The PAH patient's perspective

IF 0.8 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Daniel A. Jeffery , Wendy Gin-Sing , Radwa Bedair , Luke S. Howard
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引用次数: 0

Abstract

Pulmonary Hypertension is a serious condition which can occur in adults living with congenital heart disease. Due to advances in the care of patients with congenital heart disease, patients are living longer with the condition. Unfortunately, patients living with Pulmonary Arterial Hypertension associated with Congenital Heart Disease (PAH-CHD) face a number of different issues directly related to their condition, which range from physical limitations and uncertainty over their diagnosis, which in some cases cause significant depression and anxiety, to impact on their relationships with friends and family, financial challenges and family planning.
In this article, we interview two patients living with PAH-CHD and discuss the numerous issues that patients may face as a direct result of their condition.
PAH患者的观点
肺动脉高压是一种严重的疾病,可能发生在患有先天性心脏病的成年人身上。由于对先天性心脏病患者护理的进步,患有这种疾病的患者寿命更长。不幸的是,与先天性心脏病(PAH-CHD)相关的肺动脉高压患者面临着许多与其病情直接相关的不同问题,包括身体限制和诊断的不确定性,在某些情况下会导致严重的抑郁和焦虑,影响他们与朋友和家人的关系,财务挑战和计划生育。在这篇文章中,我们采访了两名患有PAH-CHD的患者,并讨论了患者可能面临的许多问题,这些问题是他们的病情的直接结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International journal of cardiology. Congenital heart disease
International journal of cardiology. Congenital heart disease Cardiology and Cardiovascular Medicine
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审稿时长
83 days
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