It usually manifests in patients with abnormalities of repolarization. It is usually drug related and may be either selflimiting or progressing to ventricular fibrillation. It most often occurs in the presence of a prolonged qt interval on the ecg, a slow heart rate, andor disturbances in blood electrolyte balance. First, a change in the amplitude and morphology twisting of the qrs complexes around the isoelectric line is a typical feature of. Further reading druginduced prolongation of the qt interval. Known risk of tdp kr, possible risk of tdp pr or have a conditional risk of tdp cr. A 62yearold chinese male who placed with the implanted cardioverterdefibrillator icd appeared the qtc prolongation and tdp after the concurrent administration of fluoxetine and amiodarone. Amiodarone is a wellknown class iii antiarrhythmic agent. Risk can be minimised if appropriate precautions are taken when prescribing drugs that prolong the qt interval see table 3. Read more about symptoms, diagnosis, treatment, complications, causes and prognosis. It is a polymorphic ventricular tachycardia that exhibits distinct characteristics on the electrocardiogram ecg. The ventricles are the two lower chambers of the heart that. It is a polymorphic ventricular tachycardia that exhibits distinct characteristics on the electrocardiogram.
A 62yearold chinese male who placed with the implanted. For tdp to be diagnosed, the patient has to have evidence of both pvt and qt prolongation. The vast majority of torsades results from acquired longqt. Here, we report 1 case of tdp after a coadministration of fluoxetine and amiodarone patient concerns. E uma emergencia medica e pode causar morte subita cardiaca.
Sign in below to access your subscription for full content. It is characterized by rapid, irregular qrs complexes, which appear to be twisting around the electrocardiogram ecg baseline. Torsades is lifethreatening, and can be made worse by many drugs, including some of the drugs used to treat vt. The condition can be acquired or congenital in nature. Variety of ventricular tachycardia resulting from prolongation of ventricular recovery time. The patient was treated with magnesium and potassium immediately. Please see the file description page for further information. If you do not see its contents the file may be temporarily. The initial episode is controlled with magnesium and perhaps defibrillation. Several ecg features are characteristic of tdp and are illustrated in figure 1. Pharmacological treatment of acquired qt prolongation and.
Usually the patient will be fine, but sometimes tdp does recur. Pacing at rates up to 140 bpm may prevent the ventricular pauses that allow tdp to originate. It is universally associated with congenital or acquired long qtc syndrome lqts. However, long qt syndrome can lead to tdp is left alone and unrecognized. However, the outlook for people managing the condition with the appropriate treatment is excellent. Read more about symptoms, diagnosis, treatment, complications, causes and. Overall, these new findings might improve both the decision making skills of pharmaceutical scientists to mitigate herg liability during the drug discovery process and the. Torsades usually occurs in a pause dependent fashion. Torsade des pointes an overview sciencedirect topics. The patient with torsade who is in extremis should be treated with electrical cardioversion or defibrillation. Until recently, cardiac toxicity manifesting in the form of arrhythmias related to qt interval prolongation was uncommonly appreciated within the antimicrobial class of drugs, but it was well described among antiarrhythmic agents. This can be an iatrogenic arrhythmia and due to drugs, or may be genetic in origin. The risk of tdpqtp must be considered when selecting antibiotic therapy.
Torsades definition of torsades by medical dictionary. Pointes of interest antimicrobialassociated qt interval prolongation. Ventricular tachycardia pediatrics, tachycardia syncope renal failure, chronic and. The authors wish to highlight the various responsible drugs causing tdp with. Previous cardiac investigations had been normal and after a second episode of ventricular fibrillation the patient was referred for electrophysiological studies. Torsades can be caused by either congenital longqt syndrome or acquired longqt syndrome due to electrolyte abnormalities andor medications. Behr3 1medical toxicology centre, wolfson building, institute of cellular medicine, newcastle university, newcastle upon tyne ne2 4hh,2national poisons information service newcastle unit, newcastle hospitals nhs foundation trust, newcastle upon tyne ne1 4lp and3cardiovascular. Pheochromocytomas are also extremely rare tumours in the paediatric age.
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