单纯碎裂电位指导心房颤动消融的初步临床观察

Objective To evaluate the feasibility of mdiofrequency catheter ablation of atrial fibrilla-tion (AF) guided by complex fractionated atrial electrograms (CFAEs). Methods Twenty-two patients with drug refractory and symptomatic AF(16 paroxysmal, 6 persisten) were enrolled. Using Carto, the left atrial or biatrial replica was created during spontaneous or induced AF, and areas associated with CFAEs were identi-fied. Radiofrequency ablation at the site with CFAEs was performed and the end points were to eliminate CFAEs or convert to sinus rhythm. Results Thirteen patients(59%)were converted to sinus rhythm, (7 cases conver-ted directly to sinus rhythm, and 6 via the intermediate atrial tachycardia(AT) or atrial flutter (AFL). The re-maining nine patients required cardioversion with D. C. shock or drug. Repeat ablation was performed in 6 pa-tients (5 AT/AFL, 1 paroxysmal AF). During(10.9 ±4.8) months follow-up, 16 patients (73%) were free of arrhythmia and symptoms. CFAEs were most commonly found along the left interatrial septum, pulmonary veins, left atrial roof. CFAEs ablation prolonged AFCL[(157 ± 18) ms vs (211 ± 32) ms, P < 0.05]. Only one patient had pericardial tamponade that required pericardiocentesis. Conclusion Radiofrequeney catheter abla-tion of atrial fibrillation (AF) guided by CFAEs is safe and effective.     

心房颤动与炎症及慢性幽门螺旋杆菌感染相关性研究

目的探讨心房颤动(简称房颤)与炎症及慢性幽门螺旋杆菌(Hp)感染的关系。方法选取66例房颤患者为房颤组(其中阵发性房颤44例,慢性房颤22例),另取同期住院的阵发性室上性心动过速(简称室上速)患者67例作为对照组,用间接ELISA法测定血清Hp-IgG抗体,速率散射免疫比浊法测定C反应蛋白(CRP),比较两组Hp-IgG抗体,CRP的差异并分析HP抗体滴度与房颤及其它相关因素的关系。结果房颤组与对照组的Hp-IgG阳性率Hp-IgG对数值均无差异(P均>0.05)。房颤组CRP中位数较对照组高(1.17mg/dlvs0.65mg/dl,P<0.05)。结论房颤与慢性Hp感染不相关,与炎症相关。     

特发性右室流出道室速的昼夜发作规律及临床意义

目的：探讨特发性右室流出道室速的昼夜发作规律及临床意义,方法：对12例特发性右室流出道室速患者在基础状态进行动态心电图（Holter)监测,分别记录24h中每小时内心律失常发作频数及平均心率,了解室速,室早发作的昼夜规律,结果：基础状态下,室速,连发室早,平均心率在24h内呈不均一分布（P＜0．001）,其发作规律呈白天多,夜间少,单个室呈不均一分布,但整个差异无显著性,平均心率与室速,连发室早互正相关,单个室早与平均心率无相关性,结论：左室流出道室速患者24h内室速,连发病早呈明显的昼夜节律变化,提示特发性右室流出道室速的发生与交感迷走神经平衡失调有关。     

Clinical and familial study of arrhythmogenic right ventricular cardiomyopathy

Objective　To explore the characteristics of arrhythmogenic right ventricular cardiomyopathy (ARVC). Methods　Seven patients with arrhythmogenic right ventricular cardiomyopathy and 34 members of three families were studied. All patients and family members underwent history collection, clinical examination, electrocardiogram (ECG), two-dimensional echocardiography (2-DE) and a signal averaging electrocardiogram. Programmed ventricular stimulation was performed in five patients. Results　All patients and family members had normal morphologic characteristics and normal function of the left ventricular by 2-DE. Fourteen persons had abnormal findings indicating ARVC. Five had enlargement of the right ventricular with diffused hypocontractility, eight had thin and systolic bulging in the focal anterior wall with hypokinesia and one had bulging of the inferior wall. Twenty-five persons (seven patients and 18 family members) had abnormal findings in ECG. Positive ventricular late potential was recorded in 13 persons (six patients). Two to three monomorphic ventricular tachycardia (VT) with left bundle branch block (LBBB) configurations were induced in five patients. Ventricular fibrillation was induced in two patients during the electrophysiologic study (EPS). Five patients had very high pacing threshold and/or ineffective pacing in one or many regions of the right ventricle. Two members of one family died suddenly. One member was a dwarf with ARVC. Spontaneous VT with a left bundle branch block (LBBB) configuration was recorded in five patients, polymorphic VT with extremely short coupling interval in one, and premature ventricular complexes with LBBB configuration in 12 (six patients). Conclusion　Our familial study strongly suggests that ARVC may be a hereditary disease and it is helpful in the diagnosis and detection of ARVC. The most common manifestations were abnormal structure and function of the right ventricle and abnormal ECG of repolarization and ventricular arrhythmia which originates from the right ventricle.     

心律转复除颤器植入术后电风暴的发生及其对预后的影响

目的调查单中心心律转复除颤器（ICD）植入术后电风暴（ES）的发生率、发作特征和危险因素，并探讨其对患者预后的影响。方法对本中心123例植入ICD的患者进行随访。Es定义为24h内出现3次或3次以上的快速室性心律失常（VA）导致ICD治疗，或ICD监测到持续30s以上的VA但未发放治疗。结果在（26．9±21．3）个月的随访期间，共有41（33．3％）例患者（ES组）发作139次ES（3．4±3．9）次／例，其中29（70．7％）例患者的首次发作在植入后1年内出现，Es发作呈现出6：00—10：00和14：00～17：00两个高峰。多因素Logistic回归分析表明植入ICD作为心脏性猝死二级预防是ES发生的独立危险因素（OR=4．797，P=0．044）。本组共15（12．2％）例患者死亡，Es组死亡率较无Es组（24．4％对6．1％，P=0．003）显著增高，Kaplan—Meier生存曲线分析显示Es组累计生存概率明显低于无Es组（Log—rank检验P〈0．001）。结论Es发作表现为上午和下午两个高峰，可导致死亡率增高，其首次发作多在ICD植入后1年内。植入ICD作为心脏性猝死二级预防是Es发生的独立危险因素。     

血管迷走性晕厥单中心294例结果分析

目的:对单中心33个月所做的直立倾斜试验(HUTT)结果进行分析并探讨健康教育对HUTT阳性患者再发晕厥次数的影响。方法:收集从2015年2月至2017年11月因反复晕厥或反复出现晕厥前兆在南京医科大学第一附属医院就诊并进行HUTT患者294例。根据HUTT中患者心率与血压的变化,196例HUTT呈阳性,其中混合型血管迷走神经性晕厥(Ⅰ型)146例,心脏抑制型血管迷走神经性晕厥(Ⅱ型)14例,血管抑制型迷走神经性晕厥(Ⅲ型)36例。分析各型患者HUTT阳性率并对健康教育前后HUTT阳性结果患者晕厥发生次数的差异进行比较。结果:在294例行HUTT检测的患者中,有196(66.7%)例患者出现血管迷走性晕厥,其中I型、Ⅱ型、Ⅲ型血管迷走性晕厥分别有146例(74.5%)、14例(7.1%)、36例(18.4%)。年龄>60岁患者HUTT阳性率明显高于年龄<40岁患者(77.1%vs.57.1%,P<0.01)。在196例HUTT阳性患者中,80例(40.8%)患者接受随访,随访患者接受健康教育前后,患者晕厥次数中位数从2(四分位数间距IQR:1~4)次降到0(IQR:0~0)次(P<0.001),差异有统计学意义。结论:HUTT证实,血管迷走性晕厥患者中以混合型血管迷走神经性晕厥为主,年龄较大患者HUTT阳性率较高,随访结果提示健康教育可以减少此类患者再发晕厥风险。     

沉默型动脉导管未闭的血流动力学特征及治疗探讨

目的　探讨沉默型动脉导管未闭 (patentductusarteriosus ,PDA)的血流动力学特征及治疗。方法　对临床结合超声心动图诊断的 7例沉默型PDA病人进行心导管检查 ,术后 3个月、6个月及每年随访一次。结果　 7例病人肺动脉平均压平均为 (16 0± 2 4 )mmHg ,肺循环和体循环血流量比 (Qp/Qs)为 1 0 8± 0 0 2 ,左向右分流量平均为 (0 32± 0 0 8)L/min ,左向右分流量占肺循环血流量比例平均为 0 0 98± 0 0 2 4。PDA最窄处平均直径为 (0 9± 0 2 )mm。 7例病人均未行外科手术和介入治疗。平均随访 9 5个月 (临床、心电图、超声心动图 ) ,未发现房室腔增大、肺动脉压增高 ,无感染性动脉内膜炎和心内膜炎发生。结论　沉默型PDA的左向右分流量很少 ,对病人的血流动力学影响小。沉默型PDA病人是否需要治疗尚无定论。     

致心律失常性右室心肌病患者Epsilon波的检出率

Objective To investigate the prevalence of Epsilon wave in patients with arrhythmogenic right ventrieular cardiomyopathy (ARVC). Methods The Epsilon wave was detected in 32 patients [24 men, mean age (42.3±13.3) years] with ARVC using three different electrocardiography (ECG) recording methods: standard twelve leads ECG (S-ECG), right precordial leads ECG (R-ECG) and Fontaine bipolar precordiai leads ECG (F-ECG). The Epsilon wave was defined as wiggle, small spike wave and smooth potential between the end of the QRS complex and the beginning of the ST segment. Results Epsilon wave was detected in 37.5%, 37.5% and 50.0% patients with ARVC by S-ECG, R-ECG and F-ECG respectively. The detection rates derived from the three recording methods were similar(P ＞ 0.05). The Epsilon wave was only detectable by S-ECG in one case, by R-ECG in three cases, and by F-ECG in five cases. The detection rate of Epsilon wave was 50.0% by combined use of S-ECG and R-ECG (SR-ECG), 56.3% by combined use of S-ECG and F-ECG (SF-ECG), and 65.6% by combined use of the three recording methods (SRF-ECG). The detection rate was significantly higher by SF-ECG (56.3%) and SRF-ECG (65.6%) than by S-ECG alone (37.5%, all P ＜0.05). Most Epsilon waves detected by the S-ECG, R-ECG and F-ECG were small spiked waves. Conclusion Combined use of S-ECG, F-ECG and R-ECG could increase the detection rate of Epsilon wave in patients with ARVC.     

磁导航系统遥控导管消融治疗右心室流出道室性心动过速/室性早搏

目的：探讨应用磁导航遥控导管消融治疗右心室流出道起源的室性心动过速/室性早搏（ RVOT-VT/PVCs）的安全性和有效性。方法2008年11月至2009年11月,在南京医科大学第一附属医院心血管内科行体表心电图检查,诊断为RVOT-VT/PVCs的患者共16例[女12例,男4例,平均年龄（44±15）岁],结合应用非接触标测系统和起搏标测确定靶点,磁导航遥控磁导管实施消融术,消融失败者改为手控导管消融。结果10例（63%）患者使用磁导航消融成功,6例需手控导管消融,1例术后出现动静脉瘘。平均放电（3．9±1．6）次,放电时间（240±33） s,总手术时间为（190±42） min,总X线曝光时间为（4．8±2．6） min,术者X线曝光时间平均为（3．2±2．0） min,磁导航系统遥控导管X线曝光时间为（1．6±1．0） min。结论应用磁导航系统结合非接触标测系统可安全、有效地实施遥控导管消融治疗RVOT-VT/PVCs,并可减少术者和患者的X线曝光时间。     

桥粒芯胶蛋白-2基因沉默对P19细胞向心肌细胞诱导分化的影响

目的 探讨在P19细胞诱导分化成心肌细胞过程中,桥粒芯胶蛋白-2（DSC2）基因沉默对其的影响。方法 设计并合成针对DSC2基因编码区的干扰序列,构建真核细胞表达质粒并转染P19细胞。荧光定量聚合酶链式反应（RT-PCR）和蛋白免疫印迹（Western blot）技术检测DSC2在mRNA和蛋白水平表达变化,筛选出沉默效率最佳的细胞株。二甲基亚矾诱导分化为心肌细胞,观察其超微结构和细胞凋亡等改变,以及对纤维化与脂肪化相关基因mRNA水平表达的影响。结果 成功构建了5种ShDSC2重组质粒,转染P19细胞并获得稳定转染细胞株,筛选出对DSC2基因mRNA水平（69. 47% vs 0,P〈0. 01）和蛋白水平表达（65. 62% vs 0,P〈0. 01）的抑制效率最显著的ShDSC2鄄613组,并成功诱导分化为心肌样细胞后,电镜扫描显示后者细胞出现脂滴、空泡样变性、线粒体肿胀及嵴消失,流式细胞仪检测提示细胞凋亡显著增加,RT鄄PCR示纤维化相关基因（Collal、Colla2、Col3a1）与脂肪化相关基因（Adiponectin、PPAR-γ、C/EBP-α）的mRNA表达均显著升高。结论 建立能有效抑制DSC2表达的P19细胞株并分化为心肌样细胞,表现出与致心律失常型右室心肌病（ARVC）患者病理和分子生物学特点相似的表型特征,提示其可作为深入研究ARVC致病机制的前体细胞。