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先天性主动脉瓣狭窄:关于自然病史和临床评估的一些观察

CONGENITAL AORTIC STENOSIS: SOME OBSERVATIONS ON THE NATURAL HISTORY AND CLINICAL ASSESSMENT.

作者信息

PECKHAM G B, KEITH J D, EVANS J R

出版信息

Can Med Assoc J. 1964 Sep 19;91(12):639-43.

Abstract

Three hundred patients, 30 years of age or under, with the clinical diagnosis of aortic stenosis were reviewed to provide information on the accuracy of clinical assessment and the natural history of the condition when left untreated. Sudden death was uncommon and occurred only in patients with clinical evidence of severe obstruction. In infants, the early presentation and lethal nature of aortic stenosis appeared to result from the presence of additional cardiac lesions. Correlation of clinical assessment with hemodynamic data in 83 patients indicated that important stenosis was present if the systolic murmur was accompanied by a thrill and associated with an increased left ventricular impulse, decreased brachial artery pulse pressure, or left ventricular hypertrophy on the electrocardiogram. The site of obstruction could not be established with certainty by clinical examination, but an early systolic ejection click was strong evidence against subvalvular stenosis.

摘要

对30岁及以下临床诊断为主动脉瓣狭窄的300例患者进行了回顾性研究,以提供有关临床评估准确性及未经治疗情况下该病自然病史的信息。猝死并不常见,仅发生于有严重梗阻临床证据的患者。在婴儿中,主动脉瓣狭窄的早期表现及致命性似乎是由其他心脏病变的存在所致。对83例患者的临床评估与血流动力学数据的相关性表明,如果收缩期杂音伴有震颤,并伴有左心室搏动增强、肱动脉脉压降低或心电图显示左心室肥厚,则存在重要狭窄。临床检查无法确定梗阻部位,但收缩期早期喷射性喀喇音是反对瓣下狭窄的有力证据。

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