Literature DB >> 25558950

Outcome measures for autoimmune blistering diseases.

Cathy Y Zhao1, Dédée F Murrell.   

Abstract

Outcome measures are crucial in assessing an autoimmune blistering disease's (AIBD) severity as well as its impact on the patient's quality of life (QOL). The standardization of AIBD outcome measures is pivotal to accurately monitor the patient and to pool results from randomized controlled trials for meta-analysis, and thereby provide knowledge of the optimal AIBD therapies. In the past decade, several AIBD severity outcome measures have been developed and validated. For pemphigus severity, the Pemphigus Disease Area Index (PDAI) developed by the International Pemphigus Definitions Group was shown to be the most superior, followed by the Autoimmune Bullous Skin Disorder Intensity Score (ABSIS) by the German group. For bullous pemphigoid severity, the Bullous Pemphigoid Disease Area Index (BPDAI) was shown to be an accurate and valid measure. To quantify the burden of AIBD and its treatments on QOL, the Autoimmune Bullous Disease Quality of Life (ABQOL) and the Treatment of Autoimmune Bullous Disease Quality of Life (TABQOL) were also developed, validated, and are now being validated in multiple languages and cultures.
© 2015 Japanese Dermatological Association.

Entities:  

Keywords:  Bullous Pemphigoid Disease Area Index; Pemphigus Disease Area Index; autoimmune blistering diseases; outcome measures; quality of life

Mesh:

Year:  2015        PMID: 25558950     DOI: 10.1111/1346-8138.12711

Source DB:  PubMed          Journal:  J Dermatol        ISSN: 0385-2407            Impact factor:   4.005


  9 in total

1.  Factors associated with the activity and severity of bullous pemphigoid: a review.

Authors:  Yangchun Liu; Yiman Wang; Xinyi Chen; Hongzhong Jin; Li Li
Journal:  Ann Med       Date:  2020-03-22       Impact factor: 4.709

Review 2.  Pemphigus.

Authors:  Michael Kasperkiewicz; Christoph T Ellebrecht; Hayato Takahashi; Jun Yamagami; Detlef Zillikens; Aimee S Payne; Masayuki Amagai
Journal:  Nat Rev Dis Primers       Date:  2017-05-11       Impact factor: 52.329

Review 3.  Advances in understanding and managing bullous pemphigoid.

Authors:  Cathy Y Zhao; Dedee F Murrell
Journal:  F1000Res       Date:  2015-11-20

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.  Validation studies of outcome measures in pemphigus.

Authors:  Sarah Hanna; Minhee Kim; Dedee F Murrell
Journal:  Int J Womens Dermatol       Date:  2016-12-10

Review 7.  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

8.  Autoreactive Peripheral Blood T Helper Cell Responses in Bullous Pemphigoid and Elderly Patients With Pruritic Disorders.

Authors:  Dario Didona; Luca Scarsella; Milad Fehresti; Farzan Solimani; Hazem A Juratli; Manuel Göbel; Stefan Mühlenbein; Lily Holiangu; Josquin Pieper; Vera Korff; Thomas Schmidt; Cassian Sitaru; Rüdiger Eming; Michael Hertl; Robert Pollmann
Journal:  Front Immunol       Date:  2021-03-25       Impact factor: 7.561

Review 9.  Emerging Biomarkers and Therapeutic Strategies for Refractory Bullous Pemphigoid.

Authors:  Tong Zhou; Bin Peng; Songmei Geng
Journal:  Front Immunol       Date:  2021-08-24       Impact factor: 7.561

  9 in total

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