Rindi Lorenzo Vittorio, Zaçe Drieda, Sarmati Loredana, Parrella Roberto, Russo Gianluca, Andreoni Massimo, Mastroianni Claudio Maria
Department of Systems Medicine, Infectious Diseases Clinic, University Hospital "Tor Vergata", 00133 Rome, Italy.
Respiratory Infectious Diseases Unit, Cotugno Hospital, AORN dei Colli, 80131 Naples, Italy.
Viruses. 2025 Aug 16;17(8):1128. doi: 10.3390/v17081128.
The emergence of SARS-CoV-2 Omicron subvariants characterized by increased transmissibility and immune escape has raised concerns about the efficacy of current treatments. This systematic review and meta-analysis evaluated pharmacological and non-pharmacological interventions in Omicron-infected non-hospitalized patients, focusing on key clinical outcomes such as hospitalization, respiratory failure, ICU admission, and 30-day mortality.
Searches were performed in MEDLINE, EMBASE, Web of Science, Cochrane, and ClinicalTrials.gov (last update: 13 July 2025). Eligible studies reported outcomes on antiviral agents, monoclonal antibodies, adjunctive therapies, or telemedicine. Random-effects meta-analyses were conducted when appropriate, with heterogeneity assessed by I. Publication bias was evaluated via funnel plots and Egger's test. Subgroup analyses explored sources of heterogeneity.
Eighty-eight studies were included. Meta-analyses, comparing treatment vs. no treatment, revealed that nirmatrelvir/ritonavir reduced hospitalization by 52% (RR 0.48, 95% CI 0.36-0.63) and all-cause mortality by 84% (RR 0.16, 95% CI 0.11-0.24). Remdesivir reduced hospitalization by 70% (RR 0.30, 95% CI 0.19-0.47) and respiratory failure by 89% (RR 0.11, 95% CI 0.03-0.44). Sotrovimab decreased hospitalization (RR 0.71, 95% CI 0.54-0.93) and mortality (RR 0.34, 95% CI 0.19-0.61). Molnupiravir modestly reduced hospitalization (RR 0.80, 95% CI 0.70-0.91) and respiratory failure (RR 0.45, 95% CI 0.27-0.77).
Nirmatrelvir/ritonavir and remdesivir remain important for reducing severe outcomes, while sotrovimab retains partial efficacy. Rapid access to antivirals remains an important factor in mitigating SARS-CoV-2's burden.
以传播性增强和免疫逃逸为特征的新型冠状病毒奥密克戎亚变体的出现,引发了人们对当前治疗效果的担忧。本系统评价和荟萃分析评估了针对奥密克戎感染的非住院患者的药物和非药物干预措施,重点关注住院、呼吸衰竭、入住重症监护病房(ICU)和30天死亡率等关键临床结局。
在MEDLINE、EMBASE、科学网、考克兰图书馆和美国国立医学图书馆临床试验注册库(最后更新时间:2025年7月13日)中进行检索。符合条件的研究报告了抗病毒药物、单克隆抗体、辅助治疗或远程医疗的结局。在适当情况下进行随机效应荟萃分析,采用I²评估异质性。通过漏斗图和埃格检验评估发表偏倚。亚组分析探讨了异质性来源。
纳入88项研究。比较治疗组与未治疗组的荟萃分析显示,奈玛特韦/利托那韦使住院率降低52%(风险比[RR]0.48,95%置信区间[CI]0.36 - 0.63),全因死亡率降低84%(RR 0.16,95% CI 0.11 - 0.24)。瑞德西韦使住院率降低70%(RR 0.30,95% CI 0.19 - 0.47),呼吸衰竭发生率降低89%(RR 0.11,95% CI 0.03 - 0.44)。索托维单抗降低了住院率(RR 0.71,95% CI 0.54 - 0.93)和死亡率(RR 0.34,95% CI 0.19 - 0.61)。莫努匹拉韦适度降低了住院率(RR 0.80,95% CI 0.70 - 0.91)和呼吸衰竭发生率(RR 0.45,95% CI 0.27 - 0.77)。
奈玛特韦/利托那韦和瑞德西韦对于降低严重结局仍然很重要,而索托维单抗仍保留部分疗效。快速获得抗病毒药物仍然是减轻新型冠状病毒负担的一个重要因素。