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Quality of life issues and measurement in patients with psoriasis

Authors Tan X, Feldman S, Balkrishnan R

Received 8 November 2011

Accepted for publication 24 December 2011

Published 21 February 2012 Volume 2012:2 Pages 13—23


Review by Single-blind

Peer reviewer comments 3

Xi Tan1, Steven R Feldman2, Rajesh Balkrishnan1
1Department of Clinical, Social and Administrative Sciences, College of Pharmacy, University of Michigan, Ann Arbor, MI, USA; 2Department of Dermatology, Wake Forest University School of Medicine, Winston-Salem, NC, USA

Abstract: Psoriasis is a chronic immunologic disease characterized by red papules and plaques with a silver colored scale. The impact of psoriasis on patients’ overall quality of life is significant, broad, and deep, including effects on emotional wellbeing, psychological stress, self-esteem, relationship, work, social activities, financial burden, and even physical function. Although there are various measures available for assessing health-related quality of life (HRQoL) in research studies, there is no consensus on which measure is best to use in clinical practice or for research comparing different treatments. Choosing treatments based on patients’ specific individual preferences, goal-orientation, and close, attentive cooperation between patients and their doctors may be an effective strategy that can be applied to improve patients’ quality of life.

Keywords: treatment, health related quality of life, HRQoL

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