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A randomized clinical trial for the timing of tracheotomy in critically ill patients: factors precluding inclusion in a single center study

INTRODUCTION: We investigated the potential benefits of early tracheotomy performed before day eight of mechanical ventilation (MV) compared with late tracheotomy (from day 14 if it still indicated) in reducing mortality, days of MV, days of sedation and ICU length of stay (LOS). METHODS: Randomized...

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Autores principales: Diaz-Prieto, Antonio, Mateu, Antoni, Gorriz, Maite, Ortiga, Berta, Truchero, Consol, Sampietro, Neus, Ferrer, María Jesus, Mañez, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234827/
https://www.ncbi.nlm.nih.gov/pubmed/25358451
http://dx.doi.org/10.1186/s13054-014-0585-y
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author Diaz-Prieto, Antonio
Mateu, Antoni
Gorriz, Maite
Ortiga, Berta
Truchero, Consol
Sampietro, Neus
Ferrer, María Jesus
Mañez, Rafael
author_facet Diaz-Prieto, Antonio
Mateu, Antoni
Gorriz, Maite
Ortiga, Berta
Truchero, Consol
Sampietro, Neus
Ferrer, María Jesus
Mañez, Rafael
author_sort Diaz-Prieto, Antonio
collection PubMed
description INTRODUCTION: We investigated the potential benefits of early tracheotomy performed before day eight of mechanical ventilation (MV) compared with late tracheotomy (from day 14 if it still indicated) in reducing mortality, days of MV, days of sedation and ICU length of stay (LOS). METHODS: Randomized controlled trial (RCT) including all-consecutive ICU admitted patients requiring seven or more days of MV. Between days five to seven of MV, before randomization, the attending physician (AP) was consulted about the expected duration of MV and acceptance of tracheotomy according to randomization. Only accepted patients received tracheotomy as result of randomization. An intention to treat analysis was performed including patients accepted for the AP and those rejected without exclusion criteria. RESULTS: A total of 489 patients were included in the RCT. Of 245 patients randomized to the early group, the procedure was performed for 167 patients (68.2%) whereas in the 244 patients randomized to the late group was performed for 135 patients (55.3%) (P <0.004). Mortality at day 90 was similar in both groups (25.7% versus 29.9%), but duration of sedation was shorter in the early tracheotomy group median 11 days (range 2 to 92) days compared to 14 days (range 0 to 79) in the late group (P <0.02). The AP accepted the protocol of randomization in 205 cases (42%), 101 were included in early group and 104 in the late group. In these subgroup of patients (per-protocol analysis) no differences existed in mortality at day 90 between the two groups, but the early group had more ventilator-free days, less duration of sedation and less LOS, than the late group. CONCLUSIONS: This study shows that early tracheotomy reduces the days of sedation in patients undergoing MV, but was underpowered to prove any other benefit. In those patients selected by their attending physicians as potential candidates for a tracheotomy, an early procedure can lessen the days of MV, the days of sedation and LOS. However, the imprecision of physicians to select patients who will require prolonged MV challenges the potential benefits of early tracheotomy. TRIAL REGISTRATION: Controlled-Trials.com ISRCTN22208087. Registered 27 March 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-014-0585-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-42348272014-11-19 A randomized clinical trial for the timing of tracheotomy in critically ill patients: factors precluding inclusion in a single center study Diaz-Prieto, Antonio Mateu, Antoni Gorriz, Maite Ortiga, Berta Truchero, Consol Sampietro, Neus Ferrer, María Jesus Mañez, Rafael Crit Care Research INTRODUCTION: We investigated the potential benefits of early tracheotomy performed before day eight of mechanical ventilation (MV) compared with late tracheotomy (from day 14 if it still indicated) in reducing mortality, days of MV, days of sedation and ICU length of stay (LOS). METHODS: Randomized controlled trial (RCT) including all-consecutive ICU admitted patients requiring seven or more days of MV. Between days five to seven of MV, before randomization, the attending physician (AP) was consulted about the expected duration of MV and acceptance of tracheotomy according to randomization. Only accepted patients received tracheotomy as result of randomization. An intention to treat analysis was performed including patients accepted for the AP and those rejected without exclusion criteria. RESULTS: A total of 489 patients were included in the RCT. Of 245 patients randomized to the early group, the procedure was performed for 167 patients (68.2%) whereas in the 244 patients randomized to the late group was performed for 135 patients (55.3%) (P <0.004). Mortality at day 90 was similar in both groups (25.7% versus 29.9%), but duration of sedation was shorter in the early tracheotomy group median 11 days (range 2 to 92) days compared to 14 days (range 0 to 79) in the late group (P <0.02). The AP accepted the protocol of randomization in 205 cases (42%), 101 were included in early group and 104 in the late group. In these subgroup of patients (per-protocol analysis) no differences existed in mortality at day 90 between the two groups, but the early group had more ventilator-free days, less duration of sedation and less LOS, than the late group. CONCLUSIONS: This study shows that early tracheotomy reduces the days of sedation in patients undergoing MV, but was underpowered to prove any other benefit. In those patients selected by their attending physicians as potential candidates for a tracheotomy, an early procedure can lessen the days of MV, the days of sedation and LOS. However, the imprecision of physicians to select patients who will require prolonged MV challenges the potential benefits of early tracheotomy. TRIAL REGISTRATION: Controlled-Trials.com ISRCTN22208087. Registered 27 March 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-014-0585-y) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-29 2014 /pmc/articles/PMC4234827/ /pubmed/25358451 http://dx.doi.org/10.1186/s13054-014-0585-y Text en © Diaz-Prieto et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Diaz-Prieto, Antonio
Mateu, Antoni
Gorriz, Maite
Ortiga, Berta
Truchero, Consol
Sampietro, Neus
Ferrer, María Jesus
Mañez, Rafael
A randomized clinical trial for the timing of tracheotomy in critically ill patients: factors precluding inclusion in a single center study
title A randomized clinical trial for the timing of tracheotomy in critically ill patients: factors precluding inclusion in a single center study
title_full A randomized clinical trial for the timing of tracheotomy in critically ill patients: factors precluding inclusion in a single center study
title_fullStr A randomized clinical trial for the timing of tracheotomy in critically ill patients: factors precluding inclusion in a single center study
title_full_unstemmed A randomized clinical trial for the timing of tracheotomy in critically ill patients: factors precluding inclusion in a single center study
title_short A randomized clinical trial for the timing of tracheotomy in critically ill patients: factors precluding inclusion in a single center study
title_sort randomized clinical trial for the timing of tracheotomy in critically ill patients: factors precluding inclusion in a single center study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234827/
https://www.ncbi.nlm.nih.gov/pubmed/25358451
http://dx.doi.org/10.1186/s13054-014-0585-y
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