S.P.A.N.C.

This blog is meant to be a place for Sunnybrook Peri-Anesthesia Nurses (Pre-Admission Centre, Same Day Surgery, Post Anesthetic Are Unit and Surgical Short Stay Unit) to stay in communication with each other and to be up-to-date with concerns regarding the Peri-Anesthesia Department. The Purpose of S.P.A.N.C is •To re-implement a unit based council •to identify the unique role of the Peri-anesthesia nurse and to help staff from other areas understand what it is that we do •to create a collegial atmosphere for sharing our professional experiences within the subgroups of Peri-anesthesia •to facilitate open discussion and priority of issues relating to professional practice, education and research that impact on the quality of our work life and thereby affect positive outcomes for our patients and their families.

Wednesday, July 22, 2009

Automated Dispensing Cabinets

We are currently working with pharmacy to get the McKessin cabinets up and running. I found this article on Medscape and thought I would share it on the blog. Happy reading!

From Topics in Advanced Practice Nursing eJournal > Commentary
Automated Dispensing Cabinets: Getting It Right in the Age of Automation
Barbara L. Olson, MS, RN-BC, FISMP


Just as the brand name Kleenex® is commonly used for facial tissues, automated dispensing cabinets (ADCs) are often recognized by manufacturer or product names such as AcuDose®, Omnicell®, and Pyxis®. Currently, 83% of US hospitals report that they use ADCs, indicating widespread acceptance of touchscreen-activated drug storage vaults.[1] Generally welcome additions to busy clinical settings, ADCs provide ready availability of medications (a key component of acute care) while streamlining the process of drug charging.
But ADCs are more than automated teller machines for drugs. These unit-based medication repositories incorporate sophisticated software and electronic interfaces to synthesize high-risk steps in the medication use process. Today's cabinets reflect design advances as well as an appreciation for how specific technologies, such as barcode scanning and clinical decision support, can improve medication safety. Over the years, ADCs have been adapted to facilitate compliance with emerging regulatory requirements such as pharmacy review of medication orders and safe practice recommendations.


Promoting Medication Safety
The "5 rights" of medication administration, a set of objectives well-known to nurses and other frontline clinicians, are often used to describe medication safety goals. When used to their greatest potential, ADCs can increase the reliability of the "5 rights": the right drug, the right dose, the right patient, the right route, and the right time. The mirror image of each medication right is a wrong -- wrong drug, wrong dose, wrong patient, wrong route, and wrong time -- representing a risk point that a strong system design can help to avert.
However, sophisticated, accessible drug storage systems alone do not guarantee safety. Selection, design, implementation, and monitoring of ADCs are also important to mitigate the risk associated with medication use.
In 2008, the Institute for Safe Medication Practices published Guidance on the Interdisciplinary Safe Use of Automated Dispensing Cabinets to help organizations and individuals understand and adopt practices that maximize the safety of ADCs.
[2] Twelve distinct core processes that promote safest practices and secure handling of drugs are addressed in this document. While these guidelines do not represent standards of care, they do provide organizations and frontline users with measures for each stage of ADC implementation, from deciding how the technology will be used to staff education and long-term monitoring.
The ISMP guidance document, coupled with other relevant literature and reports of error and near-miss events associated with ADC use, inform the recommendations provided below. These quick-read recommendations are by no means inclusive, but may serve to bridge understanding between executive decision makers, medication safety experts, and frontline clinicians during high-stakes decision processes that involve resource allocation, work-flow, and patient safety. Teams charged with ADC implementation or re-evaluation as well as those interested in defining pharmacy-specific processes to enhance ADC safety are advised to consult ISMP's complete document.
[2]

Wrong Drug/Wrong Dose Errors
Wrong drug and wrong dose errors are the most common errors associated with ADC use. Look-alike drug names and drug packages are variables that can lead to wrong-drug/wrong-container selection errors. Morphine and hydromorphone (Dilaudid®), for example, are 2 different opioid analgesics that top the list of the most frequently confused drugs.
[3] Alprazolam and lorazepam are another pair of look-alike, sound-alike drugs that are frequently confused.
Environmental factors (such as distraction and lighting) influence how well humans perform tasks involving product selection. Patient information at the point of dispensing, such as allergies and potential contraindications, allow a final cognitive check (matching prescribed drug, dispensed drug, and indication for use) to occur.
Consider this comment, made by a seasoned nurse who responded to a post entitled
"Meds & Mindfulness" on Medscape's On Your Meds blog in April 2009:
I have been an RN since 1974 and have worked in many settings. I am currently on a geriatric psychiatric unit and I just wanted to share that my morning med pass is just about the most unnerving thing I have ever done. The area where 2 of us prepare our meds is a small hallway through which people must pass to reach our unit tube system. Folks squeeze by often as we work. On the other end of our small area is our Pixis (sic) machine, which the pharmacy tech comes to stock during the time we are setting up our meds...... Interruption is the name of the game.
This nurse's observations highlight several of the well-known risk points in the medication use process that contribute to wrong drug/wrong dose errors.


Recommendations to Prevent Wrong Drug/Wrong Dose Errors With Automated Dispensing Cabinet Use
System Level Recommendations
System-level considerations that may diminish the risk of wrong drug and wrong dose errors when drugs are retrieved from ADCs include:
-Evaluate unit geography when planning for ADC installation or upgrades;
Minimize the potential for ADC users who stock and remove drugs, to be distracted while working at the ADC;
-Match ADC stock to unit needs meticulously, using unit-dose packaging whenever possible. Overstocking medications predisposes to wrong-dose errors, specifically overdoses, while stocking drugs that are not routinely used predisposes to wrong drug errors;
-Store drugs with look-alike, sound-alike names in different locations within ADCs. Consult published lists such as the
ISMP's list of frequently confused drug names to determine which medications stored in each of the facility's ADCs pose the greatest potential to be mixed up in the selection process;
-Examine interdisciplinary workflow issues and eliminate scheduling conflicts so that routine drug stocking and retrieval activities do not overlap;
-Establish procedures for medication administration that avoid distractions related to other duties, especially in settings where nurses care for multiple patients.
[4,5] Drug selection is a high-stakes activity, one that may be compared to safety-sensitive tasks that occur during pre-flight activities in the aviation industry. System leaders should evaluate expectations, especially those that involve multi-tasking, to ensure that staff members are not routinely disrupted at high-stakes junctures in medication administration. (If you wouldn't want the captain of your airliner to greet passengers while simultaneously performing pre-flight checks, you should advocate for processes that allow nurse to similar attention to detail during drug selection);
-Maximize the use of barcode technology with ADCs to make sure that the correct products (intended drug in the correct dose units or container size) are stocked in each clinical setting.
[6] Bar-code product verification at point of retrieval (or point of administration) further diminishes the likelihood of wrong drug or wrong dose errors. When barcode verification is not possible, high alert drugs should be verified both by the person stocking the ADC and a unit-based nurse;
-Ensure that patient medication administration records (MAR) are accessible to practitioners while they are removing medications from an ADC. To make this a practice norm, select workstations that can be positioned near the ADC. When purchasing hardware (such as wheeled workstations), weigh cost-benefits of integrated patient information repositories in light of nursing time and patient safety. (The process used to deliver food to your table at the average chain restaurant should not be more reliable -- and less cumbersome -- than the process used to bring ordered medications to your bedside in a community hospital);
-The ADC should display drug information in a nonambiguous fashion, matching information provided on the MAR;
-Require pharmacy review of medication orders (which includes measures such as checking the order against known allergies; reviewing appropriateness of the prescribed dose; and evaluating potential for drug-drug interactions) prior to removal of medications, except in emergency situations.
[6] Once pharmacy review has occurred, a readily identifiable flag/symbol should signal "go" to frontline clinicians;
-Use computerized alerts, ideally pop-ups that require a confirmation, when medications with high potential for mix-up (look-alike, sound-alike medications) in a given setting are selected. Bring the possibility of drug product confusion to the attention of the clinician at the point of retrieval, especially for other high alert drugs that have look-alike, sound-like qualities. For example, to minimize morphine and hydromorphone confusion risk, the ADC screen may prompt, "This is DILAUDID. Is that correct?" whenever hydromorphone is selected
[7];
-Monitor how well ADCs, as configured, support care goals established by frontline providers and expected by patients and other stakeholders. This may be accomplished through proactive order set/clinical pathway review and retrospective review of medication overrides. Investigate causes of ADC overrides, considering the possibility of production pressure, especially in settings where turnover goals may compete with meticulous adherence to safest medication practices;
-Teach front line clinicians, especially those who participate in unit-based practice councils and multidisciplinary committees, the principles that inform safest use of ADCs, especially those that relate to medication stocking and availability. Solicit their input proactively to prepare for anticipated practice changes involving medication use and medication storage;
-Consider providing unit-based practice councils and multidisciplinary teams in specialty units to review ADC metrics (such as results of override reports). With this knowledge, it will be possible to identify deviations from targeted benchmarks, identify barriers to compliance, and champion safest practices;
-Ensure that knowledge of high alert medications and look-alike/sound-alike drugs (particular to a given clinical setting) are included in orientation and initial competency validation measures of individuals who dispense, stock, or administer medications; and
-Create a culture in which concerns voiced by frontline clinicians are seen as valuable. Develop a visible "rapid response" when ADC near-misses or discrepancies are reported.


Individual Level Recommendations
Considerations for individuals that may diminish the risk of wrong drug and wrong dose errors when drugs are retrieved from ADCs include:
-Recognize that medication retrieval from ADCs is a high-risk activity, one in which human error has the potential to cause irreparable harm;
-Utilize bar-code scanning to the fullest extent possible in your practice setting. Report barriers to compliance immediately, using system-wide, near-miss reporting systems. For example, if barcode scanning is prevented by mechanical failures, battery life, or the availability of scanning equipment during high volume medication administration times -- these are reportable events;
-Upon removal of a drug from an ADC, validate that the drug name on the label of the drug-in-hand matches the drug name displayed on the patient's MAR (or prescriber's order if MAR has not been generated);
-Validate that the drug-in-hand is the ordered concentration, dose, and dosage form;
Be suspicious of any dose that would require removal of more than 3 packages/ampules/vials to administer a single dose;
-Avoid excessive use of the override function; it should be limited to true emergencies;
-Be aware that distractions undermine performance. Reduce distractions within your control when you are removing medications from ADCs. Although duties related to medication administration occupy a significant amount of nursing time, accurate performance cannot be assured simply because tasks are familiar. For example, answering cell phones while performing high-stakes activities impairs accuracy. Social exchanges with colleagues, patients, and family members should not occur at the ADC;
-Advocate for practice models that promote the least amount of distraction during medication preparation and administration. If multi-tasking while accessing medications from an ADC is a performance expectation, use professional practice councils and near-miss reporting systems to call attention to this risk;
-Become familiar with the rationale behind the system-level interventions (listed above) that promote safest use of ADCs; and
-Report deviations from ideal or standard practices as near-misses. This may seem "picky," but having a highly reliable medication use system involves meticulous attention to detail, something which requires a high degree of standardization. A system that has to undergo individual interpretation to accomplish routine tasks -- like a 9:00 am medication pass -- is error-prone. Fixing a system is difficult, but possible (in a way that fixing a lethal wrong-drug medication error is not). Here are a few things worth reporting when you notice them: A discrepancy between the way the drug name is displayed on the MAR and on the ADC screen; for example, when tall-man letters used to differentiate a known look-alike, sound-alike drug pair throughout your organization are not used on the pick list of your ADC screen; or when you find a syringe labeled "hydromorphone" in a bin labeled "morphine."


Summing Up: Seeing Beyond "The Box"
ADCs, particularly when they interface with computerized redundancies such as bar-coding and electronic MARS, give front line clinicians powerful tools to deliver reliable results. But reaping the benefits of technology involves more than selecting "the best box."
Knowledge of how automated dispensing cabinets are used by clinicians is essential for realizing the potential of these devices to improve safety, just as they have improved efficiency and charge capture for medications. Individual performance is one aspect of medication safety: how individuals perform is affected by the knowledge and competency each brings to the task at hand along with personal practice habits and choices under each individual's control. But key elements of performance are also influenced by the system in which care is delivered and by factors controlled at the organizational level.
To maximize the benefits of ADCs, organizations should identify and manage risk points that predictably occur when humans, often busy and working under stress, interface with machines to deliver high-stakes therapies. Interdisciplinary guidance, such as those published by ISMP, identify these risk-points and recommend risk-reduction strategies, enabling organizations to align work-flow and performance expectations so that the safety benefits of ADCs are fully realized.

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