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
  • [1] A systematic literature review of the disease burden in patients with recessive dystrophic epidermolysis bullosa
    Jean Yuh Tang
    M. Peter Marinkovich
    Eleanor Lucas
    Emily Gorell
    Albert Chiou
    Ying Lu
    Jodie Gillon
    Dipen Patel
    Dan Rudin
    Orphanet Journal of Rare Diseases, 16
  • [2] THE ECONOMIC AND HUMANISTIC BURDEN OF DYSTROPHIC EPIDERMOLYSIS BULLOSA (DEB): A SYSTEMATIC LITERATURE REVIEW
    Harricharan, S.
    Richard, M. E.
    Roman, J.
    Forsythe, A.
    VALUE IN HEALTH, 2021, 24 : S221 - S221
  • [3] ECONOMIC BURDEN AND COST DRIVERS OF DYSTROPHIC EPIDERMOLYSIS BULLOSA: A SYSTEMATIC LITERATURE REVIEW
    Bodke, A.
    Knott, C.
    Crossley, O.
    Samuels, E.
    Tang, M.
    VALUE IN HEALTH, 2023, 26 (12) : S126 - S127
  • [4] A systematic review of the natural history of recessive dystrophic epidermolysis bullosa
    Mellerio, J.
    Robertson, S.
    Pillay, E.
    Denyer, J.
    Wedgeworth, E.
    Batten, E.
    Martinez, A.
    BRITISH JOURNAL OF DERMATOLOGY, 2015, 173 : 42 - 42
  • [5] TARGETED LITERATURE REVIEW EXPLORING BURDEN OF DISEASE IN JUNCTIONAL AND DYSTROPHIC EPIDERMOLYSIS BULLOSA
    Kaler, N.
    Rudow, M.
    Stevenson, A.
    Dorling, P.
    VALUE IN HEALTH, 2024, 27 (06) : S21 - S21
  • [6] RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA
    CATTELL, A
    WADDINGTON, E
    BRITISH JOURNAL OF DERMATOLOGY, 1973, 89 : 67 - 71
  • [7] Quality of Life and Economic Burden in Recessive Dystrophic Epidermolysis Bullosa
    Jeon, In Kyung
    On, Hye Rang
    Kim, Soo-Chan
    ANNALS OF DERMATOLOGY, 2016, 28 (01) : 6 - 14
  • [8] A cephalometric analysis of patients with recessive dystrophic epidermolysis bullosa
    Shah, H
    McDonald, F
    Lucas, V
    Ashley, P
    Roberts, G
    ANGLE ORTHODONTIST, 2002, 72 (01) : 55 - 60
  • [9] Transcriptome profiling in recessive dystrophic epidermolysis bullosa patients
    Zauner, R.
    Wimmer, M.
    Lettner, T.
    Gruber, C.
    Murauer, E. M.
    Reichelt, J.
    Strunk, D.
    Bauer, J. W.
    Wally, V.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2017, 137 (10) : S288 - S288
  • [10] The Importance of Esophagography in Patients With Recessive Dystrophic Epidermolysis Bullosa
    Dante Guerra-Leal, Jesus
    Meester, Irene
    Ramon Cantu-Gonzalez, Juan
    Ornelas-Cortinas, Gerardo
    Montemayor-Martinez, Alberto
    Salas-Alanis, Julio C.
    AMERICAN JOURNAL OF ROENTGENOLOGY, 2016, 207 (04) : 778 - 781