Literature DB >> 28930362

Rapid Development of Specialty Population Registries and Quality Measures from Electronic Health Record Data*. An Agile Framework.

Vaishnavi Kannan, Jason S Fish, Jacqueline M Mutz, Angela R Carrington, Ki Lai, Lisa S Davis, Josh E Youngblood, Mark R Rauschuber, Kathryn A Flores, Evan J Sara, Deepa G Bhat, DuWayne L Willett.   

Abstract

BACKGROUND: Creation of a new electronic health record (EHR)-based registry often can be a "one-off" complex endeavor: first developing new EHR data collection and clinical decision support tools, followed by developing registry-specific data extractions from the EHR for analysis. Each development phase typically has its own long development and testing time, leading to a prolonged overall cycle time for delivering one functioning registry with companion reporting into production. The next registry request then starts from scratch. Such an approach will not scale to meet the emerging demand for specialty registries to support population health and value-based care.
OBJECTIVE: To determine if the creation of EHR-based specialty registries could be markedly accelerated by employing (a) a finite core set of EHR data collection principles and methods, (b) concurrent engineering of data extraction and data warehouse design using a common dimensional data model for all registries, and (c) agile development methods commonly employed in new product development.
METHODS: We adopted as guiding principles to (a) capture data as a byproduct of care of the patient, (b) reinforce optimal EHR use by clinicians, (c) employ a finite but robust set of EHR data capture tool types, and (d) leverage our existing technology toolkit. Registries were defined by a shared condition (recorded on the Problem List) or a shared exposure to a procedure (recorded on the Surgical History) or to a medication (recorded on the Medication List). Any EHR fields needed - either to determine registry membership or to calculate a registry-associated clinical quality measure (CQM) - were included in the enterprise data warehouse (EDW) shared dimensional data model. Extract-transform-load (ETL) code was written to pull data at defined "grains" from the EHR into the EDW model. All calculated CQM values were stored in a single Fact table in the EDW crossing all registries. Registry-specific dashboards were created in the EHR to display both (a) real-time patient lists of registry patients and (b) EDW-generated CQM data. Agile project management methods were employed, including co-development, lightweight requirements documentation with User Stories and acceptance criteria, and time-boxed iterative development of EHR features in 2-week "sprints" for rapid-cycle feedback and refinement.
RESULTS: Using this approach, in calendar year 2015 we developed a total of 43 specialty chronic disease registries, with 111 new EHR data collection and clinical decision support tools, 163 new clinical quality measures, and 30 clinic-specific dashboards reporting on both real-time patient care gaps and summarized and vetted CQM measure performance trends.
CONCLUSIONS: This study suggests concurrent design of EHR data collection tools and reporting can quickly yield useful EHR structured data for chronic disease registries, and bodes well for efforts to migrate away from manual abstraction. This work also supports the view that in new EHR-based registry development, as in new product development, adopting agile principles and practices can help deliver valued, high-quality features early and often.

Entities:  

Keywords:  Registries; agile development; data collection; data warehouse; electronic health records; information storage and retrieval; outcome and process assessment (health care); population health; quality indicators

Mesh:

Year:  2017        PMID: 28930362      PMCID: PMC5608102          DOI: 10.3414/ME16-02-0031

Source DB:  PubMed          Journal:  Methods Inf Med        ISSN: 0026-1270            Impact factor:   2.176


  12 in total

1.  Use of 13 disease registries in 5 countries demonstrates the potential to use outcome data to improve health care's value.

Authors:  Stefan Larsson; Peter Lawyer; Göran Garellick; Bertil Lindahl; Mats Lundström
Journal:  Health Aff (Millwood)       Date:  2011-12-07       Impact factor: 6.301

2.  What is value in health care?

Authors:  Michael E Porter
Journal:  N Engl J Med       Date:  2010-12-08       Impact factor: 91.245

3.  The future state of clinical data capture and documentation: a report from AMIA's 2011 Policy Meeting.

Authors:  Caitlin M Cusack; George Hripcsak; Meryl Bloomrosen; S Trent Rosenbloom; Charlotte A Weaver; Adam Wright; David K Vawdrey; Jim Walker; Lena Mamykina
Journal:  J Am Med Inform Assoc       Date:  2012-09-08       Impact factor: 4.497

Review 4.  Review of 103 Swedish Healthcare Quality Registries.

Authors:  L Emilsson; B Lindahl; M Köster; M Lambe; J F Ludvigsson
Journal:  J Intern Med       Date:  2014-09-27       Impact factor: 8.989

5.  Caring for High-Need, High-Cost Patients - An Urgent Priority.

Authors:  David Blumenthal; Bruce Chernof; Terry Fulmer; John Lumpkin; Jeffrey Selberg
Journal:  N Engl J Med       Date:  2016-07-27       Impact factor: 91.245

6.  Diabetes and hypertension quality measurement in four safety-net sites: lessons learned after implementation of the same commercial electronic health record.

Authors:  R Benkert; P Dennehy; J White; A Hamilton; C Tanner; J M Pohl
Journal:  Appl Clin Inform       Date:  2014-08-20       Impact factor: 2.342

7.  Clinical Case Registries: simultaneous local and national disease registries for population quality management.

Authors:  Lisa I Backus; Sergey Gavrilov; Timothy P Loomis; James P Halloran; Barbara R Phillips; Pamela S Belperio; Larry A Mole
Journal:  J Am Med Inform Assoc       Date:  2009-08-28       Impact factor: 4.497

8.  Combining Health Data Uses to Ignite Health System Learning.

Authors:  J Ainsworth; I Buchan
Journal:  Methods Inf Med       Date:  2015-09-17       Impact factor: 2.176

9.  Problem list completeness in electronic health records: A multi-site study and assessment of success factors.

Authors:  Adam Wright; Allison B McCoy; Thu-Trang T Hickman; Daniel St Hilaire; Damian Borbolla; Watson A Bowes; William G Dixon; David A Dorr; Michael Krall; Sameer Malholtra; David W Bates; Dean F Sittig
Journal:  Int J Med Inform       Date:  2015-07-17       Impact factor: 4.046

10.  Ability to generate patient registries among practices with and without electronic health records.

Authors:  Adam Wright; Elizabeth A McGlinchey; Eric G Poon; Chelsea A Jenter; David W Bates; Steven R Simon
Journal:  J Med Internet Res       Date:  2009-08-10       Impact factor: 5.428

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  14 in total

1.  Electronic health record-based disease surveillance systems: A systematic literature review on challenges and solutions.

Authors:  Ali Aliabadi; Abbas Sheikhtaheri; Hossein Ansari
Journal:  J Am Med Inform Assoc       Date:  2020-12-09       Impact factor: 4.497

2.  Count me in: using a patient portal to minimize implicit bias in clinical research recruitment.

Authors:  Vaishnavi Kannan; Kathleen E Wilkinson; Mereeja Varghese; Sarah Lynch-Medick; Duwayne L Willett; Teresa A Bosler; Ling Chu; Samantha I Gates; M E Blair Holbein; Mallory M Willett; Sharon C Reimold; Robert D Toto
Journal:  J Am Med Inform Assoc       Date:  2019-08-01       Impact factor: 4.497

3.  Translating Research into Agile Development (TRIAD): Development of Electronic Health Record Tools for Primary Care Settings.

Authors:  K D Clark; T T Woodson; R J Holden; R Gunn; D J Cohen
Journal:  Methods Inf Med       Date:  2019-07-05       Impact factor: 2.176

4.  Automating the Capture of Structured Pathology Data for Prostate Cancer Clinical Care and Research.

Authors:  Anobel Y Odisho; Mark Bridge; Mitchell Webb; Niloufar Ameli; Renu S Eapen; Frank Stauf; Janet E Cowan; Samuel L Washington; Annika Herlemann; Peter R Carroll; Matthew R Cooperberg
Journal:  JCO Clin Cancer Inform       Date:  2019-07

5.  Designing Tailored Displays for Clinical Practice Feedback: Developing Requirements with User Stories.

Authors:  Veena Panicker; Dahee Lee; Marisa Wetmore; James Rampton; Roger Smith; Michelle Moniz; Zach Landis-Lewis
Journal:  Stud Health Technol Inform       Date:  2019-08-21

6.  Factors Affecting the Adoption of Electronic Data Reporting and Outcomes Among Selected Central Cancer Registries of the National Program of Cancer Registries.

Authors:  Florence K L Tangka; Patrick Edwards; Paran Pordell; Reda Wilson; Wendy Blumenthal; Sandy F Jones; Madeleine Jones; Jenny Beizer; Amarilys Bernacet; Maggie Cole-Beebe; Sujha Subramanian
Journal:  JCO Clin Cancer Inform       Date:  2021-08

7.  Agile Co-Development for Clinical Adoption and Adaptation of Innovative Technologies.

Authors:  Vaishnavi Kannan; Mujeeb A Basit; Josh E Youngblood; Trenton D Bryson; Seth M Toomay; Jason S Fish; Duwayne L Willett
Journal:  Health Innov Point Care Conf       Date:  2017-11

8.  The use of automated data extraction tools to develop a solid organ transplant registry: Proof of concept study of bloodstream infections.

Authors:  Ricardo M La Hoz; Terrence Liu; Donglu Xie; Beverley Adams-Huet; DuWayne L Willett; Robert W Haley; David E Greenberg
Journal:  J Infect       Date:  2020-10-07       Impact factor: 6.072

Review 9.  Can antiepileptic efficacy and epilepsy variables be studied from electronic health records? A review of current approaches.

Authors:  Barbara M Decker; Chloé E Hill; Steven N Baldassano; Pouya Khankhanian
Journal:  Seizure       Date:  2021-01-13       Impact factor: 3.184

10.  Agile Acceptance Test-Driven Development of Clinical Decision Support Advisories: Feasibility of Using Open Source Software.

Authors:  Mujeeb A Basit; Krystal L Baldwin; Vaishnavi Kannan; Emily L Flahaven; Cassandra J Parks; Jason M Ott; Duwayne L Willett
Journal:  JMIR Med Inform       Date:  2018-04-13
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