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Clinical Assessment of the Ambu® Aura-i™ as an Independent Ventilatory Device and Conduit for Fiberoptic-Guided Endotracheal Intubation in Adults
Background and aim A novel supraglottic airway device of the second generation is the Ambu® Aura-i™. It is designed to accommodate standard cuffed tracheal tubes and is phthalate-free and compatible with MRI. The primary objectives of the research were to examine the properties and efficiency of Amb...
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description | Background and aim A novel supraglottic airway device of the second generation is the Ambu® Aura-i™. It is designed to accommodate standard cuffed tracheal tubes and is phthalate-free and compatible with MRI. The primary objectives of the research were to examine the properties and efficiency of Ambu® Aura-i™ as a means of enabling fiberoptic-guided intubation, the view of the glottis during fiber optic examination, the duration of intubation in fiber optic bronchoscopy, the ease of intubation, the success rate of intubation, and the duration for device removal from the tracheal tube. Methodology A hospital-based descriptive observational study was conducted with 80 patients. An adequately sized Ambu® Aura-i™ was placed after general anesthesia was induced. Following a fiberoptic examination of the view of the glottis through the Ambu® Aura-i™, the trachea was intubated under fiberoptic guidance. The Ambu® Aura-i™ insertion time, glottic view grading, ease of intubation, and time required for fiberoptic-guided intubation were recorded. Also, the time taken to remove the Ambu® Aura-i™ was documented. Results Similar levels of ease were experienced by both groups after inserting the Ambu® Aura-i™, being easy in both group 1 (37/40) and in group 2 (38/40). In group 1, the average time taken to insert the Ambu® Aura-i™ was 13.53±1.91 seconds, while in group 2, it was 13.98±2.4 seconds. The average time required for fiberoptic-guided intubation was found to be 14.95±1.85 seconds in group 1 and 14.15±1.37 seconds in group 2, indicating a statistically negligible variation. Conclusion The low cost of Ambu® Aura-i™, size suitability and availability for almost all age groups, compatibility with MRI machines, and availability in phthalate-free versions contribute to it being a more appealing and useful ventilatory device, as well as an intubation tool for both normal and emergency airway management. |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11103625</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3057695494</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2159-151e921dba473d0a15c907bc78fb4d72977568d154f899427ca58f2c8e03de2e3</originalsourceid><addsrcrecordid>eNpdkU1uFDEUhFsIRKKQHWtkiQ0LOtjudtteodGQhJEisQG2ltt-zTjqtgf_RMqeI3CCHCCH4CicBMOEKLApW3qfyq9cTfOc4BPOmXxjSoSSTpgYqHzUHFIyiFYQ0T9-cD9ojlO6xBgTzCnm-Glz0AnOcc-6w-b7enbeGT2jVUqQ0gI-ozChvAW0Wsby4xatStSt-_ntBumEtEcbb2EHVSr5uYqbdQ7xGr2DK2egEhatg7fFZTSFiM7cCDHssjPteXEWLDr1NuSozRbqsxufy6izCx45j1a2zDk9a55Mek5wfHceNZ_OTj-u37cXH84369VFayhhsiWMgKTEjrrnncWaMCMxHw0X09hbTmX9okFYwvpJSNlTbjQTEzUCcGeBQnfUvN377sq4gDU1TNSz2kW36Hitgnbq34l3W_UlXClCCO4GyqrDqzuHGL4WSFktLhmYZ-0hlKQ6zPggWS_7ir78D70MJfqar1IDFV3Xc1mp13vKxJBShOl-G4LV78rVvnL1p_KKv3iY4B7-W3D3Cw3nq7U</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3062833479</pqid></control><display><type>article</type><title>Clinical Assessment of the Ambu® Aura-i™ as an Independent Ventilatory Device and Conduit for Fiberoptic-Guided Endotracheal Intubation in Adults</title><source>Publicly Available Content (ProQuest)</source><source>PubMed Central</source><creator>Mishra, Navya ; Sinha, Nitesh ; Kharwar, Ramesh K ; Prakash, Jay</creator><creatorcontrib>Mishra, Navya ; Sinha, Nitesh ; Kharwar, Ramesh K ; Prakash, Jay</creatorcontrib><description>Background and aim A novel supraglottic airway device of the second generation is the Ambu® Aura-i™. It is designed to accommodate standard cuffed tracheal tubes and is phthalate-free and compatible with MRI. The primary objectives of the research were to examine the properties and efficiency of Ambu® Aura-i™ as a means of enabling fiberoptic-guided intubation, the view of the glottis during fiber optic examination, the duration of intubation in fiber optic bronchoscopy, the ease of intubation, the success rate of intubation, and the duration for device removal from the tracheal tube. Methodology A hospital-based descriptive observational study was conducted with 80 patients. An adequately sized Ambu® Aura-i™ was placed after general anesthesia was induced. Following a fiberoptic examination of the view of the glottis through the Ambu® Aura-i™, the trachea was intubated under fiberoptic guidance. The Ambu® Aura-i™ insertion time, glottic view grading, ease of intubation, and time required for fiberoptic-guided intubation were recorded. Also, the time taken to remove the Ambu® Aura-i™ was documented. Results Similar levels of ease were experienced by both groups after inserting the Ambu® Aura-i™, being easy in both group 1 (37/40) and in group 2 (38/40). In group 1, the average time taken to insert the Ambu® Aura-i™ was 13.53±1.91 seconds, while in group 2, it was 13.98±2.4 seconds. The average time required for fiberoptic-guided intubation was found to be 14.95±1.85 seconds in group 1 and 14.15±1.37 seconds in group 2, indicating a statistically negligible variation. Conclusion The low cost of Ambu® Aura-i™, size suitability and availability for almost all age groups, compatibility with MRI machines, and availability in phthalate-free versions contribute to it being a more appealing and useful ventilatory device, as well as an intubation tool for both normal and emergency airway management.</description><identifier>ISSN: 2168-8184</identifier><identifier>EISSN: 2168-8184</identifier><identifier>DOI: 10.7759/cureus.58629</identifier><identifier>PMID: 38770453</identifier><language>eng</language><publisher>United States: Cureus Inc</publisher><subject>Airway management ; Anesthesia ; Anesthesiology ; Elective surgery ; Epiglottis ; Intubation ; Laryngoscopy ; Larynx ; Nitrous oxide ; Patients</subject><ispartof>Curēus (Palo Alto, CA), 2024-04, Vol.16 (4), p.e58629-e58629</ispartof><rights>Copyright © 2024, Mishra et al.</rights><rights>Copyright © 2024, Mishra et al. This work is published under https://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>Copyright © 2024, Mishra et al. 2024 Mishra et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2159-151e921dba473d0a15c907bc78fb4d72977568d154f899427ca58f2c8e03de2e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3062833479/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3062833479?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53770,53772,74873</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38770453$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mishra, Navya</creatorcontrib><creatorcontrib>Sinha, Nitesh</creatorcontrib><creatorcontrib>Kharwar, Ramesh K</creatorcontrib><creatorcontrib>Prakash, Jay</creatorcontrib><title>Clinical Assessment of the Ambu® Aura-i™ as an Independent Ventilatory Device and Conduit for Fiberoptic-Guided Endotracheal Intubation in Adults</title><title>Curēus (Palo Alto, CA)</title><addtitle>Cureus</addtitle><description>Background and aim A novel supraglottic airway device of the second generation is the Ambu® Aura-i™. It is designed to accommodate standard cuffed tracheal tubes and is phthalate-free and compatible with MRI. The primary objectives of the research were to examine the properties and efficiency of Ambu® Aura-i™ as a means of enabling fiberoptic-guided intubation, the view of the glottis during fiber optic examination, the duration of intubation in fiber optic bronchoscopy, the ease of intubation, the success rate of intubation, and the duration for device removal from the tracheal tube. Methodology A hospital-based descriptive observational study was conducted with 80 patients. An adequately sized Ambu® Aura-i™ was placed after general anesthesia was induced. Following a fiberoptic examination of the view of the glottis through the Ambu® Aura-i™, the trachea was intubated under fiberoptic guidance. The Ambu® Aura-i™ insertion time, glottic view grading, ease of intubation, and time required for fiberoptic-guided intubation were recorded. Also, the time taken to remove the Ambu® Aura-i™ was documented. Results Similar levels of ease were experienced by both groups after inserting the Ambu® Aura-i™, being easy in both group 1 (37/40) and in group 2 (38/40). In group 1, the average time taken to insert the Ambu® Aura-i™ was 13.53±1.91 seconds, while in group 2, it was 13.98±2.4 seconds. The average time required for fiberoptic-guided intubation was found to be 14.95±1.85 seconds in group 1 and 14.15±1.37 seconds in group 2, indicating a statistically negligible variation. Conclusion The low cost of Ambu® Aura-i™, size suitability and availability for almost all age groups, compatibility with MRI machines, and availability in phthalate-free versions contribute to it being a more appealing and useful ventilatory device, as well as an intubation tool for both normal and emergency airway management.</description><subject>Airway management</subject><subject>Anesthesia</subject><subject>Anesthesiology</subject><subject>Elective surgery</subject><subject>Epiglottis</subject><subject>Intubation</subject><subject>Laryngoscopy</subject><subject>Larynx</subject><subject>Nitrous oxide</subject><subject>Patients</subject><issn>2168-8184</issn><issn>2168-8184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkU1uFDEUhFsIRKKQHWtkiQ0LOtjudtteodGQhJEisQG2ltt-zTjqtgf_RMqeI3CCHCCH4CicBMOEKLApW3qfyq9cTfOc4BPOmXxjSoSSTpgYqHzUHFIyiFYQ0T9-cD9ojlO6xBgTzCnm-Glz0AnOcc-6w-b7enbeGT2jVUqQ0gI-ozChvAW0Wsby4xatStSt-_ntBumEtEcbb2EHVSr5uYqbdQ7xGr2DK2egEhatg7fFZTSFiM7cCDHssjPteXEWLDr1NuSozRbqsxufy6izCx45j1a2zDk9a55Mek5wfHceNZ_OTj-u37cXH84369VFayhhsiWMgKTEjrrnncWaMCMxHw0X09hbTmX9okFYwvpJSNlTbjQTEzUCcGeBQnfUvN377sq4gDU1TNSz2kW36Hitgnbq34l3W_UlXClCCO4GyqrDqzuHGL4WSFktLhmYZ-0hlKQ6zPggWS_7ir78D70MJfqar1IDFV3Xc1mp13vKxJBShOl-G4LV78rVvnL1p_KKv3iY4B7-W3D3Cw3nq7U</recordid><startdate>20240420</startdate><enddate>20240420</enddate><creator>Mishra, Navya</creator><creator>Sinha, Nitesh</creator><creator>Kharwar, Ramesh K</creator><creator>Prakash, Jay</creator><general>Cureus Inc</general><general>Cureus</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</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>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240420</creationdate><title>Clinical Assessment of the Ambu® Aura-i™ as an Independent Ventilatory Device and Conduit for Fiberoptic-Guided Endotracheal Intubation in Adults</title><author>Mishra, Navya ; Sinha, Nitesh ; Kharwar, Ramesh K ; Prakash, Jay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2159-151e921dba473d0a15c907bc78fb4d72977568d154f899427ca58f2c8e03de2e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Airway management</topic><topic>Anesthesia</topic><topic>Anesthesiology</topic><topic>Elective surgery</topic><topic>Epiglottis</topic><topic>Intubation</topic><topic>Laryngoscopy</topic><topic>Larynx</topic><topic>Nitrous oxide</topic><topic>Patients</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mishra, Navya</creatorcontrib><creatorcontrib>Sinha, Nitesh</creatorcontrib><creatorcontrib>Kharwar, Ramesh K</creatorcontrib><creatorcontrib>Prakash, Jay</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Curēus (Palo Alto, CA)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mishra, Navya</au><au>Sinha, Nitesh</au><au>Kharwar, Ramesh K</au><au>Prakash, Jay</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Assessment of the Ambu® Aura-i™ as an Independent Ventilatory Device and Conduit for Fiberoptic-Guided Endotracheal Intubation in Adults</atitle><jtitle>Curēus (Palo Alto, CA)</jtitle><addtitle>Cureus</addtitle><date>2024-04-20</date><risdate>2024</risdate><volume>16</volume><issue>4</issue><spage>e58629</spage><epage>e58629</epage><pages>e58629-e58629</pages><issn>2168-8184</issn><eissn>2168-8184</eissn><abstract>Background and aim A novel supraglottic airway device of the second generation is the Ambu® Aura-i™. It is designed to accommodate standard cuffed tracheal tubes and is phthalate-free and compatible with MRI. The primary objectives of the research were to examine the properties and efficiency of Ambu® Aura-i™ as a means of enabling fiberoptic-guided intubation, the view of the glottis during fiber optic examination, the duration of intubation in fiber optic bronchoscopy, the ease of intubation, the success rate of intubation, and the duration for device removal from the tracheal tube. Methodology A hospital-based descriptive observational study was conducted with 80 patients. An adequately sized Ambu® Aura-i™ was placed after general anesthesia was induced. Following a fiberoptic examination of the view of the glottis through the Ambu® Aura-i™, the trachea was intubated under fiberoptic guidance. The Ambu® Aura-i™ insertion time, glottic view grading, ease of intubation, and time required for fiberoptic-guided intubation were recorded. Also, the time taken to remove the Ambu® Aura-i™ was documented. Results Similar levels of ease were experienced by both groups after inserting the Ambu® Aura-i™, being easy in both group 1 (37/40) and in group 2 (38/40). In group 1, the average time taken to insert the Ambu® Aura-i™ was 13.53±1.91 seconds, while in group 2, it was 13.98±2.4 seconds. The average time required for fiberoptic-guided intubation was found to be 14.95±1.85 seconds in group 1 and 14.15±1.37 seconds in group 2, indicating a statistically negligible variation. Conclusion The low cost of Ambu® Aura-i™, size suitability and availability for almost all age groups, compatibility with MRI machines, and availability in phthalate-free versions contribute to it being a more appealing and useful ventilatory device, as well as an intubation tool for both normal and emergency airway management.</abstract><cop>United States</cop><pub>Cureus Inc</pub><pmid>38770453</pmid><doi>10.7759/cureus.58629</doi><oa>free_for_read</oa></addata></record> |
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subjects | Airway management Anesthesia Anesthesiology Elective surgery Epiglottis Intubation Laryngoscopy Larynx Nitrous oxide Patients |
title | Clinical Assessment of the Ambu® Aura-i™ as an Independent Ventilatory Device and Conduit for Fiberoptic-Guided Endotracheal Intubation in Adults |
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