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Historically, a
physician’s order has been required to convert non-formulary
histamine-type 2 (H-2) antagonist agents and proton proton pump
inhibitors (PPIs) to famotidine and pantoprazole, respectively, as well
as to change from the intravenous (IV) to oral (PO) route when
appropriate. According to two initiatives approved by the Pharmacy and
Therapeutics (P&T) Committee, these steps are no longer necessary. These
initiatives maintain famotidine as the exclusive formulary H-2
antagonist and pantoprazole as the proton pump inhibitor. Orders for H-2
antagonists will be automatically converted to famotidine; orders for
PPIs will be converted to pantoprazole. Pharmacy may initiate an
intravenous to oral conversion of these dosage forms. The aim of these
initiatives is to streamline the provision of quality, cost-effective
patient care. Automatic Therapeutic Interchange This
pharmacy-based initiative allows for the interchange of non-formulary H2
antagonists and proton pump inhibitors. Each order for these agents will
be converted to therapeutically equivalent doses. This applies to both
the intravenous (IV) and the oral (PO) routes of administration.
Documentation of this interchange will be made in the medication
administration record (MAR). The roles of each health care
professional are detailed below. · Convert order to the proper dose and route of famotidine or pantoprazole. · Document the conversion in the notes field of the MAR. Nurses · Identify the conversion to formulary agent in the notes field on the MAR. Physicians · Physicians are encouraged to prescribe the formulary agent initially. IV to PO Conversion This pharmacy-based initiative allows for the conversion of IV famotidine or pantoprazole to the oral dosage form when: · The patient has a functioning GI tract, defined as tolerating tube feeds at 40 ml/hr or 1000 ml/day of fluids by the enteral/PO route; AND · The patient is tolerating other oral medications. Both criteria must be met before a patient qualifies for conversion to PO therapy. Documentation of this conversion will be made in the progress notes and orders section of the medical record. The roles of each health care professional are detailed below. Pharmacy · A list of patients on IV famotidine or pantoprazole will be generated each day for review. Each patient on the list will be assessed for possible conversion according to the criteria described above. · Eligible patients will be converted to PO agents. · For each patient converted under this policy, there will be documentation in the progress notes of the medical record. A verbal order will be written by the pharmacist as "IV to PO conversion per P&T Committee/ [Pharmacist’s Signature]". Nursing
Physicians
Table 1. Proton Pump Inhibitor Therapeutic Interchange
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Product Ordered |
Pantoprazole Conversion |
Nexium® |
PO/PT |
Esomeprazole 20 mg qday |
40 mg qday |
|
Esomeprazole 40 mg qday |
40 mg qday |
|
Esomeprazole 20 mg bid |
40 mg qday |
|
Esomeprazole >40 mg qday |
Clarify with physician |
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Prevacid® |
PO/PT |
|
Lansoprazole 15 mg qday |
40 mg qday |
|
Lansoprazole 30 mg qday |
40 mg qday |
Lansoprazole 15 mg bid |
40 mg qday |
|
Lansoprazole >30 mg qday |
Clarify with physician |
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Prilosec® |
PO/PT |
Omeprazole 20 mg qday |
40 mg qday |
|
Omeprazole 40 mg qday |
40 mg qday |
|
Omeprazole 20 mg bid |
40 mg qday |
|
Omeprazole >40 mg qday |
Clarify with physician |
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Aciphex® |
PO/PT |
|
Rabeprazole 20 mg qday |
40 mg qday |
Table 2. Famotidine Dosage Recommendations
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Oral Administration - Adults |
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| Duodenal or gastric ulcer |
40 mg qhs |
| GERD |
20 mg bid |
| Stress ulcer prophylaxis |
20 mg bid |
| Hypersecretory conditions |
20 mg q6h, may increase to 160 mg q6h |
| CrCl <50 ml/min |
20 mg qday OR 40 mg q48h |
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IV Administration - Adults |
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| Adequate renal function |
20 mg q12h |
| CrCl <50 ml/min |
20 mg qday |
_________________________________________________________________________________________________________
Approved by P&T
Committee: 12/05
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Posted on: 12/30/05
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For Internal University of Kentucky Chandler Medical Center Use Only
Comments to
Ann Hamlin,
Last Modified:
August 13, 2006
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