Variables | All (n = 32) | Survivors (n = 18) | Non-Survivors (n = 14) | P Value |
---|---|---|---|---|
Age, years, median (IQR) | 73 (64–78) | 69 (56–74) | 78 (74–80) | 0.001 |
Males N (%) | 27 (84) | 15 (84) | 12 (86) | 0.85 |
SAPS II score, median (IQR) | 36 (23–42) | 28 (19–36) | 40 (31–56) | 0.017 |
SOFA score at ICU admission, median (IQR) | 3 (2–6) | 3 (2–4) | 4 (3–8) | 0.115 |
PaO2/FiO2 ratio at study inclusion, median (IQR) | 150 (127–179) | 169 (132–181) | 143 (113–153) | 0.11 |
Noradrenaline at study inclusion, N (%) | 12 (37.5) | 4 (22) | 8 (57) | 0.07 |
Comorbidities, N (%) | ||||
Hypertension | 16 (50) | 9(50) | 7 (50) | 1 |
Cardiovascular disease | 9 (28) | 4 (22) | 5 (36) | 0.4 |
Chronic treatment with ACEi and/or ARBs, N (%) | 11 (34.3) | 4 (22.2) | 7 (50) | 0.25 |
ACEi and/or ARBs at study inclusion N (%)(‡) | 4 (12.5) | 2 (11.1) | 2 (14.2) | 1 |
ARDS (†) categories at study inclusion N (%) | ||||
Mild | 9 (28) | 5 (28) | 4 (29) | 1 |
Moderate | 23 (72) | 13 (72) | 10 (71) | |
Respiratory support throughout the ICU stay N (%) | ||||
NIV/HFNC | 11 (34) | 11(61) | 0 (0) | < 0.0004 |
IMV | 21 (66) | 7 (39) | 14 (100) | |
AKI (††) at study inclusion, N (%) | 5 (15.6) | 1 (5.5) | 4 (28.5) | 0.13 |
ICU LoS, days, median (IQR) | 8.5 (5–17) | 8 (4–13) | 10.5 (7–18) | 0.189 |
RAS peptides levels at study inclusion (*) | ||||
Renin, pg/mL median (IQR) | 16.5 (6.27–105) | 13 (4.47–31.77) | 56.7 (11–255) | 0.04 |
Angiotensin I, pg/mL, median (IQR) | 655 (445–1175) | 685 (580–1500) | 475 (410–690) | 0.03 |
Angiotensin II, pg/mL, median (IQR) | 350 (230–650) | 470 (300–920) | 250 (220–350) | 0.01 |
Angiotensin 1–7, pg/mL, median (IQR) (**) | 230 (170–350) | 320 (210–440) | 210 (160–250) | 0.023 |
Angiotensin I/Angiotensin II ratio, median (IQR) | 1.8 (1.3–2.4) | 1.6 (1.3–2.0) | 1.9 (1.2–2.9) | 0.42 |
Angiotensin II/ Angiotensin 1–7 ratio, median (IQR) | 1.6 (0.96–1.92) | 1.66 (0.97–2) | 1.58 (0.71–1.72) | 0.39 |