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Presentation Outline ICHP Annual Meeting September 13-15

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Background<br />

• Lack of comprehensive published guidelines<br />

– Available recommendations:<br />

• Multidisciplinary teams<br />

• Monitoring in operating rooms<br />

• Investigative process<br />

• Drug diversion software<br />

• Intervention process<br />

O’Neal B, Siegel J. Diversion in the Pharmacy. Hosp Pharm. 2007;42(2):145-148<br />

Siegel J, Wierwille C, O’neal B. The Investigative Process. Hosp Pharm. 2007:42(2);466469<br />

Siegel J, O’Neal B. Code N: Multidisciplinary Approach to Proactive Drug Diversion Prevention. Hosp<br />

Pharm. 2007:42(2);244-248<br />

Project Objectives<br />

• Primary:<br />

– Develop and implement a standardized process to<br />

identify users with risk of controlled substance<br />

diversion<br />

Monthly<br />

Report<br />

Methods<br />

•Pharmacist to upload monthly ADM data to vendor<br />

•Pharmacist organizes vendor report to identify high risk users<br />

•Pharmacist prints controlled substance removals from previous 30<br />

days for identified users<br />

UUser AAudit di • NNurse Manager M audits di transactions i for f appropriate i ddocumentation i<br />

Follow Up<br />

•Users with potential diversion episodes are assessed by pharmacist<br />

and nurse manager for further diversion risks<br />

Background<br />

• University Health System Consortium Survey<br />

– Operating Room Practices: 44‐63% reconciled<br />

against dispensing records<br />

– Use of diversion software: 79%<br />

• “Sometimes” or “Always” investigate flagged individuals<br />

identified by software: 88‐99%<br />

– Discrepancies “always” investigated: 92‐98%<br />

McClure SR, O’Neal BC, Grauer D, Couldry RJ, King AR. Compliance with Recommendations for<br />

Prevention and Detection of Controlled-substance Diversion in Hospitals. Am J Health-Syst Pharm.<br />

2011;68(8):689-94.<br />

Project Objectives<br />

• Secondary:<br />

– Quantify potential controlled substance diversion<br />

opportunities in users with identified risk of<br />

controlled substance diversion<br />

– Assess the type of controlled substance<br />

discrepancies occurring based on controlled<br />

substance documentation<br />

Methods: Identifying Users<br />

Report 1: Compares removals of all controlled substances<br />

by one user to all users<br />

Report 2: Compares all removals of given controlled<br />

substance by one user to all users of same ADM<br />

Report 3: Compares removals of given<br />

controlled substance by one user to all<br />

users of that class/medication<br />

Report 4: Compares daily average removals<br />

for one user for<br />

given controlled substance<br />

to all users of same<br />

ADM<br />

8/29/2012<br />

2

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