Are physicians in primary health care able to recognize pulmonary fibrosis?

Background: The early diagnosis of idiopathic pulmonary fibrosis (IPF) has become increasingly important due to evolving treatment options. IPF patients experience a significant delay in receiving an accurate diagnosis, thus delayed access to tertiary care is associated with higher mortality indepen...

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Main Authors: Minna Purokivi, Ulla Hodgson, Marjukka Myllärniemi, Eija-Riitta Salomaa, Riitta Kaarteenaho
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:European Clinical Respiratory Journal
Subjects:
Online Access:http://dx.doi.org/10.1080/20018525.2017.1290339
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spelling doaj-85626d7e85564a5fa4020b591b721df32020-12-07T18:06:37ZengTaylor & Francis GroupEuropean Clinical Respiratory Journal2001-85252017-01-014110.1080/20018525.2017.12903391290339Are physicians in primary health care able to recognize pulmonary fibrosis?Minna Purokivi0Ulla Hodgson1Marjukka Myllärniemi2Eija-Riitta Salomaa3Riitta Kaarteenaho4Kuopio University HospitalHeart and Lung CenterHeart and Lung CenterUniversity of TurkuKuopio University HospitalBackground: The early diagnosis of idiopathic pulmonary fibrosis (IPF) has become increasingly important due to evolving treatment options. IPF patients experience a significant delay in receiving an accurate diagnosis, thus delayed access to tertiary care is associated with higher mortality independently from disease severity. Objective: The aims were to evaluate whether there had been a delay in the referral process, and to determine whether the referring doctors had suspected IPF or other interstitial lung disease (ILD) already during the time of referral. Methods: Ninety-five referral letters of patients with IPF identified from the FinnishIPF registry were evaluated with respect to time of referral, referring unit, grounds for referral, symptoms, smoking status, occupational history, clinical examinations, co-morbidities, medication, radiological findings and lung function. Results: Fifty-nine percent of referral letters originated from primary public health care. The time from symptom onset to referral was reported in 60% of cases, mean time being 1.5 (0.8–2.3) (95%CI) years. The main reason for referral was a suspicion of interstitial lung disease (ILD) (63%); changes in chest X-ray were one reason for referring in 53% of cases. Lung auscultation was reported in 70% and inspiratory crackles in 52% of referral letters. Conclusions: Primary care doctors suspected lung fibrosis early in the course of disease. Lung auscultation and chest X-rays were the most common investigational abnormalities in the referrals. Providing general practitioners with more information of ILDs might shorten the delay from symptom onset to referral.http://dx.doi.org/10.1080/20018525.2017.1290339referral letteridiopathic pulmonary fibrosisinterstitial lung diseaseprimary caretertiary careregistry
collection DOAJ
language English
format Article
sources DOAJ
author Minna Purokivi
Ulla Hodgson
Marjukka Myllärniemi
Eija-Riitta Salomaa
Riitta Kaarteenaho
spellingShingle Minna Purokivi
Ulla Hodgson
Marjukka Myllärniemi
Eija-Riitta Salomaa
Riitta Kaarteenaho
Are physicians in primary health care able to recognize pulmonary fibrosis?
European Clinical Respiratory Journal
referral letter
idiopathic pulmonary fibrosis
interstitial lung disease
primary care
tertiary care
registry
author_facet Minna Purokivi
Ulla Hodgson
Marjukka Myllärniemi
Eija-Riitta Salomaa
Riitta Kaarteenaho
author_sort Minna Purokivi
title Are physicians in primary health care able to recognize pulmonary fibrosis?
title_short Are physicians in primary health care able to recognize pulmonary fibrosis?
title_full Are physicians in primary health care able to recognize pulmonary fibrosis?
title_fullStr Are physicians in primary health care able to recognize pulmonary fibrosis?
title_full_unstemmed Are physicians in primary health care able to recognize pulmonary fibrosis?
title_sort are physicians in primary health care able to recognize pulmonary fibrosis?
publisher Taylor & Francis Group
series European Clinical Respiratory Journal
issn 2001-8525
publishDate 2017-01-01
description Background: The early diagnosis of idiopathic pulmonary fibrosis (IPF) has become increasingly important due to evolving treatment options. IPF patients experience a significant delay in receiving an accurate diagnosis, thus delayed access to tertiary care is associated with higher mortality independently from disease severity. Objective: The aims were to evaluate whether there had been a delay in the referral process, and to determine whether the referring doctors had suspected IPF or other interstitial lung disease (ILD) already during the time of referral. Methods: Ninety-five referral letters of patients with IPF identified from the FinnishIPF registry were evaluated with respect to time of referral, referring unit, grounds for referral, symptoms, smoking status, occupational history, clinical examinations, co-morbidities, medication, radiological findings and lung function. Results: Fifty-nine percent of referral letters originated from primary public health care. The time from symptom onset to referral was reported in 60% of cases, mean time being 1.5 (0.8–2.3) (95%CI) years. The main reason for referral was a suspicion of interstitial lung disease (ILD) (63%); changes in chest X-ray were one reason for referring in 53% of cases. Lung auscultation was reported in 70% and inspiratory crackles in 52% of referral letters. Conclusions: Primary care doctors suspected lung fibrosis early in the course of disease. Lung auscultation and chest X-rays were the most common investigational abnormalities in the referrals. Providing general practitioners with more information of ILDs might shorten the delay from symptom onset to referral.
topic referral letter
idiopathic pulmonary fibrosis
interstitial lung disease
primary care
tertiary care
registry
url http://dx.doi.org/10.1080/20018525.2017.1290339
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