Medication Administration Errors Exceeded Allowed Rate
Summary
The facility failed to keep the medication error rate below 5 percent. Survey observations, interviews, record review, and policy review identified multiple medication administration errors involving resident self-administration, insulin administration, and a mislabeled medication card. The observed errors resulted in a medication error rate of 14.29%. Resident 24, whose BIMS score was 14 and whose diagnoses included anxiety, PTSD, epilepsy, weakness, and chronic pain, was observed with Seroquel 50 mg left in a medicine cup on the bedside table by a CMA, who did not watch the resident take the medication. The resident’s record showed an order for Seroquel 50 mg once daily with no special instructions for self-administration. Although the resident had orders allowing self-administration of certain topical and nasal medications, her self-administration assessment stated she did not want to administer pill forms and had difficulty with her left arm and weak hand grip. Resident 37, whose BIMS score was 15 and whose diagnoses included COPD, hemiplegia, presbyopia, emphysema, dysphagia, and aphasia, was observed receiving Ipratropium-Albuterol nebulizer medication from a CMA who then left the room after turning on the machine. The resident had orders allowing self-administration of eye drops and an inhaler, but no order for self-administration of the nebulizer medication. Resident 36, whose BIMS score was 10 and whose diagnoses included type 2 diabetes mellitus with diabetic polyneuropathy, chronic kidney disease stage 3, hypo-osmolality, hyponatremia, chronic systolic heart failure, rheumatic mitral stenosis, nonrheumatic mitral insufficiency, and pulmonary hypertension, was observed receiving Novolog FlexPen insulin. The RN removed the pen from the resident’s abdomen before the dose was fully dispensed, and insulin was seen expelling onto the resident’s skin. Resident 38, whose BIMS score was 12 and whose diagnoses included weakness, age-related osteoporosis without current pathological fracture, and chronic kidney disease stage 3, was observed with morning calcium/vitamin D/vitamin K blister packs labeled differently than the physician’s order in the EMR. The CMA acknowledged the mismatch between the blister pack label and the order, and the DON confirmed the label was incorrect.
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