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Pathophysiologically Based Ventilatory Management of Severe Bronchopulmonary Dysplasia

Both “new” and “old” bronchopulmonary dysplasia features overlap in preterm infants with severe bronchopulmonary dysplasia. The optimal ventilation strategy for infants with severe bronchopulmonary dysplasia has not been clarified yet. Principally, the lung is a multi-compartmental heterogeneous tis...

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Autores principales: Özkan, Hasan, Duman, Nuray, Tüzün, Funda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Pediatrics Association 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322119/
https://www.ncbi.nlm.nih.gov/pubmed/35822469
http://dx.doi.org/10.5152/TurkArchPediatr.2022.22112
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author Özkan, Hasan
Duman, Nuray
Tüzün, Funda
author_facet Özkan, Hasan
Duman, Nuray
Tüzün, Funda
author_sort Özkan, Hasan
collection PubMed
description Both “new” and “old” bronchopulmonary dysplasia features overlap in preterm infants with severe bronchopulmonary dysplasia. The optimal ventilation strategy for infants with severe bronchopulmonary dysplasia has not been clarified yet. Principally, the lung is a multi-compartmental heterogeneous tissue with regionally varying compliance and resistance. Generally, 2 critical strategical errors are common while ventilating infants with established bronchopulmonary dysplasia: (i) ventilatory management as if they are still in the acute phase of respiratory distress syndrome and (ii) early extubation attempts with the aim of reducing ventilator-induced lung injury. Considering the heterogeneous character of bronchopulmonary dysplasia, although there is no unique formulation for optimal ventilation, the most physiologically appropriate ventilation mode may be the combined mode of volume-guaranteed synchronized intermittent mechanical ventilation and pressure support ventilation. With the volume-guaranteed synchronized intermittent mechanical ventilation mode, slow compartments of the lung with high resistance and low compliance can be adequately ventilated, while fast compartments having relatively normal resistance and compliance can be ventilated well with the pressure support ventilation mode. The following settings are advisable: frequency = 12-20 breaths per minute, tidal volume = 10-15 mL/min, positive end expiratory pressure = 7-12 cmH(2)O, and inspiratory to expiratory time ratio = 1 : 5. Higher oxygen saturations such as 92%-95% should be targeted to avoid subsequent pulmonary hypertension. In conclusion, there is no evidence-based ventilation recommendation for infants with severe bronchopulmonary dysplasia. However, given the changing pattern of the disease and the underlying pathophysiology, these infants should not be ventilated as if they were in the acute phase of respiratory distress syndrome.
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spelling pubmed-93221192022-07-29 Pathophysiologically Based Ventilatory Management of Severe Bronchopulmonary Dysplasia Özkan, Hasan Duman, Nuray Tüzün, Funda Turk Arch Pediatr Review Both “new” and “old” bronchopulmonary dysplasia features overlap in preterm infants with severe bronchopulmonary dysplasia. The optimal ventilation strategy for infants with severe bronchopulmonary dysplasia has not been clarified yet. Principally, the lung is a multi-compartmental heterogeneous tissue with regionally varying compliance and resistance. Generally, 2 critical strategical errors are common while ventilating infants with established bronchopulmonary dysplasia: (i) ventilatory management as if they are still in the acute phase of respiratory distress syndrome and (ii) early extubation attempts with the aim of reducing ventilator-induced lung injury. Considering the heterogeneous character of bronchopulmonary dysplasia, although there is no unique formulation for optimal ventilation, the most physiologically appropriate ventilation mode may be the combined mode of volume-guaranteed synchronized intermittent mechanical ventilation and pressure support ventilation. With the volume-guaranteed synchronized intermittent mechanical ventilation mode, slow compartments of the lung with high resistance and low compliance can be adequately ventilated, while fast compartments having relatively normal resistance and compliance can be ventilated well with the pressure support ventilation mode. The following settings are advisable: frequency = 12-20 breaths per minute, tidal volume = 10-15 mL/min, positive end expiratory pressure = 7-12 cmH(2)O, and inspiratory to expiratory time ratio = 1 : 5. Higher oxygen saturations such as 92%-95% should be targeted to avoid subsequent pulmonary hypertension. In conclusion, there is no evidence-based ventilation recommendation for infants with severe bronchopulmonary dysplasia. However, given the changing pattern of the disease and the underlying pathophysiology, these infants should not be ventilated as if they were in the acute phase of respiratory distress syndrome. Turkish Pediatrics Association 2022-07-01 /pmc/articles/PMC9322119/ /pubmed/35822469 http://dx.doi.org/10.5152/TurkArchPediatr.2022.22112 Text en © Copyright 2022 by The Turkish Archives of Pediatrics https://creativecommons.org/licenses/by-nc/4.0/Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Review
Özkan, Hasan
Duman, Nuray
Tüzün, Funda
Pathophysiologically Based Ventilatory Management of Severe Bronchopulmonary Dysplasia
title Pathophysiologically Based Ventilatory Management of Severe Bronchopulmonary Dysplasia
title_full Pathophysiologically Based Ventilatory Management of Severe Bronchopulmonary Dysplasia
title_fullStr Pathophysiologically Based Ventilatory Management of Severe Bronchopulmonary Dysplasia
title_full_unstemmed Pathophysiologically Based Ventilatory Management of Severe Bronchopulmonary Dysplasia
title_short Pathophysiologically Based Ventilatory Management of Severe Bronchopulmonary Dysplasia
title_sort pathophysiologically based ventilatory management of severe bronchopulmonary dysplasia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322119/
https://www.ncbi.nlm.nih.gov/pubmed/35822469
http://dx.doi.org/10.5152/TurkArchPediatr.2022.22112
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