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Bronchoscopy as a supplement to computed tomography in patients with haemoptysis may be unnecessary

BACKGROUND: Haemoptysis is a common symptom and can be an early sign of lung cancer. Careful investigation of patients with haemoptysis may lead to early diagnosis. The strategy for investigation of these patients, however, is still being debated. OBJECTIVES: We studied whether the combination of co...

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Autores principales: Nielsen, Klaus, Gottlieb, Magnus, Colella, Sara, Saghir, Zaigham, Larsen, Klaus R., Clementsen, Paul F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920935/
https://www.ncbi.nlm.nih.gov/pubmed/27343164
http://dx.doi.org/10.3402/ecrj.v3.31802
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author Nielsen, Klaus
Gottlieb, Magnus
Colella, Sara
Saghir, Zaigham
Larsen, Klaus R.
Clementsen, Paul F.
author_facet Nielsen, Klaus
Gottlieb, Magnus
Colella, Sara
Saghir, Zaigham
Larsen, Klaus R.
Clementsen, Paul F.
author_sort Nielsen, Klaus
collection PubMed
description BACKGROUND: Haemoptysis is a common symptom and can be an early sign of lung cancer. Careful investigation of patients with haemoptysis may lead to early diagnosis. The strategy for investigation of these patients, however, is still being debated. OBJECTIVES: We studied whether the combination of computed tomography (CT) and bronchoscopy had a higher sensitivity for malignant and non-malignant causes of haemoptysis than CT alone. METHODS: The study was a retrospective, non-randomised, two-centre study and included patients who were referred from primary care for the investigation of haemoptysis. RESULTS: A total of 326 patients were included in the study (mean age 60.5 [SD 15.3] years, 63.3% male). The most common aetiologies of haemoptysis were cryptogenic (52.5%), pneumonia (16.3%), emphysema (8.0%), bronchiectasis (5.8%) and lung cancer (4.0%). In patients diagnosed with lung cancer, bronchoscopy, CT and the combination of bronchoscopy and CT had a sensitivity of 0.61, 0.92 (p<0.05) and 0.97 (p=0.58), respectively. In patients with non-malignant causes of haemoptysis, most aetiologies were diagnosed by CT and comprised mainly pneumonia, emphysema and bronchiectasis. Bronchoscopy did not reveal these conditions and the sensitivity to these conditions was not increased by combining CT and bronchoscopy. CONCLUSIONS: CT can stand alone as a diagnostic workup for patients with haemoptysis referred to an outpatient clinic. Bronchoscopy does not identify any malignant aetiologies not already diagnosed by CT. Combining the two test modalities does not result in a significant increase in sensitivity for malignant or non-malignant causes of haemoptysis.
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spelling pubmed-49209352016-07-15 Bronchoscopy as a supplement to computed tomography in patients with haemoptysis may be unnecessary Nielsen, Klaus Gottlieb, Magnus Colella, Sara Saghir, Zaigham Larsen, Klaus R. Clementsen, Paul F. Eur Clin Respir J Original Article BACKGROUND: Haemoptysis is a common symptom and can be an early sign of lung cancer. Careful investigation of patients with haemoptysis may lead to early diagnosis. The strategy for investigation of these patients, however, is still being debated. OBJECTIVES: We studied whether the combination of computed tomography (CT) and bronchoscopy had a higher sensitivity for malignant and non-malignant causes of haemoptysis than CT alone. METHODS: The study was a retrospective, non-randomised, two-centre study and included patients who were referred from primary care for the investigation of haemoptysis. RESULTS: A total of 326 patients were included in the study (mean age 60.5 [SD 15.3] years, 63.3% male). The most common aetiologies of haemoptysis were cryptogenic (52.5%), pneumonia (16.3%), emphysema (8.0%), bronchiectasis (5.8%) and lung cancer (4.0%). In patients diagnosed with lung cancer, bronchoscopy, CT and the combination of bronchoscopy and CT had a sensitivity of 0.61, 0.92 (p<0.05) and 0.97 (p=0.58), respectively. In patients with non-malignant causes of haemoptysis, most aetiologies were diagnosed by CT and comprised mainly pneumonia, emphysema and bronchiectasis. Bronchoscopy did not reveal these conditions and the sensitivity to these conditions was not increased by combining CT and bronchoscopy. CONCLUSIONS: CT can stand alone as a diagnostic workup for patients with haemoptysis referred to an outpatient clinic. Bronchoscopy does not identify any malignant aetiologies not already diagnosed by CT. Combining the two test modalities does not result in a significant increase in sensitivity for malignant or non-malignant causes of haemoptysis. Co-Action Publishing 2016-06-23 /pmc/articles/PMC4920935/ /pubmed/27343164 http://dx.doi.org/10.3402/ecrj.v3.31802 Text en © 2016 Klaus Nielsen et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.
spellingShingle Original Article
Nielsen, Klaus
Gottlieb, Magnus
Colella, Sara
Saghir, Zaigham
Larsen, Klaus R.
Clementsen, Paul F.
Bronchoscopy as a supplement to computed tomography in patients with haemoptysis may be unnecessary
title Bronchoscopy as a supplement to computed tomography in patients with haemoptysis may be unnecessary
title_full Bronchoscopy as a supplement to computed tomography in patients with haemoptysis may be unnecessary
title_fullStr Bronchoscopy as a supplement to computed tomography in patients with haemoptysis may be unnecessary
title_full_unstemmed Bronchoscopy as a supplement to computed tomography in patients with haemoptysis may be unnecessary
title_short Bronchoscopy as a supplement to computed tomography in patients with haemoptysis may be unnecessary
title_sort bronchoscopy as a supplement to computed tomography in patients with haemoptysis may be unnecessary
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920935/
https://www.ncbi.nlm.nih.gov/pubmed/27343164
http://dx.doi.org/10.3402/ecrj.v3.31802
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