1 Risk of composite adverse events |
28 |
2298 |
Risk Ratio (M‐H, Random, 95% CI) |
0.60 [0.49, 0.74] |
2 Composite adverse events: subgroup analysis for dosage |
28 |
2298 |
Risk Ratio (M‐H, Random, 95% CI) |
0.60 [0.49, 0.73] |
2.1 Sugammadex 2 mg/kg vs neostigmine 0.04 mg/kg |
1 |
21 |
Risk Ratio (M‐H, Random, 95% CI) |
0.45 [0.05, 4.28] |
2.2 Sugammadex 2 mg/kg vs neostigmine 0.05 mg/kg |
12 |
1076 |
Risk Ratio (M‐H, Random, 95% CI) |
0.52 [0.34, 0.80] |
2.3 Sugammadex 2 mg/kg vs neostigmine 0.07 mg/kg |
2 |
131 |
Risk Ratio (M‐H, Random, 95% CI) |
0.91 [0.57, 1.44] |
2.4 Sugammadex 2 mg/kg vs neostigmine 2.5 mg |
1 |
40 |
Risk Ratio (M‐H, Random, 95% CI) |
0.0 [0.0, 0.0] |
2.5 Sugammadex 3 mg/kg vs neostigmine 0.03 mg/kg |
1 |
90 |
Risk Ratio (M‐H, Random, 95% CI) |
0.0 [0.0, 0.0] |
2.6 Sugammadex 4 mg/kg vs neostigmine 0.05 mg/kg |
4 |
333 |
Risk Ratio (M‐H, Random, 95% CI) |
0.66 [0.49, 0.88] |
2.7 Sugammadex 4 mg/kg vs neostigmine 0.07 mg/kg |
3 |
197 |
Risk Ratio (M‐H, Random, 95% CI) |
0.49 [0.25, 0.93] |
2.8 Sugammadex, several doses vs neostigmine, several doses |
4 |
410 |
Risk Ratio (M‐H, Random, 95% CI) |
0.60 [0.40, 0.90] |
3 Composite adverse events: subgroup analysis ‐ TIVA vs volatile anaesthetics |
28 |
2298 |
Risk Ratio (M‐H, Random, 95% CI) |
0.60 [0.49, 0.73] |
3.1 TIVA |
7 |
748 |
Risk Ratio (M‐H, Random, 95% CI) |
0.51 [0.20, 1.31] |
3.2 Volatile anaesthetic |
20 |
1510 |
Risk Ratio (M‐H, Random, 95% CI) |
0.64 [0.55, 0.73] |
3.3 No information |
1 |
40 |
Risk Ratio (M‐H, Random, 95% CI) |
0.0 [0.0, 0.0] |
4 Composite adverse events: sensitivity analysis ‐ excluding meeting abstracts |
24 |
2091 |
Risk Ratio (M‐H, Random, 95% CI) |
0.60 [0.49, 0.73] |
5 Participants with ≥ adverse event |
19 |
1766 |
Risk Ratio (M‐H, Random, 95% CI) |
0.62 [0.48, 0.81] |
6 Bradycardia: subgroup analysis ‐ atropine vs glycopyrrolate |
11 |
1218 |
Risk Ratio (M‐H, Random, 95% CI) |
0.16 [0.07, 0.34] |
6.1 Atropine |
6 |
667 |
Risk Ratio (M‐H, Random, 95% CI) |
0.14 [0.05, 0.36] |
6.2 Glycopyrrolate |
5 |
551 |
Risk Ratio (M‐H, Random, 95% CI) |
0.20 [0.06, 0.69] |
7 PONV: subgroup analysis ‐ TIVA vs volatile anaesthetics |
6 |
389 |
Risk Ratio (M‐H, Random, 95% CI) |
0.52 [0.28, 0.97] |
7.1 TIVA |
1 |
94 |
Risk Ratio (M‐H, Random, 95% CI) |
3.55 [0.15, 84.86] |
7.2 Volatile anaesthetics |
5 |
295 |
Risk Ratio (M‐H, Random, 95% CI) |
0.48 [0.25, 0.91] |
8 Desaturation |
2 |
134 |
Risk Ratio (M‐H, Random, 95% CI) |
0.23 [0.06, 0.83] |
9 Procedural complications |
2 |
168 |
Risk Ratio (M‐H, Random, 95% CI) |
0.12 [0.02, 0.97] |
10 Transitory oxygen supplementation |
2 |
76 |
Risk Ratio (M‐H, Random, 95% CI) |
0.24 [0.09, 0.66] |
11 Not able to perform 5 second head‐lift after extubation |
6 |
395 |
Risk Ratio (M‐H, Random, 95% CI) |
0.34 [0.15, 0.78] |
12 General muscle weakness after extubation |
4 |
288 |
Risk Ratio (M‐H, Random, 95% CI) |
0.61 [0.31, 1.18] |
13 Nausea |
9 |
719 |
Risk Ratio (M‐H, Random, 95% CI) |
0.83 [0.44, 1.56] |
14 Vomiting |
4 |
297 |
Risk Ratio (M‐H, Random, 95% CI) |
2.05 [0.50, 8.48] |
15 Postprocedural nausea |
2 |
168 |
Risk Ratio (M‐H, Random, 95% CI) |
1.39 [0.27, 7.12] |
16 Headache |
4 |
388 |
Risk Ratio (M‐H, Random, 95% CI) |
1.02 [0.48, 2.18] |
17 Hypertension |
3 |
287 |
Risk Ratio (M‐H, Random, 95% CI) |
1.45 [0.23, 9.05] |
18 Hypotension |
4 |
465 |
Risk Ratio (M‐H, Random, 95% CI) |
1.23 [0.38, 3.96] |
19 Cough |
3 |
200 |
Risk Ratio (M‐H, Random, 95% CI) |
1.42 [0.42, 4.81] |
20 Dry mouth |
3 |
289 |
Risk Ratio (M‐H, Random, 95% CI) |
0.44 [0.10, 1.87] |
21 Dizziness |
2 |
168 |
Risk Ratio (M‐H, Random, 95% CI) |
0.98 [0.10, 9.23] |
22 Tachycardia |
3 |
338 |
Risk Ratio (M‐H, Random, 95% CI) |
0.44 [0.09, 2.22] |
23 Pruritus |
2 |
175 |
Risk Ratio (M‐H, Random, 95% CI) |
1.62 [0.20, 12.88] |
24 Pyrexia |
3 |
264 |
Risk Ratio (M‐H, Random, 95% CI) |
1.43 [0.23, 8.91] |
25 Shivering |
3 |
190 |
Risk Ratio (M‐H, Random, 95% CI) |
0.75 [0.40, 1.43] |
26 Chills |
2 |
166 |
Risk Ratio (M‐H, Random, 95% CI) |
4.04 [0.46, 35.85] |
27 Rash |
5 |
701 |
Risk Ratio (M‐H, Random, 95% CI) |
0.83 [0.17, 3.96] |
28 Supraventricular extrasystoles |
2 |
189 |
Risk Ratio (M‐H, Random, 95% CI) |
0.32 [0.03, 3.05] |
29 Laryngospasm |
2 |
100 |
Risk Ratio (M‐H, Random, 95% CI) |
0.34 [0.07, 1.65] |
30 Increased upper airway secretion |
2 |
442 |
Risk Ratio (M‐H, Random, 95% CI) |
0.37 [0.09, 1.59] |
31 Procedural hypertension |
3 |
267 |
Risk Ratio (M‐H, Random, 95% CI) |
1.65 [0.33, 8.21] |
32 Procedural hypotension |
2 |
391 |
Risk Ratio (M‐H, Random, 95% CI) |
0.49 [0.02, 14.15] |
33 Abdominal pain |
2 |
196 |
Risk Ratio (M‐H, Random, 95% CI) |
0.98 [0.10, 9.27] |
34 Clinical signs of residual NMB |
7 |
646 |
Risk Ratio (M‐H, Random, 95% CI) |
0.0 [0.0, 0.0] |
35 Clinical signs of inadequate reversal of NMB |
4 |
368 |
Risk Ratio (M‐H, Random, 95% CI) |
0.11 [0.01, 2.02] |
36 Clinical signs of recurrence of residual NMB |
13 |
1289 |
Risk Ratio (M‐H, Random, 95% CI) |
0.74 [0.05, 10.74] |
37 General muscle weakness at PACU discharge |
5 |
410 |
Risk Ratio (M‐H, Random, 95% CI) |
0.49 [0.12, 1.90] |
38 Not able to perform 5 second head‐lift at PACU discharge |
5 |
399 |
Risk Ratio (M‐H, Random, 95% CI) |
0.0 [0.0, 0.0] |
39 Overall signs of postoperative residual paralysis |
15 |
1474 |
Risk Ratio (M‐H, Random, 95% CI) |
0.40 [0.28, 0.57] |
40 Risk of composite serious adverse events |
10 |
959 |
Risk Ratio (M‐H, Random, 95% CI) |
0.54 [0.13, 2.25] |
41 Participants with ≥ 1 serious adverse event |
10 |
959 |
Risk Ratio (M‐H, Random, 95% CI) |
0.54 [0.13, 2.25] |