N0450B - GDR Attempted, Step-by-Step

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N0450B - GDR Attempted, Step-by-Step

Step-by-Step Coding Guide for Item Set N0450B - GDR Attempted

1. Review of Medical Records

  • Objective: Determine if a Gradual Dose Reduction (GDR) has been attempted for the resident within the review period.
  • Process: Thoroughly examine the resident's medical records, including Medication Administration Records (MAR), physician's orders, and pharmacy consultations, for documented evidence of GDR attempts.

2. Understanding Definitions

  • Gradual Dose Reduction (GDR): A systematic approach to reducing the dose of a medication, or discontinuing it if possible, to minimize the risk of adverse effects and to promote the resident's highest level of functioning. It is especially relevant for medications that carry a higher risk of side effects, such as psychotropics and antipsychotics.

3. Coding Instructions

  • Code "Yes" if there is documentation of at least one attempt at GDR for any medication during the look-back period.
  • Code "No" if there is no documentation of a GDR attempt for any medication during this period.

4. Coding Tips

  • Focus on medications known for needing GDR, such as psychotropics, antipsychotics, and other high-risk drug classes.
  • Pay attention to any documentation that specifies a reduction in dosage or discontinuation of medication as part of a GDR attempt.
  • Clarify any ambiguous documentation with the prescribing physician or the pharmacy to ensure accurate coding.

5. Documentation

  • Clearly document any GDR attempts, including the medication involved, the rationale for the reduction, the new dosage (if applicable), and the outcome of the attempt.
  • Include notes from interdisciplinary team meetings where GDR was discussed, highlighting the decision-making process.
  • Ensure informed consent is obtained and documented when necessary, especially when adjusting medications for conditions like dementia.

6. Common Errors to Avoid

  • Missing documentation of GDR attempts because they were not clearly labeled as such in the medical records.
  • Confusing dose changes made for reasons other than GDR (e.g., renal function adjustment) as GDR attempts.
  • Overlooking GDR attempts because they were documented in less commonly reviewed parts of the medical record, such as progress notes or pharmacy consultations.

7. Practical Application

  • Example: A resident on a long-term antipsychotic for behavioral symptoms related to dementia undergoes a GDR attempt due to stabilized behavior and potential side effects. The interdisciplinary team, including the pharmacist, reviews the resident's current status and agrees to reduce the dosage by 25%. The MAR and progress notes reflect this change, including follow-up observations indicating the resident maintained stabilized behavior post-reduction. Illustrations could include a flowchart of the GDR decision-making process and a before-and-after comparison of the medication dosage, emphasizing the importance of documentation and interdisciplinary communication.

 

 

 

Please note that the information provided in this guide for MDS 3.0 Item N0450B: Type of Record 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. 

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