Severity of COVID-19 Omicron Variants: A Global Systematic Review.

IF 5.6 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2026-07-01 Epub Date: 2026-05-17 DOI:10.1007/s40121-026-01352-1
Deepa Malhotra, Rajeev M Nepal, Irini Zografaki, Moe H Kyaw, Pinelopi Nikolopoulou, Rodrigo Sini de Almeida, Santiago M C Lopez, Stephen Wiblin, Fraser Williams, Sophie Pope, Isabelle Whittle, Fiona Pearson, Daniel Curcio
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引用次数: 0

Abstract

Introduction: The continual emergence of new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants drives the need to update evidence on coronavirus disease 2019 (COVID-19) severity and disease burden, and better understand the impact on prevention, treatment, and healthcare systems.

Methods: This systematic review aimed to determine relative disease severity, through comparative measures of hospitalization, intensive care unit admission and mortality, between SARS-CoV-2 variants of concern emerging since Omicron was first identified. A protocol was registered a priori (PROSPERO ID: CRD42024619193). Systematic searches of MEDLINE and EMBASE databases were conducted in November 2024 and supplemented by conference searches from 2022-2024. Population, Exposure, Comparisons, Outcomes (PECO) criteria were used to screen publications for inclusion. Critical appraisal tools published in the Joanna Briggs Institute (JBI) Handbook for Evidence Synthesis were used to assess the risk of bias of the primary studies included. The outcomes associated with Omicron variants, identified by sequencing or predominance periods, included hospitalization, admission to intensive care, death, and various composite endpoints.

Results: Thirty-two studies fulfilled the eligibility criteria, most reported on relative disease severity for early Omicron BA.5 (n = 23) and XBB (n = 24) variants. Overall, COVID-19 severity appeared largely comparable across the various Omicron subvariants. Among the subset of studies that directly compared various severity outcomes to earlier SARS-CoV-2 variants (n = 7), some reported modest increases or decreases in severity. However, these differences were generally not statistically significant. Five studies stratifying outcomes by the presence of comorbid conditions noted that comorbidities were predictors of significantly worse COVID-19 disease outcomes (p = 0.000-0.027).

Conclusions: Overall, this systematic review found the severity of COVID-19 disease to be comparable among Omicron subvariants. As SARS-CoV-2 subvariants continue to emerge, these results highlight the continuing need for vaccination against SARS-CoV-2 infection alongside early antiviral intervention to support short-term management and long-term reduction of COVID-19-associated morbidity and mortality.

COVID-19组粒变异的严重程度:一项全球系统综述
导论:随着严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)新变体的不断出现,需要更新关于2019年冠状病毒病(COVID-19)严重程度和疾病负担的证据,并更好地了解其对预防、治疗和卫生保健系统的影响。方法:本系统综述旨在通过住院率、重症监护病房住院率和死亡率的比较措施,确定自首次发现欧米克隆以来出现的令人关注的SARS-CoV-2变体之间的相对疾病严重程度。日志含义协议先验注册(PROSPERO ID: CRD42024619193)。2024年11月对MEDLINE和EMBASE数据库进行系统检索,并辅以2022-2024年的会议检索。人群、暴露、比较、结果(PECO)标准用于筛选出版物纳入。使用乔安娜布里格斯研究所(JBI)证据综合手册中发表的关键评估工具来评估纳入的主要研究的偏倚风险。通过测序或优势期确定的与Omicron变异相关的结局包括住院、入住重症监护、死亡和各种复合终点。结果:32项研究符合资格标准,大多数报告了早期Omicron BA.5 (n = 23)和XBB (n = 24)变异的相对疾病严重程度。总体而言,COVID-19的严重程度在各种欧米克隆亚变体之间似乎具有很大的可比性。在直接将各种严重程度结果与早期SARS-CoV-2变体(n = 7)进行比较的研究子集中,一些研究报告了严重程度的适度增加或减少。然而,这些差异通常没有统计学意义。根据合并症的存在对结果进行分层的五项研究指出,合并症是COVID-19疾病结局显著恶化的预测因素(p = 0.000-0.027)。结论:总体而言,本系统综述发现,不同基因组亚变体的COVID-19疾病严重程度具有可比性。随着SARS-CoV-2亚变体的不断出现,这些结果强调了继续需要针对SARS-CoV-2感染接种疫苗,同时进行早期抗病毒干预,以支持短期管理和长期降低covid -19相关发病率和死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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