Evidence map›Paper›PMID 32474425›Full record

ArticleBMJ open2020

Historical database cohort study addressing the clinical patterns prior to idiopathic pulmonary fibrosis (IPF) diagnosis in UK primary care.

David Thickett, Jaco Voorham, Ronan Ryan, Rupert Jones, Robina Coker, Andrew M Wilson, Sen Yang, Mandy Yl Ow, Priyanka Raju, Isha Chaudhry and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2020. 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
0.8field-weighted citation impact, top 25% 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, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Idiopathic pulmonary fibrosis: Current and future treatment.The clinical respiratory journal · 2022
    Review
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

13 authors at 6 institutions in 2 countries.

David ThickettInstitute of Inflammation, University of Birmingham, Birmingham, UK.
Jaco VoorhamObservational and Pragmatic Research Institute Pte Ltd, Singapore.
Ronan RyanObservational and Pragmatic Research Institute Pte Ltd, Singapore.
Rupert JonesPeninsula Medical School, University of Plymouth, Plymouth, Devon, UK.
Robina CokerImperial College London, London, UK.
Andrew M WilsonRespiratory and Airways Group, Norwich Medical School, University of East Anglia, Norwich, UK.
Sen YangObservational and Pragmatic Research Institute Pte Ltd, Singapore.
Mandy Yl OwObservational and Pragmatic Research Institute Pte Ltd, Singapore.
Priyanka RajuObservational and Pragmatic Research Institute Pte Ltd, Singapore.
Isha ChaudhryObservational and Pragmatic Research Institute Pte Ltd, Singapore.
Antony HardjojoObservational and Pragmatic Research Institute Pte Ltd, Singapore.
Victoria CarterObservational and Pragmatic Research Institute Pte Ltd, Singapore.
David B PriceObservational and Pragmatic Research Institute Pte Ltd, Singapore dprice@opri.sg.ORCID 0000-0002-9728-9992
Observational & Pragmatic Research Institute · SGImperial College London · GBUniversity of Aberdeen · GBUniversity of Birmingham · GBUniversity of East Anglia · GBUniversity of Plymouth · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the clinical pathways, including signs and symptoms, and symptom progression patterns preceding idiopathic pulmonary fibrosis (IPF) diagnosis. DESIGN AND

settingA historical cohort study was conducted using primary care patient records from the Optimum Patient Care Research Database.

participantsPatients included were at least 30 years, had IPF diagnosis, identified via clinical-coding and free-text records and had a consultation with a chest specialist prior to IPF diagnosis. OUTCOME MEASURES: The signs and symptoms in the year prior to IPF diagnosis from clinical codes and free-text in primary care electronic records included: cough, dyspnoea, dry cough, weight loss, fatigue/malaise, loss of appetite, crackles and clubbed fingers. The time course of presentations of clinical features and investigations in the years prior to IPF diagnosis were mapped.

resultsWithin 462 patients identified, the majority (77.9%) had a respiratory consultation within 365 days prior to the chest specialist visit preceding the IPF diagnosis recorded in their primary care records. The most common symptoms recorded in the 1 year prior to IPF diagnosis were dyspnoea (48.7%) and cough (40.9%); other signs and symptoms were rarely recorded (<5%). The majority of patients with cough (58.0%) and dyspnoea (55.0%) in the 1 year before IPF diagnosis had multiple recordings of the respective symptoms. Both cough and dyspnoea were recorded in 23.4% of patients in the year prior to diagnosis. Consultation rates for cough, dyspnoea and both, but not other signs or symptoms, began to increase 4 to 5 years prior diagnosis, with the sharpest increase in the last year. Cough and dyspnoea were often preceded by a reduction in measured weight over 5 years leading to IPF diagnosis.

conclusionProlonged cough and/or progressive dyspnoea, especially if accompanied with weight loss, should signal for a referral to specialist assessment at the earliest opportunity.

Indexed as

Idiopathic Pulmonary FibrosisCohort StudiesCoughHumansPrimary Health CareUnited Kingdomfree-text recordinterstitial lung diseasepathway featuresprincipal component analysis

Identifiers

PMID32474425
PMCPMC7264834
OpenAlexW3012107336

What OpenQuestion holds

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LicenceCC BY-NC
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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.