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Table 5 Adverse events during the PACU period

From: Effects of lidocaine, dexmedetomidine, and their combination infusion on postoperative nausea and vomiting following laparoscopic hysterectomy: a randomized controlled trial

Adverse events

Group C (n = 60)

Group L (n = 60)

Group D (n = 60)

Group LD (n = 60)

P-value

Mouth dry, n (%)

1 (1.7%)

2 (3.3%)

15 (25%)*✩

17 (28.3%)*✩

 < 0.001

Bradycardia, n (%)

1 (1.7%)

3 (5.0%)

12 (20.0%)*

18 (30.0%)*✩

 < 0.001

Ramsay sedation score (≥ 4), n (%)

2 (3.3%)

4 (6.7%)

11 (18.3%)*

21 (35.0%)*✩

 < 0.001

Patients with agitation, n (%)

11 (18.3%)

9 (15.0%)

5 (8.3%)

4 (6.7%)

0.162

Patients with shivering, n (%)

14 (23.3%)

12 (20.0%)

9 (15.0%)

7 (11.7%)

0.341

  1. Data are present as number (%)
  2. Group C Control group, Group L Lidocaine group, Group D Dexmedetomidine group, Group LD Lidocaine combined with dexmedetomidine group, PACU Post-anesthesia care unit
  3. *P versus Group C, ✩P versus Group L