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. 2024 Jan 4;25:9. doi: 10.1186/s12931-023-02648-3

Table 1.

Characteristics of the 215 subjects with influenza-related ARDS

All patients Prolonged mechanical ventilation (PMV) Weaning in PMV
Characteristics Yes No p Value Success Failure p Value
(n = 215) (n = 78) (n = 137) (n = 44) (n = 34)
Baseline data
 Age (years) 59.27(± 14.48) 58.22(± 11.74) 59.88(± 15.83) 0.38 59.25(± 12.12) 56.88(± 11.27) 038
 Male sex 134(62.3%) 50(64.1%) 84(61.3%) 0.69 31(70.5%) 19(55.9%) 0.18
 Body mass index BMI (kg/m2) 25.67(± 5.78) 26.84(± 4.77) 25.53(± 5.70) 0.087 26.65(± 4.19) 27.09(± 5.48) 0.68
 BMI > 25 (kg/m2) 124(57.7%) 56(71.8%) 68(49.6%)** 0.002 23(67.6%) 33(75%) 0.47
 Malignancy 26(12.1%) 12(15.4%) 14(10.2%) 0.26 7(15.9%) 5(14.7%) 0.88
 Type II diabetes mellitus 63(29.3%) 22(28.2%) 41(29.9%) 0.79 11 (25%) 11(32.4%) 0.47
 Cerebrovascular disease 14(6.5%) 4(5.1%) 10(7.3%) 0.54 4 0 0.13
 Liver disease 22(10.2%) 9(11.5%) 13(9.5%) 0.63 4(11.8%) 5(11.4%) 1.0
 Cardiac disease 25(11.6%) 5(6.4%) 20(14.6%) 0.072 3(8.8%) 2(4.5%) 0.65
 Hypertension 93(43.3%) 35(44.9%) 58(42.3%) 0.72 19(43.2%) 16(47.1%) 0.73
 Immunosuppressantb use before influenza infection 10(4.7%) 5(6.4%) 5(3.6%) 0.5 1(2.3%) 3(8.8%) 0.31
 Autoimmune disease 14(6.5%) 6(7.7%) 8(5.8%) 0.60 2(4.5%) 4(11.8%) 0.40
 End-stage renal disease 14(6.5%) 7(9.0%) 7(5.1%) 0.27 4(9.1%) 3(8.8%) 1.0
Severity scores
 APACHE II score 22.59(± 8.13) 24.14(± 8.52) 21.7(± 7.8)* 0.034 23.30 ± 8.74 25.24(± 8.23) 0.32
ARDS a Severity 0.18 0.76
 Severe 122(56.7%) 49(62.8%) 73(53.3%) 27(61.4%) 22(64.7%)
 Mild to moderate 93(43.3%) 29(37.2%) 64(46.7%) 17(38.6%) 12(35.3%)
Treatments and clinical outcome
 Prone 49(22.8%) 23(29.5%) 26(19%) 0.08 14(31.8%) 9(26.5%) 0.61
 ECMO 34(15.8%) 26(33.3%) 8(5.8%)**  < 0.01 8(18.2%) 18(52.9%)**  < 0.01
 Combined with bacterial pneumonia onset before D21 67(31.2%) 39(50%) 28(20.4%)**  < 0.01 26(59.1%) 22(64.7%) 0.61
 Bacteremia onset before D21 34(15.8%) 19(24.4%) 15(10.9%)** 0.01 6(13.6%) 13(38.2%)* 0.012
 Steroid user 127(59.1%) 46(59%) 81(59.1%) 0.98 23(52.3%) 23(67.6%) 0.17
 Sedation 159(74%) 60(76.9%) 99(72.3%) 0.45 32(72.7%) 28(82.4%) 0.32
 Neuromuscular blockade > 48 h 119(55.3%) 59(75.6%) 60(43.8%)***  < 0.001 32(72.7%) 27(79.4%) 0.5
 Need for vasopressor agents 103(47.9%) 49(62.8%) 54(39.4%)***  < 0.01 25(56.8%) 24(70.6%) 0.21
 Renal replacement therapy c 19(8.8%) 11(14.1%) 8(5.8%)* 0.04 6(13.6%) 5(14.7%) 1.0
 Ventilator-duration (days) 21.18(± 17.74) 39.24(± 17.77) 10.90(± 4.77)***  < 0.001 36.12(± 14.60) 43.29(± 20.72) 0.09
 ICU stay (days) 22.32(± 18) 38.18(± 20.65) 13.22(± 6.24)***  < 0.001 36(± 19.22) 41(± 22.34) 0.29
 Hospital-stay (days) 37.59(± 27.38) 54.12(± 32.73) 28.11(± 18)***  < 0.001 58.90(± 29.70) 47.92(± 35.77) 0.14
 In hospital Mortality 42(19.5%) 31(39.7%) 11(8%)***  < 0.001 5(11.4%) 26(76.5%)***  < 0.001

Data are presented as the mean ± standard deviation and number (%)

APACHE II Acute Physiology and Chronic Health Evaluation, ARDS acute respiratory distress syndrome, ECMO extracorporeal membrane oxygenation

aIn accordance with Berlin definition

bOral prednisolone equivalent dosage > 5 mg/day or > 150 mg cumulative dose within 1 month before influenza infection; or regular treatment using other immunosuppressants within 1month before influenza infection

cExcluding those with end-stage renal disease receiving regular hemodialysis

*< 0.05

**0 < 0.01

***0 < 0.001