Duke University Medical Center (Electrophysiology), 2301 Erwin Road, 3174, Durham, NC, 27710, USA.
William S. Middleton Memorial Veterans Hospital (Pharmacy), Madison, WI, USA.
Am J Cardiovasc Drugs. 2023 Nov;23(6):709-719. doi: 10.1007/s40256-023-00612-6. Epub 2023 Oct 6.
There is evidence to suggest that colchicine reduces the risk of recurrent atrial fibrillation (AF) after catheter ablation; however, the tolerability and safety of colchicine in routine practice is unknown.
Patients undergoing catheter ablation for AF who received colchicine after ablation were matched 1:1 to patients who did not by age, sex, and renal function. Recurrent AF was compared between groups categorically at 12 months and via propensity weighted Cox proportional hazards models with and without a 3-month blanking period.
Overall, 180 patients (n = 90 colchicine and n = 90 matched controls) were followed for a median (Q1, Q3) of 10.3 (7.0, 12.0) months. Mean age was 65.3 ± 9.1 years, 33.9% were women, mean CHADS-VASc score was 2.9 ± 1.5, and 51.1% had persistent AF. Most patients (70%) received colchicine 0.6 mg daily for a median of 30 days. In the colchicine group, 55 patients (61.1%) were receiving at least one known interacting medication with colchicine. After ablation, one patient required colchicine dose reduction and four patients required discontinuation. After adjusting for covariate imbalance using propensity weighting, no significant association between colchicine use and AF recurrence was identified (adjusted hazard ratio 0.94, 95% confidence interval [CI] 0.48-1.85; p = 0.853). No significant association was found between colchicine use and all-cause hospitalizations (adjusted odds ratio 0.74, 95% CI 0.28-1.96; p = 0.548).
Despite the frequent presence of drug-drug interactions, a 30-day course of colchicine is well-tolerated after AF ablation; however, we did not observe any association between colchicine and lower rates of AF recurrence or hospitalization.
有证据表明,秋水仙碱可降低导管消融后复发性心房颤动(AF)的风险;然而,秋水仙碱在常规实践中的耐受性和安全性尚不清楚。
接受导管消融治疗 AF 的患者,在消融后接受秋水仙碱治疗,与未接受秋水仙碱治疗的患者按年龄、性别和肾功能进行 1:1 匹配。通过 12 个月的分类比较和有无 3 个月洗脱期的倾向性加权 Cox 比例风险模型比较两组之间的复发性 AF。
共有 180 例患者(n=90 例秋水仙碱组和 n=90 例匹配对照组)接受中位(Q1,Q3)10.3(7.0,12.0)个月的随访。平均年龄为 65.3±9.1 岁,33.9%为女性,平均 CHADS-VASc 评分为 2.9±1.5,51.1%为持续性 AF。大多数患者(70%)接受 0.6mg/d 的秋水仙碱治疗,中位时间为 30 天。在秋水仙碱组中,55 例(61.1%)患者正在服用至少一种已知与秋水仙碱相互作用的药物。消融后,1 例患者需要减少秋水仙碱剂量,4 例患者需要停药。使用倾向性评分调整协变量失衡后,秋水仙碱使用与 AF 复发之间无显著相关性(调整后的危险比 0.94,95%置信区间[CI]0.48-1.85;p=0.853)。未发现秋水仙碱使用与全因住院之间存在显著相关性(调整后的优势比 0.74,95%CI0.28-1.96;p=0.548)。
尽管存在频繁的药物相互作用,但 AF 消融后使用 30 天的秋水仙碱是可以耐受的;然而,我们没有观察到秋水仙碱与较低的 AF 复发率或住院率之间存在任何关联。