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 3

Postoperative pain assessed by a visual analogue scale (VAS) and postoperative nausea and vomiting (PONV).

L groupH group

T3
 VAS24 ± 1726 ± 140.37
 PONV incidence111.00
 PONV scale0.02 ± 0.130.06 ± 0.131.00
 Analgesic430.70
 Antiemetic001.00
 Rhodes index
T4
 VAS31 ± 1234 ± 100.06
 PONV incidence870.90
 PONV scale0.13 ± 0.340.13 ± 0.380.90
 Analgesic551.00
 Antiemetic001.00
 Rhodes index
T5
 VAS24 ± 1222 ± 120.22
 PONV incidence9100.88
 PONV scale0.22 ± 0.630.24 ± 0.620.88
 Analgesic200.15
 Antiemetic010.32
 Rhodes index1.11 ± 3.721.25 ± 3.860.88
T6
 VAS13 ± 910 ± 100.06
 PONV incidence740.64
 PONV scale0.18 ± 0.580.10 ± 0.430.64
 Analgesic001.00
 Antiemetic001.00
 Rhodes index0.64 ± 2.250.35 ± 1.740.63

Values are expressed as mean ± standard deviation or number of patients.
L group: propofol-low dose remifentanil group; H group: propofol-high dose remifentanil group; T3: on arrival at post-anesthetic care unit (PACU); T4: after 30 minutes on arrival at PACU; T5: at 6 hours after discharge from PACU; T6: at 24 hours after discharge from PACU; PONV scale: PONV assessed using a three-point ordinal scale (0 = none, 1 = nausea, 2 = retching, and 3 = vomiting).