Propafenone versus amiodarone for supraventricular arrhythmias in septic shock: a randomised controlled trial
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu randomizované kontrolované studie, časopisecké články
Grantová podpora
NV18-06-00417
Agentura Pro Zdravotnický Výzkum České Republiky
PubMed
37698594
DOI
10.1007/s00134-023-07208-3
PII: 10.1007/s00134-023-07208-3
Knihovny.cz E-zdroje
- Klíčová slova
- Amiodarone, Atrial fibrillation, Atrial flutter, Cardioversion, Propafenone, Septic shock, Supraventricular arrhythmia,
- MeSH
- amiodaron * terapeutické užití MeSH
- antiarytmika terapeutické užití MeSH
- fibrilace síní * terapie MeSH
- funkce levé komory srdeční MeSH
- lidé MeSH
- propafenon terapeutické užití MeSH
- prospektivní studie MeSH
- septický šok * komplikace farmakoterapie MeSH
- tepový objem MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- amiodaron * MeSH
- antiarytmika MeSH
- propafenon MeSH
PURPOSE: Acute onset supraventricular arrhythmias can contribute to haemodynamic compromise in septic shock. Both amiodarone and propafenone are available interventions, but their clinical effects have not yet been directly compared. METHODS: In this two-centre, prospective controlled parallel group double blind trial we recruited 209 septic shock patients with new-onset arrhythmia and a left ventricular ejection fraction above 35%. The patients were randomised in a 1:1 ratio to receive either intravenous propafenone (70 mg bolus followed by 400-840 mg/24 h) or amiodarone (300 mg bolus followed by 600-1800 mg/24 h). The primary outcomes were the proportion of patients who had sinus rhythm 24 h after the start of the infusion, time to restoration of the first sinus rhythm and the proportion of patients with arrhythmia recurrence. RESULTS: Out of 209 randomized patients, 200 (96%) received the study drug. After 24 h, 77 (72.8%) and 71 (67.3%) were in sinus rhythm (p = 0.4), restored after a median of 3.7 h (95% CI 2.3-6.8) and 7.3 h (95% CI 5-11), p = 0.02, with propafenone and amiodarone, respectively. The arrhythmia recurred in 54 (52%) patients treated with propafenone and in 80 (76%) with amiodarone, p < 0.001. Patients with a dilated left atrium had better rhythm control with amiodarone (6.4 h (95% CI 3.5; 14.1) until cardioversion vs 18 h (95% CI 2.8; 24.7) in propafenone, p = 0.05). CONCLUSION: Propafenone does not provide better rhythm control at 24 h yet offers faster cardioversion with fewer arrhythmia recurrences than with amiodarone, especially in patients with a non-dilated left atrium. No differences between propafenone and amiodarone on the prespecified short- and long-term outcomes were observed.
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