TY - JOUR
T1 - Psychotropic Drugs Associated With Corrected QT Interval Prolongation
AU - Noord, Charlotte
AU - Straus, SMJM (Sabine)
AU - Sturkenboom, MCJM
AU - Hofman, Bert
AU - Aarnoudse, ALHJ (Albert-Jan)
AU - Bagnardi, V
AU - Kors, Jan
AU - Newton-Cheh, C
AU - Witteman, JCM
AU - Stricker, Bruno
PY - 2009
Y1 - 2009
N2 - Aims: To study whether listed putative corrected QT (QTc)-prolonging psychotropic drugs indeed prolong the QTc interval under everyday circumstances and to evaluate whether this is a class effect or an individual drue effect. we conducted a prospective population-based cohort study. Methods: This study was conducted as part of the Rotterdam Study and included 3377 men and 4845 women (>= 55 years) who had triennial electrocardiograms (ECGs). The primary end point,; of the study were the length of the QTc interval at each ECG. the difference in QTc interval between consecutive ECGs within one person, and the risk of ail abnormally prolonged QTc interval. Drug use at the index date was obtained from automated dispensing records. The associations were examined by means of a repeated measurement analysis, adjusted for age. sex, diabetes mellitus. hypertension, myocardial infarction, heart failure. and use of class I QTc-prolonging drugs. Results: Of the 8222 participants. 813 participants (9.9%) developed QTc prolongation during follow-up and 492 participants (74.4% women) used psychotropic drugs at the time of an ECG. Starting tricyclic antidepressants increased the QTc interval significantly with 6.9 milliseconds (95% confidence interval [CI], 3.1-10.7 milliseconds) between consecutive ECGs in comparison With Consecutive ECGs of participants not using tricyclic antidepressants. in particular starting amitriptyline (8.5 milliseconds: 95% CI. 2.8-14.2 milliseconds), maprotiline (13.9 milliseconds: 9 % CI, 3.6-24.3 milliseconds), and nortriptyline (35.3 milliseconds: 95% CI. 8.0-62.6 milliseconds). Starting lithium also increased the QTc interval significantly (18.6 milliseconds; 95% Cl 4.8-32.4 milliseconds). Conclusions: In this population-based prospective cohort Stud),, we confirmed the importance of antidepressants and antipsychotics as potential contributors to QTc prolongation. Especially, starting tricyclic antidepressant drugs (as a class) is associated with a significant intraindividual increase in the QTc interval in comparison to the change in nonusers. The tricyclic antidepressants seem to prolong the QTc interval as a class effect.
AB - Aims: To study whether listed putative corrected QT (QTc)-prolonging psychotropic drugs indeed prolong the QTc interval under everyday circumstances and to evaluate whether this is a class effect or an individual drue effect. we conducted a prospective population-based cohort study. Methods: This study was conducted as part of the Rotterdam Study and included 3377 men and 4845 women (>= 55 years) who had triennial electrocardiograms (ECGs). The primary end point,; of the study were the length of the QTc interval at each ECG. the difference in QTc interval between consecutive ECGs within one person, and the risk of ail abnormally prolonged QTc interval. Drug use at the index date was obtained from automated dispensing records. The associations were examined by means of a repeated measurement analysis, adjusted for age. sex, diabetes mellitus. hypertension, myocardial infarction, heart failure. and use of class I QTc-prolonging drugs. Results: Of the 8222 participants. 813 participants (9.9%) developed QTc prolongation during follow-up and 492 participants (74.4% women) used psychotropic drugs at the time of an ECG. Starting tricyclic antidepressants increased the QTc interval significantly with 6.9 milliseconds (95% confidence interval [CI], 3.1-10.7 milliseconds) between consecutive ECGs in comparison With Consecutive ECGs of participants not using tricyclic antidepressants. in particular starting amitriptyline (8.5 milliseconds: 95% CI. 2.8-14.2 milliseconds), maprotiline (13.9 milliseconds: 9 % CI, 3.6-24.3 milliseconds), and nortriptyline (35.3 milliseconds: 95% CI. 8.0-62.6 milliseconds). Starting lithium also increased the QTc interval significantly (18.6 milliseconds; 95% Cl 4.8-32.4 milliseconds). Conclusions: In this population-based prospective cohort Stud),, we confirmed the importance of antidepressants and antipsychotics as potential contributors to QTc prolongation. Especially, starting tricyclic antidepressant drugs (as a class) is associated with a significant intraindividual increase in the QTc interval in comparison to the change in nonusers. The tricyclic antidepressants seem to prolong the QTc interval as a class effect.
U2 - 10.1097/JCP.0b013e318191c6a8
DO - 10.1097/JCP.0b013e318191c6a8
M3 - Article
SN - 0271-0749
VL - 29
SP - 9
EP - 15
JO - Journal of Clinical Psychopharmacology
JF - Journal of Clinical Psychopharmacology
IS - 1
ER -