IV Admixture Automation Previous State › As IV compounding became more prevalent in the hospital pharmacy environment. More staff resources were needed to perform IV admixtures. – These activities are highly repetitive and create a large workload for staff. – Documentation of each step of the compounding process required manual checks and calculations by both the pharmacy technician and the pharmacist. – Paper compounding logs and documentation of IV admixtures was a tedious process and was not conducive to audit reporting. – A new decentralized pharmacist workflow limited the availability of staff to check products being prepared in central pharmacy. Phase 1 - Doseedge › The decision was made to install an IV workflow manager which allowed for documentation of the IV admixture process from start to finish via camera technology. › This allowed the pharmacist to validated the process remotely while logging important regulatory information along the way. › It also automated the calculations necessary and enabled bar code validation of products which helped reduce costly mistakes and miscalculations. Phase 2 – Outsourcing › Despite having technology to streamline the IV compounding process, our IV admixture volume was only increasing and we were seeing staff preparing product in batches at an increased volume. › The decision was made to outsource to a compounding pharmacy for standard doses of many medications. – These drugs, while expensive, have longer shelf lives(45-90 days vs 714 days) resulting in less waste and allowed us to pivot technicians and pharmacists to more value added tasks. Current State › With increasing regulations regarding USP797 and the coming USP800, we’re looking to minimize risk to both patients and workers while ensuring compliance with these regulations. – While outsourcing is crucial because increasing our production capacity is difficult while keeping staffing resources static, there are options available. › We’ve also seen delays and allocations from our outsourcing pharmacies recently as they struggle to meet demand. This has forced us to increase in house manufacturing without increasing staffing levels. Phase 3 – IV Automation Phase 3 – IV Automation › How do we bring back the manufacturing of premixed IVs to the hospital without straining tight staff resources and in a cost efficient manner? – We leverage our 340B and GPO purchasing power for raw ingredients which will in turn cover the cost of leasing the equipment. – We analyze our current waste of premixed products and show how we can get by with lower par levels of stock while still serving the hospital with the product it needs, when it needs it. Phase 3 – IV Automation(cont.) – Fact Sheet › Annual spend of approx. $330,000 on outsources premix products. › Analysis shows if we bring this back inhouse, our cost for ingredients would run around $76,000. – This leaves us with a delta of approx. $254,000. ServiceDescription 5 mg/mL Morphine Sulfate (Preservative Free) (Contains Sulfites) in 0.9% Sodium Chloride 50 mL in 60 cc Monoject Syringe 4% Sodium Citrate (Preservative Free) 3 mL in 5 mL BD Syringe No Overwrap 20 mg/mL Succinylcholine Chloride Injection (Preserved) 5 mL in 5 mL BD Syringe NDCNumber Latest Total Units Pharmedium Unit Total Pharmedium Est. Production cost Est. total Cost Savings with 2016 Price Price per unit [GPO/340b] production cost production % of Delta 61553-625-75 130 $ 10.32 $ 1,341.60 $ - 0.0% 61553-481-34 2208 $ 3.15 $ 6,955.20 $ - 0.0% 61553-357-33 2725 $ 19.39 $ 52,837.75 $ 0.05 $ 136.25 $ 52,701.50 21.8% 40 mcg/ml Phenylephrine HCl (Preservative Free) (Contains Sulfites) in 0.9% Sodium Chloride 10 mL in 10 mL BD Syringe 61553-312-65 3900 $ 5.01 $ 19,539.00 $ 0.13 $ 507.00 $ 19,032.00 7.9% 5 mg/mL Ephedrine Sulfate (Preservative Free) in 0.9% Sodium Chloride 5 mL in 5 mL BD Syringe 61553-301-33 3800 $ 38.21 $ 145,198.00 $ 12.54 $ 47,652.00 $ 97,546.00 40.4% 2 mcg/mL Fentanyl Citrate and 0.1% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride 250 mL in 250 mL Intravia Bag 61553-131-02 60 $ 23.14 $ 1,388.40 $ 5.07 $ 304.20 $ 1,084.20 0.4% 61553-123-48 545 $ 17.03 $ 9,281.35 $ 2.17 $ 1,182.65 $ 8,098.70 3.4% 61553-397-72 725 $ 25.70 $ 18,632.50 $ 3.92 $ 2,842.00 $ 15,790.50 6.5% 61553-149-78 130 $ 36.27 $ 4,715.10 $ 18.23 $ 2,369.90 $ 2,345.20 1.0% 61553-009-02 1104 $ 14.53 $ 16,041.12 $ 4.81 $ 5,310.24 $ 10,730.88 4.4% 61553-078-02 1128 $ 18.70 $ 21,093.60 $ 6.42 $ 7,241.76 $ 13,851.84 5.7% 61553-163-75 950 $ 10.34 $ 9,823.00 $ 1.25 $ 1,187.50 $ 8,635.50 3.6% 61553-167-75 1185 $ 14.95 $ 17,715.75 $ 6.23 $ 7,382.55 $ 10,333.20 4.3% 61553-498-39 285 $ 13.93 $ 3,970.05 $ - 61553-649-75 170 $ 8.83 $ 1,501.10 $ 71.40 2 mcg/mL Fentanyl Citrate and 0.1% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride 100 mL in 150 mL Intravia Bag 10 mg/mL Methohexital Sodium (Preservative Free) in Sterile Water for Injection 10 mL in 10 mL BD Syringe 10 mg/mL Methadone HCl Injection 1 mL in 3 mL BD Syringe 1.25 g Vancomycin HCl (Preservative Free) added to 0.9% Sodium Chloride Injection USP 250 mL in 250 mL Viaflex Bag 1.5 g Vancomycin HCl (Preservative Free) added to 0.9% Sodium Chloride Injection USP 250 mL in 250 mL Viaflex Bag 0.2 mg/mL HYDROmorphone HCl in 0.9% Sodium Chloride 50 mL in 60 cc Monoject Syringe 1 mg/mL HYDROmorphone HCl in 0.9% Sodium Chloride 50 mL in 60 cc Monoject Syringe 1 mg/mL Morphine Sulfate (Preservative Free) in 0.9% Sodium Chloride 100 mL in 150 mL Intravia Bag 1 mg/mL Morphine Sulfate in 0.9% Sodium Chloride 50 mL in 60 mL BD Syringe **Bold = 340b Pricing** Total $ 0.42 0.0% $ 1,429.70 Pharmedium Inhouse Difference $ $ $ 330,033.52 76,187.45 241,579.22 0.6% 100.0% Phase 3 – IV Automation(cont.) – Other Factors › Decreased reliance on compounding pharmacies isolates the institution from product allocations and some supply chain problems. › We now have complete control over the accuracy of compounding and have a very visible documentation process so we can more easily look for signs of variance should an adverse event occur. › We also have a mechanism to further comply with coming regulations as a result of USP 800 and have another means of isolating the compounding process as it relates to hazardous drug prep without costly physical construction.
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