Table 3.
Comparison of clinical outcomes in propensity-matched groups.
| Clinical outcomes | CBP group (n = 213) | non-CBP group (n = 213) | aOR (95% CI); p‡ |
|---|---|---|---|
| VPA serum concentration (mg/L), median (IQR) | 15.8 (7.5-24.9); (n = 192) | 60.8 (48.3-79.0); (n = 191) | p < 0.0001* |
| Epileptic seizures during concomitant administration, n (%) | 109 (51.2) | 69 (32.4) | 2.19 (1.48–3.24); p < 0.0001 |
| Status epilepticus during concomitant administration, n (%) | 29 (13.6) | 10 (4.7) | 3.20 (1.51–6.74); p = 0.0014 |
| In-hospital mortality rate, n (%) | 72 (33.8) | 53 (24.9) | 1.57 (1.03–2.20); p = 0.036 |
| Length of hospital stay after concomitant administration (days), median (IQR) | 41 (23–66) | 30 (26–48) | p < 0.001* |
| Expenditure of healthcare, U.S. dollars, median (IQR) | 20,970 (13,321.4-34,549.1) | 12,848 (7,314.4-22,831.6) | p < 0.0001* |
aOR, adjusted odds ratio; CBP, carbapenem antibiotics; CI, confidence interval; IQR, interquartile range; n, number;
P-value is reported for Chi-square test unless otherwise stated;
P-value is reported for Wilcoxon test; VPA, valproic acid.