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The optimal concentration of remifentanil required for i-gel insertion in patients with simulated difficult airways
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 전우재 | - |
| dc.contributor.author | 조상윤 | - |
| dc.contributor.author | 김경헌 | - |
| dc.contributor.author | 권용덕 | - |
| dc.date.accessioned | 2022-07-16T02:36:51Z | - |
| dc.date.available | 2022-07-16T02:36:51Z | - |
| dc.date.issued | 2014-10 | - |
| dc.identifier.issn | 1975-5171 | - |
| dc.identifier.issn | 2383-7977 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/158927 | - |
| dc.description.abstract | Background: Because difficult airways are not commonlyencountered, simulation of a difficult airway using a cervical collarhas become a well-established technique of for modeling difficultlaryngoscopic views and evaluating interventions for use in difficultairway scenarios. In this study, we have determined the optimalremifentanil concentrations (EC50 and EC95) required for i-gelinsertion in anesthetized patients fitted with cervical collars atpropofol effect-site concentrations of 4.0 and 6.0 μg/ml (group 4.0and group 6.0). Methods: The remifentanil dosage for each propofol effect-siteconcentration group was determined by the modified Dixon’sup-and-down method using previous results. The experiment wasstarted using a 4.0 ng/ml effect-site remifentanil concentration, andthe dose was reduced by 0.5 ng/ml for the next attempt when tubeinsertion was successful; if tube insertion failed, the dose for thenext attempt was increased by 0.5 ng/ml. Results: EC50 and EC95 were respectively 2.11 ng/ml (95% CI,1.78–2.26 ng/ml) and 2.44 ng/ml (95% CI, 2.28–3.67 ng/ml) for the4.0 group, and 0.42 ng/ml (95% CI, −1.30 to 0.77 ng/ml) and 0.75ng/ml (0.56–14.3 ng/ml) for the 6.0 group. Conclusions: In this study, a cervical collar was attached andhead fixation was performed to induce a difficult airway. The optimalconcentration of remifentanil at a propofol effect-site concentrationof 4.0 μg/ml was greater than 2.44 ng/ml (95% CI, 2.28–3.67 ng/ml),and that at the propofol effect-site concentration of 6.0 μg/ml wasgreater than 0.75 ng/ml (0.56–14.3 ng/ml). | - |
| dc.format.extent | 5 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | 대한마취통증의학회 | - |
| dc.title | The optimal concentration of remifentanil required for i-gel insertion in patients with simulated difficult airways | - |
| dc.type | Article | - |
| dc.publisher.location | 대한민국 | - |
| dc.identifier.bibliographicCitation | Anesthesia and Pain Medicine, v.9, no.4, pp 258 - 262 | - |
| dc.citation.title | Anesthesia and Pain Medicine | - |
| dc.citation.volume | 9 | - |
| dc.citation.number | 4 | - |
| dc.citation.startPage | 258 | - |
| dc.citation.endPage | 262 | - |
| dc.identifier.kciid | ART001922753 | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | kciCandi | - |
| dc.subject.keywordAuthor | Airway | - |
| dc.subject.keywordAuthor | Equipment | - |
| dc.subject.keywordAuthor | Remifentanil | - |
| dc.identifier.url | https://www.anesth-pain-med.org/journal/view.php?number=360 | - |
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