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Table 1 Baseline Characteristics and pain

From: Nasal nalbuphine analgesia in prehospital trauma managed by first-responder personnel on ski slopes in Switzerland: an observational cohort study

Variable

Total n = 267

Age in years

 Mean, ± SD

33.3 ± 18.2

  < 20, n (%)

84 (31.5)

 20–60, n (%)

163 (61.1)

  ≥ 60, n (%)

20 (7.5)

Male sex, n (%)

157 (58.8)

Pain (NRS)

 Initial, median (IQR)

8 (7 to 9)

 After nalbuphine

5 (4 to 7)

 Missing, n (%)

19 (7.1)

Pain reduction (NRS)

 Median (IQR)

−3 (−4 to −1)

 Clinically relevant pain reduction, n (%)

145 (58.5)

 Missing, n (%)

19 (7.1)

Dose of Nalbuphine

 5 mg, n (%)

24 (9.0)

 10 mg, n (%)

128 (47.9)

 15 mg, n (%)

35 (13.1)

 20 mg, n (%)

80 (30.0)

Location of Trauma

 Shoulder, n (%)

63 (23.6)

 Upper arm, n (%)

22 (8.2)

 Elbow, n (%)

1 (0.4)

 Forearm or hand, n (%)

32 (12.0)

 Hip or femur, n (%)

22 (8.2)

 Knee, n (%)

32 (12.0)

 Lower leg, n (%)

39 (14.6)

 Foot, n (%)

1 (0.4)

 Neck, n (%)

0 (0.0)

 Back, n (%)

8 (3.0)

 Thorax or clavicula, n (%)

18 (6.7)

 Abdomen, n (%)

1 (0.4)

 Missing, n (%)

28 (10.5)

Adverse Events

 None, n (%)

252 (94.4)

 Nausea or vomiting, n (%)

3 (1.1)

 Retching, n (%)

5 (1.9)

 Nasal discomfort, n (%)

3 (1.1)

 Major adverse events, n (%)

0 (0)

Technical device problem, n (%)

4 (1.5)

  1. Footnote:
  2. No missing data if not stated explicitly. SD Standard Deviation, IQR Inter Quartile Range