ArticleMethods of information in medicine2017
Rapid Development of Specialty Population Registries and Quality Measures from Electronic Health Record Data*. An Agile Framework.
Article in Methods of information in medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
23 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Can antiepileptic efficacy and epilepsy variables be studied from electronic health records? A review of current approaches.Seizure · 2021Pooled it
- Electronic health record-based disease surveillance systems: A systematic literature review on challenges and solutions.Journal of the American Medical Informatics Association : JAMIA · 2020Pooled it
- Exploring Technological Solutions for Interoperability Between Patient Electronic Medical Records and Clinical Registries: Scoping Review.Journal of medical Internet research · 2026Article
- Artificial intelligence: Applications in cardio-oncology and potential impact on racial disparities.American heart journal plus : cardiology research and practice · 2024Article
- P2Y12 Inhibitors Refill Gap Predicts Death in Medicare Beneficiaries on Chronic Dialysis.Kidney international reports · 2024Article
- Advancing Newborn Screening Long-Term Follow-Up: Integration ofInternational journal of neonatal screening · 2024Article
- Health data space nodes for privacy-preserving linkage of medical data to support collaborative secondary analyses.Frontiers in medicine · 2024Article
- Perspectives of Patients About Immediate Access to Test Results Through an Online Patient Portal.JAMA network open · 2023Article
- Factors Affecting the Adoption of Electronic Data Reporting and Outcomes Among Selected Central Cancer Registries of the National Program of Cancer Registries.JCO clinical cancer informatics · 2021Article
- Electronic Health Records-Based Cardio-Oncology Registry for Care Gap Identification and Pragmatic Research: Procedure and Observational Study.JMIR cardio · 2021Article
- Coupled Effect of Electronic Medical Record Modifications and Lean Six Sigma Methodology on Rheumatoid Arthritis Disease Activity Measurement and Treat-to-Target Outcomes.ACR open rheumatology · 2021Article
- The use of automated data extraction tools to develop a solid organ transplant registry: Proof of concept study of bloodstream infections.The Journal of infection · 2021Article
- Implementing electronic health system in Nigeria: perspective assessment in a specialist hospital.African health sciences · 2020Article
- User stories as lightweight requirements for agile clinical decision support development.Journal of the American Medical Informatics Association : JAMIA · 2019Article
- Designing Tailored Displays for Clinical Practice Feedback: Developing Requirements with User Stories.Studies in health technology and informatics · 2019Article
- Count me in: using a patient portal to minimize implicit bias in clinical research recruitment.Journal of the American Medical Informatics Association : JAMIA · 2019Observational
- Automating the Capture of Structured Pathology Data for Prostate Cancer Clinical Care and Research.JCO clinical cancer informatics · 2019Article
- Translating Research into Agile Development (TRIAD): Development of Electronic Health Record Tools for Primary Care Settings.Methods of information in medicine · 2019Article
- SNOMED CT Concept Hierarchies for Computable Clinical Phenotypes From Electronic Health Record Data: Comparison of Intensional Versus Extensional Value Sets.JMIR medical informatics · 2019Article
- Developing a set of consensus indicators to support maternity service quality improvement: using Core Outcome Set methodology including a Delphi process.BJOG : an international journal of obstetrics and gynaecology · 2018Article
Corrections and comments
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Authors and funding
12 authors.
Funding
Abstract
backgroundCreation 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.
objectiveTo 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.
methodsWe 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.
resultsUsing 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.
conclusionsThis 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.
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