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本文引用的文献

1
Assessing myocardial bridging and left ventricular configuration by 64-slice computed tomography in patients with apical hypertrophic cardiomyopathy presenting with chest pain.64层计算机断层扫描评估胸痛型心尖肥厚型心肌病患者的心肌桥和左心室形态
J Comput Assist Tomogr. 2010 Jan;34(1):70-4. doi: 10.1097/RCT.0b013e3181b66d31.
2
Phenotypic spectrum and clinical characteristics of apical hypertrophic cardiomyopathy: multicenter echo-Doppler study.心尖肥厚型心肌病的表型谱及临床特征:多中心超声多普勒研究
Cardiology. 2008;110(1):53-61. doi: 10.1159/000109407. Epub 2007 Oct 10.
3
Clinical features and outcome of patients with apical hypertrophic cardiomyopathy in Taiwan.台湾地区肥厚型心肌病患者的临床特征与预后
Cardiology. 2006;106(1):29-35. doi: 10.1159/000092590. Epub 2006 Apr 7.
4
Sustained cavity obliteration and apical aneurysm formation in apical hypertrophic cardiomyopathy.肥厚型心肌病心尖部持续的心腔闭塞及心尖部动脉瘤形成
J Am Coll Cardiol. 2003 Jul 16;42(2):288-95. doi: 10.1016/s0735-1097(03)00576-x.
5
Novel insights into the natural history of apical hypertrophic cardiomyopathy during long-term follow-up.长期随访期间对肥厚型心肌病自然史的新见解。
Isr Med Assoc J. 2002 Mar;4(3):166-9.
6
Long-term outcome in patients with apical hypertrophic cardiomyopathy.肥厚型心肌病患者的长期预后。
J Am Coll Cardiol. 2002 Feb 20;39(4):638-45. doi: 10.1016/s0735-1097(01)01778-8.
7
Apical hypertrophic cardiomyopathy (apical hypertrophy): an overview.心尖肥厚型心肌病(心尖肥厚):概述
J Cardiol. 2001;37 Suppl 1:161-78.
8
Left ventricular aneurysm without coronary artery disease, incidence and clinical features: clinical analysis of 11 cases.无冠状动脉疾病的左心室动脉瘤:发病率及临床特征——11例临床分析
Intern Med. 2000 Jul;39(7):531-6. doi: 10.2169/internalmedicine.39.531.
9
Apical hypertrophic cardiomyopathy: clinical and two-dimensional echocardiographic assessment.心尖肥厚型心肌病:临床与二维超声心动图评估
Ann Intern Med. 1987 May;106(5):663-70. doi: 10.7326/0003-4819-106-5-663.
10
[Apical sequestration in hypertrophic cardiomyopathy: its clinical features and pathophysiology].[肥厚型心肌病的心尖部机化:其临床特征与病理生理学]
J Cardiol. 1991;21(2):361-74.

心尖肥厚型心肌病:超声心动图参数、冠状动脉左心室形态与临床预后的相关性。

Apical hypertrophic cardiomyopathy: correlations between echocardiographic parameters, angiographic left ventricular morphology, and clinical outcomes.

机构信息

Division of Cardiology, Department of Medicine, Lo-Tung Poh-Ai Hospital, I-Lan, Taiwan.

出版信息

Clin Cardiol. 2011 Apr;34(4):233-8. doi: 10.1002/clc.20874. Epub 2011 Mar 13.

DOI:10.1002/clc.20874
PMID:21400548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6652360/
Abstract

BACKGROUND

Echocardiographic parameters could be implicated in the development of apical asynergy (characterized by apical sequestration or apical aneurysm) and worse cardiovascular outcome in patients with apical hypertrophic cardiomyopathy (ApHCM).

HYPOTHESIS

Echocardiographic parameters and morphological patterns of left ventriculograms are associated with cardiovascular morbidity and mortality in patients with ApHCM.

METHODS

We followed 47 cases with echocardiographically documented ApHCM. Echocardiographic findings of the extent and degree of hypertrophy, sustained cavity obliteration, and paradoxical diastolic jet flow were measured. All patients underwent a cardiac catheterization except for the cases whose informed consent was not acquired. The clinical manifestations were assessed and recorded by the attending physicians during 35.4 ± 23.7 months follow-up.

RESULTS

Among the 47 patients with ApHCM, 30 patients presented as the "pure" form and 17 patients present as the "mixed" form. Seventeen of 28 patients with sustained cavity obliteration showed paradoxical flow by echocardiography. Thirty-one underwent left ventriculograms and showed morphological abnormalities, including "ace-of-spades" configuration (15/31), apical sequestration (12/31), and apical aneurysm (4/31). The results demonstrated that cardiovascular morbidities occurred in 21 of 47 patients and were closely related to the presence of mixed form ApHCM, cavity obliteration, and paradoxical flow by univariate and multivariate Cox analysis. During the period of follow-up, 4 patients (9.5%) died, and among them 3 had concomitant apical aneurysm.

CONCLUSIONS

We concluded that detection of cavity obliteration and paradoxical flow and discrimination of pure form from mixed form by echocardiography, as well apical sequestration from apical aneurysm in ApHCM patients, is warranted.

摘要

背景

超声心动图参数可能与心尖肥厚型心肌病(ApHCM)患者心尖无运动(表现为心尖隔离或心尖动脉瘤)和心血管不良预后有关。

假说

ApHCM 患者的超声心动图参数和左心室造影的形态模式与心血管发病率和死亡率相关。

方法

我们随访了 47 例经超声心动图证实的 ApHCM 患者。测量了肥厚程度和范围、持续腔闭塞和矛盾性舒张射流的超声心动图发现。除未获得知情同意的病例外,所有患者均接受了心导管检查。在 35.4±23.7 个月的随访期间,由主治医生评估和记录临床表现。

结果

在 47 例 ApHCM 患者中,30 例为“单纯”型,17 例为“混合”型。28 例持续腔闭塞患者中,17 例超声心动图显示矛盾性血流。31 例行左心室造影,显示形态异常,包括“黑桃 ACE”构型(15/31)、心尖隔离(12/31)和心尖动脉瘤(4/31)。结果表明,47 例患者中有 21 例发生心血管并发症,单因素和多因素 Cox 分析表明,混合型 ApHCM、腔闭塞和矛盾性血流与心血管并发症密切相关。在随访期间,4 例患者(9.5%)死亡,其中 3 例合并心尖动脉瘤。

结论

我们的结论是,ApHCM 患者应通过超声心动图检测腔闭塞和矛盾性血流,并区分单纯型和混合型,以及心尖隔离和心尖动脉瘤。