Skip to main content

Table 1 Baseline characteristics

From: Oral transmucosal fentanyl citrate analgesia in prehospital trauma care: an observational cohort study

Variable

Total n = 177

Age in years

Mean, ± SD

40 ± 17

< 20, n (%)

25 (14.1)

20–60, n (%)

130 (73.5)

≥ 60, n (%)

22 (12.4)

Male gender, n (%)

106 (59.9)

Pain (NRS)

Initial, median (IQR)

7 (6 to 8)

After OTFC

4 (3 to 5)

Mean pain reduction

3 (2 to 4)

Dose of OTFC

600 µg, n (%)

65 (36.7)

800 µg, n (%)

112 (63.3)

Location of Trauma

Upper extremity, n (%)

90 (50.8)

Lower extremity, n (%)

81 (45.8)

Thorax, n (%)

5 (2.8)

Abdomen, n (%)

2 (1.1)

Spinal column, n (%)

3 (1.7)

Adverse Events

None, n (%)

159 (89.8)

Nausea/Vomiting, n (%)

8 (4.5)

Vertigo, n (%)

10 (5.6)

Bradypnea, n (%)

1 (0.5)

Tachypnea, n (%)

3 (1.6)

Major adverse events, n (%)

0 (0)

Transport mode to Hospital

Ground EMS, n (%)

137 (77.4)

Helicopter EMS, n (%)

40 (22.6)

Helicopter EMS treatment

Additional i.v. line, n (%)

26 (14)

Additional i.v. medication, n (%)

14 (53.9)

Fentanyl, Ketamine, midazolam, n (%)

2 (14.3)

Ketamine, Midazolam, n (%)

3 (21.3)

Ketamine, Fentanyl, n (%)

2 (14.3)

Fentanyl, n (%)

5 (35.7)

Ketamine, n (%)

2 (14.3)

  1. No missing data
  2. SD Standard Deviation, IQR Inter-Quartile Range, OTFC Oral Transmucosal fentanyl citrate