Incidence of post-acute COVID-19 symptoms across healthcare settings in seven countries: an international retrospective cohort study using routinely-collected data.

IF 9.6 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
EClinicalMedicine Pub Date : 2024-10-30 eCollection Date: 2024-11-01 DOI:10.1016/j.eclinm.2024.102903
Junqing Xie, Kim López-Güell, Daniel Dedman, Talita Duarte-Salles, Raivo Kolde, Raúl López-Blasco, Álvaro Martínez, Gregoire Mercier, Alicia Abellan, Johnmary T Arinze, Zara Cuccu, Antonella Delmestri, Dominique Delseny, Sara Khalid, Chungsoo Kim, Ji-Woo Kim, Kristin Kostka, Cora Loste, Lourdes Mateu, Miguel A Mayer, Jaime Meléndez-Cardiel, Núria Mercadé-Besora, Mees Mosseveld, Akihito Nishimura, Hedvig M E Nordeng, Jessie O Oyinlola, Laura Pérez-Crespo, Marta Pineda-Moncusí, Juan Manuel Ramírez-Anguita, Nhung T H Trinh, Anneli Uusküla, Bernardo Valdivieso, Theresa Burkard, Edward Burn, Martí Català, Daniel Prieto-Alhambra, Roger Paredes, Annika M Jödicke
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We conducted an international network cohort study to estimate the burden of these symptoms in North American, European, and Asian populations.</p><p><strong>Methods: </strong>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.</p><p><strong>Findings: </strong>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. 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引用次数: 0

Abstract

Background: 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.

Methods: 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.

Findings: 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).

Interpretation: 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.

Funding: 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).

七个国家医疗机构中 COVID-19 急性发作后症状的发生率:一项利用常规收集数据进行的国际回顾性队列研究。
背景:世界卫生组织(WHO)已确定了一系列症状表现,以帮助临床诊断 COVID 后病症,在此称为急性 COVID-19 后症状。我们开展了一项国际网络队列研究,以估计这些症状在北美、欧洲和亚洲人群中的负担:我们进行了一项联合分析,包括来自英国、荷兰、挪威、爱沙尼亚、西班牙、法国、韩国和美国的 10 个数据库,时间跨度从 2020 年 9 月 1 日到最新数据提供日(从 2021 年 12 月 31 日到 2023 年 2 月 28 日),涵盖初级和二级护理、全国范围的登记和索赔数据,所有数据均映射到观察性医疗结果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:SARS-CoV-2 感染队列(聚合酶链反应(PCR)或快速侧流试验(LFT)结果呈阳性或临床 COVID-19 诊断)和普通人群队列。既往病史少于 365 天或随访时间少于 120 天的个体被排除在外。我们估算了世界卫生组织提出的 25 种 COVID-19 急性期后症状的发病率 (IR),考虑了指数日期后≥90 天和≤365 天出现的症状,排除了指数事件发生前 180 天出现相应症状的个体。按年龄和性别进行了分层分析。将感染人群的发病率与普通人群的发病率进行比较,计算出发病率比(IRR)。使用随机效应荟萃分析将不同数据库的结果进行合并:感染人群中有 3,019,408 人。其中 1,585,160 人为女性,1,434,248 人为男性。普通人群组包括 929 351 505 人。其中 461 195 036 人为女性,466 022 004 人为男性。在COVID-19感染人群中,任何COVID-19急性感染后症状的1年IR在不同数据库中差异显著,从每100人年4.4(95% CI 3.8-5.1)到103.9(95% CI 103.2-104.7)不等。最常见的五种症状是关节痛(从 1.6 (95% CI 1.3-1.9) 到 14.3 (95% CI 14.1-14.6))、腹痛(从 0.3 (95% CI 0.1-0.5) 到 9.9 (95% CI 9.7-10.1))、胃肠道问题(从 0.6(95% CI 0.4-0.9)到13.3(95% CI 13.1-13.6))、咳嗽(从0.3(95% CI 0.2-0.5)到9.1(95% CI 8.9-9.3))和焦虑(从0.8(95% CI 0.6-1.2)到11.4(95% CI 11.2-11.6));而肌肉痉挛(从0.8)、认知功能障碍(从 0.007(95% CI 0.004-0.01)到 0.6(95% CI 0.4-0.8))以及嗅觉和/或味觉改变(从 0.04(95% CI 0.03-0.04)到 0.7(95% CI 0.6-0.8))最不常见。COVID-19急性期后症状的发病率一般随年龄增长而增加,某些症状在中年人(焦虑、抑郁障碍、头痛、嗅觉和味觉改变)中达到高峰,而其他症状则在学龄前儿童(肠胃问题和咳嗽)中达到高峰。在大多数症状中,女性的发病率较高。根据随机效应模型,感染人群中任何 COVID-19 后急性症状的发病率均高于普通人群,元分析发病率比为 1.4(1-2)。所有单个症状的情况也类似。元分析发病率比最高的是抑郁障碍(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/或味觉改变的元内比值为 1.9 (1.3-2.8):解释:COVID-19感染后通常会出现世界卫生组织列出的COVID-19急性期后症状。然而,即使在研究方法标准化后,不同医疗机构和地理位置的发病率仍存在显著的异质性。这是国际上首次使用世界卫生组织列出的症状对 COVID-19 急性感染后症状的流行病学进行研究。研究结果有助于从多国角度了解这种疾病的流行病学。这项研究的局限性包括对急性 COVID-19 后症状的定义缺乏共识,以及现有数据集难以反映急性 COVID-19 后症状对日常生活的影响:本研究由欧洲健康数据证据网络(EHDEN)通过证据生成基金(Evidence Generation Fund Grant)和英国国家健康与护理研究所(NIHR)牛津生物医学研究中心(BRC)资助。
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
EClinicalMedicine
EClinicalMedicine Medicine-Medicine (all)
CiteScore
18.90
自引率
1.30%
发文量
506
审稿时长
22 days
期刊介绍: eClinicalMedicine is a gold open-access clinical journal designed to support frontline health professionals in addressing the complex and rapid health transitions affecting societies globally. The journal aims to assist practitioners in overcoming healthcare challenges across diverse communities, spanning diagnosis, treatment, prevention, and health promotion. Integrating disciplines from various specialties and life stages, it seeks to enhance health systems as fundamental institutions within societies. With a forward-thinking approach, eClinicalMedicine aims to redefine the future of healthcare.
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