M189 - Conference Slide Deck for...

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Keynote Speaker Dr. William Geerts, MD, FRCPC Professor, Department of Medicine, University of Toronto, Director, Thromboembolism Program, Sunnybrook Health Sciences Centre, Toronto, ON

Transcript of M189 - Conference Slide Deck for...

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Keynote Speaker

Dr. William Geerts, MD, FRCPCProfessor, Department of Medicine, University of Toronto,

Director, Thromboembolism Program, Sunnybrook Health Sciences Centre, Toronto, ON

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Faculty/Presenter Disclosure

• Faculty: Dr. William Geerts• Relationships with commercial interests:*

– Grants/Research Support: NA– Speakers Bureau/Honoraria: Bayer, Leo Pharma, Sanofi– Advisory Boards: Bristol-Myers Squibb, Leo Pharma– Other: Bayer, GSK, Sanofi

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Disclosure of Commercial Support• This program has received financial support from Alexion Canada, Leo

Pharma, Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Covidien, Novartis, Octapharma, BMS/Pfizer Alliance, Pfizer Canada Injectables, Aspen Pharmacare and Sanofi in the form of an Unrestricted Educational Grant

• This program has not received in-kind support from any commercial organization

• Potential for conflict(s) of interest:– Dr. William Geerts has received payment from Bayer, Leo Pharma,

Sanofi.– Bayer, Leo Pharma and Sanofi developed/licenses/distributes/benefits

from the sale of a product that will be discussed in this program:

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Mitigating Potential Bias

• No commercial or other non-commercial organization have had any input to the content of this program

• No commercial or other non-commercial organization have been present at or privy to any discussions, meetings, or other activities related to the content of this program

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Reducing Hospital-Acquired VTE: A “Nomadic” Quality

Improvement JourneyBill Geerts, MD, FRCPC

Director Thromboembolism Program, Sunnybrook HSCProfessor of Medicine, University of Toronto

Executive, Thrombosis CanadaNational Lead, VTE Prevention, Safer Healthcare Now!

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Brief, selective and personal discussion of the road to improved patient safety through the optimal use of thromboprophylaxis

Outline

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Is it a problem?

Hospital-Acquired VTE

Can it be fixed?

Can it be fixed consistently?

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Is it a problem?

Hospital-Acquired VTE

Can it be fixed?

Can it be fixed consistently?

Clinical research

Practice guidelines

QI – local, national

QI research

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Why are we concerned about thromboprophylaxis?

1. Because 60% of all venous thromboembolism (VTE) in the population is hospital-acquired

2. Because VTE causes substantial harm

3. Because HA-VTE can be prevented (effectively, safely, inexpensively)

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Consequences of Unprevented VTE

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Burden of Hospital-Acquired VTE

Population of Ontario, 201413,679,000

Annual VTE rate13,679

Hospital-acquired VTE rate8,000/year

1/1,000/yr

60%

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1. More than 450 randomized trials show that VTE can be safely prevented

2. Guidelines have recommended routine thromboprophylaxis for 28 years

3. Thromboprophylaxis is standard of care for almost all hospital patients in 2014

Evidence for Thromboprophylaxis

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What is the evidence?

Consistent 60-70% reduction in asymptomatic VTE without a significant increase in major bleeding

But, does prophylaxis improve clinically-important outcomes?

4 recent examples

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QI improves Thromboprophylaxis

54% 67% 80% 90% 98%

Maynard – J Hosp Med 2010;5:10

1

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QI efforts also reduce VTE

Maynard – J Hosp Med 2010;5:10

Risk assessment tool linked to recommended prophylaxis options Active monitoring, feedback and interventions to improve adherence

2005 2007 P

Patients at risk 9,720 11,207

Appropriate prophylaxis 58% 98% <0.001

Hospital-acquired VTE

131 92 <0.001

Preventable hospital-acquired VTE

44 7 <0.001

1

2

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Thromboprophylaxis leads to Fewer Adverse Outcomes

Zeidan – Am J Hematol 2013;88:545

2.5%

1.1%

0%

0.5%

1.0%

1.5%

2.0%

2.5%

Symptomatic VTE

Preventable VTE

Clinical Events at 90 days

Major bleeding

0.7%

0%0.3%

0.1%

Pre‐intervention (N=1,000)

Post‐intervention (N=942)

Medical patients at Johns Hopkins

2 Increased Thromboprophylaxis leads to Fewer Adverse Outcomes

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QI project at King’s College Hospital, London launched in 2010

Developed a local VTE Prevention Program Mandatory, documented VTE risk assessment VTE prophylaxis guidance Mandatory VTE education for staff Identification of hospital-associated VTE Root cause analysis with subsequent targeted

QI interventions

Effect of a VTE Prevention Program on HA-VTE

Roberts – Chest 2013;144:1276

3

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Patients with a VTE Risk Assessment

Roberts – Chest 2013;144:1276

% o

f pat

ient

s

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QI project at King’s College Hospital, London, 2010-12

VTE Prevention Program Reduces HA-VTE

Roberts – Chest 2013;144:1276

2010-11 2011-12 p

VTE risk assessment

63% (38-88) 93% (90-97)

HA-VTE

Per 1,000 admissions

23619.7/mo

1.5

18915.8/mo

1.0

0.014

Potentially preventable HA-VTE 43% 32% 0.005

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Hospital-Acquired VTE in the UK

Lester – Heart – 2013;99:1734

Readmissions with VTE 8,578 In-hospital fatal VTE 4,334 Fatal VTE disch-90 days 1,651 In-hosp/post-disch fatal VTE 5,985

4,141,000 admissions >3 days in all 163 NHS hospital

trusts, 2010-12

1. 1/500 admissions are readmitted with VTE

2. 1/700 admissions die of VTE <90 days

4

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All patients admitted to all 163 NHS trusts, 2010-12 Mandatory reporting of use of the VTE risk tool

Use of the UK National VTE Risk Assessment Tool

Lester – Heart – 2013;99:1734

Rate of VTE risk

assessments performed

[IQR]

100%

0%

50%

July 2010 March 2012

51% [27,71]

93% [91,96]

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All 4 million patients admitted to all 163 NHS hospital trusts >3 days, 2010-12

Hospital-Acquired Fatal VTE is Reduced in Adherent Hospitals

Lester – Heart – 2013;99:1734

Fatal VTE <90 days after hospital discharge

Rel Risk for hospitals with VTE risk assessment

>90% vs <90% All 0.85 [0.75-0.96; p=0.01]

Post-discharge 0.81 [0.67-0.79; p=0.03]

Achieving >90% VTE risk assessment is associated with significant lower VTE mortality

Hospital-Acquired Fatal VTE is Reduced in Adherent Hospitals

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National VTE Mortality DataEngland

Year VTE listed as cause of death

2007 6,1212008 6,1702009 6,2182010 6,2822011 4,5622012 4,668

From R. Arya - Office for National Statistics, 2013

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Better Prophylaxis Options Reduce the Risk of DVT after TJR

60%

50%

40%

30%

20%

10%

0

DVT

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2006 Routine Use of Recommended Prophylaxis in 195 Canadian Hospitals

100%

75%

50%

25%

0 86%94% 30% 32% 11%36% 33%

Appropriate use

Knowledge-care gap

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Prophylaxis use in 8 Toronto hospitals

100%

80%

60%

40%

20%

0Hip         Major general      Medical             Combined 

fracture          surgery            patients (n=341)                (n=416)                 (n=418)                    (n=1,175)     

79%

43%

31%

49%

Knowledge-care gap

Appropriate use

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Oral Rivaroxaban after THR/TKR

Turpie – Thromb Haemost 2011;105:444

%

10

8

6

4

2

0

9.4%

4.2%

Risk reduction

55% p<0.001

0.3% 0.4 %

All VTE Symptomatic Major VTE bleeding

enoxaparin(n=6,200)

rivaroxaban(n=6,183)

P=0.141.0% 0.5%

Risk reduction

50% p=0.001

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Advantages of rivaroxaban Thromboprophylaxis in TJR

More effective and as safe as LMWH

Oral, once daily

No lab monitoring

Cheaper than LMWH (~$3/day in Canada; in Ontario, covered by ODB for TJR)

Post-discharge prophylaxis is simple and inexpensive high compliance

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0 1 2 3 4 5 6 7 8 9 10 14 21 28days

rivaroxaban 10 mg PO once daily low molecular weight heparin SC

Admit

ORDischargeor rehab

Prophylaxis in Hip and Knee Arthroplasty start postop

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2014 Thromboprophylaxis Summary

Patient Group Options DurationAcute medical illness

LMWH Discharge

Surgery: general, gyne, thorac, urol

LMWH Discharge (up to 4 wks for selected cancer patients)

Major orthopedics - THR, TKR

- Hip fracture surg

rivaroxaban LMWH

LMWH

2-6 weeks

2-6 weeks

High bleeding risk mechanical Until LMWH can start

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Prophylaxis Use in Medical Patients 1,894 consecutive patients in 29 hospitals in 6 provinces

Khan – Thromb Res 2007;119:145

90%Prophylaxis Prophylaxis

Recommendedindicated given

prophylaxis

23% 15%

100%

75%

50%

25%

0

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Looks like ol’ Bill’s tryin’ uh git dem

surgeons to use duh prophylaxis guidelines

agin.

Yah Pa, poor fool. But ah heared the cavalry’s

comin’!

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ACCREDITATION CANADA VTE Prophylaxis Required

Organizational Practice (ROP)

Hospital accreditation requirement started January, 2011

www.accreditation.ca

The hospital “identifies medical and surgical clients at risk of venous thromboembolism (DVT and PE) and provides appropriate thromboprophylaxis.”

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ACCREDITATION CANADA VTE Prophylaxis ROP

1. The hospital has an organization-wide, written thromboprophylaxis policy or guideline.

2. Identifies patients at risk for VTE and provides appropriate, evidence-based VTE prophylaxis.

3. Establishes measures for appropriate thromboprophylaxis use, audits its implementation, and uses this for quality improvement.

4. Identifies major orthopedic surgery patients who require post-discharge prophylaxis and provides it.

5. Educates health professionals and patients about VTE and its prevention.

www.accreditation.ca

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April 10 to 18, 2013

118 centers, 4,667 patients, 9 provinces coast to coast

General medical and general surgical patients at risk for VTE

Analyses conducted by Central Measurement Team on data from Patient Safety Metrics (PS Metrics)

2013 VTE Audit Day2013 National VTE Audit

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Overall, appropriate thromboprophylaxis use = 81%

- Very good (but with room for improvement)

Thromboprophylaxis Use 2013 National VTE Audit

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Appropriate Thromboprophylaxis -by Province (2013)

% o

f pat

ient

s

100%

65%

Appropriate Thromboprophylaxis by Province (2013)

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Receiving Appropriate Thromboprophylaxis and Preprinted Order Sets

N=4,518

Order set used

Order set not used

91%

71%

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9%

2003 2007  2008  2009  2010  2011  2012  2013   2014       

21%

100%

75%

50%

25%

0

60%

94%72%

79%

Appropriate Prophylaxis* Use in General IM Patients

91%

Baseline Education, commitment Order sets, audit & feedback

90% 87%

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Improving Thromboprophylaxis

1. Institutional commitment + resource support2. PLUS multidisciplinary team, committee or sub-3. PLUS input from similar organizations (Baycrest,

Providence, etc)4. PLUS develop written hospital policy5. PLUS embed into order sets6. PLUS audit adherence with 4.7. PLUS QI initiative – education, re-audit +

feedback8. PLUS periodically re-assess approach

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It’s all about the patient . . .At your hospital, do 100% of

patients considered to be at risk for VTE receive appropriate

prophylaxis 100% of the time?Yes No

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Take Home Messages National/provincial incentives are important to

achieve widespread impact Local practice change (= a culture change)

requires multi-faceted approaches and a lot of patience

QI almost always takes longer than you think VTE prophylaxis is a real success story in

Canada

Measure

Make changes

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“Bill, for goodness sake, stop asking if we’re there yet. We’re nomads*, we’ll never be there.”

*quality improvement workers

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Congratulations, to all of you for making thromboprophylaxis such

a success story in Canada