Target-controlled infusion of propofol for fibreoptic intubation
被引:22
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作者:
Knolle, E
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Univ Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, AustriaUniv Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, Austria
Knolle, E
[1
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Oehmke, MJ
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机构:
Univ Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, AustriaUniv Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, Austria
Oehmke, MJ
[1
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Gustorff, B
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Univ Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, AustriaUniv Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, Austria
Gustorff, B
[1
]
Hellwagner, K
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Univ Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, AustriaUniv Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, Austria
Hellwagner, K
[1
]
Kress, HG
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Univ Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, AustriaUniv Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, Austria
Kress, HG
[1
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机构:
[1] Univ Vienna, Dept Anaesthesiol & Gen Intens Care B, A-1090 Vienna, Austria
Background and objective: In a retrospective study, we examined the suitability of a departmental clinical protocol for anaesthesia induction with target-controlled infusion of propofol developed for fibreoptic intubation in spontaneously breathing patients scheduled for outpatient oral surgery at the dental clinic of the Vienna University Hospital. Methods: Propofol was administered using target-controlled infusion (Diprifusor(R)) at increasing target plasma concentrations starting at 2.5 mug mL(-1). After 10 min, an intravenous dose of alfentanil (5-10 mug kg(-1)) was given for pain reduction. After a further 2 min, the patient was evaluated for response to auditory stimulation. If unresponsive, fibreoptic intubation was performed, otherwise the target concentration was increased by 0.2 mug mL(-1) every 2 min until non-responsiveness was attained. Results: Tracheal intubation was successful in all patients without any haemodynamic instability. However, one patient required facemask ventilation for 2 min. No patient was aware of intubation. The plasma concentration required for non-responsiveness was 2.8 +/- 0.4 mug mL(-1) (mean +/- SD). Conclusions: When using a target-controlled infusion of propofol, fibreoptic intubation can be performed with complete amnesia of the procedure for the patient. However, assisted ventilation of the lungs may be necessary as spontaneous ventilation may cease.
机构:
Chinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R ChinaChinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R China
Luo, AL
Yi, J
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Chinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R ChinaChinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R China
Yi, J
Guo, XY
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Chinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R ChinaChinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R China
Guo, XY
Ren, HZ
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Chinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R ChinaChinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R China
Ren, HZ
Huang, YG
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Chinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R ChinaChinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R China
Huang, YG
Ye, TH
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Chinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R ChinaChinese Acad Med Sci, Peking Union Med Hosp, Peking Union Med Coll, Dept Anesthesiol, Beijing 100730, Peoples R China
机构:
Czech Technical University in Prague,Department of Biomedical Technology, Faculty of Biomedical EngineeringCzech Technical University in Prague,Department of Biomedical Technology, Faculty of Biomedical Engineering
Pavla Šafránková
Jan Bruthans
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Czech Technical University in Prague,Department of Biomedical Technology, Faculty of Biomedical EngineeringCzech Technical University in Prague,Department of Biomedical Technology, Faculty of Biomedical Engineering