隐性萎缩性表皮松解症(RDEB)中的疼痛:前瞻性表皮松解症纵向评估研究(PEBLES)的发现。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2024-10-11 DOI:10.1186/s13023-024-03349-w
Eunice Jeffs, Elizabeth I Pillay, Lesedi Ledwaba-Chapman, Alessandra Bisquera, Susan J Robertson, John A McGrath, Yanzhong Wang, Anna E Martinez, Jemima E Mellerio
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引用次数: 0

摘要

背景:遗传性皮肤脆性疾病表皮松解症(EB)患者常因皮肤和粘膜损伤、炎症以及粘膜外部位疼痛。EB患者认为疼痛是改善治疗的首要问题:前瞻性 EB 纵向评估研究(PEBLES)是一项前瞻性登记研究,旨在探索 RDEB 从出生到死亡各年龄段的自然史。在此,我们调查了不同 RDEB 亚型的疼痛特征和治疗方法:方法:我们收集了不同 RDEB 亚型患者 8 年来的信息。数据包括背景疼痛和程序性疼痛的视觉模拟量表(VAS)评分、疼痛的部位、强度、对睡眠的影响以及疼痛药物治疗情况。疾病严重程度评分和生活质量测量与疼痛评分相关:61 名参与者(13 名儿童,48 名成人)共完成了 361 次复查。疼痛是一种常见病,93%的参与者在进行指数复查时都会感到疼痛,其中80%的患者同时伴有背景疼痛和手术疼痛。在所有 RDEB 患者中,背景疼痛的 VAS 中位数为 40(满分 100 分)[四分位数范围为 20,60],对于定期更换敷料的患者,程序性疼痛的中位数为 52 [40,80]。严重组(RDEB-S)和瘙痒组(RDEB-Pru)与背景疼痛相比,程序性疼痛的增幅最大,分别为 20 分和 22 分 VAS。在大多数组别中,尤其是在 RDEB-S 组别中,都观察到了疾病严重程度与生活质量受损之间的相关性。超过一半的受试者经常或持续感到疼痛,三分之一的受试者每周至少有四个晚上因疼痛而无法入睡。在所有亚型中,皮肤是最常见的疼痛源,但倒置型 RDEB 除外,其主要疼痛部位是口腔。尽管经常出现剧烈疼痛,但三分之一的参与者没有使用任何止痛药物,而在使用药物的参与者中,疼痛程度仍然很高,这表明目前的止痛方法效果不佳,而且 RDEB 中的大量需求尚未得到满足:结论:所有 RDEB 患者的疼痛频率、严重程度和影响都很大,尤其是 RDEB-S 和 RDEB-Pru。我们的研究结果表明,目前的 RDEB 疼痛治疗效果不佳,需要进一步研究来解决这一症状。
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Pain in recessive dystrophic epidermolysis bullosa (RDEB): findings of the Prospective Epidermolysis Bullosa Longitudinal Evaluation Study (PEBLES).

Background: Pain is common in the genetic skin fragility disorder epidermolysis bullosa (EB), from skin and mucosal injury and inflammation as well as extra-mucocutaneous sites. Individuals living with EB have identified pain as a priority for better treatments.

Objectives: The Prospective EB Longitudinal Evaluation Study (PEBLES) is a prospective register study exploring the natural history of RDEB across all ages from birth to death. Here, we investigated the characteristics and treatment of pain in different RDEB subtypes.

Methods: Information was collected from individuals with different RDEB subtypes over an 8-year period. Data included visual analogue scale (VAS) ratings of background and procedural pain, its location, intensity and impact on sleep, as well as pain medication. Disease severity scores and quality of life measures were correlated to pain scores.

Results: Sixty-one participants (13 children, 48 adults) completed a total of 361 reviews. Pain was common, experienced by 93% of participants at index review, with 80% suffering both background and procedural pain. Across all RDEB patients, the median VAS for background pain was 40 (out of 100) [interquartile range 20,60] and for those having regular dressing changes, median procedural pain was 52 [40,80]. Severe (RDEB-S) and pruriginosa (RDEB-Pru) groups had the greatest increase in procedural compared to background pain of 20 and 22 VAS points, respectively. Correlations between disease severity and quality of life impairment were observed across most groups, particularly RDEB-S. Over half of those studied experienced pain frequently or constantly, and in one third pain disturbed sleep at least 4 nights per week. Skin was the commonest source of pain in all subtypes except inversa RDEB where the mouth was the main site. Despite frequent and severe pain, one third of participants used no medication for pain and, in those that did, pain levels remained high suggesting ineffectiveness of current pain management approaches and a significant unmet need in RDEB.

Conclusion: The frequency, severity, and impact of pain in all RDEB patients is significant, particularly in RDEB-S and RDEB-Pru. Our findings highlight that current RDEB pain management is poorly effective and that further research is needed to address this symptom.

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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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