Medication Safety: The Important Role of Pharmacy Technicians



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Medication Safety: The Important Role of Pharmacy Technicians CAPT - Alberta Pharmacy Technician Conference 2004 Sheraton Cavalier Hotel Calgary, Alberta September 11, 2004 David U President & CEO, ISMP Canada

Agenda ISMP Canada s s vision, mission and programs How safe is our healthcare system? Needs Cultural changes Pharmacy related errors/issues Pharmacy Technicians role Human Factors Engineering and Environmental Factors Regulated Pharmacy Technician issues

ISMP Canada Vision Independent nonprofit organization Established for the collection & analysis of medication error reports and the development of recommendations for the enhancement of patient safety Intends to serve as a national resource for promoting safe medication practices throughout the healthcare community in Canada

Mission Committed to the safe use of medication through improvement in drug distribution, naming, packaging, labeling, computer program design and drug delivery system design. Collaborate with healthcare practitioners and institutions, schools, professional organizations, pharmaceutical industry and regulatory & government agencies to provide education about adverse drug events and their prevention

Voluntary Practitioner Error Reporting System A voluntary, non-punitive reporting stimulates participation in reporting programs Front-line practitioners provide detailed, unrestricted information on incidents Errors, near-misses and hazardous situations Provides expert analysis, disseminates high- leverage safety strategies effectively

ISMP Recent Projects CMIRPS partner Systems Analysis of Medication Errors (SAME) Ontario medication error database Safe Medication Support Service Potassium Chloride Opiate Narcotics Infusion Pump Survey

Programs Medication errors and near-misses reports Analysis and Recommendation for prevention strategies Publication and distribution of Medication Safety Alert Newsletters Application of the Analyze-Err program Application of the Medication Safety Self Assessment (A QA tool)

Canadian Collaboratives CMIRPS CCHSA CPSI Provincial Ontario Manitoba Saskatchewan Nova Scotia British Columbia Alberta

Medication Safety Alerts Newsletters Monthly newsletters on safe medication practices and special alerts Format similar to ISMP Medication Safety Alert! newsletters Distributed to healthcare institutions, community practice, practitioners and professional organizations By subscription

Medication Safety Self Assessment (Community version) Developed by ISMP Implemented by over 1300 hospitals in US Derived from years of experience from analysis of medication errors reported Adapted to Canadian version Ready to be launched in Canadian hospitals

How Safe Is Health Care? Harvard Medical Practice Study found adverse events occurred in 3.7% of hospitalizations; Australian study found 16.6% of hospital admissions were associated with an adverse event 5% of these patients died IOM Report in US estimates 44,000 to 98,000 deaths yearly due to error

Incidence From Other Chart Review Studies Country Australia N Charts 14,000 Year 1995 Incidence of AE 16.6% Preventable? 51% USA (Utah( & Colorado) 15,000 2000 2.9% -- England 1014 2001 11.7% 50% New Zealand Denmark 1326 1097 2001 2001 10.7% 9.0% 71.8% 40.4%

Canadian Study CIHI and CIHR joint Study Retrospective chart review study on ADEs Applying the Australian study using predefined triggers Hospitals in 5 provinces Results published on May 25, 2004

The Canadian Study Study Goals To identify the incidence of adverse events in a sample of Canadian hospitals To compare the incidence between medical and surgical patients and between different types of hospitals To compare the incidence to results from similar studies in England, Australia, New Zealand and elsewhere To compare results from chart based review obtained from administrative data and hospital incident reporting systems

Canadian Adverse Events Study Based on methods used in the Harvard Medical Practice Study These methods have been further developed in studies in the Australia and UK Uses chart reviews of hospital records to identify adverse events and assess whether these events might be prevented

Canadian Study (results) 7.5% AE (1 in 13 hospitalizations) 37 % preventable App. 45% involved surgical events App. 25% involved drugs and fluids

Why Medication Safety? One of the leading causes of adverse events in many studies High visibility and high cost Many key technology and information management strategies are already developed

Research Highlights Boston hospitals 1997 (Bates et al) additional length of stay for preventable ADE = 4.6 days increase in cost for preventable ADE = $5857 cost for preventable ADE in 700-bed teaching hospital = $2.8 million

Annual Projections per Hospital (US data) 6,000,000 medication orders 300,000 medication errors 1900 ADEs 530 preventable ADEs 1370 non-preventable ADEs 1600 potential ADEs

Another Canadian Study Adverse events among medical patients after discharge from hospital by Alan Forster 328 patients: 76 experienced AE (23%) Most common AEs are ADEs (72%)

Incidence and Severity of Adverse Events after Discharge 400 medical inpatients Adverse event rate 19% 6% preventable 48% of ADEs resulting in at least non-permanent disability preventable 6% ameliorable Of adverse events 66% were ADEs 17% procedure-related related Forster et al, Ann Intern Med, 2003

Pre-hospitalized AE Study (Forster) 502 adult patients in Ottawa Hospital 64 adverse events (12.7%) One third deemed preventable Most events due to Drug Treatment 25 after admission; 39 pre-hospitalized Safety must be addressed in ambulatory care front

ISMP Canada Ontario Medication Error Study Ontario MOHLTC funded study Prospective medication errors tracking Analyze-ERR software program Data on errors/near misses and root causes 14 hospitals in Ontario / 12 months data collection Over 4,600 records

Ontario Medication Error Study (continued) Type of error Outcome description Severity Code Drug s s therapeutic classification Stages when error occurs Time of the day of error Age and gender of patient Program/service where error occur

Relationships Between Med Errors, Potential ADEs and ADEs Medication Errors Pot ADEs Preventable ADEs Non- Preventable ADEs (ADRs)

Error Stage for Preventable ADEs and PADEs (n=264) Admin 26% Dispensing 14% Transcrip 11% Ordering 49%

Sharp End, Blunt End Error investigations always concentrate on sharp end (front line staff) where patient/caregiver interaction occurs Contributing factors and latent errors often originate at the blunt end where organizational policies, procedures and resource allocation decisions are made

Latent (Blunt( End) ) Failures Incomplete information about the patient Unclear communication of drug order Lack of unit dose system Lack of independent check before dispensing Lack of computer warning about excessive dose Ambiguous drug references Conflicting requirements for staff competency to prescribe Warning not placed prominently on syringe

Culture Change Provide leadership Job design: avoid reliance on memory, simplification and standardization (dispel the belief that healthcare workers are perfect) Promote effective team functioning Anticipate the unexpected; design for recovery Create a learning environment Dispel the fear of litigation and discovery

Shared Accountability Sharp End Error detection and reporting Seek out errors and voluntarily report them Speak out about patient safety issues Share personal knowledge of what went wrong Recommend error reduction strategies Error reduction efforts Facilitate implementation of system-based error reduction strategies

Shared Accountability Sharp End Safe professional practice habits Follow the safety literature Seek out education to maintain competencies Willingness to change practices Ask for help when needed Value teamwork Support colleagues

Shared Accountability Blunt End Position patient safety as job one Promote and reward error detection and reporting Communicate directly with staff Safety enhancements Discuss mission, vision, values, strategic goals Learn about the barriers to safe practice

Shared Accountability Blunt End Establish safe workloads Support system enhancements as recommended by front-line Lead proactive improvement efforts Require periodic self assessment of safety Engage the community in patient safety

Medication Errors A New Way of Thinking FROM: Who did it? Punishment Errors are rare Physicians don t participate Add more layers Calculating error rates TO: What allowed it? Thank you! Errors are everywhere Physicians, RNs, RPh, QA/ RM involved Simplify/standardize No thresholds

Emphasis on Multi-factorial Nature of Errors Assume that slips, lapses and mistakes are inevitable Many factors, latent and active, must be present and in proper alignment for error to occur Emphasis on redesign of system to make it more difficult to err

Errors Involved in Dispensing Stage Wrong patient Wrong drug(s) Wrong dose Wrong route Wrong frequency Missing drug/dose Drugs given without an order Incorrect labeling

Opportunities for Mishaps Prepackaging Manual unit dose filling Point of Care dispensing cabinets Robot and ATC dispensing Floor stock I.V. Admixture/TPN Chemotherapy preparation

Rank Order of Error Reduction Strategies Forcing functions and constraints Automation and computerization Simplify and standardize Reminders, check lists and double check systems Rules and policies Education Information Punishment (no value)

Changes Needed to Improve Medication Use Process Computerization of medication use process Use of machine readable codes for most administered medications More consumer involvement in medication safety Improved access to drug information, error alerts in monographs, electronic reminders

Primary Principles in Error Reduction Reduce or Eliminate the Possibility of Errors Failure mode analysis Root cause analysis System redesign Make Errors Visible computer alerts warnings/reminders double check systems triggers (markers)

Most Frequent Serious Error Types Insulin Free flow IV pumps PCA devices Parenteral narcotics Lidocaine Cancer chemotherapy Neuromuscular blockers Conscious sedation Concentrated electrolytes (potassium, magnesium, phosphate)

High Alert Medications Adrenergic agonists Intravenous adrenergic antagonists Amiodarone & amrinone Benzodiazepines (primarily midazolam) Intravenous calcium Chemotherapeutic agents Chloral hydrate liquid in pediatrics Intravenous digoxin Dopamine & dobutamine Heparin (intravenous) and warfarin Insulin Lidocaine Intravenous magnesium sulfate Opiate narcotics Neuromuscular blocking agents Intravenous potassium phosphate & potassium choride Intravenous sodium chloride, high concentrations Theophylline

Safe Practice Recommendations for Automated Dispensing Units Minimize drug supply and stock drugs in unit dose, smallest dose/container size, single concentration Establish maximum dose range for high alert medications Educate staff to remove single selected dose only. Returns to pharmacy, not dispensing unit Adequate check system to assure accurate restocking Allergy reminders for specific drugs on appropriate storage pockets or drawers

Drug Labeling, Packaging and Nomenclature Unclear manufacturer labeling and packaging Similar drug names, packaging or labeling Unlabeled syringes prepared by staff Computer-generated labels difficult to read

Drug Storage, Stock and Distribution Consistent brands/strengths Bins and stock organization Returned medication Expired medication Unit dose packaging and dispensing Traditional dispensing and wardstock Chemotherapy preparation I.V. admixture

Confirmation Bias It leads one to see information that confirms our expectation rather than to see information that contradict our expectation.

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Pharmacy Technicians Key Roles Participate in Safe Medication Practice Committee Open communication with colleagues Be vigilant on questionable orders Be alert on high risk drugs: purchase labeling dispensing

Pharmacy Technicians Key Roles Update on new technologies bar-coding point-of of-care dispensing cabinet wireless hand-held held scanner Robot/ATC COPE and Pharmacy computer system

Emerging Issues New Treatments New Drugs New Technologies Privacy Issues Patient Safety Changing roles

Challenges and Barriers Political and economic factors Education to keep up Certification principle and practice Patient/clients centre care Increasing workload

Staff Competency & Education Competency validation Certification process Staff development New and unfamiliar drugs Orientation process Asking questions and challenging pharmacist

Environmental Factors Workload issue Staff morale issue Air circulation, lighting, noise and space Workflow Interruptions Employee safety

Quality Processes & Risk Management QA audit on unit dose bin fill QA audit on i.v. admixture Perform independent checks High risk drugs and high risk patient population

Independent Checking Keep prescription, label, and medication container together Verify prescriptions prepared by technicians Calculations Standard concentrations Automated compounding equipment Davis NM. American Pharmacy 1994; NS 34: 22-23. Cohen MR. Medication Errors. Causes, Prevention, and Risk Management; 9.1-11.19.

Independent Checking: Does it work? Two practitioners going through the same calculation or reading the same labels not exactly independent System induced errors hard to check Need proper training Double check on high alert drugs Double check on high risk patients

Human Factors Engineering 101 HFE: a discipline concerned with design of systems, tools, processes, machines that take into account human capabilities, limitations, and characteristics HFE = Ergonomics = usability engineering = user centered design

Human Factors - Guiding Principle Fit the task or tool to the human, not the other way around

Goals of Process Design Minimize additional work/tasks Provide relevant info needed to get job done Provide suitable work area to get job done

Goals of Tool Design Simple, concise, natural language & familiar terms Logical layout of info Located close to where task is carried out (minimize working memory) Easily identifiable as reference (should not require reading) Provides enough info and detail for new user Provides quick shortcuts for familiar users

Some Human Factors Themes Working Memory / Workload / Task Demands time pressure, cognitive demands, stress, information overload, multi-tasking tasking Task Flow / Information flow Confirmation Bias or Cognitive Tunnel Vision Repetition, Fatigue, Sleep Deprivation Interface Design (order forms, drug packages & labels, etc.) High Noise-to to-signal Ratio (information overload) Work Area Design & Environmental Factors (lighting, noise, distractions)

Human Factors Engineering (HFE) Medical devices such as infusion pumps Computer software design Point of care dispensing cabinets Labeling and packaging of pharmaceuticals Distribution system Protocols/Policies and Procedures

Environmental Factors Work pace Illumination Noise, Interruptions Staffing

Organization Dynamics Cultural issues Supervisory practices Organization support

Personal Qualities Demeanor Patience Ability to manager stress Interpersonal relationship

What is Happening in Alberta Interests expressed in part of regulated health professional A need for Defining standards of practice Introducing code of Ethics Ensuring competency

www.ismp-canada.org