SARS-CoV-2 viral load is linked to remdesivir efficacy in severe Covid-19 admitted to intensive care
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
AZV NU22-B-147
Agentura Pro Zdravotnický Výzkum České Republiky
PubMed
39242658
PubMed Central
PMC11379941
DOI
10.1038/s41598-024-71588-9
PII: 10.1038/s41598-024-71588-9
Knihovny.cz E-zdroje
- Klíčová slova
- Antigen testing, Intensive care, Real-time PCR, Remdesivir, SARS-CoV-2, Viral load,
- MeSH
- adenosinmonofosfát * analogy a deriváty terapeutické užití MeSH
- alanin * analogy a deriváty terapeutické užití MeSH
- antivirové látky * terapeutické užití MeSH
- COVID-19 * virologie mortalita MeSH
- farmakoterapie COVID-19 * MeSH
- jednotky intenzivní péče MeSH
- lidé středního věku MeSH
- lidé MeSH
- péče o pacienty v kritickém stavu MeSH
- retrospektivní studie MeSH
- SARS-CoV-2 * účinky léků izolace a purifikace fyziologie MeSH
- senioři MeSH
- stupeň závažnosti nemoci MeSH
- virová nálož * účinky léků MeSH
- výsledek terapie 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
- remdesivir MeSH Prohlížeč
Remdesivir therapy has been declared as efficient in the early stages of Covid-19. Of the 339 patients (males 55.8%, age 71(59;77) years) with a detectable viral load, 140 were treated with remdesivir (of those 103 in the ICU and 57 immunosuppressed) and retrospectively compared with 199 patients (of those 82 in the ICU and 28 immunosuppressed) who were denied therapy due to advanced Covid-19. The viral load was estimated by detecting nucleocapsid antigen in serum (n = 155, median 217(28;1524)pg/ml), antigen in sputum (n = 18, COI 18(4.6;32)), nasopharyngeal antigen (n = 44, COI 17(8;35)) and the real-time PCR (n = 122, Ct 21(18;27)). After adjustment for confounders, patients on remdesivir had better 12-month survival (HR 0.66 (0.44;0.98), p = 0.039), particularly when admitted to the ICU (HR 0.49 (0.29;0.81), p = 0.006). For the immunocompromised patients, the difference did not reach statistical significance (HR 0.55 (0.18;1.69), p = 0.3). The other most significant confounders were age, ICU admission, mechanical ventilation, leukocyte/lymphocyte ratio, admission creatinine and immunosuppression. The impact of monoclonal antibodies or previous vaccinations was not significant. Despite frequent immune suppression including haemato-oncology diseases, lymphopenia, and higher inflammatory markers in the remdesivir group, the results support remdesivir administration with respect to widely available estimates of viral load in patients with high illness severity.
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