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Affiliation(s)

Captain James A. Lovell Federal Health Care Center, North Chicago, USA

ABSTRACT

QTc prolongation is a common black box warning within medication labeling. However, it is unclear if QTc prolonging drugs carry the same risk for torsade de pointes as primary or congenital prolongation. The majority of previous studies regarding antipsychotics are limited by a variety of factors. This was a retrospective, cohort study amongst 114 patients at the FHCC to examine the risk of developing QTc prolongation and torsade de pointes in relation to antipsychotic dosing. The primary objective is to determine the incidence rate and mean of QTc prolongation stratified to dose of five antipsychotics. The secondary objective is to determine the incidence of QTc of ≥ 500 msecs and torsades de pointes stratified to dose. The frequency of QTc prolongation was analyzed using chi-square and Fischer’s exact test as appropriate with a p < 0.05 being labeled as significant. The average length of QTc prolongation stratified to the dose of antipsychotic was analyzed using linear regression analysis. Dose dependency of QTc prolongation with the five antipsychotic drugs of interest (haloperidol, ziprasidone, olanzapine, risperidone, and ziprasidone) was not supported in this study based on the non-significant linear regression analyses. However, the frequency of torsade de pointes and changes of > 60 msec in the QTc were relatively rare. Thus frequent monitoring is likely unnecessary unless the patient has a prolonged QT at baseline or other risk factors.

KEYWORDS

antipsychotics, QTc prolongation, torsade de pointes, haloperidol, risperidone, olanzapine, quetiapine ziprasidone

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