Evidence map›Paper›PMID 37004203›Full record

ArticleQJM : monthly journal of the Association of Physicians2023

Classifying the unclassifiable-a Delphi study to reach consensus on the fibrotic nature of diseases.

G M Massen, R J Allen, O C Leavy, N M Selby, G P Aithal, N Oliver, H Parfrey, L V Wain, G Jenkins, I Stewart and 1 more

Erratum issuedAbstract readConsensus Statement
In one paragraph

Article in QJM : monthly journal of the Association of Physicians, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Observational
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

G M MassenNational Heart and Lung Institute, Imperial College London, London, W12 0BZ, UK.ORCID 0000-0003-4355-6546
R J AllenDepartment of Population Health Sciences, University of Leicester, Leicester, LE1 7RH, UK.
O C LeavyDepartment of Population Health Sciences, University of Leicester, Leicester, LE1 7RH, UK.
N M SelbyDepartment of Renal Medicine,, Derby Hospitals Foundation Trust, Derby, DE22 3NE,UK.
G P AithalNIHR Nottingham Digestive Diseases Biomedical Research Unit, University of Nottingham, Nottingham, NG7 2UH, UK.
N OliverDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, SW7 2AZUK.ORCID 0000-0003-3525-3633
H ParfreyCambridge Interstitial Lung Disease Unit, Royal Papworth Hospital, Cambridge, CB2 0AY, UK.
L V WainDepartment of Population Health Sciences, University of Leicester, Leicester, LE1 7RH, UK.
G JenkinsNational Heart and Lung Institute, Imperial College London, London, W12 0BZ, UK.
I StewartNational Heart and Lung Institute, Imperial College London, London, W12 0BZ, UK.
J K QuintNational Heart and Lung Institute, Imperial College London, London, W12 0BZ, UK.

Funding

Medical Research Council MR/V005324/1Medical Research Council MR/W014491/1
6 · The paper itself

Abstract

backgroundTraditionally, clinical research has focused on individual fibrotic diseases or fibrosis in a particular organ. However, it is possible for people to have multiple fibrotic diseases. While multi-organ fibrosis may suggest shared pathogenic mechanisms, yet there is no consensus on what constitutes a fibrotic disease and therefore fibrotic multimorbidity.

aimA Delphi study was performed to reach consensus on which diseases may be described as fibrotic.

methodsParticipants were asked to rate a list of diseases, sub-grouped according to eight body regions, as 'fibrotic manifestation always present', 'can develop fibrotic manifestations', 'associated with fibrotic manifestations' or 'not fibrotic nor associated'. Classifications of 'fibrotic manifestation always present' and 'can develop fibrotic manifestations' were merged and termed 'fibrotic'. Clinical consensus was defined according to the interquartile range, having met a minimum number of responses. Clinical agreement was used for classification where diseases did not meet the minimum number of responses (required for consensus measure), were only classified if there was 100% consensus on disease classification.

resultsAfter consulting experts, searching the literature and coding dictionaries, a total of 323 non-overlapping diseases which might be considered fibrotic were identified; 92 clinical specialists responded to the first round of the survey. Over three survey rounds, 240 diseases were categorized as fibrotic via clinical consensus and 25 additional diseases through clinical agreement.

conclusionUsing a robust methodology, an extensive list of diseases was classified. The findings lay the foundations for studies estimating the burden of fibrotic multimorbidity, as well as investigating shared mechanisms and therapies.

Indexed as

MultimorbidityDelphi TechniqueFibrosisHumansSurveys and Questionnaires

Identifiers

PMID37004203
PMCPMC10250078

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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.