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Clinical characteristics of chylothorax: results from the International Collaborative Effusion database

BACKGROUND: Chylothorax is an uncommon medical condition for which limited data are available regarding the contemporary aetiology, management and outcomes. The goal of this study was to better define these poorly characterised features. METHODS: The medical records of adult patients diagnosed with...

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Autores principales: Porcel, José M., Bielsa, Silvia, Civit, Carmen, Aujayeb, Avinash, Janssen, Julius, Bodtger, Uffe, Fjaellegaard, Katrine, Petersen, Jesper Koefod, Welch, Hugh, Symonds, Jenny, Mitchell, Michael A., Grabczak, Elżbieta Magdalena, Ellayeh, Mohamed, Addala, Dinesh, Wrightson, John M., Rahman, Najib M., Munavvar, Mohammed, Koegelenberg, Coenraad F.N., Labarca, Gonzalo, Mei, Federico, Maskell, Nick, Bhatnagar, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577597/
https://www.ncbi.nlm.nih.gov/pubmed/37850216
http://dx.doi.org/10.1183/23120541.00091-2023
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author Porcel, José M.
Bielsa, Silvia
Civit, Carmen
Aujayeb, Avinash
Janssen, Julius
Bodtger, Uffe
Fjaellegaard, Katrine
Petersen, Jesper Koefod
Welch, Hugh
Symonds, Jenny
Mitchell, Michael A.
Grabczak, Elżbieta Magdalena
Ellayeh, Mohamed
Addala, Dinesh
Wrightson, John M.
Rahman, Najib M.
Munavvar, Mohammed
Koegelenberg, Coenraad F.N.
Labarca, Gonzalo
Mei, Federico
Maskell, Nick
Bhatnagar, Rahul
author_facet Porcel, José M.
Bielsa, Silvia
Civit, Carmen
Aujayeb, Avinash
Janssen, Julius
Bodtger, Uffe
Fjaellegaard, Katrine
Petersen, Jesper Koefod
Welch, Hugh
Symonds, Jenny
Mitchell, Michael A.
Grabczak, Elżbieta Magdalena
Ellayeh, Mohamed
Addala, Dinesh
Wrightson, John M.
Rahman, Najib M.
Munavvar, Mohammed
Koegelenberg, Coenraad F.N.
Labarca, Gonzalo
Mei, Federico
Maskell, Nick
Bhatnagar, Rahul
author_sort Porcel, José M.
collection PubMed
description BACKGROUND: Chylothorax is an uncommon medical condition for which limited data are available regarding the contemporary aetiology, management and outcomes. The goal of this study was to better define these poorly characterised features. METHODS: The medical records of adult patients diagnosed with chylothorax at 12 centres across Europe, America and South Africa from 2009–2021 were retrospectively reviewed. Descriptive and inferential statistics were performed. RESULTS: 77 patients (median age 69 years, male to female ratio 1.5) were included. Subacute dyspnoea was the most typical presenting symptom (66%). The commonest cause of chylothorax was malignancy (68.8%), with lymphoma accounting for 62% of these cases. Other aetiologies were trauma (13%), inflammatory/miscellaneous conditions (11.7%) and idiopathic cases (6.5%). At the initial thoracentesis, the pleural fluid appeared milky in 73%, was exudative in 89% and exhibited triglyceride concentrations >100 mg·dL(−1) in 88%. Lymphangiography/lymphoscintigraphy were rarely ordered (3%), and demonstration of chylomicrons in pleural fluid was never ascertained. 67% of patients required interventional pleural procedures. Dietary measures were infrequently followed (36%). No patient underwent thoracic duct ligation or embolisation. Morbidity included infections (18%), and thrombosis in malignant aetiologies (16%). The 1-year mortality was 47%. Pleural fluid protein >3.5 mg·dL(−1) (sub-distribution hazard ratio (SHR) 4.346) or lactate dehydrogenase <500 U·L(−1) (SHR 10.21) increased the likelihood of effusion resolution. Pleural fluid protein ≤3.5 mg·dL(−1) (HR 4.047), bilateral effusions (HR 2.749) and a history of respiratory disease (HR 2.428) negatively influenced survival. CONCLUSION: Chylothoraces have a poor prognosis and most require pleural interventions. Despite the standard recommendations, lymphatic imaging is seldom used, nor are dietary restrictions followed.
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spelling pubmed-105775972023-10-17 Clinical characteristics of chylothorax: results from the International Collaborative Effusion database Porcel, José M. Bielsa, Silvia Civit, Carmen Aujayeb, Avinash Janssen, Julius Bodtger, Uffe Fjaellegaard, Katrine Petersen, Jesper Koefod Welch, Hugh Symonds, Jenny Mitchell, Michael A. Grabczak, Elżbieta Magdalena Ellayeh, Mohamed Addala, Dinesh Wrightson, John M. Rahman, Najib M. Munavvar, Mohammed Koegelenberg, Coenraad F.N. Labarca, Gonzalo Mei, Federico Maskell, Nick Bhatnagar, Rahul ERJ Open Res Original Research Articles BACKGROUND: Chylothorax is an uncommon medical condition for which limited data are available regarding the contemporary aetiology, management and outcomes. The goal of this study was to better define these poorly characterised features. METHODS: The medical records of adult patients diagnosed with chylothorax at 12 centres across Europe, America and South Africa from 2009–2021 were retrospectively reviewed. Descriptive and inferential statistics were performed. RESULTS: 77 patients (median age 69 years, male to female ratio 1.5) were included. Subacute dyspnoea was the most typical presenting symptom (66%). The commonest cause of chylothorax was malignancy (68.8%), with lymphoma accounting for 62% of these cases. Other aetiologies were trauma (13%), inflammatory/miscellaneous conditions (11.7%) and idiopathic cases (6.5%). At the initial thoracentesis, the pleural fluid appeared milky in 73%, was exudative in 89% and exhibited triglyceride concentrations >100 mg·dL(−1) in 88%. Lymphangiography/lymphoscintigraphy were rarely ordered (3%), and demonstration of chylomicrons in pleural fluid was never ascertained. 67% of patients required interventional pleural procedures. Dietary measures were infrequently followed (36%). No patient underwent thoracic duct ligation or embolisation. Morbidity included infections (18%), and thrombosis in malignant aetiologies (16%). The 1-year mortality was 47%. Pleural fluid protein >3.5 mg·dL(−1) (sub-distribution hazard ratio (SHR) 4.346) or lactate dehydrogenase <500 U·L(−1) (SHR 10.21) increased the likelihood of effusion resolution. Pleural fluid protein ≤3.5 mg·dL(−1) (HR 4.047), bilateral effusions (HR 2.749) and a history of respiratory disease (HR 2.428) negatively influenced survival. CONCLUSION: Chylothoraces have a poor prognosis and most require pleural interventions. Despite the standard recommendations, lymphatic imaging is seldom used, nor are dietary restrictions followed. European Respiratory Society 2023-10-16 /pmc/articles/PMC10577597/ /pubmed/37850216 http://dx.doi.org/10.1183/23120541.00091-2023 Text en Copyright ©The authors 2023 https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org)
spellingShingle Original Research Articles
Porcel, José M.
Bielsa, Silvia
Civit, Carmen
Aujayeb, Avinash
Janssen, Julius
Bodtger, Uffe
Fjaellegaard, Katrine
Petersen, Jesper Koefod
Welch, Hugh
Symonds, Jenny
Mitchell, Michael A.
Grabczak, Elżbieta Magdalena
Ellayeh, Mohamed
Addala, Dinesh
Wrightson, John M.
Rahman, Najib M.
Munavvar, Mohammed
Koegelenberg, Coenraad F.N.
Labarca, Gonzalo
Mei, Federico
Maskell, Nick
Bhatnagar, Rahul
Clinical characteristics of chylothorax: results from the International Collaborative Effusion database
title Clinical characteristics of chylothorax: results from the International Collaborative Effusion database
title_full Clinical characteristics of chylothorax: results from the International Collaborative Effusion database
title_fullStr Clinical characteristics of chylothorax: results from the International Collaborative Effusion database
title_full_unstemmed Clinical characteristics of chylothorax: results from the International Collaborative Effusion database
title_short Clinical characteristics of chylothorax: results from the International Collaborative Effusion database
title_sort clinical characteristics of chylothorax: results from the international collaborative effusion database
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577597/
https://www.ncbi.nlm.nih.gov/pubmed/37850216
http://dx.doi.org/10.1183/23120541.00091-2023
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