Use of the high-flow helmet CPAP non-invasive ventilation device designed in Peru in patients with severe acute respiratory syndrome (COVID-19): A prospective multicenter study

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High-flow non-invasive ventilation (NIV) devices reduce the morbidity and mortality of COVID-19. The objective was to evaluate the use of the non-invasive ventilation device with high-flow helmet CPAP designed in Peru in patients with severe acute respiratory syndrome (COVID-19) hospitalized in the...

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Detalles Bibliográficos
Autores: Mantari, José Luis, Bonifacio, Diego, Hinostroza, Fany Ponce, Panduro, Roy, Oliden, José, Cuba, Lizbeth Mónica, Salazar, José Luis, Tito, Jenny, García, Jorge A., Bendezú, María R., Pariona Llanos, Ricardo, Aguilar Ramirez, Priscilia, Alvarado, Angel T.
Formato: artículo
Fecha de Publicación:2024
Institución:Universidad Nacional San Luis Gonzaga de Ica
Repositorio:UNICA-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.unica.edu.pe:20.500.13028/7399
Enlace del recurso:https://hdl.handle.net/20.500.13028/7399
Nivel de acceso:acceso abierto
Materia:COVID-19
Respiratory failure
CPAP helmet
High-flow ventilation
Ventilatory support
https://purl.org/pe-repo/ocde/ford#3.02.00
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dc.title.none.fl_str_mv Use of the high-flow helmet CPAP non-invasive ventilation device designed in Peru in patients with severe acute respiratory syndrome (COVID-19): A prospective multicenter study
title Use of the high-flow helmet CPAP non-invasive ventilation device designed in Peru in patients with severe acute respiratory syndrome (COVID-19): A prospective multicenter study
spellingShingle Use of the high-flow helmet CPAP non-invasive ventilation device designed in Peru in patients with severe acute respiratory syndrome (COVID-19): A prospective multicenter study
Mantari, José Luis
COVID-19
Respiratory failure
CPAP helmet
High-flow ventilation
Ventilatory support
https://purl.org/pe-repo/ocde/ford#3.02.00
title_short Use of the high-flow helmet CPAP non-invasive ventilation device designed in Peru in patients with severe acute respiratory syndrome (COVID-19): A prospective multicenter study
title_full Use of the high-flow helmet CPAP non-invasive ventilation device designed in Peru in patients with severe acute respiratory syndrome (COVID-19): A prospective multicenter study
title_fullStr Use of the high-flow helmet CPAP non-invasive ventilation device designed in Peru in patients with severe acute respiratory syndrome (COVID-19): A prospective multicenter study
title_full_unstemmed Use of the high-flow helmet CPAP non-invasive ventilation device designed in Peru in patients with severe acute respiratory syndrome (COVID-19): A prospective multicenter study
title_sort Use of the high-flow helmet CPAP non-invasive ventilation device designed in Peru in patients with severe acute respiratory syndrome (COVID-19): A prospective multicenter study
author Mantari, José Luis
author_facet Mantari, José Luis
Bonifacio, Diego
Hinostroza, Fany Ponce
Panduro, Roy
Oliden, José
Cuba, Lizbeth Mónica
Salazar, José Luis
Tito, Jenny
García, Jorge A.
Bendezú, María R.
Pariona Llanos, Ricardo
Aguilar Ramirez, Priscilia
Alvarado, Angel T.
author_role author
author2 Bonifacio, Diego
Hinostroza, Fany Ponce
Panduro, Roy
Oliden, José
Cuba, Lizbeth Mónica
Salazar, José Luis
Tito, Jenny
García, Jorge A.
Bendezú, María R.
Pariona Llanos, Ricardo
Aguilar Ramirez, Priscilia
Alvarado, Angel T.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Mantari, José Luis
Bonifacio, Diego
Hinostroza, Fany Ponce
Panduro, Roy
Oliden, José
Cuba, Lizbeth Mónica
Salazar, José Luis
Tito, Jenny
García, Jorge A.
Bendezú, María R.
Pariona Llanos, Ricardo
Aguilar Ramirez, Priscilia
Alvarado, Angel T.
dc.subject.none.fl_str_mv COVID-19
Respiratory failure
CPAP helmet
High-flow ventilation
Ventilatory support
topic COVID-19
Respiratory failure
CPAP helmet
High-flow ventilation
Ventilatory support
https://purl.org/pe-repo/ocde/ford#3.02.00
dc.subject.ocde.none.fl_str_mv https://purl.org/pe-repo/ocde/ford#3.02.00
description High-flow non-invasive ventilation (NIV) devices reduce the morbidity and mortality of COVID-19. The objective was to evaluate the use of the non-invasive ventilation device with high-flow helmet CPAP designed in Peru in patients with severe acute respiratory syndrome (COVID-19) hospitalized in the emergency services of five hospitals. Prospective multicenter and cross-sectional observational study from five hospitals from July to August 2020. 19 patients were recruited and divided into two groups (G-1 n = 10; G-2 n = 9) applying clinical and gasometric parameters as indicators of disease evolution upon hospital admission and within 24 hours. A progressive increase in these parameters was observed in those patients who used the NIV CPAP helmet within the first 24 hours. In G-01, improvement was evident in 90% (n = 9/10): PaO2 (range 48–137; average: 82.49 ± 8.07; p-value = 0.008), CO2 (25.2–51.0; 36.62 ± 2.62; p-value p = 0.327), and the PaO2/FiO2 coefficient (87–318; 191.5 ± 18.68). 10% of patients did not progress optimally, being subjected to endotracheal intubation and invasive mechanical ventilation. In G-02 the values ​​were %SatO2 (range 92–98; 96 ± 0.76) and the SaO2/FiO2 coefficient (214–228; 223.2 ± 1.80), indicating significant improvement within 24 hours (p < 0.001). It is concluded that the use of the CPAP helmet non-invasive ventilation (NIV) device contributes to improving gasometric values ​​and clinical condition. Being an alternative to recover typical cases of COVID-19 in all hospitals in Peru.
publishDate 2024
dc.date.accessioned.none.fl_str_mv 2026-03-30T16:08:36Z
dc.date.available.none.fl_str_mv 2026-03-30T16:08:36Z
dc.date.issued.fl_str_mv 2024
dc.type.none.fl_str_mv info:eu-repo/semantics/article
dc.type.version.none.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.13028/7399
dc.identifier.doi.none.fl_str_mv 10.3897/PHARMACIA.71.E135653
url https://hdl.handle.net/20.500.13028/7399
identifier_str_mv 10.3897/PHARMACIA.71.E135653
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Pharmacia
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eu_rights_str_mv openAccess
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Pensoft Publishers
publisher.none.fl_str_mv Pensoft Publishers
dc.source.none.fl_str_mv reponame:UNICA-Institucional
instname:Universidad Nacional San Luis Gonzaga de Ica
instacron:UNICA
instname_str Universidad Nacional San Luis Gonzaga de Ica
instacron_str UNICA
institution UNICA
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spelling Mantari, José LuisBonifacio, DiegoHinostroza, Fany PoncePanduro, RoyOliden, JoséCuba, Lizbeth MónicaSalazar, José LuisTito, JennyGarcía, Jorge A.Bendezú, María R.Pariona Llanos, RicardoAguilar Ramirez, PrisciliaAlvarado, Angel T.2026-03-30T16:08:36Z2026-03-30T16:08:36Z2024https://hdl.handle.net/20.500.13028/739910.3897/PHARMACIA.71.E135653High-flow non-invasive ventilation (NIV) devices reduce the morbidity and mortality of COVID-19. The objective was to evaluate the use of the non-invasive ventilation device with high-flow helmet CPAP designed in Peru in patients with severe acute respiratory syndrome (COVID-19) hospitalized in the emergency services of five hospitals. Prospective multicenter and cross-sectional observational study from five hospitals from July to August 2020. 19 patients were recruited and divided into two groups (G-1 n = 10; G-2 n = 9) applying clinical and gasometric parameters as indicators of disease evolution upon hospital admission and within 24 hours. A progressive increase in these parameters was observed in those patients who used the NIV CPAP helmet within the first 24 hours. In G-01, improvement was evident in 90% (n = 9/10): PaO2 (range 48–137; average: 82.49 ± 8.07; p-value = 0.008), CO2 (25.2–51.0; 36.62 ± 2.62; p-value p = 0.327), and the PaO2/FiO2 coefficient (87–318; 191.5 ± 18.68). 10% of patients did not progress optimally, being subjected to endotracheal intubation and invasive mechanical ventilation. In G-02 the values ​​were %SatO2 (range 92–98; 96 ± 0.76) and the SaO2/FiO2 coefficient (214–228; 223.2 ± 1.80), indicating significant improvement within 24 hours (p < 0.001). It is concluded that the use of the CPAP helmet non-invasive ventilation (NIV) device contributes to improving gasometric values ​​and clinical condition. 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