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. 2017 Jun 14;71(1):43–47. doi: 10.4097/kjae.2018.71.1.43

Table 3. Number of Patients Exhibiting Adverse Events.

Adverse event Group 1 (n = 68) Group 2 (n = 70) Group 3 (n = 72)
Desaturation 5 (7.35%) 4 (5.71%) 5 (6.94%)
Hypotension 4 (5.88%) 4 (5.71%) 3 (4.16%)
Coughing 2 (2.94%) 5 (7.14%) 7 (9.72%)
Hiccups 24 (35.2%) 28 (40%) 30 (41.67%)

Values are given as number (%). Patients in Group 1 received propofol only, Group 2 received fentanyl + propofol, and Group 3 received ketamine + propofol.