Clinical Study

Total Intravenous Anaesthesia with High-Dose Remifentanil Does Not Aggravate Postoperative Nausea and Vomiting and Pain, Compared with Low-Dose Remifentanil: A Double-Blind and Randomized Trial

Table 1

Demographic data from the L and H groups.

L group ( )H group ( )

Age (years)47 ± 1247 ± 90.95
Height (cm)158 ± 7158 ± 50.91
Weight (kg)57 ± 1058 ± 80.55
Smoking (pack × years)0 ± 11 ± 40.64
Hx of motion sickness470.34
Hx of PONV111.00
Remifentanil (μg)1013 ± 4361894 ± 735<0.001
Propofol (mg)580 ± 294428 ± 138<0.001
Anaesthesia time (min)104 ± 3895 ± 350.15
Operation time (min)69 ± 3661 ± 330.23
Recovery time (min)14 ± 613 ± 40.82

Values are expressed as number of patients or mean ± standard deviation.
L group: propofol-low dose remifentanil group; H group: propofol-high dose remifentanil group; Hx: history; PONV: postoperative nausea and vomiting.