成人主动脉瓣闭锁修复后猝死:基于性别的风险因素案例

IF 0.8 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Lauren Lastinger , Marc Lee , Lauren Hassen , Omer Cavus , Saurabh Rajpal , Jeremy P. Moore , May Ling Mah , Elisa A. Bradley
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引用次数: 0

摘要

背景心脏性猝死(SCD)是成人主动脉瓣闭锁修复术(rCoA)患者的一个重要风险。我们的目的是确定成人 rCoA 患者是否存在 SCD 的临床风险因素。方法和结果评估了一家三级医疗中心所有成人 rCoA 患者的 SCD 事件和临床数据(2007-2017 年)。在 167 名成人 rCoA 患者(39 ± 11 岁,75(45%)为女性)中,有 8 人(5%)发生了 SCD(与年龄匹配的成人相比为 0.9%)。SCD 患者的 QTc 明显延长(QTc:479 ± 16 vs. 434 ± 30 毫秒,p < 0.001)。总体而言,患有 rCoA 和性别正常 QTc 间期延长的成年人发生 SCD 的风险增加了 12 倍(ᵡ2 (1) = 12.3,p < 0.001),男性发生 SCD 的年龄更小(42 ± 13 岁 vs. 女性 60 ± 10 岁,p < 0.05)。多元逻辑回归模型显示,QTc 延长仅在男性中选择性地增加了 SCD 风险(ᵡ2 QTc 延长 8.46,p < 0.005,ᵡ2 年龄 0.29,p = 0.587),而在女性中,年龄与 SCD 风险相关(ᵡ2 QTc 延长 2.84,p = 0.092,ᵡ2 年龄 7.81,p = 0.005)。非持续性室性心动过速、心室功能障碍和心肌纤维化对 SCD 风险没有显著影响。未来对 rCoA 性别特异性 SCD 风险的研究对于更好地了解这种疾病及其晚期表型非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sudden death in adults with repaired coarctation of the aorta: A case for sex-based risk factors

Background

Sudden cardiac death (SCD) is an important risk for adults with repaired coarctation of the aorta (rCoA). We aimed determine if there are clinical risk factors for SCD in adults with rCoA.

Methods and results

SCD events and clinical data from all adults with rCoA at a tertiary care center (2007–2017) were evaluated. In 167 adults with rCoA (39 ± 11 years old, 75 (45%) female) SCD occurred in 8 (5%) (vs. age-matched adults 0.9%). Those with SCD demonstrated significant QTc prolongation (QTc: 479 ± 16 vs. 434 ± 30 msec, p < 0.001). Overall, adults with rCoA and a prolonged sex-normative QTc interval had a 12-fold increased risk of SCD (ᵡ2 (1) = 12.3, p < 0.001), with men sustaining SCD at younger ages (42 ± 13 years vs. women 60 ± 10 years, p < 0.05). Multiple logistic regression modeling demonstrated that prolonged QTc selectively advanced risk for SCD in men only (ᵡ2 QTc prolongation 8.46, p < 0.005 and ᵡ2 age 0.29, p = 0.587), whereas in women, age was associated with SCD risk (ᵡ2 QTc prolongation 2.84, p = 0.092 and ᵡ2 age 7.81, p = 0.005). Non-sustained ventricular tachycardia, ventricular dysfunction, and myocardial fibrosis did not significantly impact SCD risk.

Conclusions

There is an unanticipated high burden of SCD in adults with rCoA, occurring in men at younger age than women, suspicious for primary electrophysiologic dysfunction. Future investigation of sex-specific SCD risk in rCoA is important to better understand this disease and its late phenotype.

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来源期刊
International journal of cardiology. Congenital heart disease
International journal of cardiology. Congenital heart disease Cardiology and Cardiovascular Medicine
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