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Published on: February 26, 2013
Implantable atrial flow regulator for severe, irreversible pulmonary arterial hypertension
Mehul B Patel1, Bennett P Samuel, Reda E Girgis
1Congenital Heart Center, Helen DeVos Children's Hospital of Spectrum Health, Grand Rapids, MI, USA.
Abstract:
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.
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