The European Voice of the Patient living with pulmonary hypertension associated with interstitial lung disease: Diagnosis, symptoms, impacts, and treatments.

IF 2.2 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Pulmonary Circulation Pub Date : 2024-06-22 eCollection Date: 2024-04-01 DOI:10.1002/pul2.12405
Lucilla Piccari, Gabor Kovacs, Steve Jones, Hall Skaara, Claudia Roca Herms, Gabriela Silvina Bacchini Jeanneret, Melquiades Calzado Vinardell, Nuria Gonzalez-Rojas Guix, Miriam Fernandez Delgado, Héctor Gálvez García, David Schwicker
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Abstract

Pulmonary hypertension (PH) adds a substantial disease burden, including higher mortality, when associated with interstitial lung disease (ILD), a severe, chronic, progressive condition. Yet little is known of the lived experiences, perspectives, priorities, and viewpoints of patients and carers living with PH-ILD. The Voice of the Patient meeting at the center of this qualitative research study aims to provide these difficult-to-obtain insights from a European perspective for the first time. The multistakeholder approach brought together four PH-ILD patients, three primary caregivers, two patient associations, clinical experts, sponsor representatives, and a facilitator. Of the six major themes identified in the thematic analysis, symptoms, and physical limitations were the most impactful. Shortness of breath was the most bothersome symptom affecting patients daily. Further symptoms included fatigue, cough, dizziness, syncope, edema, and palpitations. Physical limitations focused on reduced mobility, impacting patients' ability to perform daily tasks, hobbies, sports, and to enjoy travel. Existing antifibrotic and pulmonary arterial hypertension-targeted treatments were perceived as beneficial. However, despite advances in treatment, severe disease burdens and high unmet medical needs persist from the perspectives of patients. Most meaningful to patients' daily wellbeing was supplemental oxygen, enabling greater mobility. Patients and carers reported difficulties and barriers in navigating the healthcare system and obtaining adequate information to reduce their considerable uncertainties, documenting the substantial challenges that rare and complex conditions such as PH-ILD pose for routine clinical practice beyond PH expert centers and indicating an urgent need for high-quality patient- and clinician-directed information to support patient-centered care.

欧洲间质性肺病肺动脉高压患者之声:诊断、症状、影响和治疗。
肺动脉高压(PH)与间质性肺病(ILD)(一种严重、慢性、进展性疾病)并发时,会增加很大的疾病负担,包括增加死亡率。然而,人们对 PH-ILD 患者和照护者的生活经历、视角、优先事项和观点知之甚少。患者之声 "会议是这项定性研究的核心,旨在首次从欧洲的视角提供这些难以获得的见解。多方利益相关者方法汇集了四名 PH-ILD 患者、三名主要护理人员、两个患者协会、临床专家、赞助商代表和一名主持人。在主题分析中确定的六大主题中,症状和身体限制影响最大。呼吸急促是影响患者日常生活的最令人烦恼的症状。其他症状包括疲劳、咳嗽、头晕、晕厥、水肿和心悸。身体上的限制主要集中在行动不便,影响患者完成日常任务、业余爱好、体育运动和享受旅行的能力。现有的抗纤维化和肺动脉高压靶向治疗被认为是有益的。然而,尽管治疗取得了进展,但从患者的角度来看,严重的疾病负担和大量未满足的医疗需求依然存在。对患者的日常福祉最有意义的是补充氧气,使他们能够更加灵活地行动。患者和照护者报告了他们在驾驭医疗系统和获取足够信息以减少相当大的不确定性方面遇到的困难和障碍,记录了 PH-ILD 等罕见和复杂疾病给 PH 专家中心以外的常规临床实践带来的巨大挑战,并表明迫切需要以患者和临床医生为导向的高质量信息,以支持以患者为中心的护理。
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
Pulmonary Circulation
Pulmonary Circulation Medicine-Pulmonary and Respiratory Medicine
CiteScore
4.20
自引率
11.50%
发文量
153
审稿时长
15 weeks
期刊介绍: Pulmonary Circulation''s main goal is to encourage basic, translational, and clinical research by investigators, physician-scientists, and clinicans, in the hope of increasing survival rates for pulmonary hypertension and other pulmonary vascular diseases worldwide, and developing new therapeutic approaches for the diseases. Freely available online, Pulmonary Circulation allows diverse knowledge of research, techniques, and case studies to reach a wide readership of specialists in order to improve patient care and treatment outcomes.
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