Investigating factors associated with quality of life of vitiligo patients in Singapore

Authors


  • Contributions:

    Study design: MFC and TLC; Data collection: BKG, CWDA, TGST, TLC and SML

    Data analysis: MFC; Preparation: MFC, BKG, CWDA, TGST, TLC and SML

    Conflict of interests: The authors declare that they have no conflict of interests.

Correspondence: Moon Fai Chan, Alice Lee Centre for Nursing Studies, National University of Singapore, Singapore 117597. Email: nurcmf@nus.edu.sg

Abstract

Skin disease is often visible to others. People who have dermatological condition may also suffer from its psychological consequences. The purpose of this study is to explore the quality of life of patients with vitiligo and to identify factors associated with their quality of life. A descriptive correlational study was conducted with 222 patients with vitiligo recruited from two skin centres in Singapore from 2009 to 2011. Data were collected by a structured questionnaire. Three outcome variables were measured in the study: predisposal, clinical and psychological outcomes. Results showed that almost two-thirds of the participants reported vitiligo had moderate to extreme impact on their quality of life. Multiple regression analyses showed that patients who were depressed, had thyroid disease and had not used multiclear treatment were more likely to report poor quality of life. It is recommended that providing health care consultation for patients with vitiligo may help reduce depressive symptoms and maintain their psychological health, thus enhance their quality of life.

Ancillary