Evidence map›Paper›PMID 29321018›Full record

ArticleBMC pulmonary medicine2018

Management and attitudes about IPF (Idiopathic Pulmonary Fibrosis) among physicians from Latin America.

Iván Cherrez-Ojeda, Vincent Cottin, Juan Carlos Calderón, César Delgado, Erick Calero, Daniel Simanca-Racines, Silvia Quadrelli, Annia Cherrez

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC pulmonary medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Safety and tolerability of nintedanib in patients with idiopathic pulmonary fibrosis in Brazil.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2019
    Article
  8. 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 at 6 institutions in 4 countries.

Iván Cherrez-OjedaUniversidad de Especialidades Espíritu Santo, Samborondón, Ecuador. ivancherrez@gmail.com.ORCID http://orcid.org/0000-0002-1610-239X
Vincent CottinLouis Pradel Hospital, Reference center for rare pulmonary diseases, Auvernia-Ródano-Alpes, Lyon, France.
Juan Carlos CalderónUniversidad de Especialidades Espíritu Santo, Samborondón, Ecuador.
César DelgadoHospital Metropolitano, Quito, Ecuador.
Erick CaleroUniversidad de Especialidades Espíritu Santo, Samborondón, Ecuador.
Daniel Simanca-RacinesCentro de Investigación en Salud Pública y Epidemiología Clínica. Facultad de Ciencias de la Salud Eugenio Espejo. Universidad Tecnológica Equinoccial., Quito, Ecuador.
Silvia QuadrelliHospital Británico, Buenos Aires, Argentina.
Annia CherrezRespiralab, Respiralab Research Group, Guayaquil, Ecuador.
Universidad de Especialidades Espíritu Santo · ECHeidelberg University · DEHelios Salud · ARHôpital Louis Pradel · FRHospital Metropolitano · ECUniversidad UTE · EC

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of our study was to assess current practice patterns and attitudes towards diagnosis and management of idiopathic pulmonary fibrosis (IPF) patients in Latin America.

methodsA Cross-sectional survey was developed and up to 455 physicians were enrolled. We used a rigorous method of validation using the translated version of the AIR Survey.

resultsMean age was 47.5 years (SD 12.6) with 20.4 years (SD 12.3) of practice. In around 30% of physicians were reported access to radiologist, pathologist and multidisciplinary team. Despite almost all physicians reported that (ATS/ERS/JRS/ALAT) guidelines are useful, half of them prescribed corticoids for treatment of disease. Most respondents (69.9%) reported cough as the presenting symptom. Around 80% considered IPF to be an important clinical disorder, and felt that identifying patients at risk for IPF was important or extremely important. However, only 59.7% felt confident in managing patients with IPF, and similar numbers (60.8%) felt confident about their knowledge. Pulmonologist have more confidence and management of IPF that no pulmonologist.

conclusionThe results of this survey of Latin American physicians could help to fill gaps regarding awareness, management and treatment of IPF and improve earlier diagnosis of IPF.

Indexed as

Attitude of Health PersonnelPractice Patterns, Physicians'Pulmonary MedicineAdultClinical CompetenceCross-Sectional StudiesDisease ProgressionFemaleHumansIdiopathic Pulmonary FibrosisLatin AmericaMaleMiddle AgedPathologyPatient Care TeamPractice Guidelines as TopicAttitudesHealth knowledgeIdiopathic pulmonary fibrosisLatin AmericaPhysiciansPracticeSurveys and questionnaires

Identifiers

PMID29321018
PMCPMC5763612
OpenAlexW2783641600

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.