Assessment of quality of life in vitiligo patients in terms of clinical severity and psychological burden in a tertiary care hospital: An observational study

Background: Vitiligo is characterized depigmented macules and patches over the skin. It has a major impact on the quality of life (QoL) of patients, many of whom feel distressed and stigmatized by their condition. Aim: To assess QoL in vitiligo patients in terms of clinical severity and psychologica...

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Main Authors: Cyril Sajan, Priyanshi R Shah, Rashmi Mahajan, Vikas Chandrakar, Disha Baxi, Hiral Patel
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2023-01-01
Series:Journal of the Scientific Society
Subjects:
Online Access:http://www.jscisociety.com/article.asp?issn=0974-5009;year=2023;volume=50;issue=1;spage=45;epage=54;aulast=Sajan
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author Cyril Sajan
Priyanshi R Shah
Rashmi Mahajan
Vikas Chandrakar
Disha Baxi
Hiral Patel
author_facet Cyril Sajan
Priyanshi R Shah
Rashmi Mahajan
Vikas Chandrakar
Disha Baxi
Hiral Patel
author_sort Cyril Sajan
collection DOAJ
description Background: Vitiligo is characterized depigmented macules and patches over the skin. It has a major impact on the quality of life (QoL) of patients, many of whom feel distressed and stigmatized by their condition. Aim: To assess QoL in vitiligo patients in terms of clinical severity and psychological burden. Materials and Methods: An observational study on 60 patients with age ≥16 years was conducted at an outpatient department of a tertiary care hospital. Data were collected in a predesigned pro forma. The QoL of patients and family members was assessed using Dermatology Life Quality Index (DLQI) and Family DLQI (FDLQI), respectively. The clinical severity was measured using Vitiligo Area Severity Index (VASI) and psychological burden by Vitiligo Impact Score-22 (VIS-22) questionnaire. Results: Sixty patients were included in the study. The mean age was 35.27 ± 2.24. Male-to-female ratio was 1.1:1. About 51.7% of patients were married. Majority of patients were students (30%). The time of presentation after disease onset was 5 years. About 20% of subjects had positive family history. The common sites were face (75%), lower limb (71.67%), and upper limb (60%), with leukotrichia in 11.7% of patients. The mean VASI score at baseline and at 1-month of follow-up after starting treatment was 4.11 ± 0.38 and 3.59 ± 0.58, respectively. The mean DLQI, FDLQI and VIS-22 score were 11.73 ± 0.80, 10.58 ± 0.71, and 37.32 ± 1.53, respectively. VIS-22 and VASI score correlated with changes in DLQI (P < 0.059). Conclusion: Vitiligo largely impairs the QoL of patients. The more the clinical severity (high VASI score), the higher the psychological burden, impairing QoL of patients, and family members.
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spelling doaj.art-49d9482f4cb54822ada6d4445ca534cf2023-07-21T12:07:14ZengWolters Kluwer Medknow PublicationsJournal of the Scientific Society0974-50092023-01-01501455410.4103/jss.jss_119_22Assessment of quality of life in vitiligo patients in terms of clinical severity and psychological burden in a tertiary care hospital: An observational studyCyril SajanPriyanshi R ShahRashmi MahajanVikas ChandrakarDisha BaxiHiral PatelBackground: Vitiligo is characterized depigmented macules and patches over the skin. It has a major impact on the quality of life (QoL) of patients, many of whom feel distressed and stigmatized by their condition. Aim: To assess QoL in vitiligo patients in terms of clinical severity and psychological burden. Materials and Methods: An observational study on 60 patients with age ≥16 years was conducted at an outpatient department of a tertiary care hospital. Data were collected in a predesigned pro forma. The QoL of patients and family members was assessed using Dermatology Life Quality Index (DLQI) and Family DLQI (FDLQI), respectively. The clinical severity was measured using Vitiligo Area Severity Index (VASI) and psychological burden by Vitiligo Impact Score-22 (VIS-22) questionnaire. Results: Sixty patients were included in the study. The mean age was 35.27 ± 2.24. Male-to-female ratio was 1.1:1. About 51.7% of patients were married. Majority of patients were students (30%). The time of presentation after disease onset was 5 years. About 20% of subjects had positive family history. The common sites were face (75%), lower limb (71.67%), and upper limb (60%), with leukotrichia in 11.7% of patients. The mean VASI score at baseline and at 1-month of follow-up after starting treatment was 4.11 ± 0.38 and 3.59 ± 0.58, respectively. The mean DLQI, FDLQI and VIS-22 score were 11.73 ± 0.80, 10.58 ± 0.71, and 37.32 ± 1.53, respectively. VIS-22 and VASI score correlated with changes in DLQI (P < 0.059). Conclusion: Vitiligo largely impairs the QoL of patients. The more the clinical severity (high VASI score), the higher the psychological burden, impairing QoL of patients, and family members.http://www.jscisociety.com/article.asp?issn=0974-5009;year=2023;volume=50;issue=1;spage=45;epage=54;aulast=Sajandermatology life quality indexquality of lifevitiligo area severity indexvitiligo impact score-22 questionnairevitiligo vulgaris
spellingShingle Cyril Sajan
Priyanshi R Shah
Rashmi Mahajan
Vikas Chandrakar
Disha Baxi
Hiral Patel
Assessment of quality of life in vitiligo patients in terms of clinical severity and psychological burden in a tertiary care hospital: An observational study
Journal of the Scientific Society
dermatology life quality index
quality of life
vitiligo area severity index
vitiligo impact score-22 questionnaire
vitiligo vulgaris
title Assessment of quality of life in vitiligo patients in terms of clinical severity and psychological burden in a tertiary care hospital: An observational study
title_full Assessment of quality of life in vitiligo patients in terms of clinical severity and psychological burden in a tertiary care hospital: An observational study
title_fullStr Assessment of quality of life in vitiligo patients in terms of clinical severity and psychological burden in a tertiary care hospital: An observational study
title_full_unstemmed Assessment of quality of life in vitiligo patients in terms of clinical severity and psychological burden in a tertiary care hospital: An observational study
title_short Assessment of quality of life in vitiligo patients in terms of clinical severity and psychological burden in a tertiary care hospital: An observational study
title_sort assessment of quality of life in vitiligo patients in terms of clinical severity and psychological burden in a tertiary care hospital an observational study
topic dermatology life quality index
quality of life
vitiligo area severity index
vitiligo impact score-22 questionnaire
vitiligo vulgaris
url http://www.jscisociety.com/article.asp?issn=0974-5009;year=2023;volume=50;issue=1;spage=45;epage=54;aulast=Sajan
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