Department of Medicine, Cardiovascular Division, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts.
Department of Medicine, Cardiovascular Division, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts; Radiology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts.
JACC Cardiovasc Imaging. 2020 Sep;13(9):1917-1930. doi: 10.1016/j.jcmg.2020.03.014. Epub 2020 Jul 9.
This study sought to determine whether myocardial tissue heterogeneity scanned by native T mapping could improve risk stratification in patients with nonischemic dilated cardiomyopathy (NICM) evaluated for primary prevention by ICD.
The benefit of insertable cardiac-defibrillator (ICD) as primary prevention ICD in patients with NICM remains to be fully clarified.
A total of 115 NICM candidates for primary prevention and 55 healthy controls with similar distributions of age and sex were prospectively enrolled. Imaging was performed at 1.5-T using a protocol that included cine magnetic resonance for left ventricular function, late gadolinium enhancement (LGE) for focal scarring, and 5-slice native T mapping for diffuse fibrosis and heterogeneity. The last method was assessed by mean absolute deviation of the segmental pixel-SD from the average pixel-SD (Mad-SD). The primary endpoint was a composite of appropriate ICD therapy and sudden cardiac death.
During a median follow-up of 24 months, 13 patients (11%) experienced the primary endpoint. Dichotomized Mad-SD >0.24 provided a comparable outcome to the presence of LGE for the primary endpoint (annual event rate: 9.8% vs. 10.9%). The integration of Mad-SD to global native T showed excellent arrhythmic event-free survival (annual event rate: 0%), and high sensitivity of 85% (95% confidence interval [CI]: 55% to 98%) and moderate specificity of 72% (95% CI: 62% to 80%), with a C-statistic of 0.76 (95% CI: 0.64 to 0.87), which was comparable to the presence, location, or extent of LGE in its ability to predict arrhythmic events.
Combined myocardium tissue heterogeneity and interstitial fibrosis assessment by native T mapping is an important predictor of ventricular tachycardia and ventricular fibrillation and provides additive risk stratification for primary prevention ICD in NICM patients without the need for gadolinium contrast.
本研究旨在确定通过原生 T 映射扫描心肌组织异质性是否可以提高非缺血性扩张型心肌病(NICM)患者的风险分层,这些患者正在接受 ICD 进行一级预防评估。
可植入心脏除颤器(ICD)作为 NICM 患者一级预防 ICD 的益处仍有待充分阐明。
共前瞻性纳入 115 名 NICM 一级预防候选者和 55 名年龄和性别分布相似的健康对照者。使用包括左心室功能电影磁共振成像、局灶性瘢痕的晚期钆增强(LGE)和 5 层原生 T 映射弥漫性纤维化和异质性的方案在 1.5-T 进行成像。最后一种方法通过节段像素-SD 与平均像素-SD 的绝对偏差(Mad-SD)进行评估。主要终点是适当的 ICD 治疗和心脏性猝死的复合终点。
在中位随访 24 个月期间,13 名患者(11%)经历了主要终点。Mad-SD >0.24 的二分法与 LGE 对主要终点的存在提供了相当的结果(年事件率:9.8% vs. 10.9%)。将 Mad-SD 整合到整体原生 T 中显示出极好的心律失常无事件生存(年事件率:0%),并且具有 85%的高灵敏度(95%置信区间[CI]:55%至 98%)和 72%的中度特异性(95%CI:62%至 80%),C 统计量为 0.76(95%CI:0.64 至 0.87),与 LGE 的存在、位置或程度相比,预测心律失常事件的能力相当。
通过原生 T 映射评估心肌组织异质性和间质纤维化的组合是室性心动过速和室颤的重要预测指标,并为 NICM 患者的 ICD 一级预防提供了附加的风险分层,而无需使用钆对比剂。