Table of Contents    
ORIGINAL ARTICLE
Year : 2016  |  Volume : 7  |  Issue : 1  |  Page : 27-32  

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


1 Department of Dermatology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India
2 Department of Dermatology, LN Medical College and JK Hospital, Bhopal, Madhya Pradesh, India
3 Department of Community and Family Medicine, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India
4 Department of Preventive and Social Medicine, LN Medical College and JK Hospital, Bhopal, Madhya Pradesh, India

Date of Web Publication28-Jan-2016

Correspondence Address:
Dinesh Prasad Asati
Assistant Professor, Department of Dermatology, All India Institute of Medical Sciences, Saket Nagar, Bhopal - 462 024, Madhya Pradesh
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0976-9668.175021

Rights and Permissions
   Abstract 

Background: Vitiligo is one of the common stigmatizing dermatosis in the Indian society and the vitiligo patients have to face significant psychological hurt and social neglect. The severity of the stigma is related to the society's attitude and knowledge about it. Aims and Objectives: To document the prevalent knowledge and attitude in general public towards vitiligo patients, and to identify the determinants of good/poor knowledge and attitude. Materials and Methods: A systematic random sampling technique was adopted to enroll 700 adult participants visiting an urban tertiary healthcare facility of central India. We developed a questionnaire to collect information on knowledge and attitude of the participants. A composite score was developed for good knowledge and attitude and performance of the participants was compared with the selected determinants. Data analysis was conducted by Stata software version 11. Results: The overall knowledge score was good for 66.3% (95% confidence interval [CI]: 62.8%, 69.8%) of the participants. However, the score for attitude was comparatively poor i.e., only 16.9% (95% CI: 13.9%, 19.5%). None of the studied parameters could be significantly correlated with the knowledge score. Being married and being engaged in a health care related occupation were significant predictors of good attitude levels with P = 0.042 and 0.034 respectively, whereas female gender was the significant predictor for poor attitude with an odds ratio of 0.54 (95% CI: 0.33, 0.9) and P = 0.018. Conclusions: There were widespread myths prevalent about vitiligo in the studied population. The knowledge scores were better than attitude scores.

Keywords: Attitude, knowledge, myths, society perceptions, vitiligo


How to cite this article:
Asati DP, Gupta C M, Tiwari S, Kumar S, Jamra V. A hospital-based study on knowledge and attitude related to vitiligo among adults visiting a tertiary health facility of central India. J Nat Sc Biol Med 2016;7:27-32

How to cite this URL:
Asati DP, Gupta C M, Tiwari S, Kumar S, Jamra V. A hospital-based study on knowledge and attitude related to vitiligo among adults visiting a tertiary health facility of central India. J Nat Sc Biol Med [serial online] 2016 [cited 2020 Jan 29];7:27-32. Available from: http://www.jnsbm.org/text.asp?2016/7/1/27/175021


   Introduction Top


Vitiligo is a common, autoimmune acquired disorder of the skin, which causes milky white depigmented macules on various parts of the body. These macules are commonly aesthetically disfiguring, especially in dark colored individuals. Vitiligo downbeats affected persons' thinking, emotions, and daily activities. The severity of this negative impact is related to the knowledge and attitude of the society regarding that disease along with the patients' demographic or personal characters and individual life situations. [1] Common peoples' misconceptions and undue apprehension associated with vitiligo are the result of inadequate knowledge about this otherwise benign and harmless condition. The present study attempted to document the prevalent knowledge and attitude in the general public regarding vitiligo and to identify the determinants of good/poor knowledge and attitude. There is a severe scarcity of similar studies across the worldwide literature, and we could not find any from the Indian subcontinent.


   Materials and Methods Top


Design of the study

A prospective, hospital-based questionnaire survey was carried out over about 3 months from January to March 2012 at a tertiary care center hospital in central India. We recruited caregivers or other visitors of the dermatology outpatient facilities by systematic random sampling method. The participants included attendants and patients from various socioeconomic groups visiting the hospital. We excluded the individuals having vitiligo themselves, children below 16 years of age and mentally subnormal persons. This study was approved by the Ethics Committee of our institute and informed consent was taken from all the participants. Confidentiality and privacy of the participants were ensured by excluding identification details from the study instrument.

Sample size estimation

We considered 75% as the anticipated good knowledge level in our study population. At a confidence level of 95% and a power of 80% for a two-tailed test and with 12% relative precision, our primary outcome (overall good knowledge) was expected to lie between 66% and 84%. We got a sample size of 89 with the above criteria. It was proposed to recruit at least 150 participants for the study to account for the anticipated 60% response rate. For robust sub-group analysis of different variables included in the study, we kept 150 as the sample size for each of the 4 age wise sub-groups. Thus, the final minimum sample size was 600 for the study. We recruited 700 participants for the study.

Each participant was provided a questionnaire in the local language (Hindi), which was devised to include participants' demographic characteristics, questions related to their knowledge of vitiligo and their attitude toward persons with vitiligo. Each question was given open as well as close-ended options to mark in the affirmative, negative, or as not knowing and had the freedom to describe if the participant's opinion was not fitting in any given options for that question [Table 1] and [Table 2]. Answers to all these were ranked at different marks and a scoring system (indicative only as the scoring was an empirical device) was formulated for knowledge and attitude estimation. For knowledge component of the study instrument, the total score was 20, while it was 14 for the attitude component.
Table 1: Knowledge and prevalent myths in the study participants*

Click here to view
Table 2: Attitude of the participants towards vitiligo patients*

Click here to view


Study outcomes

The study indicated the proportion of participants having overall good knowledge and attitude and correlation of their knowledge/attitude with selected sociodemographic characteristics of the study participants.

Statistical analysis

The data were entered into Microsoft Excel version 2010, and data analysis was done with the help of statistical software Stata version 11 (College Station, Texas). Descriptive statistics was presented as means and standard deviations for continuous variables, and counts and percentages with confidence intervals (CIs) for categorical variables. Sub-group analysis was done to find out the association of outcome variable with the determinants studied. Appropriate statistical tests were used for continuous (t-test, ANOVA) and discrete variables (Chi-square test, Z-test). We also performed multivariate analysis using logistic regression method to identify the significant predictors of knowledge and attitude levels.


   Results Top


A total of 700 participants (499 males and 201 females) were included the study. Their sociodemographic characteristics are charted in [Table 3]. The majority were from urban areas of Bhopal city, and most were well educated.
Table 3: Demographic characteristics of the study participants

Click here to view


The majority (487; 69.6%) perceived vitiligo to be an uncommon condition that is rarely seen around. A quarter of the participants (178; 25.4%) had some close family member/neighbor/friend affected with vitiligo (parent/sibling/child/spouse = 26, other relative = 27, friend = 61, neighbour = 64). The white patches on the exposed body parts of the patients such as face and hand were the most common to be recalled by the participants (314; 44.9% and 321; 45.9% respectively, followed by the whole body (209; 29.9%) and scalp (82; 11.7%).

The participants' knowledge about vitiligo is summarized in [Table 1]. Few participants (46; 6.6%) thought vitiligo to be a lethal disease. The majority of the recruited subjects (482; 68.9%) were hopeful about a possible cure by various treatments. A large number of people (390; 55.7%) in our study had belief in probable complete cure by using alternative (homeopathic or Ayurvedic) medicines while 362 (51.7%) had belief in the efficacy of allopathy treatment. 152 (21.7%) believed that there is no effective treatment, 130 (18.6%) even thought that the treatment might further aggravate the disease. Only 188 (26.9%) participants made a clear distinction between vitiligo and Hansen's disease. There are widespread myths prevalent about the disease [Table 1]. The attitude of the participants towards vitiligo patients also varied [Table 2].

Knowledge and attitude scores

[Table 1] and [Table 2] depict the assessment of the participants' knowledge and attitude scores, respectively. 66.3% of the participants achieved knowledge score of >10 (out of 20), the rest (33.7%) reported poor score. The attitude was assessed with a 14 point score and only 16.9% were found to have satisfactorily good (≥7) attitude score. [Table 2] discloses reluctance observed in the participants to have friendship, share meal or have close social relation or marriage with a vitiligo affected a person. Thoughts of fear, hate or pity toward the affected person were also not uncommon. A total of 161 (23.0%) participants had witnessed marital difficulties for vitiligo affected persons. Discrimination at the workplace was also reported by a large number (198; 28.3%) of participants.

The possible correlation of knowledge and attitude scores with sociodemographic profile of the participants was checked. Good knowledge was not associated with any of the sociodemographic factors used in the bivariate analysis [Table 4]. The participants with a relative or friend with vitiligo had no significant difference in knowledge or attitude scores from other participants. Attitude score was significantly better among males, younger age-groups, the married and the participants indulging in healthcare related occupation or the unemployed [Table 5]. After multivariate analysis, married participants had an odds ratio (OR) of 1.51 (95% CI: 1.01, 2.44) as compared to unmarried participants for having good attitude. After controlling other factors, female gender was the only other significant factor for poor attitude score with an OR of 0.54 (95% CI: 0.33, 0.9) and a P = 0.018.
Table 4: Observed relationship of knowledge about vitiligo with sociodemographic characteristics

Click here to view
Table 5: Observed relationship of attitude about vitiligo with sociodemographic characteristics

Click here to view



   Discussion Top


Although it is mostly an asymptomatic ailment, vitiligo may be a painful condition to live with because of the associated stigmas. The negative impact on the patients' psyche is much more in Indians as most of the population is colored (Fitzpatrick scale IV or V). [2],[3] Various tools like dermatology life quality index and quality of life have been used to measure the negative impact on vitiligo affected persons in India. All of these studies have underlined the psychological trauma and physical disfigurement caused by vitiligo. [4],[5],[6],[7] However, none of these studies has explored the community outlook towards vitiligo patients in India.

Vitiligo affected persons are often subjected to whispered comments, taunts, and social rejection. Sometimes the patients themselves withdraw from all social interaction in anticipation of the guilt and humiliation. [4],[8],[9] Many of our participants had reservations in having a friendship (27.7%) and in sharing meals (24.0%) with vitiligo patients. The thoughts of pity, hate or fear to touch, or talk with a patient around were also noticed in our study. There is no Indian study available with which these data could be compared, however, one recent study from Saudi Arabia has focused on public perceptions and attitudes toward vitiligo patients. [10] The causes assumed by the participants in that study included autoimmunity (41.2%), heredity (40.50%), diet (30.50%), poor hygiene (22.5%), and evil eye (29.3%). The notion of contagiousness was maintained by less number (8.0%) of the participants in that study as compared to ours (17.0%). [10] In comparison, heredity was the most prevalent theory noticed in our society as the cause of vitiligo.

Vitiligo is recognized since antiquity. It is mentioned in the old testament, Ayurveda, Vinaypitika, Ebers Papyrus (1550 B.C.) and described even at the time of Aushooryan (2200 B.C.). [11] Such a long history has added many myths in the general understanding related to its causes, spreadability, complications, and treatment options. The notion of infectiousness (119; 17% of our participants) or contagiousness (82; 11.7%) of the disease is still prevalent in our society. A part of this could be because of its confusion (73; 10.4% of the participants) with Hansen's disease. Kilasa or external Kushta (vitiligo) and Switra (leprosy) were described in Ayurveda together and were thought to have a similar etiology. In fact, the suffix "Kushta" was used for all skin diseases in Ayurveda. [11] However, it became synonymous with leprosy later. The fallacy carries a huge and culturally deep-rooted negative impact.

Another major problem in our society is regarding the difficulties faced by the vitiligo patients and their close family members in getting married. 69.14% of our study participants were unwilling to marry a vitiligo patient even when he or she was otherwise a suitable match. The study from Saudi Arabia had reported that 56.1% of their subjects were unwilling for the same. [10] Only about one-third of the participants in this study were agreeable for marriage relations with a family having a vitiligo patient.

Many diet related myths are prevalent as evidenced in this study (almost one-third of the participants believed in them), like implicating sour food/white food/fish, etc.

Around 3-4% (about thirty million) of the general Indian population is suffering from vitiligo. [2] Despite it being such a common disease, nearly about 70% of our study participants perceived vitiligo to be an uncommon condition. This might be because many cases have localized or sometimes widespread patches on unexposed parts.

Vitiligo patients are more likely to adopt alternative medicines as compared to other cosmetic dermatoses, in which allopathy is commonly used by them. [12] Marginally more number (55.7%) of our study participants had belief in the efficacy of alternative medicine as compared to 51.7% having confidence in allopathy. Overall, the majority (68.9%) of the enrolled people were optimistic about improvement with treatment in vitiligo.

The majority (66.3%) of the participants had good knowledge score (11/20), while only 16.9% had good attitude score (8/14). There are no published studies with which these data could be compared. We had excluded persons affected with vitiligo themselves from the study, but the results of our study can be corroborated with another Indian study, which analyzed the views and concerns of vitiligo affected persons themselves. This qualitative study also looked in depth into their psychological burden and highlighted the feelings of guilt, insult, marital problems, gender differences, social isolation and coping strategies adopted by vitiligo affected persons. [4]

Various coping techniques like cognitive behavioral therapy have been tried in patients to decrease the psychological burden, [13] The use of camouflage on exposed white patches has also been encouraged as a harmless procedure. [14] Understanding and interacting with society regarding its vitiligo related knowledge and attitude would be important steps towards decreasing the vitiligo patients' emotional burden.


   Conclusion Top


There were widespread myths and misconceptions regarding vitiligo prevalent in the studied population. The knowledge scores were better than attitude scores. A better designed, community based study should be planned to get deeper insight into the problem.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Chaturvedi SK, Singh G, Gupta N. Stigma experience in skin disorders: An Indian perspective. Dermatol Clin 2005;23:635-42.  Back to cited text no. 1
    
2.
Dhar S, Dutta P, Malakar R. Pigmentary disorders. In: Valia RG, Valia AR, editors. IADVL Textbook of Dermatology. 3 rd ed. Mumbai: Bhalani Publishing House; 2008. p. 736-98.  Back to cited text no. 2
    
3.
Mattoo SK, Handa S, Kaur I, Gupta N, Malhotra R. Psychiatric morbidity in vitiligo: Prevalence and correlates in India. J Eur Acad Dermatol Venereol 2002;16:573-8.  Back to cited text no. 3
    
4.
Pahwa P, Mehta M, Khaitan BK, Sharma VK, Ramam M. The psychosocial impact of vitiligo in Indian patients. Indian J Dermatol Venereol Leprol 2013;79:679-85.  Back to cited text no. 4
[PUBMED]  Medknow Journal  
5.
Kent G, al-Abadie M. Factors affecting responses on dermatology life quality index items among vitiligo sufferers. Clin Exp Dermatol 1996;21:330-3.  Back to cited text no. 5
    
6.
Parsad D, Pandhi R, Dogra S, Kanwar AJ, Kumar B. Dermatology life quality index score in vitiligo and its impact on the treatment outcome. Br J Dermatol 2003;148:373-4.  Back to cited text no. 6
    
7.
Kiprono S, Chaula B, Makwaya C, Naafs B, Masenga J. Quality of life of patients with vitiligo attending the regional dermatology training center in Northern Tanzania. Int J Dermatol 2013;52:191-4.  Back to cited text no. 7
    
8.
Pichaimuthu R, Ramaswamy P, Bikash K, Joseph R. A measurement of the stigma among vitiligo and psoriasis patients in India. Indian J Dermatol Venereol Leprol 2011;77:300-6.  Back to cited text no. 8
[PUBMED]  Medknow Journal  
9.
Parsad D, Dogra S, Kanwar AJ. Quality of life in patients with vitiligo. Health Qual Life Outcomes 2003;1:58.  Back to cited text no. 9
    
10.
Alghamdi KM, Moussa NA, Mandil A, Alkofidi M, Madani A, Aldaham N, et al. Public perceptions and attitudes toward vitiligo. J Cutan Med Surg 2012;16:334-40.  Back to cited text no. 10
    
11.
Prasad PV, Bhatnagar VK. Medico-historical study of "Kilasa" (vitiligo/leucoderma) a common skin disorder. Bull Indian Inst Hist Med Hyderabad 2003;33:113-27.  Back to cited text no. 11
    
12.
Bhalla M, Thami GP. Factors predicting the preference of complementary and alternative systems of medicine in treatment of vitiligo. Indian J Dermatol Venereol Leprol 2010;76:705-7.  Back to cited text no. 12
[PUBMED]  Medknow Journal  
13.
Papadopoulos L, Bor R, Legg C. Coping with the disfiguring effects of vitiligo: A preliminary investigation into the effects of cognitive-behavioural therapy. Br J Med Psychol 1999;72 (Pt 3):385-96.  Back to cited text no. 13
    
14.
Ongenae K, Dierckxsens L, Brochez L, van Geel N, Naeyaert JM. Quality of life and stigmatization profile in a cohort of vitiligo patients and effect of the use of camouflage. Dermatology 2005;210:279-85  Back to cited text no. 14
    



 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5]


This article has been cited by
1 Knowledge and attitudes towards vitiligo in the general population: Asurvey based on the simulation video of a real situation
Premjit Juntongjin,Chulaphan Rachawong,Winitra Nuallaong
Dermatologica Sinica. 2017;
[Pubmed] | [DOI]



 

Top
  
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Introduction
    Materials and Me...
   Results
   Discussion
   Conclusion
    References
    Article Tables

 Article Access Statistics
    Viewed2120    
    Printed27    
    Emailed0    
    PDF Downloaded275    
    Comments [Add]    
    Cited by others 1    

Recommend this journal