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DOI 10.1016/j.jacep.2022.02.018

Медицинская библиотека · JACC. Clinical electrophysiology · 2022

Reduction in Ventricular Tachyarrhythmia Burden in Patients Enrolled in the RAID Trial.

Younis Arwa, Goldenberg Ilan, Farooq Shamroz, Yavin Hagai, Daubert James, Raitt Merritt, Mazur Alexander, Huang David T, Mitchell Brent L, Rashtian Mayer R, Winters Stephen, Vloka Margot, Aktas Mehmet, Bernabei Matthew A, Beck Christopher A, McNitt Scott, Zareba Wojciech

СтатьяРандомизированное исследованиеПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаПеревод пока не подготовлен

Аннотация

BACKGROUND

The RAID (Ranolazine Implantable Cardioverter-Defibrillator) randomized placebo-controlled trial showed that ranolazine treatment was associated with reduction in recurrent ventricular tachycardia (VT) requiring appropriate implantable cardioverter-defibrillator (ICD) therapy.

OBJECTIVES

This study aimed to identify groups of patients in whom ranolazine treatment would result in the highest reduction of ventricular tachyarrhythmia (VTA) burden.

METHODS

Andersen-Gill analyses were performed to identify variables associated with risk for VTA burden among 1,012 patients enrolled in RAID. The primary endpoint was VTA burden defined as VTA episodes requiring appropriate treatment.

RESULTS

Multivariate analysis identified 7 factors associated with increased VTA burden: history of VTA, age ≥65 years, New York Heart Association functional class ≥III, QRS complex (≥130 ms), low ejection fraction (<30%), atrial fibrillation (AF), and concomitant antiarrhythmic drug (AAD) therapy. The effect of ranolazine on VTA burden was seen among patients without concomitant AAD therapy (HR [HR]: 0.68; 95% CI: 0.55-0.84; P < 0.001), whereas no effect was seen among those who are concomitantly treated with other AADs (HR: 1.33; 95% CI: 0.90-1.96; P = 0.16); P = 0.003 for interaction. In patients with cardiac resynchronization therapy (CRT) ICDs, ranolazine treatment was associated with a 36% risk reduction for VTA recurrence (HR: 0.64; 95% CI: 0.47-0.86; P < 0.001), whereas among patients with ICDs without CRT no significant effect was noted (HR: 0.94; 95% CI: 0.74-1.18; P = 0.57); P = 0.047 for interaction.

CONCLUSIONS

In patients with high risk for VTA, ranolazine is effective in reducing VTA burden, with significantly greater effect in CRT-treated patients, those without AF, and those not treated with concomitant AADs. In patients already on AADs or those with AF, the addition of ranolazine did not affect VTA burden. (Ranolazine Implantable Cardioverter-Defibrillator Trial [RAID]; NCT01215253).

Для цитирования: Younis Arwa, Goldenberg Ilan, Farooq Shamroz, Yavin Hagai, Daubert James, Raitt Merritt, Mazur Alexander, Huang David T, Mitchell Brent L, Rashtian Mayer R, Winters Stephen, Vloka Margot, Aktas Mehmet, Bernabei Matthew A, Beck Christopher A, McNitt Scott, Zareba Wojciech. Reduction in Ventricular Tachyarrhythmia Burden in Patients Enrolled in the RAID Trial.. JACC. Clinical electrophysiology. 2022. DOI: 10.1016/j.jacep.2022.02.018.

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