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. 2021 Dec 1;21:299. doi: 10.1186/s12871-021-01525-0

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