (LQTS) is an inherited primary arrhythmia syndrome associated with life-threatening ventricular arrhythmias and sudden death. This study aimed to report the clinical and genetic characteristics and outcomes of children diagnosed as having LQTS in a tertiary pediatric cardiology center in Turkey.
METHODS: This was a retrospective review of pediatric patients diagnosed as having LQTS at our center from January 2011 to April 2020.
RESULTS: A total of 145 patients (76 males) were included, with a mean age of 9.2±4.5 years and a mean weight of 35.7±18.5 kg; 38 (26.2%) were identified as having LQTS during family screening, whereas a significant proportion of patients were asymptomatic at presentation, 15 patients (10.3%) were diagnosed after previous cardiac arrest, and 26 patients (18%) had syncope. The mean Schwartz score was 4.5 points (range, 3-7.5 points). Furthermore, 107 patients (82%) were confirmed to have a pathogenic mutation for LQTS genes. All patients received beta-blockers. Implantable cardioverter-defibrillator insertion was performed in 34 patients (23.4%). Left or bilateral cardiac sympathetic denervation was performed in 9 patients (6.2%). Median follow-up time was 35.6±25.8 months. Five (3.4%) patients died during the follow-up. Statistical analyses of risk factors for major cardiac events revealed that the QTc was >500 ms and that T wave alternans, high Schwartz score, and Jervell and Lange-Nielsen syndrome were strong and significant predictors of cardiac events.
CONCLUSION: LQTS has a variety of clinical manifestations. Patients' symptoms ranged between asymptomatic and sudden cardiac death (SCD). By raising the awareness of physicians regarding the disease, SCD might be prevented in the early period.

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Mesh:

Year:  2021        PMID: 33830046      PMCID: PMC8923495          DOI: 10.14744/AnatolJCardiol.2020.08791

Source DB:  PubMed          Journal:  Anatol J Cardiol        ISSN: 2149-2263            Impact factor:   1.596


  26 in total

Review 1.  HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.

Authors:  Silvia G Priori; Arthur A Wilde; Minoru Horie; Yongkeun Cho; Elijah R Behr; Charles Berul; Nico Blom; Josep Brugada; Chern-En Chiang; Heikki Huikuri; Prince Kannankeril; Andrew Krahn; Antoine Leenhardt; Arthur Moss; Peter J Schwartz; Wataru Shimizu; Gordon Tomaselli; Cynthia Tracy
Journal:  Heart Rhythm       Date:  2013-08-30       Impact factor: 6.343

2.  Clinical and genetic profile of congenital long QT syndrome in Hong Kong: a 20-year experience in paediatrics.

Authors:  S Y Kwok; A Py Liu; C Yy Chan; K S Lun; J Lf Fung; C Cy Mak; B Hy Chung; T C Yung
Journal:  Hong Kong Med J       Date:  2018-12-03       Impact factor: 2.227

3.  Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome.

Authors:  Jenny B Hobbs; Derick R Peterson; Arthur J Moss; Scott McNitt; Wojciech Zareba; Ilan Goldenberg; Ming Qi; Jennifer L Robinson; Andrew J Sauer; Michael J Ackerman; Jesaia Benhorin; Elizabeth S Kaufman; Emanuela H Locati; Carlo Napolitano; Silvia G Priori; Jeffrey A Towbin; G Michael Vincent; Li Zhang
Journal:  JAMA       Date:  2006-09-13       Impact factor: 56.272

Review 4.  Long-QT syndrome: from genetics to management.

Authors:  Peter J Schwartz; Lia Crotti; Roberto Insolia
Journal:  Circ Arrhythm Electrophysiol       Date:  2012-08-01

5.  Long QT syndrome in adults.

Authors:  Andrew J Sauer; Arthur J Moss; Scott McNitt; Derick R Peterson; Wojciech Zareba; Jennifer L Robinson; Ming Qi; Ilan Goldenberg; Jenny B Hobbs; Michael J Ackerman; Jesaia Benhorin; W Jackson Hall; Elizabeth S Kaufman; Emanuela H Locati; Carlo Napolitano; Silvia G Priori; Peter J Schwartz; Jeffrey A Towbin; G Michael Vincent; Li Zhang
Journal:  J Am Coll Cardiol       Date:  2007-01-04       Impact factor: 24.094

6.  In utero diagnosis of long QT syndrome by magnetocardiography.

Authors:  Bettina F Cuneo; Janette F Strasburger; Suhong Yu; Hitoshi Horigome; Takayoshi Hosono; Akihiko Kandori; Ronald T Wakai
Journal:  Circulation       Date:  2013-11-12       Impact factor: 29.690

7.  Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome.

Authors:  Ilan Goldenberg; Arthur J Moss; Derick R Peterson; Scott McNitt; Wojciech Zareba; Mark L Andrews; Jennifer L Robinson; Emanuela H Locati; Michael J Ackerman; Jesaia Benhorin; Elizabeth S Kaufman; Carlo Napolitano; Silvia G Priori; Ming Qi; Peter J Schwartz; Jeffrey A Towbin; G Michael Vincent; Li Zhang
Journal:  Circulation       Date:  2008-04-21       Impact factor: 29.690

8.  T-wave alternans in long QT syndrome.

Authors:  Siddharth Narayan Gadage
Journal:  Ann Pediatr Cardiol       Date:  2018 May-Aug

9.  Bilateral cardiac sympathetic denervation in children with long-QT syndrome and catecholaminergic polymorphic ventricular tachycardia.

Authors:  Murat Akkuş; Yunus Seyrek; Hasan Candaş Kafalı; Yakup Ergül
Journal:  J Electrocardiol       Date:  2020-05-22       Impact factor: 1.438

10.  Long QT syndrome: a Korean single center study.

Authors:  Yun-Sik Lee; Bo-Sang Kwon; Gi-Beom Kim; Se-Il Oh; Eun-Jung Bae; Sung-Sup Park; Chung-Il Noh
Journal:  J Korean Med Sci       Date:  2013-09-25       Impact factor: 2.153

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  2 in total

1.  Secondary genomic findings in the 2020 China Neonatal Genomes Project participants.

Authors:  Hui Xiao; Jian-Tao Zhang; Xin-Ran Dong; Yu-Lan Lu; Bing-Bing Wu; Hui-Jun Wang; Zheng-Yan Zhao; Lin Yang; Wen-Hao Zhou
Journal:  World J Pediatr       Date:  2022-06-21       Impact factor: 9.186

Review 2.  Cardiac sympathetic denervation in the prevention of genetically mediated life-threatening ventricular arrhythmias.

Authors:  Peter J Schwartz; Michael J Ackerman
Journal:  Eur Heart J       Date:  2022-06-06       Impact factor: 35.855

  2 in total

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