Evidence map›Paper›PMID 37505797›Full record

ArticleJMIR formative research2023

Using Patient Blogs on Social Media to Assess the Content Validity of Patient-Reported Outcome Measures: Qualitative Analysis of Patient-Written Blogs.

Diana M J Delnoij, Meggie Derks, Laura Koolen, Shuka Shekary, Jozua Suitela

Abstract read
In one paragraph

Article in JMIR formative research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

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

2 citing papers in PubMed.

  1. Review
  2. 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.

Diana M J DelnoijErasmus School of Health Policy & Management, Erasmus University Rotterdam, Rotterdam, Netherlands.ORCID https://orcid.org/0000-0002-2066-9604
Meggie DerksErasmus School of Health Policy & Management, Erasmus University Rotterdam, Rotterdam, Netherlands.ORCID https://orcid.org/0009-0002-9019-7371
Laura KoolenErasmus School of Health Policy & Management, Erasmus University Rotterdam, Rotterdam, Netherlands.ORCID https://orcid.org/0000-0001-9974-4058
Shuka ShekaryErasmus School of Health Policy & Management, Erasmus University Rotterdam, Rotterdam, Netherlands.ORCID https://orcid.org/0009-0006-0571-4979
Jozua SuitelaErasmus School of Health Policy & Management, Erasmus University Rotterdam, Rotterdam, Netherlands.ORCID https://orcid.org/0009-0001-4637-8573

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatient-reported outcome measures (PROMs) are questionnaires that measure patient outcomes related to quality of life, health, and functioning, and are increasingly used to assess important outcomes from the patient's perspective. For PROMs to contribute to better health and better care, it is vital that their content validity be adequate. This requires patient involvement in various steps of PROM development. PROM developers not only recognize the benefits of patient involvement but also report difficulties in recruiting patients and experience patient involvement as time-consuming, logistically challenging, and expensive.

objectiveThis study seeks to explore different strategies for disclosing the experiential knowledge of patients, namely through analyzing patient stories on the web and social media. The research questions are as follows: (1) how do bloggers living with a disease experience their health-related quality of life? (2) How are these experiences reflected in the domains and items of PROMs related to their disease?

methodsFirst, a qualitative analysis of blogs written by patients was performed. Second, subthemes and underlying codes resulting from this qualitative analysis were systematically compared with the domains and items in PROMs for the respective diseases that the bloggers write about. Blogs were identified via the Google search engine between December 2019 and May 2021.

resultsBloggers describe a wide range of experiences regarding their physical functioning and health; mental well-being; social network and support; daily life, education, work, and leisure; coping; and self-management. Bloggers also write about their positive and negative experiences with health care delivery, the organization of health care, and health care professionals. In general, patients' experiences as described in blogs were reflected in the domains and items of the PROMs related to their disease. However, except for diabetes mellitus, in all the sets of PROMs, potentially missing topics could be identified. Similarly, with the exception of Parkinson disease, all PROMs address issues that patients did not write about in their blogs and that might therefore be redundant.

conclusionsWeb-based patient stories in the form of blogs reveal how people living with a certain disease experience their health-related quality of life. These stories enable analyses of patients' experiences that can be used to assess the content validity of PROMs. This can be a useful step for researchers who are looking for sets of measuring instruments that match their purposes.

Indexed as

bloggerbreast cancercancerchronic diseasecontent analysiscontent validitycross sectionalcross-sectionaldata dictionarydiabetesexperienceexperientialHAQHealth Assessment QuestionnaireICHOMinductiveinductive codeInternational Consortium for Health Outcome MeasurementnarrativeNCDnoncommunicable diseasesoncologyParkinson disease, diabetes mellitusParkinson Disease Quality of Life Questionnairepatient-reported outcome measurepatient storiespatient storyPDQPROMqualitativerheumatoid arthritissocial mediastorytellingtype II diabetes

Identifiers

PMID37505797
PMCPMC10422175

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Registered trials

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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.