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Table 3 Risk assessment for primary and secondary outcomes in the entire population and in septic and non-septic subgroups

From: Urinary [TIMP-2] × [IGFBP7] and serum procalcitonin to predict and assess the risk for short-term outcomes in septic and non-septic critically ill patients

Variables

Analysis cohort

Sepsis

Non-sepsis

OR

95% CI

p-value

OR

95% CI

p-value

OR

95% CI

p-value

Primary outcome

 AKI within 48 h

  [TIMP-2] × [IGFBP7] > 0.3

3.93a

2.14–7.20

< 0.001

5.92a

2.53–13.82

< 0.001

3.27a

1.53–6.97

< 0.001

PCT > 0.5

3.67a

2.17–6.19

< 0.001

2.74a

0.87–8.57

0.083

4.85a

2.37–9.94

< 0.001

  Single-marker positivity

4.08

1.90–8.76

< 0.001

2.27

0.45–11.23

0.316

4.93

2.05–11.82

< 0.001

  Double-marker positivity

26.41

12.32–56.62

< 0.001

19.5

4.20–90.44

< 0.001

25.11

9.58–65.79

< 0.001

Secondary outcomes

 AKD at 7 days

  Single-marker positivity

4.73

1.04–21.60

0.045

2.28

0.26–20.02

0.15

3.24

0.65–16.20

0.151

  Double-marker positivity

15.92

3.67–68.97

0.001

4.57

0.48–36.25

0.15

15.36

3.21–73.57

0.001

Mortality within 7 days

 Single-marker positivity

1.16

0.51–2.65

0.724

0.86

0.77–2.75

0.494

1.59

0.63–4.05

0.329

 Double-marker positivity

2.75

1.34–5.65

0.006

4.1

1.41–11.78

0.001

2.01

0.75–5.40

0.166

  1. A single-marker positivity was defined by the presence of [TIMP-2] × [IGFBP7] above the cut-off of 0.3 or PCT above the cut-off of 0.5; the double-marker positivity was defined by the presence of [TIMP-2] × [IGFBP7] measurements above 0.3 and the concomitant presence of PCT levels above 0.5
  2. [TIMP-2] × [IGFBP7] tissue inhibitor metalloproteinase-2 and insulin-growth factor binding protein 7 product, PCT procalcitonin
  3. a Odds ratios (OR) were adjusted for Sequential Organ Failure Assessment (SOFA) and estimated glomerular filtration rate (eGFR) at the time of admission