Electrophysiology Section, Cardiovascular Division, Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
J Am Coll Cardiol. 2012 Nov 20;60(21):2194-204. doi: 10.1016/j.jacc.2012.08.977. Epub 2012 Oct 24.
This study sought to assess the value of left ventricular (LV) endocardial unipolar electroanatomical mapping (EAM) in identifying irreversibility of LV systolic dysfunction in patients with left ventricular nonischemic cardiomyopathy (LVCM).
Identifying irreversibility of LVCM would be helpful but cannot be reliably accomplished by bipolar EAM or cardiac magnetic resonance identification of macroscopic scar.
Detailed endocardial LV EAM was performed in 3 groups: 1) 24 patients with irreversible LVCM (I-LVCM) but with no or minimal macroscopic scar (<15% LV surface) evidenced on bipolar voltage EAM and/or cardiac magnetic resonance; 2) 14 patients with reversible ventricular premature depolarization-mediated LVCM (R-LVCM); and 3) 17 patients with structurally normal hearts. LV endocardial unipolar electrogram amplitude and area of unipolar amplitude abnormality were defined after excluding macroscopic scar.
Unipolar amplitude differed in the 3 groups: median of 7.6 (interquartile range [IQR]: 5.5 to 9.7) mV in I-LVCM group, 13.2 (IQR: 10.4 to 16.2) mV in R-LVCM group, and 16.3 (IQR: 13.6 to 19.8) mV in structurally normal hearts group (p < 0.001). Areas of unipolar abnormality represented a large proportion of total LV surface in I-LVCM, 64.7% (IQR: 47.5% to 75.9%) compared with R-LVCM, 5.2% (IQR: 0.0% to 19.1%) and structurally normal hearts, 0.1% (IQR: 0.0% to 0.9%), groups (p < 0.001). A unipolar abnormality area cutoff of 32% of total LV surface was 96% sensitive and 100% specific in identifying irreversible cardiomyopathy among patients with LV dysfunction (I-LVCM and R-LVCM), p < 0.001.
Detailed unipolar voltage mapping can identify irreversible myocardial dysfunction consistent with fibrosis, even in the absence of bipolar EAM or cardiac magnetic resonance abnormalities, and may serve as valuable prognostic tool in patients presenting with LVCM to facilitate clinical decision making.
本研究旨在评估左心室(LV)心内膜单极电解剖图(EAM)在识别左心室非缺血性心肌病(LVCM)患者左心室收缩功能不可逆性中的价值。
确定 LVCM 的不可逆性是有帮助的,但不能通过双极 EAM 或心脏磁共振确定宏观瘢痕来可靠地完成。
对 3 组患者进行详细的心内膜 LV EAM:1)24 例不可逆 LVCM(I-LVCM)患者,但双极电压 EAM 和/或心脏磁共振未见或仅有微量宏观瘢痕(<15%LV 表面);2)14 例由室性早搏介导的可逆性 LVCM(R-LVCM)患者;3)17 例结构正常的心脏患者。排除宏观瘢痕后,定义 LV 心内膜单极电图幅度和单极幅度异常面积。
3 组间单极幅度不同:I-LVCM 组中位数为 7.6(四分位距 [IQR]:5.5 至 9.7)mV,R-LVCM 组为 13.2(IQR:10.4 至 16.2)mV,结构正常心脏组为 16.3(IQR:13.6 至 19.8)mV(p<0.001)。I-LVCM 中单极异常面积占 LV 总表面积的很大比例,为 64.7%(IQR:47.5%至 75.9%),而 R-LVCM 为 5.2%(IQR:0.0%至 19.1%)和结构正常心脏组为 0.1%(IQR:0.0%至 0.9%)(p<0.001)。单极异常面积截断值为总 LV 表面的 32%,在 LV 功能障碍患者(I-LVCM 和 R-LVCM)中识别不可逆性心肌病的敏感性为 96%,特异性为 100%,p<0.001。
详细的单极电压图可以识别与纤维化一致的不可逆性心肌功能障碍,即使在没有双极 EAM 或心脏磁共振异常的情况下,也可以作为 LVCM 患者的有价值的预后工具,有助于临床决策。