T-wave morphology as a covariate in drug-induced QTc prolongation

Claus Graff*, J. Matz, M. P. Andersen, J. K. Kanters, J. Nielsen, J. Q. Xue, E. Toft, J. J. Struijk

*Corresponding author af dette arbejde

Abstract

QT interval prolongation is one of the most common causes of delays and non-approvals in drug development due to the qualitative relationship between this interval and Torsade de Pointes (TdP) arrhythmia. However, not all drugs that prolong the QT interval to the same extent carry the same risk for TdP. Other indications, such as abnormal T-wave morphology, may play a role in differentiating between safe and unsafe drugs. We used moxifloxacin and d,l-sotalol to investigate whether concurrent changes for QTc and T-wave morphology could be used to describe the discrepancy in proarrhythmic risk between the two drugs. Our results provide evidence that these drugs have significantly different morphology-duration profiles at similar QTc prolongations. We propose to investigate whether concurrent assessment of QTc and T-wave morphology has general validity for drug safety evaluation.

OriginalsprogEngelsk
TitelComputers in Cardiology 2009, CinC 2009
Antal sider4
Vol/bind36
Publikationsdato1 dec. 2009
Sider589-592
Artikelnummer5445339
ISBN (Trykt)9781424472819
StatusUdgivet - 1 dec. 2009
Begivenhed36th Annual Conference of Computers in Cardiology, CinC 2009 - Park City, UT, USA
Varighed: 13 sep. 200916 sep. 2009

Konference

Konference36th Annual Conference of Computers in Cardiology, CinC 2009
Land/OmrådeUSA
ByPark City, UT
Periode13/09/200916/09/2009
SponsorEMB, IEEE, Medtronic, CareFusion, Biosense Webster

Fingeraftryk

Dyk ned i forskningsemnerne om 'T-wave morphology as a covariate in drug-induced QTc prolongation'. Sammen danner de et unikt fingeraftryk.

Citationsformater