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. 2022 Aug 20;22:391. doi: 10.1186/s12876-022-02467-8

Table 4.

Adverse events

Group P Group PK1 Group PK2 Group PK3 P value
Injection pain 3 (4.6%) 7 (10.8%) 2 (3.1%) 1 (1.5%) 0.149
Hypoxemia 14 (21.5%) 16 (24.6%) 23 (35.4%) 16 (24.6%) 0.297
Hypotension 11 (16.9%) 8 (12.3%) 3 (4.6%) 4 (6.2%) 0.072
Cough 46 (70.8%) 34 (52.3%) 37 (56.9%) 31 (47.7%)※ 0.048
Body movement 54 (83.1%) 55 (84.6%) 42 (64.6%) 39 (60.0%)※† 0.001
Dizziness 7 (10.8%) 9 (13.8%) 6 (9.2%) 11 (16.9%) 0.563
Excessive oral secretion 0 (0%) 0 (0%) 0 (0%) 2 (3.1%) 0.247
Hypertension 0 (0%) 1 (1.5%) 0 (0%) 0 (0%) 1.000
Arrhythmia 0 (0%) 0 (0%) 0 (0%) 0 (0%) 1.000
Nausea and vomiting 0 (0%) 0 (0%) 0 (0%) 0 (0%) 1.000
Apnea 0 (0%) 0 (0%) 0 (0%) 0 (0%) 1.000

Data are presented as number (%); ※P < 0.05 compared with group P, †P < 0.05 compared with group PK1