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首页> 外文期刊>Cardiology Research >Treating a Structural Heart Disease Using a Non-structural Approach: Role of Cardiac Pacing in Hypertrophic Cardiomyopathy
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Treating a Structural Heart Disease Using a Non-structural Approach: Role of Cardiac Pacing in Hypertrophic Cardiomyopathy

机译:使用非结构性方法治疗结构性心脏病:心脏起搏在肥厚型心肌病中的作用

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Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease characterized by a thickened non-dilated ventricle in the absence of another cardiac or systemic condition. Its most important hemodynamic consequence is left ventricular outflow tract (LVOT) obstruction. The primary management strategy of this condition is surgical septal myectomy, but an acceptable alternative treatment in patients who are not suitable for (or who refuse) surgery is alcohol septal ablation (ASA). However, in patients with unfavorable coronary anatomy which precludes ASA (i.e. absence of major septal perforator branch of the left anterior descending (LAD) artery), another reasonable option is dual chamber pacemaker implantation to decrease LVOT outflow gradient. A 77-year-old female, known hypertensive, diabetic with a history of coronary artery disease, presented with 1-week history of worsening chest pain and shortness of breath. She was admitted as a case of acute coronary syndrome and pneumonia. On workup, 2DED revealed hypertrophic obstructive cardiomyopathy (HOCM) with a demonstrated systolic anterior motion (SAM) of the mitral valve with a peak instantaneous gradient of 194 mm Hg across the basal LV cavity. The patient refused surgical myectomy, and ASA was the preferred treatment option. On coronary angiography, there was an incidental finding of absent major septal perforator branch of the LAD coronary artery, rendering her unsuitable for septal ablation. She was referred to electrophysiology for evaluation. She underwent dual chamber pacemaker implantation and documented significant decrease in the peak instantaneous gradient from 194 to 37 mm Hg, with complete obliteration of SAM and improvement in overall wall motion. She remained stable and asymptomatic after pacemaker insertion until her recent outpatient follow-up (1 year after implantation). We present a case of HCM with congenitally absent major septal perforator branch coronary artery treated with dual chamber pacemaker implantation. To our knowledge, this is the first reported angiographically absent first (major) septal perforator coronary anatomy in the setting of HCM, and also the first description of dual chamber pacemaker implantation to relieve the LVOT obstruction. Although the role of dual chamber pacing has become limited in HCM because surgical myectomy and septal ablation have resulted in better decrease in LV outflow gradient and symptom improvement, this modality remains essential and may still be considered as the treatment strategy-of-choice in patients who are unsuitable for surgical myectomy and ASA.Cardiol Res. 2017;8(1):20-25doi: https://doi.org/10.14740/cr512w
机译:肥厚型心肌病(HCM)是最常见的遗传性心血管疾病,其特征是在没有其他心脏病或全身性疾病的情况下,心室增厚,未扩张。它最重要的血液动力学后果是左室流出道(LVOT)阻塞。这种情况的主要治疗策略是手术间隔肌切除术,但是对于不适合(或拒绝)手术的患者,可接受的替代治疗方法是酒精中隔消融术(ASA)。但是,对于冠状动脉解剖不利于ASA(即不存在左前降支(LAD)动脉的主要间隔穿孔分支)的患者,另一个合理的选择是双腔起搏器植入以降低LVOT流出梯度。一名77岁的女性,患有高血压,患有糖尿病,有冠状动脉疾病的病史,有1周的病史,即胸痛和呼吸急促恶化。她因急性冠状动脉综合征和肺炎而入院。在检查中,2DED显示出肥厚性梗阻性心肌病(HOCM),并显示二尖瓣的收缩前运动(SAM),整个基底LV腔的瞬时峰值为194 mm Hg。该患者拒绝进行外科手术切除术,而ASA是首选的治疗选择。在冠状动脉造影上,偶然发现了LAD冠状动脉的主要中隔穿支支脉缺失,因此不适合进行中隔消融。她被转介至电生理学进行评估。她接受了双腔起搏器植入术,并记录了峰值瞬时梯度从194到37 mm Hg的显着降低,同时完全消除了SAM并改善了整体壁运动。植入起搏器后,她保持稳定且无症状,直到最近的门诊随访(植入后1年)为止。我们提出了一例伴有双腔起搏器植入的先天性大间隔隔膜穿孔冠状动脉缺席的HCM。据我们所知,这是第一个在HCM背景下首次在血管造影上未见到的第一(主要)间隔穿孔冠状动脉解剖,也是对双腔起搏器植入以缓解LVOT阻塞的首次描述。尽管双腔起搏在HCM中的作用已经受到限制,因为外科手术的肌瘤切除术和间隔消融术可更好地降低LV流出梯度并改善症状,但这种方式仍然必不可少,仍可能被视为患者的首选治疗策略不适合外科手术和ASA的患者。 2017; 8(1):20-25doi:https://doi.org/10.14740/cr512w

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