Avoiding Unnecessary Prophylaxis: HMS VTE Low Risk Webinar O C T O B E R 1,

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Avoiding Unnecessary Prophylaxis: HMS VTE Low Risk Webinar O C T O B E R 1, 2 0 1 8

Agenda Overview & Current State Hospital Specific Examples Discussion

Overview & Current State S C O T T F L A N D E R S, M D

At Risk Patients with No Contraindications: Pharmacologic Prophylaxis on Admission At Risk = Caprini > 2; 97% of cohort (non-surgical / non-icu patients) 30% Increase!

Do Higher Prophylaxis Rates for ALL Patients Reduce VTE Rates? (n=31,000) 86% 73% 55% Flanders, et. al., JAMA IM. 2014

VTE-Free Survival by Hospital Prophylaxis Performance In Hospital VTE Rate: 0.2% 90-Day VTE Rate: 1.0% Flanders, et. al., JAMA IM. 2014

Why? Pharmacologic prophylaxis trials Highly selected patients Average LOS > 7-10 days Treated an average of 10 +/- days Outcomes: screening dopplers for DVT Pharmacologic prophylaxis in today s hospitals Applied to all patients Median LOS 4-5 days Mobility enhancement Prophylaxis ends at discharge Outcomes: symptomatic VTE

Risk Models Evaluated Kucher Padua IMPROVE Intermountain Caprini Bottom Line Only 20% of patients were at risk (non-icu, non-surgical) For all models, VTE rate in at risk pts was 3x that in not at risk pts Very hard to identify population which benefits from prophylaxis NNT 500-750 (ARR < 0.25%)

Low Risk Patients Regardless of Risk Score Used Majority of non-surgical, non-icu medical patients are low risk HMS registry: no benefit of prophylaxis in this group Risks > benefits with pharmacologic prophylaxis Bleeding Patient discomfort Nursing time Cost Mechanical prophylaxis not recommended for low VTE risk patients or high VTE risk patients (without bleeding risk)

A Path Forward for HMS Risk assessment is critical Pharmacologic Prophylaxis Groups with 90 day risk of VTE > 1% Caprini > 5 Padua > 4 Active bleeding and high VTE risk Mechanical prophylaxis Not at Risk for VTE No prophylaxis Ambulation for everyone!

Consistent with National Guidelines American College of Chest Physicians (ACCP) 2.4. For acutely ill hospitalized medical patients at low risk of thrombosis, we recommend against the use of pharmacologic prophylaxis or mechanical prophylaxis (Grade 1B) Definition of low risk ACCP: Padua risk score <4 HMS: Padua risk score <4 OR Caprini <3 (very low risk) Kahn SR. Chest. 2012 Feb;141(2 Suppl):e195S-226S. PMID: 22315261

Pharmacologic Prophylaxis Low Risk (p<.0001) 100% 90% 80% 70% 60% 50% 40% 65.0% 64.1% 63.3% 64.4% 61.9% 58.6% 50.3% 51.9% 51.8% 48.8% 47.5% 46.4% 56.1% 57.7% 57.0% 56.4% 42.8% 43.4% 42.5% 42.8% 52.8% 40.1% 30% 20% 10% 0% Caprini Padua

HMS Publication on Excess VTE Prophylaxis in Medical Patients Excessive prophylaxis in the low risk population Risk stratification between high and low risk is critical

Excess VTE Prophylaxis 79.7% 32.8% Grant, P et al. JAMA Int Med 2018

865 842 878 833 845 877 820 887 851 884 824 858 861 880 835 841 844 897 885 874 859 852 801 898 873 817 894 890 886 896 802 893 857 822 891 804 828 870 818 846 867 840 834 VTE Pharmacologic Prophylaxis Low Risk Caprini by Hospital 2017-2018 100% Collaborative = 44% 90% 80% 70% 60% 50% 40% 30% 20% 10% 0% 2018 Performance Index Collaborative Measure Goal: < 40%

VTE Pharmacologic Prophylaxis Low Risk Caprini by Hospital Quarter 2 2018 Collaborative Average = 48% 2018 Performance Index Collaborative Measure Goal: < 40%

VTE Pharmacologic Prophylaxis Low Risk Caprini by Quarter 2018 Performance Index Collaborative Measure Goal: < 40%

VTE Pharmacologic Prophylaxis Low Risk Padua by Hospital Quarter 2 2018 Collaborative Average = 65.5% 2018 Performance Index Collaborative Measure Goal: < 60%

VTE Pharmacologic Prophylaxis Low Risk Padua by Quarter 2018 Performance Index Collaborative Measure Goal: < 60%

Hospital Specific Examples

Metro Health - University of Michigan Health CHALLENGES WITH OVER-PROPHYLAXIS OF PATIENTS AT LOW RISK FOR VTE

VTE Low Risk Project Interventions 22 Our challenge has been inaccurate assignment of patients to moderate/high risk group. If accurately assessed as low risk, the patients typically do not receive orders for pharmacological prophylaxis. Added VTE Risk Assessment to Admission Order Set for all medicine patients (2013) o o Used 3 Bucket model similar to UC San Diego (Greg Maynard) Strengths: Simple and easy to use; no calculations required Reliable assessment of patients at moderate/high risk for VTE Accepted by medical staff

VTE Low Risk Project Interventions o Limitations/Barriers: 23 Initially, the threshold for moderate risk was set quite low ( 1 VTE risk factors) & very few patients fell into low risk category Most VTE assessments are completed by residents/apps who tend to be more cautious in assessing low risk & more hesitant to withhold VTE prophylaxis Even if attending hospitalist changes the initial order & discontinues pharmacological prophylaxis upon review, the first dose may have already been given, resulting in a fallout

VTE Low Risk Project Interventions Implemented revisions to the VTE Risk Assessment to more accurately identify low risk patients (still using 3 bucket model) & increased provider education/feedback o Results Started to see improvement in compliance to indicator 24 When VTE project changed to maintenance mode, compliance to this indicator began to decrease again because sepsis/acute infection was a risk factor that placed patient in moderate risk category (and VTE cases were associated with ABX project)

VTE Low Risk Project Interventions Revised VTE Risk Assessment again to more accurately identify low risk patients (still using 3 bucket model) o Risk factors are placed into 2 categories & weighted as high and moderate risk factors o Ongoing education is provided to the various groups with multiple methods to try to impact this indicator o Have not had sufficient time to assess results of this last change 25

VTE Risk Assessment in Medical Non-surgical, Non-ICU, Non-paralyzed HFHS Inpatients A Paradigm Shift in VTE Prophylaxis Scott Kaatz, DO, MSc, Division of Hospital Medicine, Henry Ford Hospital

Potential Conflict of Interest for Scott Kaatz Consultant Janssen Pfizer Portola Roche Research funding (to institution) Janssen Board membership (non-profit) AC Forum Thrombosis and Hemostasis Societies of North America National Certification Board of Anticoagulation Providers National Blood Clot Alliance Medical and Scientific Advisory Board None in over 12 months Consultant Bristol Myer Squibb Boehringer Ingelheim Daiichi Sankyo The Medicines Company Speaker honorarium Janssen Boehringer-Ingelheim Bristol Myer Squibb Pfizer Daiichi Sankyo CSL Behring

Acknowledgment We d like to collectively thank all the team members on the HFHS VTE taskforce for their efforts on this project. VTE Taskforce Members Arace, Alicia; Blasses, Cynthia; Bradley, Lisa; Caumartin, Elizabeth; Charara, Abdul-Nasser; Chu, Betty; Cooper, Michelle; Davies, Jennifer; Eichenhorn, Michael; Finch, Kimberly; Humayun, Fawwaz; Jordan, Jack; Kaatz, Scott; Marashi, Seyed Mani; Orta, Mary; Palombit, Margaret; Piotrowski, Megan; Punnoose, Maxin; Reddy, Vikram; Savage, Colleen; Schembri, Sherry; Schweyen, Deborah; Toth, Nicole; Valerio, Cynthia; Walsh, Kathleen; White, Cheryl

Joint Commission VTE Prevention Hospital Acquired Potentially-Preventable Venous Thromboembolism This measure assesses the number of patients diagnosed with confirmed VTE during hospitalization (not present at admission) who did not receive VTE prophylaxis between hospital admission and the day before the VTE diagnostic testing order date. Specifications Manual for National Hospital Inpatient Quality Measures Discharges 07-01-18 (3Q18) through 12-31-18 (4Q18) Version 5.4a Explicit documentation that the patient does not need VTE prophylaxis ALL INCLUSIVE VALIDATED RISK ASSESSMENTS: Caprini DVT Risk Assessment Padua Prediction Score International Medical Prevention Registry on Venous Thromboembolism (IMPROVE) http://www.jointcommission.org/specifications_manual_for_national_hospital_inpatient_quality_measures.aspx

Risk Assessment Models Using Mobility Criteria No consistent criteria for mobility No accepted mobility standard Ye F. J Thromb Thrombolysis. 2017 Jul;44(1):94-103. PMID: 28484939.

Frequently Cited Risk Assessment Models 90 day post admission VTE rates < 1% for low risk in all models ~ 2.5% for high risk in all models Greene MT. Am J Med. 2016 Sep;129(9):1001.e9-1001.e18. PMID: 27107925

Risk Factor History of DVT or PE? History of thrombophilia? Does patient have active cancer? Age greater than or equal to 60? Score Yes = 3 points; No = 0 points Yes = 3 points; No = 0 points Yes = 1 point; No = 0 points Yes = 1 point; No = 0 points Score Interpretation Low risk - score of 0-1 and predicted VTE 1.0% High score 2 indicates a considerably greater 3-month VTE risk of 2% IMPROVE Risk Assessment Model

LOW VTE RISK orderset NO VTE prophylaxis option is preselected

Discussion

Questions?