Table 1: Baseline patients’ characteristics.
Data are expressed as mean ± SD, median (interquartile range), or number and
percentage (%).
|
HFO
Group N = 111 |
Control
Group N = 111 |
P |
Age, years |
62.9 ± 16.1 |
64.5 ± 13.7 |
0.4 |
Male sex |
70 (63%) |
73 (66%) |
0.7 |
Comorbidities: |
|
|
|
COPD |
37 (33%) |
34 (31%) |
0.7 |
Heart disease |
22 (20%) |
23 (21%) |
0.9 |
Diagnosis at admission: |
|
|
|
Medical |
66 (59%) |
66 (59%) |
1 |
Respiratory primary failure* |
46 (41.4%) |
41 (36.9%) |
|
Cardiologic primary failure |
2 (1.8%) |
3 (2.7%) |
|
Abdominal |
6 (5.4%) |
10 (9.1%) |
|
Sepsis (other focus) |
5 (4.5%) |
8 (7.2%) |
|
Other |
7 (6.3%) |
4 (3.6%) |
|
Surgical |
51 (45.9%) |
47 (42.3%) |
0.8 |
Scheduled surgery |
31 (27.9%) |
38 (34.2%) |
|
Urgent surgery |
20 (18.1%) |
9 (8.1%) |
|
Body mass index |
27 ± 6.9 |
27 ± 7.1 |
0.8 |
APACHE II at ICU admission |
15.1 ± 6.6 |
15.8 ± 7.5 |
0.6 |
APACHE II at extubation |
9.6 ± 6.2 |
9.9 ± 7.1 |
0.8 |
PaO2/FiO2 at end of SBT |
175
± 21 |
180
± 32 |
0.8 |
Length of mechanical ventilation before extubation,
days |
9.7 ± 4.8 |
10.1 ± 4.6 |
0.5 |
ICU-acquired paresis (MRC score <
48 points) |
10 (9%) |
7 (6%) |
0.6 |
Corticosteroids (> 12 h before
extubation) |
16 (14%) |
18 (16%) |
0.8 |
High risk variables for reintubation: |
66 (59%) |
66 (59%) |
1 |
Age > 65 years |
54 (49%) |
53 (48%) |
|
Intubation due to heart failure |
2 (2%) |
1 (1%) |
|
Moderate-to-severe COPD |
29 (26%) |
30 (27%) |
|
APACHE II > 12 at extubation |
52 (47%) |
51 (46%) |
|
Body mass index > 30 |
22 (20%) |
24 (22%) |
|
Inability to deal with respiratory
secretions |
1 (1%) |
0 (0%) |
|
Difficult or prolonged weaning |
29 (26%) |
27 (24%) |
|
≥ 2 comorbidities |
34 (31%) |
33 (30%) |
|
Mechanical ventilation > 7 days |
56 (50%) |
58 (52%) |
|
Laryngeal edema
after extubation |
0 (0%) |
4 (4%) |
0.1 |
APACHE
= acute physiology and chronic health evaluation; ARDS = acute respiratory
distress syndrome; COPD = chronic obstructive pulmonary disease; MRC = Medical
Research Council score; SBT = spontaneous breathing trial.
*
Primary respiratory failure included severe pneumonia (23/21),
aspiration (3/3), asthma exacerbation (2/1), pulmonary embolism (4/2), and COPD
exacerbation (11/12), ARDS (3/2), respectively.