gordon “gordy” schiff, md kathy duncan, rn critical values expedition...gordon “gordy”...
TRANSCRIPT
7/26/2011
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Gordon “Gordy” Schiff, MD
Kathy Duncan, RN
These presenters have nothing to disclose
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Agenda
• Welcome and Introductions
• The Expedition Process
• Overview of Critical Values Communication
• Assignment & Planning for Next Session
• Final Questions & Close
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Chat Time!
What is your goal for participating in this
Expedition?
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Join Passport to:
• Get unlimited access to Expeditions, two- to four-month,
interactive, web-based programs designed to help front-line teams
make rapid improvements.
• Train your middle managers to effectively lead quality
improvement initiatives.
• Enhance your strategic planning with customized whole systems
data and selected benchmarking information.
. . . and much, much more for $5,000 per year! •
• Visit www.IHI.org/passport for details.
• To enroll, call 617-301-4800 or email [email protected].
7/26/2011
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What is an Expedition?
ex•pe•di•tion (noun)
1. an excursion, journey, or voyage made for
some specific purpose
2. the group of persons engaged in such an
activity
3. promptness or speed in accomplishing
something
Where are you joining from?
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Our Expedition Director
Kathy D. Duncan, RN, Faculty, Institute for Healthcare
Improvement (IHI), is co-leader of IHI's National Learning
Network and coordinates the Improvement Map support care
processes. Previously she co-led the 5 Million Lives
Campaign National Field Team and was faculty for the
Improving Outcomes for High Risk and Critically Ill Patients
Innovation Community. Ms. Duncan was responsible for the
Prevention of Pressure Ulcers and Deployment of Rapid
Response Teams content areas for the 5 Million Lives
Campaign. She is a member of the Scientific Advisory Board
for the AHA NRCPR, NQF's Coordination of Care Advisory
Panel, and NDNQI's Pressure Ulcer Advisory Committee.
She has served in a variety of staff and management
positions, including director of critical care for a large
community hospital, where she led an initiative to decrease
ICU mortality and morbidity by reducing ventilator-associated
pneumonia and ICU length of stay.
What We Expect of You
• “All Teach, All Learn” philosophy
• Join and participate on all calls
• Participate in the listserv discussion
• Test, test, test
• Share what you’ve learned (challenges as
well as successes and insights)
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Overall Program Aim
The overall goal of the Expedition is for
participants to build the foundation of an efficient
process for communicating critical tests results
consistently and promptly.
Objectives
Upon completion of this expedition, participants will be able to:
• Identify opportunities to improve their current process of
communicating critical test results
• Identify safe practice recommendations for communicating
critical test results
• Develop a reliable process for communicating critical test
results
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7/26/2011
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Gordon “Gordy” Schiff, MD
Gordon “Gordy” Schiff, MD, Associate Director,
Center for Patient Safety Research and Practice,
Brigham and Women’s Hospital, is also Associate
Professor of Medicine at Harvard Medical School. He
is a founding member and past president of Physicians
for a National Health Program (PHNP), and he is
author of PNHP’s JAMA paper on quality health care
reform. Dr. Schiff was previously professor of medicine
at Rush University and senior attending physician at
Cook County Hospital, where he worked for more than
30 years as director of clinical quality research and
improvement for the department of medicine. During
the 1990s he was director of Cook County’s large
general medical clinic. He is clinical director of the
recently awarded TOP-MED (Tools for Optimizing
Prescribing, Monitoring and Education) CERT (Center
for Education and Research in Therapeutics) based at
the UIC College of Pharmacy.
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Outline
• Personal introduction – 3 studies
– Theophylline Potassium TSH
• Review of selected literature
– Methods Studies
• Reliability science
– Key concepts for results management
• 6 requirements to reliable test result f/up
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• -67 y.o. woman w/ hx of HBP, COPD,
asymptomatic gallstone
• -Presents acute MI
• -Develops CHF, treated w/ usual meds including
digoxin, diuretic, theophylline
• -Acute nausea vomiting abdom pain, rushed to
operating room for cholecystectomy
• -Chart review 1 yr later--theophylline level 37.0 .
Schiff Ann Intern Med 1990
Abnormal Lab Belatedly Discovered
ERROR (N=40) # %
Delay (>10 hrs) toxic level draw to MD action 20 50%
Excessively high (>1.5) doses CHF, liver dis 17 43%
Miss obvious GI,CNS,cardiac sx/signs toxicity 16 40%
Recurrent toxicity: unaware; failure adjust dose 11 28%
Dosing errors for non CHF pts 9 23%
ED rx despite pretreatment level already toxic 6 15%
Inadvertent overlap of i.v. and p.o. rx 6 15%
Interacting drugs (w/ failure to adjust dose) 5 13%
Discharged on same dose came in toxic 5 13%
Discharged w/ no noted MD awareness of toxicty 4 10%
Theophylline Toxicity, Schiff, Ann Internal Med 1991
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Potassium Prescriptions
N = 32,563
(12,825 unique patients)
Potassium Levels 5.3
N = 9,790
(4,188 patients)
Positive “Screen” = Match Found in Both Databases N=1,781 Prescriptions (701 Unique Patients)
Last K 5.3 N=498 1.53%
No Error N=1107
Same Day K 5.3 N=276 0.84%
Detailed Review all Potassium Levels
Schiff, Am J Med 2000
NAME UNITNO DATE RESULT GENERIC_NM QUANTITY
JEFFERSON, RUTH 116996 09/06/95 5.2
JEFFERSON,RUTH 116996 09/11/95 POTASSIUM CHLORIDE 100
JONES, BILL 122441 03/11/95 6.0
JONES, BILL 122441 03/20/95 POTASSIUM CHLORIDE 60
SMITH, MARY 125565 05/16/95 5.3
SMITH, MARY 125565 05/16/95 POTASSIUM CHLORIDE 30
SMITH, MARY 125565 11/19/95 7.0
STOKES,WILL 137995 01/03/95 POTASSIUM CHLORIDE 30
STOKES,WILL 137995 01/03/95 5.3
CULLEN, CORA 148341 03/30/95 5.3
CULLEN, CORA 148341 04/01/95 POTASSIUM CHLORIDE 14
CULLEN, CORA 148341 04/12/95 POTASSIUM CHLORIDE 60
CULLEN, CORA 148341 06/14/95 POTASSIUM CHLORIDE 30
PABST, POLLY 155103 01/11/95 5.3
PABST, POLLY 155103 04/12/95 POTASSIUM CHLORIDE 240
KENNEDY,JOE 156828 02/22/95 5.6
KENNEDY,JOE 156828 03/06/95 POTASSIUM CHLORIDE 240
KENNEDY,JOE 156828 04/05/95 4.9
KENNEDY,JOE 156828 05/09/95 6.6
KENNEDY,JOE 156828 05/10/95 POTASSIUM CHLORIDE 20
KENNEDY,JOE 156828 05/23/95 5.2
KENNEDY,JOE 156828 05/24/95 POTASSIUM CHLORIDE 30
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NAME UNITNO DATE RESULT GENERIC_NM QUANTITY
JEFFERSON, RUTH 116996 09/06/95 5.2
JEFFERSON,RUTH 116996 09/11/95 POTASSIUM CHLORIDE 100
JONES, BILL 122441 03/11/95 6.0
JONES, BILL 122441 03/20/95 POTASSIUM CHLORIDE 60
SMITH, MARY 125565 05/16/95 5.3
SMITH, MARY 125565 05/16/95 POTASSIUM CHLORIDE 30
SMITH, MARY 125565 11/19/95 7.0
STOKES,WILL 137995 01/03/95 POTASSIUM CHLORIDE 30
STOKES,WILL 137995 01/03/95 5.3
CULLEN, CORA 148341 03/30/95 5.3
CULLEN, CORA 148341 04/01/95 POTASSIUM CHLORIDE 14
CULLEN, CORA 148341 04/12/95 POTASSIUM CHLORIDE 60
CULLEN, CORA 148341 06/14/95 POTASSIUM CHLORIDE 30
PABST, POLLY 155103 01/11/95 5.3
PABST, POLLY 155103 04/12/95 POTASSIUM CHLORIDE 240
KENNEDY,JOE 156828 02/22/95 5.6
KENNEDY,JOE 156828 03/06/95 POTASSIUM CHLORIDE 240
KENNEDY,JOE 156828 04/05/95 4.9
KENNEDY,JOE 156828 05/09/95 6.6
KENNEDY,JOE 156828 05/10/95 POTASSIUM CHLORIDE 20
KENNEDY,JOE 156828 05/23/95 5.2
KENNEDY,JOE 156828 05/24/95 POTASSIUM CHLORIDE 30
Potassium
Level
Most
Recent
Value High
Same
Day High Total %
5.3 137 27 164 24.30% 674 62.30%
5.4 86 23 109 16.20% 510 47.10%
5.5 48 22 70 10.40% 401 37.10%
5.6 51 19 70 10.40% 331 30.60%
5.7 32 11 43 6.40% 261 24.10%
5.8 24 17 41 6.10% 218 20.10%
5.9 13 5 18 2.70% 177 16.40%
6.0 16 6 22 3.30% 159 14.70%
6.1 11 8 19 2.80% 137 12.70%
6.2 10 3 13 1.90% 118 10.90%
6.3 9 3 12 1.80% 105 9.70%
6.4 3 7 10 1.50% 93 8.60%
6.5 4 3 7 1.00% 83 7.70%
6.6 8 2 10 1.50% 76 7.00%
6.7 2 2 4 0.60% 66 6.10%
6.8 4 1 5 0.70% 62 5.70%
6.9 1 3 4 0.60% 57 5.30%
>7.0 39 14 53 7.90% 53 4.90%
Total 498 176 674 100.00%
= or > K+ Level
N %
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TSH > 20
470
Rx Outside Pharmacy
17
On Thyroxine
390
Baby
3 +/-Awareness
4
Hyperthyroid Rx
17
Lost F/up; Died
27
Missed Dx
Hypothyroidism
12
Hypothyroid
63
No Rx
19
No Thyroxine
80
(5.7%)
(0.9%) (2.6%)
Schiff Arch Intern Med 2005
Year
N % N %
Total TSH done 22,076 24,524
Unique patients 17,467 19,293
TSH levels > 20 1,334 744
TSH > 20 unique patients 470 512
On thyroxine 390 415
No thyroxine 80 17.0% 97 18.9%
Hyperthyroid Rx 17 3.6% 20 3.9%
Rx outside pharmacy 17 3.6% 34 6.6%
No Rx 19 4.0% 16 3.1%
Lost F/up or died 27 5.7% 27 5.3%
Babies 3 3
Awareness but failed F/up 4 2
Missed Dx hypothyroidism 12 2.6% 11 2.1%
2000 2001
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Year
N % N %
Total TSH done 22,076 24,524
Unique patients 17,467 19,293
TSH levels > 20 1,334 744
TSH > 20 unique patients 470 512
On thyroxine 390 415
No thyroxine 80 17.0% 97 18.9%
Hyperthyroid Rx 17 3.6% 20 3.9%
Rx outside pharmacy 17 3.6% 34 6.6%
No Rx 19 4.0% 16 3.1%
Lost F/up or died 27 5.7% 27 5.3%
Babies 3 3
Awareness but failed F/up 4 2
Missed Dx hypothyroidism 12 2.6% 11 2.1%
2000 2001
Every system is perfectly
designed to deliver the
results it does
Don Berwick IHI
Perfectly designed system to “miss” 12 patients a year (and lose another 27 follow-up)
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Poon Arch Intern Med 2004
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Poon Arch Intern Med 2004
2.5 Missed Results per MD
= 25,000 “ Harvard CRICO MD’s
150,000 Missed Tests/Yr
Methods to Measure
Failed Test Result Follow-up • MD survey- how often missing results
• Chart review: failure, delay in documenting result
• Patient survey- whether aware of result
• Failure follow-up action as signal
• Tracer studies-working backward from dx
• Action suggesting unaware of result – Linking pharmacy data
• Malpractice studies
• PRO Citations
• Lab Frustrations
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Methodologic Issues • Time frame; abnormal criteria
• Type of result (Lab, x-ray, other)
• Inpatient vs. outpatient vs. ED – Labs at discharge
• Failure to document vs. failure to act
• MD notification by lab vs. Pt notification by MD
• Recall biases
• Generalizability: VA, academic centers
• Denominators
• Notification vs. Action
• Lost letters; unopened electronic messages
• Follow-up action in future
Casalino Arch Intern Med 2009
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Singh Arch Intern Med 2009
Lack of
Timely f/up Timely F/up
N=92
(7.7%)
N=1104
(92.3%)
Acknowledged 71 (77.2) 908 (82.2)
Not
Acknowledged 21 (22.8) 196 (17.8)
Acknowledged Alerts for Abnormal Imaging Exams
No Better in Timely Follow-up
Singh Arch Intern Med 2009
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Gordon Ann Intern Med 2009
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Reliability Science 10 Key Improvement Concepts
1. Situational awareness and anticipation of needs
2. Need for closed-loop
3. Attention to hand-offs and teamwork
4. Continuous flow systems w/out batching
5. Doing everything “just-in-time”
6. Culture of stopping to fix problems
7. Forcing functions, simplification, standardization
8. Visual cues- facilitate work, ensure probs not hidden
9. Use only reliable thoroughly tested technology
10.Go see for self to thoroughly understand
(Genchi Genbutsu)
Schiff, JAMA 2011
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High Reliability Results Management
1. Track tests from ordering to completion to
receipt/acknowledgement and action on
results.
2. Standardized approach for all test areas to
define and flag clinically significant
abnormal results
3. Eliminate ambiguities regarding how to
return a result or who to contact
4. Patients should be informed about all
test results, even normals
5. Importance of tracking and system
oversight monitoring
6. Advanced systems to support clinicians
in result management activities
High Reliability Results Management
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Questions?
• Raise your hand
or
• Use the chat box
The Model for Improvement
Critical Values Reporting and
Communication
July 26, 2011
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Fundamental Questions for Improvement
• What are we trying to accomplish?
• How will we know that a change is an improvement?
• What changes can we make that will result in an improvement?
Langley, G.J., Nolan, K.M., Nolan, T.W, Norman, C.L., & Provost, L.P.
(2009). The improvement guide: A practical approach to enhancing
organizational performance (2nd Ed.). San Francisco: Jossey-Bass.
What are we trying to accomplish?
How will we know that a change is an improvement?
What change can we make that will result in improvement?
Model for Improvement
Act Plan
Study Do
From:: Associates in
Process Improvement
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The PDSA Cycle
for Learning and Improvement
PlanAct
DoStudy
- Objective- Questions and predictions (Why?)- Plan to carry out the cycle(who, what, where, when)- Plan for Data collection
- Carry out the plan- Document problems and unexpected observations- Begin analysis of the data
- Complete the analysis of the data - Compare data to predictions - Summarize what was learned
- What changes are to be made?
- Next cycle?
Source:
Improvement
Guide p 60
Repeated Use of the Cycle
Hunches
Theories
Ideas
Changes That
Result in
Improvement
A P
S D
A P
S D
What are we trying to accomplish?
How will we know that a change is an improvement?
What change can we make that will result in improvement?
Model for Improvement
Source: Improvement Guide, p 10
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Successful Cycles to Test
Changes
• Plan multiple cycles for a test of a change
• Think a couple of cycles ahead
• Initially, scale down size of test (# of patients, clinicians,
locations)
• Test with volunteers
• Do not try to get buy-in or consensus for test cycles
• Be innovative to make test feasible
• Collect useful data during each test
• In latter cycles, test over a wide range of conditions
Developing the team’s
Aim Statement
Question #1: What are we trying to accomplish?
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What are we trying to accomplish?
• Defines the aim of the
improvement effort.
• Time specific and
measureable.
Aim Example
• Reduce adverse drug events (ADEs) in
critical care by 75% within 1 year.
• Increase the number of surgical cases
between cases with a surgical site
infection by 50% within 1 year.
• Reduce the average length of stay for
Medical ICU patients by 50% within 9
months.
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Tips for Creating Aim Statements
• State the aims clearly (What do you
want to accomplish? How good, by
when?)
• Define location or population
• Set stretch goals
• Include numerical goals/targets
Homework: Due Next week
• Assess Current work
• State your Aim
─Simple
─What, Where, By when
• State 2 measures
─“How do you know you have made an
improvement?”
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Things to Consider in Aim Setting
• What happens to results that return after patient
discharged?
• Who is responsible and what is process for incidental
finding on pre-op CXR ?
• What happens when the ordering MD does not answer
page for panic result?
• How are cross coverage test result issues handled?
• When is the PCP vs. specialist responsible for results of
tests specialist orders?
• What does it mean to have a test “acknowledged?”
• How are patients informed of test results; how
documented?
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Things to Consider in Aim Setting
• How do you insure that proper follow-up occurs (“repeat
in 6 mos”) ?
• What happens when test result is returned to an MD and
he/says “this is not my patient?”
• Are there ways to know when a “normal” result (e.g. INR)
is not normal?
• Are there ways to link test results to drugs (elevated
CPK on statin) ?
• How easy do you make it for your clinicians, in and
outpatient, to manage results?
• How do you handle results that return to the ED for a
patient who has been admitted?
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Volunteers…….
1.__________
2.__________
3.__________
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Upcoming Sessions
• Session 2: August 2, 2:00 PM – 3:00 PM ET
Topic: Getting Started
• Session 3: August 23, 2:00 PM – 3:00 PM ET
Topic: Developing Your Aim Statement
• Session 4: September 6, 2:00 PM – 3:00 PM ET
Topic: Testing Process Changes
• Session 5: September 20, 2:00 PM – 3:00 PM ET
Topic: Safe Practice Recommendations
• Session 6: October 4, 2:00 PM – 3:00 PM ET
Topic: Participant Report-outs and Continuing
Your Work
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