Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, University of Barcelona, Barcelona, Spain.
Department of Microbiology, Hospital Clinic of Barcelona, University of Barcelona, Barcelona, Spain.
Clin Infect Dis. 2023 Jan 6;76(1):32-38. doi: 10.1093/cid/ciac760.
There is no reliable microbiological marker to guide the indication and the response to antiviral treatment in patients with coronavirus disease 2019 (COVID-19). We aimed to evaluate the dynamics of subgenomic RNA (sgRNA) in patients with COVID-19 before and after receiving treatment with remdesivir.
We included consecutive patients admitted for COVID-19 who received remdesivir according to our institutional protocol and accepted to participate in the study. A nasopharyngeal swab for quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) was collected at baseline and after 3 and 5 days of treatment with remdesivir. Genomic and sgRNA were analyzed in those samples and main comorbidities and evolution were collected for the analyses. The main outcomes were early discharge (≤10 days) and 30-day mortality.
A total of 117 patients were included in the study, of whom 24 had a negative sgRNA at baseline, with 62.5% (15/24) receiving early discharge (≤10 days) and no deaths in this group. From the 93 remaining patients, 62 had a negative sgRNA at day 5 with 37/62 (59.6%) with early discharge and a mortality rate of 4.8% (3/62). In the subgroup of 31 patients with positive sgRNA after 5 days of remdesivir, the early discharge rate was 29% (9/31) and the mortality rate was 16.1% (5/31). In multivariable analyses, the variables associated with early discharge were negative sgRNA at day 3 and not needing treatment with corticosteroids or intensive care unit admission.
Qualitative sgRNA could help in monitoring the virological response in patients who receive remdesivir. Further studies are needed to confirm these findings.
目前尚无可靠的微生物标志物来指导 2019 年冠状病毒病(COVID-19)患者的抗病毒治疗适应证和判断治疗应答。我们旨在评估接受瑞德西韦治疗前后 COVID-19 患者的亚基因组 RNA(sgRNA)动态变化。
我们连续纳入了根据我院方案接受瑞德西韦治疗并同意参与研究的 COVID-19 住院患者。在基线时以及接受瑞德西韦治疗 3 天和 5 天后采集鼻咽拭子进行定量逆转录聚合酶链反应(qRT-PCR)。对这些样本进行基因组和 sgRNA 分析,并收集主要合并症和转归数据进行分析。主要结局是早期出院(≤10 天)和 30 天死亡率。
共纳入 117 例患者,其中基线时 sgRNA 阴性的有 24 例,其中 62.5%(15/24)患者早期出院(≤10 天),且该组无死亡病例。在其余 93 例患者中,62 例患者在第 5 天 sgRNA 阴性,其中 37/62(59.6%)患者早期出院,死亡率为 4.8%(3/62)。在 5 天后瑞德西韦治疗 sgRNA 阳性的 31 例患者亚组中,早期出院率为 29%(9/31),死亡率为 16.1%(5/31)。多变量分析显示,第 3 天 sgRNA 阴性和无需皮质类固醇治疗或入住重症监护病房与早期出院相关。
定性 sgRNA 可帮助监测接受瑞德西韦治疗的患者的病毒学应答。需要进一步的研究来证实这些发现。