Sotalolo e amiodarone
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Restoration of Sinus Rhythm Between randomization and day 28, 70 of patients in the amiodarone group Sebbene la maggior parte dei casi di torsione di punta siano autolimitantisi, possono essere associati a sintomi es.: The presence of atrial fibrillation or atrial flutter was confirmed by the concordance of two transtelephonic measurements or of a lead ECG and a transtelephonic measurement obtained less than 24 hours apart.
Journal of the American College of Cardiology Insulina e ipoglicemizzanti orali: CrossRef 91 Jonathan P. David Burkhardt, Andrea Natale.
Among the patients who actually received the assigned study drug, 13 died in the amiodarone group, 10 died in the sotalol group, and 2 died in the placebo group; the mortality ratios were 2. Management of patients with atrial fibrillation. Therefore, DFT reassessment after the institution of antiarrhythmic drug therapy with amiodarone or sotalol is not routinely required. A Companion to Braunwald's Heart Disease, Todd Rudo, Peter Kowey.
European Heart Journal 35 Management of patients with atrial fibrillation: CrossRef 65 Gerald V. Frontiers in Physiology 8. Follow-up visits were scheduled every four weeks and included a clinical evaluation, lead ECG recordings, and measurements of digoxin levels and the INR; the patient's rhythm was monitored transtelephonically weekly.
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CrossRef Giovanni B. SOTALEX dovrebbe essere somministrato con estrema cautela insieme ad altri farmaci che prolungano l'intervallo QT come gli antiaritmici di Classe I, le fenotiazine, gli antidepressivi triciclicila terfenadina e l'astemizolo, ed alcuni antibiotici chinolonici vedi Avvertenze Speciali. There also was a trend toward a longer period of sustained sinus rhythm with sotalol therapy in patients with ischemic heart disease than in those without ischemic heart disease.
Heart Failure Clinics 9 Long-term efficacy of amiodarone for the maintenance of normal sinus rhythm in patients with refractory atrial fibrillation or flutter. Address reprint requests to Dr.
To account for differences in the duration of follow-up among the study groups, the rates of adverse events were calculated as the number of patients who had a particular adverse event at least once per patient-years of follow-up. Patients with atrial flutter or paroxysmal atrial fibrillation were excluded.
Episodi di sovradosaggio, intenzionale o accidentale, hanno raramente causato il decesso.