Whitaker John, Neji Radhouene, Kim Steven, Connolly Adam, Aubriot Thierry, Calvo Justo Juliá, Karim Rashed, Roney Caroline H, Murfin Brendan, Richardson Carla, Morgan Stephen, Ismail Tevfik F, Harrison James, de Vos Judith, Aalders Maurice C G, Williams Steven E, Mukherjee Rahul, O'Neill Louisa, Chubb Henry, Tschabrunn Cory, Anter Elad, Camporota Luigi, Niederer Steven, Roujol Sébastien, Bishop Martin J, Wright Matthew, Silberbauer John, Razavi Reza, O'Neill Mark
School of Biomedical Engineering and Imaging Sciences, King's College, London, United Kingdom.
Siemens Healthcare, Frimley, United Kingdom.
Front Cardiovasc Med. 2021 Oct 26;8:744779. doi: 10.3389/fcvm.2021.744779. eCollection 2021.
The majority of data regarding tissue substrate for post myocardial infarction (MI) VT has been collected during hemodynamically tolerated VT, which may be distinct from the substrate responsible for VT with hemodynamic compromise (VT-HC). This study aimed to characterize tissue at diastolic locations of VT-HC in a porcine model. Late Gadolinium Enhancement (LGE) cardiovascular magnetic resonance (CMR) imaging was performed in eight pigs with healed antero-septal infarcts. Seven pigs underwent electrophysiology study with venous arterial-extra corporeal membrane oxygenation (VA-ECMO) support. Tissue thickness, scar and heterogeneous tissue (HT) transmurality were calculated at the location of the diastolic electrograms of mapped VT-HC. Diastolic locations had median scar transmurality of 33.1% and a median HT transmurality 7.6%. Diastolic activation was found within areas of non-transmural scar in 80.1% of cases. Tissue activated during the diastolic component of VT circuits was thinner than healthy tissue (median thickness: 5.5 mm vs. 8.2 mm healthy tissue, < 0.0001) and closer to HT (median distance diastolic tissue: 2.8 mm vs. 11.4 mm healthy tissue, < 0.0001). Non-scarred regions with diastolic activation were closer to steep gradients in thickness than non-scarred locations with normal EGMs (diastolic locations distance = 1.19 mm vs. 9.67 mm for non-diastolic locations, < 0.0001). Sites activated late in diastole were closest to steep gradients in tissue thickness. Non-transmural scar, mildly decreased tissue thickness, and steep gradients in tissue thickness represent the structural characteristics of the diastolic component of reentrant circuits in VT-HC in this porcine model and could form the basis for imaging criteria to define ablation targets in future trials.
大多数关于心肌梗死后(MI)室性心动过速(VT)组织基质的数据是在血流动力学耐受的室性心动过速期间收集的,这可能与导致血流动力学受损的室性心动过速(VT-HC)的基质不同。本研究旨在在猪模型中对VT-HC舒张期位置的组织进行特征描述。对八只患有愈合的前间隔梗死的猪进行了延迟钆增强(LGE)心血管磁共振(CMR)成像。七只猪在静脉-动脉体外膜肺氧合(VA-ECMO)支持下接受了电生理研究。在映射的VT-HC舒张期电图位置计算组织厚度、瘢痕和异质组织(HT)透壁性。舒张期位置的瘢痕透壁性中位数为33.1%,HT透壁性中位数为7.6%。在80.1%的病例中,舒张期激活出现在非透壁瘢痕区域。在VT环路舒张期成分期间激活的组织比健康组织薄(中位数厚度:5.5毫米对8.2毫米健康组织,<0.0001),并且更接近HT(舒张期组织的中位数距离:2.8毫米对11.4毫米健康组织,<0.0001)。与具有正常心电图的非瘢痕位置相比,具有舒张期激活的非瘢痕区域更接近厚度的陡峭梯度(舒张期位置距离=1.19毫米对非舒张期位置的9.67毫米,<0.0001)。在舒张期末期激活的部位最接近组织厚度的陡峭梯度。非透壁瘢痕、组织厚度轻度降低以及组织厚度的陡峭梯度代表了该猪模型中VT-HC折返环路舒张期成分的结构特征,并可为未来试验中定义消融靶点的成像标准奠定基础。