Giovana Alves Santos, Carlos Laranjeira, Lígia Carreira, Vanessa Denardi Antoniassi Baldissera, Maria Fernanda do Prado Tostes, Viviani Camboin Meireles, Rosella Santoro Ageno, Maria Aparecida Salci
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引用次数: 0
Abstract
Introduction
The majority of those infected with COVID-19 undergo a brief duration of clinical illness. In certain instances, symptoms endure for months or years after the initial viral exposure—a condition characterized as Long COVID (LC). The experience of this illness remains largely unexplored as it has only recently surfaced. This study aims to understand the repercussions of persistent respiratory post-COVID symptoms in Brazilian adults 12 months after SARS-CoV-2 infection.
Methods
A constructivist grounded theory study was employed. Data were collected through individual interviews with adults with persistent respiratory symptoms of Long COVID in Brazil. Data collection took place between September 2023 and February 2024. Data analysis was performed on a constant comparative basis and concurrent with data collection to understand the findings.
Results
Twenty-four individuals (12 females, 12 males) with a median age of 43.29 ± 9.09 years participated. The data analysis generated a central category—living with the long-term effects of COVID-19: breathlessness pervades everything—around which three categories emerged: (1) imbalance between life before and after being infected by COVID-19; (2) living with acute post-COVID respiratory symptoms; and (3) struggling with persistent post-COVID respiratory symptoms.
Conclusion
Our analysis of the perceived needs of individuals with Long COVID underscores the urgent necessity for legislative reform to acknowledge LC as a disability that requires clear diagnostic criteria. Approaches to treatment and rehabilitation are required to evaluate the extent to which functioning and disability improve. Lastly, this study highlights the complex problems encountered by individuals with Long COVID, including employment uncertainties, everyday tasks and social relationships.
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.