Literature DB >> 22284144

Quality-of-life measurement in blistering diseases.

Deshan F Sebaratnam1, John W Frew, Fereydoun Davatchi, Dédée F Murrell.   

Abstract

Both congenital and acquired bullous dermatoses have the potential to impose a significant burden of disease, and the impact exerted on the quality of life (QOL) of patients is often multifaceted. The qualitative and quantitative studies reviewing QOL in patients with bullous dermatoses have all reported a significant decrease in QOL scores compared with the greater population using a range of patient-based measures. Formal evaluation of QOL in the setting of bullous dermatoses facilitates the assessment of disease severity and mapping of disease trajectory and can capture outcomes of therapeutic intervention relevant to the patient.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22284144     DOI: 10.1016/j.det.2011.11.008

Source DB:  PubMed          Journal:  Dermatol Clin        ISSN: 0733-8635            Impact factor:   3.478


  11 in total

1.  A Comprehensive Review of Quality of Life Surveys for Trauma-Affected Communities.

Authors:  Kimberly A Peterson; Leming Zhou; Valerie J M Watzlaf
Journal:  Perspect Health Inf Manag       Date:  2019-01-01

Review 2.  Autoimmune Subepidermal Bullous Diseases of the Skin and Mucosae: Clinical Features, Diagnosis, and Management.

Authors:  Kyle T Amber; Dedee F Murrell; Enno Schmidt; Pascal Joly; Luca Borradori
Journal:  Clin Rev Allergy Immunol       Date:  2018-02       Impact factor: 8.667

Review 3.  Psychosocial impact of inherited and autoimmune blistering diseases.

Authors:  Swaranjali V Jain; Dedee F Murrell
Journal:  Int J Womens Dermatol       Date:  2018-01-08

4.  Reliability of the autoimmune bullous disease quality of life (ABQOL) questionnaire in the USA.

Authors:  Deshan F Sebaratnam; Joyce Okawa; Aimee Payne; Dédée F Murrell; Victoria P Werth
Journal:  Qual Life Res       Date:  2015-03-21       Impact factor: 4.147

5.  Specific causes of death in patients with bullous pemphigoid as measured by death certificate data: a retrospective cohort study.

Authors:  Benjamin J Barrick; Christine M Lohse; Julia S Lehman
Journal:  Int J Dermatol       Date:  2013-12-30       Impact factor: 2.736

6.  Quality of life, depression, anxiety and loneliness in patients with bullous pemphigoid. A case control study.

Authors:  Anargyros Kouris; Eftychia Platsidaki; Christos Christodoulou; Kalliopi Armyra; Panagiota Korkoliakou; Christina Stefanaki; Revekka Tsatovidou; Dimitrios Rigopoulos; George Kontochristopoulos
Journal:  An Bras Dermatol       Date:  2016 Sep-Oct       Impact factor: 1.896

7.  Health literacy in patients with epidermolysis bullosa in Iran.

Authors:  Mohammad Mahdi Parvizi; Kamran Bagheri Lankarani; Farhad Handjani; Sulmaz Ghahramani; Zahra Parvizi; Sara Rousta
Journal:  J Educ Health Promot       Date:  2017-12-04

Review 8.  The effects of autoimmune blistering diseases on work productivity: A review.

Authors:  Esther Q Wang; M Adriana Castrillón Velásquez; Dedee F Murrell
Journal:  Int J Womens Dermatol       Date:  2018-02-09

Review 9.  Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines.

Authors:  K Martin; S Geuens; J K Asche; R Bodan; F Browne; A Downe; N García García; G Jaega; B Kennedy; P J Mauritz; F Pérez; K Soon; V Zmazek; K M Mayre-Chilton
Journal:  Orphanet J Rare Dis       Date:  2019-06-11       Impact factor: 4.123

10.  Inherited epidermolysis bullosa: clinical and therapeutic aspects.

Authors:  Vanessa Lys Simas Yamakawa Boeira; Erica Sales Souza; Bruno de Oliveira Rocha; Pedro Dantas Oliveira; Maria de Fátima Santos Paim de Oliveira; Vitória Regina Pedreira de Almeida Rêgo; Ivonise Follador
Journal:  An Bras Dermatol       Date:  2013 Mar-Apr       Impact factor: 1.896

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