a. Univariate analysis of primary and secondary endpoint | ||||||
Serious secondary headache | Composite endpoint mortality or hospitalization | |||||
Predictors | OR | 95%CI | p | OR | 95%CI | p |
Copeptin (lna) | 2.03 | 1.52–2.70 | <0.0001 | 1.45 | 1.12.1.88 | 0.005 |
Age > 50 | 2.83 | 1.69–4.74 | <0.0001 | 2.77 | 1.72–4.46 | <0.0001 |
Male gender | 2.12 | 1.27–3.52 | 0.004 | 1.41 | 0.88–2.27 | 0.150 |
Focal-neurological symptoms | 3.50 | 1.99–6.14 | <0.0001 | 4.23 | 2.47–7.24 | <0.0001 |
Thunderclap onset | 4.23 | 2.38–7.52 | <0.0001 | 3.04 | 1.75–5.29 | <0.0001 |
Scenario 4* | 0.46 | 0.24–0.87 | 0.018 | 0.56 | 0.32–0.97 | 0.040 |
D-Dimer (lna) | 1.50 | 1.00–2.27 | 0.052 | 1.28 | 0.87–1.89 | 0.205 |
Fibrinogen (lna) | 2.95 | 1.10–7.89 | 0.031 | 2.29 | 0.91–5.80 | 0.080 |
C-reactive protein (lna) | 1.06 | 0.87–1.30 | 0.544 | 1.31 | 1.07–1.60 | 0.010 |
Leukocyte count (lna) | 2.04 | 1.01–4.13 | 0.046 | 0.63 | 0.34–1.16 | 0.136 |
b. Multivariate model 1: Copeptin and clinical variables | ||||||
Serious secondary headache | Composite endpoint mortality or hospitalization | |||||
Predictors | OR | 95%CI | Predictors | OR | 95%CI | p |
Copeptin (lna) | 1.73 | 1.26–2.40 | 0.001 | 1.23 | 0.91–1.65 | 0.173 |
Age > 50 | 2.25 | 1.28–3.96 | 0.005 | 2.34 | 1.41–3.89 | 0.001 |
Male gender | 1.84 | 1.04–3.26 | 0.035 | |||
Focal-neurological symptoms | 2.63 | 1.40–4.92 | 0.003 | 3.41 | 1.94–6.02 | <0.0001 |
Thunderclap onset | 2.90 | 1.49–5.65 | 0.002 | 2.21 | 1.18–4.15 | 0.013 |
Scenario 4b | 0.73 | 0.35–1.50 | 0.388 | 0.81 | 0.43–1.51 | 0.503 |
c. Multivariate model 2: Copeptin and laboratory variablesa | ||||||
Serious secondary headache** | Composite endpoint mortality or hospitalization*** | |||||
Predictors | OR | 95%CI | p | OR | 95%CI | p |
Copeptin (ln) | 1.80 | 1.33–2.44 | <0.0001 | 1.39 | 1.0–1.94 | 0.050 |
Fibrinogen (ln) | 1.22 | 0.93–1.61 | 0.158 | |||
Leukocyte count (ln) | 1.78 | 0.82–3.83 | 0.143 | |||
C-reactive protein (ln) | 1.27 | 1.04–1.56 | 0.021 |