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Automated Guidelines
for Healthcare
Reimbursement Series
Three FREE Online Presentations/Micro-Events
Dr. John Svirbely, MD
Chief Medical Informatics Officer (CMIO),
jsvirbely@Trisotech.com
Denis Gagne
Chief Executive Officer (CEO),
dgagne@Trisotech.com
Automated Healthcare Reimbursement
Guidelines Series
1. Orthopedic Surgery Preauthorization (Sep 30)
2. Preauthorization for Targeted Drug Therapy and
Streamlining of the Appeals Process (Oct 21)
3. Documentation of Medical Necessity for CMS
Home Services (Nov 18)
Some logistics
1. Recording and slides will be
made available to all
attendees
2. Q&A – Send your questions in
Healthcare Reimbursement
authorization (as by an insurer) that is required prior to or after
the performance of a health-care service (such as a surgery or
prescription of a drug)
involves a series of processes to determine if a patient has
insurance coverage for a healthcare service or good . A healthcare
service or good without preauthorization, or medical necessity, is
normally not paid for by the insurance company
https://www.merriam-webster.com/dictionary/pre-authorization
Automatable
Guidelines
An Automatable Guideline is a visual decision
model that is both human readable and machine
automatable.
Such a standardized workflow can improve the
efficiency and quality of healthcare processes.
Our Objective
Promote the modeling of Automatable
Guidelines using open standards to:
• Disambiguate Guidelines creation and
interpretation
• Inform care coordination workflows
so that:
• Clinical Knowledge is delivered at the point of
care
• A single visual Knowledge Artefact is created for
clinicians and for automation
Benefits
Payer
•Effectiveness: Complete and correct information at submission
•Efficiency : Increased decisions throughput
•ROI: Reallocation of resources
Patient
Necessary care with minimum delay
Reduced stress and anxiety
No incurred financial surprises
Provider
Real time adjudication
Clear understanding of the acceptance criteria
Lower administrative burden
Marrying two sets of standards
www.OMG.org www.HL7.org
Established to foster the sharing and
promulgation of best-practices
around modeling and sharing:
• clinical pathways,
• clinical guidelines, and
• other healthcare knowledge
A robust and thriving community-
of-practice of healthcare
institutions, professional societies,
and vendors
www.BPM-plus.org
OMG BPM+ Standards
Open standards for: 1) machine interpretable models based on 2) unambiguous graphical
notations visual languages (MN)
Language Provides Examples
BP (Business Processes) MN Process diagram
(Prescriptive)
Flow diagram, guideline
CM (Case Management) MN Unstructured
processes
(Declarative ECA)
Personalized patient care
D (Decision) MN Decision
(Stateless)
Decision tables, logical
expressions
www.OMG.org
Overview
Preapproval of Targeted Drug Therapy
Modern therapies using humanized monoclonal antibodies are
very expensive.
A monoclonal antibody is a cancer treatment that enlists natural immune system
functions to fight cancer, i.e. it stimulates the body's immune system to fight cancer
cells.
Some have therapeutic use beyond the conditions for which they
have regulatory approval.
Cost of Targeted Therapy – Two Examples
Targeted Drug Brand
Name
Target Cost per Year
rituximab Rituxan CD20 $33,000
pembrolizumab Keytruda PD-1 receptor $110,000
Approved Indications (”On Label”)
Rituximab Therapy (”On Label”)
Submitting an Appeal for Off Label
Usage
• The details of the process vary between insurers.
• This is expensive since it requires review by clinicians working
for the payer.
• It usually requires submission of evidence justifying its use,
which may be of varying quality.
Levels of Evidence of Efficacy for
Off Label Use
No
Evidence
Weak
Evidence
Some
Evidence
Good
Evidence
Approved
Off-Label
Appeal
worthy
Clinal trial
worthy
On-Label
Desired Usage?
Evidence of efficacy?
Potential Outcome?
Rejected
Required Evidence (“Off Label”)
Off Label Drug Request
Nonstandard Evidence of Efficacy
Off Label Drug
Use
Demo
Introducing AI
Conclusion
Combining OMG BPM+ standards with HL7 standards provides:
• An automated way of confirming On Label drug use
• An automated way of appealing and reviewing Off Label drug use
• Standardizing preauthorization while reducing the burden of
human review
Over 900 Automatable Guidelines (Models) are openly available here: https://cds.trisotech.com
Any questions?
THANKS!
Recording and slides will be made available to all attendees at www.Trisotech.com

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Preauthorization for Targeted Drug Therapy Automated Guidelines for Healthcare Reimbursement Guidelines Series

  • 1. Automated Guidelines for Healthcare Reimbursement Series Three FREE Online Presentations/Micro-Events Dr. John Svirbely, MD Chief Medical Informatics Officer (CMIO), jsvirbely@Trisotech.com Denis Gagne Chief Executive Officer (CEO), dgagne@Trisotech.com
  • 2. Automated Healthcare Reimbursement Guidelines Series 1. Orthopedic Surgery Preauthorization (Sep 30) 2. Preauthorization for Targeted Drug Therapy and Streamlining of the Appeals Process (Oct 21) 3. Documentation of Medical Necessity for CMS Home Services (Nov 18)
  • 3. Some logistics 1. Recording and slides will be made available to all attendees 2. Q&A – Send your questions in
  • 4. Healthcare Reimbursement authorization (as by an insurer) that is required prior to or after the performance of a health-care service (such as a surgery or prescription of a drug) involves a series of processes to determine if a patient has insurance coverage for a healthcare service or good . A healthcare service or good without preauthorization, or medical necessity, is normally not paid for by the insurance company https://www.merriam-webster.com/dictionary/pre-authorization
  • 5. Automatable Guidelines An Automatable Guideline is a visual decision model that is both human readable and machine automatable. Such a standardized workflow can improve the efficiency and quality of healthcare processes.
  • 6. Our Objective Promote the modeling of Automatable Guidelines using open standards to: • Disambiguate Guidelines creation and interpretation • Inform care coordination workflows so that: • Clinical Knowledge is delivered at the point of care • A single visual Knowledge Artefact is created for clinicians and for automation
  • 7. Benefits Payer •Effectiveness: Complete and correct information at submission •Efficiency : Increased decisions throughput •ROI: Reallocation of resources Patient Necessary care with minimum delay Reduced stress and anxiety No incurred financial surprises Provider Real time adjudication Clear understanding of the acceptance criteria Lower administrative burden
  • 8. Marrying two sets of standards www.OMG.org www.HL7.org
  • 9. Established to foster the sharing and promulgation of best-practices around modeling and sharing: • clinical pathways, • clinical guidelines, and • other healthcare knowledge A robust and thriving community- of-practice of healthcare institutions, professional societies, and vendors www.BPM-plus.org
  • 10. OMG BPM+ Standards Open standards for: 1) machine interpretable models based on 2) unambiguous graphical notations visual languages (MN) Language Provides Examples BP (Business Processes) MN Process diagram (Prescriptive) Flow diagram, guideline CM (Case Management) MN Unstructured processes (Declarative ECA) Personalized patient care D (Decision) MN Decision (Stateless) Decision tables, logical expressions www.OMG.org
  • 12. Preapproval of Targeted Drug Therapy Modern therapies using humanized monoclonal antibodies are very expensive. A monoclonal antibody is a cancer treatment that enlists natural immune system functions to fight cancer, i.e. it stimulates the body's immune system to fight cancer cells. Some have therapeutic use beyond the conditions for which they have regulatory approval.
  • 13. Cost of Targeted Therapy – Two Examples Targeted Drug Brand Name Target Cost per Year rituximab Rituxan CD20 $33,000 pembrolizumab Keytruda PD-1 receptor $110,000
  • 16. Submitting an Appeal for Off Label Usage • The details of the process vary between insurers. • This is expensive since it requires review by clinicians working for the payer. • It usually requires submission of evidence justifying its use, which may be of varying quality.
  • 17. Levels of Evidence of Efficacy for Off Label Use No Evidence Weak Evidence Some Evidence Good Evidence Approved Off-Label Appeal worthy Clinal trial worthy On-Label Desired Usage? Evidence of efficacy? Potential Outcome? Rejected
  • 19. Off Label Drug Request
  • 23. Conclusion Combining OMG BPM+ standards with HL7 standards provides: • An automated way of confirming On Label drug use • An automated way of appealing and reviewing Off Label drug use • Standardizing preauthorization while reducing the burden of human review Over 900 Automatable Guidelines (Models) are openly available here: https://cds.trisotech.com
  • 24. Any questions? THANKS! Recording and slides will be made available to all attendees at www.Trisotech.com