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2023年澳大利亚高疫苗接种人群中的长期新冠症状群、相关因素及预测指标

Long Covid Symptom Clusters, Correlates and Predictors in a Highly Vaccinated Australian Population in 2023.

作者信息

Tawfiq Essa, Chen Rosalie, Honeyman Damian Alexander, Dawson Rebecca, Kunasekaran Mohana, Notaras Adriana, Gurdasani Deepti, Skouteris Helen, Ayton Darshini, MacIntyre Chandini Raina

机构信息

Biosecurity Program, The Kirby Institute, Faculty of Medicine and Health, The University of New South Wales, Sydney, Australia.

University of Western Australia Medical School, University of Western Australia, Perth, Australia.

出版信息

Health Expect. 2025 Jun;28(3):e70273. doi: 10.1111/hex.70273.

Abstract

BACKGROUND

Limited data exists regarding long Covid burden following Omicron infection in highly vaccinated populations.

OBJECTIVE

To (1) characterise long Covid prevalence and predictors and (2) identify key symptom clusters and their correlates among long Covid patients, during an Omicron-predominant period in a highly vaccinated population.

DESIGN

Anonymous, online, cross-sectional survey.

SETTING

January 2023, Australia.

PARTICIPANTS

Residents aged ≥ 18 years with self-reported history of test-positive Covid-19. The main variables studied were socio-demographic characteristics, Covid-19 risk factors, vaccination, infection history and experiences with long Covid.

MAIN OUTCOME MEASURES

Long Covid symptoms. Symptom-based clustering was used to identify long Covid symptom clusters and their functional correlates. Predictors of long Covid occurrence and severity were assessed using multivariable logistic regression.

RESULTS

Overall, 240/1205 participants (19.9%) reported long Covid. Long Covid risk was significantly higher for women OR 1.71 (95% CI: 1.17-2.51), people with comorbidities 2.19 (95% CI: 1.56-3.08) and those using steroid inhalers for Covid-19 treatment (2.34 [95% CI: 1.29-4.24]). Long-Covid risk increased with increasing Covid-19 infection severity (moderately severe symptoms: 2.23 [95% CI: 1.50-3.30], extremely severe symptoms: 5.80 [95% CI: 3.48-9.66], presented to ED/hospitalised: 7.22 [95% CI: 3.06-17.03]). We found no significant difference in the likelihood of long Covid between the Omicron and pre-Omicron periods, vaccination status and participant age. We identified two long Covid clusters (pauci-symptomatic, n = 170, vs. polysymptomatic, n = 66). Polysymptomatic cluster membership was associated with worse functioning (impacts on work, moderate activity, emotions and energy). Severity acute infection was strongly predictive of polysymptomatic cluster membership (5.72 [2.04-17.58]). Monoclonal antibody treatment was strongly associated with pauci-symptomatic cluster membership (0.02 [0.00-0.13]).

DISCUSSION

Our study shows that long Covid is an important health burden in Australia, including during the Omicron era, and identifies several risk factors. We found a subgroup of patients characterised by more symptoms and worse functional outcomes. Our findings can inform policies for protecting vulnerable populations and frameworks for long Covid risk assessment and management.

CONCLUSIONS

One-in-five people may suffer long Covid after acute Covid-19 infection, with similar risk across age groups. Omicron variants appear not to have a lower risk compared to earlier variants in our study. A cumulative number of symptoms can help triage long Covid patients.

PATIENT OR PUBLIC CONTRIBUTION

We did not involve patients or the public in the design of the questionnaire. However, after a soft launch, we revised some survey questions by reviewing early responses from patients and the public.

摘要

背景

关于高疫苗接种人群感染奥密克戎后长期新冠负担的数据有限。

目的

在高疫苗接种人群以奥密克戎为主的时期,(1)描述长期新冠的患病率及预测因素,(2)识别长期新冠患者的关键症状群及其关联因素。

设计

匿名在线横断面调查。

地点

2023年1月,澳大利亚。

参与者

年龄≥18岁且自我报告新冠病毒检测呈阳性病史的居民。研究的主要变量包括社会人口学特征、新冠病毒风险因素、疫苗接种情况、感染史以及长期新冠经历。

主要观察指标

长期新冠症状。基于症状的聚类用于识别长期新冠症状群及其功能关联因素。使用多变量逻辑回归评估长期新冠发生和严重程度的预测因素。

结果

总体而言,240/1205名参与者(19.9%)报告有长期新冠。女性患长期新冠的风险显著更高,比值比为1.71(95%置信区间:1.17 - 2.51),患有合并症者为2.19(95%置信区间:1.56 - 3.08),以及使用类固醇吸入器治疗新冠的患者为2.34(95%置信区间:1.29 - 4.24)。长期新冠风险随新冠病毒感染严重程度增加而升高(中度严重症状:2.23 [95%置信区间:1.50 - 3.30],极其严重症状:5.80 [95%置信区间:3.48 - 9.66],前往急诊科就诊/住院:7.22 [95%置信区间:3.06 - 17.03])。我们发现奥密克戎时期与奥密克戎之前时期、疫苗接种状况以及参与者年龄之间,长期新冠的发生可能性无显著差异。我们识别出两个长期新冠症状群(症状较少群,n = 170,与症状较多群,n = 66)。症状较多群与功能较差相关(对工作、适度活动、情绪和精力有影响)。严重急性感染强烈预测症状较多群成员身份(5.72 [2.04 - 17.58])。单克隆抗体治疗与症状较少群成员身份密切相关(0.02 [0.00 - 0.13])。

讨论

我们的研究表明,长期新冠在澳大利亚是一项重要的健康负担,包括在奥密克戎时代,并识别出了几个风险因素。我们发现了一个以症状更多和功能结局更差为特征的患者亚组。我们的研究结果可为保护弱势群体的政策以及长期新冠风险评估和管理框架提供参考。

结论

五分之一的人在急性新冠病毒感染后可能会患长期新冠,各年龄组风险相似。在我们的研究中,奥密克戎变异株似乎与早期变异株相比风险并未降低。累积的症状数量有助于对长期新冠患者进行分类。

患者或公众参与

我们在问卷设计中未纳入患者或公众。然而,在软启动后,我们通过审查患者和公众的早期回复对一些调查问题进行了修订。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aa0/12059467/d4b8387c3a1d/HEX-28-e70273-g001.jpg

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