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Registry Participation 101:A Simple Step-by-Step Guide to Understanding What You Really Need
to Know from AJRR
Joe Greene
University of Wisconsin—Department of Orthopedics and Rehabilitation
AJRR Staff:
Phil Dwyer, Program Coordinator
Caryn Etkin, PhD, MPH, Director of Analytics
September Cahue, MPH, Senior Registry Analyst
Topics and Agenda
Agenda:
• Introduction to clinical data registries Phil Dwyer
• University of Wisconsin experience Joe Greene
• Patient-Reported Outcome Measures September Cahue
• Quality programs Caryn Etkin
Topics:
• What is a clinical data registry
• Who is using registry information and why
• Value of registry data
• Additional information, resources
Origin of Registries –Sweden
What is a Registry?
• A clinical data registry records information about the
health status of patients and the health care they receive
over varying periods of time
• Designed to capture clinical data of importance to health
care practitioners, providers, and patient. Generally,
registries focus on clinical data for specific populations
based on:
– A disease/condition (e.g. cystic fibrosis, spina bifida)
– Procedure (e.g. coronary artery bypass graft)
– Device or drug (e.g. total joint replacement)
• More frequently are able to capture data from multiple
EHRs
• Designed for quality improvement efforts, payment,
research, etc.
Who Manages Registries?
• Medical Specialty Societies
• Health Plans
• Patient Advocacy Organizations
• Federal and State Governments
• For-profit Companies and Non-profit
Organizations
Who is Interested in Registries?
• Hospitals, health systems
• Private practice groups
• Health plans and other payers
• Researchers
• Patient and consumer organizations
• Federal, state, and local government
Look at Some of the National Options!
How Does a Registry Collect Data?
How Does a Registry Collect Data?
• Push
• Pull
• Certification
model
• Manual
• Linking with
different
databases
• Departmental
systems
• Direct from
patients
• From devices
Electronic Health Records
Other IT systems
Patients
Clinical Registry Information Flow
Provider documents patient care
EHR
RegistryProvider
performance report
Provider reviews report
Patients can
enter their own
data into some
registries
How can I improve my
performance?
More Patients, Less Burden
Clinical
registries
Collecting
structured data
On more patient
populations
Data pull
from EHRs
Is becoming less
dependent on
chart abstraction
Lowering
barriers
Source: https://download.ama-assn.org/resources/doc/cqi/x-pub/pcpi-richardson-102915.pdf
AJRR is a multi-stakeholder, independent, not-for-profit with diverse national constituents led by top orthopaedists
We optimize patient outcomes through collection of data on all primary and revision total joint replacement procedures in the US
Our mission is to enhance patient safety, improve quality of care, and reduce the cost of care
Our goal is to capture 90% of all total joint replacement
procedures in the U.S.
AJRR Mission and Vision
AJRR is supported by hospitals, health insurers, and
the following groups:
Supporters
20 2656
79
122
158177
219242
269292
388
417
467
522
612677
0
50
100
150
200
250
300
350
400
450
500
550
600
650
700
Jan July Jan July Jan July Jan Jul Currently
Total # ofhospitals*
20152012 2013
Nu
mb
er o
f H
osp
ital
s
2014N=24,971
procedures from 63 hospital ls
N= 43,823procedures from
123 hospitals
AJRR 2012-2016 Progress
N= 211,721procedures from
252 hospitals
N= 350,154 procedures from
464 hospitals
Where Are We Now?
September 2014
The National Registry:All 50 States
Participating Institution Types
Participating Institution Types
• Hospitals
• Academic Medical Centers
• Multiple Health Systems/Networks
• Ambulatory Surgery Centers
• Private Practice Groups
• Solo Practitioners
• Hospital bed count
– Small = 1-99 beds
– Medium = 100-399 beds
– Large = 400+ beds
Teaching
25%
Rural
9%
Univ/
Research
11% Major Teaching (21.0%)
Minor Teaching (35.6%)
Non-Teaching (43.3%)
Small (21.1%)
Medium (48.0%)
Large (30.9%)
Demand Reporting &
Electronic Dashboard System
TrainingAccessing and ComparingYour Data
AJRR Dashboard
AJRR Dashboard – Reports
AJRR Dashboard
AJRR Dashboard
AJRR Dashboard
AJRR Dashboard
Joe GreeneUniversity of Wisconsin
Department of Orthopedics and Rehabilitation
Registry Participation 101
A Simple Step-by-Step Guide from AJRR
The Acquisition and Reporting of Patient
Reported Outcomes
Joe GreeneUniversity of Wisconsin
Department of Orthopedics and Rehabilitation
Objectives
Outline the UW Health System approach to PRO
questionnaire deployment
Define current AJRR reporting status and goals
Describe Phase 1: The pilot collection of PRO
data in orthopedics
Outline Phase 2: Full implementation of PRO
data collection and reporting
Discuss lessons learned throughout
UW Health Orthopedics and
Rehabilitation
UW Health Orthopedic Service Line
• 600+ employees
• Highly profitable service line with UW Health
• Highly comprehensive
Department of Orthopedics and Rehabilitation
• 29 orthopedic surgeons and 16 rehabilitation providers
• 20+ PA’s and APNP’s
• 5 primary care sports medicine providers
Research and Education
• 25 residents and 4 fellows
• 4 PhD Level Scientists and multiple post-doc’s
• Robust stem cell and regenerative medicine research
• Strong clinical research program
AJRR Data Elements
Level 1 Data
• Patient, Surgeon, and Procedure Data
Level 2 Data
• Risk Factors and Co-Morbidities
Level 3 Data
• Patient Reported Outcomes
Level 4 Data
• Radiographic Images
Current Status: AJRR Reporting
Level 1 Reporting
• Automated since June, 2014
Level 2 Reporting
• Goal of automating by monthly Epic extract by
June, 2016
Level 3 Reporting
• Automate by monthly extract of PRO data from
Epic by July, 2016
Level 4 Reporting
• Automate when AJRR is ready to accept
UW Health System Considerations
Patient Assessment Tools Workgroup
Epic vs Third Party Solution
Getting data in/out of Epic
IT and operational workflows implications
Tablet vs Kiosk vs Portal
Real time access to results
Copyright and cost implications
Discrete data storage within EMR
Reporting customization
Multiple data entry mechanisms
Meaningful Use benefits
No interface required
Leveraged Epic investment
Epic will improve over time
Decision: Develop Epic Solution
Streamlined collection processes
Eloquent and attractive user interfaces
Better than EMR functionality at present
My Recommendations
Strongly consider reporting capability
Interfacing ability is paramount
Consider depth of their questionnaire build
Third Party Solutions
Phase 1
Pilot Collection of PRO Data
6 Clinics at 2 different locations and approximately 100 users including
Staff affected : Physicians, AT’s, PT’s, PA’s, RN’s, MA’s, Schedulers
Phase 1
Project Overview Resources
UW Epic teams – 1024.75 hours
• EpicCare Ambulatory
• Cadence
• MyChart
• Prelude/Welcome
• Training Team
• Project Management
• Security
• Clinical Center for Knowledge
Management
• Server and Desktop
• Programming
Consultants (10 months)
• MyChart
• Programmer
• Reporting
Phase 1
Questionnaires ACL Reconstruction (Clinics: Sports Med, Sports Rehab)
• VR-12 Physical & Psychological Health Form
• IKDC Knee Evaluation Form
• ACL-RSI Return to Sport After Injury Scale
• MARX Activity Rating Scale
• SANE - Single Assessment Numeric Evaluation
Total Hip Replacement (Clinic: Ortho)
• VR-12 Physical & Psychological Health Form
• HOOS Hip Disability & Osteoarthritis Score Survey
• UCLA Activity-Level Rating Form
• Modified Harris Hip Form
Low Back Pain (Clinics: Spine Ortho, Neuro, Spine PT)
• VR-12 Physical & Psychological Health Form
• Oswestry Low Back Pain Form
Phase 1
Project Overview Workflows
Assign Questionnaire Series
• Option 1: Scheduling question; Reporting
Workbench used by Scheduler
• Option 2: Order placed by clinician
Assign a Questionnaire
• Patient Entered Questionnaire Activity
Available on DAR and Multi-provider schedule
Patient entered questionnaires
• MyChart
• Welcome (Tablet Solution)
Initially sought a Windows 7 tablet
• Located a product and began testing
• Lack of device quantity made the decision to use Windows 8
Windows 8 models were tested (need about 75)
• Dell Model: Cost ~ $600.00 (Now about $800.00)
• Storage Units: Cost ~ $800.00 (Now about $800.00)
Extensive testing completed
• 40 hours testing
Every questionnaire
Saved responses
Response filing
Ease of answering
Single item on each page
Auto advance
Tablet Selection and Testing
Questionnaire Volume
Pilot Go-Live
October 16th
Questionnaire Volume
Pilot Go-Live
October 16th
% QNRs completed in MyChart
% MyChart Active Patients per #
of Encounters
Phase 2
Full Implementation
Build and validate all remaining orthopedic
questionnaires
Deploy at all orthopedic locations
Identify and implement all reporting Needs
Consider research and HS-IRB implications
Phase 2 Considerations
Quality and Outcomes
Research
Clinical Reporting
Registry Reporting
Government and Reporting
Third Party Payors and Bundling
Marketing
Phase 2
New Questionnaire Build
FAAM
FAAM Sport
NDI
SRS 22
UWRI
SILS (CJR)
Ped’s QL 4.0
• 5-7, 8-12, 13-18
quickDASH
KOOS
Knee Society Score
PSFS (Flowsheet)
Phase 2
Reporting Automation
Clinical and Marketing Reporting
• Automate Quarterly
Registry Reporting
• AJRR Level 3
VR-12, HOOS, KOOS
(Why? : WOMAC, Historical Database, CJR)
Pre-op and 1 year
Payor and Government Reporting
• CJR
VR-12, HOOS, KOOS Pre-op and 1 year
SILS and Oswestry
Total Painful Joint Count
Lessons Learned
Integrated tablet and portal solution was critical
Coordinated IT and Orthopedic project
management is imperative
An Epic solution was right for the UW, but may
not be the best, easiest or cost effective in many
cases
Consider reporting needs early
Physician and Management Champions are
essential!
Questions
Joe Greene ([email protected])
Orthopedics Project Manager
Ryley O’Brien (RO’[email protected])
Patient Assessment Tools Workgroup Facilitator
Sara Balster and Johnna Bledsoe
IS Project Managers
Leandra Frank ([email protected])
IS Analyst, Hardware
Bret Wagner ([email protected])
Huron Consulting, Director of Portals and Population Health
AJRR Patient Reported Outcome Measures (Level III) Platform
• Electronic submission of PRO scores (already captured at
your hospital/clinic)
• AJRR will provide a data specification file – you submit data to us
(similar to Level I submission)
• Selected EHR vendors can submit to AJRR on your behalf
• Collection direct from patients (or facilitated by clinician) via
AJRR’s Level III platform
How AJRR Can Accept Data
Information can be found in our PRO Guide on www.ajrr.net
How to Start a PRO Program
1. Define your PRO team
2. Define your PRO goals
3. Determine the PRO measure/s you
would like to use
4. Define the frequency for data collection
5. Develop workflow for data capture
• Most likely, a core group of colleagues have decided that including PROs in your practice of care for TJA may provide important information to improve patient outcomes. Beyond this core group, it will be critical to involve stakeholders at each level of patient care
• Some groups to be considered:
• Orthopaedic Department
• Orthopaedic practice groups and clinics
• Quality Department
• Information Technology
• Orthopaedic Service Line
• Research
• Rehabilitation
• Hospital Administration
• Patient Advocate/Patient Representative
• Institutional Review Board (guidance/review)
Define Your PRO team
Define Your PRO goals• For those interested in a PRO program, you and your
colleagues will need to determine the reasons you would
like to launch a PRO program
• You may consider asking yourselves questions such as:
• Are we launching a research initiative with specific aims?
• Are we seeking comparative benchmarks to our peers?
• Are we wanting to quantify our outcomes from our patients’
perspective?
• Do we want to measure if patients have improved function or
reduced pain?
• Do we want to measure whether our patients’ overall health has
improved?
• What are the requirements of the payer-specific program for which
we are hoping to qualify?
Determine the PRO Measure/s• Your reasons for implementing PRO program will direct your
team to a certain instrument(s) that will allow you to meet your objectives.
• For example, if your institution has decided to collect PROMs for research initiatives, you may choose an instrument that measures multiple domains.
• However, if you are focused on measuring patients’ outcomes as part of your clinical care, a shorter instrument will suffice as long as it is able to detect change.
Consider:
1. What does the measure assess – quality of life or
function?
2. What is the cost (licensing fee) to use the form?
3. What is the associated patient burden?a. What is the length of form?
b. How easy/hard is the form to complete?
4. What is the associated staff burden (FTE time)?
Define Frequency for PRO Data Collection
• PROMs guidelines from the International Consortium for
Health Outcome Measurement (ICHOM) have
recommended pre-op (baseline) and one-year follow-up
as appropriate time points for data collection to provide
meaningful data for comparing outcomes across
providers
• The CJR Final Rule also advises that post-operative surveys be
collected between 270 and 365 days post-surgery
• AJRR’s platform will allow for other time points (e.g.,
three-month, six-months, etc.) to be submitted and
stored in AJRR’s database. However, national benchmarks
will only be reported for pre-op and one-year outcomes.
• Each time point will have a two-month window for data
collection
Develop Workflow for Data Capture
Consider the following:
1. Points of patient contact
2. Staff responsibilities
3. Electronic completion versus paper capture of forms
4. Collection at clinic or allow patients to complete on
their own
5. Will surgeon be using the measure responses during
the patient encounter?
Other PROM resources
• Patient-Reported Outcomes in Performance Measurement
RTI document
• International Consortium for Health Outcomes Measurement - Hip & Knee Osteoarthritis Data Collection Reference Guide
ICHOM document
• National Quality Forum – Patient Reported Outcomes (PROs) in Performance Measurement
NQF document
• International Society for Quality of Life Research -User’s Guide to Implementing Patient-Reported Outcomes Assessment in Clinical Practice
ISOQOL document
Health-Related Quality of Life Measures• VR-12: VR-12
• PROMIS-10 Global: PROMIS-10 Global
• SF-12: SF-12
• SF-36: SF-36
• EQ-5D: EQ-5D
Joint-Specific Measures• HOOS and KOOS: HOOS and KOOS
• HOOS, JR and KOOS JR.: HOOS JR and KOOS JR
• Oxford Hip: Oxford Hip
• Oxford Knee: Oxford Knee
• KSS: Knee Society Knee Scoring System
• Harris Hip Score: Harris Hip Score
• WOMAC: WOMAC
Other PROM resources
AJRR and Quality Programs
• Comprehensive Care for Joint Replacement (CJR) – CJR Final Rule
– AJRR's efforts related to CJR
• AJRR is also a Qualified Clinical Data Registry
(QCDR), which means Eligible Professionals can
use our platform for the Physician Quality
Reporting System (PQRS) – AJRR's QCDR Platform
– QCDR Reporting
• Meaningful Use
Additional Registry Resources• National Quality Registry Network NQRN Home Page
– Registry inventory, “What is a registry” handout, registry vendor
assessment
• CMS Qualified Clinical Data Registries QCDR Home Page
• AHRQ Registry of Patient Registries (RoPR)
• Numerous other efforts:
Questions
American Joint Replacement Registry
847.292.0530
http://www.ajrr.net
65
Managing Orthopedic Episodes of Care
www.wellbe.me
Wellbe is an authorized vendor to submit your PRO data to AJRR!