St. John's Institute of Dermatology , Guy's and St Thomas' NHS Foundation Trust, London, UK.
Department of Population Health Sciences, King's College London, London, UK.
Orphanet J Rare Dis. 2024 Oct 11;19(1):375. doi: 10.1186/s13023-024-03349-w.
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.
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.
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.
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.
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.
疼痛在遗传性皮肤脆弱性疾病大疱性表皮松解症(EB)中很常见,可由皮肤和黏膜损伤及炎症以及黏膜外部位引起。患有 EB 的个体将疼痛确定为更好治疗的优先事项。
前瞻性 EB 纵向评估研究(PEBLES)是一项前瞻性登记研究,探索从出生到死亡的所有年龄段 RDEB 的自然史。在这里,我们研究了不同 RDEB 亚型的疼痛特征和治疗方法。
在 8 年的时间里,从不同 RDEB 亚型的个体收集信息。数据包括背景和程序疼痛的视觉模拟量表(VAS)评分、其位置、强度以及对睡眠的影响,以及疼痛药物。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 名成年人)完成了总共 361 次复查。疼痛很常见,索引复查时 93%的参与者有疼痛,80%的参与者同时患有背景疼痛和程序疼痛。在所有 RDEB 患者中,背景疼痛的中位数 VAS 为 40(满分 100)[20,60],而对于那些定期换衣的患者,程序疼痛的中位数为 52[40,80]。严重型(RDEB-S)和瘙痒型(RDEB-Pru)组在程序疼痛方面的增加最大,分别为 20 和 22 VAS 点。在大多数组中观察到疾病严重程度和生活质量受损之间的相关性,尤其是 RDEB-S。超过一半的研究对象经常或持续感到疼痛,三分之一的人每周至少有 4 个晚上因疼痛而睡眠受到干扰。除了反转型 RDEB 以外,皮肤是所有亚型中疼痛的最常见来源,在反转型 RDEB 中,口腔是主要部位。尽管疼痛频繁且严重,但三分之一的参与者没有使用任何药物治疗疼痛,而在使用药物的参与者中,疼痛水平仍然很高,这表明目前的疼痛管理方法效果不佳,RDEB 存在显著的未满足需求。
所有 RDEB 患者的疼痛频率、严重程度和影响都很显著,尤其是 RDEB-S 和 RDEB-Pru。我们的发现强调,目前 RDEB 的疼痛管理效果不佳,需要进一步研究来解决这一症状。