Abstract
Abstract. Chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) describes a condition of
chronic weakness that cannot be alleviated by rest and it is associated with lower quality of life and
higher health care utilization. In western countries, its prevalence ranges from 0.2 to 1%. Despite
the many efforts carried out during the last decades to investigate the nature of this syndrome, there
are still uncertainties and controversies with respect to its definition, diagnosis, and treatment. Some
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authors suggest that there may be a non-negligible percentage of patients that are not yet diagnosed
with this pathology, due to the difficulty in identifying the symptoms. Henceforth, the economic
burden of the disease is still unclear, though it is highly recognized that costs are mainly related to
productivity loss. The present literature review investigates this topic, by considering, through a
chronological perspective, the most relevant contributions focused on the economic costs and
consequences of CFS/ME. It describes how the economic burden of CFS has been gradually and
increasingly considered through the years by researchers and addresses the aspects that should
deserve more attention in the next future.
| Titolo tradotto del contributo | [Machine translation] The economic and social costs of chronic fatigue syndrome/myalgic encephalomyelitis: a first review of the literature on the subject |
|---|---|
| Lingua originale | Italian |
| pagine (da-a) | 1-15 |
| Numero di pagine | 15 |
| Rivista | POLITICHE SANITARIE |
| Volume | 19 |
| Numero di pubblicazione | 2 Aprile_Giugno 2018 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 2018 |
Keywords
- CFS/ME
- diagnosis
- economic burden of the disease
- indirect costs