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Effects of time-controlled adaptive ventilation on cardiorespiratory parameters and inflammatory response in experimental emphysema.
Oliveira, Milena Vasconcellos de; Magalhães, Raquel Ferreira de; Rocha, Nazareth de Novaes; Fernandes, Marcus Vinicius; Antunes, Mariana Alves; Morales, Marcelo Marcos; Capelozzi, Vera Luiza; Satalin, Joshua; Andrews, Penny; Habashi, Nader M; Nieman, Gary; Rocco, Patricia Rieken Macedo; Silva, Pedro Leme.
Afiliação
  • Oliveira MV; Laboratory of Pulmonary Investigation, Carlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Magalhães RF; Laboratory of Pulmonary Investigation, Carlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Rocha NN; Laboratory of Pulmonary Investigation, Carlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Fernandes MV; Department of Physiology and Pharmacology, Biomedical Institute, Fluminense Federal University, Rio de Janeiro, Brazil.
  • Antunes MA; Laboratory of Pulmonary Investigation, Carlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Morales MM; Laboratory of Pulmonary Investigation, Carlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Capelozzi VL; Laboratory of Cellular and Molecular Physiology, Carlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Satalin J; Department of Pathology, São Paulo University, São Paulo, Brazil.
  • Andrews P; Department of Surgery, State University of New York Upstate Medical University, Syracuse, New York.
  • Habashi NM; Department of Surgical Critical Care, R Adams Cowley Shock Trauma Center, Baltimore, Maryland.
  • Nieman G; Department of Surgical Critical Care, R Adams Cowley Shock Trauma Center, Baltimore, Maryland.
  • Rocco PRM; Department of Surgery, State University of New York Upstate Medical University, Syracuse, New York.
  • Silva PL; Laboratory of Pulmonary Investigation, Carlos Chagas Filho Biophysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
J Appl Physiol (1985) ; 132(2): 564-574, 2022 02 01.
Article em En | MEDLINE | ID: mdl-34989651
ABSTRACT
The time-controlled adaptive ventilation (TCAV) method attenuates lung damage in acute respiratory distress syndrome. However, so far, no study has evaluated the impact of the TCAV method on ventilator-induced lung injury (VILI) and cardiac function in emphysema. We hypothesized that the use of the TCAV method to achieve an expiratory flow termination/expiratory peak flow (EFT/EPF) of 25% could reduce VILI and improve right ventricular function in elastase-induced lung emphysema in rats. Five weeks after the last intratracheal instillation of elastase, animals were anesthetized and mechanically ventilated for 1 h using TCAV adjusted to either EFT/EPF 25% or EFT/EPF 75%, the latter often applied in acute respiratory distress syndrome (ARDS). Pressure-controlled ventilation (PCV) groups with positive end-expiratory pressure levels similar to positive end-release pressure in TCAV with EFT/EPF 25% and EFT/EPF 75% were also analyzed. Echocardiography and lung ultrasonography were monitored. Lung morphometry, alveolar heterogeneity, and biological markers related to inflammation [interleukin 6 (IL-6), CINC-1], alveolar pulmonary stretch (amphiregulin), lung matrix damage [metalloproteinase 9 (MMP-9)] were assessed. EFT/EPF 25% reduced respiratory system peak pressure, mean linear intercept, B lines at lung ultrasonography, and increased pulmonary acceleration time/pulmonary ejection time ratio compared with EFT/EPF 75%. The volume fraction of mononuclear cells, neutrophils, and expression of IL-6, CINC-1, amphiregulin, and MMP-9 were lower with EFT/EPF 25% than with EFT/EPF 75%. In conclusion, TCAV with EFT/EPF 25%, compared with EFT/EPF 75%, led to less lung inflammation, hyperinflation, and pulmonary arterial hypertension, which may be a promising strategy for patients with emphysema.NEW & NOTEWORTHY The TCAV method reduces lung damage in ARDS. However, so far, no study has evaluated the impact of the TCAV method on ventilator-induced lung injury and cardiac function in experimental emphysema. The TCAV method at EFT/EPF ratio of 25%, compared with EFT/EPF of 75% (frequently used in ARDS), reduced lung inflammation, alveolar heterogeneity and hyperinflation, and pulmonary arterial hypertension in elastase-induced emphysema. TCAV may be a promising and personalized ventilation strategy for patients with emphysema.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enfisema Pulmonar / Enfisema / Lesão Pulmonar Induzida por Ventilação Mecânica Limite: Animals / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Enfisema Pulmonar / Enfisema / Lesão Pulmonar Induzida por Ventilação Mecânica Limite: Animals / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article