Literature DB >> 21508568

A measurement of the stigma among vitiligo and psoriasis patients in India.

Rajan Pichaimuthu1, Premkumar Ramaswamy, Kar Bikash, Richard Joseph.   

Abstract

BACKGROUND AND AIM: The aim is to measure and to compare the level of social participation experienced by vitiligo and psoriasis patients in their domestic and social life in an Indian context.
METHODS: A cross-sectional comparative study with a sample of 150 cases each of psoriasis and vitiligo, a total of 300 subjects. A detailed clinical assessment of these two conditions, including the extent of lesions on the affected body parts, socioeconomic status and participation levels in social and domestic lives, was done.
RESULTS: The result showed that, 17.3% of vitiligo patients participated minimally in domestic and social life, whereas 28% of psoriasis patients had this problem (P=0.027). Extreme participation restriction was observed only among psoriasis patients (2.7%). Psoriasis patients also faced significantly more restrictions in a number of day-to-day life situations such as, less confidence in learning and applying knowledge, difficulties in meaningfully participating in major life areas like, work, education and employment, and also in community, social and civic life (all three domains P<0.0001), to vitiligo patients.
CONCLUSION: Both psoriasis and vitiligo patients suffered moderate to severe restriction while participating in their domestic and social life. Of these two groups, psoriasis patients faced significantly more restrictions in a number of day-to-day life situations. The Indian population of this study was predominantly dark-skinned and hypo-pigmentation as seen in vitiligo is much more noticeable than psoriatic red patches. However, the results showed that the component of hypo or hyperpigmentation of the skin is not the only factor leading to participation restrictions.

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Year:  2011        PMID: 21508568     DOI: 10.4103/0378-6323.79699

Source DB:  PubMed          Journal:  Indian J Dermatol Venereol Leprol        ISSN: 0378-6323            Impact factor:   2.545


  9 in total

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Journal:  J Arthropod Borne Dis       Date:  2018-06-13       Impact factor: 1.198

2.  Gender Differences in Depression, Coping, Stigma, and Quality of Life in Patients of Vitiligo.

Authors:  Neena S Sawant; Nakul A Vanjari; Uday Khopkar
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Authors:  Sandeep Grover; Aseem Mehra; Sunil Dogra; Nandita Hazari; Nidhi Malhora; Tarun Narang; Swapanjeet Sahoo; Sunil Sharma; Sanjeev Handa; Ajit Avasthi
Journal:  Indian Dermatol Online J       Date:  2020-09-28

Review 4.  Stigmatization in Patients With Psoriasis: A Mini Review.

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Journal:  Front Immunol       Date:  2021-11-15       Impact factor: 7.561

5.  Psychosocial Effects of Vitiligo: A Systematic Literature Review.

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7.  A hospital-based study on knowledge and attitude related to vitiligo among adults visiting a tertiary health facility of central India.

Authors:  Dinesh Prasad Asati; C M Gupta; Shreyansh Tiwari; Sanjeev Kumar; Vishal Jamra
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8.  Clinic-based Group Multi-professional Education Causes Significant Decline in Psoriasis Severity: A Randomized Open Label Pilot Study.

Authors:  Shubh Mohan Singh; Tarun Narang; Keshavamurthy Vinay; Aditi Sharma; Ashirbad Satapathy; Sanjeev Handa; Sunil Dogra
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Review 9.  The psychosocial adaptation of patients with skin disease: a scoping review.

Authors:  Xiu-Jie Zhang; Ai-Ping Wang; Tie-Ying Shi; Jun Zhang; Hui Xu; Da-Qiu Wang; Li Feng
Journal:  BMC Public Health       Date:  2019-10-29       Impact factor: 3.295

  9 in total

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