From Paper Files to Web-Based Application for Data-Driven Monitoring of HIV Programs: Nigeria's Journey to a National Data Repository for Decision-Making and Patient Care.
IF 1.3 4区 医学Q3 COMPUTER SCIENCE, INFORMATION SYSTEMS
Ibrahim Dalhatu, Chinedu Aniekwe, Adebobola Bashorun, Alhassan Abdulkadir, Emilio Dirlikov, Stephen Ohakanu, Oluwasanmi Adedokun, Ademola Oladipo, Ibrahim Jahun, Lisa Murie, Steven Yoon, Mubarak G Abdu-Aguye, Ahmed Sylvanus, Samuel Indyer, Isah Abbas, Mustapha Bello, Nannim Nalda, Matthias Alagi, Solomon Odafe, Sylvia Adebajo, Otse Ogorry, Murphy Akpu, Ifeanyi Okoye, Kunle Kakanfo, Amobi Andrew Onovo, Gregory Ashefor, Charles Nzelu, Akudo Ikpeazu, Gambo Aliyu, Tedd Ellerbrock, Mary Boyd, Kristen A Stafford, Mahesh Swaminathan
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引用次数: 0
Abstract
Background: Timely and reliable data are crucial for clinical, epidemiologic, and program management decision making. Electronic health information systems provide platforms for managing large longitudinal patient records. Nigeria implemented the National Data Repository (NDR) to create a central data warehouse of all people living with human immunodeficiency virus (PLHIV) while providing useful functionalities to aid decision making at different levels of program implementation.
Objective: We describe the Nigeria NDR and its development process, including its use for surveillance, research, and national HIV program monitoring toward achieving HIV epidemic control.
Methods: Stakeholder engagement meetings were held in 2013 to gather information on data elements and vocabulary standards for reporting patient-level information, technical infrastructure, human capacity requirements, and information flow. Findings from these meetings guided the development of the NDR. An implementation guide provided common terminologies and data reporting structures for data exchange between the NDR and the electronic medical record (EMR) systems. Data from the EMR were encoded in extensible markup language and sent to the NDR over secure hypertext transfer protocol after going through a series of validation processes.
Results: By June 30, 2021, the NDR had up-to-date records of 1,477,064 (94.4%) patients receiving HIV treatment across 1,985 health facilities, of which 1,266,512 (85.7%) patient records had fingerprint template data to support unique patient identification and record linkage to prevent registration of the same patient under different identities. Data from the NDR was used to support HIV program monitoring, case-based surveillance and production of products like the monthly lists of patients who have treatment interruptions and dashboards for monitoring HIV test and start.
Conclusion: The NDR enabled the availability of reliable and timely data for surveillance, research, and HIV program monitoring to guide program improvements to accelerate progress toward epidemic control.
期刊介绍:
Good medicine and good healthcare demand good information. Since the journal''s founding in 1962, Methods of Information in Medicine has stressed the methodology and scientific fundamentals of organizing, representing and analyzing data, information and knowledge in biomedicine and health care. Covering publications in the fields of biomedical and health informatics, medical biometry, and epidemiology, the journal publishes original papers, reviews, reports, opinion papers, editorials, and letters to the editor. From time to time, the journal publishes articles on particular focus themes as part of a journal''s issue.