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First experience of treating patients with atrial fibrillation using thoracoscopic isolation with left atrial appendage excision in the North-Western State Medical University named after I.I. Mechnikov 以 I.I. Mechnikov 命名的西北国立医科大学利用胸腔镜隔离术和左心房阑尾切除术治疗心房颤动患者的首次经验
Pub Date : 2024-06-12 DOI: 10.17816/cardar625555
D. A. Yakovlev, Andrey I. Lenkin, Vera V. Stepanova, V. A. Marinin, Nikolai V. Petrov, Vladislav K. Verendeev
The given article describes the first experience of a thoracoscopic isolation of pulmonary veins and left atrial appendage excision in the North-Western State Medical University named after I.I. Mechnikov. The clinical case features a woman with a long history of paroxysmal atrial fibrillation, severe left atrium dilation, failure in a pace control drug therapy and no effect of radiofrequency catheter isolation of pulmonary veins. Additionally, there outlined the advantages and the significance of employing the method of thoracoscopic ablation in patients with symptomatic paroxysmal and long-term persistent atrial fibrillation, — in case if antiarrythmic drugs and radiofrequency catheter ablation proved ineffective, as well as in patients with a long-term persistent atrial fibrillation along with a severe left atrium dilation.
本文介绍了以 I.I. Mechnikov 命名的西北国立医科大学首次开展胸腔镜肺静脉隔离术和左心房阑尾切除术的经验。该临床病例的特点是,一名女性长期患有阵发性心房颤动,左心房严重扩张,步伐控制药物治疗失败,而肺静脉射频导管隔离术效果不佳。此外,该报告还概述了对有症状的阵发性和长期持续性心房颤动患者采用胸腔镜消融方法的优势和意义--在抗心律失常药物和射频导管消融无效的情况下,以及对长期持续性心房颤动并伴有严重左心房扩张的患者。
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引用次数: 0
Multifaces of hypertrophic cardiomyopathy: a case of transformation of hypertrophic phenotype into dilated 多面肥厚型心肌病:一例由肥厚表型转变为扩张型的病例
Pub Date : 2024-06-12 DOI: 10.17816/cardar630134
T. N. Novikova, Alina E. Andreeva, F. I. Bitakova, Vladimir I. Novikov, Kristina A. Gladysheva, Polina V. Petrova, Polina A. Stalnova, Nadezhda A. Tokareva
The article presents a clinical case of a rather rare course of hypertrophic cardiomyopathy with the transformation of a hypertrophic phenotype into a dilated phenotype against the background of the “burned-out phase” phenomenon, ventricular and supraventricular rhythm disturbances, and multiple genetic mutations. Timely started disease-modifying therapy (quadruple therapy) for chronic heart failure led to reverse positive remodeling of the left chambers of the heart.
文章介绍了一例相当罕见的肥厚型心肌病临床病例,该病例在 "衰竭期 "现象、心室和室上性节律紊乱以及多种基因突变的背景下,由肥厚表型转变为扩张表型。及时开始的慢性心力衰竭疾病修饰疗法(四联疗法)导致心脏左腔逆向正重塑。
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引用次数: 0
Obstructive sleep apnea as a potentially reversible cause of nighttime bradyarrhythmias. Clinical case 阻塞性睡眠呼吸暂停是导致夜间缓性心律失常的潜在可逆原因。临床病例
Pub Date : 2024-06-12 DOI: 10.17816/cardar626655
Natalia G. Kucherenko, A. Bebekh, Irina A. Umarova, Aigul R. Abukova
Obstructive sleep apnea syndrome is a common condition, especially among obese patients. Patients with obstructive sleep apnea syndrome have an increased risk of developing arterial hypertension and cardiovascular events, as well as cardiac arrhythmias, which include reflexively occurring bradyarrhythmias and episodes of asystole at night. Treatment of obstructive sleep apnea syndrome leads to an improvement in the patient’s quality of life and also reduces cardiovascular risk and eliminates associated bradyarrhythmias during night sleep.
阻塞性睡眠呼吸暂停综合征是一种常见病,尤其是在肥胖患者中。患有阻塞性睡眠呼吸暂停综合征的患者罹患动脉高血压和心血管事件以及心律失常(包括反射性缓性心律失常和夜间阵发性心跳骤停)的风险会增加。治疗阻塞性睡眠呼吸暂停综合症可改善患者的生活质量,降低心血管风险,消除夜间睡眠中相关的缓慢性心律失常。
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引用次数: 0
Opportunities of metabolic treatment in paroxysmal atrial fibrillation patients with obesity, arterial hypertension and/or ischemic heart disease 伴有肥胖、动脉高血压和/或缺血性心脏病的阵发性心房颤动患者接受代谢治疗的机会
Pub Date : 2024-06-12 DOI: 10.17816/cardar629168
Tatiana I. Balabanovich, Valentina S. Golyshko, Irina A. Sinkevich, Elen S. Shkuta, Elizaveta A. Veniadziktova, Pavel V. Baliuk, Alexei V. Knysh
This article provides the experience of examination and treatment of paroxysmal atrial fibrillation patients with concomitant obesity, arterial hypertension and/or ischemic heart disease, who were prescribed levocarnitine in addition to traditional therapy. The addition of levocarnitine in management of atrial fibrillation was found to be capable of reducing the atrial fibrillation burden after cardioversion and improve the functional state of the patients.
本文介绍了对伴有肥胖、动脉高血压和/或缺血性心脏病的阵发性心房颤动患者进行检查和治疗的经验。研究发现,在心房颤动治疗中添加左卡尼汀能够减轻心脏复律后的心房颤动负担,并改善患者的功能状态。
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引用次数: 0
Clinical and genetic characterization of patients with catecholaminergic polymorphic ventricular tachycardia: a case series 儿茶酚胺能多态性室性心动过速患者的临床和遗传特征:一个病例系列
Pub Date : 2024-01-16 DOI: 10.17816/cardar568180
S. Komissarova, N. Rineiska, N. Chakova, S. Niyazova, L. Plashchinskaya, Veronika Ch. Barsukevich, Olga V. Podpalova
AIM: of the study was to evaluate the clinical and genetic characteristics, including the development of adverse events and outcomes in patients with catecholaminergic polymorphic ventricular tachycardia (CPVT). MATERIALS AND METHODS: The clinical phenotype of eight patients with CPVT, two of whom were relatives of probands, was observed over 4 years. The clinical and instrumental study included ECG-12, 24-hour Holter ECG monitoring, genealogical history collection and family history of sudden cardiac death (SCD), transthoracic echocardiography and cardiac magnetic resonance imaging to detect structural myocardial changes, electrophysiologic study according to indications, and ICD monitoring. High-throughput sequencing (NGS) was utilized to search for mutations in genes linked to the onset of channelopathies and other inherited rhythm disorders. RESULTS: In 8 patients, nucleotide variants of pathogenicity classes III-V were identified according to the ACMG (2015) criteria in the RYR2 gene associated with CPVT. Pathogenic (IV-V class) and likely pathogenic (IV class) mutations in the RYR2 gene were found in 6 (75%) probands, variants with uncertain clinical significance (VUS, class III) were found in 2 patients. At the time of diagnosis, transient QTc interval prolongation of more than 480 ms was detected in 4 (50%) patients; bradycardia less than 54 beats/min — in 2 (25%) patients, sequences of supraventricular tachycardia and ventricular tachyarrhythmia — in 2 (25%) patients. The most severe form of the disease with marked clinical manifestations and an episode of clinical death with subsequent resuscitation, as well as a transient QTc interval prolongation exceeding 500 ms was observed in patients with mutations c.11814C A (p.Ser3938Arg, rs794728704); c.463G A (p.Gly155Arg) and c.14876G A (p.Arg4959Gln, rs794728811) in the RYR2 gene. Three (37.5%) patients underwent ICD implantation; one for primary SCD prevention and two for secondary prevention. CONCLUSION: In this study, the spectrum of clinical manifestations in patients with genetically confirmed CPVT was examined. The findings highlight transient QTc interval extensions, significant sinus bradycardia, and sequences of supraventricular tachyarrhythmias, which can escalate into life-threatening ventricular tachyarrhythmias in CPVT patients.
研究目的:评估儿茶酚胺能多形性室性心动过速(CPVT)患者的临床和遗传特征,包括不良事件的发生和结局。材料与方法:对 8 名 CPVT 患者的临床表型进行了长达 4 年的观察,其中 2 人是原发性 CPVT 患者的亲属。临床和仪器研究包括心电图(ECG-12)、24 小时 Holter 心电图监测、家谱史收集和心脏性猝死(SCD)家族史、经胸超声心动图和心脏磁共振成像以检测心肌结构变化、根据适应症进行电生理研究和 ICD 监测。利用高通量测序(NGS)寻找与通道病和其他遗传性心律失常发病有关的基因突变。结果:根据 ACMG(2015 年)标准,在 8 例患者中发现了与 CPVT 相关的 RYR2 基因中 III-V 类致病性核苷酸变异。在 6 名(75%)患者中发现了 RYR2 基因的致病性(IV-V 级)和可能致病性(IV 级)变异,在 2 名患者中发现了临床意义不确定的变异(VUS,III 级)。在确诊时,4 名患者(50%)的 QTc 间期一过性延长超过 480 毫秒;2 名患者(25%)的心动过缓低于 54 次/分,2 名患者(25%)出现室上性心动过速和室性心动过速。在 RYR2 基因突变为 c.11814C A(p.Ser3938Arg,rs794728704)、c.463G A(p.Gly155Arg)和 c.14876G A(p.Arg4959Gln,rs794728811)的患者中,观察到了最严重的疾病形式,临床表现明显,并在随后的抢救中出现临床死亡,以及一过性 QTc 间期延长超过 500 毫秒。三名(37.5%)患者接受了 ICD 植入术;其中一名用于 SCD 一级预防,两名用于二级预防。结论:本研究探讨了经基因证实的 CPVT 患者的临床表现谱。研究结果表明,CPVT 患者会出现一过性 QTc 间期延长、明显的窦性心动过缓和室上性快速性心律失常序列,这些症状可升级为危及生命的室性快速性心律失常。
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引用次数: 0
Analysis of the endocardial stage of treatment of tachyarhythmias after open interventions for atrial fibrillation. Experience of one center 分析心房颤动开放介入治疗后快速性心律失常的心内膜治疗阶段。一个中心的经验
Pub Date : 2024-01-16 DOI: 10.17816/cardar529671
A. S. Postol, G. N. Antipov, A. V. Ivanchenko, Vitaliy V. Lyashenko, D. A. Kalinin, S. Kotov, A. B. Vygovsky, Yuriy A. Shneider
AIM: To study EFI parameters and features of recurrent atrial tachyarrhythmias in patients who underwent surgical correction of AF. MATERIALS AND METHODS: from January 2013 to December 2021, 447 combined interventions were performed to eliminate AF using the labyrinth-3 and left atrial labyrinth techniques with correction of CHD (congenital heart disease) and/or coronary artery disease. Rhythm disturbances were detected in 57 (12.7%) patients at various follow-up periods. Endovascular interventions were performed in 39 patients. The average follow-up period after the endocardial stage was 34.37 (standard deviation 24.32) months. The median age of patients was 64 (58–67) years, 21 (54%) were men. The patients were divided into 2 groups: group 1 — after the classic biatrial (BA) labyrinth-3 — 23 (59%) patients, group 2 — after the left-atrial variant (LA) labyrinth-3 — 16 (41%) patients. At the endocardial stage, electrophysiological studies (EFI) were performed to clarify the mechanism of arrhythmia, and ablation eliminated tachyarrhythmia. EFI protocol: revision of the pulmonary veins, determination of the isolation of the posterior wall of the LA assessment of atrial arrhythmia, elimination of arrhythmia, control induction of arrhythmia after ablation. After repeated intervention, patients were observed in the operating clinic every 3 months. RESULTS: After the endocardial stage, a regular rhythm was determined in 19 (82.6%) patients of the BA group, 13 (92.9%) patients of the LA group (p = 0.914). Relapses in the form of AF were noted in 5 patients (4 — group 1 and 1 — group 2) group (p = 0.306) All relapses of tachyarrhythmia with an irregular cycle (AF) were detected in patients with AF before the endovascular stage In both groups, there were cases of restoration of conduction in the pulmonary veins — 10 (43.5%) patients after BA ablation and 1 (5.3%) patient after LA ablation. There are no recurrences of atrial arrhythmia after ablation of atrial flutter (arrhythmia with a stable cycle). CONCLUSION: The endocardial stage is highly effective and demonstrates subsequent freedom from atrial arrhythmia in patients who have tachycardia with a regular cycle after both methods of surgical ablation of AF. Recurrent tachyarrhythmia in the form of AF (irregular cycle) is associated with a low probability of maintaining a regular atrial rhythm after a repeated endocardial procedure, due to the presence of structural and electrophysiological changes in the atrial myocardium.
目的:研究接受房颤手术矫正的患者的 EFI 参数和复发性房性快速性心律失常的特征。材料和方法:2013 年 1 月至 2021 年 12 月,447 例患者在接受了 CHD(先天性心脏病)和/或冠状动脉疾病矫治的同时,接受了迷宫-3 和左心房迷宫技术的联合介入治疗,以消除房颤。在不同的随访期间,有 57 名患者(12.7%)被检测出心律失常。39名患者接受了血管内介入治疗。心内膜阶段后的平均随访时间为 34.37 个月(标准差为 24.32 个月)。患者的中位年龄为 64(58-67)岁,21(54%)人为男性。患者被分为两组:第1组--经典双心房(BA)迷宫-3术后--23名(59%)患者,第2组--左心房变异(LA)迷宫-3术后--16名(41%)患者。在心内膜阶段,进行了电生理学研究(EFI)以明确心律失常的机制,消融术消除了快速性心律失常。EFI 方案:修改肺静脉,确定 LA 后壁隔离评估房性心律失常,消除心律失常,控制消融后诱发心律失常。反复干预后,每 3 个月在手术室对患者进行观察。结果:心内膜阶段后,BA 组有 19 名(82.6%)患者的心律正常,LA 组有 13 名(92.9%)患者的心律正常(P = 0.914)。在两组患者中,均有肺静脉传导恢复的病例--BA消融术后有10例(43.5%)患者,LA消融术后有1例(5.3%)患者。心房扑动(周期稳定的心律失常)消融术后,心房心律失常没有复发。结论:心内膜阶段效果显著,两种房颤手术消融方法均可使周期规律的心动过速患者随后不再出现房性心律失常。房颤(周期不规则)形式的复发性快速心律失常与重复心内膜手术后维持规律心房节律的可能性较低有关,这是因为心房心肌存在结构和电生理变化。
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Cardiac Arrhythmias
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