A systematic literature review of the disease burden in patients with recessive dystrophic epidermolysis bullosa

被引:50
|
作者
Tang, Jean Yuh [1 ]
Marinkovich, M. Peter [1 ]
Lucas, Eleanor [2 ]
Gorell, Emily [1 ]
Chiou, Albert [1 ]
Lu, Ying [1 ]
Gillon, Jodie [3 ]
Patel, Dipen [2 ]
Rudin, Dan [3 ]
机构
[1] Stanford Univ, Dept Dermatol, Sch Med, 291 Campus Dr, Stanford, CA 94305 USA
[2] Pharmerit OPEN Hlth Co, 4350 East West Highway,Suite 1100, Bethesda, MD 20814 USA
[3] Abeona Therapeut Inc, 1330 Ave Amer, New York, NY 10019 USA
关键词
Recessive dystrophic epidermolysis bullosa; Burden of disease; Systematic literature review; QUALITY-OF-LIFE; SQUAMOUS-CELL CARCINOMA; GASTROINTESTINAL COMPLICATIONS; VENTRICULAR DYSFUNCTION; DILATED CARDIOMYOPATHY; CUMULATIVE EXPERIENCE; ESOPHAGEAL STRICTURES; NATURAL-HISTORY; AORTIC DILATION; CHILDREN;
D O I
10.1186/s13023-021-01811-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background/objectiveRecessive dystrophic epidermolysis bullosa (RDEB) is a genetic collagen disorder characterized by skin fragility leading to blistering, wounds, and scarring. There are currently no approved curative therapies. The objective of this manuscript is to provide a comprehensive literature review of the disease burden caused by RDEB.MethodsA systematic literature review was conducted in MEDLINE and Embase in accordance with PRISMA guidelines. Observational and interventional studies on the economic, clinical, or humanistic burden of RDEB were included.ResultsSixty-five studies were included in the review. Patients had considerable wound burden, with 60% reporting wounds covering more than 30% of their body. Increases in pain and itch were seen with larger wound size. Chronic wounds were larger and more painful than recurrent wounds. Commonly reported symptoms and complications included lesions and blistering, anemia, nail dystrophy and loss, milia, infections, musculoskeletal contractures, strictures or stenoses, constipation, malnutrition/nutritional problems, pseudosyndactyly, ocular manifestations, and dental caries. Many patients underwent esophageal dilation (29-74%; median dilations, 2-6) and gastrostomy tube placement (8-58%). In the severely affected population, risk of squamous cell carcinoma (SCC) was 76% and mortality from SCC reached 84% by age 40. Patients with RDEB experienced worsened quality of life (QOL), decreased functioning and social activities, and increased pain and itch when compared to other EB subtypes, other skin diseases, and the general population. Families of patients reported experiencing high rates of burden including financial burden (50-54%) and negative impact on private life (79%). Direct medical costs were high, though reported in few studies; annual payer-borne total medical costs in Ireland were $84,534 and annual patient-borne medical costs in Korea were $7392. Estimated annual US costs for wound dressings ranged from $4000 to $245,000. Patients spent considerable time changing dressings: often daily (13-54% of patients) with up to three hours per change (15-40%).ConclusionPatients with RDEB and their families/caregivers experience significant economic, humanistic, and clinical burden. Further research is needed to better understand the costs of disease, how the burden of disease changes over the patient lifetime and to better characterize QOL impact, and how RDEB compares with other chronic, debilitating disorders.
引用
收藏
页数:25
相关论文
共 50 条
  • [31] Oral lesions in recessive dystrophic epidermolysis bullosa
    Serrano-Martínez, MC
    Bagán, JV
    Silvestre, FJ
    Viguer, MT
    ORAL DISEASES, 2003, 9 (05) : 264 - 268
  • [32] DIGESTIVE INVOLVEMENT IN DYSTROPHIC RECESSIVE EPIDERMOLYSIS BULLOSA
    FORTIERBEAULIEU, M
    DEPROST, Y
    ARCHIVES OF DERMATOLOGY, 1988, 124 (12) : 1870 - 1870
  • [33] THERAPEUTIC CONSIDERATIONS IN RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA
    BAUER, EA
    COOPER, TW
    ARCHIVES OF DERMATOLOGY, 1981, 117 (09) : 529 - 530
  • [35] ALTERED COLLAGENASE IN RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA
    BAUER, EA
    CLINICAL RESEARCH, 1977, 25 (03): : A461 - A461
  • [36] CARDIOVASCULAR FINDINGS IN RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA
    Jefferies, John L.
    Towbin, Jeffrey
    Ryan, Thomas
    Lucky, Anne
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2013, 61 (10) : E589 - E589
  • [37] Identification of isomiRs in recessive dystrophic epidermolysis bullosa
    Zauner, R.
    Wimmer, M.
    Lettner, T.
    Niklas, N.
    Atzmueller, S.
    Reichelt, J.
    Bauer, J. W.
    Wally, V.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2016, 136 (09) : S187 - S187
  • [38] Gene Therapy for Recessive Dystrophic Epidermolysis Bullosa
    Titeux, Matthias
    Pendaries, Valerie
    Hovnanian, Alain
    DERMATOLOGIC CLINICS, 2010, 28 (02) : 361 - +
  • [39] Epidermolysis Bullosa Nevus in a Patient With Recessive Dystrophic Epidermolysis Bullosa: A Case Report
    Fening, Katherine
    Theos, Amy
    Andea, Aleodor
    Vincent, Bethaney
    Busam, Klaus
    McKay, Kristopher
    AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2014, 36 (12) : E194 - E197
  • [40] Somatic mosaic recessive dystrophic epidermolysis bullosa
    Shipman, A. R.
    Halpern, J.
    Lai-Cheong, J. E.
    McGrath, J. A.
    Heagerty, A. H. M.
    BRITISH JOURNAL OF DERMATOLOGY, 2012, 167 : 25 - 25