无痛性全身肥大细胞增多症的症状负担和症状管理的患者和高级医生观点。

Sandra Kurtin, Susan Woodward, Erin Kolb, Shonna Snyder, Shawna Hull
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引用次数: 0

摘要

背景:症状负担是懒散全身性肥大细胞增多症(ISM)患者求医的主要原因,无论他们是否被诊断出来。目的:本研究旨在探讨高级医师(AP)和ISM患者对ISM症状负担、ISM多学科诊断和管理、症状管理障碍、ISM协同管理策略和ISM患者沟通健康素养的看法。方法:由AP领导的指导委员会制定了ISM患者调查和AP调查,包括有效的工具来衡量症状负担、症状负担影响、障碍和改善症状负担的策略。调查嵌入在Qualtrics中,由Conexiant在2024年12月22日至2025年2月3日期间部署到血液/肿瘤高级从业者协会(APSHO)的AP成员,美国肥大细胞疾病倡议的AP成员以及肥大细胞疾病协会附属患者的方便样本中。结果:50例ap患者和53例ISM患者均100%完成了相应的问卷问题。使用惰性全身性肥大细胞增多症症状评估表(ISM-SAF)来确定最常见、最具挑战性和对生活质量影响最大的症状,所描述的症状负担与本调查中发表的患者数据一致。只有24% (n = 13)的ISM患者表示他们的疾病得到了良好控制,而76%的ap表示他们的ISM患者的疾病得到了良好控制(n = 38)。大多数ap(68%)在调查中表示,他们每年看到一到五名ISM患者,但对管理ISM相关症状感到满意(54%,n = 27)。描述了分诊、多学科管理和共同决策的实践模式。结论:这是第一个以ISM症状负担为重点的调查,提供了对血液学/肿瘤学、过敏和免疫学患者对APs的反应的直接比较。惰性全身性肥大细胞增多症的症状负担测量和症状负担减轻仍然具有挑战性,在本研究中发现了几个障碍和差距。与本研究同时开发的系统性肥大细胞增多症APSHO工具包,为克服本研究中发现的一些障碍和差距提供了一个以ap为重点的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patient and Advanced Practitioner Perspectives on Symptom Burden and Symptom Management in Indolent Systemic Mastocytosis.

Background: Symptom burden is the primary driver for patients with indolent systemic mastocytosis (ISM) to seek medical care, whether or not they are diagnosed.

Purpose: This descriptive study aimed to describe the advanced practitioner (AP) and ISM patient perspective relative to the symptom burden of ISM, multidisciplinary diagnosis and management of ISM, barriers to symptom management, strategies for collaborative management of ISM, and communicative health literacy in patients with ISM.

Methods: An ISM patient survey and AP survey were developed by an AP-led steering committee incorporating validated tools to measure symptom burden, symptom burden impact, barriers, and strategies for improving symptom burden. Surveys were embedded in Qualtrics and were deployed by Conexiant to a convenience sample of AP members of the Advanced Practitioner Society for Hematology/Oncology (APSHO), AP members of the American Initiative in Mast Cell Diseases, and patients affiliated with The Mast Cell Disease Society between December 22, 2024, and February 3, 2025.

Findings: 50 APs and 53 ISM patients completed 100% of the questions on the corresponding surveys. The symptom burden described using the Indolent Systemic Mastocytosis Symptom Assessment Form (ISM-SAF) to identify the symptoms that are most common, most challenging, and have the greatest impact on quality of life aligns with published data for patients in this survey. Only 24% (n = 13) of ISM patients indicated their disease was well controlled, while 76% of APs indicated greater than 50% of their ISM patients had well-controlled disease (n = 38). Most APs (68%) in the survey indicated they saw one to five ISM patients per year but were comfortable with managing ISM-related symptoms (54%, n = 27). Practice patterns for triage, multidisciplinary management, and shared decision-making are described.

Conclusions: This is the first ISM symptom burden-focused survey to provide a direct comparison of patient responses to those of APs in hematology/oncology and allergy and immunology. Indolent systemic mastocytosis symptom burden measurement and symptom burden reduction remain challenging, with several barriers and gaps identified in this study. The APSHO Toolkit for Systemic Mastocytosis, developed in parallel to this study, provides an AP-focused resource for overcoming some of the barriers and gaps identified in this study.

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