Exploring Long Covid Prevalence and Patient Uncertainty by Sociodemographic Characteristics Using GP Patient Survey Data

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Health Expectations Pub Date : 2025-03-17 DOI:10.1111/hex.70202
Mirembe Woodrow, Nida Ziauddeen, Dianna Smith, Nisreen A. Alwan
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Abstract

Background

The high global burden of Long Covid (LC) has significant implications for population well-being, health care, social care and national economies.

Aim

To explore associations between patient sociodemographic and health characteristics with two outcomes: having LC and expressing uncertainty about having LC, as described by general practice (GP) survey respondents.

Design and Setting

Analysis of GP Patient Survey (England), a random sample of 759,149 patients aged 16 years+ registered with a GP in England (2023).

Method

Multivariable logistic regression modelling comparing those with and without LC, and those who were unsure in relation to patient characteristics.

Results

4.8% of respondents reported having LC, and 9.1% were unsure. Significant adjusted associations indicating higher risk of LC included age (highest odds 35−54 years), sex (females), ethnicity (White Gypsy/Irish Traveller, mixed/multiple ethnic groups), sexual orientation (gay/lesbian or bisexual), living in a deprived area, being a carer or a parent and having a long-term condition (LTC). Those aged ≤ 25 years, males, non-binary, heterosexual, not parents or carers, from other White, Indian, Bangladeshi, Chinese, Black or Arab backgrounds, former and current smokers, and with no defined LTC were more likely in adjusted analysis to be unsure about having LC compared to answering ‘yes’.

Conclusion

There is an unequal distribution of LC in England, with the condition being more prevalent in minoritised and disadvantaged groups. There are also high levels of uncertainty about having LC. Improved awareness is needed amongst the general population and health care professionals to ensure those most vulnerable in society are identified and provided with care and support.

Patient or Public Contribution

The analysis builds on previous studies co-created with people with lived experience. A public contributor advised on discussions on dissemination towards optimal impact of this study's findings. Study findings will inform the next phases of the research in which the research questions and design will be co-created with public partners.

How This Fits in

In England there is high prevalence of Long Covid, a COVID-19 infection-induced chronic condition that can limit daily activities significantly. The burden of ill health from Long Covid is unequal, with minoritised groups experiencing higher prevalence. This study adds further evidence of inequality in the prevalence of Long Covid, but also reveals that there are more people who are unsure whether they have Long Covid than those who are confident they have it, with certain groups that are already disadvantaged being more likely to be uncertain if they have the condition. Findings underline a need for greater awareness of Long Covid amongst the public and health care professionals, and for diagnosis, treatment and support to be better distributed according to need.

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Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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