Upon completion of this activity, the participant should be able to:



Similar documents
FMEA and FTA Analysis

Objective. Failure Modes & Effects Analysis: A U-500 Insulin Case Study. What is a FMEA? Assembling a Team. Steps to Conducting a FMEA 5/12/2011

Proactive Risk Assessment: Using FMEA in Healthcare. Shelly Jeffcott PhD Senior Research Fellow

FMEA Failure Risk Scoring Schemes

Strengthening Risk Evaluation and Mitigation Strategies (REMS) Through Systematic Analysis, Standardized Design, and Evidence-Based Assessment

ExCPT Certified Pharmacy Technician (CPhT) Detailed Test Plan* 100 scored items, 20 pretest items Exam time: 2 hours 10 minutes

Mona Osman MD, MPH, MBA

How To Prevent Medication Errors

The Massachusetts Coalition for the Prevention of Medical Errors. MHA Best Practice Recommendations to Reduce Medication Errors

Implementing an Evidence Based Hospital Discharge Process

Human Error and Safety Federal Aviation Human Error and Safety Administration Risk Analysis HESRA

Problem Management Overview HDI Capital Area Chapter September 16, 2009 Hugo Mendoza, Column Technologies

7/24/2015. Disclosure. Preventing Medication Errors in a Just Culture Environment. Blame Free Culture. Objectives.

Quality Risk Management Tools Quality Risk Management Tool Selection When to Select FMEA: QRM Tool Selection Matrix

Pathways for Medication Safety. Looking. Collectively. At Risk. A Partnership: American Hospital Association. Health Research and Educational Trust

High-Reliability Health Care: Getting There from Here

Types of Medical Errors Understanding Why Errors Happen Error Active Errors Placing a topical steroid on an active Herpetic epithelial keratitis

AHE 232 Introduction to Clinical Software. Week six:

RISK MANAGEMENT FOR INFRASTRUCTURE

Guidance for Industry: Quality Risk Management

Risk Assessment and Management. Allen L. Burgenson Manager, Regulatory Affairs Lonza Walkersville Inc.

How To Manage Risk

Application of Quality Risk Management to Pharmaceutical Operations. Eldon Henson, Vice President, Quality Operations

Beyond the Quick Fix: The Medical Director s Role in Quality Assurance Performance Improvement (QAPI) By: Jane Pederson, M.D.

Administrative Policies and Procedures for MOH hospitals /PHC Centers. TITLE: Organization & Management Of Medication Use APPLIES TO: Hospital-wide

Pharmacy Technician Structured Practical Training Program Logbook

ASPH Education Committee Master s Degree in Public Health Core Competency Development Project

The consensus of the Pharmacy Practice Model Summit Am J Health-Syst Pharm. 2011; 68: This list of the Pharmacy Practice

Edwin Lindsay Principal Consultant. Compliance Solutions (Life Sciences) Ltd, Tel: + 44 (0) elindsay@blueyonder.co.

Controlling Risks Risk Assessment

What Is Patient Safety?

ROOT CAUSE ANALYSIS (RCA)

Reducing Medical Errors with an Electronic Medical Records System

Risk Assessment & Enterprise Risk Management

Part 1 Overview of clinical governance Clinical governance the concept 1-3

ENTERPRISE RISK MANAGEMENT FRAMEWORK

SafetyFirst Alert. Errors in Transcribing and Administering Medications

Risk Management in Community Pharmacy

Fifteenth Annual ASHP Conference for Leaders in Health-System Pharmacy Implementing Medication-Use Systems: Meeting Stakeholders Requirements

The MPH. ability to. areas. program. planning, the following. Competencies: research. 4. Distinguish. among the for selection

CNA and NSO Risk Control Self-assessment Checklist for Nurse Practitioners 1. Self-assessment topic Yes No Actions needed to reduce risks

HIMSS Electronic Health Record Definitional Model Version 1.0

Risk and Quality Management Program Self-Assessment

Online MPH Program Supplemental Application Handbook

Concept Series Paper on Disease Management

Root Cause Analysis Concepts and Best Practices for IT Problem Managers

Hazard Identification and Risk Assessment for the Use of Booster Fans in Underground Coal Mines

Using RE-AIM to Assess a Medication Safety Intervention for Generalizability and Potential for Translation to Clinical Practice. David Magid, MD, MPH

Frequently Asked Questions

Nova Scotia EMO. Hazard Risk Vulnerability Assessment (HRVA) Model. Guidelines for Use. October, 2010

Focus on Pharmacy Management PHYSICIAN DISPENSING

Failure Modes and Effects Analysis (FMEA)

Journal of Business & Economics Research July 2008 Volume 6, Number 7

7Questions Toward. More Effective Workers Comp Programs. by Ron Skrocki. benefits magazine november 2014 MAGAZINE

The Systems Approach to Quality Assurance for Pharmacy Practice: A Framework for Mitigating Risk

Improving Medication Errors and Near Miss Reporting Without Spending Money. Jacob Thompson, PharmD, MS Associate Director of Pharmacy

Evaluating the impact of REMS on burden and patient access

3.4.4 Description of risk management plan Unofficial Translation Only the Thai version of the text is legally binding.

Staff should not feel that the Quality Management staff are policing them. These thoughts

APPENDIX I. Best Practices: Ten design Principles for Performance Management 1 1) Reflect your company's performance values.


Reliability Analysis A Tool Set for. Aron Brall

DISCHARGE FOCUS PUTS HOSPITAL CAPACITY ISSUE TO BED By Terry Maher, Healthcare Practice Leader, USC Consulting Group

SKF Asset Management Services. Your trusted resource for life cycle support and sustainability of physical assets

10/1/2015. National Library of Medicine definition of medical informatics:

A STRATIFIED APPROACH TO PATIENT SAFETY THROUGH HEALTH INFORMATION TECHNOLOGY

Quality Risk Management in Pharmaceutical Industry: A Review

Risk Management Primer

U.S. DEPARTMENT OF TRANSPORTATION FEDERAL AVIATION ADMINISTRATION. Air Traffic Organization Policy

Project Risk Management

Subcutaneous Insulin Audit Tool

Medication Errors. Prevention and Reduction Guidelines. Approved by PEIPB November 2004

POL ENTERPRISE RISK MANAGEMENT SC51. Executive Services Department BUSINESS UNIT: Executive Support Services SERVICE UNIT:

PLAN OF CORRECTION. Provider's Plan of Correction (Each corrective action must be cross-referenced to the appropriate deficiency.)

A To Do List to Improve Supply Chain Risk Management Capabilities

How To Improve Safety In The Nhs

A Risk Management Standard

Media fills Periodic performance qualification (Re-Validation)

MEDICATION ERRORS A CASE STUDY

Responsibilities of Public Health Departments to Control Tuberculosis

Pharmacy Leadership. Preceptors: Richmond, Michele; Gierhart, Kent; Hitzke, Ron

Improved Utilization of Self-Inspection Programs within the GMP Environment A Quality Risk Management Approach

Transcription:

The Utility of Root Cause Analysis and Failure Mode and Effects Analysis in the Hospital Setting Learning objectives: Upon completion of this activity, the participant should be able to: 1. Discuss the prevalence of medication errors in the United States; 2. Describe the utility of root cause analysis (RCA) in the health care setting; 3. Outline the steps involved in a failure mode and effects analysis (FMEA); 4. Summarize the benefits of drawing from a multidisciplinary team to complete patient safety evaluations; and 5. List 4 strategies that can be employed in the pharmacy to help reduce medication errors. Post-test/Rationale 1. According to IOM estimates, how many people die each year as a result of medication errors in the United States? A. 7000*** B. 98,000 C. 1.5 million D. 3.5 billion An estimated 98,000 people die every year as the result of preventable adverse events, and 7000 of these deaths are due to medication errors. 2. Which of the following statements is true regarding medication errors? A. Medication errors are usually the fault of a single individual or event B. Medication errors can occur at any stage of the medication-use process*** C. Medication errors only occur while a medication is in the control of a health care professional D. All of the above Correct Answer: B

Most medication errors are not the fault of a single individual or event, but, rather, are caused by professionals operating in a highly variable and complex system of health care delivery and medication use. Medication errors can be made during any step of the medication-use process and can occur when the medication is in the control of the health care professional, patient, or consumer. It is estimated that one-third of medication errors that occur in hospitals take place in the dispensing or administration phases. 3. Which of the following strategies strengthens the findings and recommendations of a root cause analysis? A. Implementing additional education for health care professionals after an error has occurred B. Gathering knowledge only from the individuals directly involved in a safety-related incident C. Excluding human factors from the investigation D. Supporting workplace transparency and learning across the organization*** Correct Answer: D Weak recommendations or improvement strategies undermine the utility of a root cause analysis. Education and new policies and procedures are considered weak interventions, as are repeating existing policies or confirming previous recommendations. RCA teams must investigate similar errors or incidents outside the system or in literature to learn from others experiences. Human error should be investigated to determine factors that influenced performance, such as task complexity, workflow, time availability, process design, experience, training, fatigue, and stress. Managers and administrators can encourage workplace transparency, sharing of concerns, and learning across the organization, which will support and empower all staff involved in patient care to make and sustain improvements in patient safety. 4. Which of the following pairs of statements is true regarding root cause analysis (RCA) and failure mode and effects analysis (FMEA)? A. RCA is a proactive approach to risk reduction and FMEA is a reactive approach to risk reduction B. RCA identifies sources of potential failure and FMEA identifies where processes have failed in the past C. RCA is conducted after an error occurs and FMEA can be conducted before a process is implemented*** D. RCA is a quantitative assessment of the severity, likelihood, and detectability of an error and FMEA is a qualitative assessment of latent system weaknesses

Correct Answer: C An RCA asks Why did the system fail in the past?, and an FMEA asks How could the system fail in the future? An RCA is conducted after an incident has occurred and FMEA is used to identify potential sources of before an incident occurs. FMEA quantifies the severity, likelihood, and detectability of potential failures to determine where change is needed. 5. Which of the following steps is essential to the application of an FMEA? A. Assembly of an appropriate team B. Develop a process map C. Conduct a risk or hazard analysis for each process and subprocess D. Develop an action plan and follow up on the actions taken E. All of the above*** Correct Answer: E For the best use in health care settings, an FMEA should include the following steps: Define the topic, Assemble a committed team, Develop a process map, Conduct a risk or hazard analysis for each process and subprocess, Develop an action plan and Follow up on the actions taken. 6. Which process would be identified as most in need of change on the basis of its criticality index (CI)? A. A process with a likelihood rank of 7, a severity rank of 3, and a detectability rank of 4 B. A process with a likelihood rank of 3, a severity rank of 2, and a detectability rank of 1 C. A process with a likelihood rank of 8, a severity rank of 5, and a detectability rank of 3*** D. A process with a likelihood rank of 2, a severity rank of 3, and a detectability rank of 2 Correct Answer: C A CI is calculated by multiplying the severity rating, the probability rating, and the detectability rating. Failure modes with low CIs are unlikely to affect patient outcomes and do not require immediate attention. Failure modes with the highest CIs are prioritized for corrective action. Process A has an RPN of 84, process B, 6, process C, 120, and process D, 12.

7. Which of the following strategies has not been shown to reduce rates of mediation errors? A. False-positive safety alerts*** B. Barcode-assisted medication administration C. Computerized order entry D. Decision-support software Technology plays a key role in patient safety and computerized order entry systems, decision support software, automated dispensing, and barcode-assisted medication administration have improved medication safety. Safety alerts have value in prescribing and order processing software, but many alerts are false positives or clinically irrelevant, which decreases the value of system alerts. 8. A multidisciplinary approach to health care and patient safety has led to which of the following outcomes? A. Decreased adverse events*** B. Lost productivity in the health care system C. Reduced medication use D. Expanded patient safety training in professional education Multidisciplinary teams limit adverse events, improve outcomes, and enhance patient and employee satisfaction. Currently, patient safety education and training is limited in most health care disciplines. 9. Which of the following is a common cause of medication errors? A. Using tall-man lettering to differentiate look-alike sound-alike products B. Storing high-risk medications separate from standard drug stock C. Using abbreviations to communicate instructions for medication use*** D. Allowing patients to review their medical records Correct Answer: C

Communication among multidisciplinary health care team members is facilitated by using clear and unambiguous prescribing vocabulary and designations. Unapproved abbreviations and symbols should be avoided, since they contribute to errors in communication and misinterpretation of medication information. Storage strategies and tall-man lettering can reduce the occurrence of errors, especially those related to high-risk medications. Patients are sometimes able to detect medication errors and, in some settings, patients are encouraged to view their medication records, to remind staff about medication administration times, to provide information to assist shift changes and transitions of care, and to ask questions of physicians, pharmacists, and nurses. 10. Which is true of a nonpunitive approach to safety in health care? A. Medication errors are viewed as opportunities for learning and improving the system*** B. One individual is identified as the root cause of an error C. Error reduction strategies focus on human performance D. None of the above An organizational commitment to patient safety and the promotion of a non-punitive environment will improve the recognition, evaluation, and mitigation of safety risks within the system. Health care team members must be willing to consistently report errors and near-misses without fear of punishment. Error reporting should not be a burden of work, and errors should be viewed as opportunities to learn and improve patient care. Focusing only on the individual who committed the error, instead of the system weaknesses that allowed for the error, is ineffective as a long-term safety improvement strategy.