2018 Detailed Annual Report
© Society for Vascular Surgery Patient Safety Organization, 2018. All rights reserved. TABLE OF CONTENTS
1. Executive Summary: The Value of Participation in the VQI 3 2. VQI Members Profile 5 3. Outcomes and Data Quality Dashboards 6 4. Regional Quality Groups 7 5. Quality Improvement Projects: Learning from the Data 8 6. VQI National QI Projects 9 7. VQI Data Analysis 12 8. Using VQI Data for Collaborative Projects 12 9. Future Developments 15
APPENDICES
A. Participating Sites 17 B. SVS Patient Safety Organization 19 C. Medstreaming/M2S Technology Partner 19 D. VQI Registry Dashboards 20 E. Sample COPI Report (Endovascular AAA Length of Stay) and Best Practice Dashboard (Center-level) 32 F. VQI Regional Quality Groups and Leadership 37 G. VQI Quality Improvement Projects 2017/18 38 H. National Approved Project List, October 2017 – September 2018 39 I. National Publications, October 2017 – September 2018 44 J. SVS PSO Councils and Registry Committees 49
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SVS VQI 2018 Annual Report 1. EXECUTIVE SUMMARY—THE VALUE OF PARTICIPATION IN THE VASCULAR QUALITY INITIATIVE (VQI)
“If you can’t measure it, you can’t improve it.” This management catchphrase has been attributed to Edwards Deming, Peter Drucker, Lord Kelvin and others, but it could serve as the founding principle of the Vascular Quality Initiative. Our mission is to gath- er data to help hospitals and providers assess their performance and provide better vascular care.
VQI’s 12 registries contain demographic, clinical, use the strength of different societies (VQI, NCDR, procedural and outcomes data from more and SIR) to enhance device evaluation and than 500,000 vascular procedures performed to develop objective performance criteria for nationwide and in Canada. Each record the endovascular treatment of lower-extremity includes information from the patient’s initial arterial occlusive disease. VQI also works with hospitalization and at one-year follow-up. The industry to provide clinically detailed data for wealth of data allows centers and providers to device performance, post-market surveillance, compare their performance to regional and and label expansion. VQI has partnered with national benchmarks. All centers and providers vascular registries from Europe and Asia to receive biannual dashboards and regular form the International Consortium of Vascular performance reports, so they can use their Registries (ICVR) to bring a global perspective to data to support quality improvement initiatives. improving vascular care and device evaluation. Biannual regional meetings allow physicians of different specialties, nurses, data managers, quality officers, and others to meet, share information and ideas, and learn from each other in a positive and supportive environment. Members have used VQI data to significantly new56 centers improve the delivery of vascular care at local and national levels, reducing complications and 502 expenses. total centers
Investigators have used VQI data for risk 519,178 stratification, outcomes analysis, quality procedures improvement, defining best clinical practices, comparative effectiveness research and new99 data reducing resource utilization. This work has analysis projects resulted in more than 140 scientific publications in peer-reviewed journals since 2011. VQI 63 membership also facilitates participation new published journal articles in clinical trials and other medical device evaluation efforts.
The VQI collaborates with multiple organizations, 18 including the American College of Cardiology, new quality Society of Interventional Radiology, governmental improvement regulatory agencies, device manufacturers, and abstracts and payers. The Registry Assessment of Peripheral posters Interventional Devices (RAPID) is a collaboration of VQI with these other groups. RAPID plans to
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www.VQI.org Activities for 2017/2018 INTRODUCTION TO THE VQI 1. Center and procedure growth: As of September The Vascular Quality Initiative® (VQI®) is a 2018, VQI had reached two new milestones, with more collaboration of the Society for Vascular Surgery than 500 member centers and more than 500,000 Patient Safety Organization (SVS PSO), 18 vascular procedures in its registries. regional quality improvement groups organized under the SVS PSO, and Medstreaming/M2S, its 2. Projects and journal articles: In the past year, commercial technology partner. Other partners VQI’s Research Advisory Council approved 99 data include the American Venous Forum (AVF), the analysis projects using VQI data, and 63 articles were Society for Vascular Medicine (SVM), Vascular published in peer reviewed journals. Access Society of America (VASA) and the Society of Vascular Ultrasound (SVU), along 3. National quality improvement initiatives: The SVS with an additional 15 endorsing societies (see PSO launched two major quality initiatives, working Appendix B for the full list). with regional quality groups and centers to develop strategies to 1) increase the prescription of appropri- The mission of VQI is to improve the quality, ate discharge medications for secondary prevention safety, effectiveness and cost of vascular and 2) increase the use of imaging for long-term healthcare. follow-up of endovascular AAA patients. The SVS PSO is a wholly-owned LLC of the 4. Quality project program: There are 55 VQI centers Society for Vascular Surgery, with headquarters working on specific quality improvement projects. Re- in Chicago. The SVS PSO governs all functions sults will be presented as posters and abstracts at the of VQI, including the specification of data VQI@VAM meeting to take place in June 2019. elements captured in each registry, the types of standard reports made available to regional 5. Dashboards and Center Opportunity Profile groups, member hospitals and physicians, for Improvement (COPI) reports: The center-level and national quality improvement projects and physician-level dashboard reports are produced sponsored by VQI. quarterly for each VQI registry to report outcomes and provide benchmarks. COPI reports use VQI data to The SVS PSO is supported by 170 physician highlight process of care for improvement. volunteers who dedicate their time and effort in support of VQI’s mission. These physicians 6. VQI@VAM: The SVS PSO hosts this annual meeting in provide governance, clinical support to all conjunction with the SVS Vascular Annual Meeting to the registries and data analyses and ad-hoc present the latest quality activities, including in-depth support in areas such as industry partnerships case reviews, case study presentations, and outcomes and communications. In addition, all centers analysis as well as presentations from quality experts. and regions have lead physicians and regional VQI@VAM19 will be held at National Harbour, MD. medical directors to provide guidance, identify best practices and develop regional initiatives. 7. Industry projects: Five post-approval surveillance projects are currently underway in VQI. In addition, the The SVS PSO is funded by annual registry Transcarotid Surveillance Project (TSP) allows centers subscription fees from participating hospitals or to participate in the study and receive reimburse- physician groups, and additional contributions ment for eligible cases. VQI allows data collection for VQI projects are provided by corporate for CREST-2 participation and works with industry and supporters. regulatory agencies in the Registry Assessment of Pe- ripheral Interventional Devices (RAPID) and Superficial Popliteal EvidEnce Development (SPEED) projects.
8. Development: The SVS PSO is currently working on enhancements to VQI’s PVI and Hemodialysis regis- tries, and two new registries are nearing completion – the Vascular Medicine Registry and the Venous Stent VascularVascularRegistry. Quality Quality Initiative® Initiative®
4 SVS VQI 2018 Annual Report YEAR IN REVIEW 2017/2018 YEAR IN REVIEW 2017/2018
Bard LifeStent® Popliteal Artery Initial work has been completed on defining a Technology Improvements VQI Activity Stent Project set of core data elements as well as unique with External This post-approval surveillance project is device identifiers.The current phase involves Through M2S Outcomes Reporting designed to further evaluate the Bard analyzing device performance. The 4th Annual Stakeholders LifeStent® for treatment of popliteal artery Meeting was held recently in Silver Spring, MD. atherosclerosis. It will enroll 74 patients with Daniel Bertges, MD, University of Vermont Registry Revisions New Quarterly Dashboards Medical Center, presented a preliminary MEDICAL DEVICE two-year follow up, and remains open for Transition to the newly revised CAS registry was completed, with These Registry-specific reports allow physicians and centers to compare member participation. analysis of endovascular device performance in MANUFACTURE PROJECTS the superficial femoral and popliteal artery mapping of old registry data elements such that all data are available to their performance to regional and national benchmarks on dozens of location. The goal is to share data from multiple centers in the Analytic Engine. Enhancements to the PVI registry included process and outcome measures. Medtronic IN.PACT Admiral DCB the addition of drawings to illustrate TASC grading and regular updates to TCAR Surveillance Project registries to provide a larger database for ISR Project analysis. The FDA hopes to use this real-world devices through GUDID data importing. Semi-Annual Regional Reporting This project is designed to collect one-year This post-approval surveillance project is experience to assist in regulatory decision The SVS PSO produces de-identified reports in the spring and fall that follow up data to assess the real-world making. IVC Filter Retrieval Report & Email Notification outcomes of trans-carotid artery revasculariza- designed to confirm that IN.PACT Admiral drug give centers detailed information about their performance on more than tion (TCAR) in comparison with carotid coated balloons are safe and effective for This report identifies patients with a temporary IVC filter at the time that 20 key measures, such as postop stroke and length of stay, across all treatment of in-stent restenosis lesions in the removal is indicated and notifies the provider or staff by email to assist registries. These reports, which show how each center compares to other endarterectomy as performed in VQI centers. In International Consortium of September 2016, CMS approved reimburse- superficial femoral and popliteal arteries. This YEAR thisIN process. REVIEW This report facilitates 2017/2018 physician and office workflow centers2. in VQI its region MEMBERS and to other centers nationally,PROFILE are the principalYEAR IN REVIEW 2017/2018 ment for physicians and centers that perform project will enroll 300 patients with three-year Vascular Registries (ICVR) facilitating improved patient care. topic of discussion2. VQI Members at the spring Profile and fall meetings of the VQI regional follow-up and remains open for member groups. Reports are distributed to all users directly in secure file formats. THE VQI REGISTRIES TCAR procedures on both symptomatic and VQI and 11 other national vascular registries Figure 2.1: Growth of VQI Centers (YTD September 2018) participation. asymptomatic medical high-risk patients, from Europe and Australasia combined data to Audit & Supplemental Data Query Worklist As of September 2017, there were 12 VQI reg- Figure 2.1: Growth of VQI Centers (YTD September 2018) provided that those procedures and follow-up analyze variation in treatment of carotid and This new tool within PATHWAYS allows VQI participants to respond to Center Outcome Performance for Improvement istries that contained 413,905 vascular pro- COLLABORATIVE PROJECTS aortic aneurysm disease across countries. are entered into the VQI CAS Registry. The SVS Bard LifeStent® Poplitealdata audits Artery and queries initiatedInitial workby the has SVSbeen PSO. completed It provides on defininga rapid a Reports (COPI)Growth of VQI Centers cedures. During the past year (October 2017 PSO Steering Committee will make periodic WITH OTHER VQI CurrentActivity projects are analyzing volume-outcome YEARinterface IN with REVIEW Pathways data such2017/2018 that users can easily edit or add Technology ImprovementsYEAR IN REVIEW 2017/2018 Stent Project set of core data elements as well as unique The SVS PSO produces periodic analyses that look in depth at a single key through September 2018), there were over data analyses. Publication of data collected in ORGANIZATIONS relationships and variations between countries needed data identified bydevice SVS PSO identifiers.The audits. current phase involves outcome, determine patient and procedural factors that increase risk of withfor Externalcarotid and AAA treatment, as well asThis post-approval surveillance project is Through500 M2S 100,000Outcomes procedures addedReporting to the registries, for a this project which will help inform future CMS designed to further evaluate the Bard analyzing device performance. The 4th Annual that outcome, and show centers how they compare to their region and CAS coverage decisions and two abstracts will developing a core dataset for future PAD QCDR and MIPS Meeting was held recently in Silver Spring, MD. the nation on each of those risk factors. Recent topics have included LOS total of 519,178. Registry Assessment of PeripheralStakeholders projects. A project to evaluate EVAR devicesLifeStent® for treatment of popliteal artery be presented by the TCAR Steering Committee atherosclerosis. It will enrollM2S 74 was patients approved with by CMSDaniel as a QualifiedBertges, MD, Clinical University Data Registryof Vermont (QCDR) afterRegistry CEA and hematomaRevisions after PVI. New Quarterly Dashboards Interventional Devices (RAPID) used to treat ruptured AAA is underway. Medical Center, presented a preliminary at VAM18. two-yearBard follow LifeStent® up, and remainsfor Popliteal the open2018 forProgramArtery Year. ThisInitial is the 10thwork hasconsecutive been completed year thaton definingthe M2S a 400 VQI is an active participant in RAPID, whichMEDICAL has DEVICE analysis of endovascular device performance in TransitionTechnology to the newly revised CAS Improvementsregistry was completed, with These Registry-specific reports allow physicians and centers to compare VQI Activity member participation. has been involved in CMS’s PQRSset program,of core data and elements the 4th as year well that as unique the M2S mapping of old registry data elements such that all data are available to their performance to regional and national benchmarks on dozens of developed a minimum core dataset for the MANUFACTURE PROJECTS Stent Project the superficial femoral and popliteal artery TEVAR Dissection Project CREST-2 Registry has been an approved QCDR. Baseddevice on identifiers.The the VQI Registry, current M2S phase supports involves centers in the Analytic Engine. Enhancements to the PVI registry included process and outcome measures. evaluation of endovascular peripheral arterial with External This post-approval surveillance project is location. The goal is to share data from multiple This project, initiated in 2014, has demonstrat- This randomized controlled clinical trial Medtronic IN.PACTreporting Admiral of DCB 12 MIPS individualanalyzing measures device and performance.13 QCDR non-MIPS The 4th Annual the additionThrough of drawings to illustrateM2S TASC grading and regular updates to Outcomes Reporting devices from multiple data sources. RAPID is a designed to further evaluate the Bard registries to provide a larger database for 300 ed the value of expanding surveillance to real TCAR Surveillancecompares CEA Project and CAS to best medical therapy. individual measures for the 2018Meeting MIPS reportingwas held recently period, in whichSilver areSpring, MD. devices through GUDID data importing. Total Procedures Public Private Partnership between the FDA, Stakeholders ISR LifeStent®Project for treatment of popliteal artery analysis. The FDA hopes to use this real-world Semi-Annual Regional Reporting world device performance while meeting FDA This projectInvestigators is designed to use collect VQI one-yearto report CAS proceduresatherosclerosis. It willavailable enroll 74 to patients all VQI physicianwith experience members.Daniel toBertges, assist inMD, regulatory University decision of Vermont professional societies (SVS, ACC, SIR), academia, This post-approval surveillance project is Registry Revisions The SVSNew PSOCaptured Quarterly produces de-identified Dashboards reports5 in 1the9 spring,1 7and8 fall that requirements, with faster patient enrollment follow up todata become to assess qualified the real-world for this trial and then two-year follow up, and remains open for making.Medical Center, presented a preliminary IVC Filter Retrieval Report & Email Notification industry, payers, and others to support a outcomesMEDICAL of trans-carotid DEVICE artery revasculariza- designed to confirm that IN.PACT Admiral drug analysis of endovascular device performance in Transition to the newly revised CAS registry was completed, with give centersThese Registry-specific detailed information reports about allow their physicians performance and centers on more to compare than compared to traditional study methodology. In report non-randomized procedures during themember participation. 200 national medical device evaluation system. tionIn MANUFACTURE(TCAR) in comparison with PROJECTS carotid coated balloons are safe and effective for the superficial femoral and popliteal artery This reportmapping identifies of old registry patients data with elements a temporary such thatIVC allfilter data at arethe availabletime that to 20 keytheir measures, performance such as to postop regional stroke and nationaland length benchmarks of stay, across on dozensall of partnership with Gore and Medtronic, the SVS trial. This year more than 90 interventioniststreatment of in-stent restenosis lesions in the process and outcome measures. Phase 2, VQI data is being used to develop endarterectomy as performed in VQI centers. In location. The goal is to share data from multiple removalcenters is indicated in the Analytic and notifies Engine. the Enhancements provider or staff to theby emailPVI registry to assist included registries. These reports, which show how each center compares to other PSO and M2S completed enrollment of the used VQI to report more than 800 CAS superficialMedtronic femoral andIN.PACT popliteal Admiral arteries. This DCB International Consortium of this process.the addition This reportof drawings facilitates to illustrate physician TASC and gradingoffice workflow and regular updates to centersPeripheral in its region Vascular and to other Intervention centers nationally,164,793 are the principal objective performance criteria (OPC) for SeptemberTCAR 2016, Surveillance CMS approved Project reimburse - registries to provide a larger database for five-year cohort with annual follow ups procedures for the CREST-2 Registry project.project will enroll 300 patients with three-year Vascularanalysis. Registries The FDA hopes (ICVR) to use this real-world facilitatingdevices improved through GUDIDpatient data care. importing. topic of discussion at the spring and fall meetings of the VQI regional contemporary interventional treatment of ment for physicians and centers that perform ISR Project 100 Semi-Annual Regional Reporting continuing for five years, and the one-year This project is designed to collect one-year follow-up and remains open for member VQI and 11 other national vascular registries groups.Carotid Reports Endarterectomy are distributed to all users directly108,485 in secure file formats. SFA-popliteal arteries. TCAR procedures on both symptomatic and This post-approval surveillance project is experience to assist in regulatory decision The SVS PSO produces de-identified reports in the spring and fall that cohort of 200 patients otherwise recorded in asymptomaticfollow up datamedical to assess high-risk the real-worldpatients, participation. frommaking. Europe and Australasia combined data to AuditIVC & Filter Supplemental Retrieval ReportData Query & Email Worklist Notification outcomes of trans-carotid artery revasculariza- designed to confirm that IN.PACT Admiral drug Infra-Inguinalgive centers detailed Bypass information about their48,350 performance on more than the TEVAR registry. provided that those procedures and follow-up coated balloons are safe and effective for analyze variation in treatment of carotid and This newThis reporttool within identifies PATHWAYS patients allows with VQI a participantstemporary IVC to filterrespond at the to time that Center20 key Outcome measures, suchPerformance as postop stroke for and Improvement length of stay, across all tion (TCAR) in comparison with carotid COLLABORATIVE PROJECTS aortic aneurysm disease across countries. are entered into the VQI CAS Registry. The SVS data 0audits and queries initiated by the SVS PSO. It provides a rapid Reports (COPI) endarterectomy as performed in VQI centers. In treatment of in-stent restenosis lesions in the removalJan-10 Jan-11 is indicatedJan-12 Jan-13 andJan-14 notifiesJan-15 Jan-16 the providerJan-17 Jan-18 or staff by email to assist Endovascularregistries. These reports,AAA Repair which show how each43,773 center compares to other PSO Steering Committee will make periodic WITHsuperficial OTHER femoral and popliteal arteries. This CurrentInternational projects are analyzing Consortium volume-outcome of interfacethis process.with Pathways This report data facilitatessuch that usersphysician can easilyand office edit workflowor add The SVScenters PSO inproduces its region periodic and to analysesother centers that look nationally, in depth are at thea single principal key September 2016, CMS approved reimburse- relationships and variations between countries needed data identified by SVS PSO audits. data analyses. Publication of data collected in ORGANIZATIONSproject will enroll 300 patients with three-year Vascular Registries (ICVR) facilitating improved patient care. outcome,topic determineof discussion patient at the andspring procedural and fall meetingsfactors that of increase the VQI regionalrisk of this projectment for which physicians will help and inform centers future that CMSperform for carotid andVQI AAA treatment, Member as well as Characteristics Hemodialysis Access 42,967 TCAR procedures on both symptomatic and follow-up and remains open for member VQI and 11 other national vascular registries that outcome,groups. Reports and show are distributedcenters how to they all users compare directly to their in secure region file and formats. CAS coverage decisions and two abstracts will participation. developing a core dataset for future PAD QCDRSource: M2S and PATHWAYS MIPS Data, September 2018 the nation on each of those risk factors. Recent topics have included LOS asymptomatic medical high-risk patients, Registry Assessment of Peripheral projects.from A Europe project and to evaluate Australasia EVAR combined devices data to Audit & Supplemental Data Query Worklist Carotid Artery Stent 24,077 be presented by the TCAR Steering Committee FIGURE 2 FIGUREM2S 3 was approved by CMS as a Qualified Clinical Data Registry (QCDR) after CEA and hematoma after PVI. provided that those procedures and follow-up Interventional Devices (RAPID) used analyzeto treat variation ruptured inAAA treatment is underway. of carotid and This new tool within PATHWAYS allows VQI participants to respond to Center Outcome Performance for Improvement at VAM18. COLLABORATIVE PROJECTS aortic aneurysm disease across countries. FigureforFigure the 2.2: 20182.2: VQI Program Participating Participating Year. Hospital This is TypesHospital the 10th consecutiveTypes year that the M2S Industry Support are entered into the VQI CAS Registry. The SVS VQI is an active participant in RAPID, which has data audits and queries initiated by the SVS PSO. It provides a rapid VaricoseReports Vein (COPI) 23,526 Current projects are analyzing volume-outcome has been involved in CMS’s PQRS program, and the 4th year that the M2S PSO Steering Committee will make periodic developedWITH a minimum OTHER core dataset for the interface with Pathways data such that users can easily edit or add The SVS PSO produces periodic analyses that look in depth at a single key TEVAR Dissection Project VQI PhysicianCREST-2 Specialtyrelationships Registry andDistribution variations between countries hasTypes been an approved of Affiliation, QCDR. Based on theVQI VQI Registry,Centers M2S supports Quality Champions data analyses.Quality Publication Partners of data collected in evaluationORGANIZATIONS of endovascular peripheral arterial needed data identified by SVS PSO audits. Supra-Inguinaloutcome, determine Bypass patient and procedural 16,197factors that increase risk of This project, initiated in 2014, has demonstrat- This randomizedfor carotid andcontrolled AAA treatment, clinical trial as well as reporting of 12 MIPS individual measures and 13 QCDR non-MIPS this project which will help inform future CMS devices from multiple data sources. RAPID is a that outcome, and show centers how they compare to their region and ed the value of expanding surveillance to real comparesdeveloping CEA and a core CAS datasetto best formedical future therapy. PAD individual measures7% for the 2018 MIPS reporting period, which are CAS coverage decisions and two abstracts will Public Private Partnership between the FDA, QCDR and MIPS Thoracicthe nation & on Complex each of those EVAR risk factors. Recent12,665 topics have included LOS world device performance while meeting FDA Registry Assessment of Peripheral Investigatorsprojects. Ause project VQI to to report evaluate CAS EVAR procedures devices available to all VQI physician members. be presented by the TCAR Steering Committee professional societies (SVS, ACC, SIR), academia, M2S was approved by CMS as a Qualified Clinical Data Registry (QCDR) after CEA and hematoma after PVI. requirements, with faster patient enrollment Interventional Devices (RAPID) to becomeused to qualified treat ruptured for this AAAtrial isand underway. then at VAM18. industry, payers, and others to support a for the 2018 Program Year. This is the 10th consecutive year that the M2S compared to traditional study methodology. In report non-randomized procedures during the Lower Extremity Amputations 12,098 nationalVQI is medicalan active device participant evaluation in system.RAPID, whichIn has has been involved in CMS’s PQRS program, and the 4th year that the M2S partnership with Gore and Medtronic, the SVS trial. This year more than 90 interventionists 37% TEVAR Dissection Project Phasedeveloped 2, VQI data a minimumis being used core to dataset develop for the CREST-2 Registry has been an approved QCDR. Based on the VQI Registry, M2S supports PSO and M2S completed enrollment of the evaluation of endovascular peripheral arterial used VQI to report more than 800 CAS 27% Open AAA Repair 11,377 This project, initiated in 2014, has demonstrat- objective performance criteria (OPC) for This randomized controlled clinical trial reporting of 12 MIPS individual measures and 13 QCDR non-MIPS five-year cohort with annual follow ups devices from multiple data sources. RAPID is a procedures for the CREST-2 Registry project. ed the value of expanding surveillance to real contemporary interventional treatment of compares CEA and CAS to best medical therapy. individual measures for the 2018 MIPS reporting period, which are continuing for five years, and the one-year Public Private Partnership between the FDA, IVC Filter 10,870 world device performance while meeting FDA SFA-popliteal arteries. Investigators use VQI to report CAS procedures available to all VQI physician members. cohort of 200 patients otherwise recorded in professional societies (SVS, ACC, SIR), academia, requirements, with faster patient enrollment to become qualified for this trial and then the TEVAR registry. industry, payers, and others to support a compared to traditional study methodology. In report non-randomized procedures during the national medical device evaluation system. In partnership with Gore and Medtronic, the SVS trial. This year more than 90 interventionists Phase 2, VQI data is being used to develop PSO and M2S completed enrollment of the used VQI to report more than 800 CAS objective performance criteria (OPC) for five-year cohort with annual follow ups procedures for the CREST-2 Registry project. 29% VQI Member Characteristics continuing for five years, and the one-year contemporary interventional treatment of SFA-popliteal arteries. cohort of 200 patients otherwise recorded in FIGURE 2 FIGURE 3 the TEVAR registry. Industry Support Figure 2.3: Distribution of VQI Physician Specialties 6 www.vqi.org Quality Champions Quality Partners www.vqi.org VQI Physician Specialty Distribution 3 Types of Affiliation, VQI Centers 5% 3% VQI Member Characteristics 8% Industry Support FIGURE 2 FIGURE 3 9% Quality Champions Quality Partners VQI Physician Specialty43% Distribution Types of Affiliation, VQI Centers
15%
17%
6 www.vqi.org www.vqi.org 35 www.VQI.org
6 www.vqi.org www.vqi.org 3 3. OUTCOMES & DATA QUALITY DASHBOARDS
The VQI dashboards allow physicians and centers to compare their performance to regional and national benchmarks. The SVS PSO registry committees selected outcome measures to be reported in the dashboards, which are distributed quarterly to VQI members. The dashboards provide each physician his or her individual results, along with results for the physician’s center, region and across all VQI. Results that are in the top 25th percentile are highlighted in green and those in the bottom 25th percentile are highlighted in red.
Table 3.1: Sample Physician Dashboard, PVI Registry
Your Your Your VQI Category Outcome/Complication Results Center Region Overall Case Data Number of cases reviewed 3 46 2466 28817 Hematoma Any Hematoma 0% 4.4% 4.2% 2.4% Moderate/Major Hematoma 0% 0% 0.7% 0.7% Discharge Medications (excludes death in Antiplatelet 100% 95.3% 96.1% 94.1% hospital) Statin 100% 93% 86.1% 82.3% Smoking in Claudicants Never 0% 0% 9.5% 11.4% Prior 0% 22.2% 56.7% 49.3% Current 100% 77.8% 33.8% 39.3% 9-Month Outcomes Your Your Your VQI (JulyCategory 2015-June 2016 Outcome/Complication9-Month AFS* for CLI No cases 100% 90.8% 87.4%*** Results Center Region Overall with 9-month LTFU) 9-Month MALE** for CLI No cases 0% 13% 20.6%*** Long term follow-up (July 2015-June 2016) Long term follow-up rate No cases 87.5% 88.9% 71.4%
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4. REGIONAL QUALITY GROUPS
Regional quality groups distinguish VQI from almost all other registries. Each of the 18 groups hold biannual meetings that provide a forum for discussion and work on quality improvement.
Figure 4.1: VQI Regional Group Map
During each region’s biannual meeting, members review and discuss their region’s data. Many groups identify an area for improvement and launch region-wide efforts to improve care. Topics that the groups have chosen to focus on include:
• Use of ultrasound guidance for peripheral interventions
• Increased recording of hemodynamic data (ABI/TBI) prior to peripheral intervention
• Measuring aneurysm sac diameter one year following EVAR and TEVAR
• Renal protection from contrast administration during peripheral interventions
• Increasing rates of IVC filter retrieval • Reducing LOS for multiple registries
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www.VQI.org 5. QUALITY IMPROVEMENT QUALITY IMPROVEMENT PROJECTS PROJECTS: LEARNING FROM In response to this new charter initiative, THE DATA 55 VQI centers have submitted charters in 2018. The charters included the two The QI Community national initiatives, Discharge Medications The SVS PSO is encouraging centers to submit and EVAR LTFU Imaging, as well as clinical quality improvement charters on projects using and documentation topics. Selected VQI data. This process has helped the SVS PSO charter projects are listed below. identify groups working on similar initiatives and Table 5.1 – Quality Improvement Projects to Date facilitate networking opportunities. All members are encouraged to participate in focused group PARTICIPATING calls whether or not they have a charter. As CENTERS these projects reach completion, the SVS PSO will TOPICS aggregate data and share best practices with the full VQI membership. Discharge Medications 20 (National Initiative)
The SVS PSO also provides resources to assist VQI LOS (CEA and EVAR) 11 centers with their QI projects: LTFU (including EVAR Imaging, a 8 National Initiative), IVCF Retrieval • QI Project Guide and National Initiative Supplement: These booklets provide the Clinical: Blood Transfusion, 6 foundation and step-by-step guidance to begin AAA Processes, Limb Salvage, SSI and complete a QI project. The QI Project Smoking Cessation 5 Guide is designed to assist centers that are just beginning a QI project but may be useful Documentation: Epic Workflow, 5 at any stage of the QI process. Subsequently, Preop ABI, PVI Documentation the SVS PSO created a National Initiative TOTAL 55 Supplement, which focused on the progress with the two national QI priorities: Optimal Discharge Medications for Vascular Patients and Endovascular AAA Long-Term Follow-Up with Imaging.
• The “Members Only” area of the VQI website (www.vqi.org) offers access to national QI materials, including presentations and videos, as well as a QI discussion forum to encourage interaction among centers.
• National and regional meetings and quarterly calls help VQI data managers share best practices and QI project ideas.
8 SVS VQI 2018 Annual Report 6. NATIONAL QUALITY From January 2012 to the present, the prescription of antiplatelets and statins at IMPROVEMENT INITIATIVES— discharge has risen steadily among VQI DISCHARGE MEDICATIONS members as information about its benefits was disseminated through presentation of the data AND EVAR LONG-TERM analysis, publication of the results and sharing of FOLLOW-UP IMAGING reports with centers and physicians. In addition to the original data analysis and publication led Experienced VQI centers have applied registry by Randall DeMartino, MD, the SVS PSO provided data and implemented innovative approaches webinars and presentations at the VQI Annual to improve success rates for these initiatives. Meeting as part of this national QI initiative. The SVS PSO seeks to build on these efforts and Individual QI charters and regional presentations help these QI initiatives expand from clusters of continue to reinforce the importance and innovation to coast-to-coast improvements. success of these efforts. Optimal Discharge Medications for Vascular Figure 6.2: Discharge Medications and Statin Rate for 123 VQIFigure Hospitals 6.2: Discharge (2012 Medications to Date) and Statin Rate for 123 VQI Hospitals (2012 to Date) Patients The VQI’s first national QI initiative is the prescribing of antiplatelet agents and statins at discharge to improve patients’ long-term vascular health. Discharge medications was selected because it is a treatment that affects most vascular surgery patients and is readily actionable. There is strong evidence that antiplatelet agents and statins increase patient survival.
VQI data has shown that patients undergoing arterial procedures who received a discharge SOURCE: VQI prescription of antiplatelet medications and a statin had significantly better 5-year survival. The SOURCE: VQI For example, South Bend Hospital used VQI data VQI provided physicians with individual reports For example, South Bend Hospital used VQI data to show that only 65.9% of their patients in 2014 received antiplatelet showing their prescribing rates for discharge toand show statin medications. that only They 65.9% used a combinationof their patients of clinical protocols, in 2014 education and workforce reallocation to increase medications and how they compared to their receivedthe rate to 97.9 antiplatelet% in early 2016. Theand SVS statin PSO is now medications. developing a program designed specifically to help centers with peers. The VQI also disseminated evidence- Theythe greatest used opportunity a combination for improvement. of clinical protocols based information and tools for providers and at discharge following a vascular operation, patients, such as templated communications to educationNational QI Initiative: and EVAR workforce Long Term Followreallocation-Up (LTFU) Imaging to EVAR requires long-term monitoring to ensure the durability of repair. EVAR patients are susceptible to the late development of primary care physicians, to increase the number increaseendoleaks, which the can rate occur in to up to97.9% 20% of patientsin early and may2016. result The in rupture SVS. To ensure that patients achieve successful of patients receiving optimal medications. PSOoutcomes is now after EVAR, developing long-term follow a-up program imaging is essential designed, though recent studies have demonstrated low compliance rates specificallywith long-term follow to-up helpimaging aftercenters EVAR. with the greatest
opportunity for improvement. ______EVAR(SIDEBAR/Quote Long-Term from Dr. Scali) Follow-Up (LTFU) Imaging
EVAR “Endovascular requires aortic aneurysm long-term repair (EVAR) monitoring is a non-curative to treatment ensure of infrarenalthe abdominal aortic aneurysm disease. When durabilitycommercially available of repair. devices areEVAR used withinpatients their instructions are susceptible for use, excellent long-term rupture-free survival can be toantic theipated. late However, development due to the persistent of presence endoleaks, of the aneurysm which and the life-long risk of device related failure and/or canendoleak occur, up to 20% in ofup patients to 20%may experience of patients some form and of aorta may-related result re-intervention after EVAR. For this reason, long-term follow-up (LTFU) imaging after EVAR is mandatory, and patients need to be educated about this preoperatively and repeatedly induring rupture. follow-up. Recent It is the obligation studies of the haveoperating demonstrated surgeon to stress the need for life-long imaging surveillance and integrate lowdiscuss complianceions about LTFU into ratesall stages with of AAA long-termEVAR care to ensure follow- that their patients achieve durable outcomes.” —Salvatore upScali, imaging MD after EVAR. To ensure that patients
achieve______successful outcomes after EVAR, long- term follow-up imaging is essential.
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www.VQI.org SAMPLE NATIONAL QI INITIATIVE DASHBOARD:
Discharge Medications (2018 Procedures) Excludes patients who died in hospital and patients who were not treated for medical reason or non- compliant.Includes CEA, CAS, OAAA, EVAR, TEVAR, INFRA, SUPRA, PVI and LEAMP procedures entered in the VQI as of March 31,2018. For theExcludes 2018 patients Participation who died inAwards, hospital centersand patients that who are were above not treated the 2018 for medical 75th percentile reason or non-compliant. for the rate of dischargeIncludes antiplatelet+statinCEA, CAS, OAAA, EVAR, willTEVAR, receive INFRA, a SUPRA, point PVI toward and LEAMP their procedures final award entered (as inlong the VQIas theiras of Marchrate is 31, not 2018.significantly lower than their 2017 rate). Centers that are below the 75th percentile but show statisticallyFor the significant 2018 Participation improvement Awards, centers (p-value<.05) that are above overthe 2018 their 75th 2017 percentile rate forwill the also rate receive of discharge a point toward theirantiplatelet+statin final award. will receive a point toward their final award (as long as their rate is not significantly lower than their 2017 rate). Centers that are below the 75th percentile but show statistically significant improvement (p-value<.05) over their 2017 The ratefirst will two also lines receive of a thepoint table toward belowtheir final show award. your center’s current antiplatelet+statin rate for 2018 cases. OtherThe first rows two lines show of the the table rate below of discharge show your center’s antiplatelet+statin current antiplatelet+statin that must rate forbe 2018 achieved cases. Other among rows your expectedshow the numberrate of discharge of remaining antiplatelet+statin 2018 cases that must for be your achieved center among to yourreach expected the 75thnumber percentile of remaining for 2018 2017, cases or to showfor statistically your center to significantreach the 75th improvement percentile for 2017, over or to its show 2017 statistically rate. Note significant that improvementthe 75th percentile over its 2017 for rate. 2017 has been providedNote that the as 75tha benchmark, percentile for 2017but hasthe been 75th provided percentile as a benchmark, for 2018 but cases the 75th will percentile likely be for different 2018 cases than will it waslikely for 2017.be different Thus, than reaching it was for the 2017. 75th Thus, percentile reaching the 75thfor 2017 percentile will notfor 2017 guarantee will not guarantee that your that yourcenter center is isabove the above75th thepercentile 75th percentile for 2018. for 2018. Results Number of 2018 procedures meeting inclusion criteria that your center had entered as of March 31, 112 2018 N (%) of 2018 patients receiving antiplatelet+statin 105 (94%) 75th percentile of antiplatelet+statin rates among VQI centers for 2017 89% Your center’s antiplatelet+statin rate for 2017 cases 90% Estimated total number of procedures your center will enter for 2018* 493 Estimated number of cases remaining to be entered 381 If your center is above the 75th percentile for 2017, minimum rate among estimated remaining 2018 cases to stay there 336/381 (88%) If your center is below the 75th percentile for 2017, minimum rate among estimated remaining 2018 cases to reach the 75th percentile or show statistically significant improvement over your 2017 rate NA (above 75th percentile)
*Extrapolated from your center’s case volume for Jan-Mar 2018.
Follow-Up Imaging After EVAR (2016 Procedures) Excludes patients who died within 21 months of surgery. “Imaging” includes CT, CTA, MR, MRA, duplex, and/orFollow-Up angiogram imaging Imaging between After 9 and EVAR 21 months (2016 of surgery. procedures) Time from surgery to imaging = Date of follow-up visit where surgery was recorded — surgery date. Excludes patients who died within 21 months of surgery. “Imaging” includes CT, CTA, MR, MRA, duplex, and/or angiogram imaging between 9 and 21 months of surgery. Time from surgery to imaging = Date of follow-up visit EVARwhere is used surgery to wastreat recorded AAA to — preventsurgery date. rupture and improve survival. Patients must have good survival and successful aneurysm exclusion to offset the risk of operation and gain benefit. All EVAR patients EVAR is used to treat AAA to prevent rupture and improve survival. Patients must have good survival and successful should undergo annual imaging to confirm success of the procedure and demonstrate absence of aneurysm exclusion to offset the risk of operation and gain benefit. All EVAR patients should undergo annual imaging to endoleak,confirm success which of could the procedure lead toand rupture. demonstrate absence of endoleak, which could lead to rupture.
For the For2018 the Participation 2018 Participation Awards, Awards, centerscenters that that are above are abovethe 2016 the75th 2016percentile 75th for percentile EVAR follow-up for imaging EVAR willfollow- receive a point toward their final award (as long as their rate is not significantly lower than their 2015 rate). Centers that are up imagingbelow the 75thwill percentilereceive buta point show statisticallytoward their significant final improvement award (as over long their as2015 their EVAR rate follow-up is not imaging significantly rate will alsolower thanreceive their a 2015 point towardrate). theirCenters final award. that are below the 75th percentile but show statistically significant improvement over their 2015 EVAR follow-up imaging rate will also receive a point toward their final The table below shows your center’s current imaging rate for 2016 cases and the number of additional cases with award. imaging that must be reported for your center to reach the 75th percentile for 2015, or to show statistically significant improvement over its 2015 imaging rate. 10 SVS VQI 2018 Annual Report Excludes patients who died in hospital and patients who were not treated for medical reason or non-compliant. Includes CEA, CAS, OAAA, EVAR, TEVAR, INFRA, SUPRA, PVI and LEAMP procedures entered in the VQI as of March 31, 2018. The tableFor below the 2018 shows Participation your Awards,center’s centers current that are imaging above the rate 2018 for 75th 2016 percentile cases for and the rate the of numberdischarge of additionalantiplatelet+statin cases with will receive imaging a point that toward must their be final reported award (as for long your as their center rate is tonot reachsignificantly the lower 75th than percentile their 2017 for 2015,rate). or toCenters show that statistically are below the significant 75th percentile improvement but show statistically over significant its 2015 improvementimaging rate. (p-value<.05) over their 2017 rate will also receive a point toward their final award. Note thatThe the first 75thtwo lines percentile of the table for below 2015 show has your been center’s provided current antiplatelet+statin as a benchmark rate for because 2018 cases. centers Other rows have hadshow a full the 21 rate months of discharge to enter antiplatelet+statin follow-up thatfor mustthose be cases,achieved but among the your 75th expected percentile number for of remaining 2016 cases 2018 willcases likely be differentfor your center than to itreach was the for 75th 2015. percentile Thus, forreaching 2017, or tothe show 75th statistically percentile significant for 2015improvement will not over guarantee its 2017 rate. that your centerNote thatis above the 75th the percentile 75th percentilefor 2017 has been for 2016. provided as a benchmark, but the 75th percentile for 2018 cases will likely be different than it was for 2017. Thus, reaching the 75th percentile for 2017 will not guarantee that your center is above the 75th percentile for 2018. Results Number of 2018 procedures meeting inclusion criteria that your center had entered as of March 31, 112 2018 N (%) of 2018 patients receiving antiplatelet+statin 105 (94%) 75th percentile of antiplatelet+statin rates among VQI centers for 2017 89% Your center’s antiplatelet+statin rate for 2017 cases 90% Estimated total number of procedures your center will enter for 2018* 493 Estimated number of cases remaining to be entered 381 If your center is above the 75th percentile for 2017, minimum rate among estimated remaining 2018 cases to stay there 336/381 (88%) If your center is below the 75th percentile for 2017, minimum rate among estimated remaining 2018 cases to reach the 75th percentile or show statistically significant improvement over your 2017 rate NA (above 75th percentile)
*Extrapolated from your center’s case volume for Jan-Mar 2018.
Follow-Up Imaging After EVAR (2016 procedures) Excludes patients who died within 21 months of surgery. “Imaging” includes CT, CTA, MR, MRA, duplex, and/or angiogram imaging between 9 and 21 months of surgery. Time from surgery to imaging = Date of follow-up visit where surgery was recorded — surgery date. “Endovascular aortic aneurysm repair (EVAR) is a non-curative treatment of infrarenal EVAR is used to treat AAA to prevent rupture and improve survival. Patients must have good survival and successful abdominalaneurysm exclusion aortic to aneurysmoffset the risk disease. of operation When and gain commercially benefit. All EVAR available patients should devices undergo are annual used imaging within to their instructionsconfirm success for of use, the procedureexcellent and long-term demonstrate rupture-free absence of endoleak, survival which can could be lead anticipated. to rupture. However, due to the persistent presence of the aneurysm and the life-long risk of device-related failure and/ For the 2018 Participation Awards, centers that are above the 2016 75th percentile for EVAR follow-up imaging will orreceive endoleak, a point towardup to their20% final of patientsaward (as long may as theirexperience rate is not significantlysome form lower of aorta-relatedthan their 2015 rate). re-intervention Centers that are afterbelow EVAR. the 75th For percentile this reason, but show long-term statistically follow-up significant improvement (LTFU) imaging over their after 2015 EVAR EVAR follow-upis mandatory, imaging rateand will also patientsreceive a pointneed toward to be their educated final award. about this preoperatively and repeatedly during follow-up. It is the obligation of the operating surgeon to stress the need for life-long imaging surveillance and The table below shows your center’s current imaging rate for 2016 cases and the number of additional cases with integrateimaging that discussions must be reported about for yourLTFU center into toall reach stages the 75th of AAA percentile EVAR for care 2015, orto to ensure show statistically that their significant patients achieveimprovement durable over its outcomes.” 2015 imaging rate. —Salvatore Scali, MD, Professor of Surgery, University of Florida
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www.VQI.org the use of protamine and carotid patching from the Vascular tudy roup of e England and for discharge medications from the V . As of ctober the RA has approved pro ects and of those have resulted in peer revie ed publications. n the past year pro ects ere approved and have been published.