Literature DB >> 22137233

Quality of life in patients with bullous dermatoses.

Deshan F Sebaratnam1, James R McMillan, Victoria P Werth, Dédée F Murrell.   

Abstract

Genetic and acquired bullous dermatoses can severely affect multiple domains of a patient's quality of life (QOL). Integrating formal evaluation of QOL into the clinical evaluation of patients facilitates an objective assessment of disease severity, mapping of disease trajectory, and captures therapeutic intervention outcomes. There have been 5 studies evaluating QOL in autoimmune dermatoses and 4 studies reviewing QOL in the genodermatoses. All literature to date indicates a significant disease burden in this setting. The development of formal QOL instruments has facilitated quantification of QOL deficits in this arena and offers promising tools for patient assessment in the future.
Copyright © 2012 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2012        PMID: 22137233      PMCID: PMC3883428          DOI: 10.1016/j.clindermatol.2011.03.016

Source DB:  PubMed          Journal:  Clin Dermatol        ISSN: 0738-081X            Impact factor:   3.541


  26 in total

Review 1.  Critical review of generic and dermatology-specific health-related quality of life instruments.

Authors:  Hilde Both; Marie-Louise Essink-Bot; Jan Busschbach; Tamar Nijsten
Journal:  J Invest Dermatol       Date:  2007-11-08       Impact factor: 8.551

2.  Main problems experienced by children with epidermolysis bullosa: a qualitative study with semi-structured interviews.

Authors:  Corinne van Scheppingen; Ant T Lettinga; José C Duipmans; Carel G B Maathuis; Marcel F Jonkman
Journal:  Acta Derm Venereol       Date:  2008       Impact factor: 4.437

3.  Highlights from the report of the working group on "Core measures of the burden of skin diseases".

Authors:  Marta VanBeek; Scott Beach; Lawrence Braslow; Judith B Braslow; Suephy C Chen; Mary Margaret Chren; David Margolis; Sarah Chamlin; George Torrance; Tom Hodgson
Journal:  J Invest Dermatol       Date:  2007-12       Impact factor: 8.551

4.  Dermatology quality of life instruments: sorting out the quagmire.

Authors:  Suephy C Chen
Journal:  J Invest Dermatol       Date:  2007-12       Impact factor: 8.551

5.  Quality of life evaluation in epidermolysis bullosa (EB) through the development of the QOLEB questionnaire: an EB-specific quality of life instrument.

Authors:  J W Frew; L K Martin; T Nijsten; D F Murrell
Journal:  Br J Dermatol       Date:  2009-06-11       Impact factor: 9.302

6.  Quality of life in epidermolysis bullosa.

Authors:  H M Horn; M J Tidman
Journal:  Clin Exp Dermatol       Date:  2002-11       Impact factor: 3.470

7.  The health impact of pemphigus vulgaris and pemphigus foliaceus assessed using the Medical Outcomes Study 36-item short form health survey questionnaire.

Authors:  S Tabolli; A Mozzetta; V Antinone; S Alfani; G Cianchini; D Abeni
Journal:  Br J Dermatol       Date:  2008-02-22       Impact factor: 9.302

8.  Quality of life in patients with epidermolysis bullosa.

Authors:  S Tabolli; F Sampogna; C Di Pietro; A Paradisi; C Uras; P Zotti; D Castiglia; G Zambruno; D Abeni
Journal:  Br J Dermatol       Date:  2009-05-11       Impact factor: 9.302

9.  Reliability and convergent validity of two outcome instruments for pemphigus.

Authors:  Misha Rosenbach; Dedee F Murrell; Jean-Claude Bystryn; Sam Dulay; Sarah Dick; Steve Fakharzadeh; Russell Hall; Neil J Korman; Julie Lin; Joyce Okawa; Amit G Pandya; Aimee S Payne; Mathew Rose; David Rubenstein; David Woodley; Carmela Vittorio; Benjamin B Werth; Erik A Williams; Lynne Taylor; Andrea B Troxel; Victoria P Werth
Journal:  J Invest Dermatol       Date:  2009-04-09       Impact factor: 8.551

10.  Quality-of-life assessment in patients with pemphigus using a minimum set of evaluation tools.

Authors:  Andrea Paradisi; Francesca Sampogna; Cristina Di Pietro; Giuseppe Cianchini; Biagio Didona; Rossana Ferri; Damiano Abeni; Stefano Tabolli
Journal:  J Am Acad Dermatol       Date:  2008-11-11       Impact factor: 11.527

View more
  12 in total

1.  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

2.  Characteristics of Pruritus in Bullous Pemphigoid and Impact on Quality of Life: A Prospective Cohort Study.

Authors:  Clémence Briand; Greta Gourier; Florence Poizeau; Lamia Jelti; Marie Bachelerie; Gaëlle Quéreux; Géraldine Jeudy; Marie Acquitter; Saskia Ingen-Housz-Oro; Frédéric Caux; Catherine Prost; Anne-Sophie Darrigade; Diane Heron Mermin; Emmanuel Mahé; Catherine Picart Dahan; Marie-Aleth Richard; Caroline Jade Clerc; Camille Salle De Chou; Julie Plée; Claire Abasq-Thomas; Laurent Misery; Emilie Brenaut
Journal:  Acta Derm Venereol       Date:  2020-11-12       Impact factor: 3.875

3.  Quality of life index in autoimmune bullous dermatosis patients.

Authors:  Mariana Álvares Penha; Joyce Godoy Farat; Hélio Amante Miot; Sílvia Regina Catharino Sartori Barraviera
Journal:  An Bras Dermatol       Date:  2015 Mar-Apr       Impact factor: 1.896

4.  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

5.  Reliability and validity of the Chinese version of the autoimmune bullous disease quality of life (ABQOL) questionnaire.

Authors:  Baoqi Yang; Guo Chen; Qing Yang; Xiaoxiao Yan; Zhaoxia Zhang; Dédée F Murrell; Furen Zhang
Journal:  Health Qual Life Outcomes       Date:  2017-02-02       Impact factor: 3.186

Review 6.  Autoimmune blistering diseases in females: a review.

Authors:  Cathy Y Zhao; Dédée F Murrell
Journal:  Int J Womens Dermatol       Date:  2015-02-26

Review 7.  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

8.  Illness perception of patients with pemphigus vulgaris.

Authors:  Maryam Nasimi; Robabe Abedini; Maryam Daneshpazjooh; Afsane Esmaeilpour; Forugh Ghaedi; Amir Teimourpour; Shahab Abtahi
Journal:  Int J Womens Dermatol       Date:  2018-11-19

Review 9.  Depression and Anxiety in Patients with Bullous Pemphigoid: Impact and Management Challenges.

Authors:  Nicolas Kluger; Anna Pankakoski; Jaana Panelius
Journal:  Clin Cosmet Investig Dermatol       Date:  2020-01-21

10.  Assessing the Correlation Between Disease Severity Indices and Quality of Life Measurement Tools in Pemphigus.

Authors:  Rebecca L Krain; Carolyn J Kushner; Meera Tarazi; Rebecca G Gaffney; Andrea C Yeguez; Danielle E Zamalin; David R Pearson; Rui Feng; Aimee S Payne; Victoria P Werth
Journal:  Front Immunol       Date:  2019-11-06       Impact factor: 7.561

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.