Skip to main content
. 2022 May 17;26:141. doi: 10.1186/s13054-022-03983-5

Table 1.

Demographic and clinical characteristics upon intensive care unit admission of patients who received or did not receive NMBA treatment

Unmatched cohort
(N = 1953)
Propensity score-matched cohort
(N = 420)
Parameter Control (N = 1711) NMBA treatment
(N = 242)
Control (N = 210) NMBA treatment
(N = 210)
Age (years) mean (SD) 61.8 (12.3) 58.9 (12.2) 61.2 (14.2) 59.4 (12.1)
Age (years) n (%)
 < 50 268 (15.7%) 50 (20.7%) 42 (20.0%) 40 (19.0%)
50–59 366 (21.4%) 66 (27.3%) 45 (21.4%) 56 (26.7%)
60–69 578 (33.8%) 80 (33.1%) 57 (27.1%) 73 (34.8%)
70–79 448 (26.2%) 43 (17.8%) 59 (28.1%) 39 (18.6%)
 ≥ 80 51 (3.0%) 3 (1.2%) 7 (3.3%) 2 (1.0%)
Male n (%) 1,196 (70.0%) 175 (72.3%) 144 (68.6%) 152 (72.4%)
Duration of symptom onset to hospital admission (days) median (IQR) 6.0 (4.0–9.0) 7.0 (4.0–9.0) 6.0 (4.0–9.0) 7.0 (3.0–9.0)
Duration of symptom onset to ICU admission (days) median (IQR) 11.0 (8.0–15.0) 10.0 (7.0–13.0) 10.0 (8.0–15.0) 10.0 (7.0–13.0)
Duration of symptom onset to first use of mechanical ventilation (days) median (IQR) 11.0 (8.0–15.0) 10.0 (7.0–13.0) 10.0 (8.0–15.0) 10.0 (7.0–13.0)
Ethnicity
Aboriginal 5 (0.3%) 0 (0.0%) 3 (1.4%) 0 (0%)
Arab 59 (3.4%) 6 (2.5%) 8 (3.8%) 4 (1.9%)
Black 53 (3.1%) 21 (8.7%) 11 (5.2%) 20 (9.5%)
East Asian 18 (1.1%) 5 (2.1%) 7 (3.3%) 5 (2.4%)
Latin American 108 (6.3%) 31 (12.8%) 25 (11.9%) 27 (12.9%)
South Asian 75 (4.4%) 9 (3.7%) 8 (3.8%) 9 (4.3%)
West Asian 5 (0.3%) 1 (0.4%) 1 (0.5%) 1 (0.5%)
White 163 (9.5%) 54 (22.3%) 18 (8.6%) 48 (22.9%)
Mixed 11 (0.6%) 8 (3.3%) 4 (1.9%) 5 (2.4%)
Other 22 (1.3%) 10 (4.1%) 1 (0.5%) 10 (4.8%)
Missing 1192 (69.7%) 97 (40.1%) 124 (59.0%) 81 (38.6%)
Continent
Africa n (%) 19 (1.1%) 18 (7.4%) 14 (6.7%) 14 (6.7%)
Asia n (%) 148 (8.6%) 19 (7.9%) 12 (5.7%) 18 (8.6%)
Europe n (%) 1237 (72.3%) 135 (55.8%) 121 (57.6%) 114 (54.3%)
North America n (%) 175 (10.2%) 43 (17.8%) 42 (20.0%) 43 (20.5%)
Oceania n (%) 30 (1.8%) 7 (2.9%) 3 (1.4%) 5 (2.4%)
South/Central America n (%) 102 (6.0%) 20 (8.3%) 18 (8.6%) 16 (7.6%)
Healthcare or laboratory worker n (%) 42 (2.6%) 10 (4.5%) 8 (4.0%) 9 (4.7%)
Comorbidities
Smoking n (%) 525 (31.0%) 76 (32.1%) 62 (29.5%) 65 (31.4%)
Obesity* n (%) 622 (36.7%) 97 (40.8%) 88 (41.9%) 84 (40.2%)
Hypertension n (%) 916 (53.9%) 125 (52.7%) 123 (58.6%) 116 (55.2%)
Chronic cardiac disease n (%) 227 (13.4%) 21 (8.9%) 17 (8.1%) 19 (9.0%)
Diabetes n (%) 502 (29.8%) 65 (27.9%) 65 (31.0%) 60 (29.1%)
Malignant neoplasm n (%) 66 (3.9%) 8 (3.4%) 9 (4.3%) 8 (3.8%)
Chronic pulmonary disease n (%) 171 (10.1%) 30 (12.6%) 32 (15.2%) 27 (12.9%)
Severe liver disease n (%) 30 (1.8%) 6 (2.5%) 4 (1.9%) 6 (2.9%)
Chronic kidney disease n (%) 152 (9.0%) 12 (5.0%) 12 (5.7%) 12 (5.7%)
BMI mean (SD) 30.2 (6.4) 30.9 (6.8) 30.3 (6.2) 30.6 (6.6)
Severity of illness
APACHE II mean (SD) 18.5 (10.5) 17.8 (11.0) 21.2 (12.3) 18.3 (11.0)
SOFA mean (SD) 6.0 (3.9) 5.3 (3.5) 6.1 (4.7) 5.4 (3.6)
Laboratory results upon ICU admission
WBC count (10*3/µL) median (IQR) 9.6 (6.1–13.0) 8.8 (7.1–11.7) 10.0 (6.4–14.1) 8.7 (7.1–11.4)
Lymphocyte count (10*3/µL) median (IQR) 0.7 (0.5–1.1) 0.8 (0.5–1.0) 0.8 (0.5–1.2) 0.8 (0.5–1.0)
Neutrophils/lymphocyte ratio median (IQR) 9.9 (5.8–17.9) 10.6 (6.2–15.8) 9.8 (5.5–17.8) 10.4 (6.0–15.2)
Temperature (°C) mean (SD) 37.3 (1.1) 37.4 (1.1) 37.2 (1.0) 37.4 (1.0)
Creatinine (mg/dL) median (IQR) 0.9 (0.7–1.2) 0.8 (0.7–1.1) 1.0 (0.7–1.4) 0.8 (0.7–1.1)
C-reactive protein level (mg/dL) median (IQR) 104.8 (30.0–192.0) 86.3 (22.6–185.4) 126.3 (40.9–228.6) 82.8 (20.8–172.1)
D-dimer (mcg/mL) median (IQR) 0.9 (0.5–2.2) 1.0 (0.5–2.3) 1.0 (0.6–2.9) 1.1 (0.5–2.3)
Lactate (mmol/L) median (IQR) 1.5 (1.1–2.1) 1.6 (1.1–2.1) 1.6 (1.1–2.0) 1.5 (1.1–2.1)
Ferritin (ng/mL) median (IQR) 2.9 (1.4–4.8) 2.8 (1.7–5.6) 3.4 (1.7–5.9) 3.2 (1.7–5.6)
IL-6 (ng/L) median (IQR) 124.7 (51.2–268.0) 79.4 (28.9–108.2) 83.0 (47.8–173.3) 75.9 (26.3–100.1)

Demographic and clinical characteristics upon intensive care unit admission of patients who received or did not receive neuromuscular blocking agents (NMBA). NMBA treatment was defined as at least 2 days of continuous use of NMBAs or up to 3 days, within 48 h from commencement of IMV

IMV, invasive mechanical ventilation; BMI, body mass index; APACHE II, acute physiology and chronic health evaluation; SOFA, sequential organ failure assessment; WBC, white blood cells; IL, interleukin