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. 2017 May 19;17:65. doi: 10.1186/s12871-017-0357-8

Table 2.

Incidence of postoperative nausea and vomiting, use of rescue emetics and complete response

Parameter Group G (n = 40) Group R (n = 44) Group GR (n = 40) P overall (P 1, P 2)
Postoperative 0–2 h
 Nausea (0/1/2/3) 22*/4/10/4 22*/6/4/8 32/2/1/5 0.042
(0.017, 0.038)
 Emetic episode 4 (10.0%) 4 (9.1%) 4 (10.0%) 0.987
 Rescue antiemetics 4 (10.0%) 5 (11.4%) 5 (12.5%) 0.939
Postoperative 2–24 h
 Nausea (0/1/2/3) 21*/7/8/4 22*/12/6/4 30/3/5/2 0.041
(0.036, 0.018)
 Emetic episode 11 (27.5%) 10 (25.0%) 7 (17.5%) 0.564
 Rescue antiemetics 5 (12.5%) 6 (13.6%) 4 (10.0%) 0.874
Postoperative 24–48 h
 Nausea (0/1/2/3) 29*/8/1/2 29*/9/4/2 36/3/1/0 0.030
(0.045, 0.008)
 Emetic episode 2 (5.0%) 4 (9.1%) 1 (2.5%) 0.416
 Rescue antiemetics 2 (5.0%) 2 (4.5%) 1 (2.5%) 0.831
Postoperative 0–48 h
 Severe nausea 9 (22.5%) 11 (25.0%) 6 (15.0%) 0.510
 Emetic episode 14 (35.0%) 15 (34.1%) 9 (22.5%) 0.396
 Rescue antiemetics 10 (25.0%) 9 (20.5%) 8 (20.0%) 0.834
 Complete response 16 (40.0%)* 18 (40.9%)* 26 (65.0%) 0.038
(0.025, 0.027)

Data presented as n (%) of patients

Group G, patients received oral gabapentin 300 mg 1 h before induction of anesthesia; Group R, patients received intravenous ramosetron 0.3 mg at the end of surgery; Group GR, patients received oral gabapentin 300 mg 1 h before induction of anesthesia and intravenous ramosetron 0.3 mg at the end of surgery

Nausea: 0, none; 1, mild; 2, moderate; 3, severe; emetic episode: retching or vomiting; complete response: absence of postoperative nausea and vomiting and no need for rescue antiemetic therapy during the 48-h postoperative period

P 1 = group G vs group GR; P 2 = group R versus group GR

* P < 0.05 compared with group GR