Patient and caregiver experiences with a patient-support program for setmelanotide treatment of patients with Bardet-Biedl syndrome.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Ilja Finkelberg, Ioanna M Polichronidou, Tom Hühne, Pia Brensing, Sinem Karaterzi, Johannes Jaegers, Anja Gäckler, Lars Pape, Metin Cetiner
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引用次数: 0

Abstract

Background: Bardet-Biedl syndrome (BBS) is a rare genetic disease caused by impaired cilium function and characterized by a plethora of symptoms, including hyperphagia and early-onset obesity, that negatively affect patient and caregiver quality of life. Here, we assessed real-world patient expectations and experiences before and during treatment with setmelanotide, a melanocortin-4 receptor agonist shown to reduce hunger and body weight in patients with BBS.

Methods: An online survey was conducted to capture the real-world experience of patients with BBS and their caregivers regarding setmelanotide treatment and the use of a specialist nurse support service aimed at educating patients and their caregivers, and enabling them to administer injections independently. The survey was administered between January 2024 and May 2024 to participants who began treatment between June 2023 and December 2023 at a single center in Germany.

Results: Of the 35 respondents, 10 were pediatric patients, 13 were adult patients, and 12 were caregivers. Prior to treatment, the most commonly reported symptoms by pediatric patients and caregivers were insatiable hunger (80% and 83%, respectively) and obesity (50% and 92%, respectively); for adult patients, key symptoms were vision loss (92%) and obesity (69%). Setmelanotide reduced feelings of insatiable hunger and had a positive effect on body weight: ≥ 92% of respondents across survey groups reported feeling less hunger, feeling satiated after meals, and a stable body weight or weight loss (mean BMI z-score ± SD at start: 3.12 ± 0.89, change after 6 months: -0.47 ± 0.37). Improvements in mobility, mood, and behavior were also reported. The specialist nurse support service was rated excellent by all respondents. The personalized approach contributed to high patient and caregiver satisfaction, enabled most of them to administer the drug independently, and ensured high treatment adherence, without any patients discontinuing setmelanotide treatment.

Conclusion: Based on this real-world survey of patients with BBS and their caregivers, setmelanotide improved key symptoms related to insatiable hunger and obesity. Personalized multidimensional nursing support at the start of treatment can help address unmet support needs in BBS and may contribute to high rates of treatment satisfaction and adherence.

患者和护理人员对setmelanotide治疗Bardet-Biedl综合征患者的患者支持计划的经验。
背景:Bardet-Biedl综合征(BBS)是一种罕见的遗传性疾病,由纤毛功能受损引起,其特征是大量的症状,包括贪食和早发性肥胖,对患者和护理者的生活质量产生负面影响。在这里,我们评估了现实世界患者在使用setmelanotide之前和期间的期望和体验,setmelanotide是一种黑素皮质素-4受体激动剂,可以减少BBS患者的饥饿感和体重。方法:通过一项在线调查,收集BBS患者及其护理人员关于setmelanotide治疗的真实体验,并使用专业护士支持服务,旨在教育患者及其护理人员,使他们能够独立进行注射。该调查于2024年1月至2024年5月在德国的一个中心进行,参与者于2023年6月至2023年12月开始接受治疗。结果:35名受访者中,10名儿童患者,13名成人患者,12名护理人员。在治疗前,儿科患者和护理人员最常报告的症状是无法满足的饥饿(分别为80%和83%)和肥胖(分别为50%和92%);成人患者的主要症状是视力下降(92%)和肥胖(69%)。Setmelanotide减少了无法满足的饥饿感,并对体重有积极影响:研究组中≥92%的受访者报告饥饿感减少,饭后感到饱腹,体重稳定或体重减轻(开始时平均BMI z-score±SD: 3.12±0.89,6个月后的变化:-0.47±0.37)。在行动能力、情绪和行为方面也有改善。专家护士支持服务被所有受访者评为优秀。个性化方法有助于提高患者和护理人员的满意度,使他们中的大多数人能够独立给药,并确保高治疗依从性,没有任何患者停止setmelanotide治疗。结论:基于对BBS患者及其护理人员的真实世界调查,setmelanotide改善了与无法满足的饥饿和肥胖相关的关键症状。治疗开始时的个性化多维护理支持可以帮助解决BBS患者未满足的支持需求,并有助于提高治疗满意度和依从性。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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