Evidence map›Paper›PMID 33302933›Full record

ArticleBMC dermatology2020

Quality of life of patients living with psoriasis: a qualitative study.

Silmara Meneguin, Natália Aparecida de Godoy, Camila Fernandes Pollo, Hélio Amante Miot, Cesar de Oliveira

Open access · diamondAbstract read
In one paragraph

Article in BMC dermatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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  6. Exploring the content validity of the EQ-5D-5L and four bolt-ons (skin irritation, self-confidence, sleep, social relationships) in atopic dermatitis and chronic urticaria.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2025
    Article
  7. Review
  8. Observational
  9. Psoriasis and Fibromyalgia: A Systematic Review.Journal of personalized medicine · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Observational
  17. Article
  18. Review
  19. Impact of Psoriasis on Quality of Life.Indian journal of dermatology
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Silmara MeneguinDepartment of Nursing, Botucatu Medical School, Paulista State University, São Paulo, Brazil. s.meneguin@unesp.br.ORCID 0000-0003-3853-5134
Natália Aparecida de GodoyDepartment of Nursing, Botucatu Medical School, Paulista State University, São Paulo, Brazil.
Camila Fernandes PolloDepartment of Nursing, Botucatu Medical School, Paulista State University, São Paulo, Brazil.
Hélio Amante MiotDepartment of Dermatology, Botucatu Medical School, Paulista State University, São Paulo, Brazil.
Cesar de OliveiraDepartment of Epidemiology & Public health, University College London, London, UK.
Universidade Estadual Paulista (Unesp) · BRUniversity College London · GB

Funding

the Economic and Social Research Council Grant ES/T008822/11
6 · The paper itself

Abstract

backgroundPsoriasis is a multifactorial inflammatory disease prevalent in dermatology. We aimed to understand the perceptions of patients living with psoriasis in relation to their quality of life and to identify aspects to improve it.

methodsThis is qualitative research carried out in a dermatology outpatient clinic of the São Paulo State University (UNESP) medical school, Botucatu, Brazil, with 81 psoriasis patients. The interviews were transcribed and analysed using the Discourse of the Collective Subject method (DCS).

resultsQuality of life was linked to well-being, happiness, leisure, good food and financial stability. However, disease symptoms, social and clothing restrictions, impairment of professional activities and the absence of a cure, negatively influenced their perceptions. Suggestions for improvements included an increase of public awareness, stress reduction, disease acceptance and multidisciplinary care.

conclusionThe meanings of quality of life revealed by the participants are subjective, multidimensional, linked to moments experienced by them and to the health-disease process. Public health policies promoting reduction in social stigma and stress as well as multidisciplinary approaches towards care can contribute to improvements of QoL in psoriasis.

Indexed as

Quality of LifeSocial StigmaAdultBrazilFemaleHumansMaleMiddle AgedPsoriasisQualitative ResearchSelf ConceptStress, PsychologicalSurveys and QuestionnairesYoung AdultDermatologyNursingPsoriasisQuality of life

Identifiers

PMID33302933
PMCPMC7727128
OpenAlexW3107553880

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.