Ann Dermatol AD Annals of Dermatology 1013-9087 2005-3894 Korean Dermatological Association; The Korean Society for Investigative Dermatology 10.5021/ad.2016.28.1.6 Original Article Quality of Life and Economic Burden in Recessive Dystrophic Epidermolysis Bullosa Jeon In Kyung On Hye Rang Kim Soo-Chan Department of Dermatology, Gangnam Severance Hospital, Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea. Corresponding author: Soo-Chan Kim, Department of Dermatology, Gangnam Severance Hospital, Yonsei University College of Medicine, 211 Eonju-ro, Gangnam-gu, Seoul 06273, Korea. Tel: 82-2-2019-3360, Fax: 82-2-3463-6136, kimsc@yuhs.ac 02 2016 28 01 2016 28 1 6 14 24 10 2014 06 03 2015 27 04 2015 Copyright © 2016 The Korean Dermatological Association and The Korean Society for Investigative Dermatology 2016 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Background

Patients with recessive dystrophic epidermolysis bullosa (RDEB) exhibit blisters and erosions since birth, causing pain, pruritus and various complications. RDEB affects quality of life (QoL) in physical, emotional and social aspects. Furthermore, interminable dressing changes and supportive therapies impose a significant economic burden on the patient's family.

 Objective

We assessed the QoL and economic burden in patients with RDEB.

 Methods

Sixteen patients with RDEB were surveyed to assess the QoL and economic burden. Patients answered questionnaires consisting of a visual analogue scale (VAS) on pain and pruritus, Skindex-29, Quality of Life in EB questionnaire (QOLEB), and the economic burden due to EB.

 Results

Thirteen patients with RDEB completed the questionnaire. Female patients presented higher VAS, QOLEB and total Skindex-29 scores than male patients. Patients with RDEB showed severe levels of pruritus, which was more intolerable than pain. Mean VAS score on pain in RDEB was higher than in oral lichen planus and post-herpetic neuralgia. VAS score on pruritus was similar to those in chronic urticaria, atopic dermatitis, and prurigo nodularis. Compared with other dermatologic conditions, patients with RDEB were profoundly affected in all three scales of skindex-29. Mean "medical cost" in a month was $257.54 (USD) (±169.39) and mean "dressing cost" was $358.41 (USD) (±312.55), which was negatively related to patient age.

 Conclusion

RDEB had a profound impact on QoL and economic burden. Compared with other dermatologic diseases, RDEB showed severe symptoms and QoL was seriously impaired. Most patients sustained economic burdens, especially on preparing dressing materials. Younger patients experienced more economic burdens.

 Dressing Economic burden Quality of life Recessive dystrophic epidermolysis bullosa INTRODUCTION

Epidermolysis bullosa (EB) encompasses a heterogeneous group of inherited skin diseases characterized by blistering and erosion of the skin after minor mechanical trauma or friction. The four major types of EB are defined according to differences in their level of separation within the dermal-epidermal junction on electron microscopy and immunofluorescence mapping: the epidermis in EB simplex (EBS), the lamina lucida in junctional EB (JEB), the sublamina densa in dystrophic EB (DEB), and mixed in Kindler syndrome1.

Recessive DEB (RDEB) is caused by mutations in the COL7A1 gene and is inherited in an autosomal recessive manner. The two major subtypes of RDEB, generalized severe subtype (RDEB-gen sev), previously called Hallopeau-Siemens type, and RDEB generalized intermediate (RDEB-gen intermed) subtype, exhibit generalized blistering, nail dystrophy, ocular and oral involvement, contractures, severe deformities of the hands and feet, as well as multiple extracutaneous impairments1. These physical impairments affect the physical, emotional, and social domains of quality of life (QoL) in patients with RDEB. Several studies on QoL in EB have been reported in the United States, Australia, and Italy2345, meanwhile, studies have yet to evaluate QoL in patients with EB throughout Asia.

Although promising cell-based treatments are under investigation67, treatment of EB mainly relies on supportive therapies (e.g., avoiding trauma, wound dressing, and management of extracutaneous complications). Nevertheless, although interminable dressing changes and supportive therapies impose a significant economic burden on the family members of patients with EB, studies have yet to measure the economic burden thereof8. Accordingly, in this study, we aimed to assess QoL and costs related to treatment in patients with RDEB to obtain a better understanding of the overall burden of EB.

 MATERIALS AND METHODS Study design

This cross-sectional, observational study included patients with RDEB who were diagnosed at the Department of Dermatology, Gangnam Severance Hospital, Seoul, Korea. All diagnoses were confirmed by transmission electron microscopy, immunofluorescence mapping, and mutational analysis. The study was approved by the Institutional Review Board in Gangnam Severance Hospital (3-2012-0028).

Sixteen patients with RDEB were surveyed for QoL and economic burden. Patients were oriented about the questionnaires, and written consents were obtained before the survey. The documents were mailed to the patients who were unable to visit. Completed questionnaires and signed consent forms were returned by mail.

Patients answered questionnaires consisting of the visual analogue scale (VAS) on pain and pruritus, Skindex-29, Quality of Life in EB (QOLEB), and questions addressing economic burden of treatment. Information about accompanying complications, body surface area (BSA) involved, perceived disease severity by patient global assessment (PGA), and days of hospitalization because of EB in the previous year were also obtained. Accompanying complications included infection, poor wound healing, anemia, nutritional problems, growth retardation, esophageal stricture, constipation, eye lesions, dental problems, urinary dysfunction, contractures, nail dystrophy, depression, and others. For children under 7-years old, main caregivers were asked to participate in the survey to answer the questionnaires.

 Measurement tools 1) Visual analogue scale

The VAS has been demonstrated to be a reliable and valid method for measuring pain and pruritus910. Average degrees of daily disease-related pain and pruritus were assessed by a linear 10-score visual analogue scale, ranging from 0 (no symptom) to 10 (intolerable symptom). VAS scores of RDEB were compared to other dermatologic diseases reported in the literature1112131415. VAS differences of 6~10 mm were considered as clinically meaningful16.

 2) Skindex-29

Skindex-29 is a reliable dermatology-specific instrument to measure QoL17. The Korean version of Sindex-29 has been translated and has proven value in evaluating QoL for various dermatologic diseases18192021. The questionnaire included 29 questions consisting of three scales (symptom, functioning, emotional burden). Patients were requested to answer these questions concerning the preceding 4-week period using a 5-point scale. (from never=0, to all the time=4). In each scale, the score was represented as a percentage of the highest score, from 0 to 100; higher values indicate a poor QoL. We also compared Skindex-29 scores of RDEB with other dermatologic diseases reported in the literature22.

 3) QOLEB questionnaire

To our knowledge, this is the first disease-specific QoL tool for EB, and is a valid and reliable measurement tool reflecting the inability of a patient with EB to perform certain tasks4. Patients were asked to answer 17 questions using a 4-point scale (from least=0, to most impact=3).

 4) Patient global assessment

Subjective disease severity perceived by the patients was assessed using PGA, which consists of a 5-point scale (from very mild=0, to very severe=4).

 5) Economic burden

Average monthly expenses for "dressing costs" and "medical costs" were investigated. "Dressing costs" were defined as total expenses for preparing dressings, fixing materials, topical agents, and medicines used during dressing changes. "Medical costs" were defined as other expenses due to EB, excluding "dressing costs".

 6) Dressing burden

To clarify the burden of dressings, additional questions were presented: "Do you experience an economic burden with preparing dressings/fixing materials?"; "How often do you change your dressings?"; "How long does it take to change your dressings?"; "Are specialized dressings/fixing materials better in function than general dressings/fixing materials?"; "What is the most important factor when you purchase dressings/fixing materials?".

 Statistical analysis

Results were expressed as mean±standard deviations. Statistical analysis was performed using SAS software (version 9.1.3; SAS Institute Inc., Cary, NC, USA) using Student's sample t-test, analysis of variance, and Spearman's rank correlation coefficient. p-value<0.05 was considered implying statistical significance.

 RESULTS

Among 16 patients invited, 13 (81.3%) completed the questionnaires. Uncompleted questionnaires were excluded from data analysis.

Patient demographics and subjective disease severity

Basic patient characteristics are summarized in Table 1. Three patients were aged below 7 years and their main caregivers participated in the survey together. Nine patients (69.2%) were male and 4 patients (30.8%) were female. The mean accompanying numbers of complications were 7.77±2.92, with a range of 3 to 12.

According to the EB classification1, 7 patients (53.8%) were RDEB-gen sev, and 6 patients (46.2%) were RDEB-gen intermed. All patients had skin lesions involving more than 30% of BSA. Five patients (38.5%) were hospitalized for more than 7 days because of EB in the previous year, 1 patient (7.7%) for less than 7 days, and 7 patients (53.8%) were not hospitalized at all. Eleven patients (84.6%) perceived their disease as 'very severe' and 2 patients as 'severe' (15.4%).

 QoL results 1) Visual analogue scale

Table 2 shows the VAS, QOLEB and Skindex-29 scores for different clinical variables. Female patients had higher VAS scores in pain and pruritus than male patients. Compared with RDEB-gen intermed, RDEB-gen sev had higher VAS score in pruritus, but had similar VAS scores in pain. VAS scores in pain and pruritus were not significantly different among hospitalization days or between perceived disease severities. Patient age and accompanying complication numbers had no correlation with VAS scores in pain or pruritus.

Compared with other dermatologic diseases, the mean pain scale was higher than for oral lichen planus and herpes zoster (Fig. 1A). The mean pruritus scale was similar to that in chronic urticaria, atopic dermatitis, and prurigo nodularis (Fig. 1B).

 2) Skindex-29

The mean score was 86.31±10.38 on the symptoms scale, 75.23±15.76 in emotions, and 76.69±12.09 in functioning (Table 2). Male patients had higher scores in symptoms, and female patients presented higher scores in emotions and functioning; however, these results were not statistically significant. Skindex-29 was not significantly different among the hospitalization days or between EB subtypes. On the function scale, patients with perceived disease severity of 'very severe' reported significantly higher scores than those with 'severe' (p<0.05). Patient age and accompanying complication numbers had no correlation with Skindex-29. Compared with other dermatologic conditions, patients with RDEB were profoundly affected in all three scales of Skindex-29 (Table 3).

 3) QOLEB

Mean QOLEB score was 26.62±7.61 (Table 2). Higher scores were observed for female patients, patients with hospitalization days greater than 7 days, and RDEB-gen sev subtype; these results were not statistically significant. Patients with perceived disease severity of 'very severe' reported significantly higher scores than that of 'severe' (p<0.05). Patient age and accompanying complication numbers had no correlation with QOLEB.

 4) Economic burden

Table 4 shows the "medical costs" and "dressing costs" for different clinical variables. "Dressing costs" were greater than "medical costs": the mean monthly "medical cost" was $257.53±169.39 (USD); the mean monthly "dressing cost" was $358.41±312.55(USD). The mean monthly total cost was $615.97±32.09 (USD). Patients with hospitalization days greater than 7 days and RDEB-gen sev subtype spent more on "medical costs" and "dressing costs" than did other patients. "Medical costs" and "dressing costs" were negatively related to patient age (Spearman rho=–0.68, p=0.01 and Spearman rho=–0.56, p=0.049), representing a statistically meaningful correlation. Perceived disease severities and accompanying complication numbers had no correlation with economic burden. "Medical costs" and "dressing costs" had no correlation with VAS, QOLEB, and Skindex-29.

 5) Dressing burden

Regarding additional questions about the burden of dressings, 7 patients (53.8%) answered that they have experienced an economic burden on dressing materials "always", and 3 (23.1%) answered "often" (Fig. 2A). Regarding dressing change frequency, 7 patients (53.8%) changed the dressing every day and 4 patients (30.8%) changed three times a week (Fig. 2B). Seven patients (53.8%) answered that they require 1~2 hours to change the dressings and 4 (30.8%) required less than 1 hour (Fig. 2C).

Eleven patients (84.6%) answered that specialized dressings are better or much better in function than general dressings (Fig. 2D). Price was the most important factor (38.5%) when purchasing dressings, followed by pain during dressing change (30.8%) (Fig. 2E). Regarding fixing materials, 12 patients (92.3%) answered that specialized fixing materials are better than general fixing materials (Fig. 2F). Price (38.5%) and fixing ability (38.5%) were two important factors considered when selecting fixing materials (Fig. 2G).

 DISCUSSION

The present study evaluated the QoL and economic burden of patients with RDEB. To our knowledge, this study is the first to assess the economic burden of EB and to evaluate the QoL of patients with RDEB in Asia.

The female sex is reportedly correlated with QoL and psychological morbidity8, reported in EB as well as in other dermatological diseases523. In the present study, female patients presented higher VAS, QOLEB, and total Skindex-29 scores than male patients. While VAS scores were more severe in females, symptom scores on the Skindex-29 scale were higher in males. VAS assesses symptoms according to severity, whereas Skindex-29 evaluates symptoms according to frequency. QOLEB also evaluates pain according to frequency. Notwithstanding, Frew et al.4 suggested that VAS is more accurate for actual assessment of pain and pruritus. Moreover, VAS is easy and quick to perform, and could be useful during consultation of patients with for accurate symptom management.

Compared to other dermatologic diseases in the literature, the patients with RDEB included in this study suffered from more severe pain: VAS scores on pain were higher for RDEB than in oral lichen planus and post-herpetic neuralgia. Meanwhile, Fine et al.24 reported that severe levels of pain were most often seen in JEB-Herlitz type and RDEB Hallopeau–Siemens type. However, in the present study, VAS scores on pain were similar between RDEB-gen intermed and RDEB-gen sev subtypes. Additionally, compared with other dermatologic diseases, patients with RDEB showed higher Skindex-29 scores in all three scales, further reflecting the disease burden of RDEB. Compared with a previous survey of patients with EB in Italy5, Skindex-29 scale scores for RDEB were higher in our study; however, the previous survey seems to have enrolled more participants with a milder phenotype than the present did: all patients in the present study had skin involvement greater than 30% patients who had more than 30% skin involvement in the Italian study showed higher symptom. Seven scale scores than the other patients in the study. Nevertheless, the present study still showed higher Skindex-29 scores. This discrepancy could be related to different cultural backgrounds concerning symptoms, emotions, and social relationships between Asian and Western countries.

Pruritus is a common symptom among patients with EB. Nevertheless, the etiology of pruritus in these patients is unknown. Abnormal chronic skin inflammation, overheating caused by dressings, dry skin, healing wounds, and weather are potential contributing factors225. Pruritus has been reported to be the biggest concern of patients with EB, followed by pain2. In our study, patients with RDEB showed severe pruritus. VAS scores for pruritus among patients with RDEB were similar to those for chronic urticaria, atopic dermatitis, and prurigo nodularis. However, among these, pruritus in EB would be more influential to QoL, as it usually starts at birth or early childhood, lasts the lifetime of the patient, and scarcely shows satisfactory responses to medication.

Herein, we hypothesized that patients with the severe subtype, RDEB-gen sev, would show greater impairment in QoL than those with other subtypes. However, patients with RDEB subtypes showed no significant differences in QoL. In a previous report5, Sindex-29 also showed no significant differences between the types or subtypes of EB. This could be explained by heterogeneity within the disease8. Notwithstanding, in our study, other objective indices (hospitalization days, number of accompanying complications) also showed no significant differences in QoL. Meanwhile, perceived disease severity according to patient global assessment was significantly associated with QOLEB scores and Skindex-29 scores. Although establishing a causal relationship was not possible in this observational, cross-sectional study, impairments in daily activity and social relationships might have considerable influence when patients with EB recognize their disease.

In this study, we also assessed economic burden. Most patients reported economic burdens related to preparing dressing materials. "Dressing costs" were higher than "medical costs," demonstrating that dressings are the main cause of economic burdens in patients with RDEB. In the present study, patients reported using various kinds of general and special dressings/fixing materials. Many stated that specialized dressings/fixing materials were better than general dressings/fixing materials with regards to functional aspects. Nevertheless, in addition to their functional aspects, the price of dressing materials also considerably influenced patients' decisions to purchase one material over another. In Korea, specialized dressing materials are not covered by insurance, although three sheets of specialized dressings weekly are covered by insurance for patients with JEB or DEB. Patients with a "rare and incurable disease," including those with RDEB, are responsible for 10% of their total expenses. For instance, patients with RDEB are covered for three sheets of Mepilex lite (Mölnlycke Health Care, Göteborg, Sweden) 20×50 cm for approximately $14 (USD) weekly. However, total monthly "dressing costs" are much more expensive for patients with RDEB because they usually require numerous sheets of dressing material across the whole body. Most patients change the dressings every day or every other day, imposing a tremendous economic burden.

As skin lesions enlarge, higher economic burden from dressing materials is incurred. As all participants in this study had skin lesions larger than 30%, comparing "dressing costs" according to the involved BSA was not possible. Moreover, blisters and erosions can occur at any area of the skin in patients with EB; therefore, investigating accurate area involvement was not feasible. The BSA of infants or children is smaller than in adults; thus, they are expected to incur lower expenses than adults. Interestingly, however, younger patients in this study accrued more "dressing costs" and "medical costs" than those incurred by adults. In infancy and early childhood, physical adjustment ability has not developed fully, and self-induced mechanical trauma occurs more frequently, making it difficult to maintain dressings. Moreover, secondary complications due to skin barrier disruptions and immunologic immaturity might increase the "medical costs" in younger patients with RDEB. Furthermore, older patients would be expected to have milder phenotypes than others who have died from their disease.

There are several limitations to our study. First, there is the potential for selection bias because our study was conducted at a single institute; our sample may not represent the general population with EB. Nevertheless, our institute is the only institute that can perform laboratory diagnosis of EB; almost all patients in Korea with EB are referred to our institute. Second, the small sample size of this study also acts as a limitation, although incidence of RDEB is very low. Third, patients with severe RDEB were over-represented because these patients are usually referred to our institute. Indeed, all patients included in this study had skin lesions involving more than 30% of their body surface area and averaged seven complications. Fourthly, the main caregivers of children under 7 years old completed the questionnaire. Their answers, which cannot be taken to represent the actual QoL of the children, were also included for analysis. Finally, the potential for recall bias exists in this questionnaire-based study.

In conclusion, RDEB had a profound impact on QoL and economic burden. The present study could help expand the understanding of QoL and economic burden associated with RDEB, and in turn, better meet the needs of patients with this disease.

 Fine JD Bruckner-Tuderman L Eady RA Bauer EA Bauer JW Has C Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification J Am Acad Dermatol 2014 70 1103 1126 van Scheppingen C Lettinga AT Duipmans JC Maathuis CG Jonkman MF Main problems experienced by children with epidermolysis bullosa: a qualitative study with semi-structured interviews Acta Derm Venereol 2008 88 143 150 Frew JW Murrell DF Quality of life measurements in epidermolysis bullosa: tools for clinical research and patient care Dermatol Clin 2010 28 185 190 Frew JW Martin LK Nijsten T Murrell DF Quality of life evaluation in epidermolysis bullosa (EB) through the development of the QOLEB questionnaire: an EB-specific quality of life instrument Br J Dermatol 2009 161 1323 1330 Tabolli S Sampogna F Di Pietro C Paradisi A Uras C Zotti P Quality of life in patients with epidermolysis bullosa Br J Dermatol 2009 161 869 877 Wagner JE Ishida-Yamamoto A McGrath JA Hordinsky M Keene DR Woodley DT Bone marrow transplantation for recessive dystrophic epidermolysis bullosa N Engl J Med 2010 363 629 639 Conget P Rodriguez F Kramer S Allers C Simon V Palisson F Replenishment of type VII collagen and re-epithelialization of chronically ulcerated skin after intradermal administration of allogeneic mesenchymal stromal cells in two patients with recessive dystrophic epidermolysis bullosa Cytotherapy 2010 12 429 431 Pagliarello C Tabolli S Factors affecting quality of life in epidermolysis bullosa Expert Rev Pharmacoecon Outcomes Res 2010 10 329 338 Lundqvist C Benth JS Grande RB Aaseth K Russell MB A vertical VAS is a valid instrument for monitoring headache pain intensity Cephalalgia 2009 29 1034 1041 Reich A Heisig M Phan NQ Taneda K Takamori K Takeuchi S Visual analogue scale: evaluation of the instrument for the assessment of pruritus Acta Derm Venereol 2012 92 497 501 Mansourian A Momen-Heravi F Saheb-Jamee M Esfehani M Khalilzadeh O Momen-Beitollahi J Comparison of aloe vera mouthwash with triamcinolone acetonide 0.1% on oral lichen planus: a randomized double-blinded clinical trial Am J Med Sci 2011 342 447 451 Park J Jang WS Park KY Li K Seo SJ Hong CK Thermography as a predictor of postherpetic neuralgia in acute herpes zoster patients: a preliminary study Skin Res Technol 2012 18 88 93 Aydogan K Karadogan SK Tunali S Saricaoglu H Narrowband ultraviolet B (311 nm, TL01) phototherapy in chronic ordinary urticaria Int J Dermatol 2012 51 98 103 Chrostowska-Plak D Reich A Szepietowski JC Relationship between itch and psychological status of patients with atopic dermatitis J Eur Acad Dermatol Venereol 2013 27 e239 e242 Ständer S Siepmann D Herrgott I Sunderkötter C Luger TA Targeting the neurokinin receptor 1 with aprepitant: a novel antipruritic strategy PLoS One 2010 5 e10968 Arenberger P Arenbergerová M Drozenová H Hladíková M Holcová S Effect of topical heparin and levomenol on atopic dermatitis: a randomized four-arm, placebo-controlled, double-blind clinical study J Eur Acad Dermatol Venereol 2011 25 688 694 Nijsten T Dermatology life quality index: time to move forward J Invest Dermatol 2012 132 11 13 Ahn BK Lee SJ Namkoong K Chung YL Lee SH The Korean version of skindex-29 Korean J Dermatol 2004 42 9 15 Ahn BK Lee SJ Namkoong K Chung YL Lee SH Quality of life of acne patients Korean J Dermatol 2005 43 6 14 Ryu JH Kim KH Kim KJ Kim SJ Quality of life in patients with psoriasis Korean J Dermatol 2004 42 264 271 Han SH Byun JW Lee WS Kang H Kye YC Kim KH Quality of life assessment in male patients with androgenetic alopecia: result of a prospective, multicenter study Ann Dermatol 2012 24 311 318 Klein R Moghadam-Kia S Taylor L Coley C Okawa J LoMonico J Quality of life in cutaneous lupus erythematosus J Am Acad Dermatol 2011 64 849 858 Sampogna F Picardi A Chren MM Melchi CF Pasquini P Masini C Association between poorer quality of life and psychiatric morbidity in patients with different dermatological conditions Psychosom Med 2004 66 620 624 Fine JD Johnson LB Weiner M Suchindran C Assessment of mobility, activities and pain in different subtypes of epidermolysis bullosa Clin Exp Dermatol 2004 29 122 127 Pope E Lara-Corrales I Mellerio J Martinez A Schultz G Burrell R A consensus approach to wound care in epidermolysis bullosa J Am Acad Dermatol 2012 67 904 917 Visual analogue scale (VAS) in (A) pain and (B) pruritus. VAS differences of 6~10 mm are considered as clinically meaningful. (A) The mean pain scale in recessive dystrophic epidermolysis bullosa (RDEB) is higher than in oral lichen planus and herpes zoster (post-herpetic neuralgia). (B) The mean pruritus scale is similar to that in chronic urticaria, atopic dermatitis, and prurigo nodularis. Questions and answers about economic burden and dressing materials. (A) Seven patients answer that they experienced economic burden on dressing materials "always", and 3 patients answered "often". (B) Seven patients change the dressing every day, and 4 patients change three times a week. (C) Seven patients answer that they require 1~2 hours to change their dressings, and 4 patients answered less than 1 hour. (D) Eleven patients (84.6%) answer that specialized dressings are better or much better in function than general dressings. (E) Price is the most important factor when purchasing dressings, followed by pain during dressing change. (F) Regarding fixing materials, 12 patients answer that the specialized fixing materials are better than general fixing materials. (G) Price and fixing ability are two important factors when selecting fixing materials. Basic patient characteristics
Clinical variable Result
Total case 13
Age (yr) 21.57±17.61
Gender
 Male 9 (69.2)
 Female 4 (30.8)
Complication 7.77±2.92 (3~12)
EB subtype
 RDEB-gen sev 7 (53.8)
 RDEB-gen intermed 6 (46.2)
Area of body surface involved (%)
 >30 13 (100)
 10~30 0 (0)
 <10 0 (0)
Hospitalization due to EB in the last year (d)
 >7 5 (38.5)
 ≤7 1 (7.7)
 0 7 (53.8)
PGA
 Very severe 11 (84.6)
 Severe 2 (15.4)
 Moderate 0 (0)
 Mild 0 (0)
 Very mild 0 (0)

Values are presented as mean±standard deviation (range) or number (%). EB: epidermolysis bullosa, RDEB: recessive dystrophic EB, RDEB-gen sev: RDEB generalized severe, RDEB-gen intermed: RDEB generalized intermediate, PGA: perceived disease severity.

 Quality of life results
Clinical variable VAS QOLEB Skindex-29
Pain Pruritus Symptom Emotion Function
Total cases (n=13) 6.54±1.56 7.54±2.07 26.62±7.61 86.31±10.38 75.23±15.76 76.69±12.09
Gender
 Male (n=4) 5.75±0.95 6.75±2.63 25.75±8.22 90.00±14.21 65.00±20.94 75.00±17.68
 Female (n=9) 6.88±1.69 7.88±1.83 27.44±7.78 84.67±8.72 79.78±11.51 77.44±10.00
Hospitalization due to EB in the last year (d)
 0 (n=7) 6.57±1.39 7.14±2.27 25.14±7.35 80.71±10.67 79.14±10.38 77.71±12.22
 ≤7 (n=1) 6 10 25 91 94 88
 >7 (n=5) 6.60±2.07 7.60±1.82 29.80±8.70 93.20±5.72 66.00±19.02 73.00±12.81
EB subtype
 RDEB-gen sev (n=7) 6.57±1.72 8.00±1.29 30.14±8.82 90.57±8.96 70.29±17.41 79.00±14.19
 RDEB-gen intermed (n=6) 6.50±1.52 7.00±2.76 23.17±3.76 81.33±10.35 81.00±12.57 74.00±9.65
Perceived disease severity
 Very severe (n=11) 6.54±1.69 7.54±2.25 28±7.82* 86.72±10.39 78.54±13.97 79.54±10.82*
 Severe (n=2) 6.50±0.71 7.50±0.71 21* 84.00±14.14 57.00±15.55 61.00±1.41*

Values are presented as mean±standard deviation. VAS: visual analogue scale, QOLEB: quality of life in EB questionnaire, EB: epidermolysis bullosa, RDEB: recessive dystrophic EB, RDEB-gen sev: RDEB generalized severe, RDEB-gen intermed: RDEB generalized intermediate. *p<0.05.

 RDEB versus other skin conditions (Skindex-29)
Clinical variable Sample size Symptom Emotion Function
RDEB 13 86 (10) 75 (16) 77 (12)
Other skin condition22
 Dermatomyositis 22 42 (25) 45 (27) 28 (29)
 Vulvodynia 280 50 (17) 50 (20) 44 (22)
 Psoriasis 44 42 (21) 39 (27) 23 (27)
 Eczema 102 48 (23) 41 (27) 26 (26)
 Acne vulgaris 63 30 (19) 41 (25) 16 (16)
 Alopecia 7 31 (24) 27 (33) 14 (23)
 Rosacea 29 33 (20) 33 (20) 16 (18)
 Without skin disease 107 14 (2) 9 (13) 4 (8)

Values are presented as mean (standard deviation). RDEB: recessive dystrophic epidermolysis bullosa.

 Economic burden of RDEB patients in a month
Clinical variable Medical cost (USD) Dressing cost (USD)
Total case (n=13) 257.54±169.39 (93~465) 358.41±312.55 (93~930)
Gender
 Male (n=4) 267.40±229.00 488.30±411.60
 Female (n=9) 253.20±152.70 300.70±266.10
Hospitalization due to EB in the last year (d)
 0 (n=7) 219.21±148.79 273.69±298.32
 ≤7 (n=1) 46.50 93.00
 >7 (n=5) 353.40±166.36 503.10±304.21
EB subtype
 RDEB-gen sev (n=7) 298.90±177.80 431.80±299.80
 RDEB-gen intermed (n=6) 209.30±160.40 272.80±332.00

Values are presented as mean±standard deviation (range). RDEB: recessive dystrophic EB, EB: epidermolysis bullosa, RDEB-gen sev: RDEB generalized severe, RDEB-gen intermed: RDEB generalized intermediate, USD: United States Dollar.