Evidence map›Paper›PMID 32163363›Full record

ArticleTurkish thoracic journal2020

Survey of Physician's Knowledge, Attitudes, and Practices Regarding Idiopathic Pulmonary Fibrosis in Turkey.

Haluk Türktaş, Gülfer Okumuş, Oğuz Uzun, Özlem Özdemir Kumbasar, Göksel Altınışık, Züleyha Bingöl, Şermin Börekçi, Vincent Cottin, Benan Müsellim

Open access · diamondAbstract read
In one paragraph

Article in Turkish thoracic journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 81% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Observational
  2. 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

9 authors at 2 institutions in 1 country.

Haluk TürktaşDepartment of Pulmonary Diseases, Gazi University School of Medicine, Ankara, Turkey.ORCID https://orcid.org/0000-0002-2598-6553
Gülfer OkumuşDepartment of Pulmonary Diseases, İstanbul University İstanbul School of Medicine, İstanbul, Turkey.ORCID https://orcid.org/0000-0001-8309-1216
Oğuz UzunDepartment of Pulmonary Diseases, Ondokuz Mayıs University School of Medicine, Samsun, Turkey.ORCID https://orcid.org/0000-0002-0475-4198
Özlem Özdemir KumbasarDepartment of Pulmonary Diseases, Ankara University School of Medicine, Ankara, Turkey.ORCID https://orcid.org/0000-0003-4599-1461
Göksel AltınışıkDepartment of Pulmonary Diseases, Pamukkale University School of Medicine, Denizli, Turkey.ORCID https://orcid.org/0000-0001-6869-1301
Züleyha BingölDepartment of Pulmonary Diseases, İstanbul University İstanbul School of Medicine, İstanbul, Turkey.ORCID https://orcid.org/0000-0002-1414-617X
Şermin BörekçiDepartment of Pulmonary Diseases, İstanbul University-Cerrahpaşa, Cerrahpaşa School of Medicine, İstanbul, Turkey.ORCID https://orcid.org/0000-0002-0089-1312
Vincent CottinClaude Bernard University, Reference Center for Rare Pulmonary Diseases, UMR754, Lyon, France.ORCID https://orcid.org/0000-0002-5591-0955
Benan MüsellimDepartment of Pulmonary Diseases, İstanbul University-Cerrahpaşa, Cerrahpaşa School of Medicine, İstanbul, Turkey.ORCID https://orcid.org/0000-0002-7678-3393
Ankara University · TRGazi University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe aim of this study is to evaluate the approaches of Turkish pulmonologists to the diagnosis and treatment of idiopathic pulmonary fibrosis (IPF) in daily clinical practice. MATERIALS AND

methodsA questionnaire containing 38 questions about the IPF diagnosis and treatment was given to pulmonologists between January 22 and 29, 2018, and the data of 158 physicians who responded to the questionnaire were evaluated.

resultsThis survey showed that the mean number of patients that physicians followed up and managed annually was 8.3 and 5, respectively. The mean symptom duration before the diagnosis was 9-12 months. Patients were seen on average by three physicians prior to confirmed diagnosis. Almost 80% of the physicians have an opportunity to access a pathologist and radiologist specialized in IPF. However, only 26% of them have an opportunity to access regular multidisciplinary meetings. Although antifibrotics were the most commonly prescribed drugs, approximately 10% of patients were prescribed steroids, N-acetylcysteine, and immunosuppressants. Most of the physicians (81%) were aware of international guidelines; however, the Turkish Thoracic Society IPF Diagnosis and Treatment Consensus Report was read by only 41% of them.

conclusionThis survey may lead to the IPF awareness in Turkey, and it may help to close the gaps regarding the diagnosis and treatment.

Identifiers

PMID32163363
PMCPMC7020893
OpenAlexW2978184112

What OpenQuestion holds

Textmetadata
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.