Cardiology, Christchurch Hospital, Christchurch, New Zealand.
Biostatistics, Christchurch Hospital, Christchurch, New Zealand.
BMJ Open. 2019 May 5;9(5):e025253. doi: 10.1136/bmjopen-2018-025253.
In takotsubo syndrome, QTc prolongation is a measure of risk of potentially fatal arrhythmia. It is not known how this risk, or derangement of other markers, differs across the echo variants of takotsubo syndrome. Therefore, we sought to explore whether apical takotsubo syndrome differs from the variants of the syndrome in more ways than just regional wall motion pattern. As the region of affected myocardium is usually larger, we hypothesised that patients with the classic apical ballooning form of takotsubo syndrome would have more severe derangement of their markers.
Observational study of patients gathered from a prospective database (2010-2018) and by retrospective review (2006-2009).
The sole tertiary hospital from a New Zealand region in which case clusters of takotsubo syndrome were precipitated by large earthquakes in 2010, 2011 and 2016.
A total of 222 patients who met a modified version of the Mayo criteria for takotsubo syndrome were included. All patients had digitally archived echocardiograms that were over-read by a second echocardiologist blinded to the clinical report.
Ejection fraction, peak troponin and QTc interval.
Patients with the apical form were older (p=0.011), had a lower initial left ventricular ejection fraction (35% vs 44%, p<0.0001) and a higher peak high-sensitivity troponin I (hsTnI) (p=0.01) than those with variant forms. There was no difference in the electrical abnormalities between the variants (QTc interval, heart rate, PR interval, QRS duration or T-wave axis). There was also no correlation between any of peak hsTnI, peak QTc and ejection fraction. QTc interval increased on day 2 and peaked on day 3 before falling steeply (p<0.0001).
The variants of takotsubo syndrome differ in more ways than just their echo pattern but do not differ in their electrical abnormalities. There is a dissociation between the structural and electrical abnormalities. QTc peaks on day 3 and then falls steeply.
在应激性心肌病中,QTc 延长是潜在致命性心律失常风险的指标。目前尚不清楚这种风险,或其他标志物的紊乱,在应激性心肌病的不同心尖球囊样变中如何不同。因此,我们试图探索心尖型应激性心肌病是否与该综合征的其他变体在多个方面存在差异,而不仅仅是区域性壁运动模式。由于受影响的心肌区域通常更大,我们假设经典的心尖球囊样变应激性心肌病患者的标志物紊乱会更严重。
对前瞻性数据库(2010-2018 年)和回顾性研究(2006-2009 年)中收集的患者进行观察性研究。
这是新西兰一个地区的唯一一家三级医院,该地区的应激性心肌病病例群是由 2010 年、2011 年和 2016 年的大地震引发的。
共纳入 222 名符合改良梅奥应激性心肌病标准的患者。所有患者均有数字化存档的超声心动图,由第二位对临床报告不知情的超声心动图专家进行二次阅片。
射血分数、峰值肌钙蛋白和 QTc 间期。
心尖型患者年龄较大(p=0.011),左心室射血分数初始值较低(35% vs 44%,p<0.0001),峰值高敏肌钙蛋白 I(hsTnI)较高(p=0.01)。在变体之间,电异常没有差异(QTc 间期、心率、PR 间期、QRS 持续时间或 T 波轴)。峰值 hsTnI、峰值 QTc 和射血分数之间也没有相关性。QTc 间期在第 2 天增加,第 3 天达到峰值,然后急剧下降(p<0.0001)。
应激性心肌病的变体在多个方面存在差异,而不仅仅是其超声心动图模式,但电异常没有差异。结构和电异常之间存在分离。QTc 在第 3 天达到峰值,然后急剧下降。