Information for Funeral and Crematory Practitioners (2024)

Purpose

Practitioners at funeral homes, cemeteries, and crematories must balance dealing with infectious diseases while still serving families whose loved one has died. Dealing with patients who died of Creutzfeldt-Jakob Disease (CJD) is no exception. Safety measures can help protect staff while taking care of the decedent and their family.

Information for Funeral and Crematory Practitioners (1)

Background

CJD is not spread between people by normal contact or through environmental contamination. For example, it is not spread by airborne droplets or by blood or sexual contact as other diseases are.

Standard disinfection procedures and routine embalming solutions are ineffective against prions, infectious proteins that cause CJD. However, studies show that chemical solutions and physical processes involving bleach, sodium hydroxide, or autoclaving can inactivate prions.

It is important to protect yourself and your staff as you transport and prepare the bodies of people who had CJD.

If the bodies of CJD patients weren't autopsied, funeral preparation activities can be safely performed with strict adherence to standard precautions. These activities include transportation, preparation, disinfection, and final disposition.

Transporting

Funeral service workers can safely transport the CJD patient's body from the place they died to the funeral home. Workers should use appropriate standard infection control measures, including wearing personal protective gear.

The World Health Organization (WHO) recommends placing the body in a leak-proof pouch prior to moving. The bag should be lined with absorbent material to prevent leakage of body fluids. If there is excess fluid, a double bag can be utilized. After transporting, all surfaces (i.e. stretchers, cots) should be disinfected with bleach.

Preparation and dressing

An autopsied or traumatized body of a suspected or confirmed CJD patient can be embalmed. Funeral workers should use the precautions outlined in the WHO CJD infection control guidelines.

CJD patients who have not been autopsied or whose bodies have not been traumatized can be embalmed using standard precautions.

Family members should be advised to avoid contact with the CJD patient's body if they were autopsied. This includes touching or kissing their loved one's face. However, if the patient has not been autopsied, such contact does not need to be discouraged.

Embalming bodies not autopsied

Embalming bodies of CJD patients who have not been autopsied can be performed using standard precautions.

However, it may be prudent to place the body on a waterproof sheet to collect bodily fluids and use disposable instruments. The bodily fluids should be collected in a suitable container.

Incision sites should be closed with super glue, wiped down with bleach and the body washed prior to dressing. Cosmetic restorative work may also be undertaken.

Embalming bodies autopsied

Embalming bodies of CJD patients who have been autopsied can also be safely performed. Adherence to standard infection control measures is paramount when embalming an autopsied body of a suspected or clinically-diagnosed CJD patient.

Autopsies on these individuals are often restricted to removal of the brain. Therefore, special precautions should be taken including placing a plastic sheet with absorbent wadding and raised edges underneath the head. This will ensure containment of fluids and prevent any spillage.

If sutures do not control leaking, pack the cranial cavity with absorbent material soaked with bleach, and tightly suture.

Bodies of autopsied CJD patients

Bodies of autopsied CJD patients should be placed on a waterproof sheet to collect all fluids.

It is strongly recommended that disposable instruments, masks, gowns, and puncture resistant gloves be used whenever possible.

The entire body should be washed with bleach, rinsed, and sanitized before dressing.

Special care should be taken to limit fluid leakage when performing restorative work on a CJD patient. All fluids should be collected in a suitable container.

Casketing and viewing

Avoid unnecessary manipulation of the body that would force purging of body fluids and risk opening of incision sites. If warranted, the casket can be lined with a leak proof sheet.

An open casket for viewing should not be prohibited. However, if an autopsy has been performed, family members of CJD patients should be advised to avoid contact with the body. This would include touching or kissing the patient’s face.

Terminal disinfection and waste removal

According to WHO guidelines, disinfect all collected fluids by adding 40 grams of sodium hydroxide pellets per liter of fluid. Stir the mixture after a few minutes. Be careful to avoid spilling the fluid, as it will be hot. Leave it undisturbed for at least one hour. Then, dispose of it like other mortuary waste.

Plastic sheets and other disposable items that have been exposed to bodily fluids should be incinerated.

Mortuary working surfaces that have become contaminated should be flooded with sodium hydroxide or bleach. Then, leave undisturbed for at least one hour. Then don gloves and mop up with absorbent, disposable rags. Finally, swab the surface with water needed to remove any residual disinfectant solution.

Use of disposable instruments is preferred. However, reusable instruments and tools can be cleaned and disinfected by using CDC's CJD sterilization protocols.

All contaminated solid materials should be disposed of as hazardous waste. Dispose of body fluids/tissues and hazardous chemicals in accordance with funeral home policy, state, and federal regulations.

Final disposition - cremation and burial

There are no special interment, entombment, inurnment, or cremation requirements for patients with CJD.

Interment of bodies in closed caskets does not present a significant risk of environmental contamination.

Cremated remains can be considered sterile, as the infectious agent does not survive incineration-range temperatures.

Information for Funeral and Crematory Practitioners (2024)

FAQs

Why do CJD patients have to be cremated? ›

No special interment, entombment, cremation, or inurnment requirements are needed. Interment of closed caskets do not present a significant risk of environmental contamination. Cremated remains are considered sterile. The CJD agent does not survive incineration temperatures.

Is CJD contagious after death? ›

As above, there is no evidence that CJD can be passed from one person to another by contact with the skin or hair. Therefore, the body bag can be opened to allow relatives to dress the body and wash the hair.

Is genetic CJD contagious? ›

Is CJD contagious? CJD is not contagious in the typical sense, and is not transmitted person to person by direct contact, airborne spread, or the environment. CJD transmission can occur during invasive medical procedures involving the central nervous system due to exposure to contaminated brain tissue.

How do you prevent Creutzfeldt Jakob disease? ›

Prevention. There's no known way to prevent sporadic CJD . If you have a family history of neurological disease, you may benefit from talking with a genetics counselor. A counselor can help you sort through your risks.

What is the life expectancy of someone with CJD? ›

The disorder is fatal in a short time, usually within 8 months. People who have variant CJD get worse more slowly, but the condition is still fatal. A few people survive for as long as 1 or 2 years. The cause of death is usually infection, heart failure, or respiratory failure.

What are the final stages of CJD? ›

As the condition progresses to its final stages, people with all forms of CJD will become totally bedridden. They often become totally unaware of their surroundings and require around-the-clock care. They also often lose the ability to speak and can't communicate with their carers.

What is the main cause of Creutzfeldt-Jakob disease? ›

Creutzfeldt-Jakob disease (CJD) is caused by an abnormal infectious protein in the brain called a prion. Proteins are molecules made up of amino acids that help the cells in our body function. They begin as a string of amino acids that then fold themselves into a 3-dimensional shape.

What is the longest someone has lived with CJD? ›

She received long-term home care with regularly visiting nursing services and died of pneumonia 198 months (16 years) after symptom onset. Conclusion: To our knowledge, this is the first report of CJD who lived more than 16 years after onset.

What are three symptoms of CJD? ›

Overview Creutzfeldt-Jakob disease
  • loss of intellect and memory.
  • changes in personality.
  • loss of balance and co-ordination.
  • slurred speech.
  • vision problems and blindness.
  • abnormal jerking movements.
  • progressive loss of brain function and mobility.

What meat causes Creutzfeldt-Jakob disease? ›

The human version of BSE is called variant Creutzfeldt-Jakob disease (vCJD). There's strong evidence people can get vCJD by eating beef products with central nervous system tissue, such as brain and spinal cord, from cattle infected with mad cow disease.

Who is more prone to CJD? ›

CJD usually occurs in people over the age of 60. Sporadic CJD (sCJD) occurs spontaneously and is the most common type of CJD in the United States accounting for ~85% of cases. Genetic CJD (gCJD) is inherited through a genetic mutation and is ~5-15% of cases worldwide and ~10% of cases in the United States.

Has anyone ever recovered from CJD? ›

There's no proven cure for Creutzfeldt-Jakob disease (CJD), but clinical studies are under way at the National Prion Clinic to investigate possible treatments. At present, treatment involves trying to keep the person as comfortable as possible and reducing symptoms with medicines.

What puts you at risk of CJD? ›

In each of the studies, a family history of dementia, history of psychotic disease, employment as a health professional, and exposure to cows and sheep was associated with an increased CJD risk.

Why is CJD not treatable? ›

With CJD, faulty proteins, known as prions, build up in your brain cells, damaging and destroying those cells. The condition is very severe, and its effects develop and worsen quickly. It's ultimately fatal, and unfortunately, there's no way to cure, treat or even slow down the progress of this disease.

What is the rarest brain disorder? ›

Creutzfeldt-Jakob disease, or CJD, is a rare degenerative brain disease that is incurable and fatal. It is caused by prions, infectious, misshapen versions of normal proteins, which build up in the brain, damaging brain cells.

Can a person with CJD be embalmed? ›

An autopsied or traumatized body of a suspected or confirmed CJD patient can be embalmed. Funeral workers should use the precautions outlined in the WHO CJD infection control guidelines. CJD patients who have not been autopsied or whose bodies have not been traumatized can be embalmed using standard precautions.

Does cremation destroy prions? ›

Incineration of prion-contaminated material is considered the most effective method of disposal. Combustion at 1,000°C can destroy prion infectivity, however, low infectivity remains after treatment at 600°C.

Do CJD patients feel pain? ›

They may feel discomfort, and some of the symptoms of the disease such as myoclonus are distressing to caregivers. Neurologists believe there is no pain associated with the disease itself. For example, there is no rise in pressure in the head which could cause headache or any other obvious cause of pain.

How long can CJD lay dormant? ›

CJD-related disease can incubate for 50 years.

References

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