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A long-lasting porcine model of ARDS caused by pneumonia and ventilator-induced lung injury
Animal models of acute respiratory distress syndrome (ARDS) do not completely resemble human ARDS, struggling translational research. We aimed to characterize a porcine model of ARDS induced by pneumonia-the most common risk factor in humans-and analyze the additional effect of ventilator-induced lu...
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Published in: | Critical care (London, England) England), 2023-06, Vol.27 (1), p.239-239, Article 239 |
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creator | Barbeta, Enric Arrieta, Marta Motos, Ana Bobi, Joaquim Yang, Hua Yang, Minlan Tanzella, Giacomo Di Ginnatale, Pierluigi Nogas, Stefano Vargas, Carmen Rosa Cabrera, Roberto Battaglini, Denise Meli, Andrea Kiarostami, Kasra Vázquez, Nil Fernández-Barat, Laia Rigol, Montserrat Mellado-Artigas, Ricard Frigola, Gerard Camprubí-Rimblas, Marta Ferrer, Pau Martinez, Daniel Artigas, Antonio Ferrando, Carlos Ferrer, Miquel Torres, Antoni |
description | Animal models of acute respiratory distress syndrome (ARDS) do not completely resemble human ARDS, struggling translational research. We aimed to characterize a porcine model of ARDS induced by pneumonia-the most common risk factor in humans-and analyze the additional effect of ventilator-induced lung injury (VILI).
Bronchoscopy-guided instillation of a multidrug-resistant Pseudomonas aeruginosa strain was performed in ten healthy pigs. In six animals (pneumonia-with-VILI group), pulmonary damage was further increased by VILI applied 3 h before instillation and until ARDS was diagnosed by PaO
/FiO
|
doi_str_mv | 10.1186/s13054-023-04512-8 |
format | article |
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Bronchoscopy-guided instillation of a multidrug-resistant Pseudomonas aeruginosa strain was performed in ten healthy pigs. In six animals (pneumonia-with-VILI group), pulmonary damage was further increased by VILI applied 3 h before instillation and until ARDS was diagnosed by PaO
/FiO
< 150 mmHg. Four animals (pneumonia-without-VILI group) were protectively ventilated 3 h before inoculum and thereafter. Gas exchange, respiratory mechanics, hemodynamics, microbiological studies and inflammatory markers were analyzed during the 96-h experiment. During necropsy, lobar samples were also analyzed.
All animals from pneumonia-with-VILI group reached Berlin criteria for ARDS diagnosis until the end of experiment. The mean duration under ARDS diagnosis was 46.8 ± 7.7 h; the lowest PaO
/FiO
was 83 ± 5.45 mmHg. The group of pigs that were not subjected to VILI did not meet ARDS criteria, even when presenting with bilateral pneumonia. Animals developing ARDS presented hemodynamic instability as well as severe hypercapnia despite high-minute ventilation. Unlike the pneumonia-without-VILI group, the ARDS animals presented lower static compliance (p = 0.011) and increased pulmonary permeability (p = 0.013). The highest burden of P. aeruginosa was found at pneumonia diagnosis in all animals, as well as a high inflammatory response shown by a release of interleukin (IL)-6 and IL-8. At histological examination, only animals comprising the pneumonia-with-VILI group presented signs consistent with diffuse alveolar damage.
In conclusion, we established an accurate pulmonary sepsis-induced ARDS model.</description><identifier>ISSN: 1364-8535</identifier><identifier>EISSN: 1466-609X</identifier><identifier>EISSN: 1364-8535</identifier><identifier>EISSN: 1366-609X</identifier><identifier>DOI: 10.1186/s13054-023-04512-8</identifier><identifier>PMID: 37328874</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acute respiratory distress syndrome ; Animals ; ARDS ; Bronchoscopy ; Care and treatment ; Complications and side effects ; Critical care ; Development and progression ; Double hit ; Drug resistance in microorganisms ; Experiments ; Hemodynamics ; Injurious mechanical ventilation ; Mechanics ; Patient outcomes ; Pneumonia ; Porcine model ; Prevention ; Respiratory system ; Ventilation ; Ventilator-associated pneumonia ; Ventilator-induced lung injury ; Ventilators</subject><ispartof>Critical care (London, England), 2023-06, Vol.27 (1), p.239-239, Article 239</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c564t-41437932076928d38061955890a4bb97f0c0cf95c9240ff6bdd99f6d34fb92ea3</citedby><cites>FETCH-LOGICAL-c564t-41437932076928d38061955890a4bb97f0c0cf95c9240ff6bdd99f6d34fb92ea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276390/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2827103376?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37328874$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barbeta, Enric</creatorcontrib><creatorcontrib>Arrieta, Marta</creatorcontrib><creatorcontrib>Motos, Ana</creatorcontrib><creatorcontrib>Bobi, Joaquim</creatorcontrib><creatorcontrib>Yang, Hua</creatorcontrib><creatorcontrib>Yang, Minlan</creatorcontrib><creatorcontrib>Tanzella, Giacomo</creatorcontrib><creatorcontrib>Di Ginnatale, Pierluigi</creatorcontrib><creatorcontrib>Nogas, Stefano</creatorcontrib><creatorcontrib>Vargas, Carmen Rosa</creatorcontrib><creatorcontrib>Cabrera, Roberto</creatorcontrib><creatorcontrib>Battaglini, Denise</creatorcontrib><creatorcontrib>Meli, Andrea</creatorcontrib><creatorcontrib>Kiarostami, Kasra</creatorcontrib><creatorcontrib>Vázquez, Nil</creatorcontrib><creatorcontrib>Fernández-Barat, Laia</creatorcontrib><creatorcontrib>Rigol, Montserrat</creatorcontrib><creatorcontrib>Mellado-Artigas, Ricard</creatorcontrib><creatorcontrib>Frigola, Gerard</creatorcontrib><creatorcontrib>Camprubí-Rimblas, Marta</creatorcontrib><creatorcontrib>Ferrer, Pau</creatorcontrib><creatorcontrib>Martinez, Daniel</creatorcontrib><creatorcontrib>Artigas, Antonio</creatorcontrib><creatorcontrib>Ferrando, Carlos</creatorcontrib><creatorcontrib>Ferrer, Miquel</creatorcontrib><creatorcontrib>Torres, Antoni</creatorcontrib><title>A long-lasting porcine model of ARDS caused by pneumonia and ventilator-induced lung injury</title><title>Critical care (London, England)</title><addtitle>Crit Care</addtitle><description>Animal models of acute respiratory distress syndrome (ARDS) do not completely resemble human ARDS, struggling translational research. We aimed to characterize a porcine model of ARDS induced by pneumonia-the most common risk factor in humans-and analyze the additional effect of ventilator-induced lung injury (VILI).
Bronchoscopy-guided instillation of a multidrug-resistant Pseudomonas aeruginosa strain was performed in ten healthy pigs. In six animals (pneumonia-with-VILI group), pulmonary damage was further increased by VILI applied 3 h before instillation and until ARDS was diagnosed by PaO
/FiO
< 150 mmHg. Four animals (pneumonia-without-VILI group) were protectively ventilated 3 h before inoculum and thereafter. Gas exchange, respiratory mechanics, hemodynamics, microbiological studies and inflammatory markers were analyzed during the 96-h experiment. During necropsy, lobar samples were also analyzed.
All animals from pneumonia-with-VILI group reached Berlin criteria for ARDS diagnosis until the end of experiment. The mean duration under ARDS diagnosis was 46.8 ± 7.7 h; the lowest PaO
/FiO
was 83 ± 5.45 mmHg. The group of pigs that were not subjected to VILI did not meet ARDS criteria, even when presenting with bilateral pneumonia. Animals developing ARDS presented hemodynamic instability as well as severe hypercapnia despite high-minute ventilation. Unlike the pneumonia-without-VILI group, the ARDS animals presented lower static compliance (p = 0.011) and increased pulmonary permeability (p = 0.013). The highest burden of P. aeruginosa was found at pneumonia diagnosis in all animals, as well as a high inflammatory response shown by a release of interleukin (IL)-6 and IL-8. At histological examination, only animals comprising the pneumonia-with-VILI group presented signs consistent with diffuse alveolar damage.
In conclusion, we established an accurate pulmonary sepsis-induced ARDS model.</description><subject>Acute respiratory distress syndrome</subject><subject>Animals</subject><subject>ARDS</subject><subject>Bronchoscopy</subject><subject>Care and treatment</subject><subject>Complications and side effects</subject><subject>Critical care</subject><subject>Development and progression</subject><subject>Double hit</subject><subject>Drug resistance in microorganisms</subject><subject>Experiments</subject><subject>Hemodynamics</subject><subject>Injurious mechanical ventilation</subject><subject>Mechanics</subject><subject>Patient outcomes</subject><subject>Pneumonia</subject><subject>Porcine model</subject><subject>Prevention</subject><subject>Respiratory system</subject><subject>Ventilation</subject><subject>Ventilator-associated pneumonia</subject><subject>Ventilator-induced lung injury</subject><subject>Ventilators</subject><issn>1364-8535</issn><issn>1466-609X</issn><issn>1364-8535</issn><issn>1366-609X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkkuLFDEQxxtR3HX0C3iQBi9eeq08Op2cZFhfCwuCDxA8hHQebYbuZEy6F-bbm5lZB0ckh4TKv36Vqvyr6jmCK4Q4e50RgZY2gEkDtEW44Q-qS0QZaxiI7w_LmTDa8Ja0F9WTnDcAqOOMPK4uSEcw5x29rH6s6zGGoRlVnn0Y6m1M2gdbT9HYsY6uXn9--6XWasnW1P2u3ga7TDF4Vatg6jsbZj-qOabGB7PoohmXQvFhs6Td0-qRU2O2z-73VfXt_buv1x-b208fbq7Xt41uGZ0biijpBMHQMYG5IRwYEm3LBSja96JzoEE70WqBKTjHemOEcMwQ6nqBrSKr6ubINVFt5Db5SaWdjMrLQyCmQao0ez1aaTQYLQSnwjjaUc01IcwB6UmpxIgorDdH1nbpJ2t0aTCp8Qx6fhP8TznEO4kAdwUAhfDqnpDir8XmWU4-azuOKti4ZIk57jADoLxIX_4j3cQlhTKrgwoBIYV5Ug2qdOCDi6Ww3kPlumtJYaHyn6vq6j-qsoydvI7BOl_iZwn4mKBTzDlZd2oSgdz7Sx79JYu_5MFfcv_iF3-P55Tyx1DkN0tHyP8</recordid><startdate>20230616</startdate><enddate>20230616</enddate><creator>Barbeta, Enric</creator><creator>Arrieta, Marta</creator><creator>Motos, Ana</creator><creator>Bobi, Joaquim</creator><creator>Yang, Hua</creator><creator>Yang, Minlan</creator><creator>Tanzella, Giacomo</creator><creator>Di Ginnatale, Pierluigi</creator><creator>Nogas, Stefano</creator><creator>Vargas, Carmen Rosa</creator><creator>Cabrera, Roberto</creator><creator>Battaglini, Denise</creator><creator>Meli, Andrea</creator><creator>Kiarostami, Kasra</creator><creator>Vázquez, Nil</creator><creator>Fernández-Barat, Laia</creator><creator>Rigol, Montserrat</creator><creator>Mellado-Artigas, Ricard</creator><creator>Frigola, Gerard</creator><creator>Camprubí-Rimblas, Marta</creator><creator>Ferrer, Pau</creator><creator>Martinez, Daniel</creator><creator>Artigas, Antonio</creator><creator>Ferrando, Carlos</creator><creator>Ferrer, Miquel</creator><creator>Torres, Antoni</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230616</creationdate><title>A long-lasting porcine model of ARDS caused by pneumonia and ventilator-induced lung injury</title><author>Barbeta, Enric ; Arrieta, Marta ; Motos, Ana ; Bobi, Joaquim ; Yang, Hua ; Yang, Minlan ; Tanzella, Giacomo ; Di Ginnatale, Pierluigi ; Nogas, Stefano ; Vargas, Carmen Rosa ; Cabrera, Roberto ; Battaglini, Denise ; Meli, Andrea ; Kiarostami, Kasra ; Vázquez, Nil ; Fernández-Barat, Laia ; Rigol, Montserrat ; Mellado-Artigas, Ricard ; Frigola, Gerard ; Camprubí-Rimblas, Marta ; Ferrer, Pau ; Martinez, Daniel ; Artigas, Antonio ; Ferrando, Carlos ; Ferrer, Miquel ; Torres, Antoni</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c564t-41437932076928d38061955890a4bb97f0c0cf95c9240ff6bdd99f6d34fb92ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acute respiratory distress syndrome</topic><topic>Animals</topic><topic>ARDS</topic><topic>Bronchoscopy</topic><topic>Care and treatment</topic><topic>Complications and side effects</topic><topic>Critical care</topic><topic>Development and progression</topic><topic>Double hit</topic><topic>Drug resistance in microorganisms</topic><topic>Experiments</topic><topic>Hemodynamics</topic><topic>Injurious mechanical ventilation</topic><topic>Mechanics</topic><topic>Patient outcomes</topic><topic>Pneumonia</topic><topic>Porcine model</topic><topic>Prevention</topic><topic>Respiratory system</topic><topic>Ventilation</topic><topic>Ventilator-associated pneumonia</topic><topic>Ventilator-induced lung injury</topic><topic>Ventilators</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbeta, Enric</creatorcontrib><creatorcontrib>Arrieta, Marta</creatorcontrib><creatorcontrib>Motos, Ana</creatorcontrib><creatorcontrib>Bobi, Joaquim</creatorcontrib><creatorcontrib>Yang, Hua</creatorcontrib><creatorcontrib>Yang, Minlan</creatorcontrib><creatorcontrib>Tanzella, Giacomo</creatorcontrib><creatorcontrib>Di Ginnatale, Pierluigi</creatorcontrib><creatorcontrib>Nogas, Stefano</creatorcontrib><creatorcontrib>Vargas, Carmen Rosa</creatorcontrib><creatorcontrib>Cabrera, Roberto</creatorcontrib><creatorcontrib>Battaglini, Denise</creatorcontrib><creatorcontrib>Meli, 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Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Critical care (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barbeta, Enric</au><au>Arrieta, Marta</au><au>Motos, Ana</au><au>Bobi, Joaquim</au><au>Yang, Hua</au><au>Yang, Minlan</au><au>Tanzella, Giacomo</au><au>Di Ginnatale, Pierluigi</au><au>Nogas, Stefano</au><au>Vargas, Carmen Rosa</au><au>Cabrera, Roberto</au><au>Battaglini, Denise</au><au>Meli, Andrea</au><au>Kiarostami, Kasra</au><au>Vázquez, Nil</au><au>Fernández-Barat, Laia</au><au>Rigol, Montserrat</au><au>Mellado-Artigas, Ricard</au><au>Frigola, Gerard</au><au>Camprubí-Rimblas, Marta</au><au>Ferrer, Pau</au><au>Martinez, Daniel</au><au>Artigas, Antonio</au><au>Ferrando, Carlos</au><au>Ferrer, Miquel</au><au>Torres, Antoni</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A long-lasting porcine model of ARDS caused by pneumonia and ventilator-induced lung injury</atitle><jtitle>Critical care (London, England)</jtitle><addtitle>Crit Care</addtitle><date>2023-06-16</date><risdate>2023</risdate><volume>27</volume><issue>1</issue><spage>239</spage><epage>239</epage><pages>239-239</pages><artnum>239</artnum><issn>1364-8535</issn><eissn>1466-609X</eissn><eissn>1364-8535</eissn><eissn>1366-609X</eissn><abstract>Animal models of acute respiratory distress syndrome (ARDS) do not completely resemble human ARDS, struggling translational research. We aimed to characterize a porcine model of ARDS induced by pneumonia-the most common risk factor in humans-and analyze the additional effect of ventilator-induced lung injury (VILI).
Bronchoscopy-guided instillation of a multidrug-resistant Pseudomonas aeruginosa strain was performed in ten healthy pigs. In six animals (pneumonia-with-VILI group), pulmonary damage was further increased by VILI applied 3 h before instillation and until ARDS was diagnosed by PaO
/FiO
< 150 mmHg. Four animals (pneumonia-without-VILI group) were protectively ventilated 3 h before inoculum and thereafter. Gas exchange, respiratory mechanics, hemodynamics, microbiological studies and inflammatory markers were analyzed during the 96-h experiment. During necropsy, lobar samples were also analyzed.
All animals from pneumonia-with-VILI group reached Berlin criteria for ARDS diagnosis until the end of experiment. The mean duration under ARDS diagnosis was 46.8 ± 7.7 h; the lowest PaO
/FiO
was 83 ± 5.45 mmHg. The group of pigs that were not subjected to VILI did not meet ARDS criteria, even when presenting with bilateral pneumonia. Animals developing ARDS presented hemodynamic instability as well as severe hypercapnia despite high-minute ventilation. Unlike the pneumonia-without-VILI group, the ARDS animals presented lower static compliance (p = 0.011) and increased pulmonary permeability (p = 0.013). The highest burden of P. aeruginosa was found at pneumonia diagnosis in all animals, as well as a high inflammatory response shown by a release of interleukin (IL)-6 and IL-8. At histological examination, only animals comprising the pneumonia-with-VILI group presented signs consistent with diffuse alveolar damage.
In conclusion, we established an accurate pulmonary sepsis-induced ARDS model.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37328874</pmid><doi>10.1186/s13054-023-04512-8</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 1364-8535 |
ispartof | Critical care (London, England), 2023-06, Vol.27 (1), p.239-239, Article 239 |
issn | 1364-8535 1466-609X 1364-8535 1366-609X |
language | eng |
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source | Open Access: PubMed Central; Publicly Available Content (ProQuest) |
subjects | Acute respiratory distress syndrome Animals ARDS Bronchoscopy Care and treatment Complications and side effects Critical care Development and progression Double hit Drug resistance in microorganisms Experiments Hemodynamics Injurious mechanical ventilation Mechanics Patient outcomes Pneumonia Porcine model Prevention Respiratory system Ventilation Ventilator-associated pneumonia Ventilator-induced lung injury Ventilators |
title | A long-lasting porcine model of ARDS caused by pneumonia and ventilator-induced lung injury |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T15%3A25%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20long-lasting%20porcine%20model%20of%20ARDS%20caused%20by%20pneumonia%20and%20ventilator-induced%20lung%20injury&rft.jtitle=Critical%20care%20(London,%20England)&rft.au=Barbeta,%20Enric&rft.date=2023-06-16&rft.volume=27&rft.issue=1&rft.spage=239&rft.epage=239&rft.pages=239-239&rft.artnum=239&rft.issn=1364-8535&rft.eissn=1466-609X&rft_id=info:doi/10.1186/s13054-023-04512-8&rft_dat=%3Cgale_doaj_%3EA753260137%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c564t-41437932076928d38061955890a4bb97f0c0cf95c9240ff6bdd99f6d34fb92ea3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2827103376&rft_id=info:pmid/37328874&rft_galeid=A753260137&rfr_iscdi=true |