Xie Junqing, López-Güell Kim, Dedman Daniel, Duarte-Salles Talita, Kolde Raivo, López-Blasco Raúl, Martínez Álvaro, Mercier Gregoire, Abellan Alicia, Arinze Johnmary T, Cuccu Zara, Delmestri Antonella, Delseny Dominique, Khalid Sara, Kim Chungsoo, Kim Ji-Woo, Kostka Kristin, Loste Cora, Mateu Lourdes, Mayer Miguel A, Meléndez-Cardiel Jaime, Mercadé-Besora Núria, Mosseveld Mees, Nishimura Akihito, Nordeng Hedvig M E, Oyinlola Jessie O, Pérez-Crespo Laura, Pineda-Moncusí Marta, Ramírez-Anguita Juan Manuel, Trinh Nhung T H, Uusküla Anneli, Valdivieso Bernardo, Burkard Theresa, Burn Edward, Català Martí, Prieto-Alhambra Daniel, Paredes Roger, Jödicke Annika M
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
CPRD, Medicines and Healthcare Products Regulatory Agency, London, UK.
EClinicalMedicine. 2024 Oct 30;77:102903. doi: 10.1016/j.eclinm.2024.102903. eCollection 2024 Nov.
The World Health Organisation (WHO) has identified a range of symptomatic manifestations to aid in the clinical diagnosis of post-COVID conditions, herein referred to as post-acute COVID-19 symptoms. We conducted an international network cohort study to estimate the burden of these symptoms in North American, European, and Asian populations.
A federated analysis was conducted including 10 databases from the United Kingdom, Netherlands, Norway, Estonia, Spain, France, South Korea, and the United States, between September 1st 2020 and latest data availability (which varied from December 31st 2021 to February 28th 2023), covering primary and secondary care, nationwide registries, and claims data, all mapped to the Observational Medical Outcomes Partnership Common Data Model (OMOP CDM). We defined two cohorts for the main analyses: a SARS-CoV-2 infection cohort [positive polymerase chain reaction (PCR) or rapid lateral flow test (LFT) result or clinical COVID-19 diagnosis] and a general population cohort. Individuals with less than 365 days of prior history or 120 days of follow-up were excluded. We estimated incidence rates (IRs) of the 25 WHO-proposed post-acute COVID-19 symptoms, considering symptoms that occurred ≥90 and ≤365 days after index date, excluding individuals with the respective symptoms 180 days prior to the index event. Stratified analyses were conducted by age and sex. Incidence rate ratios (IRRs) were calculated comparing rates in the infected cohort versus the general population. Results from the different databases were combined using random-effects meta-analyses.
3,019,408 individuals were included in the infection cohort. 1,585,160 of them were female and 1,434,248 of them male. 929,351,505 individuals were included in the general population group. 461,195,036 of them were female and 466,022,004 of them male. The 1-year IR of any post-acute COVID-19 symptom in the COVID-19 infection cohort varied significantly across databases, from 4.4 (95% CI 3.8-5.1) per 100 person-years to 103.9 (95% CI 103.2-104.7). The five most common symptoms were joint pain (from 1.6 (95% CI 1.3-1.9) to 14.3 (95% CI 14.1-14.6)), abdominal pain (from 0.3 (95% CI 0.1-0.5) to 9.9 (95% CI 9.7-10.1)), gastrointestinal issues (from 0.6 (95% CI 0.4-0.9) to 13.3 (95% CI 13.1-13.6)), cough (from 0.3 (95% CI 0.2-0.5) to 9.1 (95% CI 8.9-9.3)), and anxiety (from 0.8 (95% CI 0.6-1.2) to 11.4 (95% CI 11.2-11.6)); whereas muscle spasms (from 0.01 (95% CI 0.008-0.2) to 1.7 (95% CI 1.6-1.8)), pins and needles (from 0.05 (95% CI 0.03-0.0.9) to 1.5 (95% CI 1.4-1.6)), memory issues (from 0.03 (95% CI 0.02-0.06) to 0.8 (95% CI 0.7-0.8)), cognitive dysfunction (from 0.007 (95% CI 0.004-0.01) to 0.6 (95% CI 0.4-0.8)), and altered smell and/or taste (from 0.04 (95% CI 0.03-0.04) to 0.7 (95% CI 0.6-0.8)) were least common. Incidence rates of any post-acute COVID-19 symptoms generally increased with age, with certain symptoms peaking in middle-aged adults (anxiety, depressive disorders, headache, altered smell and taste) and others in pre-school children (gastrointestinal issues and cough). Females had higher incidence rates for most symptoms. Based on the random-effects model, the infected cohort had a higher incidence of any post-acute COVID-19 symptom than the general population, with a meta-analytic incidence rate ratio (meta-IRR) of 1.4 (1-2). A similar pattern was seen for all individual symptoms. The highest meta-IRRs were depressive disorder, 2.6 (1.7-3.9); anxiety, 2.3 (1.4-3.8); allergy, 2.1 (1.7-2.8) and sleep disorders, 2.1 (1.5-2.6). The meta-IRR for altered smell and/or taste was 1.9 (1.3-2.8).
Post-acute COVID-19 symptoms, as listed by the WHO, were commonly observed following COVID-19 infection. However, even after standardising research methods, there was significant heterogeneity in the incidence rates from different healthcare settings and geographical locations. This is the first international study of the epidemiology of post-acute COVID-19 symptoms using the WHO-listed symptoms. Its findings contibute to understand the epidemiology of this condition from a multinational approach. Limitations of this study include the lack of consensus of the post-acute COVID-19 definition, as well as the difficulty to capture the impact on daily life of the post-acute COVID-19 symptoms in the available datasets.
This work has been funded by the European Health Data Evidence Network (EHDEN) through an Evidence Generation Fund Grant and by the National Institute for Health and Care Research (NIHR) Oxford Biomedical Research Centre (BRC).
世界卫生组织(WHO)已确定了一系列症状表现,以辅助新冠后状况的临床诊断,在此称为新冠后急性症状。我们开展了一项国际网络队列研究,以评估北美、欧洲和亚洲人群中这些症状的负担。
进行了一项联合分析,纳入了来自英国、荷兰、挪威、爱沙尼亚、西班牙、法国、韩国和美国的10个数据库,时间跨度为2020年9月1日至最新数据可用时间(从2021年12月31日至2023年2月28日不等),涵盖初级和二级医疗保健、全国登记处及理赔数据,所有数据均映射到观察性医疗结局合作组织通用数据模型(OMOP CDM)。我们为主要分析定义了两个队列:一个新冠病毒感染队列[聚合酶链反应(PCR)或快速侧向流动检测(LFT)结果为阳性或临床诊断为新冠]和一个普通人群队列。排除既往病史少于365天或随访少于120天的个体。我们估计了世界卫生组织提出的25种新冠后急性症状的发病率,考虑在索引日期后≥90天且≤365天出现的症状,排除在索引事件前180天有相应症状的个体。按年龄和性别进行分层分析。计算感染队列与普通人群的发病率比值(IRR)。使用随机效应荟萃分析合并不同数据库的结果。
感染队列纳入了3,019,408人。其中女性1,585,160人,男性1,434,248人。普通人群组纳入了929,351,505人。其中女性461,195,036人,男性466,022,004人。新冠感染队列中任何新冠后急性症状的1年发病率在不同数据库间差异显著,从每100人年4.4(95%置信区间3.8 - 5.1)到103.9(95%置信区间103.2 - 104.7)。最常见的五种症状为关节疼痛(从1.6(95%置信区间1.3 - 1.9)到14.3(95%置信区间14.1 - 14.6))、腹痛(从0.3(95%置信区间0.1 - 0.5)到9.9(95%置信区间9.7 - 10.1))、胃肠道问题(从0.6(95%置信区间0.4 - 0.9)到13.3(95%置信区间13.1 - 13.6))、咳嗽(从0.3(95%置信区间0.2 - 0.5)到9.1(95%置信区间8.9 - 9.3))和焦虑(从0.8(95%置信区间0.6 - 1.2)到11.4(95%置信区间11.2 - 11.6));而肌肉痉挛(从0.01(95%置信区间0.008 - 0.2)到1.7(95%置信区间1.6 - 1.8))、刺痛感(从0.05(95%置信区间0.03 - 0.0.9)到1.5(95%置信区间1.4 - 1.6))、记忆问题(从0.03(95%置信区间0.02 - 0.06)到0.8(95%置信区间0.7 - 0.8))、认知功能障碍(从0.007(95%置信区间0.004 - 0.01)到0.6(95%置信区间0.4 - 0.8))以及嗅觉和/或味觉改变(从0.04(95%置信区间0.03 - 0.04)到0.7(95%置信区间0.6 - 0.8))最为少见。任何新冠后急性症状的发病率一般随年龄增长而升高,某些症状在中年成年人中达到峰值(焦虑、抑郁障碍、头痛、嗅觉和味觉改变),而其他症状在学龄前儿童中达到峰值(胃肠道问题和咳嗽)。女性大多数症状的发病率更高。基于随机效应模型,感染队列中任何新冠后急性症状的发病率高于普通人群,荟萃分析发病率比值(meta - IRR)为1.4(1 - 2)。所有个体症状均呈现类似模式。最高的meta - IRR为抑郁障碍,2.6(1.7 - 3.9);焦虑,2.3(1.4 - 3.8);过敏,2.1(1.7 - 2.8)和睡眠障碍,2.1(1.5 - 2.6)。嗅觉和/或味觉改变的meta - IRR为1.9(1.3 - 2.8)。
世界卫生组织列出的新冠后急性症状在新冠感染后普遍存在。然而,即使在标准化研究方法后,不同医疗环境和地理位置的发病率仍存在显著异质性。这是第一项使用世界卫生组织列出的症状对新冠后急性症状流行病学进行的国际研究。其结果有助于从多国角度理解这种状况的流行病学。本研究的局限性包括新冠后急性定义缺乏共识,以及在现有数据集中难以捕捉新冠后急性症状对日常生活的影响。
本研究由欧洲卫生数据证据网络(EHDEN)通过证据生成基金资助,并由国家卫生与保健研究机构(NIHR)牛津生物医学研究中心(BRC)提供资金。