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2008
DOI: 10.1016/j.ahj.2007.08.033
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A randomized comparison of amiodarone and class IC antiarrhythmic drugs to treat atrial fibrillation in patients paced for sinus node disease: The Prevention Investigation and Treatment: A Group for Observation and Research on Atrial arrhythmias (PITAGORA) trial

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Cited by 28 publications
(8 citation statements)
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“…On the other hand, AADs are always required to control tachycardia‐related symptoms. The Prevention Investigation and Treatment: A Group for Observation and Research on Atrial arrhythmias (PITAGORA) trial had compared the efficacy and safety of amiodarone and Class IC AADs to treat AF in patients paced for SND; the authors found that only 40% of the amiodarone group and 28% of the Class IC AADs group were free from atrial tachyarrhythmias (episodes > 10 minutes) after 20 ± 9 months of follow‐up . In our study, only about one‐fifth of the patients in the PM group maintained sinus rhythm even though many patients were still on AADs at the end of follow‐up.…”
Section: Prolonged Sinus Pauses On Af Termination: Pace or Ablate?mentioning
confidence: 61%
“…On the other hand, AADs are always required to control tachycardia‐related symptoms. The Prevention Investigation and Treatment: A Group for Observation and Research on Atrial arrhythmias (PITAGORA) trial had compared the efficacy and safety of amiodarone and Class IC AADs to treat AF in patients paced for SND; the authors found that only 40% of the amiodarone group and 28% of the Class IC AADs group were free from atrial tachyarrhythmias (episodes > 10 minutes) after 20 ± 9 months of follow‐up . In our study, only about one‐fifth of the patients in the PM group maintained sinus rhythm even though many patients were still on AADs at the end of follow‐up.…”
Section: Prolonged Sinus Pauses On Af Termination: Pace or Ablate?mentioning
confidence: 61%
“…In our observational cohort, there were eight deaths during flecainide treatment, three of which were classified as SCD. Earlier studies revealed a total number of eight deaths in the AF population receiving flecainide (three because of noncardiac causes, four because of structural heart disease, and information was not available in the remaining case) [16–21]. In cases in which information was available, the occurrence of death ranged from 1 day to 2 months after flecainide treatment initiation.…”
Section: Discussionmentioning
confidence: 99%
“…A few clinical studies have identified an overall increase in respiratory adverse effects [16,17]; however, none have specifically identified ALI/ARDS as being increased, either around the time of surgery [18,19] or with long-term use [2023]. One clinical trial that did find a significant increase in ARDS was a nonblinded study of Belgian patients randomized to prophylactic placebo, verapamil, or amiodarone for the prevention of atrial fibrillation after lung cancer surgery [7].…”
Section: Discussionmentioning
confidence: 99%