Case Report: Dual-chamber pacemaker for hypertrophic cardiomyopathy with bradyarrhythmia and idiopathic pericardial effusion: a report of two cases and literature review.

IF 2.8 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Frontiers in Cardiovascular Medicine Pub Date : 2025-02-27 eCollection Date: 2025-01-01 DOI:10.3389/fcvm.2025.1518000
Chang Liu, Fei Zheng, Yuxia Gao, Zheming Wang, Xinyu Zhang, Xiuqing Tian
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Abstract

Background: Hypertrophic cardiomyopathy (HCM) is an autosomal dominant disorder characterized by asymmetric hypertrophy of the ventricles and the ventricular septum, leading to subsequent left ventricular outflow tract (LVOT) obstruction and diastolic dysfunction. Typically, patients with HCM experience sinus tachycardia and sinus arrest relatively infrequently. In addition, the concurrent occurrence of HCM with non-surgically induced (ablation or myectomy) bradyarrhythmia and idiopathic pericardial effusion in adult patients has not been previously reported.

Case summary: In this report, we present two elderly female patients with HCM who exhibited sinus bradycardia and sinus arrest, one of whom also presented with moderate pericardial effusion, they all presented with chest tightness. To manage the complex comorbidities, we opted for dual-chamber pacemaker implantation. Subsequent examinations and follow-up revealed that pacing significantly reduced LVOT obstruction and corrected heart rhythm. Additionally, there was no significant progression of pericardial effusion.

Discussion: The primary strategies for alleviating LVOT obstruction involve altering the structure of the septum, including septal myectomy (SME), alcohol septal ablation (ASA), and septal radiofrequency ablation. Meanwhile, a dual-chamber pacemaker can treat HCM by changing the sequence of myocardial contraction. Although pacemakers have been considered an inferior alternative due to their relatively large residual obstruction, their benefits may be significantly underestimated. This report underscores the additional efficacy of dual-chamber pacemakers in managing HCM, particularly in patients complicated by sinus node dysfunction and idiopathic pericardial effusion.

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病例报告:双腔起搏器治疗肥厚型心肌病伴缓慢性心律失常和特发性心包积液:两例病例报告和文献综述。
背景:肥厚性心肌病(HCM)是一种常染色体显性遗传病,其特征是心室和室间隔不对称肥大,导致随后的左心室流出道(LVOT)阻塞和舒张功能障碍。通常,HCM患者出现窦性心动过速和窦性骤停的频率相对较低。此外,HCM与非手术诱导(消融或肌瘤切除术)慢速心律失常和特发性心包积液同时发生在成人患者中,此前未见报道。病例总结:在本报告中,我们报告了两名老年女性HCM患者,他们表现为窦性心动过缓和窦性骤停,其中一人还表现为中度心包积液,他们都表现为胸闷。为了控制复杂的合并症,我们选择了双腔起搏器植入。随后的检查和随访显示起搏明显减少LVOT阻塞和纠正心律。此外,没有明显的心包积液进展。讨论:缓解LVOT梗阻的主要策略包括改变室间隔结构,包括室间隔肌切除术(SME)、酒精室间隔消融(ASA)和室间隔射频消融。同时,双室起搏器可以通过改变心肌收缩顺序来治疗HCM。尽管起搏器由于其相对较大的残余阻塞而被认为是一种较差的选择,但其益处可能被大大低估。本报告强调了双腔起搏器在治疗HCM方面的额外功效,特别是在并发窦房结功能障碍和特发性心包积液的患者中。
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来源期刊
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.80
自引率
11.10%
发文量
3529
审稿时长
14 weeks
期刊介绍: Frontiers? Which frontiers? Where exactly are the frontiers of cardiovascular medicine? And who should be defining these frontiers? At Frontiers in Cardiovascular Medicine we believe it is worth being curious to foresee and explore beyond the current frontiers. In other words, we would like, through the articles published by our community journal Frontiers in Cardiovascular Medicine, to anticipate the future of cardiovascular medicine, and thus better prevent cardiovascular disorders and improve therapeutic options and outcomes of our patients.
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