经皮治疗肺动脉高压伴心房间隔缺损患者的左冠状动脉主干受压。

IF 0.9 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Muhammed Furkan Deniz, Mit Ya Ar Sinan, Ahmet Y Ld Z, Emir Bar Zg R K N, Mehmet Serdar K Ko Lu
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引用次数: 1

摘要

尽管近年来在治疗(新药物和新的联合策略)方面取得了种种进展,但肺动脉高压仍然是一种预后不良的致命疾病。患者表现出不同的症状,这些症状并非疾病特有(呼吸困难、心绞痛、心悸和晕厥)。心绞痛可能继发于心肌缺血,原因是负荷增加(氧气供应和需求不匹配)或左主冠状动脉受到外部压迫。左冠状动脉主干受压与肺动脉高压患者运动后心源性猝死有关。在鉴别诊断肺动脉高压患者心绞痛时应牢记这一点,并应立即治疗。在此,我们报告了一名肺动脉高压患者,该患者伴有继发性房间隔缺损,表现为肺动脉扩张引起的左冠状动脉口主动脉压迫,并接受了血管内超声引导下的经皮冠状动脉介入治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Percutaneous Treatment of Left Main Coronary Artery Compression in a Pulmonary Artery Hypertension Patient Associated with Atrial Septal Defect.

Pulmonary arterial hypertension is still a fatal disease persisting with poor prognosis, despite all the advances in treatment (new agents and new combination strategies) in recent years. Patients present with different symptoms which are not specific to the disease (dyspnea, angina, palpitation, and syncope). Angina may occur secondary to myocardial ischemia due to increased right ventricular after load (oxygen supply and demand mismatch) or external compression on the left main coronary artery. Left main coronary artery compression is associated with post-exercise sudden cardiac death in pulmonary arterial hypertension patients. It should be kept in mind in the differential diagnosis of angina in patients with pulmonary arterial hypertension and should be treated immediately. Here, we report a pulmonary arterial hypertension patient associated with secundum-type atrial septal defect presented with ostial left main coronary artery compression caused by an enlarged pulmonary artery and treated with intravascular ultrasound-guided percutaneous coronary intervention.

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来源期刊
CiteScore
1.30
自引率
12.50%
发文量
124
审稿时长
32 weeks
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