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Phase II study comparing nasal pressure monitoring with capnography during invasive endoscopic procedures: a single-center, single-arm trial
Nasal pressure signal is commonly used to evaluate obstructive sleep apnea. This study aimed to assess its safety for respiratory monitoring during sedation. A total of 45 adult patients undergoing sedation with propofol and fentanyl for invasive endoscopic procedures were enrolled. While both nasal...
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Published in: | Scientific reports 2023-01, Vol.13 (1), p.1265-10, Article 1265 |
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creator | Nagashima, Hiroki Mikata, Rintaro Isono, Shiroh Ogasawara, Sadahisa Sugiyama, Harutoshi Ohno, Izumi Yasui, Shin Matsumura, Tomoaki Koroki, Keisuke Kusakabe, Yuko Miura, Yoshifumi Kan, Motoyasu Maruta, Shikiko Yamada, Toshihito Takemura, Ryo Sato, Yasunori Kato, Jun Kato, Naoya |
description | Nasal pressure signal is commonly used to evaluate obstructive sleep apnea. This study aimed to assess its safety for respiratory monitoring during sedation. A total of 45 adult patients undergoing sedation with propofol and fentanyl for invasive endoscopic procedures were enrolled. While both nasal pressure and capnograph signals were continuously recorded, only the nasal pressure signal was displayed. The primary outcome was the incidence of oxygen desaturation below 90%. The secondary outcomes were the ability to predict the desaturation and incidence of harmful events and false alarms, defined as an apnea waveform lasting more than 3 min without desaturation. Of the 45 participants, 43 completed the study. At least one desaturation event occurred in 12 patients (27.9%; 95% confidence interval 15.3–43.7%). In these 12 patients, more than half of the desaturation events were predictable in 9 patients by capnography and 11 patients by nasal pressure monitoring (
p
= 0.59). In the 43 patients, false alarms were detected in 7 patients with capnography and 11 patients with nasal pressure monitoring (
p
= 0.427). Harmful events unrelated to nasal pressure monitoring occurred in 2 patients. Nasal pressure monitoring is safe and possibly useful for respiratory monitoring despite false alarms during sedation. |
doi_str_mv | 10.1038/s41598-023-28213-y |
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p
= 0.59). In the 43 patients, false alarms were detected in 7 patients with capnography and 11 patients with nasal pressure monitoring (
p
= 0.427). Harmful events unrelated to nasal pressure monitoring occurred in 2 patients. Nasal pressure monitoring is safe and possibly useful for respiratory monitoring despite false alarms during sedation.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-023-28213-y</identifier><identifier>PMID: 36690708</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/308 ; 692/4020 ; Adult ; Anesthesia ; Apnea ; Capnography - methods ; Carbon dioxide ; Endoscopy ; False alarms ; Fentanyl ; Humanities and Social Sciences ; Humans ; Monitoring ; Monitoring, Physiologic - methods ; multidisciplinary ; Pressure ; Propofol ; Propofol - adverse effects ; Science ; Science (multidisciplinary) ; Sleep Apnea, Obstructive - chemically induced ; Sleep disorders</subject><ispartof>Scientific reports, 2023-01, Vol.13 (1), p.1265-10, Article 1265</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c491t-24e92a5ce54b96608dc3ae9f8fe890f9bd0fb15eb9e5141ad71772a5e0377b703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2768595987/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2768595987?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25733,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36690708$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagashima, Hiroki</creatorcontrib><creatorcontrib>Mikata, Rintaro</creatorcontrib><creatorcontrib>Isono, Shiroh</creatorcontrib><creatorcontrib>Ogasawara, Sadahisa</creatorcontrib><creatorcontrib>Sugiyama, Harutoshi</creatorcontrib><creatorcontrib>Ohno, Izumi</creatorcontrib><creatorcontrib>Yasui, Shin</creatorcontrib><creatorcontrib>Matsumura, Tomoaki</creatorcontrib><creatorcontrib>Koroki, Keisuke</creatorcontrib><creatorcontrib>Kusakabe, Yuko</creatorcontrib><creatorcontrib>Miura, Yoshifumi</creatorcontrib><creatorcontrib>Kan, Motoyasu</creatorcontrib><creatorcontrib>Maruta, Shikiko</creatorcontrib><creatorcontrib>Yamada, Toshihito</creatorcontrib><creatorcontrib>Takemura, Ryo</creatorcontrib><creatorcontrib>Sato, Yasunori</creatorcontrib><creatorcontrib>Kato, Jun</creatorcontrib><creatorcontrib>Kato, Naoya</creatorcontrib><title>Phase II study comparing nasal pressure monitoring with capnography during invasive endoscopic procedures: a single-center, single-arm trial</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Nasal pressure signal is commonly used to evaluate obstructive sleep apnea. This study aimed to assess its safety for respiratory monitoring during sedation. A total of 45 adult patients undergoing sedation with propofol and fentanyl for invasive endoscopic procedures were enrolled. While both nasal pressure and capnograph signals were continuously recorded, only the nasal pressure signal was displayed. The primary outcome was the incidence of oxygen desaturation below 90%. The secondary outcomes were the ability to predict the desaturation and incidence of harmful events and false alarms, defined as an apnea waveform lasting more than 3 min without desaturation. Of the 45 participants, 43 completed the study. At least one desaturation event occurred in 12 patients (27.9%; 95% confidence interval 15.3–43.7%). In these 12 patients, more than half of the desaturation events were predictable in 9 patients by capnography and 11 patients by nasal pressure monitoring (
p
= 0.59). In the 43 patients, false alarms were detected in 7 patients with capnography and 11 patients with nasal pressure monitoring (
p
= 0.427). Harmful events unrelated to nasal pressure monitoring occurred in 2 patients. Nasal pressure monitoring is safe and possibly useful for respiratory monitoring despite false alarms during sedation.</description><subject>692/308</subject><subject>692/4020</subject><subject>Adult</subject><subject>Anesthesia</subject><subject>Apnea</subject><subject>Capnography - methods</subject><subject>Carbon dioxide</subject><subject>Endoscopy</subject><subject>False alarms</subject><subject>Fentanyl</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Monitoring</subject><subject>Monitoring, Physiologic - methods</subject><subject>multidisciplinary</subject><subject>Pressure</subject><subject>Propofol</subject><subject>Propofol - adverse effects</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Sleep Apnea, Obstructive - chemically induced</subject><subject>Sleep disorders</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9Uk1v1DAQjRCIVqV_gAOyxIUDAduJ45gDEqr4WKkSHOBsTZzJrleJHexkUf4DPxrvpi0tB3yxPfPeG4_nZdlzRt8wWtRvY8mEqnPKi5zXnBX58ig757QUOS84f3zvfJZdxrinaQmuSqaeZmdFVSkqaX2e_f62g4hksyFxmtuFGD-MEKzbEgcRejIGjHEOSAbv7ORPmV922hEDo_PbAONuIe18ilt3gGgPSNC1Pho_WpP43mDKY3xHgMQE6zE36CYMr2-vEAYyBQv9s-xJB33Ey5v9Ivvx6eP3qy_59dfPm6sP17kpFZtyXqLiIAyKslFVRevWFICqqzusFe1U09KuYQIbhYKVDFrJpEwEpIWUjaTFRbZZdVsPez0GO0BYtAerTwEfthrCZE2PWoJou4qmiqYrS2VUA1wKmjR51XHFktb7VWucmwHbY2sB-geiDzPO7vTWH7SqJUvTSwKvbgSC_zljnPRgo8G-B4d-jprLShWy5FWVoC__ge79HFz6qiOqFio5QiYUX1Em-BgDdnePYVQfvaNX7-hUXZ-8o5dEenG_jTvKrVMSoFgBcTwOG8Pf2v-R_QOQHtNc</recordid><startdate>20230123</startdate><enddate>20230123</enddate><creator>Nagashima, Hiroki</creator><creator>Mikata, Rintaro</creator><creator>Isono, Shiroh</creator><creator>Ogasawara, Sadahisa</creator><creator>Sugiyama, Harutoshi</creator><creator>Ohno, Izumi</creator><creator>Yasui, Shin</creator><creator>Matsumura, Tomoaki</creator><creator>Koroki, Keisuke</creator><creator>Kusakabe, Yuko</creator><creator>Miura, Yoshifumi</creator><creator>Kan, Motoyasu</creator><creator>Maruta, Shikiko</creator><creator>Yamada, Toshihito</creator><creator>Takemura, Ryo</creator><creator>Sato, Yasunori</creator><creator>Kato, Jun</creator><creator>Kato, Naoya</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Portfolio</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230123</creationdate><title>Phase II study comparing nasal pressure monitoring with capnography during invasive endoscopic procedures: a single-center, single-arm trial</title><author>Nagashima, Hiroki ; Mikata, Rintaro ; Isono, Shiroh ; Ogasawara, Sadahisa ; Sugiyama, Harutoshi ; Ohno, Izumi ; Yasui, Shin ; Matsumura, Tomoaki ; Koroki, Keisuke ; Kusakabe, Yuko ; Miura, Yoshifumi ; Kan, Motoyasu ; Maruta, Shikiko ; Yamada, Toshihito ; Takemura, Ryo ; Sato, Yasunori ; Kato, Jun ; Kato, Naoya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c491t-24e92a5ce54b96608dc3ae9f8fe890f9bd0fb15eb9e5141ad71772a5e0377b703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>692/308</topic><topic>692/4020</topic><topic>Adult</topic><topic>Anesthesia</topic><topic>Apnea</topic><topic>Capnography - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagashima, Hiroki</au><au>Mikata, Rintaro</au><au>Isono, Shiroh</au><au>Ogasawara, Sadahisa</au><au>Sugiyama, Harutoshi</au><au>Ohno, Izumi</au><au>Yasui, Shin</au><au>Matsumura, Tomoaki</au><au>Koroki, Keisuke</au><au>Kusakabe, Yuko</au><au>Miura, Yoshifumi</au><au>Kan, Motoyasu</au><au>Maruta, Shikiko</au><au>Yamada, Toshihito</au><au>Takemura, Ryo</au><au>Sato, Yasunori</au><au>Kato, Jun</au><au>Kato, Naoya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phase II study comparing nasal pressure monitoring with capnography during invasive endoscopic procedures: a single-center, single-arm trial</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2023-01-23</date><risdate>2023</risdate><volume>13</volume><issue>1</issue><spage>1265</spage><epage>10</epage><pages>1265-10</pages><artnum>1265</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Nasal pressure signal is commonly used to evaluate obstructive sleep apnea. This study aimed to assess its safety for respiratory monitoring during sedation. A total of 45 adult patients undergoing sedation with propofol and fentanyl for invasive endoscopic procedures were enrolled. While both nasal pressure and capnograph signals were continuously recorded, only the nasal pressure signal was displayed. The primary outcome was the incidence of oxygen desaturation below 90%. The secondary outcomes were the ability to predict the desaturation and incidence of harmful events and false alarms, defined as an apnea waveform lasting more than 3 min without desaturation. Of the 45 participants, 43 completed the study. At least one desaturation event occurred in 12 patients (27.9%; 95% confidence interval 15.3–43.7%). In these 12 patients, more than half of the desaturation events were predictable in 9 patients by capnography and 11 patients by nasal pressure monitoring (
p
= 0.59). In the 43 patients, false alarms were detected in 7 patients with capnography and 11 patients with nasal pressure monitoring (
p
= 0.427). Harmful events unrelated to nasal pressure monitoring occurred in 2 patients. Nasal pressure monitoring is safe and possibly useful for respiratory monitoring despite false alarms during sedation.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>36690708</pmid><doi>10.1038/s41598-023-28213-y</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 692/308 692/4020 Adult Anesthesia Apnea Capnography - methods Carbon dioxide Endoscopy False alarms Fentanyl Humanities and Social Sciences Humans Monitoring Monitoring, Physiologic - methods multidisciplinary Pressure Propofol Propofol - adverse effects Science Science (multidisciplinary) Sleep Apnea, Obstructive - chemically induced Sleep disorders |
title | Phase II study comparing nasal pressure monitoring with capnography during invasive endoscopic procedures: a single-center, single-arm trial |
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