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Role of bronchoscopy during non invasive ventilation in hypercapnic respiratory failure

INTRODUCTION: Non invasive positive pressure ventilation (NIPPV) is the first line treatment for hypercapnic acute respiratory failure (ARF) secondary to COPD exacerbation in selected patients. Limited data exist supporting the use of fiberoptic bronchoscopy (FOB) during this clinical setting. The a...

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Autores principales: Rady, W., Abouelela, A., Abdallah, A., Youssef, W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Egyptian Society of Chest Diseases and Tuberculosis. Production and hosting by Elsevier B.V. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132652/
https://www.ncbi.nlm.nih.gov/pubmed/32288127
http://dx.doi.org/10.1016/j.ejcdt.2014.06.015
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author Rady, W.
Abouelela, A.
Abdallah, A.
Youssef, W.
author_facet Rady, W.
Abouelela, A.
Abdallah, A.
Youssef, W.
author_sort Rady, W.
collection PubMed
description INTRODUCTION: Non invasive positive pressure ventilation (NIPPV) is the first line treatment for hypercapnic acute respiratory failure (ARF) secondary to COPD exacerbation in selected patients. Limited data exist supporting the use of fiberoptic bronchoscopy (FOB) during this clinical setting. The aim of this study is to assess the role of FOB during NIPPV in patients with decompensated COPD acute exacerbation. METHODS: This study is a randomized prospective case control pilot study carried out on 50 patients - admitted to critical care units at Alexandria University Hospital, Egypt - suffering from hypercapnic ARF secondary to COPD exacerbation with Kelly Matthay Score from 2 to 4. All patients received NIPPV. Patients were divided randomly into 2 equal groups: group I (cases) (25 patients) was subjected to additional intervention of early FOB during the first 6–12 h from admission while group II (control) (25 patients) received the conventional treatment and NIPPV only. Outcome parameters measured were changes in ABG data, duration of NIPPV, rate of its success, ICU stay and mortality as well as the safety of FOB and possible complications. RESULTS: No significant difference was detected between the 2 groups regarding the baseline characteristics. No serious complications happened from FOB, and Oxygen desaturation happened in 4/25 patients (16%), Tachycardia in 2/25 patients (8%). In group I, 23 patients (92%) were successfully weaned from NIPPV versus 16 patients (64%) in group II (p = 0.037). Total duration of NIPPV was 28.52 h in group I versus 56.25 h in group II (p = 0.001). Length of ICU stay was 4.84 days in group I versus 8.68 days in group II (p = 0.001). Only 1 patient died in group I versus 3 patients in group II (p = 0.609). CONCLUSION: The early application of FOB during NIPPV in patients with ARF due to COPD exacerbation was shown to be safe. Significant improvement in the outcome of patients who underwent FOB was noticed in terms of improved ABG data, shorter duration of NIPPV, higher percentage of success and shorter ICU stay while no significant difference was detected in mortality.
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spelling pubmed-71326522020-04-08 Role of bronchoscopy during non invasive ventilation in hypercapnic respiratory failure Rady, W. Abouelela, A. Abdallah, A. Youssef, W. Egypt J Chest Dis Tuberc Article INTRODUCTION: Non invasive positive pressure ventilation (NIPPV) is the first line treatment for hypercapnic acute respiratory failure (ARF) secondary to COPD exacerbation in selected patients. Limited data exist supporting the use of fiberoptic bronchoscopy (FOB) during this clinical setting. The aim of this study is to assess the role of FOB during NIPPV in patients with decompensated COPD acute exacerbation. METHODS: This study is a randomized prospective case control pilot study carried out on 50 patients - admitted to critical care units at Alexandria University Hospital, Egypt - suffering from hypercapnic ARF secondary to COPD exacerbation with Kelly Matthay Score from 2 to 4. All patients received NIPPV. Patients were divided randomly into 2 equal groups: group I (cases) (25 patients) was subjected to additional intervention of early FOB during the first 6–12 h from admission while group II (control) (25 patients) received the conventional treatment and NIPPV only. Outcome parameters measured were changes in ABG data, duration of NIPPV, rate of its success, ICU stay and mortality as well as the safety of FOB and possible complications. RESULTS: No significant difference was detected between the 2 groups regarding the baseline characteristics. No serious complications happened from FOB, and Oxygen desaturation happened in 4/25 patients (16%), Tachycardia in 2/25 patients (8%). In group I, 23 patients (92%) were successfully weaned from NIPPV versus 16 patients (64%) in group II (p = 0.037). Total duration of NIPPV was 28.52 h in group I versus 56.25 h in group II (p = 0.001). Length of ICU stay was 4.84 days in group I versus 8.68 days in group II (p = 0.001). Only 1 patient died in group I versus 3 patients in group II (p = 0.609). CONCLUSION: The early application of FOB during NIPPV in patients with ARF due to COPD exacerbation was shown to be safe. Significant improvement in the outcome of patients who underwent FOB was noticed in terms of improved ABG data, shorter duration of NIPPV, higher percentage of success and shorter ICU stay while no significant difference was detected in mortality. The Egyptian Society of Chest Diseases and Tuberculosis. Production and hosting by Elsevier B.V. 2014-10 2014-07-22 /pmc/articles/PMC7132652/ /pubmed/32288127 http://dx.doi.org/10.1016/j.ejcdt.2014.06.015 Text en Copyright © 2014 The Egyptian Society of Chest Diseases and Tuberculosis. Production and hosting by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Rady, W.
Abouelela, A.
Abdallah, A.
Youssef, W.
Role of bronchoscopy during non invasive ventilation in hypercapnic respiratory failure
title Role of bronchoscopy during non invasive ventilation in hypercapnic respiratory failure
title_full Role of bronchoscopy during non invasive ventilation in hypercapnic respiratory failure
title_fullStr Role of bronchoscopy during non invasive ventilation in hypercapnic respiratory failure
title_full_unstemmed Role of bronchoscopy during non invasive ventilation in hypercapnic respiratory failure
title_short Role of bronchoscopy during non invasive ventilation in hypercapnic respiratory failure
title_sort role of bronchoscopy during non invasive ventilation in hypercapnic respiratory failure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132652/
https://www.ncbi.nlm.nih.gov/pubmed/32288127
http://dx.doi.org/10.1016/j.ejcdt.2014.06.015
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