Outpatient Surgery Magazine - Subscribers

Thumbs Up on Safety Scalpels - Outpatient Surgery Magazine - May 2019

Outpatient Surgery Magazine, providing current information on Surgical Services, Surgical Facility Administration, Outpatient Surgery News and Trends, OR Excellence and more.

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It takes a village Physicians will always err. It's up to other healthcare professionals to serve as checks and balances to help prevent patient harm. When a physician orders a medication for a procedure, whomever at the facili- ty orders the drug should review the order before delivering the med- ication to the point of care or to the automated dispensing system. Again, the FDA's label change for Kenalog had been in place for 2 years before the woman's incident, so someone at the facility had a duty to protect the patient — and all back pain patients at the center — by alerting ordering physicians about the potential risks of Kenalog for ESI, and perhaps even restricting it from the facility's formulary. The patient's nurse also had a responsibility to the patient in terms of the 5 rights of medication administration: right patient, right drug, right dose, right route and right time. Most surgical facilities specialize in a limited array of procedures, so nurses routinely become familiar with various procedures and associated perioperative medications. Nurses often witness or play a role in informed consent, so they had an additional opportunity to prevent the use of Kenalog by ensuring that the patient understood what was going to happen. If the nursing team wasn't familiar with Kenalog, then it was their responsibility to educate themselves so they could advocate for the patient and ensure the 5 rights. In the Colorado case, that would have afforded another opportunity to confer with the pharmacist and order- ing physician to avoid a catastrophic error. The surgery center itself also had an administrative duty because it employed the nursing and pharmacy teams, and should have been aware that Kenalog was routinely purchased and administered for epidural injections despite explicit FDA and manufacturer warnings. Medical Malpractice MM 3 0 • O U T PA T I E N T S U R G E R Y M A G A Z I N E • M A Y 2 0 1 9

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