Dexmedetomidine versus Remifentanil for Sedation during Awake Fiberoptic Intubation

This study compared remifentanil and dexmedetomidine as awake fiberoptic intubation (AFOI) anesthetics. Thirty-four adult ASA I-III patients were enrolled in a double-blinded randomized pilot study to receive remifentanil (REM) or dexmedetomidine (DEX) for sedation during AFOI (nasal and oral). Thi...

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Main Authors: Davide Cattano, Nicholas C. Lam, Lara Ferrario, Carmen Seitan, Kash Vahdat, Darrell W. Wilcox, Carin A. Hagberg
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Anesthesiology Research and Practice
Online Access:http://dx.doi.org/10.1155/2012/753107
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author Davide Cattano
Nicholas C. Lam
Lara Ferrario
Carmen Seitan
Kash Vahdat
Darrell W. Wilcox
Carin A. Hagberg
author_facet Davide Cattano
Nicholas C. Lam
Lara Ferrario
Carmen Seitan
Kash Vahdat
Darrell W. Wilcox
Carin A. Hagberg
author_sort Davide Cattano
collection DOAJ
description This study compared remifentanil and dexmedetomidine as awake fiberoptic intubation (AFOI) anesthetics. Thirty-four adult ASA I-III patients were enrolled in a double-blinded randomized pilot study to receive remifentanil (REM) or dexmedetomidine (DEX) for sedation during AFOI (nasal and oral). Thirty patients completed the study and received 2 mg midazolam IV and topical anesthesia. The REM group received a loading dose of 0.75 mcg/kg followed by an infusion of 0.075 mcg/kg/min. The DEX group received a loading dose of 0.4 mcg/kg followed by an infusion of 0.7 mcg/kg/hr. Time to sedation, number of intubation attempts, Ramsay sedation scale (RSS) score, bispectral index (BIS), and memory recall were recorded. All thirty patients were successfully intubated by AFOI (22 oral intubations/8 nasal). First attempt success rate with AFOI was higher in the REM group than the DEX group, 72% and 38% (P=0.02), respectively. The DEX group took longer to attain RSS of ≥3 and to achieve BIS <80, as compared to the REM group. Postloading dose verbal recall was poorer in the DEX group. Dexmedetomidine seems a useful adjunct for patients undergoing AFOI but is dependent on dosage and time. Further studies in the use of dexmedetomidine for AFOI are warranted.
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spelling doaj-art-f21e7ba642da4c4ba458cbb19a28c2b92025-02-03T06:11:45ZengWileyAnesthesiology Research and Practice1687-69621687-69702012-01-01201210.1155/2012/753107753107Dexmedetomidine versus Remifentanil for Sedation during Awake Fiberoptic IntubationDavide Cattano0Nicholas C. Lam1Lara Ferrario2Carmen Seitan3Kash Vahdat4Darrell W. Wilcox5Carin A. Hagberg6Department of Anesthesiology, The University of Texas Medical School at Houston, Houston, TX 77030, USADepartment of Anesthesiology, The University of Texas Medical School at Houston, Houston, TX 77030, USADepartment of Anesthesiology, The University of Texas Medical School at Houston, Houston, TX 77030, USADepartment of Anesthesiology, The University of Texas Medical School at Houston, Houston, TX 77030, USADepartment of Internal Medicine, Vanderbilt University, Nashville, TN 37240, USADepartment of Anesthesia, Duke University School of Medicine, Durham, NC 27710, USADepartment of Anesthesiology, The University of Texas Medical School at Houston, Houston, TX 77030, USAThis study compared remifentanil and dexmedetomidine as awake fiberoptic intubation (AFOI) anesthetics. Thirty-four adult ASA I-III patients were enrolled in a double-blinded randomized pilot study to receive remifentanil (REM) or dexmedetomidine (DEX) for sedation during AFOI (nasal and oral). Thirty patients completed the study and received 2 mg midazolam IV and topical anesthesia. The REM group received a loading dose of 0.75 mcg/kg followed by an infusion of 0.075 mcg/kg/min. The DEX group received a loading dose of 0.4 mcg/kg followed by an infusion of 0.7 mcg/kg/hr. Time to sedation, number of intubation attempts, Ramsay sedation scale (RSS) score, bispectral index (BIS), and memory recall were recorded. All thirty patients were successfully intubated by AFOI (22 oral intubations/8 nasal). First attempt success rate with AFOI was higher in the REM group than the DEX group, 72% and 38% (P=0.02), respectively. The DEX group took longer to attain RSS of ≥3 and to achieve BIS <80, as compared to the REM group. Postloading dose verbal recall was poorer in the DEX group. Dexmedetomidine seems a useful adjunct for patients undergoing AFOI but is dependent on dosage and time. Further studies in the use of dexmedetomidine for AFOI are warranted.http://dx.doi.org/10.1155/2012/753107
spellingShingle Davide Cattano
Nicholas C. Lam
Lara Ferrario
Carmen Seitan
Kash Vahdat
Darrell W. Wilcox
Carin A. Hagberg
Dexmedetomidine versus Remifentanil for Sedation during Awake Fiberoptic Intubation
Anesthesiology Research and Practice
title Dexmedetomidine versus Remifentanil for Sedation during Awake Fiberoptic Intubation
title_full Dexmedetomidine versus Remifentanil for Sedation during Awake Fiberoptic Intubation
title_fullStr Dexmedetomidine versus Remifentanil for Sedation during Awake Fiberoptic Intubation
title_full_unstemmed Dexmedetomidine versus Remifentanil for Sedation during Awake Fiberoptic Intubation
title_short Dexmedetomidine versus Remifentanil for Sedation during Awake Fiberoptic Intubation
title_sort dexmedetomidine versus remifentanil for sedation during awake fiberoptic intubation
url http://dx.doi.org/10.1155/2012/753107
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