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The 411 of MIROW: Navigation to Implementation Presentation Obj ective This session will provide A detailed overview of best practice guides for immunization information systems operations User testimonials about leveraging


  1. The ‘ 411’ of MIROW: Navigation to Implementation

  2. Presentation Obj ective • This session will provide • A detailed overview of best practice guides for immunization information systems operations • User testimonials about leveraging these guides in various j urisdictions

  3. Directory of Presentation S lides Topic Slides MIROW background, process, documents 4-11 Vaccine Level Deduplication in IIS Guide 12-29 Data Quality Assurance: Incoming Data, S elected 30-46 Aspects Management of Patient Active/ Inactive S tatus in 47-65 Immunization Information S ystems What’s Next for MIROW Guide Development? 66-68

  4. What is MIROW? • The Modeling of Immunization Registry Operations Workgroup • Formed in 2005 • AIRA in part nership IIS S B at t he CDC • Obj ective • Develop and promot e IIS Best Pract ices • Goal • Provide t he basis and support for uniform alignment of IIS processes Inconsist ency among IIS negat ively af f ect s overall dat a qualit y, comparabilit y, operat ional cost , and usef ulness of inf ormat ion.

  5. MIROW Documents Mini-guide (brochure) Complete Guide 4 to 8 pages – 100+ pages Download MIROW documents at: ht t p:/ / www.immregist ries.org/ pubs/ mirow.ht ml AIRA web site: CDC web site: www.cdc.gov/ vaccines/ programs/ iis/ activities/ mirow.html 5

  6. Typical S tructure of the MIROW Documents • Principles: provide a high level direction that helps to guide the development of business rules • Business rules: represent specific requirements and decision- making logic for various aspects of the topic • Domain Model: describes the main concepts, terms, and definitions related to the topic

  7. MIROW Efforts in Context Generic IIS Functional Standards Level 1 Functional Requirements for IIS Level 2 Specific MIROW Best Practices Level 3 IIS Software Level 4

  8. How MIROW Works • Oversight from the MIROW S teering Committee • Business analysis and development process support provided by IIS S B/ CDC • Organizational support for in-person meetings from AIRA staff • Facilitation support for in-person meetings provided by external consultants • Volunteering subj ect matter experts from the IIS community • MIROW S teering Committee is working on developing a new process in response to the changing landscape

  9. The MIROW Process Brainstorming Discussing Consensus = “ I can live wit h t hat and support it ” Reaching Consensus

  10. The Buy-In!

  11. The MIROW Process – YES !

  12. Vaccination Level Deduplication in Immunization Information S ystems

  13. Deduplication can be Daunting … .

  14. Deduplication: S cope of the Guide • Deduplication of immunization records is a two-fold problem that includes deduplication • at the vaccination event level (e.g. two records describe the same immunization) This is in scope • at the demographic/ patient level (e.g. two records describe the same patient) This is out of scope

  15. Why Vaccine Deduplication? • Create and maintain an accurate and timely record of an individual’s immunizations • More accurately forecast vaccine administrat ion in accordance with Advisory Committee on Immunization Practices (ACIP) recommendations

  16. Changes in Data Coming into the IIS • IIS often receive vaccinat ion data from multiple sources • Frequently contain multiple records for the same vaccinat ion event. • Do similar records = same vaccinat ion event? • What to do with these duplicates?

  17. Incoming Data Issues … .

  18. Why is this guide important? • Inconsistency across immunization information systems (IIS ) • Uniform alignment of the vaccination level deduplication processes across different immunization information systems

  19. Vaccination level deduplication can be addressed in three phases: Phase 1. SELECTION : Identify and group multiple vaccinat ion records that potentially belong to the same vaccination event. Phase 2. EVALUA TION : Evaluate pairs of potentially duplicate immunization records for match/ differ decisions.  Results in three possible outcomes:  records match (are duplicates)  they differ  don’ t know Phase 3. RESOLUTION : Produce a ‘ BES T’ record to represent the vaccinat ion.

  20. Consistency … .

  21. S election Phase: Principles and Business Rules • P04 We would like to be more inclusive than exclusive. • BR02 A record for the vaccinat ion event must be compared with all and any of the vaccinat ion event records with the same Vaccine – Family/ Group. • BR03 Identical records should not be selected for deduplication.

  22. Evaluation Phase: Principles and Business Rules (Excerpt) • P11: If vaccinat ion encounter dates are different in records under evaluation, the proximity of these dates has to be taken in consideration. • BR09: Records selected for evaluation at the S election phase should be considered different until proven to be duplicates. • BR10: If vaccine lot numbers are different in evaluated records, these records are most likely to be different (not duplicates).

  23. Resolution Phase: Principles and Business Rules (excerpt) • P15 Business Rules should be applied completely, in a specified sequence. • BR21 The record with more complete data should be selected. • BR22 The record with more specific data should be selected. • BR25 Records with an earlier or later date should be selected consistently within a particular IIS .

  24. Resolution: Not a Duplicate Record

  25. Testimonials: Direct Uses of the Guide* • 16/ 25 indicated the guide was helpful • 9 programs used guide to develop/ refine existing vaccination-level deduplication algorithm • 1 program used guide for potential future changes • 8 programs used guide in planning features of a new IIS • 3 programs used guide as internal reference on best practices • 3 programs used guide to develop manual deduplication decision-making processes *Immunization Registry Operational Guidelines Evaluation – Final Report

  26. 26 *Immunization Registry Operational Guidelines Evaluation – Final Report

  27. Use of Guide in Massachusetts • MIIS Developers use all MIROW Guides when starting any requirements effort • Used Guide when defining deduplication algorithm • S equential Approach to Evaluation • Applied guidelines in the Guide to assign confidence level to a record • MIIS S taff applied most principles and business rules in developing its process for de-duplicating vaccinations • MIIS applies a 10-day window for deduplication

  28. Vaccination Level Deduplication in IIS – Reading Paths Immunization Program Managers Technical Developers Program S taff • Executive S ummary • Chapter 2: Process Overview • Appendix A: Domain Model • Chapter 2: Process Overview • Chapter 3: S election Phase • Chapter 2: Process Overview • • • Chapter 7: Conclusions Chapter 4: Evaluation Phase Chapter 3: S election Phase • • • Appendix B: Merging Data from Chapter 5: Resolution Phase Chapter 4: Evaluation Phase Duplicate Records • • Chapter 6: Additional Chapter 5: Resolution Phase Miscellaneous Recommendations • Appendix B: Merging Data from • Appendix B: Merging Data from Duplicate Records Duplicate Records

  29. Don’ t be Complacent!

  30. Data Quality Assurance: Incoming data S elected aspects

  31. Why Data Quality Assurance? • Electronic data exchange and the ongoing Meaningful Use initiative • Resulting increase in IIS -EHR collaborations • IIS and IIS partners need data quality assurance guidelines

  32. Data Quality Assurance MIROW Guides Chapter 3: Chapter 7: DQA: Incoming data DQA: Selected Aspects Publication date February 2008 May 2013 • • Main topic areas Develop principles and Develop domain model & business rules for incoming diagram • DQA Reporting facility • Describe healthcare identification management • providers’ precertification Review & update business process rules from Chapter 3 Number of principles 13 2 Number of business rules 32 27 + 27 updated business rules from Chapter 3 Number of general 0 7 recommendations

  33. DQA: Incoming data S teps to pre-certifying submitters 1. S ubmitter produces a sample file 2. IIS examines the sample file 3. IIS staff person compares the sample file to the medical chart 4. IIS periodically examines a subset of IIS data

  34. DQA: Incoming data Pre-load validation • Inspect incoming data reported by certified submitters to ensure high quality BEFORE loading it into the system • Thirteen principles used to validated immunization data • Consistency principle • Accuracy principle

  35. DQA: S elected aspects • Facility identification management • Roles of organizations • Vaccinator • Recorder • S ubmitter

  36. DQA: S elected aspects • Principles for facility identification management: • IIS should be consistent in the approaches followed for facility identification management. (P801) • IIS should clearly document the approaches followed for facility identification management (P802) • HL7 considerations • Enable submission of two organizations per message • Recommended use of MS H-22: responsible sending organization

  37. Data Quality Assurance

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