Table 2.
Propofol usage, time parameters, and incidence of adverse events
| Variable | Control group | Lidocaine group | OR | P value (95% CI) |
|---|---|---|---|---|
| Propofol induction dose, mg | 63.2 ± 10.1 | 57.4 ± 11.6 | 0.112(−13.05, 1.42) | |
| Propofol maintenance dose, mg | 136.2 ± 49.6 | 71.2 ± 26.7 | <0.001(−90.78, −39.22) | |
| Total propofol dose, mg | 199.4 ± 57.6 | 128.6 ± 30.4 | <0.001(−100.60, −41.02) | |
| Operation time, min | 25.9 ± 7.0 | 24.0 ± 5.8 | 0.357(−6.03, 2.23) | |
| Awakening time, min | 11.2 ± 2.4 | 4.8 ± 1.4 | <0.001(−7.67, −5.13) | |
| Recovery time, min | 13.7 ± 2.7 | 7.8 ± 2.1 | <0.001(−7.45, −4.35) | |
| Involuntary movement n (%) | 8 (40) | 2 (10) | 0.17 | 0.028 (0.03, 0.92) |
| Hypotension n (%) | 3 (5) | 2 (10) | 0.63 | >0.999 (0.09, 4.24) |
| Bradycardia n (%) | 1 (5) | 3 (15) | 3.35 | 0.605 (0.32, 35.36) |
| Hypoxia n (%) | 2 (10) | 1 (5) | 0.47 | >0.999 (0.04, 5.69) |
Data are presented as mean ± SD or number(%); OR Odds ratio, CI Confidence interval; P < 0.05 denotes statistical significance