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Remdesivir treatment for patients with moderate to severe COVID-19
BACKGROUND/AIM: Remdesivir, which was first developed for the treatment of Ebola disease but failed to meet expectations, has become hope in the fight against the COVID-19 pandemic. This study aimed to evaluate risk factors for mortality and prognosis of adult moderate/severe COVID-19 patients treat...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific and Technological Research Council of Turkey (TUBITAK)
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387889/ https://www.ncbi.nlm.nih.gov/pubmed/36326369 http://dx.doi.org/10.55730/1300-0144.5387 |
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author | HASANOĞLU, İmran GÜNER, Rahmet ÇELİK, İlhami KANAT, Fikret BATIREL, Ayşe TELLİ DİZMAN, Gülçin EREN, Esma YILDIZ SEVGİ, Dilek BOZKURT, İlkay KART YAŞAR, Kadriye ŞENOĞLU, Sevtap KAZAK, Esra KARAALİ, Rıdvan ÇELİKBAŞ, Aysel PULLUKÇU, Hüsnü ÇAĞATAY, Arif Atahan ÜNAL, Serhat ERDİNÇ, Şebnem TABAK, Fehmi GÜL, Ahmet ALP, Emine |
author_facet | HASANOĞLU, İmran GÜNER, Rahmet ÇELİK, İlhami KANAT, Fikret BATIREL, Ayşe TELLİ DİZMAN, Gülçin EREN, Esma YILDIZ SEVGİ, Dilek BOZKURT, İlkay KART YAŞAR, Kadriye ŞENOĞLU, Sevtap KAZAK, Esra KARAALİ, Rıdvan ÇELİKBAŞ, Aysel PULLUKÇU, Hüsnü ÇAĞATAY, Arif Atahan ÜNAL, Serhat ERDİNÇ, Şebnem TABAK, Fehmi GÜL, Ahmet ALP, Emine |
author_sort | HASANOĞLU, İmran |
collection | PubMed |
description | BACKGROUND/AIM: Remdesivir, which was first developed for the treatment of Ebola disease but failed to meet expectations, has become hope in the fight against the COVID-19 pandemic. This study aimed to evaluate risk factors for mortality and prognosis of adult moderate/severe COVID-19 patients treated with remdesivir, and safety and tolerability of 5 days of remdesivir treatment. MATERIALS AND METHODS: This multicenter prospective observational study was conducted in 14 centers in Turkey. Pregnancy or breastfeeding, multiorgan failure, or usage of vasopressors for septic shock, ALT > 5 × the upper limit of the normal range, or eGRF <30 mL/min or dialysis and receiving favipiravir were the exclusion criteria of the study. RESULTS: Among 500 patients, 494 patients were included in the study. On admission, 392 (79.3%) patients had moderate and 102 (20.6%) patients had severe COVID-19. The 28-day mortality was 10.1%. The median of the scores of the seven-category ordinal scale assessed on days 0, 3, 5, 7 were 4 and 3 on day 14. When the survival status of the patients was evaluated according to the time between the remdesivir start date and the end date of the symptoms, no statistically significant difference was found between the medians of the groups (p = 0.404). In multivariable analysis, age (OR, 1.05; 95%CI, 1.02–1.08; p = 0.003), SpO(2) level on admission (OR, 3.03; 95%CI, 1.35–6.81; p = 0.007), heart rate (OR, 2.48; 95%CI, 1.01–6.07; p = 0.047), follow-up site at the hospital (clinic/ICU) (OR, 26.4; 95%CI, 11.6–60.17; p < 0.001) were independently associated with increased mortality. Grade 3 adverse event (AE) was observed in 4 (0.8%) patients. None of the patients experienced grade 4 or 5 AEs. CONCLUSION: Remdesivir is a safe and well-tolerated drug and older age, low SpO(2) level on admission, tachycardia, and ICU admission are independently associated with increased mortality among patients with moderate/severe COVID-19 receiving remdesivir treatment. |
format | Online Article Text |
id | pubmed-10387889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Scientific and Technological Research Council of Turkey (TUBITAK) |
record_format | MEDLINE/PubMed |
spelling | pubmed-103878892023-08-01 Remdesivir treatment for patients with moderate to severe COVID-19 HASANOĞLU, İmran GÜNER, Rahmet ÇELİK, İlhami KANAT, Fikret BATIREL, Ayşe TELLİ DİZMAN, Gülçin EREN, Esma YILDIZ SEVGİ, Dilek BOZKURT, İlkay KART YAŞAR, Kadriye ŞENOĞLU, Sevtap KAZAK, Esra KARAALİ, Rıdvan ÇELİKBAŞ, Aysel PULLUKÇU, Hüsnü ÇAĞATAY, Arif Atahan ÜNAL, Serhat ERDİNÇ, Şebnem TABAK, Fehmi GÜL, Ahmet ALP, Emine Turk J Med Sci Research Article BACKGROUND/AIM: Remdesivir, which was first developed for the treatment of Ebola disease but failed to meet expectations, has become hope in the fight against the COVID-19 pandemic. This study aimed to evaluate risk factors for mortality and prognosis of adult moderate/severe COVID-19 patients treated with remdesivir, and safety and tolerability of 5 days of remdesivir treatment. MATERIALS AND METHODS: This multicenter prospective observational study was conducted in 14 centers in Turkey. Pregnancy or breastfeeding, multiorgan failure, or usage of vasopressors for septic shock, ALT > 5 × the upper limit of the normal range, or eGRF <30 mL/min or dialysis and receiving favipiravir were the exclusion criteria of the study. RESULTS: Among 500 patients, 494 patients were included in the study. On admission, 392 (79.3%) patients had moderate and 102 (20.6%) patients had severe COVID-19. The 28-day mortality was 10.1%. The median of the scores of the seven-category ordinal scale assessed on days 0, 3, 5, 7 were 4 and 3 on day 14. When the survival status of the patients was evaluated according to the time between the remdesivir start date and the end date of the symptoms, no statistically significant difference was found between the medians of the groups (p = 0.404). In multivariable analysis, age (OR, 1.05; 95%CI, 1.02–1.08; p = 0.003), SpO(2) level on admission (OR, 3.03; 95%CI, 1.35–6.81; p = 0.007), heart rate (OR, 2.48; 95%CI, 1.01–6.07; p = 0.047), follow-up site at the hospital (clinic/ICU) (OR, 26.4; 95%CI, 11.6–60.17; p < 0.001) were independently associated with increased mortality. Grade 3 adverse event (AE) was observed in 4 (0.8%) patients. None of the patients experienced grade 4 or 5 AEs. CONCLUSION: Remdesivir is a safe and well-tolerated drug and older age, low SpO(2) level on admission, tachycardia, and ICU admission are independently associated with increased mortality among patients with moderate/severe COVID-19 receiving remdesivir treatment. Scientific and Technological Research Council of Turkey (TUBITAK) 2022-04-16 /pmc/articles/PMC10387889/ /pubmed/36326369 http://dx.doi.org/10.55730/1300-0144.5387 Text en © TÜBİTAK https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. |
spellingShingle | Research Article HASANOĞLU, İmran GÜNER, Rahmet ÇELİK, İlhami KANAT, Fikret BATIREL, Ayşe TELLİ DİZMAN, Gülçin EREN, Esma YILDIZ SEVGİ, Dilek BOZKURT, İlkay KART YAŞAR, Kadriye ŞENOĞLU, Sevtap KAZAK, Esra KARAALİ, Rıdvan ÇELİKBAŞ, Aysel PULLUKÇU, Hüsnü ÇAĞATAY, Arif Atahan ÜNAL, Serhat ERDİNÇ, Şebnem TABAK, Fehmi GÜL, Ahmet ALP, Emine Remdesivir treatment for patients with moderate to severe COVID-19 |
title | Remdesivir treatment for patients with moderate to severe COVID-19 |
title_full | Remdesivir treatment for patients with moderate to severe COVID-19 |
title_fullStr | Remdesivir treatment for patients with moderate to severe COVID-19 |
title_full_unstemmed | Remdesivir treatment for patients with moderate to severe COVID-19 |
title_short | Remdesivir treatment for patients with moderate to severe COVID-19 |
title_sort | remdesivir treatment for patients with moderate to severe covid-19 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387889/ https://www.ncbi.nlm.nih.gov/pubmed/36326369 http://dx.doi.org/10.55730/1300-0144.5387 |
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