Evidence map›Paper›PMID 26557259›Full record

ArticleEuropean clinical respiratory journal2015

Organisation of diagnosis and treatment of idiopathic pulmonary fibrosis and other interstitial lung diseases in the Nordic countries.

Elisabeth Bendstrup, Charlotte Hyldgaard, Alan Altraja, Tone Sjåheim, Marjukka Myllärniemi, Gunnar Gudmundsson, Magnus Sköld, Ole Hilberg

Registry-linked trialAbstract read
In one paragraph

Article in European clinical respiratory journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06465654 (OXYWILD - Automated Oxygen Titration With O2matic During Walking in Patients With Fibrotic Interstitial Lung Diseases), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

NCT06465654 nacompletednot on this mapstarted 2024, after this paper: background citation

OXYWILD - Automated Oxygen Titration With O2matic During Walking in Patients With Fibrotic Interstitial Lung Diseases (F-ILD): A Randomized Study

TypeinterventionalSponsorJanne Hastrup JensenRan2024 to 2025Enrolled29ConditionsFibrosis Lung, Respiratory TherapyArmsAutomated variable dose oxygen treatment, Fixed dose oxygen treatment
3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Best supportive care for idiopathic pulmonary fibrosis: current gaps and future directions.European respiratory review : an official journal of the European Respiratory Society · 2018
    Review
  5. 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

8 authors.

Elisabeth BendstrupDepartment of Respiratory Diseases and Allergy, Aarhus University Hospital, Aarhus, Denmark.
Charlotte HyldgaardDepartment of Respiratory Diseases and Allergy, Aarhus University Hospital, Aarhus, Denmark.
Alan AltrajaDepartment of Respiratory Diseases, University of Tartu, Tallinn, Estonia.
Tone SjåheimDepartment of Respiratory Diseases, Oslo University Hospital, Oslo, Norway.
Marjukka MyllärniemiDepartment of Respiratory Diseases and Heart and Lung Center, University of Helsinki and Helsingin University Central Hospital, Helsinki, Finland.
Gunnar GudmundssonDepartment of Respiratory Medicine and Sleep, Landspitali, The National University Hospital of Iceland, Reykjavik, Iceland ; Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.
Magnus SköldDepartment of Medicine Solna, Karolinska Institutet, Lung Allergy Clinic, Karolinska University Hospital, Stockholm, Sweden.
Ole HilbergDepartment of Respiratory Diseases and Allergy, Aarhus University Hospital, Aarhus, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDifferences in the organisation of idiopathic pulmonary fibrosis (IPF) and interstitial lung diseases (ILDs) in the Nordic countries are not well described. Diagnostic setups, treatment modalities and follow-up plans may vary due to national, cultural and epidemiological features. The aim of the present study was to describe the different organisation of diagnostics and treatment of IPF and ILD in the Nordic countries.

methodsAll university and regional hospitals with respiratory physicians were invited to respond to a questionnaire collecting data on the number of physicians, nurses, patients with ILD/IPF, the presence of and adherence to disease-specific national and international guidelines, diagnosis and treatment including ILD-specific palliation and rehabilitation programmes.

resultsTwenty-four university and 22 regional hospitals returned the questionnaire. ILD and IPF incidence varied between 1.4 and 20/100,000 and 0.4 and 10/100,000, respectively. Denmark and Estonia have official national plans for the organisation of ILD. The majority of patients are managed at the university hospitals. The regional hospitals each manage 46 (5-200) patients with ILD and 10 (0-20) patients with IPF. There are from one to four ILD centres in each country with a median of two ILD specialists employed. Specialised ILD nurses are present in nine hospitals. None of the Nordic countries have national guidelines made by health authorities. The respiratory societies in Sweden, Norway and Denmark have developed national guidelines. All hospitals except two use the ATS/ERS/JRS/ALAT IPF guidelines from 2011. The limited number of ILD specialists, ILD-specialised radiologists and pathologists and the low volume of ILD centres were perceived as bottlenecks for implementation of guidelines. Twenty of the 24 university hospitals have multidisciplinary conferences (MDCs). Pulmonologists and radiologists take part in all MDCs while pathologists only participate at 17 hospitals. Prescription of pirfenidone is performed by all university hospitals except in Estonia. Triple therapy with steroid, azathioprine and N-acetylcysteine is not used. No hospitals have specific palliation programmes for patients with ILD/IPF, but 36 hospitals have the possibility of referring patients for palliative care, mostly based on existing oncology palliative care teams; seven hospitals have rehabilitation programmes for ILD.

conclusionThere are obvious differences between the organisations of ILD patients in the Nordic countries. We call for national plans that consider the challenge of cultural and geographical differences and suggest the establishment of national reference centres and satellite collaborative hospitals to enable development of common guidelines for diagnostics, therapy and palliation in this patient group.

Indexed as

diagnosisguidelinesidiopathic pulmonary fibrosisinterstitial lung diseaseorganisationtreatment

Identifiers

PMID26557259
PMCPMC4629764

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