sentinel events 2014. speaker john r. rosing, mha, fache accreditation and regulatory compliance...
TRANSCRIPT
SpeakerJohn R. Rosing, MHA, FACHE
Accreditation and Regulatory Compliance Consultant
Vice President and Principal Patton Healthcare Consulting
262-242-3631
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Most Frequently Reported Sentinel Events,January 1–June 30, 2013 (Source: 10/13 Perspectives)
• Wrong-patient, wrong-site, or wrong-procedure—60• Unintended retention of a foreign object—56• Delay in treatment†—56• Falls†—48• Other unanticipated events† ‡—40• Operative/postoperative complication†—37• Suicide—35• Criminal event (assault/rape/homicide)—26• Medication error†—20• Perinatal death/injury†—15
– † Resulting in death or permanent loss of function– ‡ Includes asphyxiation, burns, choking, drowning, and being
found unresponsive
Most Frequently Identified Root Causes forSentinel Events, January 1–June 30, 2013
(Source: 10/13 Perspectives)
• Human factors (such as fatigue or distraction)—314• Communication (such as among staff, across disciplines, or with patients)—292• Leadership (regarding, for example, lack of performance improvement infrastructure
or community relations)—276• Assessment (such as patient observation processes or its documentation)—246• Information management (such as patient identification or confidentiality)—101• Physical environment (such as emergency management or hazardous materials)—70• Care planning (planning and/or interdisciplinary collaboration)—49• Continuum of care (includes transfer and/or discharge of patient)—48• Medication use (such as storage/control or labeling)—48• Operative care (such as blood use or patient monitoring)—45
Sentinel Event Defined
• A sentinel event is an unexpected occurrence involving death or serious physical or psychological injury, or the risk thereof. Serious injury specifically includes loss of limb or function. The phrase “or the risk thereof” includes any process variation for which a recurrence would carry a significant chance of a serious adverse outcome.
• The terms “sentinel event” and “medical error” are not synonymous; not all sentinel events occur because of an error and not all errors result in sentinel events.
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RCA Value?• Root causes vs proximate causes
– The barn door was left open and all the horses ran away. Close the barn door now – problem solved
– Mary made a serious medication error, fire Mary – problem solved
• Could someone else forget to close the barn door, could someone else make the same error as Mary?
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RCA Value• Why was the barn door left open?
– There was no automatic door closing mechanism, inadequate training, procedural noncompliance
• Why did Mary make the medication error?– There was no bar coding support, inadequate orientation,
inadequate training, no policy guidance, no secondary check on calculation
– Procedural noncompliance – Mary duplicated all her patients wrist bands and unit dose bar codes. Still need to understand the why, but actions may be different
• Action plan and measurement phase enables you to redesign for additional safety and monitor
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RCA Value (cont’d)• Action plan – you create system changes that
help protect against the same error being repeated
• Measurement – you self assess to determine if the changes you designed are being used as anticipated and do they prevent the weakness you had previously seen. Have you sustained the improvement??
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RCA Process• The decision to pro-actively report or not
report to the Joint Commission is voluntary….
• The decision to analyze or not analyze using RCA technique is not voluntary under the standards and SE policy
• If the Joint Commission becomes aware of your sentinel event, reporting using one of their techniques, is mandatory
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When To Conduct An RCA
TJC Reportable
All events that meet your internal definition, including near misses
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RCA Process (cont’d)
• Don’t confuse reporting responsibilities and deadlines with deadlines for completing the RCA– You must complete the RCA within 45 days
of the event, or your becoming aware of the event
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Do We Ever Skip The RCA?“It was evident that our problem was a physician performance issue, should we just make the referral to peer review and skip the RCA?”
– Did your system for error prevention work as designed?
– Did your OPPE, FPPE system identify this vulnerability?
– Were prior peer evaluations thorough?– Were privileges granted appropriately?
What is a Root Cause Analysis?
• A credible process for identifying the basic or causal factors that underlie variation in performance.
• This process should be used to identify the risk that led to a sentinel event.
• Use a RCA framework to drill down to root cause; complete within 45 days
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Starting With The BasicsDefine Your Goals
• Your goal: To conduct a complete, thorough investigation of the event or near miss
• Why? To ensure you have identified the real cause or causes of the incident
• Why? So you can prevent this situation from occurring again
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Starting With The BasicsGetting Organized
Organize your RCA efforts:– Centralize coordination and oversight
responsibilities to one department• Allows for better trending of results• Provides for monitoring to ensure actions have
taken place and results are achieved– Have a written process for conducting the RCA
• Maintains process consistency• Prevents solution “short cuts”• Ensures important steps are not forgotten• Provides reporting structure and follow up
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Putting Together The RCA Team Roles and Responsibilities
• Team Leader– Select wisely– Usually someone in a leadership position
• Director, manager or higher– Usually from one of the involved departments– Should be a strong, fair person who can reign
in group members when needed– Someone who will not push to solve the
problem before all the facts are uncovered
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Putting Together The RCA Team Roles and Responsibilities (cont’d)
• Team Facilitator• Often someone in Performance Improvement,
Patient Safety or Risk Management • Experienced in facilitation• Understands how to conduct an RCA• Can provide “just in time” training for members• Familiar with tools such as brainstorming,
Fishbone & Event Flow Diagrams• Organized
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Putting Together The RCA Team Roles and Responsibilities (cont’d)
• Team Members– Rule of thumb keep the group “workable” 6-8
members is ideal– When possible include those staff/physicians
directly involved in event• Exceptions-
– Too emotionally or personally involved– May be an obstructionist to a good process
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Starting The RCAWhere Do You begin?
• Step one: What happened?• Identify the key components in the event:
– Who were the people/departments/areas involved in this event?
– What Equipment, if any was involved?– What are the key Systems, Processes and
Patient Safety Measures that were involved?
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Gathering The FactsWhat Happened?
• Gather the facts- and just the facts. Do not get bogged down in extraneous details that can actualize dilute or divert the focus off the key issues
• Ways to gather the facts include:– Interviews– Chart reviews– On-line documentation– Event reports– Other data, policies, procedures
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Gathering The Factsand Just The Facts
– Interview Tips- focus on cooperation not interrogation
– Chart reviews- documentation and sequencing of events, create a time line of events
– Event reports- Making sure it is completed with documented follow up
– Secure equipment- get it before it is gone– The other “Stuff” you need - policies, procedures,
documents
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How Deep Do You Dig?
• Getting to the root cause is somewhat like peeling back the layers of an onion until you reach the core
• A thorough RCA methodically asks the question “why” until there is no further to go- until every layer surrounding the core has been removed and you are comfortable you have reached the real root cause
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Tools To Help With The RCAConstructing “What Happened”?
Step two- Begin to put things togetherAn event flow diagram is a great place to start
putting the facts together– It is a tool that sequences the steps in the event and
provides you with a chronology of the facts surrounding the event
– It helps to focus the group on the actual steps in this event- not how things should occur
– It helps the group identify where there may have been a breakdown in process that led to the event occurring
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Tools To Help With The RCA
• Let’s walk through a very simplified example to see how we would create the event flow diagram
• This is a case of Near Miss in the emergency room
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Tools To Help With The RCA (cont’d)• Sequence of Events
– Mr. G, an unaccompanied patient, walked in the Emergency Room and signed in at the triage desk at 8:45 PM
– Triage nurse was assessing another patient when patient signed in and did not see patient. Security guard was present at desk
– 9:10 PM Patient with Chest Pain arrived in ED. Triage Nurse immediately assessed Chest Pain patient
– 10 PM Nursed called for Mr. G. and patient did not respond– 10:10 Security checked waiting room and found patient
unconscious. Waiting room was full of patients– 10:11 Emergency Code was called and patient was
transported to treatment bay– 10:13 Blood sugar found to be 37– Patient was treated, kept in observation overnight and
discharged the next morning
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Tools To Help With The RCA (cont’d)
• Simplified Event Flow
8:45 Mr. G Signs in at
Triage
9:10 PT With CP Arrives
At triage
10:00 NurseCalls for
Mr. GNo response
10:11 CodeCalled
Pt to TX bay
10:13 Mr.G’sBS 37
Mr. G treatedObserved overnight
10:10 SecurityFinds Mr. G
Unresponsive
Mr. G D/C home in
AM
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Tools To Help With The RCA (cont’d)
• Why did this happen?• Focus the group on trying to uncover “Why” this
event happened
• Identify all of the “whys”• Resist the temptation to jump to the solution • Keeping asking “Why” until you can literally go no
further- there is no additional information to be gleaned from asking “Why.”
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Tools To Help With The RCA Brainstorming
• Brainstorming is a great way to surface potential “Whys”
• It gets everyone involved in process• Unleashes and uncovers multiple ideas-
solutions or possible causes• Can be “free flowing” or “structured”
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Tools To Help With The RCABrainstorming (cont’d)
• Free Flowing-– Members speak up as they have ideas– Scribe or facilitator write ideas on flip chart
• Structured-– Members are asked to jot down ideas on sticky
notes– Go around the room using a round robin to
give each member a chance to speak. Keep going around until no one has any more ideas
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Tools To Help With The RCA Cause and Effect Diagram
• Constructing a Fishbone or Cause and Effect Diagram can help the group organize facts and information into a single picture– It helps establish possible relationships– It can help to elicit additional information
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Constructing The Diagram
Organize the results of your “Brainstorming” into the contributing factors
EXAMPLE:– Human factors– Equipment factors– Controllable environmental factors– Uncontrollable environmental factors– Other factors
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Constructing The Diagram (cont’d)
• Simplified example of Fishbone or Cause and Effect Diagram:
Human Factors Equipment Factors
Environmental Factors
Other Factors
Private waiting room design- poor visualization
Panic button in private waiting room non-functional
Second triage nurse on break- relief nurse did not show
Sign in policy does not ensure pt is seen before sitting down
Identify the Root Cause(s) Prune the list of Root Causes
– Would the problem have occurred if cause #1 had not been present?
– Will the problem recur due to same causal factor if cause #1 is corrected or eliminated?
– Will correction or elimination of cause #1 still potentially lead to similar events?
• Yes = contributing cause, No = root cause
Taking Action• The Hardest Step In The RCA: Installing
effective error prevention strategies• Make the right thing to do the easiest
thing to do and then hard-wire it• Make the process fool-proof
recognizing that nothing is outside the capability of a sufficiently talented fool!
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Taking ActionJust Do It!!
What can we do to prevent this from happening again?
• You know what has happened• You know why it happened• Now you need to decide what you can
do to prevent this from happening again• AND… actually take the steps to make
the changes happen!
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Taking ActionJust Do It!! (cont’d)
• Develop an action plan– List the Root Causes with the actions needed
to prevent this event from happening again• Present the plan
– Reporting structure should be established in your RCA policy- i.e. Patient Safety Committee
• Assign responsibilities for action steps– These can be assigned prior to reporting to
designated committee or afterwards
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Taking ActionJust Do It!! (cont’d)
• Follow up on assignments– Usually facilitator or someone in PI, RM or PS
keeps a tracking log• Report back
– Require follow up to be reported back to designated committee
• Close the loop– Monitor for lasting impact
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Taking Action StepCommon Obstacles and Problems
• Fear• Rushing to the solution• Not gathering enough information• Solving the wrong problem• Making tough recommendations• Implementing actions• Doing the follow up- making sure the
changes stick
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Taking Action• You have completed your RCA• You have your team’s list of root causes for this
event• You have drafted your action plan and
measurement strategy– Who is going to approve the RCA?– Who is going to approve the action plan?– Who is going to approve the measurement
strategy?• This should all be hard coded before you have a
sentinel event
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Importance of Approvals?• You need people to take action, change
behaviors, change policy, potentially provide resources and support
• You have a responsibility to measure change in accordance with your action plan– If there is inadequate buy in, your changes
won’t be accepted, your measurement will not work, your accreditation can be downgraded and your patients may remain at risk
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Action Plans• If your root causes include improper
patient identification techniques…..– Is it lack of training, orientation, system to
accomplish the technique, procedural non compliance or failure to provide leadership?
• If your root causes include procedural non compliance or a failure to lead or fund, your action plan will be different
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Broad The Scope?• Your SE involved incorrect patient
identification in cardiac cath lab• Your root causes identified mis-application
of the 2 identifier technique in cardiac cath• Your planned actions will focus on cardiac
cath or on your organization?– Implement actions where ever you have risk,
not just where this event occurred
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Measurement Strategy• You identify a statistically valid sampling
methodology before starting to measure and you collect audit data using that system– Try to collect passively, retrospectively– Concurrent data collection by responsible staff with new forms
may create under reporting or artificial findings– Concurrent external observer studies may be more thorough
• You average your 4 months of data and must achieve A or C level performance or if not linked to a standard 85%
• Be sure to provide rapid, departmental and aggregate feedback each month and consider graphical analysis to promote change and improvement
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Building On Success• Fostering the blame free atmosphere
– Talk about your RCA process, the system changes, the resources that flowed, display the improvement data, the enhanced safety
– This can be a positive change experience• Do analyze procedural noncompliance, was
your design reasonable?
Root causes, failures, defects, workarounds, or undesired
variation……Are usually caused by one or more
of the following……
• Poor process design• Poor transfer of knowledge• Poor validation of competency• Poor measurement of conformance• Poor management intervention
Intervention(appropriate action)
LI
NE
MA
NA
GE
RS
Measure conformancePI staff
EducateStaff dev.
Validate competencyStaff dev.
Focus/PDSA/Rapid cycle design
PI team
5 Steps to doing the Right Thing Well Sustained Execution=Continuous Readiness
Measure conformance
• Poor design?
• Inadequate education
• Ineffective competency validation
• Variation due to work-arounds
• Variation due to unit, day of week, time of day, FT/PT/agency staff, etc.
John R. Rosing, MHA, FACHE
Patton Healthcare Consulting