Evidence map›Paper›PMID 41933345›Full record

ArticleBMC medical informatics and decision making2026

Design and evaluation of an automated pediatric acute lymphoblastic leukemia registry from clinical data warehouses.

Yoona Choi, Jae Yoon Kim, Jung-Hyun Won, Ki Hoon Kim, Yujin Kim, Wona Choi, Bo Kyung Kim, Jae Won Yoo, Nack-Gyun Chung, Jae Wook Lee and 3 more

Abstract read
In one paragraph

Article in BMC medical informatics and decision making, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Yoona Choi *Department of Applied Bioengineering, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0001-8948-1880
Jae Yoon Kim *Department of Medical Informatics, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea.ORCID 0000-0001-8847-9586
Jung-Hyun WonCenter for Convergence Approaches in Drug Development, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0001-7335-8087
Ki Hoon KimDepartment of Medical Informatics, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea.ORCID 0009-0005-7426-0723
Yujin KimCenter for Convergence Approaches in Drug Development, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, Republic of Korea.ORCID 0009-0002-5582-5213
Wona ChoiDepartment of Medical Informatics, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea.ORCID 0000-0003-0269-6374
Bo Kyung KimDepartment of Pediatrics, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0003-4671-0449
Jae Won YooDepartment of Pediatrics, Catholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.ORCID 0000-0001-7970-1691
Nack-Gyun ChungDepartment of Pediatrics, Catholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.ORCID 0000-0003-4855-390X
Jae Wook LeeDepartment of Pediatrics, Catholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.ORCID 0000-0002-0735-0287
Hyoung Jin KangDepartment of Pediatrics, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0003-1009-6002
In Young Choi *Department of Medical Informatics, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea. iychoi@catholic.ac.kr.ORCID 0000-0002-2860-9411
Howard Lee *Department of Applied Bioengineering, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, Republic of Korea. howardlee@snu.ac.kr.ORCID 0000-0001-6713-5418

Funding

Korea Health Industry Development Institute (KHIDI) HI22C0464National Research Foundation of Korea (NRF) RS-2019-NR040058
6 · The paper itself

Abstract

backgroundReal-world data (RWD)–based pediatric acute lymphoblastic leukemia (ALL) registries often face scalability and reliability limits owing to manual data entry and inter-institutional heterogeneity. We evaluated the feasibility of building an automated, high-quality registry using electronic medical records (EMR) and clinical data warehouses (CDWs) to quantitatively assess the Pediatric ALL Automated Registry (PeARL) for (1) automatic extractability (ADE) (2), data quality, and (3) multicenter applicability.

methodsIn this study, we used CDWs to identify patients aged < 18 years with ALL (ICD-10 C91.0) who visited Seoul National University Hospital (SNUH) and the Catholic Medical Center (CMC). between 1990 and 2023. An automated extraction pipeline applied standard mapping, multivariate transformations, and rule-based natural language processing (NLP). Key variables were selected using the Medical Information Standards for Hematologic Cancer. Data quality was evaluated based on 228 rules across five dimensions (completeness, validity, accuracy, uniqueness, and consistency) based on DQ4HEALTH; error rates, defined as the proportion of data elements violating these rules, were calculated before and after quality management.

resultsOverall, 1,609 patients were included (CMC 946; SNUH 663). ADE for key variables was 89.7% at SNUH and 75.0% at CMC; most automations were single-field transformations (SNUH 61.8%; CMC 84.7%), with multivariate transformations and rule-based NLP addressing complex elements. Initial overall error rates were 1.858% (SNUH) and 0.129% (CMC), decreasing to 0.001% at both institutions after quality processes. Differences in CDW structure required additional preprocessing for laboratory and transplant variables, but harmonization was achieved via standardized table specifications and cross-site review.

conclusionsPeARL integrated standardized mapping, multivariate transformations, and rule-based NLP to enable large-scale automation of a pediatric ALL registry, achieving a 0.001% overall error rate under DQ4HEALTH-based quality management. This clinically guided, standardized framework enables reproducible implementation and scalable automation of pediatric ALL registry construction, supporting multicenter research and the generation of regulatory-grade real-world evidence. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Data WarehousingElectronic Health RecordsPrecursor Cell Lymphoblastic Leukemia-LymphomaRegistriesAdolescentChildChild, PreschoolData AccuracyFemaleHumansInfantMaleAcute lymphoblastic leukemia (ALL)Clinical Data Warehouse (CDW)Electronic medical recordsPediatricsRegistries

Identifiers

PMID41933345
PMCPMC13173821

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