Evidence map›Paper›PMID 33980667›Full record

SynthesisEuropean respiratory review : an official journal of the European Respiratory Society2021

The measurement properties of tests and tools used in cystic fibrosis studies: a systematic review.

Charlie McLeod, Jamie Wood, Allison Tong, André Schultz, Richard Norman, Sherie Smith, Christopher C Blyth, Steve Webb, Alan R Smyth, Thomas L Snelling

Abstract readSystematic Review
In one paragraph

Synthesis in European respiratory review : an official journal of the European Respiratory Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
–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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Thymidine-dependent Staphylococcus aureus and lung function in patients with cystic fibrosis: a 10-year retrospective case-control study.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2024
    Article
  7. Article
  8. Guidance and standard operating procedures for functional exercise testing in cystic fibrosis.European respiratory review : an official journal of the European Respiratory Society · 2023
    Review
  9. Article
  10. Article
  11. 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

10 authors.

Charlie McLeodWesfarmers Centre for Vaccines and Infectious Diseases, Telethon Kids Institute, Nedlands, Australia charlie.mcleod@health.wa.gov.au.ORCID https://orcid.org/0000-0002-3197-7493
Jamie WoodPhysiotherapy Dept, Sir Charles Gairdner Hospital, Nedlands, Australia.
Allison TongSydney School of Public Health, The University of Sydney, Sydney, Australia.
André SchultzWal-yan Respiratory Research Centre, Telethon Kids Institute, University of Western Australia, Nedlands, Australia.
Richard NormanSchool of Population Health, Curtin University, Bentley, Australia.
Sherie SmithEvidence Based Child Health Group, University of Nottingham, Queens Medical Centre, Nottingham, UK.
Christopher C BlythWesfarmers Centre for Vaccines and Infectious Diseases, Telethon Kids Institute, Nedlands, Australia.
Steve WebbSt John of God Hospital, Subiaco, Australia.
Alan R SmythEvidence Based Child Health Group, University of Nottingham, Queens Medical Centre, Nottingham, UK.
Thomas L SnellingSydney School of Public Health, The University of Sydney, Sydney, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is no consensus on how best to measure responses to interventions among children and adults with cystic fibrosis (CF). We have systematically reviewed and summarised the characteristics and measurement properties of tests and tools that have been used to capture outcomes in studies among people with CF, including their reliability, validity and responsiveness. This review is intended to guide researchers when selecting tests or tools for measuring treatment effects in CF trials. A consensus set of these tests and tools could improve consistency in how outcomes are captured and thereby facilitate comparisons and synthesis of evidence across studies.

Indexed as

Cystic FibrosisAdultChildHumansReproducibility of Results

Identifiers

PMID33980667
PMCPMC9489019

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.