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Efficacy and safety of HD-tDCS and respiratory rehabilitation for critically ill patients with COVID-19 The HD-RECOVERY randomized clinical trial

BACKGROUND AND PURPOSE: Acute Respiratory Distress Syndrome (ADRS) due to coronavirus disease 2019 (COVID-19) has been associated with muscle fatigue, corticospinal pathways dysfunction, and mortality. High-Definition transcranial Direct Current Stimulation (HD-tDCS) may be used to attenuate clinica...

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Autores principales: Andrade, Suellen Marinho, Cecília de Araújo Silvestre, Maria, Tenório de França, Eduardo Ériko, Bezerra Sales Queiroz, Maria Heloísa, de Jesus Santana, Kelly, Lima Holmes Madruga, Marcela Lais, Torres Teixeira Mendes, Cristina Katya, Araújo de Oliveira, Eliane, Bezerra, João Felipe, Barreto, Renata Gomes, Alves Fernandes da Silva, Silmara Maria, Alves de Sousa, Thais, Medeiros de Sousa, Wendy Chrystyan, Patrícia da Silva, Mariana, Cintra Ribeiro, Vanessa Meira, Lucena, Paulo, Beltrammi, Daniel, Catharino, Rodrigo Ramos, Caparelli-Dáquer, Egas, Hampstead, Benjamin M., Datta, Abhishek, Teixeira, Antonio Lucio, Fernández-Calvo, Bernardino, Sato, João Ricardo, Bikson, Marom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9093082/
https://www.ncbi.nlm.nih.gov/pubmed/35568312
http://dx.doi.org/10.1016/j.brs.2022.05.006
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author Andrade, Suellen Marinho
Cecília de Araújo Silvestre, Maria
Tenório de França, Eduardo Ériko
Bezerra Sales Queiroz, Maria Heloísa
de Jesus Santana, Kelly
Lima Holmes Madruga, Marcela Lais
Torres Teixeira Mendes, Cristina Katya
Araújo de Oliveira, Eliane
Bezerra, João Felipe
Barreto, Renata Gomes
Alves Fernandes da Silva, Silmara Maria
Alves de Sousa, Thais
Medeiros de Sousa, Wendy Chrystyan
Patrícia da Silva, Mariana
Cintra Ribeiro, Vanessa Meira
Lucena, Paulo
Beltrammi, Daniel
Catharino, Rodrigo Ramos
Caparelli-Dáquer, Egas
Hampstead, Benjamin M.
Datta, Abhishek
Teixeira, Antonio Lucio
Fernández-Calvo, Bernardino
Sato, João Ricardo
Bikson, Marom
author_facet Andrade, Suellen Marinho
Cecília de Araújo Silvestre, Maria
Tenório de França, Eduardo Ériko
Bezerra Sales Queiroz, Maria Heloísa
de Jesus Santana, Kelly
Lima Holmes Madruga, Marcela Lais
Torres Teixeira Mendes, Cristina Katya
Araújo de Oliveira, Eliane
Bezerra, João Felipe
Barreto, Renata Gomes
Alves Fernandes da Silva, Silmara Maria
Alves de Sousa, Thais
Medeiros de Sousa, Wendy Chrystyan
Patrícia da Silva, Mariana
Cintra Ribeiro, Vanessa Meira
Lucena, Paulo
Beltrammi, Daniel
Catharino, Rodrigo Ramos
Caparelli-Dáquer, Egas
Hampstead, Benjamin M.
Datta, Abhishek
Teixeira, Antonio Lucio
Fernández-Calvo, Bernardino
Sato, João Ricardo
Bikson, Marom
author_sort Andrade, Suellen Marinho
collection PubMed
description BACKGROUND AND PURPOSE: Acute Respiratory Distress Syndrome (ADRS) due to coronavirus disease 2019 (COVID-19) has been associated with muscle fatigue, corticospinal pathways dysfunction, and mortality. High-Definition transcranial Direct Current Stimulation (HD-tDCS) may be used to attenuate clinical impairment in these patients. The HD-RECOVERY randomized clinical trial was conducted to evaluate the efficacy and safety of HD-tDCS with respiratory rehabilitation in patients with moderate to severe ARDS due to COVID-19. METHODS: Fifty-six critically ill patients were randomized 1:1 to active (n = 28) or sham (n = 28) HD-tDCS (twice a day, 30-min, 3-mA) plus respiratory rehabilitation for up to 10 days or until intensive care unit discharge. The primary outcome was ventilator-free days during the first 28 days, defined as the number of days free from mechanical ventilation. Furthermore, secondary outcomes such as delirium, organ failure, hospital length of stay and adverse effects were investigated. RESULTS: Active HD-tDCS induced more ventilator-free days compared to sham HD-tDCS. Patients in the active group vs in the sham group experienced lower organ dysfunction, delirium, and length of stay rates over time. In addition, positive clinical response was higher in the active vs sham group. There was no significant difference in the prespecified secondary outcomes at 5 days. Adverse events were similar between groups. CONCLUSIONS: Among patients with COVID-19 and moderate to severe ARDS, use of active HD-tDCS compared with sham HD-tDCS plus respiratory rehabilitation resulted in a statistically significant increase in the number of ventilator-free days over 28 days. HD-tDCS combined with concurrent rehabilitation therapy is a safe, feasible, potentially add-on intervention, and further trials should examine HD-tDCS efficacy in a larger sample of patients with COVID-19 and severe hypoxemia.
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spelling pubmed-90930822022-05-12 Efficacy and safety of HD-tDCS and respiratory rehabilitation for critically ill patients with COVID-19 The HD-RECOVERY randomized clinical trial Andrade, Suellen Marinho Cecília de Araújo Silvestre, Maria Tenório de França, Eduardo Ériko Bezerra Sales Queiroz, Maria Heloísa de Jesus Santana, Kelly Lima Holmes Madruga, Marcela Lais Torres Teixeira Mendes, Cristina Katya Araújo de Oliveira, Eliane Bezerra, João Felipe Barreto, Renata Gomes Alves Fernandes da Silva, Silmara Maria Alves de Sousa, Thais Medeiros de Sousa, Wendy Chrystyan Patrícia da Silva, Mariana Cintra Ribeiro, Vanessa Meira Lucena, Paulo Beltrammi, Daniel Catharino, Rodrigo Ramos Caparelli-Dáquer, Egas Hampstead, Benjamin M. Datta, Abhishek Teixeira, Antonio Lucio Fernández-Calvo, Bernardino Sato, João Ricardo Bikson, Marom Brain Stimul Article BACKGROUND AND PURPOSE: Acute Respiratory Distress Syndrome (ADRS) due to coronavirus disease 2019 (COVID-19) has been associated with muscle fatigue, corticospinal pathways dysfunction, and mortality. High-Definition transcranial Direct Current Stimulation (HD-tDCS) may be used to attenuate clinical impairment in these patients. The HD-RECOVERY randomized clinical trial was conducted to evaluate the efficacy and safety of HD-tDCS with respiratory rehabilitation in patients with moderate to severe ARDS due to COVID-19. METHODS: Fifty-six critically ill patients were randomized 1:1 to active (n = 28) or sham (n = 28) HD-tDCS (twice a day, 30-min, 3-mA) plus respiratory rehabilitation for up to 10 days or until intensive care unit discharge. The primary outcome was ventilator-free days during the first 28 days, defined as the number of days free from mechanical ventilation. Furthermore, secondary outcomes such as delirium, organ failure, hospital length of stay and adverse effects were investigated. RESULTS: Active HD-tDCS induced more ventilator-free days compared to sham HD-tDCS. Patients in the active group vs in the sham group experienced lower organ dysfunction, delirium, and length of stay rates over time. In addition, positive clinical response was higher in the active vs sham group. There was no significant difference in the prespecified secondary outcomes at 5 days. Adverse events were similar between groups. CONCLUSIONS: Among patients with COVID-19 and moderate to severe ARDS, use of active HD-tDCS compared with sham HD-tDCS plus respiratory rehabilitation resulted in a statistically significant increase in the number of ventilator-free days over 28 days. HD-tDCS combined with concurrent rehabilitation therapy is a safe, feasible, potentially add-on intervention, and further trials should examine HD-tDCS efficacy in a larger sample of patients with COVID-19 and severe hypoxemia. Published by Elsevier Inc. 2022 2022-05-11 /pmc/articles/PMC9093082/ /pubmed/35568312 http://dx.doi.org/10.1016/j.brs.2022.05.006 Text en © 2022 Published by Elsevier Inc. 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
Andrade, Suellen Marinho
Cecília de Araújo Silvestre, Maria
Tenório de França, Eduardo Ériko
Bezerra Sales Queiroz, Maria Heloísa
de Jesus Santana, Kelly
Lima Holmes Madruga, Marcela Lais
Torres Teixeira Mendes, Cristina Katya
Araújo de Oliveira, Eliane
Bezerra, João Felipe
Barreto, Renata Gomes
Alves Fernandes da Silva, Silmara Maria
Alves de Sousa, Thais
Medeiros de Sousa, Wendy Chrystyan
Patrícia da Silva, Mariana
Cintra Ribeiro, Vanessa Meira
Lucena, Paulo
Beltrammi, Daniel
Catharino, Rodrigo Ramos
Caparelli-Dáquer, Egas
Hampstead, Benjamin M.
Datta, Abhishek
Teixeira, Antonio Lucio
Fernández-Calvo, Bernardino
Sato, João Ricardo
Bikson, Marom
Efficacy and safety of HD-tDCS and respiratory rehabilitation for critically ill patients with COVID-19 The HD-RECOVERY randomized clinical trial
title Efficacy and safety of HD-tDCS and respiratory rehabilitation for critically ill patients with COVID-19 The HD-RECOVERY randomized clinical trial
title_full Efficacy and safety of HD-tDCS and respiratory rehabilitation for critically ill patients with COVID-19 The HD-RECOVERY randomized clinical trial
title_fullStr Efficacy and safety of HD-tDCS and respiratory rehabilitation for critically ill patients with COVID-19 The HD-RECOVERY randomized clinical trial
title_full_unstemmed Efficacy and safety of HD-tDCS and respiratory rehabilitation for critically ill patients with COVID-19 The HD-RECOVERY randomized clinical trial
title_short Efficacy and safety of HD-tDCS and respiratory rehabilitation for critically ill patients with COVID-19 The HD-RECOVERY randomized clinical trial
title_sort efficacy and safety of hd-tdcs and respiratory rehabilitation for critically ill patients with covid-19 the hd-recovery randomized clinical trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9093082/
https://www.ncbi.nlm.nih.gov/pubmed/35568312
http://dx.doi.org/10.1016/j.brs.2022.05.006
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