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Wiley InterScience

British Journal of Clinical Pharmacology

British Journal of Clinical Pharmacology

Volume 61 Issue 4, Pages 464 - 469

Published Online: 24 Jan 2006

Journal compilation © 2010 The British Pharmacological Society



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QT interval prolongation associated with sibutramine treatment
Mira Harrison-Woolrych 1 , David W. J. Clark 1,2 , Geraldine R. Hill 1 , Mark I. Rees 3 & Jonathan R. Skinner 4
  1 Intensive Medicines Monitoring Programme, Department of Preventive and Social Medicine, University of Otago, New Zealand,   2 Department of Pharmacology and Toxicology, School of Medical, Sciences, University of Otago, P.O Box 913, Dunedin, New Zealand,   3 Molecular Neuroscience Group, The School of Medicine, University of Wales Swansea, Singleton Park, Swansea SA2 8PP, UK and   4 Department of Paediatric Cardiology, Starship Hospital, Park Road, Auckland, New Zealand
Correspondence to  Dr David Clark, Department of Pharmacology and Toxicology, University of Otago, PO Box 913, Dunedin, New Zealand. Tel: +64 3479 7239 Fax: +64 3479 9140
E-mail: david.clark@stonebow.otago.ac.nz
Copyright 2006 Blackwell Publishing Ltd
KEYWORDS
adverse cardiovascular events • congenital long QT syndrome (LQTS) • IKs currents • KCNQ1 • QT prolongation • sibutramine

ABSTRACT

 
Aims

To investigate a possible association of sibutramine with QT interval prolongation.

 
Methods

Post-marketing surveillance using prescription event monitoring in the New Zealand Intensive Medicines Monitoring Programme (IMMP) identified a case of QT prolongation and associated cardiac arrest in a patient taking sibutramine for 25 days. This patient was further investigated, including genotyping for long QT syndrome. Other IMMP case reports suggesting arrhythmias associated with sibutramine were assessed and further reports were obtained from the World Health Organisation (WHO) adverse drug reactions database.

 
Results

The index case displayed a novel mutation in a cardiac potassium channel subunit gene, KCNQ1, which is likely to prolong cardiac membrane depolarization and increase susceptibility to long QT intervals. Assessment of further IMMP reports identified five additional patients who experienced palpitations associated with syncope or presyncopal symptoms, one of whom had a QTc at the upper limit of normal. Assessment of reports from the WHO database identified three reports of QT prolongation and one fatal case of torsade de pointes in a patient also taking cisapride.

 
Conclusions

This case series suggests that sibutramine may be associated with QT prolongation and related dysrhythmias. Further studies are required, but in the meantime we would recommend that sibutramine should be avoided in patients with long QT syndrome and in patients taking other medicines that may prolong the QT interval.


Received 12 May 2005 Accepted 18 October 2005

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-2125.2006.02574.x About DOI

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