M1200B. Skin/ulcer treatments: pressure reducing device for bed, Step-by-Step

Step-by-Step Coding Guide for Item Set M1200B: Skin/Ulcer Treatments - Pressure Reducing Device for Bed

1. Review of Medical Records

Objective: To accurately identify the utilization of pressure-reducing devices for beds.

• Key Points:
  • Examine the resident’s medical and nursing records for mentions of pressure ulcers or risks that have led to the use of a pressure-reducing device for the bed.
  • Look for orders from healthcare providers, including physical therapists or wound care specialists, for the implementation of bed-related pressure-reducing devices.

2. Understanding Definitions

Objective: Define what constitutes a pressure-reducing device for beds.

• Key Points:
  • Pressure Reducing Device for Bed: Includes any product or technology used on a bed to alleviate pressure and distribute weight more evenly to prevent or manage pressure ulcers. Examples include specialized mattresses, mattress overlays, and air-fluidized beds.

3. Coding Instructions

Objective: Provide clear guidelines for coding the use of bed-related pressure-reducing devices in the MDS.

• Key Points:
  • Code "Yes" for M1200B if any pressure-reducing device is being utilized on the resident's bed to prevent or treat skin ulcers.
  • Devices should be coded regardless of whether they are used prophylactically or as a direct treatment for existing pressure ulcers.

4. Coding Tips

Objective: Offer advice to enhance the accuracy and completeness of M1200B coding.

• Key Points:
  • Verify the specific type of pressure-reducing device in use. Not all products may qualify as pressure-reducing according to clinical guidelines.
  • Understand the purpose of the device's use: Whether it is for the prevention of new ulcers or the treatment of existing ones.

5. Documentation

Objective: Ensure comprehensive documentation for the use of pressure-reducing devices for beds.

• Key Points:
  • Document the type of pressure-reducing device used, including brand and model if relevant, to support coding decisions.
  • Record the rationale for the device's use, detailing any specific skin integrity issues or risk factors present.
  • Include instructions for the device's maintenance and use, ensuring care staff are aware of how to properly utilize it for maximum effectiveness.

6. Common Errors to Avoid

Objective: Highlight frequent mistakes in coding and documentation for M1200B.

• Key Points:
  • Overlooking the use of pressure-reducing devices that are considered standard equipment in the facility.
  • Failing to document the initiation or discontinuation of a pressure-reducing device, leading to inaccuracies in the MDS.
  • Misclassifying devices not specifically designed for pressure reduction as such.

7. Practical Application

Objective: Apply M1200B coding instructions to a realistic example.

• Key Points:
  • Scenario: A resident with limited mobility has developed a stage II pressure ulcer on their sacrum. In response, the care team initiates the use of a gel overlay on the resident's bed to reduce pressure and support healing.
  • Coding: This scenario should be coded as "Yes" for M1200B. Documentation should include the presence of the sacral pressure ulcer, the introduction of the gel overlay as a treatment measure, and any observed outcomes following its use.
  • Follow-Up: Regularly assess the resident's skin condition and the effectiveness of the pressure-reducing device, adjusting care plans as necessary and documenting all changes.

Please note that the information provided in this guide for MDS 3.0 Item set M1200B was originally based on the CMS's RAI Version 3.0 Manual, October 2023 edition. Every effort will be made to update it to the most current version. The MDS 3.0 Manual is typically updated every October. If there are no changes to the Item Set, there will be no changes to this guide. This guidance is intended to assist healthcare professionals, particularly new nurses or MDS coordinators, in understanding and applying the correct coding procedures for this specific item within MDS 3.0. 

The guide is not a substitute for professional judgment or the facility’s policies. It is crucial to stay updated with any changes or updates in the MDS 3.0 manual or relevant CMS regulations. The guide does not cover all potential scenarios and should not be used as a sole resource for MDS 3.0 coding. 

Additionally, this guide refrains from handling personal patient data and does not provide medical or legal advice. Users are responsible for ensuring compliance with all applicable laws and regulations in their respective practices.