Evidence map›Paper›PMID 36855412›Full record

ArticleNIHR open research2022

Exploring the nature of perceived treatment burden: a study to compare treatment burden measures in adults with cystic fibrosis [version 1; peer review: 2 approved].

Rana Altabee, Siobhan B Carr, Janice Abbott, Rory Cameron, Daniel Office, Jessie Matthews, Nicholas Simmonds, Rebecca Cosgriff, David Turner, Jennifer Whitty

Open access · diamondAbstract read
In one paragraph

Article in NIHR open research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
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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

10 authors at 4 institutions in 2 countries.

Rana AltabeeHealth Economics Group, Norwich Medical School, University of East Anglia, Norwich, NR4 7TJ, UK.ORCID https://orcid.org/0000-0001-8626-5269
Siobhan B CarrDepartment of Paediatric Respiratory Medicine, Royal Brompton & Harefield NHS Trust, London, SW3 6NP, UK.ORCID https://orcid.org/0000-0003-0580-2478
Janice AbbottSchool of Psychology, University of Central Lancashire, Preston, PR1 2HE, UK.
Rory CameronHealth Economics Group, Norwich Medical School, University of East Anglia, Norwich, NR4 7TJ, UK.ORCID https://orcid.org/0000-0002-7442-0935
Daniel OfficeAdult Cystic Fibrosis Centre, Royal Brompton & Harefield NHS Trust, London, SW3 6NP, UK.
Jessie MatthewsAdult Cystic Fibrosis Centre, Royal Brompton & Harefield NHS Trust, London, SW3 6NP, UK.
Nicholas SimmondsNational Heart and Lung Institute, Imperial College London, London, SW7 2BX, UK.
Rebecca CosgriffCystic Fibrosis Trust, London, EC3N 1RE, UK.
David TurnerHealth Economics Group, Norwich Medical School, University of East Anglia, Norwich, NR4 7TJ, UK.ORCID https://orcid.org/0000-0002-1689-4147
Jennifer WhittyHealth Economics Group, Norwich Medical School, University of East Anglia, Norwich, NR4 7TJ, UK.
Royal Brompton & Harefield NHS Foundation Trust · GBUniversity of East Anglia · GBCystic Fibrosis Trust · GBUniversity of Lancashire · GB

Funding

Department of Health PB-PG-1217-20018
6 · The paper itself

Abstract

Background: Despite the importance of reducing treatment burden for people with cystic fibrosis (CF), it has not been fully understood as a concept. This study aims to quantify the treatment burden perceived by CF adults and explore the association between different validated treatment burden measures. Methods: This is a cross-sectional observational study of CF adults attending a single large UK adult center. Participants completed an online survey that contained three different treatment burden scales; CF Questionnaire-Revised (CFQ-R) subscale, CF Quality of Life (CFQoL) subscale, and the generic multimorbidity treatment burden questionnaire (MTBQ). Results: Among 101 participants, the median reported treatment burden by the CFQ-R subscale was 55.5 (IQR 33.3 - 66.6), the CFQoL subscale was 66.6 (IQR 46.6 - 86.6), and the MTBQ reversed global score was 84.6 (IQR 73.1 - 92.3). No correlation was found between respondents' demographic or clinical variables and treatment burden measured via any of the three measures. All treatment burden measures showed correlations against each other. More treatments were associated with high treatment burden as measured by the CFQ-R, CFQoL subscales, and the MTBQ. However, longer treatment time and more complex treatment plans were correlated with high treatment burden as measured by the CFQ-R and CFQoL subscales, but not with the MTBQ. Conclusions: Treatment burden is a substantial issue in CF. Currently, the only available way to evaluate it is with the CF-specific quality of life measure treatment burden subscales (CFQ-R and CFQoL); both indicated that treatment burden increases with more treatments, longer treatment time, and more complex treatments.

Indexed as

cystic fibrosispatient-reported outcomestreatment burden

Identifiers

PMID36855412
PMCPMC7614250
OpenAlexW4229377027

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.