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1.
Chinese Journal of Thoracic and Cardiovascular Surgery ; (12): 535-538, 2011.
Article in Chinese | WPRIM | ID: wpr-419908

ABSTRACT

Objective To evaluate the clinic efficacy of sufentanil and remifentanil by target- controlled infusion (TCI) combined with propofol in patients undergoing endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA).Methods Sixty patients,ASA Ⅰ ~ Ⅱ,undergoing elective EBUS-TBNA were randomly divided into group S ( sufentanil group),group R (remifentanil group) and group SR (sufentanil + remifentanil group),each group were twenty patients.The anesthesia of all groups is propofol intravenous anesthesia with 2% lidocaine topical anesthesia,to controll BIS between 50 and 60 during surgery.Heart rate(HR),mean arterial pressure(MAP) pulse oxygen saturation( SpO2 ) and respiratory rate (RR) were recorded and compared 5mins after entering room(T0),30mins after the beginning of surgery(T1 ) and after surgery(T3).Arterial blood gas and the times of cough during surgery were also recorded and compared in all groups.The use of propofol and lidocaine,the wake-up time,satisfaction with anesthesia and adverse reactions in 6 hrs after surgery were also obtained.Results ( 1 ) RR decreased distinctly in group R and PaCO2 increased distinctly in group S and group R compared with that of group SR (P <0.05) during surgery.(2)The times of cough and the wake-up time lessened distinctly in group R and group SR compared with that of group S ( P <0.05 ).(3) The use of propofol and lidocaine,satisfaction with anesthesia and adverse reactions in 6 hrs after surgery were similar in all groups ( P > 0.05 ).Conclusion Sufentanil compounded remifentanil by TCI combined with propofol is a safe and feasible anesthesia option for EBUS-TBNA,which provides better efficacy,high satisfaction and less side effects compared with using alone of sufentanil and remifentanil respectively.

2.
Journal of the Korean Ophthalmological Society ; : 53-58, 1990.
Article in Korean | WPRIM | ID: wpr-199805

ABSTRACT

To evaluate the clinical usefulness of new handheld air impulse tonometer(Pulsair, Keeler), the intraocular pressures of 147 eyes of 80 men and women at the age range of 9 to 82 year without corneal opacity or corneal edema were measured with the Goldmann applanation tonometer as well as noncontact air impulse tonometer. The IOPs measured with both tonometer were compared to evaluate the correlation coefficiency. The correlation coefficiency between two instruments is 0.89. Therefore, the new type of noncontact tonometer could be useful for clinical applications due to its accuracy, simplicity, painlessness, portability, and repeatability-especially at glaucoma screening programs.


Subject(s)
Female , Humans , Male , Corneal Edema , Corneal Opacity , Glaucoma , Intraocular Pressure , Mass Screening
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