Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Jul 27;13(15):4401.
doi: 10.3390/jcm13154401.

Creutzfeldt-Jakob Disease and Fatal Familial Insomnia: Demographics and In-Hospital Mortality in Spain

Affiliations

Creutzfeldt-Jakob Disease and Fatal Familial Insomnia: Demographics and In-Hospital Mortality in Spain

Natividad Cuadrado-Corrales et al. J Clin Med. .

Abstract

Background: Creutzfeldt-Jakob disease (CJD) and fatal familial insomnia (FFI) are prion diseases characterized by severe neurodegenerative conditions and a short duration of illness. Methods: This study explores the characteristics of hospitalizations for CJD and FFI in Spain from 2016 to 2022 using the Spanish National Hospital Discharge Database (SNHDD). Results: We identified a total of 1063 hospital discharges, including 1020 for CJD and 43 for FFI. Notably, the number of hospitalized patients with FFI showed a significant peak in 2017. The average length of hospital stay (LOHS) was 13 days for CJD and 6 days for FFI, with in-hospital mortality rates (IHM) of 36.37% for CJD and 32.56% for FFI. Among CJD patients, the average LOHS was 14 days, with a significantly longer duration for those who experienced IHM. Conclusions: The presence of sepsis or pneumonia and older age were associated with a higher IHM rate among CJD patients. The total estimated cost for managing CJD and FFI patients over the study period was EUR 6,346,868. This study offers new insights into the epidemiology and healthcare resource utilization of CJD and FFI patients, which may inform future research directions and public health strategies.

Keywords: Creutzfeldt–Jakob disease; costs; epidemiology; fatal familial insomnia: hospitalizations; mortality.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Similar articles

References

    1. Prusiner S.B. Novel proteinaceous infectious particles cause scrapie. Science. 1982;216:136–144. doi: 10.1126/science.6801762. - DOI - PubMed
    1. DeArmond S.J., Prusiner S.B. Etiology and pathogenesis of prion diseases. Am. J. Pathol. 1995;146:785–811. - PMC - PubMed
    1. Morales R. Prion strains in mammals: Different conformations leading to disease. PLoS Pathog. 2017;13:e1006323. doi: 10.1371/journal.ppat.1006323. - DOI - PMC - PubMed
    1. Brown D.R., Kretzschmar H.A. Microglia and prion disease: A review. Histol. Histopathol. 1997;12:883–892. - PubMed
    1. Piccardo P., Manson J.C., King D., Ghetti B., Barron R.M. Accumulation of prion protein in the brain that is not associated with transmissible disease. Proc. Natl. Acad. Sci. USA. 2007;104:4712–4717. doi: 10.1073/pnas.0609241104. - DOI - PMC - PubMed

LinkOut - more resources