Failure to Follow Medication Monitoring, Clarify Orders, and Document TB Testing
Summary
The facility failed to follow physician orders for medication side effect monitoring and failed to clarify a hypoglycemia order for two residents. One resident was admitted with diagnoses including left femur fracture, dementia, and hypertension, and had severely impaired cognitive skills. The resident’s January eMAR/eTAR included an anticoagulant monitoring order requiring documentation of specific side effects every shift, but nurses sometimes signed "N" without documenting in the progress note what side effect was observed, as required by the order. The same resident also had an order stating that if the resident was not alert or not able to swallow during a hypoglycemic episode, a meal or snack should be given within 1 hour, and the order was not clarified even though the instruction did not match the resident’s condition. A second resident, admitted with diagnoses including dementia, hemiplegia and hemiparesis, and hypertension, had a BIMS score of 10 out of 15 indicating moderate cognitive impairment. The resident’s January eMAR/eTAR included multiple medication monitoring orders, including anticoagulant, anticonvulsant, antidepressant, and antipsychotic monitoring. For the anticoagulant order, the record showed entries of No, NA, or Y for INR monitoring, and for the anticonvulsant order nurses documented a check mark rather than the required Y or N. The antidepressant and antipsychotic orders did not state how to document if a significant side effect was observed, and the progress notes did not include documentation of what side effect was observed for any of the documented "N" entries. The resident also had the same hypoglycemia order stating that if not alert or not able to swallow, a meal or snack should be given within 1 hour, and this order was not clarified. The facility also failed to follow appropriate TB testing and documentation for another resident. That resident was admitted with diagnoses including acute respiratory failure with hypoxia, encephalopathy, and chronic diastolic congestive heart failure, and had severe cognitive impairment with a BIMS score of 3 out of 15. The physician ordered PPD testing for TB screening, including a first dose and a second dose 14 days later only if the first dose was negative. The January eMAR showed the PPD solution documented as administered twice by two different nurses, and the PPD results were read as negative on both occasions. However, the progress notes did not document whether the PPD was actually administered or not administered on the second date, and the record did not contain documented evidence explaining the duplicate entry until after surveyor inquiry.
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