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Reactions 1290 - 27 Feb 2010 S Citalopram QT-interval prolongation in an elderly patient: case report A 76-year-old woman developed QT-interval prolongation during treatment with citalopram for chronic depression [duration of treatment to reaction onset not stated]. The woman, whose history included Alzheimer’s disease, rheumatoid arthritis and a paranoid schizophrenic episode, was hospitalised after collapsing on her way to the bathroom. On admission, she was in mildly reduced state, but showed no other conclusive pathology. An ECG revealed bradycardia of 55/min, a QT interval of 526ms and a QTc interval of 503ms; she also had hypokalaemia of 3.4 mmol/L. At that time, her medication included citalopram 20 mg/day, olanzapine, methotrexate, prednisone, folic acid and atorvastatin. Citalopram and olanzapine were discontinued. Two days later, an ECG showed a normal sinus rhythm with a HR of 65/min, and a normal QT interval of 410ms (QTc interval 428ms). Her therapy was changed to escitalopram; olanzapine was currently not indicated and therefore not restarted. On day 2, a 24h ECG was largely normal, without arrhythmias apart from isolated supraventricular and ventricular extrasystoles. A Schellong test was pathological with a 26mm Hg drop in her systolic BP. Five days after admission, a repeat ECG was normal with a HR of 58/min, a QT interval of 412ms and a QTc interval of 408ms. Her collapse was interpreted as orthostatic syncope. Review of her history later revealed several hospitalisations for syncopes during the previous years. Three years before the current event, while she was receiving citalopram 40 mg/day, the hospital work-up had disclosed a prolonged QT interval and hypokalaemia. One and a half years later, she was hospitalised while receiving citalopram, olanzapine, and after taking a dose of oxazepam; on that occasion, her QT interval had normalised following a reduction in her citalopram dosage to 20 mg/day. On her last admission about 0.5 years later, she was again receiving citalopram 40 mg/day, and had a prolonged QT interval and mild hypokalaemia. Author comment: Given the known association between citalopram intake and prolonged QT duration, immediate regression of QT duration after discontinuation or dose reduction, and new QT prolongation following re-exposure to citalopram, causality between citalopram intake and onset of QT/QTc prolongation can be considered at least likely. Bruggisser M, et al. Drug-induced long QT syndrome. Praxis 98: 1409-15, No. 24, 2 Dec 2009 [German] - Switzerland 803006452 1 Reactions 27 Feb 2010 No. 1290 0114-9954/10/1290-0001/$14.95 © 2010 Adis Data Information BV. All rights reserved

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Page 1: Citalopram

Reactions 1290 - 27 Feb 2010

SCitalopram

QT-interval prolongation in an elderly patient:case report

A 76-year-old woman developed QT-intervalprolongation during treatment with citalopram for chronicdepression [duration of treatment to reaction onset notstated].

The woman, whose history included Alzheimer’sdisease, rheumatoid arthritis and a paranoid schizophrenicepisode, was hospitalised after collapsing on her way to thebathroom. On admission, she was in mildly reduced state,but showed no other conclusive pathology. An ECGrevealed bradycardia of 55/min, a QT interval of 526ms anda QTc interval of 503ms; she also had hypokalaemia of3.4 mmol/L. At that time, her medication includedcitalopram 20 mg/day, olanzapine, methotrexate,prednisone, folic acid and atorvastatin.

Citalopram and olanzapine were discontinued. Two dayslater, an ECG showed a normal sinus rhythm with a HR of65/min, and a normal QT interval of 410ms (QTc interval428ms). Her therapy was changed to escitalopram;olanzapine was currently not indicated and therefore notrestarted. On day 2, a 24h ECG was largely normal, withoutarrhythmias apart from isolated supraventricular andventricular extrasystoles. A Schellong test was pathologicalwith a 26mm Hg drop in her systolic BP. Five days afteradmission, a repeat ECG was normal with a HR of 58/min, aQT interval of 412ms and a QTc interval of 408ms. Hercollapse was interpreted as orthostatic syncope.

Review of her history later revealed severalhospitalisations for syncopes during the previous years.Three years before the current event, while she wasreceiving citalopram 40 mg/day, the hospital work-up haddisclosed a prolonged QT interval and hypokalaemia. Oneand a half years later, she was hospitalised while receivingcitalopram, olanzapine, and after taking a dose ofoxazepam; on that occasion, her QT interval hadnormalised following a reduction in her citalopram dosageto 20 mg/day. On her last admission about 0.5 years later,she was again receiving citalopram 40 mg/day, and had aprolonged QT interval and mild hypokalaemia.

Author comment: Given the known association betweencitalopram intake and prolonged QT duration, immediateregression of QT duration after discontinuation or dosereduction, and new QT prolongation following re-exposure tocitalopram, causality between citalopram intake and onset ofQT/QTc prolongation can be considered at least likely.Bruggisser M, et al. Drug-induced long QT syndrome. Praxis 98: 1409-15, No. 24,2 Dec 2009 [German] - Switzerland 803006452

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Reactions 27 Feb 2010 No. 12900114-9954/10/1290-0001/$14.95 © 2010 Adis Data Information BV. All rights reserved