Evidence map›Paper›PMID 33008362›Full record

Observational studyBMC pulmonary medicine2020

Australasian interstitial lung disease registry (AILDR): objectives, design and rationale of a bi-national prospective database.

Irene Moore, Jeremy Wrobel, Jessica Rhodes, Qi Lin, Susanne Webster, Helen Jo, Lauren Troy, Christopher Grainge, Ian Glaspole, Tamera J Corte and 1 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMC pulmonary medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Global epidemiology and burden of interstitial lung disease.The Lancet. Respiratory medicine · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Relative incidence of interstitial lung diseases in Brazil.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. 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

11 authors at 5 institutions in 2 countries.

Irene MooreAdvanced Lung Disease Unit, Fiona Stanley Hospital, PO Box Locked Bag 100, Palmyra DC, Perth, WA, 6961, Australia. imoore03@qub.ac.uk.ORCID http://orcid.org/0000-0003-1827-4168
Jeremy WrobelAdvanced Lung Disease Unit, Fiona Stanley Hospital, PO Box Locked Bag 100, Palmyra DC, Perth, WA, 6961, Australia.
Jessica RhodesRoyal Prince Alfred Hospital, Sydney, NSW, Australia.
Qi LinRoyal Prince Alfred Hospital, Sydney, NSW, Australia.
Susanne WebsterRoyal Prince Alfred Hospital, Sydney, NSW, Australia.
Helen JoRoyal Prince Alfred Hospital, Sydney, NSW, Australia.
Lauren TroyRoyal Prince Alfred Hospital, Sydney, NSW, Australia.
Christopher GraingeJohn Hunter Hospital, Sydney, NSW, Australia.
Ian GlaspoleThe Alfred Hospital, Melbourne, VIC, Australia.
Tamera J CorteRoyal Prince Alfred Hospital, Sydney, NSW, Australia.
Australasian ILD Registry
Royal Prince Alfred Hospital · AUThe University of Sydney · AUFiona Stanley Hospital · AUJohn Hunter Hospital · AUThe Alfred Hospital · AU

Funding

National Health and Medical Research Council GNT1116371
6 · The paper itself

Abstract

backgroundInterstitial Lung Disease (ILD) is a group of respiratory conditions affecting the lung interstitium often associated with progressive respiratory failure. There is increasing recognition of the need for improved epidemiological data to help determine best practice and improve standardisation of care. The Australasian ILD Registry (AILDR) is a bi-national registry of patients with all ILD subtypes designed to establish a clinically meaningful database reflecting real world practice in Australasia with an objective to improve diagnostic and treatment pathways through research and collaboration.

methodsAILDR is a prospective observational registry recruiting patients attending ILD clinics at centres around Australia and New Zealand. Core and non-core data are stored on a secure server. The pilot phase was launched in 2016 consisting of four sites in Australia. Currently in its second phase a further 16 sites have been recruited, including three in New Zealand.

resultsA total of 1061 participants were consented during the pilot phase. Baseline data demonstrated a mean age 68.3 ± 12.5 (SD) years, mean FVC (%predicted) 79.1 ± 20.4 (SD), mean DLCO (%predicted) 58.5 ± 17.9 (SD) and nadir exertional SpO2 (%) 91 ± 6.9 (SD). Idiopathic pulmonary fibrosis (31%) and connective-tissue disease related ILD (21.7%) were the two most common subtypes. Baseline demographics and physiology were not significantly different across the four centres.

conclusionAILDR is an important clinical and research tool providing a platform for epidemiological data that will prove essential in promoting understanding of a rare cohort of lung disease and provide foundations for our aspiration to standardise investigation and treatment pathways of ILD across Australasia.

Indexed as

Lung Diseases, InterstitialOutcome Assessment, Health CareRegistriesAgedAged, 80 and overAustraliaConnective Tissue DiseasesDatabases, FactualFemaleHumansIdiopathic Pulmonary FibrosisMaleMiddle AgedNew ZealandProspective StudiesAutoimmune diseaseClinical epidemiologyInterstitial lung diseaseLung fibrosisRegistry

Identifiers

PMID33008362
PMCPMC7532571
OpenAlexW3089679280

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.