Our organization is looking to move all doses of cefazolin, ceftriaxone, and cefepime to IVP. While this may work from a clinical and financial perspective, I'm concerned about the risks associated with moving from commercially-available products to pharmacy-compounded syringes (risk of error, contamination, expired product management, etc.).
Has any other large hospital or health system moved forward with this conversion and have some "lessons learned" to share with us? Thank you in advance!
Michele
michele.holley@mchs.com