Joint Commission Do Not Use List 2024


Joint Commission Do Not Use List 2024

The Joint Commission (TJC) Do Not Use (DNU) List is a set of medical devices and supplies that have been deemed unsafe or ineffective by The Joint Commission, an independent organization that accredits healthcare organizations across the United States.

The DNU List is updated annually and is intended to help healthcare providers make informed decisions about the use of medical devices and supplies. The 2024 DNU List includes 35 devices and supplies that have been linked to serious patient harm, including infections, injuries, and even death.

The DNU List is a valuable resource for healthcare providers and can help to prevent patient harm. However, it is important to note that the DNU List is not a complete list of all unsafe or ineffective medical devices and supplies. Healthcare providers should always use their own judgment and discretion when making decisions about the use of medical devices and supplies.

Joint Commission Do Not Use List 2024

The Joint Commission (TJC) Do Not Use (DNU) List is a set of medical devices and supplies that have been deemed unsafe or ineffective by TJC.

  • 35 devices and supplies
  • Linked to serious patient harm
  • Infections, injuries, death
  • Updated annually
  • Valuable resource
  • Not a complete list
  • Use caution and judgment
  • Prevent patient harm

Healthcare providers should always use their own judgment and discretion when making decisions about the use of medical devices and supplies.

35 devices and supplies

The 35 devices and supplies on the Joint Commission Do Not Use (DNU) List 2024 include a variety of medical products, such as:

  • Implantable devices: These devices are surgically implanted into the body and include products such as:
    • AneuRx stent graft
    • Bard Recovery stent
    • Cook Celect heparin-bonded catheter

Medical equipment: These devices are used to diagnose or treat medical conditions and include products such as:

  • Alaris infusion pumps
  • Baylis Medical BridgePoint neurointerventional system
  • Stryker 510K pituitary forceps

Consumables: These are single-use items that are used during medical procedures, such as:

  • 3M Avagard antiseptic wipes
  • Cardinal Health ChloraPrep One-Step solution
  • Medtronic SynchroMed II infusion sets

The DNU List is updated annually by The Joint Commission, an independent organization that accredits healthcare organizations across the United States. The DNU List is intended to help healthcare providers make informed decisions about the use of medical devices and supplies and to prevent patient harm.

Linked to serious patient harm

The devices and supplies on the Joint Commission Do Not Use (DNU) List 2024 have been linked to a variety of serious patient harm, including:

  • Infections: Some of the devices on the DNU List have been linked to infections, including:
  • AneuRx stent graft: This device has been linked to infections in the bloodstream, heart, and lungs.
  • 3M Avagard antiseptic wipes: These wipes have been linked to infections in the surgical site and bloodstream.

Injuries: Other devices on the DNU List have been linked to injuries, including:

  • Bard Recovery stent: This device has been linked to injuries to the heart and blood vessels.
  • Stryker 510K pituitary forceps: These forceps have been linked to injuries to the brain and pituitary gland.

Death: In some cases, the devices and supplies on the DNU List have been linked to death. For example, the Cook Celect heparin-bonded catheter has been linked to deaths from blood clots.

The Joint Commission DNU List is intended to help healthcare providers make informed decisions about the use of medical devices and supplies and to prevent patient harm.

Infections, injuries, death

The devices and supplies on the Joint Commission Do Not Use (DNU) List 2024 have been linked to a variety of serious patient harm, including infections, injuries, and death.

  • Infections: Some of the devices on the DNU List have been linked to infections, including:
  • AneuRx stent graft: This device has been linked to infections in the bloodstream, heart, and lungs.
  • 3M Avagard antiseptic wipes: These wipes have been linked to infections in the surgical site and bloodstream.
  • Cardinal Health ChloraPrep One-Step solution: This solution has been linked to infections in the surgical site.

Injuries: Other devices on the DNU List have been linked to injuries, including:

  • Bard Recovery stent: This device has been linked to injuries to the heart and blood vessels.
  • Baylis Medical BridgePoint neurointerventional system: This system has been linked to injuries to the brain and nervous system.
  • Stryker 510K pituitary forceps: These forceps have been linked to injuries to the brain and pituitary gland.

Death: In some cases, the devices and supplies on the DNU List have been linked to death. For example, the Cook Celect heparin-bonded catheter has been linked to deaths from blood clots.

The Joint Commission DNU List is intended to help healthcare providers make informed decisions about the use of medical devices and supplies and to prevent patient harm.

Updated annually

The Joint Commission Do Not Use (DNU) List is updated annually to ensure that it includes the most up-to-date information on unsafe and ineffective medical devices and supplies.

  • The DNU List is updated based on a number of factors, including:
  • New reports of patient harm associated with a particular device or supply.
  • New research that shows that a device or supply is ineffective.
  • Changes to regulatory standards.

The Joint Commission also works with a variety of stakeholders to gather information about unsafe and ineffective medical devices and supplies, including:

  • Healthcare providers
  • Manufacturers
  • Patients and patient advocates

The DNU List is an important resource for healthcare providers because it helps them to make informed decisions about the use of medical devices and supplies and to prevent patient harm.

The Joint Commission encourages healthcare providers to regularly review the DNU List and to use it in conjunction with their own clinical judgment when making decisions about the use of medical devices and supplies.

Valuable resource

The Joint Commission Do Not Use (DNU) List is a valuable resource for healthcare providers because it helps them to make informed decisions about the use of medical devices and supplies and to prevent patient harm.

  • The DNU List is valuable because it:
  • Provides up-to-date information on unsafe and ineffective medical devices and supplies.
  • Is based on a rigorous review of the latest evidence.
  • Is developed by a team of experts in healthcare quality and patient safety.

Healthcare providers can use the DNU List to:

  • Identify devices and supplies that should not be used.
  • Make informed decisions about the use of devices and supplies.
  • Develop policies and procedures to prevent the use of unsafe and ineffective devices and supplies.

The DNU List is an essential tool for healthcare providers who are committed to providing safe and effective care to their patients.

The Joint Commission encourages healthcare providers to regularly review the DNU List and to use it in conjunction with their own clinical judgment when making decisions about the use of medical devices and supplies.

Not a complete list

It is important to note that the Joint Commission Do Not Use (DNU) List is not a complete list of all unsafe and ineffective medical devices and supplies.

  • The DNU List only includes devices and supplies that have been linked to serious patient harm and that have been reviewed by The Joint Commission.
  • There are many other devices and supplies that may be unsafe or ineffective, but that have not yet been identified by The Joint Commission.

Healthcare providers should always use their own clinical judgment when making decisions about the use of medical devices and supplies.

  • The DNU List should be used as a guide, but it should not be the only factor considered when making decisions about patient care.

Healthcare providers should also be aware of the latest research on medical devices and supplies and should consult with experts in the field when making decisions about patient care.

  • The DNU List is an important resource for healthcare providers, but it is not a substitute for clinical judgment and expertise.

The Joint Commission encourages healthcare providers to regularly review the DNU List and to use it in conjunction with their own clinical judgment when making decisions about the use of medical devices and supplies.

Use caution and judgment

Healthcare providers should always use caution and judgment when making decisions about the use of medical devices and supplies, even if the device or supply is not on the Joint Commission Do Not Use (DNU) List.

Some devices and supplies may be safe and effective for some patients, but not for others. For example, a particular type of stent may be safe and effective for a patient with a certain type of heart condition, but not for a patient with a different type of heart condition.

Healthcare providers should also be aware of the potential risks and benefits of using a particular device or supply. For example, a particular type of medication may be effective in treating a certain condition, but it may also have side effects. Healthcare providers should weigh the risks and benefits of using a particular device or supply before making a decision.

Healthcare providers should also consider the patient’s preferences when making decisions about the use of medical devices and supplies. Some patients may prefer to use a particular type of device or supply, even if it is not the most effective or safest option. Healthcare providers should respect the patient’s preferences and work with them to develop a treatment plan that meets their needs.

The Joint Commission encourages healthcare providers to regularly review the DNU List and to use it in conjunction with their own clinical judgment when making decisions about the use of medical devices and supplies.

Prevent patient harm

The Joint Commission Do Not Use (DNU) List is intended to help healthcare providers prevent patient harm by providing them with information on unsafe and ineffective medical devices and supplies.

  • The DNU List can help healthcare providers to:
  • Identify devices and supplies that should not be used.
  • Make informed decisions about the use of devices and supplies.
  • Develop policies and procedures to prevent the use of unsafe and ineffective devices and supplies.

By using the DNU List, healthcare providers can help to reduce the risk of patient harm and improve the quality of care.

  • The DNU List is an important tool for healthcare providers who are committed to providing safe and effective care to their patients.

The Joint Commission encourages healthcare providers to regularly review the DNU List and to use it in conjunction with their own clinical judgment when making decisions about the use of medical devices and supplies.

FAQ

The following are some frequently asked questions about the Joint Commission Do Not Use (DNU) List 2024:

Question 1: What is the Joint Commission DNU List?
Answer 1: The Joint Commission DNU List is a list of medical devices and supplies that have been deemed unsafe or ineffective by The Joint Commission, an independent organization that accredits healthcare organizations across the United States.

Question 2: Why was the DNU List created?
Answer 2: The DNU List was created to help healthcare providers make informed decisions about the use of medical devices and supplies and to prevent patient harm.

Question 3: What types of devices and supplies are on the DNU List?
Answer 3: The DNU List includes a variety of medical devices and supplies, such as implantable devices, medical equipment, and consumables.

Question 4: How often is the DNU List updated?
Answer 4: The DNU List is updated annually to ensure that it includes the most up-to-date information on unsafe and ineffective medical devices and supplies.

Question 5: How can I access the DNU List?
Answer 5: The DNU List is available on the Joint Commission’s website.

Question 6: What should I do if I am using a device or supply that is on the DNU List?
Answer 6: If you are using a device or supply that is on the DNU List, you should talk to your healthcare provider about alternative options.

Question 7: How can I report a device or supply that I believe should be on the DNU List?
Answer 7: You can report a device or supply that you believe should be on the DNU List to The Joint Commission.

The DNU List is an important resource for healthcare providers and can help to prevent patient harm. However, it is important to note that the DNU List is not a complete list of all unsafe and ineffective medical devices and supplies. Healthcare providers should always use their own judgment and discretion when making decisions about the use of medical devices and supplies.

In addition to using the DNU List, healthcare providers can also follow these tips to help prevent patient harm:

Tips

In addition to using the Joint Commission Do Not Use (DNU) List, healthcare providers can also follow these tips to help prevent patient harm:

Tip 1: Use caution when using new devices and supplies.
New devices and supplies have not been used as extensively as older devices and supplies, so there may be more unknown risks associated with their use.

Tip 2: Be aware of the potential risks and benefits of using a particular device or supply.
Before using a particular device or supply, healthcare providers should be aware of the potential risks and benefits of using it. This information can be found in the device or supply’s labeling or instructions for use.

Tip 3: Follow the manufacturer’s instructions for use.
Devices and supplies should be used according to the manufacturer’s instructions for use. This will help to ensure that the device or supply is used safely and effectively.

Tip 4: Report any adverse events to the manufacturer and The Joint Commission.
If a healthcare provider experiences any adverse events with a device or supply, they should report the event to the manufacturer and The Joint Commission. This will help to ensure that the device or supply is investigated and that appropriate action is taken.

By following these tips, healthcare providers can help to prevent patient harm and improve the quality of care.

The Joint Commission DNU List is a valuable resource for healthcare providers, but it is not a substitute for clinical judgment and expertise. Healthcare providers should always use their own judgment and discretion when making decisions about the use of medical devices and supplies.

Conclusion

The Joint Commission Do Not Use (DNU) List 2024 is a valuable resource for healthcare providers, as it provides information on medical devices and supplies that have been linked to serious patient harm. Healthcare providers should use the DNU List in conjunction with their own clinical judgment and expertise when making decisions about the use of medical devices and supplies.

The main points of this article are as follows:

  • The DNU List includes 35 devices and supplies that have been linked to serious patient harm, including infections, injuries, and death.
  • The DNU List is updated annually to ensure that it includes the most up-to-date information on unsafe and ineffective medical devices and supplies.
  • Healthcare providers should use the DNU List as a guide, but it should not be the only factor considered when making decisions about patient care.
  • Healthcare providers should always use caution and judgment when making decisions about the use of medical devices and supplies, even if the device or supply is not on the DNU List.
  • Healthcare providers can help to prevent patient harm by following the tips outlined in this article.

By using the DNU List and following the tips in this article, healthcare providers can help to ensure that their patients receive safe and effective care.

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