Prions Flashcards

1
Q

Prions should be handled as CL3 organisms

How are they transported to lab?

A

Transport as Category B (UN3373)

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2
Q

What is first aid if prion material gets on open wound?

A

Scrub with warm soapy water

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3
Q

Which of these decontamination measures are effective?

Aldehyde
Chlorine dioxide
Ethylene dioxide
Hypochlorite
Sodium Hydroxide
Phenol
Autoclave
Ionising radiation
Incineration

A

Prions when dry adhere very strongly to surfaces. Important to keep cleaning area damp/ moist

Effective:

Sodium Hydroxide - effective but irritant

Phenol - most effective but very destructive

Incineration - needs to be >850degC

Ineffective:

Aldehyde
Chlorine dioxide
Ethylene dioxide
Hypochlorite - partially effective, but very toxic
Autoclave - reduce risk, but don’t eliminate
Ionising radiation

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4
Q

In the cleaning of surgical instruments by Department of Health ACDP, what is upper limit of protein detection on surfaces?

A

5 micrograms/ side of instrument

lower for neurosurgical instruments which will be in contact with high risk tissues

thought that less protein, suggests better cleaning, and less risk of prior transmission in those who prion disease is not suspected

if patient suspected of having prion disease, their instruments should be isolated from use from others

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5
Q

Who is at risk of hereditary CJD?

A

Familial CJD is a very rare genetic condition where one of the genes a person inherits from their parent (the prion protein gene) carries a mutation that causes prions to form in their brain during adulthood, triggering the symptoms of CJD

Blood relative with known mutation

At least two blood relatives with compatible syndrome

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6
Q

Who is at risk of variant CJD?

caused by consuming meat that had bovine spongiform encephalopathy

younger people

A

consuming meat that has had bovine spongiform encephalopathy

Or

risk from others who already have vCJD:

surgery with instruments from either confirmed case OR at risk individual

Received organs or tissue from confirmed case OR at risk individual

Donor of blood to someone who then developed vCJD

Receiver of blood from donor who then developed vCJD

Receiver of blood from donor who also gave to someone who then developed vCJD

Plasma products pre-2001

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7
Q

Who is at risk of sporadic CJD?

Most common type

Due to misfolding protein appearing sometime between age 45-75

A

Random mutation causing prior disease

Or

iatrogenic:

Pituitary
hormones pre-1985 in UK, perhaps more recently overseas

Neurosurgical procedures pre-1992 with possibility of dura mater
graft

Use of any instruments that used on someone who then developed CJD

Corneal grafts

Blood with white cells, protein component -
now sourced outside UK for children

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8
Q

CJD Tissue grading

What tissues are considered high risk?

A

High risk

CNS tissue

Posterior eye tissue

Pituitary tissue

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9
Q

CJD Tissue grading

What tissues are considered medium risk?

A

spinal ganglia

Olfactory epithelium

Lymphoid tissue - gut lymph tissue, spleen, Thymus, appendix, tonsils

adrenals

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10
Q

CJD Tissue grading

What tissues are considered low risk?

A

Every other tissue which is not high or medium risk

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11
Q

Patient with confirmed or possible CJD

How are surgical instruments disposed/ cleaned?

A

High/ medium risk -
- destroy - incinerate
- quarantine - if to be used again
- try and use single use instruments as much as possible

Low risk
- normal process, but good audit trail needed

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12
Q

Patient with confirmed or possible CJD

What are the steps of quarantining instruments

A

Keep instruments separate during procedure

Wash instruments well - cover in damp cloth

normal sterilisation process

put in sealed box - either for re-use on same patient of destruction

If diagnosis confirmed as CJD - destroy instruments

If alternative diagnosis found - can bring out of quarantine

If die before diagnosis - destroy instruments

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