Failure to Monitor and Address Resident's Edema and Weight Gain
Summary
The facility failed to adequately monitor and intervene in the decline of a resident's condition who was suffering from chronic venous hypertension and congestive heart failure. The resident's care plan, dated July 2023, indicated a need for staff assistance with lower body dressing due to lymphedema and a risk of worsening CHF, with interventions to monitor and report signs of edema. However, the care plan lacked specific information regarding the resident's venous hypertension or lymphedema. Despite physician notes documenting severe lymphadenopathy and the resident's reports of inconsistent application of a lymphedema compression device, the facility did not ensure consistent use of the device as ordered. Throughout the months from February to May 2024, the resident experienced significant weight gain, indicative of fluid retention, yet there was no documentation of actions taken in response to this change. The Treatment Administration Record (TAR) showed multiple instances where the lymphedema compression pump was not documented as applied during night shifts. Observations in May 2024 revealed the resident's legs were consistently edematous, red, and uncovered, with no compression devices in use. Interviews with the resident and staff confirmed the irregular use of the compression device and a lack of awareness or response to the resident's weight gain. The Director of Nursing acknowledged that there should have been parameters for reporting weight gain to the physician and orders to reduce edema, such as compression stockings and leg elevation. The DON expected staff to apply the lymphedema compression device as ordered and document its use, but this was not consistently done. The failure to monitor and address the resident's weight gain and edema, as well as the inconsistent application of the compression device, contributed to the deficiency in care provided to the resident.
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