Table 2.
HFNO group | Venturi mask group | P value | |
---|---|---|---|
(n = 52) | (n = 48) | ||
Primary endpoint | |||
Number (%) of patients requiring mechanical ventilation | 8 (15 %) | 4 (8 %) | 0.36 |
Noninvasive mechanical ventilation | 6a | 3a | |
Invasive mechanical ventilation | 4 | 2 | |
Secondary endpoints, median [25th–75th percentile] | |||
Discomfort VAS scoreb at 120 min | 3 [1–5] | 3 [0–5] | 0.88 |
Dyspnea VAS scoreb at 120 min | 3 [2 – 6] | 3 [1–6] | 0.87 |
Thirst VAS scoreb at 120 min | 6 [3–8] | 6 [5 – 9] | 0.40 |
Respiratory rate at 120 min, breaths/min | 25 [22–29] | 25 [21–31] | |
Heart rate at 120 min, beats/min | 98 [90–110] | 99 [83–112] | 0.43 |
HFNO high-flow nasal oxygen, VAS visual analogue scale
aTwo patients in the HFNO group and one patient in the Venturi mask group received noninvasive ventilation followed by invasive mechanical ventilation
bAll three VASs ranged from 0 (absence of discomfort, dyspnea, or thirst) to 10 (worst possible discomfort, dyspnea, or thirst)