Pregled bibliografske jedinice broj: 1252023
Real-life experience with remdesivir for treatment of hospitalized coronavirus disease 2019 patients: matched case-control study from a large tertiary hospital registry
Real-life experience with remdesivir for treatment of hospitalized coronavirus disease 2019 patients: matched case-control study from a large tertiary hospital registry // Croatian medical journal, 63 (2022), 6; 536-543 doi:10.3325/cmj.2022.63.536 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1252023 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Real-life experience with remdesivir for treatment
of hospitalized coronavirus disease 2019 patients:
matched case-control study from a large tertiary
hospital registry
Autori
Lucijanić, Marko ; Bušić, Nikolina ; Bistrović, Petra ; Papić, Ivan ; Zelenika Margeta, Marina ; Babić, Paško ; Barčan, Mihaela ; Pasarić, Antica ; Mustapić, Mirna ; Piskač Živković, Nevenka ; Ortner Hadžiabdić, Maja ; Lucijanić, Tomo ; Lukšić, Ivica ; Baršić, Bruno
Izvornik
Croatian medical journal (0353-9504) 63
(2022), 6;
536-543
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
SARS-CoV-2 ; real-world effectiveness ; remdesivir ; antiviral drug
Sažetak
Aim To evaluate the association of remdesivir use and the survival of hospitalized patients with coronavirus disease 2019 (COVID-19). Methods We retrospectively reviewed the medical records of 5959 COVID-19 patients admitted to our tertiarylevel hospital from March 2020 to June 2021. A total of 876 remdesivir-treated patients were matched with 876 control patients in terms of age, sex, Charlson comorbidity index (CCI), WHO- defined COVID-19 severity on admission, and oxygen requirement at the time of remdesivir use. Results Among 1752 COVID-19 patients (median age 66 years, 61.8% men), 1405 (80.2%) had severe and 311 (17.8%) had critically severe COVID-19 on admission. Remdesivir was given at a median of one day after hospital admission and at a median of eight days from the onset of symptoms. Overall, 645 (73.6%) patients received remdesivir before high-flow oxygen therapy (HFOT) or mechanical ventilation (MV), 198 (22.6%) after HFOT institution, and 83 (9.5%) after MV institution. Remdesivir use was associated with improved survival in the entire cohort (hazard ratio 0.79, P = 0.006). Survival benefit was evident among patients receiving remdesivir during low-flow oxygen requirement (hazard ratio 0.61, P < 0.001) but not among patients who received it after starting HFOT (P = 0.499) or MV (P = 0.380). Conclusion Remdesivir, if given during low-flow oxygen therapy, might be associated with survival benefit in hospitalized COVID-19 patients.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Medicinski fakultet, Zagreb,
Klinička bolnica "Dubrava"
Profili:
Maja Ortner Hadžiabdić
(autor)
Bruno Baršić
(autor)
Petra Bistrović
(autor)
Ivica Lukšić
(autor)
Nevenka Piskać Živković
(autor)
Tomo Lucijanić
(autor)
Marko Lucijanic
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE