专题讨论会 10:从哮喘人群中发现 EGPA,以及风湿免疫科和呼吸科医生如何共同护理:病例分享

Ping-Hung Kuo
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引用次数: 0

摘要

嗜酸性粒细胞增多性多血管炎(EGPA),以前称为丘格-斯特劳斯综合征(Churg-Strauss syndrome),是一种罕见的系统性血管炎,以哮喘、嗜酸性粒细胞增多和血管性器官受累为特征。这种罕见疾病给重症哮喘的诊断带来了挑战。因此,在哮喘患者群中识别 EGPA 对于适当管理和改善患者预后至关重要。此外,风湿免疫科医生和呼吸科医生之间的有效合作对于全面护理 EGPA 患者至关重要。本科学讲座旨在讨论如何识别哮喘患者中的 EGPA,并强调风湿免疫科和呼吸科共同护理的重要性。讲座将首先概述 EGPA、其临床表现以及与严重哮喘相鉴别的挑战。讲座将讨论如何识别独特的临床特征,如难治性哮喘、外周嗜酸性粒细胞增多和全身症状,这些特征是 EGPA 存在的信标。讲座将探讨包括影像学、实验室检测和活检技术在内的诊断工具,重点介绍这些工具在区分 EGPA 和哮喘方面的作用。与此同时,讲座的重点将转移到风湿免疫科医生和呼吸科医生在管理 EGPA 患者方面所需的合作。讲座将讨论两个专科在实现患者最佳治疗效果方面的互补作用。风湿免疫科医生在诊断和治疗包括 EGPA 在内的全身性血管炎方面发挥着至关重要的作用,而呼吸科医生则在管理哮喘和呼吸系统并发症方面提供专业知识。该病例将强调开放式沟通、共同决策和协调治疗计划的重要性,以确保为 EGPA 患者提供全面护理,满足他们在风湿病和呼吸系统方面的需求。我们将分享真实案例,说明风湿病学和呼吸内科之间成功的共同管理模式。这些案例将强调多学科方法的益处,包括改善疾病管理、减少治疗相关并发症和提高患者满意度。总之,识别哮喘人群中的 EGPA 对于适当的管理至关重要,而风湿免疫科和呼吸科医生之间的有效合作对于全面护理至关重要。本科学讲座旨在提供有关发现哮喘患者中 EGPA 的见解,并强调这些专科之间共同护理的重要性,最终改善患者的预后和生活质量。
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Symposium 10: Spotting EGPA from Asthma Populations and How Co-Care Works Between Rheumatology and Respiratory Physicians: A Case Sharing
Eosinophilic Granulomatosis with Polyangiitis (EGPA), formerly known as Churg-Strauss syndrome, is a rare systemic vasculitis characterized by asthma, eosinophilia, and vasculitic organ involvement. This rare disease poses diagnostic challenges within the domain of severe asthma. Recognizing EGPA within the asthmatic cohort is therefore crucial for appropriate management and improved patient outcomes. Moreover, effective collaboration between rheumatologists and respiratory physicians is vital for the comprehensive care of EGPA patients. This scientific lecture aims to discuss the identification of EGPA in individuals with asthma and highlight the importance of co-care between rheumatology and respiratory medicine. This lecture will begin by providing an overview of EGPA, its clinical manifestations, and the challenges associated with differentiating it from severe asthma. The crucial identification of distinctive clinical features, such as refractory asthma, peripheral eosinophilia, and systemic symptoms, which serve as beacons for the presence of EGPA, will be discussed. Diagnostic tools encompassing imaging, laboratory tests, and biopsy techniques are explored, focusing on their utility in distinguishing EGPA from asthma. Concomitantly, the lecture will then shift its focus to the collaborative efforts required from rheumatologists and respiratory physicians in managing EGPA patients. The complementary roles of both specialties in achieving optimal patient outcomes will be discussed. Rheumatologists play a crucial role in the diagnosis and treatment of systemic vasculitis, including EGPA, while respiratory physicians provide expertise in managing asthma and respiratory complications. The case will highlight the importance of open communication, shared decision-making, and coordinated treatment plans to ensure comprehensive care for EGPA patients, addressing both their rheumatologic and respiratory needs. Real-life case will be shared to illustrate successful co-management models between rheumatology and respiratory medicine. These examples will underscore the benefits of a multidisciplinary approach, including improved disease management, reduced treatment-related complications, and enhanced patient satisfaction. In conclusion, identifying EGPA within the asthma population is crucial for appropriate management, and effective collaboration between rheumatology and respiratory physicians is essential for comprehensive care. This scientific lecture aims to provide insights into spotting EGPA among asthma patients and emphasize the significance of co-care between these specialties, ultimately improving patient outcomes and quality of life.
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