Table 1.
Demographic Data of Ordinary Worker and Doctor Groups
Variable | No. (%) |
---|---|
Ordinary worker (n=1,738)* | |
Age, yr | |
<40 | 1,153 (66.4) |
≥40 | 584 (33.6) |
Sex | |
Male | 811 (46.7) |
Female | 927 (53.3) |
Marital status | |
Unmarried | 841 (48.4) |
Married | 896 (51.6) |
Recognition of sedation drug | |
Propofol | 659 (37.9) |
Another | 1,079 (62.1) |
Previous state of health | |
Experience of general anesthesia | |
Yes | 517 (29.7) |
No | 1,221 (70.3) |
Experience of admission | |
Yes | 996 (57.3) |
No | 741 (42.7) |
Current state of health | |
Chronic disease | |
Yes | 158 (9.1) |
No | 1,580 (90.9) |
Confidence of health | |
Self-reported healthy | 1,321 (76.0) |
Self-reported unhealthy | 417 (24.0) |
Prior sedation experience | |
Myself | |
No | 721 (41.6) |
Yes† | 1,012 (58.4) |
Adverse event | |
No | 931 (92.2) |
Yes‡ | 79 (7.8) |
Prior experienced (n=1,012)† | |
Target procedure of sedation | |
Endoscopy | 793 (78.7) |
Medical imaging/surgery | 215 (21.3) |
Comfortability of target procedure | |
Yes | 905 (89.5) |
No | 106 (10.5) |
Sufficient explanation of sedation | |
Yes | 586 (58.0) |
No | 425 (42.0) |
Adverse event (n=79)‡ | |
Types§ | |
Awakening or inadequate sedation | 41 (51.9) |
Dyspnea | 9 (11.4) |
Hypotension | 7 (8.9) |
Delayed emergence | 25 (31.6) |
Occurrence of sequelae following adverse event | |
Yes | 15 (19.2) |
No | 63 (80.8) |
Family | |
No | 521 (30.0) |
Yes | 1,217 (70.0) |
Adverse event | |
No | 1,113 (64.1) |
Yes | 102 (5.9) |
Friends | |
No | 536 (30.9) |
Yes | 1,201 (69.1) |
Adverse event | |
No | 1,074 (61.9) |
Yes | 126 (7.3) |
Doctor (n=649) | |
Age, yr | |
<40 | 440 (67.8) |
≥40 | 209 (32.2) |
Sex | |
Male | 382 (58.9) |
Female | 267 (41.1) |
Subspecialty | |
All excluding Anesthesiology and Pain Medicine | 588 (90.6) |
Anesthesiology and Pain Medicine | 61 (9.4) |
Experience of adverse event | |
Yes | 234 (36.1) |
No | 415 (63.9) |
Sufficient explanation of sedation | |
Yes | 457 (70.4) |
No | 192 (29.6) |
Includes non-responses;
Respondents with sedation experience;
Respondents with sedation experience, as well as an adverse event during sedation;
Includes multiple responses.