Failure to Provide and Monitor Nutritional Supplements for Residents With Weight Loss
Summary
The facility failed to implement nutrition measures to maintain the health of residents with ongoing weight loss. For Resident 14, the record showed severe cognitive impairment, wandering behavior, dependence for most activities of daily living, and a mechanically altered diet with thickened liquids. The resident’s weights showed progressive loss from 142.3 pounds on admission to 120.4 pounds 176 days later, and a Mini Nutritional Assessment score of 7 indicated malnutrition. The record also showed no documented nutritional interventions in the assessment, no evidence that the significant weight loss was evaluated, and no follow-up documentation from the RD, Dietary Manager, or Nursing Department regarding the ongoing weight loss or the effectiveness of supplements. Resident 14’s RD note recommended Ensure 4 ounces daily after identifying significant weight loss, but the MARs reflected only Magic Cup twice daily, with no documentation that Ensure was actually ordered or provided. Observations on multiple days showed the resident wandering in and out of the dining room, being redirected by staff, eating meals, and no observed Magic Cup or Ensure being served or present in the resident’s room. Interviews with nursing and dietary staff confirmed the Magic Cup was the only supplement being used, that dietary staff were responsible for administering it, and that the facility was unaware of the RD recommendation for Ensure and had not implemented interventions when the resident’s weight loss was identified. For Resident 1, the record showed end stage renal disease, diabetes, non-Alzheimer’s dementia, dialysis three times weekly, assistance needed with eating and drinking, and documented weight loss of 5% or more in one month and 10% or more in six months. The care plan identified risk for altered nutrition and included fortified food/drink at meals, monitoring intake, and weight monitoring. The RD recommended Glucerna twice daily until weight stabilized, but the MARs showed the supplement was frequently refused or the resident was unavailable, with no documentation of how much was consumed when it was given. The record also showed no evidence the RD assessed the resident for extended periods, a later RD note documented significant weight loss and recommended discontinuing Glucerna and starting a different supplement, and the facility continued to document Glucerna on the MAR without evidence that the new recommendation was implemented or that fortified food/drinks were actually being provided.
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