The impact of remdesivir on renal and liver functions in severe COVID-19 patients with presence of viral load
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
AZV NU22-B-147
Czech Health Research Council
PubMed
40594535
PubMed Central
PMC12214511
DOI
10.1038/s41598-025-05541-9
PII: 10.1038/s41598-025-05541-9
Knihovny.cz E-zdroje
- Klíčová slova
- Intensive care, Liver function tests, Remdesivir, Renal function, SARS-CoV-2, Viral load,
- MeSH
- adenosinmonofosfát * analogy a deriváty terapeutické užití škodlivé účinky MeSH
- alanin * analogy a deriváty terapeutické užití škodlivé účinky MeSH
- antivirové látky * terapeutické užití škodlivé účinky MeSH
- COVID-19 * virologie patofyziologie MeSH
- farmakoterapie COVID-19 * MeSH
- jaterní testy MeSH
- játra * účinky léků patofyziologie MeSH
- kreatinin krev MeSH
- ledviny * účinky léků patofyziologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- močovina krev MeSH
- SARS-CoV-2 izolace a purifikace MeSH
- senioři MeSH
- virová nálož * účinky léků MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- adenosinmonofosfát * MeSH
- alanin * MeSH
- antivirové látky * MeSH
- kreatinin MeSH
- močovina MeSH
- remdesivir MeSH Prohlížeč
The impact of remdesivir on renal and liver functions remains a matter of concern in advanced COVID-19 patients with high illness severity and presence of viral load. The laboratory results of the 114 patients (males 55.8%, age 71 (59; 77) years) with a detectable viral load treated with remdesivir were compared with the controls. Baseline plasmatic creatinine (PCr) < 150 µmol/l in patients on remdesivir decreased equally to controls (- 6 (- 20; 9) vs. - 8 (- 24; 2) µmol/l, n = 170, p = 0.11). The similar trends were found for baseline PCr ≥ 150 µmol/l (- 57 (- 129; - 15) µmol/l for remdesivir group vs. - 65 (- 111; - 7) µmol/l, p > 0.9). Changes of PCr were independent of the remdesivir therapy, the statistically significant confounders were baseline PCr levels (p < 0.001), hospital length-of-stay (p < 0.001), leukocyte-to-lymphocyte ratio (p = 0.025). The plasmatic urea (PU) mildly increased in the remdesivir group (1 (- 2; 5) mmol/l vs. 0 (- 3; 2) mmol/l in the controls, p = 0.009), its levels were related to remdesivir (p = 0.026), age (p = 0.002), PCr (p < 0.001), hospital length-of-stay (p < 0.001), IPPV (p = 0.035). Regarding the liver function tests the significant relationships to remdesivir therapy were found only for GGT (p = 0.007) and ALT (p = 0.044). The levels of PCr were decreasing over the hospitalisation period including patients with mild-to-moderate renal insufficiency. The multivariate regression analysis excluded an impact of remdesivir on the PCr changes yet admitted an impact on the levels of urea, GGT and ALT.
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