The effect of skin diseases on quality of life in patients from different social and ethnic groups in Cape Town, South Africa
Abstract
Abstract Background Skin diseases can greatly affect the quality of life (QoL). Little is known, however, of their impact on QoL in the developing world. This study was designed to assess the effect of skin diseases in such a setting. Methods A questionnaire survey of patients using the Dermatology Life Quality Index (DLQI), modified to the cultural needs of the population. The adapted instrument was translated into Afrikaans and Xhosa. Six hundred and seven patients attending general dermatology clinics at Groote Schuur Hospital and 53 controls were recruited. Influences on QoL of clinical severity, employment, education, age, sex, and home language were examined. Results Participants included 313 (52%) English‐speaking, 215 (35%) Afrikaans‐speaking, and 79 (13%) Xhosa‐speaking dermatology patients. Independent risk factors for having a high disability score were dermatologists' assessment of severity, younger age, unemployment, and language (odds ratio, 0.13; 95% confidence interval (CI) of 0.03–0.5 for Xhosa speakers compared to Afrikaans speakers). Gender was not associated with a high score, but females were more likely to report effects of skin disease on self‐esteem, clothing choice, treatment problems, and anxiety. Conclusions In this multicultural setting, social class and language group, but not gender, influenced the impact of skin disease on overall QoL. Xhosa speakers were apparently less affected than other patients. This could be due to cultural differences in the experience of skin disease and in the perception of disability, or to biases in questionnaire responses. Anxiety and depression were relevant dimensions of QoL in this study and should be considered for inclusion in future research. The adapted and translated DLQI was valid and reliable.
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In the South African study, women reported greater impact on self-esteem, clothing choice, and treatment problems.
“Women reported greater impact on self-esteem, clothing choice, treatment problems and clothing choice in the South African study.”
From Global Burden of Skin Disease: Inequities and Innovations (2017) · cites this paper as [9]
Seniors were much more likely to experience disability due to a skin condition.
“Seniors were much more likely to experience disability due to a skin condition.”
From Global Burden of Skin Disease: Inequities and Innovations (2017) · cites this paper as [9]
In a South African study, patients with skin complaints had significantly poorer quality of life than controls in depression, anxiety, effect on work or study, clothing choice, and looking after home.
“A study of QoL in South African patients with skin complaints found that patients with these diseases had significantly poorer QoL compared to controls in realms such as depression, anxiety, effect on work or study, clothing choice, looking after one’s home”
From Global Burden of Skin Disease: Inequities and Innovations (2017) · cites this paper as [9]
Conditions with the highest disability burden often have disabling symptoms such as pruritus, including dermatitis, prurigo, and papular urticaria.
“Conditions that constitute the highest disability burden are often characterized by disabling symptoms like pruritus. These conditions include dermatitis, prurigo, and papular urticaria”
From Global Burden of Skin Disease: Inequities and Innovations (2017) · cites this paper as [9]
Increased clinical severity was an independent predictor of decreased quality of life in a study of skin conditions among South Africans.
“Increased clinical severity was an independent predictor of decreased QoL in a study of skin conditions among South Africans”
From Global Burden of Skin Disease: Inequities and Innovations (2017) · cites this paper as [9]
Dermatologic quality of life is more impaired for vulnerable groups: people of advanced age, women, and children.
“Dermatologic QoL is also more impaired for members of vulnerable groups: people of advanced age, women, and children.”
From Global Burden of Skin Disease: Inequities and Innovations (2017) · cites this paper as [9]
Far fewer studies examine quality of life in patients with skin conditions in resource-poor settings than in resource-replete settings.
“Far fewer studies exist examining the QoL of patients with skin conditions in the resource-poor world”
From Global Burden of Skin Disease: Inequities and Innovations (2017) · cites this paper as [9]
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- Authors
- Jobanputra, R., & Bachmann, M.
- Affiliations
- Southmead Hospital (GB)
- ORCID
- Bachmann, Max
- Venue
- International Journal of Dermatology
- Publisher
- Wiley
- Published
- 2000-11
- Volume
- 39
- Issue
- 11
- Pages
- 826-831
- ISSN
- 0011-9059 (ISSN-L)
- 1365-4632
- OpenAlex
- W2104263215
- Cited by
- 71
- References
- 18
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 2 · 2023: 2 · 2022: 3 · 2021: 8 · 2020: 2 · 2019: 4 · 2018: 8 · 2017: 5 · 2016: 3 · 2014: 3 · 2013: 2 · 2012: 3
- FWCI
- 0.80
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- International Journal of Dermatology (publishedVersion)
- PubMed (publishedVersion)
- UEA Digital Repository (University of East Anglia) (submittedVersion)
- Topics
- Health Sciences › Medicine › Dermatology › Dermatology and Skin Diseases
- Health Sciences › Medicine › Infectious Diseases › Dermatological diseases and infestations
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Health Systems, Economic Evaluations, Quality of Life
- Keywords
- skin diseases, quality of life, Dermatology Life Quality Index, disability, social class, language groups, Afrikaans speakers, unemployment, self-esteem, anxiety, depression, cultural adaptation of questionnaires, Cape Town
- MeSH terms
- Adult, Aged, Anxiety, Clothing, Depression, Ethnicity, Female, Humans, Male, Quality of Life, Surveys and Questionnaires, Self Concept, Skin Diseases, Social Class, South Africa, Statistics as Topic
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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