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All Studies   Meta Analysis    Recent:   

Clinical outcomes and considerations in outpatient with COVID‐19 receiving remdesivir therapy

Siami et al., Health Science Reports, doi:10.1002/hsr2.2252
Jul 2024  
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Hospitalization -70% Improvement Relative Risk Remdesivir for COVID-19  Siami et al.  EARLY TREATMENT Is early treatment with remdesivir beneficial for COVID-19? Retrospective 514 patients in Iran (May - September 2021) Higher hospitalization with remdesivir (not stat. sig., p=0.2) c19early.org Siami et al., Health Science Reports, Jul 2024 Favorsremdesivir Favorscontrol 0 0.5 1 1.5 2+
Retrospective 514 COVID-19 outpatients showing no significant benefit with remdesivir therapy.
Gérard, Zhou, Wu, Kamo, Choi show significantly increased risk of acute kidney injury with remdesivir.
risk of hospitalization, 70.0% higher, OR 1.70, p = 0.20, treatment 341, control 148, adjusted per study, multivariable, RR approximated with OR.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Siami et al., 22 Jul 2024, retrospective, Iran, peer-reviewed, 5 authors, study period May 2021 - September 2021. Contact: siami_z@yahoo.com.
This PaperRemdesivirAll
Clinical outcomes and considerations in outpatient with COVID‐19 receiving remdesivir therapy
Zeinab Siami, Aziz Rasooli, Jayran Zebardast, Illahay Jalali, Saeidreza Jamalimoghadamsiahkali
Health Science Reports, doi:10.1002/hsr2.2252
Introduction: This retrospective cross-sectional study aimed to assess the outcomes of Covid-19 patients who received remdesivir therapy at the outpatient department of Ziaian Hospital. Method: A total of 514 eligible patients were included between May and September 2021. Covid-19 diagnosis was confirmed through positive SARS-COV-2 PCR tests or chest CT scans. Due to limited hospital beds, patients received remdesivir on an outpatient basis. Results: Patients received six daily doses of remdesivir for 5 days. Those referred to a physician within 7 days of symptom onset had similar hospitalization rates compared to later referrals. Lower blood saturation levels were associated with a higher likelihood of hospital admission, indicating that earlier administration of remdesivir may be more effective. Patients with over 50% lung involvement had higher rates of disease progression despite treatment. Corticosteroids did not significantly improve outcomes in patients with saturation above 90%. Discontinuation of remdesivir due to side effects was rare, with only 1% experiencing increased liver enzymes, 1.2% facial redness and tremors, and 1.5% allergies. After 1 week of treatment, patients commonly reported symptoms such as hair loss, fatigue, body pain, lethargy, and anorexia, particularly among hospitalized patients. Discussion: Patients generally preferred outpatient treatment over hospitalization. Body mass index (BMI) did not significantly impact hospitalization rates, although average weight tended to be higher among inpatients. The study confirmed the effectiveness of remdesivir therapy with a low occurrence of side effects.
After adjusting for these variables, the odds ratio for adverse outcomes was 1.58, indicating a slightly increased risk, although this result was not statistically significant (p = 0.2). Similarly, after adjustment, the odds ratio for was 1.7, suggesting a higher likelihood of hospitalization, but this result did not reach statistical significance (p = 0.2). While we did not achieve statistical significance after adjusting for age and sex, it is important to note that the study sample size was relatively small, which may have limited the statistical power to detect significant effects. Future studies with larger sample sizes are warranted to further investigate the relationship between remdesivir and adverse outcomes or hospitalization. The safety profile of remdesivir was also evaluated in our study, and overall, the drug was well-tolerated, with no major adverse events reported during the study period. This finding aligns with previous evidence indicating the favorable safety profile of remdesivir. However, it is important to continue monitoring the safety of remdesivir as more data becomes available from larger clinical trials and real-world use. While our study provides valuable insights into the effectiveness and safety of remdesivir, there are several limitations to consider. Firstly, the study had a retrospective design, which may introduce selection bias and limit causal inference. Additionally, the sample size was relatively small, which may have affected the ability..
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