Congenital Heart Center, Helen DeVos Children's Hospital of Spectrum Health, Grand Rapids, MI, USA.
EuroIntervention. 2015 Oct;11(6):706-9. doi: 10.4244/EIJY15M07_08.
Pulmonary arterial hypertension (PAH) is a severe, progressive and fatal disease. The creation of an interatrial right-to-left shunt in patients with PAH may enhance systemic ventricular output at the expense of desaturation. However, creating sustainable restricted interatrial communication is challenging. We describe the successful use of an atrial flow regulator, a novel implantable atrial communication device, in a 54-year-old female with severe irreversible PAH.
肺动脉高压(PAH)是一种严重、进行性和致命的疾病。在 PAH 患者中创建房间隔右向左分流可以增加全身心室输出,但代价是饱和度降低。然而,创建可持续的限制性房间隔交通是具有挑战性的。我们描述了一种新型可植入房间隔通讯装置——心房流量调节器在一名 54 岁女性严重不可逆 PAH 中的成功应用。