Resources with keywords: Creutzfeldt-Jakob disease (CJD)



Prion Diseases (including Creutzfeldt-Jakob Disease)
Utah Department of Health

Lab testing, case definition

Policies and Procedures for Patients with Suspected or Confirmed Human Prion Disease (E.G., Creutzfeldt-Jakob Disease [CJD])
University of California San Francisco

Infection control measures and example of patient management ( appropriate confinement, containment, safe handling, disinfection, and disposal of contaminated materials and tissues generated during the course of hospitalization)

Human Prion Disease - Infection Control Key Points
Washington State Department of Health

Infection control measures and Recommendations for disinfection and sterilization of prion-contaminated medical devices

Safe laboratory management of prions and proteopathic seeds
The Lancet Neurology

Mead, Simon et al.
The Lancet Neurology, Volume 20, Issue 12, 981

The UK’s Advisory Committee for Dangerous Pathogens convened a subgroup to revise guidance for safe working with prions and to consider whether any measures were needed for work with proteopathic seeds, involving experts from research laboratories for prion and other neurodegenerative diseases, infectious disease specialists, pathologists, veterinarians, and health and safety experts.

UK Prions and proteopathic seeds: Safe Working and the Prevention of Infection-Laboratory containment and control measures
UK Government

Flow chart to manage samples from human or animal source

Minimise transmission risk of CJD and vCJD in healthcare settings
UK Government / National Health Service

This guidance produced by the ACDP TSE risk management subgroup aims to help minimise the risk of transmission of Creutzfeldt-Jakob disease (CJD) and variant Creutzfeldt-Jakob disease (vCJD) in healthcare and other work settings.

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