Implementation of a learning healthcare system for sickle cell disease

Author:

Miller Robin123ORCID,Coyne Erin1,Crowgey Erin L123,Eckrich Dan1,Myers Jeffrey C23,Villanueva Raymond4,Wadman Jean1,Jacobs-Allen Sidnie1,Gresh Renee123,Volchenboum Samuel L5,Kolb E Anders123

Affiliation:

1. Nemours Sickle Cell Center of Biomedical Research Excellence (COBRE), Nemours Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA

2. Nemours Center for Cancer and Blood Disorders, Nemours Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA

3. Department of Pediatrics, Nemours Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA

4. Information Systems Clinical Applications, Nemours Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA

5. Center for Research Informatics, University of Chicago, Chicago, Illinois, USA

Abstract

ABSTRCT Objective Using sickle cell disease (SCD) as a model, the objective of this study was to create a comprehensive learning healthcare system to support disease management and research. A multidisciplinary team developed a SCD clinical data dictionary to standardize bedside data entry and inform a scalable environment capable of converting complex electronic healthcare records (EHRs) into knowledge accessible in real time. Materials and Methods Clinicians expert in SCD care developed a data dictionary to describe important SCD-associated health maintenance and adverse events. The SCD data dictionary was deployed in the EHR using EPIC SmartForms, an efficient bedside data entry tool. Additional data elements were extracted from the EHR database (Clarity) using Pentaho Data Integration and stored in a data analytics database (SQL). A custom application, the Sickle Cell Knowledgebase, was developed to improve data analysis and visualization. Utilization, accuracy, and completeness of data entry were assessed. Results The SCD Knowledgebase facilitates generation of patient-level and aggregate data visualization, driving the translation of data into knowledge that can impact care. A single patient can be selected to monitor health maintenance, comorbidities, adverse event frequency and severity, and medication dosing/adherence. Conclusions Disease-specific data dictionaries used at the bedside will ultimately increase the meaningful use of EHR datasets to drive consistent clinical data entry, improve data accuracy, and support analytics that will facilitate quality improvement and research.

Funder

National Institute of General Medical Sciences of the National Institutes of Health

Institutional Development Award (IDeA) from the National Institute of General Medical Sciences of the National Institutes of Health

Patient-Centered Outcomes Research Institute

Publisher

Oxford University Press (OUP)

Subject

Health Informatics

Reference14 articles.

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2. The potential of learning health care systems;Maddox;J Am Coll Cardiol,2015

3. Differences in the clinical and genotypic presentation of sickle cell disease around the world;Saraf;Paediatr Respir Rev,2014

4. Sickle cell disease;Ware;Lancet (London, England,2017

5. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on Transcranial Doppler ultrasonography;Adams;N Engl J Med,1998

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