A novel unidirectional-valved shunt approach for end-stage pulmonary arterial hypertension: Early experience in adolescents and adults
نویسندگان
چکیده
ObjectivesDespite advances in treatment of idiopathic pulmonary arterial hypertension (IPAH), there remains no medical cure, and patients can experience disease progression leading to right heart failure, progressive exercise intolerance, death. The reversed Potts shunt (left artery descending aorta) was reintroduced for end-stage IPAH permit decompression the suprasystemic ventricle by left shunting, with preservation upper body oxygenation. has potential delay need lung transplantation offer a those who are transplant ineligible. To optimize design avoid complications bidirectional we developed novel approach using unidirectional-valved (UVS) pressure poor ventricular function.MethodsA single-center retrospective review performed UVS cases done at Columbia University Medical Center–New York Presbyterian between November 1, 2016, May 2019.ResultsFive (4 female; ages 12-22 years) underwent UVS. All had pressure, function, World Health Organization functional class IV symptoms baseline. alive transplant-free latest follow-up (range 3-33 months; median 6 ± 11 months).ConclusionsThe may an alternative solution adolescents young adults IPAH. Longer-term is needed determine ultimate impact unidirectional unloading these whether will enable broader
منابع مشابه
Characteristics of Pulmonary Vascular Remodeling in a Novel Model of Shunt-Associated Pulmonary Arterial Hypertension
BACKGROUND Establishing a shunt-induced pulmonary arterial hypertension (PAH) model in mice would be of great scientific value, but no such models have been reported to date. Here, we established a shunt-associated PAH in mice to investigate the characteristics of pulmonary vascular remodeling, which provides a new platform for the in-depth study of PAH associated with congenital heart disease ...
متن کاملPulmonary Hypertension Registry: a 10-Year Experience
Background: Pulmonary Arterial Hypertension (PAH), a fatal orphan disease, is defined as increased mean Pulmonary Arterial Pressure (mPAP) above 25 mm/Hg, Pulmonary Capillary Wedge Pressure (PCWP) below 15 mm/Hg, and pulmonary vascular Resistance over 3 Wood Unit (WU). Although Pulmonary Hypertension (PH) is a relatively prevalent disease, the idiopathic form (iPAH) is a rare disease with a pre...
متن کاملA novel mechanism for pulmonary arterial hypertension?
The pathophysiology of primary pulmonary hypertension (PPH) involves alterations in vascular reactivity, vascular structure, and interactions of the vessel wall with circulating blood elements.1 An imbalance of vasodilator and vasoconstrictor influences is likely to be an early derangement. Progressive intimal and medial thickening, due to proliferation and migration of vascular smooth muscle c...
متن کاملTransplantation in end-stage pulmonary hypertension
The Third International Right Heart Summit was organized for the purpose of bringing an interdisciplinary group of expert physician-scientists together to promote dialogue involving emerging concepts in the unique pathophysiology, clinical manifestation, and therapies of pulmonary vascular disease (PVD) and right heart failure (RHF). This review summarizes key ideas addressed in the section of ...
متن کاملTHE EFFECTS OF CAPTOPRIL ON PULMONARY AND SYS TEMIC ARTERIAL PRESSURES IN HIGHALTITUDE PULMONARY HYPERTENSION
The purpose of this investigation was to assess the effect of captopril on both systemic (P.a) and pulmonary arterial pressures (PPA) in patients with high-altitude pulmonary hypertension (HAPH). Seventeen patients (mean age 44±6.8 years) with HAPH and mild to moderate systemic arterial hypertension were included in the study. All patients underwent right heart catheterization with measurem...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: The Journal of Thoracic and Cardiovascular Surgery
سال: 2021
ISSN: ['1097-685X', '1085-8687', '0022-5223']
DOI: https://doi.org/10.1016/j.jtcvs.2019.10.149