'…completely exhausted and weak, really drained.': a multinational qualitative interview study of healthcare provider, patient, and caregiver experiences of C3 glomerulopathy and primary (idiopathic) immune complex membranoproliferative glomerulonephritis diagnosis, burden and management.

IF 2.9
Frontiers in nephrology Pub Date : 2026-05-22 eCollection Date: 2026-01-01 DOI:10.3389/fneph.2026.1770706
Sayna Norouzi, Mingyi Huang, Carly Rich, Katie Gordon, Lucia Quintana-Gallardo, Ryan Naylor, Mona Amet, Laura Mirams, Elizabeth Holdsworth, Fernando Caravaca-Fontán
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Abstract

Introduction: C3 glomerulopathy (C3G) and primary (idiopathic) immune complex membranoproliferative glomerulonephritis (IC-MPGN) are rare progressive kidney diseases. Due to the rare nature of C3G/primary IC-MPGN, there is a paucity of real-world data on the diagnosis, management, and impact of the diseases on patients and caregivers. Our study used the direct experiences of healthcare professionals (HCPs), patients, and caregivers, to provide insight into the diagnosis/management of C3G/primary IC-MPGN and its burden on patients and caregivers.

Methods: We conducted a multi-country, cross-sectional, semi-structured, qualitative interview study with HCPs, patients, and caregivers in France, Germany, Italy, Spain, the United Kingdom and the United States between July 2024-January 2025. Nephrologists or internal medicine specialists (France and Spain only) were eligible to participate if they managed at least one patient with a biopsy-confirmed C3G/primary IC-MPGN diagnosis. Patients and informal caregivers were recruited via HCPs, patient advocacy groups, online panels or social media and had to be aged ≥16 years and ≥18 years respectively. Thematic analysis was conducted to identify key response themes.

Results: A total of 21 HCPs, 13 patients, and 8 caregivers were interviewed. HCPs and patients highlighted that milder symptoms often led to diagnostic delays with HCPs highlighting lack of disease recognition, difficulties accessing specialist care, and patient reluctance to receive a biopsy as barriers to timely diagnosis. Mental and physical fatigue/exhaustion were the most burdensome symptoms according to patients and caregivers, impacting all aspects of the patient's life. Patients stated that achieving disease stability was a key goal of treatment, however HCPs, patients, and caregivers all stated that treatment options at survey (prior to approval of iptacopan and pegcetacoplan) were limited, with dialysis being particularly burdensome to patients. HCPs were hopeful about future treatment options. Caregivers reported that they provided physical and psychological support and advocated for their patient. Caregiving had a substantial impact on the caregiver's mental wellbeing.

Conclusions: Overall, C3G/primary IC-MPGN presented a substantial burden to patients and caregivers, with a need for timely diagnosis, psychological support for patients and caregivers, improved HCP-patient communication, and treatments which target the cause of C3G/primary IC-MPGN to stabilize the disease.

“……完全筋疲力尽,真的筋疲力尽。一项针对C3肾小球病变和原发性(特发性)免疫复合物膜增生性肾小球肾炎诊断、负担和管理的医疗保健提供者、患者和护理人员经验的跨国定性访谈研究。
C3肾小球病(C3G)和原发性(特发性)免疫复合物膜增殖性肾小球肾炎(IC-MPGN)是罕见的进行性肾脏疾病。由于C3G/原发性IC-MPGN的罕见性质,缺乏有关该疾病的诊断、管理以及对患者和护理人员的影响的真实数据。我们的研究使用了医疗保健专业人员(HCPs)、患者和护理人员的直接经验,以深入了解C3G/原发性IC-MPGN的诊断/管理及其对患者和护理人员的负担。方法:我们在2024年7月至2025年1月期间对法国、德国、意大利、西班牙、英国和美国的医护人员、患者和护理人员进行了一项多国、横断面、半结构化、定性访谈研究。肾内科医生或内科专家(仅限法国和西班牙)如果治疗了至少一名活检证实的C3G/原发性IC-MPGN诊断的患者,则有资格参加研究。患者和非正式护理人员通过HCPs、患者倡导团体、在线小组或社交媒体招募,年龄分别≥16岁和≥18岁。进行了专题分析,以确定关键的应对主题。结果:共访谈21名HCPs、13名患者和8名护理人员。HCPs和患者强调,较轻的症状往往导致诊断延迟,HCPs强调缺乏疾病识别、难以获得专科护理以及患者不愿接受活检是及时诊断的障碍。根据患者和护理人员的说法,精神和身体疲劳/疲惫是最繁重的症状,影响患者生活的各个方面。患者表示,实现疾病稳定性是治疗的关键目标,然而,HCPs、患者和护理人员都表示,在调查中(在批准伊普他科泮和pegcetacoplan之前),治疗选择有限,透析对患者来说尤其繁重。HCPs对未来的治疗方案充满希望。护理人员报告说,他们提供了身体和心理上的支持,并为他们的病人辩护。照顾对照顾者的心理健康有实质性的影响。结论:总体而言,C3G/原发性IC-MPGN给患者和护理人员带来了沉重的负担,需要及时诊断,为患者和护理人员提供心理支持,改善医患沟通,针对C3G/原发性IC-MPGN的病因进行治疗,以稳定病情。
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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