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Beneficial effects of loxapine on agitation and breathing patterns during weaning from mechanical ventilation

INTRODUCTION: Interruption of sedation during weaning from mechanical ventilation often leads to patient agitation because of withdrawal syndrome. We tested the short-term efficacy and tolerance of loxapine in this situation. METHODS: Nineteen mechanically ventilated patients with marked agitation a...

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Autores principales: Sztrymf, Benjamin, Chevrel, Guillaume, Bertrand, Fabrice, Margetis, Dimitri, Hurel, Dominique, Ricard, Jean-Damien, Dreyfuss, Didier
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911718/
https://www.ncbi.nlm.nih.gov/pubmed/20459867
http://dx.doi.org/10.1186/cc9015
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author Sztrymf, Benjamin
Chevrel, Guillaume
Bertrand, Fabrice
Margetis, Dimitri
Hurel, Dominique
Ricard, Jean-Damien
Dreyfuss, Didier
author_facet Sztrymf, Benjamin
Chevrel, Guillaume
Bertrand, Fabrice
Margetis, Dimitri
Hurel, Dominique
Ricard, Jean-Damien
Dreyfuss, Didier
author_sort Sztrymf, Benjamin
collection PubMed
description INTRODUCTION: Interruption of sedation during weaning from mechanical ventilation often leads to patient agitation because of withdrawal syndrome. We tested the short-term efficacy and tolerance of loxapine in this situation. METHODS: Nineteen mechanically ventilated patients with marked agitation after sedation withdrawal were included. Three agitation scales, the Richmond Agitation Sedation Scale (RASS), the Motor Activity Assessment Scale (MAAS), and the Ramsay and physiological variables (respiratory rate, airway occlusion pressure during the first 0.1 second of inspiration (P0.1), heart rate and systolic arterial blood pressure) were recorded before and after loxapine administration. RESULTS: Loxapine dramatically improved all agitation scores (RASS and MASS decreased from 2 ± 0 to -1.1 ± 2.3, and 5.4 ± 0.5 to 2.7 ± 1.6, respectively; Ramsay increased from 1.0 ± 0 to 3.5 ± 1.5, 60 minutes after loxapine administration, P < 0.05 for all scores) as well as P0.1 (6 ± 4.2 to 1.8 ± 1.8 cm H(2)O; P < 0.05) and respiratory rate (from 31.2 ± 7.2 to 23.4 ± 7.8; P < 0.05) without hemodynamic adverse events. No side effects occurred. Sixteen (84%) patients were successfully managed with loxapine, sedation was resumed in two others, and one patient self-extubated without having to be reintubated. CONCLUSIONS: Loxapine was safe and effective in treating agitation in a small group of mechanically ventilated patients and improved respiratory physiologic parameters, enabling the weaning process to be pursued. A multicenter trial is under way to confirm these promising results.
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spelling pubmed-29117182010-07-29 Beneficial effects of loxapine on agitation and breathing patterns during weaning from mechanical ventilation Sztrymf, Benjamin Chevrel, Guillaume Bertrand, Fabrice Margetis, Dimitri Hurel, Dominique Ricard, Jean-Damien Dreyfuss, Didier Crit Care Research INTRODUCTION: Interruption of sedation during weaning from mechanical ventilation often leads to patient agitation because of withdrawal syndrome. We tested the short-term efficacy and tolerance of loxapine in this situation. METHODS: Nineteen mechanically ventilated patients with marked agitation after sedation withdrawal were included. Three agitation scales, the Richmond Agitation Sedation Scale (RASS), the Motor Activity Assessment Scale (MAAS), and the Ramsay and physiological variables (respiratory rate, airway occlusion pressure during the first 0.1 second of inspiration (P0.1), heart rate and systolic arterial blood pressure) were recorded before and after loxapine administration. RESULTS: Loxapine dramatically improved all agitation scores (RASS and MASS decreased from 2 ± 0 to -1.1 ± 2.3, and 5.4 ± 0.5 to 2.7 ± 1.6, respectively; Ramsay increased from 1.0 ± 0 to 3.5 ± 1.5, 60 minutes after loxapine administration, P < 0.05 for all scores) as well as P0.1 (6 ± 4.2 to 1.8 ± 1.8 cm H(2)O; P < 0.05) and respiratory rate (from 31.2 ± 7.2 to 23.4 ± 7.8; P < 0.05) without hemodynamic adverse events. No side effects occurred. Sixteen (84%) patients were successfully managed with loxapine, sedation was resumed in two others, and one patient self-extubated without having to be reintubated. CONCLUSIONS: Loxapine was safe and effective in treating agitation in a small group of mechanically ventilated patients and improved respiratory physiologic parameters, enabling the weaning process to be pursued. A multicenter trial is under way to confirm these promising results. BioMed Central 2010 2010-05-12 /pmc/articles/PMC2911718/ /pubmed/20459867 http://dx.doi.org/10.1186/cc9015 Text en Copyright ©2010 Sztrymf et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Sztrymf, Benjamin
Chevrel, Guillaume
Bertrand, Fabrice
Margetis, Dimitri
Hurel, Dominique
Ricard, Jean-Damien
Dreyfuss, Didier
Beneficial effects of loxapine on agitation and breathing patterns during weaning from mechanical ventilation
title Beneficial effects of loxapine on agitation and breathing patterns during weaning from mechanical ventilation
title_full Beneficial effects of loxapine on agitation and breathing patterns during weaning from mechanical ventilation
title_fullStr Beneficial effects of loxapine on agitation and breathing patterns during weaning from mechanical ventilation
title_full_unstemmed Beneficial effects of loxapine on agitation and breathing patterns during weaning from mechanical ventilation
title_short Beneficial effects of loxapine on agitation and breathing patterns during weaning from mechanical ventilation
title_sort beneficial effects of loxapine on agitation and breathing patterns during weaning from mechanical ventilation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911718/
https://www.ncbi.nlm.nih.gov/pubmed/20459867
http://dx.doi.org/10.1186/cc9015
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