Evidence map›Paper›PMID 31171027›Full record

ReviewOrphanet journal of rare diseases2019

Under-utilisation of reproducible, child appropriate or patient reported outcome measures in childhood uveitis interventional research.

Ameenat L Solebo, Robert J Barry, Pearse A Keane, Jugnoo S Rahi, Alastair K Denniston

Open access · goldAbstract readReview
In one paragraph

Review in Orphanet journal of rare diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 13% 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, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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 3 institutions in 1 country.

Ameenat L SoleboNIHR Moorfields Eye Hospital Biomedical Research Centre, London, UK.
Robert J BarryInstitute of Translational Medicine, Birmingham Health Partners, University of Birmingham, Birmingham, UK.
Pearse A KeaneNIHR Moorfields Eye Hospital Biomedical Research Centre, London, UK.
Jugnoo S RahiNIHR Moorfields Eye Hospital Biomedical Research Centre, London, UK.
Alastair K DennistonInstitute of Translational Medicine, Birmingham Health Partners, University of Birmingham, Birmingham, UK. a.denniston@bham.ac.uk.ORCID 0000-0001-7849-0087
Moorfields Eye Hospital NHS Foundation Trust · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBGreat Ormond Street Hospital · GB

Funding

Department of Health CS-2014-14-023Department of Health CS-2018-18-ST2-005
6 · The paper itself

Abstract

backgroundChildhood uveitis is a collection of chronic rare inflammatory eye disorders which result in visual loss in at least one eye of one fifth of affected children. Despite the introduction of novel systemic immunochemotherapies, it remains a blinding disease. We have undertaken a systematic review of outcome measures used in interventional trials of children with, or at risk of uveitis, in order to investigate metric quality and heterogeneity, as possible barriers to the translation of clinical research into improved outcomes.

methodsSystematic review of trials registered within databases approved by the International Committee of Medical Journal Editors (ICMJE). Eligible trials for were those which involved participants aged under 18 years with or at risk of non-infectious uveitis. Data on date of study commencement, uveitis site, inclusion age criteria, and outcome measure characteristics including type, dimension and quality were extracted independently by two authors. Quality was determined using the reproducibility, validity and age-appropriateness of the metric.

resultsOf 917 identified trials, 57 were eligible for inclusion. Twenty different domains across five dimensions were used as primary outcome measures. The structure most commonly used was multiple separate outcome measures. In a quarter of studies, outcomes were assessed less than 3 months following the intervention. Disease activity was the most commonly assessed dimension, with only 30 studies (60%) using reproducible methodologies to assess activity. Only 2/12 (18%) studies on intermediate or posterior uveitis used reproducible activity grading schemes. Of 18 studies involving children aged under 6 years old which used outcome measures related to visual function, only 8/18 (44%) described the use of age-appropriate acuity assessment measures. None of the studies used a vision related quality of life metrics which had been validated for use in childhood.

conclusionThis review of outcome measures in childhood uveitis interventional trials has identified under-utilisation of reproducible or child appropriate measures, and considerable heterogeneity in metric type, and structure. Clinicians and researchers interested in improving outcomes for affected children must identify a patient and family centred core outcome set, and work to validate both objective and patient (or proxy) reported disease age appropriate outcome measures.

Indexed as

Rare DiseasesChildChild, PreschoolFemaleHumansInfantInfant, NewbornMaleQuality of LifeUveitisOutcome measuresPaediatric uveitisRare disease

Identifiers

PMID31171027
PMCPMC6555041
OpenAlexW2949033876

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.