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131

PROPOFOL AND REMIFENTANIL SEDATION FOR BRONCHIAL THERMOPLASTY

10

Table 1.

Baseline characteristics

Subjects, n

13

Bronchial Thermoplasty procedures, n

32

Gender, male/female

2/11

Age, years

42 ± 14

Pre-bronchodilator FEV1, % predicted

78 ± 26

Inhaled corticosteroids of futicasone or equivalent, μg/day

1,269 ± 525

Inhaled LABA of salmeterol or equivalent, μg/day

154 ± 97

Chronic oral corticosteroid use, n

6

Oral corticosteroids of prednisone or equivalent, mg/day

13 ± 7

Values are means ± standard deviations unless otherwise indicated. FEV1, forced expiratory volume in 1s; LABA,

long-acting β

2

agonist.

Primary endpoints

The median VAS scores assessed by the patients were: overall satisfaction 9.5 (IQR 8.5–

10.0) (Figure 1), dyspnea 0.0 (IQR 0.0–0.6), pain 0.1 (IQR 0.0–1.0), cough 0.5 (IQR 0.0–2.1),

and anxiety 0.1 (IQR 0.0–0.7) (Figure 2a; Table 2). The mean VAS scores assessed by the

bronchoscopists were: overall patient cooperation 9.1 (IQR 8.5–9.6) (Figure 1), dyspnea 0.3

(IQR 0.0–0.9), pain 0.2 (IQR 0.0–1.3), cough 1.2 (IQR 0.7–2.0), and discomfort 0.6 (IQR 0.3–1.5)

(Figure 2b; Table 2). All patients were willing to undergo the BT procedures under the same

conditions again and would recommend this form of sedation to their best friend (Table 2).

Figure 1.

Patients’ and bronchoscopists’ median VAS score for overall procedural satisfaction and

overall patient cooperation