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Incidence of adverse events
| Parameter | Group S (n = 29) | Group SD (n = 29) |
|---|---|---|
| Nausea | 6 (20.6) | 5 (17.2) |
| Vomiting | 2 (6.8) | 3 (10.3) |
| Pruritus | 6 (20.6) | 3 (10.3) |
| Uninary retention | 0 | 0 |
| Severe sedation | 0 | 0 |
Values are given as number of subjects (%)
S sufentanil group, SD sufentanil/dexmedetomidine group
