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IAP Room Entry Protocol

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30 Questions

What should be checked on each device before assembly?

Free movement of all parts and non-sticking joints

What is the purpose of the barcode label scanning in the IAP room?

To track the devices through the decontamination process

What is the consequence of not checking the screws on jointed RMD during cleaning?

The devices may become loose during the cleaning process

What is the benefit of using a computerized track and trace system in the CSSD?

Accurate tracking of devices and device trays

What is generated each time a new processing cycle begins in the computerized track and trace system?

A new unique unit number

What is used in place of a computerized track and trace system in some CSSDs?

A manual system

What is the primary reason for wearing protective clothing in the IAP room?

To minimize the risk of contamination of the clean reusable medical devices and the environment

What is the recommended frequency for changing freshly laundered scrub suits?

Daily or whenever it becomes visibly soiled or wet

What type of hat or hood is worn in the IAP room?

A clean, single-use, low-lint surgical hat or hood

What is the correct disposal method for headgear and beard masks after use?

Discard them in the appropriate waste stream

What type of jewelry is allowed to be worn in the IAP room?

Only stud earrings, as long as they are totally confined within the head cover

What is the rule regarding the use of shoes in the IAP room?

Dedicated sturdy shoes should be worn inside the IAP room and never be used outside

What is the primary purpose of packaging in a CSSD environment?

To protect the contents from physical damage and ensure sterility

What is the main advantage of sequential wrapping over simultaneous wrapping?

It is the most commonly used method in CSSD

What is the primary benefit of using a Square Fold Technique?

It is preferred for wrapping heavier items

What is the characteristic of Spunbond-meltblown-spunbond (SMS) fabrics?

They are non-woven fabrics

What is the primary purpose of using a sterilization wrap?

To create a sterile barrier for items

What is the characteristic of a good seal in sterilization wrapping?

It is resistant to tears and punctures

What is a significant improvement in rigid reusable containers compared to previous versions?

The technology has improved significantly

What is a key consideration when using rigid containers for sterilization?

The compatibility with the sterilization method

Why is it important to examine the filter plate of a rigid container?

To inspect for damage, holes, tears, or punctures

What is a benefit of using rigid containers for sterilization?

They provide sterility and customer reassurance

What should be considered when packing a rigid container for sterilization?

Packing in a manner that allows for penetration of the sterilizing agent

What happens if the filter plate of a rigid container is damaged or dislodged?

The contents are considered contaminated

What is the primary purpose of using a tip protector during sterilization?

To prevent instruments from puncturing the pouch

Why is it important to avoid folding the inner pouch during double pouching?

To prevent air removal and ensure proper sterilant penetration

What is the recommended method for labeling packages before sterilization?

Using sterilization tape, commercially available adhesive labels, or the plastic side of peel pouches

What information should be included on the label of a sterilized package?

Package contents, lot number, sterilization date, pack complete name, assembler/packager name, requesting department, and sterilizer number and cycle

Why is complete and accurate labeling of packages important?

To allow the end user to select the correct pack

What is the purpose of double pouching in the sterilization process?

To ensure aseptic presentation of the items inside the sterile field

Study Notes

Device Inspection and Assembly

  • Devices should be checked for free movement of all parts and non-sticking joints.
  • A water-based lubricant may be used if required, following the IFU for dilutions and application.
  • Check that the edges of clamping RMD meet with no overlap and that teeth mesh together properly.
  • Ensure all screws on jointed RMD are tightened, as they may become loose during cleaning.

Track and Trace Systems

  • Many CSSDs use computerized track and trace systems to accurately track devices and device trays throughout the decontamination process.
  • The system uses handheld barcode readers connected to PCs to log and store information for each tray.
  • A unique barcode label is generated for each tray, containing the serial number specific to that tray and process.

Dress Code Requirements

  • Staff must pass through a clothing change and hand-wash area when moving between dirty and clean areas.
  • Protective clothing is worn by personnel entering the IAP room to reduce the risk of contamination.
  • Managers ensure protective clothing is available, and personnel are responsible for its correct use and disposal.

Protective Clothing

  • Specialists in the IAP room wear a freshly laundered scrub suit, changed daily or when visibly soiled or wet.
  • A clean, single-use, low-lint surgical hat or hood is worn to confine all hair.
  • Headgear and beard masks are discarded in the appropriate waste stream after use.
  • Stud earrings are allowed if totally confined within the head cover.
  • Make-up and jewelry, apart from a wedding band, are not worn in the IAP.

Packaging Requirements

  • Packaging should allow for complete and secure enclosure of the item(s).
  • Packages should protect the contents from physical damage due to stacking or compression.
  • Packages should have a method of sealing that results in a complete seal and provide adequate seal integrity.
  • Packages should be resistant to tears, abrasions, and punctures.
  • Packages should ensure the seal is tamper-proof and can only be sealed once.
  • Packages should permit adequate air removal.

Sterilization Flat Wrap

  • Sterilization flat wraps are made of nonwoven Spunbond-meltblown-spunbond (SMS) fabrics and are designed as single-use products.
  • They are available in a variety of sizes and weights.
  • Two wrapping techniques are used: sequential wrapping and simultaneous wrapping.

Wrapping Techniques

  • Sequential wrapping involves wrapping two layers of wrap material individually using a fold technique.
  • Simultaneous wrapping involves wrapping both layers of wrap material together simultaneously.
  • Square fold and envelope fold techniques are used with sequential and simultaneous wrapping.

Containers

  • Rigid reusable containers are making a comeback and can be cost-effective if used properly.
  • Containers should be easily disassembled for cleaning, drying, and storage.
  • Containers should be suitable for the method of sterilization being used.
  • Containers should be compatible with the cleaning method and cleaning agent being used.
  • Containers should be suitable for the storage configuration, lockable, tamper-proof, and non-resealable.
  • Containers should be packed to allow for penetration of the sterilizing agent.

Package Labeling

  • All packages should be labeled before sterilization with complete and accurate information.
  • Labels should include package contents, lot number, sterilization date, pack complete name, assembler/packager name, requesting department, sterilizer number, and used cycle.
  • Labeling information should be written on sterilization tape, commercially available adhesive labels, or in the plastic side of peel pouches.

Learn about the essential dress code requirements for staff entering the IAP room, including protective clothing and hand-washing protocols to prevent contamination. Understand the roles of managers and personnel in maintaining a clean environment. Test your knowledge of the safeguards in place to ensure the sterilization of medical devices and the surrounding area.

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