Evidence map›Paper›PMID 21569235›Full record

ArticleBMC pediatrics2011

Balancing health benefits and social sacrifices: a qualitative study of how screening-detected celiac disease impacts adolescents' quality of life.

Anna Rosén, Anneli Ivarsson, Katrina Nordyke, Eva Karlsson, Annelie Carlsson, Lars Danielsson, Lotta Högberg, Maria Emmelin

Registry-linked trialAbstract read
In one paragraph

Article in BMC pediatrics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05923346 (Educational Intervention on Celiac Disease and Gluten-free Diet Through Social Networks), which is not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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.

NCT05923346 nacompletednot on this mapstarted 2022, after this paper: background citation

Educational Intervention on Celiac Disease and Gluten-free Diet Through Social Networks (GLUTLEARN Project).

TypeinterventionalSponsorUniversity of the Basque Country (UPV/EHU)Ran2022 to 2023Enrolled93ConditionsCeliac DiseaseArmsGLUTLEARN
3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. One-Year Outcomes Among Children Identified With Celiac Disease Through a Mass Screening Program.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2025
    Article
  6. Review
  7. Review
  8. Article
  9. Global Approach to Follow-Up of Celiac Disease.Foods (Basel, Switzerland) · 2024
    Review
  10. Article
  11. Population level screening for celiac disease: is now the time?Current opinion in gastroenterology · 2023
    Review
  12. Article
  13. The costs of celiac disease: a contingent valuation in Switzerland.The European journal of health economics : HEPAC : health economics in prevention and care · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Perceptions and experiences underlying self-management and reporting of symptoms in teens with asthma.The Journal of asthma : official journal of the Association for the Care of Asthma · 2017
    Article
  20. The Perceived Social Burden in Celiac Disease.Diseases (Basel, Switzerland) · 2015
    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

8 authors.

Anna RosénDepartment of Public Health and Clinical Medicine, Epidemiology and Global Health, Umeå University, Umeå, Sweden. anna.rosen@epiph.umu.se
Anneli Ivarsson
Katrina Nordyke
Eva Karlsson
Annelie Carlsson
Lars Danielsson
Lotta Högberg
Maria Emmelin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCeliac disease often goes undiagnosed. Mass screening might be an option to reduce the public health burden of untreated celiac disease. However, mass screening is still controversial since it is uncertain whether the benefits of early detection outweigh the possible negative consequences. Before implementation of screening programs, the experiences of those being identified as cases should be considered. The aim of our study was to explore how screening-detected celiac disease impacts adolescents' quality of life, as perceived by themselves and their parents.

methodsAll adolescents (n = 145) with screening-detected celiac disease found in a Swedish screening study, and their parents, were invited to share their experiences in a qualitative follow-up study. In total, we have information on 117 (81%) of the adolescents, either from the adolescents themselves (n = 101) and/or from their parent/s (n = 125). Written narratives were submitted by 91 adolescents and 105 parents. In addition, 14 focus group discussions involving 31 adolescents and 43 parents were conducted. Data was transcribed verbatim and analyzed based on a Grounded Theory framework.

resultsThe screening-detected celiac disease diagnosis had varying impact on quality of life that related both to changes in perceived health and to the adolescents' experiences of living with celiac disease in terms of social sacrifices. Changes in perceived health varied from "healthy as anyone else with no positive change" to "something was wrong and then changed to the better", whereas experiences of living with celiac disease ranged from "not a big deal" to "treatment not worth the price". Perceptions about living with celiac disease and related coping strategies were influenced by contextual factors, such as perceived support from significant others and availability of gluten-free products, and were developed without a direct relation to experiencing changes in perceived health.

conclusionsScreening-detected celiac disease has varying impact on adolescents' quality of life, where their perceived change in health has to be balanced against the social sacrifices the diagnosis may cause. This needs to be taken into account in any future suggestion of celiac disease mass screening and in the management of these patients.

Indexed as

Insurance BenefitsSocial ValuesAdaptation, PsychologicalAdolescentCeliac DiseaseChildFemaleHumansMaleParentsPsychology, AdolescentQualitative ResearchQuality of LifeSocial SupportSurveys and Questionnaires

Identifiers

PMID21569235
PMCPMC3120678

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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.