Influence of continuous renal replacement therapy on the plasma concentration of tigecycline in patients with septic shock: A prospective observational study
The influence of continuous renal replacement therapy (CRRT) on the steady-state plasma concentration of high-dose tigecycline was investigated in septic shock patients to provide references for drug dosing. In this prospective observational study, 17 septic shock patients presenting with severe inf...
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Veröffentlicht in: | Frontiers in pharmacology 2023-03, Vol.14, p.1118788-1118788 |
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Sprache: | eng |
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Zusammenfassung: | The influence of continuous renal replacement therapy (CRRT) on the steady-state plasma concentration of high-dose tigecycline was investigated in septic shock patients to provide references for drug dosing.
In this prospective observational study, 17 septic shock patients presenting with severe infections needing a broad-spectrum antibiotic therapy with high-dose tigecycline (100 mg per 12 h) in the intensive care unit were included and divided into CRRT group (
= 6) or non-CRRT group (
= 11). The blood samples were collected and plasma drug concentration was determined by SHIMADZU LC-20A and SHIMADZU LCMS 8040. The steady-state plasma concentration was compared between groups using unpaired
-test. Furthermore, between-groups comparisons adjusted for baseline value was also done using multivariate linear regression model.
Peak concentration (C
) of tigecycline was increased in CRRT group compared to non-CRRT group, but there were no statistical differences (505.11 ± 143.84 vs
406.29 ± 108.00 ng/mL,
-value: 0.129). Trough concentration (C
) of tigecycline was significantly higher in CRRT group than in non-CRRT group, with statistical differences (287.92 ± 41.91 vs
174.79 ± 33.15 ng/mL,
-value: 0.000, adjusted
-value: 0.000). In safety, C
was reported to be a useful predictor of hepatotoxicity with a cut-off of 474.8 ng/mL. In our studies, C
of all patients in CRRT group was lower than 474.8 ng/mL.
The plasma concentration of tigecycline was increased in septic shock patients with CRRT treatment and only C
shown statistical differences. No dose adjustment seems needed in the view of hepatotoxicity.
https://www.chictr.org.cn/, identifier ChiCTR2000037475. |
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ISSN: | 1663-9812 1663-9812 |
DOI: | 10.3389/fphar.2023.1118788 |