Literature DB >> 26611485

Ventricular fibrillation after elective surgery in an adolescent with long QT syndrome.

Sharon J Kim1, Kavitha N Pundi1, J Martijn Bos1, Michael J Ackerman1.   

Abstract

Congenital long QT syndrome (LQTS) is a potentially lethal but highly treatable channelopathy. Along with multiple risk reduction measures, a recommendation for left sympathetic cardiac denervation therapy and/or implantable cardioverter defibrillator is made for higher risk patients. Despite its relatively common incidence in paediatric patients, there are no formal recommendations regarding perioperative management and discharge criteria for LQTS patients undergoing ambulatory surgery. This report describes a 17-year-old girl, diagnosed with congenital LQTS at 9 years of age, who had an episode of ventricular fibrillation the day after elective ear, nose and throat surgery. Despite several risk factors, she had a same-day dismissal, was not adequately monitored postoperatively and her cardiologists were not notified of her procedure. For the high-risk LQTS patient, we recommend monitoring of perioperative electrolytes and rhythm, postoperative ECG, adequate β-blockade therapy, avoidance of particular pharmacological agents, consideration of overnight observation and communication with the patient's cardiologist prior to procedure, and at discharge. 2015 BMJ Publishing Group Ltd.

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Year:  2015        PMID: 26611485      PMCID: PMC4680316          DOI: 10.1136/bcr-2015-212365

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  16 in total

Review 1.  Anesthesia for patients with congenital long QT syndrome.

Authors:  Susan J Kies; Christina M Pabelick; Heather A Hurley; Roger D White; Michael J Ackerman
Journal:  Anesthesiology       Date:  2005-01       Impact factor: 7.892

Review 2.  Genotype- and phenotype-guided management of congenital long QT syndrome.

Authors:  John R Giudicessi; Michael J Ackerman
Journal:  Curr Probl Cardiol       Date:  2013-10       Impact factor: 5.200

3.  Prevalence of the congenital long-QT syndrome.

Authors:  Peter J Schwartz; Marco Stramba-Badiale; Lia Crotti; Matteo Pedrazzini; Alessandra Besana; Giuliano Bosi; Fulvio Gabbarini; Karine Goulene; Roberto Insolia; Savina Mannarino; Fabio Mosca; Luigi Nespoli; Alessandro Rimini; Enrico Rosati; Patrizia Salice; Carla Spazzolini
Journal:  Circulation       Date:  2009-10-19       Impact factor: 29.690

Review 4.  The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy.

Authors:  Peter J Schwartz; Michael J Ackerman
Journal:  Eur Heart J       Date:  2013-03-18       Impact factor: 29.983

5.  Ventricular tachycardia during general anesthesia in a patient with congenital long QT syndrome.

Authors:  Robert I Katz; Irene Quijano; Nelson Barcelon; Thomas Biancaniello
Journal:  Can J Anaesth       Date:  2003-04       Impact factor: 5.063

6.  Risk factors for recurrent syncope and subsequent fatal or near-fatal events in children and adolescents with long QT syndrome.

Authors:  Judy F Liu; Christian Jons; Arthur J Moss; Scott McNitt; Derick R Peterson; Ming Qi; Wojciech Zareba; Jennifer L Robinson; Alon Barsheshet; Michael J Ackerman; Jesaia Benhorin; Elizabeth S Kaufman; Emanuela H Locati; Carlo Napolitano; Silvia G Priori; Peter J Schwartz; Jeffrey Towbin; Michael Vincent; Li Zhang; Ilan Goldenberg
Journal:  J Am Coll Cardiol       Date:  2011-02-22       Impact factor: 24.094

7.  Acquired long QT syndrome and elective anesthesia in children.

Authors:  Timothy B Curry; Renee Gaver; Roger D White
Journal:  Paediatr Anaesth       Date:  2006-04       Impact factor: 2.556

8.  Cardiac arrest under anaesthesia in a child with previously undiagnosed Jervell and Lange-Nielsen syndrome.

Authors:  J J Holland
Journal:  Anaesthesia       Date:  1993-02       Impact factor: 6.955

9.  Ambulatory surgery in the United States, 2006.

Authors:  Karen A Cullen; Margaret J Hall; Aleksandr Golosinskiy
Journal:  Natl Health Stat Report       Date:  2009-01-28

10.  Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.

Authors:  Wojciech Zareba; Arthur J Moss; Emanuela H Locati; Michael H Lehmann; Derick R Peterson; W Jackson Hall; Peter J Schwartz; G Michael Vincent; Silvia G Priori; Jesaia Benhorin; Jeffrey A Towbin; Jennifer L Robinson; Mark L Andrews; Carlo Napolitano; Katherine Timothy; Li Zhang; Aharon Medina
Journal:  J Am Coll Cardiol       Date:  2003-07-02       Impact factor: 24.094

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  1 in total

1.  Refractory ventricular fibrillations after surgical repair of atrial septal defects in a patient with CACNA1C gene mutation - case report.

Authors:  Ai Kojima; Fumiaki Shikata; Toru Okamura; Takashi Higaki; Seiko Ohno; Minoru Horie; Shunji Uchita; Yujiro Kawanishi; Kenji Namiguchi; Takumi Yasugi; Hironori Izutani
Journal:  J Cardiothorac Surg       Date:  2017-12-19       Impact factor: 1.637

  1 in total

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