Surfactant replacement therapy in combination with different non-invasive ventilation techniques in spontaneously-breathing, surfactant-depleted adult rabbits

Nasal intermittent positive pressure ventilation (NIPPV) holds great potential as a primary ventilation support method for Respiratory Distress Syndrome (RDS). The use of NIPPV may also be of great value combined with minimally invasive surfactant delivery. Our aim was to implement an in vivo model...

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Veröffentlicht in:PloS one 2018-07, Vol.13 (7), p.e0200542-e0200542
Hauptverfasser: Ricci, Francesca, Casiraghi, Costanza, Storti, Matteo, D'Alò, Francesco, Catozzi, Chiara, Ciccimarra, Roberta, Ravanetti, Francesca, Cacchioli, Antonio, Villetti, Gino, Civelli, Maurizio, Murgia, Xabi, Carnielli, Virgilio, Salomone, Fabrizio
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container_issue 7
container_start_page e0200542
container_title PloS one
container_volume 13
creator Ricci, Francesca
Casiraghi, Costanza
Storti, Matteo
D'Alò, Francesco
Catozzi, Chiara
Ciccimarra, Roberta
Ravanetti, Francesca
Cacchioli, Antonio
Villetti, Gino
Civelli, Maurizio
Murgia, Xabi
Carnielli, Virgilio
Salomone, Fabrizio
description Nasal intermittent positive pressure ventilation (NIPPV) holds great potential as a primary ventilation support method for Respiratory Distress Syndrome (RDS). The use of NIPPV may also be of great value combined with minimally invasive surfactant delivery. Our aim was to implement an in vivo model of RDS, which can be managed with different non-invasive ventilation (NIV) strategies, including non-synchronized NIPPV, synchronized NIPPV (SNIPPV), and nasal continuous positive airway pressure (NCPAP). Forty-two surfactant-depleted adult rabbits were allocated in six different groups: three groups of animals were treated with only NIV for three hours (NIPPV, SNIPPV, and NCPAP groups), while three other groups were treated with surfactant (SF) followed by NIV (NIPPV+SF, SNIPPV+SF, and NCPAP+SF groups). Arterial gas exchange, ventilation indices, and dynamic compliance were assessed. Post-mortem the lungs were sampled for histological evaluation. Surfactant depletion was successfully achieved by repeated broncho-alveolar lavages (BALs). After BALs, all animals developed a moderate respiratory distress, which could not be reverted by merely applying NIV. Conversely, surfactant administration followed by NIV induced a rapid improvement of arterial oxygenation in all surfactant-treated groups. Breath synchronization was associated with a significantly better response in terms of gas exchange and dynamic compliance compared to non-synchronized NIPPV, showing also the lowest injury scores after histological assessment. The proposed in vivo model of surfactant deficiency was successfully managed with NCPAP, NIPPV, or SNIPPV; this model resembles a moderate respiratory distress and it is suitable for the preclinical testing of less invasive surfactant administration techniques.
doi_str_mv 10.1371/journal.pone.0200542
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The use of NIPPV may also be of great value combined with minimally invasive surfactant delivery. Our aim was to implement an in vivo model of RDS, which can be managed with different non-invasive ventilation (NIV) strategies, including non-synchronized NIPPV, synchronized NIPPV (SNIPPV), and nasal continuous positive airway pressure (NCPAP). Forty-two surfactant-depleted adult rabbits were allocated in six different groups: three groups of animals were treated with only NIV for three hours (NIPPV, SNIPPV, and NCPAP groups), while three other groups were treated with surfactant (SF) followed by NIV (NIPPV+SF, SNIPPV+SF, and NCPAP+SF groups). Arterial gas exchange, ventilation indices, and dynamic compliance were assessed. Post-mortem the lungs were sampled for histological evaluation. Surfactant depletion was successfully achieved by repeated broncho-alveolar lavages (BALs). 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Xabi</au><au>Carnielli, Virgilio</au><au>Salomone, Fabrizio</au><au>Staffieri, Francesco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surfactant replacement therapy in combination with different non-invasive ventilation techniques in spontaneously-breathing, surfactant-depleted adult rabbits</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-07-12</date><risdate>2018</risdate><volume>13</volume><issue>7</issue><spage>e0200542</spage><epage>e0200542</epage><pages>e0200542-e0200542</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Nasal intermittent positive pressure ventilation (NIPPV) holds great potential as a primary ventilation support method for Respiratory Distress Syndrome (RDS). The use of NIPPV may also be of great value combined with minimally invasive surfactant delivery. Our aim was to implement an in vivo model of RDS, which can be managed with different non-invasive ventilation (NIV) strategies, including non-synchronized NIPPV, synchronized NIPPV (SNIPPV), and nasal continuous positive airway pressure (NCPAP). Forty-two surfactant-depleted adult rabbits were allocated in six different groups: three groups of animals were treated with only NIV for three hours (NIPPV, SNIPPV, and NCPAP groups), while three other groups were treated with surfactant (SF) followed by NIV (NIPPV+SF, SNIPPV+SF, and NCPAP+SF groups). Arterial gas exchange, ventilation indices, and dynamic compliance were assessed. Post-mortem the lungs were sampled for histological evaluation. Surfactant depletion was successfully achieved by repeated broncho-alveolar lavages (BALs). After BALs, all animals developed a moderate respiratory distress, which could not be reverted by merely applying NIV. Conversely, surfactant administration followed by NIV induced a rapid improvement of arterial oxygenation in all surfactant-treated groups. Breath synchronization was associated with a significantly better response in terms of gas exchange and dynamic compliance compared to non-synchronized NIPPV, showing also the lowest injury scores after histological assessment. The proposed in vivo model of surfactant deficiency was successfully managed with NCPAP, NIPPV, or SNIPPV; this model resembles a moderate respiratory distress and it is suitable for the preclinical testing of less invasive surfactant administration techniques.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>30001410</pmid><doi>10.1371/journal.pone.0200542</doi><orcidid>https://orcid.org/0000-0001-6225-5250</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS) Journals Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry
subjects Adult respiratory distress syndrome
Airway management
Alveoli
Animals
Biology and Life Sciences
Care and treatment
Clinical trials
Continuous positive airway pressure
Depletion
Disease Models, Animal
Dosage and administration
Engineering and Technology
Gas exchange
In vivo methods and tests
Intubation
Lungs
Mechanical ventilation
Medicine and Health Sciences
Newborn babies
Oxygen therapy
Oxygenation
Pediatrics
Physical Sciences
Positive-Pressure Respiration
Pressure
Pulmonary Surfactants - pharmacology
Rabbits
Research and Analysis Methods
Respiratory distress syndrome
Respiratory Distress Syndrome, Adult - physiopathology
Respiratory Distress Syndrome, Adult - therapy
Respiratory therapy
Respiratory tract
Surface active agents
Surfactants
Synchronism
Synchronization
Ventilation
Ventilators
title Surfactant replacement therapy in combination with different non-invasive ventilation techniques in spontaneously-breathing, surfactant-depleted adult rabbits
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