MDS Coding Not Supported for IV Micronutrient Hydration
Summary
The facility failed to ensure that the MDS accurately reflected the clinical status and services provided for two sampled residents. For Resident 12, the record showed diagnoses of dementia without behavioral disturbance and anxiety, and a physician order for an intravenous micronutrient hydration infusion provided by an outside contracted nursing service. The infusion consisted of vitamins, minerals, amino acids, and 500 mL of normal saline, and it was administered and completed on December 20, 2025. Resident 12’s annual MDS coded Section K0520 as yes for parenteral/IV feeding, Section K0710 as 25 percent or less intake by artificial route and 500 mL per day or less of fluid, and Section O0110H1 as yes for IV medications. However, the clinical record did not contain documentation that the infusion provided calories as a primary nutritional source, replaced oral intake, or otherwise met the RAI Manual definition of parenteral feeding. The record also did not contain documentation supporting that the infusion met the RAI criteria for IV medication coding. For Resident 8, the record showed diagnoses of Alzheimer’s dementia and mild protein-calorie malnutrition, along with a physician order for the same type of intravenous micronutrient hydration therapy through the contracted nursing service. The infusion was administered and completed on December 20, 2025, and the quarterly MDS likewise coded Section K0520 as yes, Section K0710 as 25 percent or less and 500 mL per day or less, and Section O0110H1 as yes. The clinical record did not show documentation that the infusion constituted parenteral feeding, provided primary nutritional support, or met criteria for IV medication coding under the RAI Manual. Interviews with the RAC and RD showed they believed the contracted IV service’s information supported coding Sections K and O for micronutrient therapies. The facility also provided vendor educational material describing when IV fluids may be coded for hydration support, but the records for both residents did not contain documentation of a chronic or acute fluid deficit, dehydration findings, oral hydration interventions that failed, a condition interfering with fluid balance, or a care plan supporting the need for IV hydration. Based on the clinical documentation and RAI guidance, the coding on the MDS assessments was not supported by the residents’ records.
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