Calvo David, Rubín José M, Pérez Diego, Gómez Juan, Flórez Juan Pablo, Avanzas Pablo, García-Ruíz José Manuel, de la Hera Jesús María, Reguero Julián, Coto Eliecer, Morís César
Arrhythmia Unit, Cardiology Department.
Arrhythmia Unit, Cardiology Department.
Heart Rhythm. 2015 Feb;12(2):350-7. doi: 10.1016/j.hrthm.2014.10.036. Epub 2014 Oct 31.
Time-dependent variability of electrocardiogram (ECG) in patients with Brugada syndrome could affect the interpretation of provocative testing.
The aim of this study was to characterize ECG changes during and after flecainide infusion.
We studied 59 consecutive patients. The ECG was continuously analyzed during the first 30 minutes of provocative testing, and a single ECG was recorded 60 minutes later. We analyzed CYP2D6 and CYP3A5 variants affecting flecainide metabolism and performed blinded measurements at lead II.
At baseline, ECG patterns were classified as follows: type II in 31 patients (53%), type III in 15 (25%), and normal ECG in 13 (22%). Because of induction of type I ECG, the percentage of responders progressively increased with longer recording time periods (6.8% in 10 minutes vs 11.9% in 20-30 minutes vs 18.6% in 90 minutes; P < .01). Four patients displayed a late response, which was evidenced 90 minutes after the initiation of provocative testing. QRS width differentially increased between responders and nonresponders (P < .01), with a maximum QRS width of 110 ms during the first 30 minutes being effective for identifying possible late responders (sensitivity 100%; specificity 85.6%; positive predictive value 88%; negative predictive value 100%). The incidence of CYP2D6 variants was lower in late responders than in early or delayed responders (0% vs 75% vs 100%; P = .04), while a homogeneous distribution of CYP3A5*3/*3 was observed in our population.
Response to flecainide exhibits time-dependent variability of ECG patterns and intervals. Longer periods of ECG recording increase the recognition probability of type I ECG.
Brugada综合征患者心电图(ECG)的时间依赖性变异性可能会影响激发试验的解读。
本研究旨在描述氟卡尼输注期间及之后的心电图变化。
我们连续研究了59例患者。在激发试验的前30分钟连续分析心电图,并在60分钟后记录一份心电图。我们分析了影响氟卡尼代谢的CYP2D6和CYP3A5变体,并在II导联进行了盲法测量。
基线时,心电图模式分类如下:31例患者(53%)为II型,15例(25%)为III型,13例(22%)为正常心电图。由于I型心电图的诱导,随着记录时间延长,反应者的百分比逐渐增加(10分钟时为6.8%,20 - 30分钟时为11.9%,90分钟时为18.6%;P < 0.01)。4例患者出现延迟反应,在激发试验开始90分钟后得到证实。反应者和非反应者之间QRS波宽度差异增加(P < 0.01),在前30分钟内最大QRS波宽度为110 ms可有效识别可能的延迟反应者(敏感性100%;特异性85.6%;阳性预测值88%;阴性预测值100%)。延迟反应者中CYP2D6变体的发生率低于早期或延迟反应者(0% vs 75% vs 100%;P = 0.04),而在我们的研究人群中观察到CYP3A5*3/*3的均匀分布。
对氟卡尼的反应表现出心电图模式和间期的时间依赖性变异性。更长时间的心电图记录增加了I型心电图的识别概率。