Abstract
Objectives
Diagnostic stewardship aims to optimize laboratory testing practices by ensuring appropriate test utilization while minimizing unnecessary testing. However, the nationwide monitoring systems for laboratory test utilization remain underdeveloped. In this study, we analyzed nationwide health insurance claims data to identify inappropriate test utilization patterns and inform diagnostic stewardship interventions.
Methods
We analyzed the health insurance claims data from the Health Insurance Review and Assessment Service of Korea from January 2018 to December 2023. Three laboratory tests with concerns were evaluated. Inappropriate test utilization was classified based on adherence to recommended methodologies and institutional testing practices.
Results
The proportion of tuberculosis cultures performed using both liquid and solid media increased from 84.6 % in 2018 to 91.4 % in 2023; however, some institutions continued to perform >90 % of tests using only a single medium. Regional disparities were observed, with nonmetropolitan areas exhibiting higher rates of inappropriate tuberculosis testing. Stool ova and parasite tests showed a persistent reliance on direct smear-only methods. The correlation between endemic parasitic regions and the high proportions of direct smear-only tests suggests an urgent need for improved diagnostic methodologies. Despite longstanding recommendations against their use, bleeding time tests remained frequently ordered. The total number of bleeding time test claims exceeded 400,000 annually, with a limited decline over time.
Conclusions
Systematic monitoring frameworks based on nationwide claims data can identify inappropriate test utilization and support diagnostic stewardship efforts by informing targeted interventions, thereby optimizing laboratory resource allocation and enhancing patient safety.
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Research ethics: This study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The Institutional Review Board of Sanggye Paik Hospital waived the requirement for review of the study and the need to obtain informed consent (2023-11-012).
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Informed consent: Not applicable.
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Author contributions: Conceptualization: Park K. Data curation: Koo S. Investigation: Koo S and Kim J. Writing – original draft: Koo S. Writing – review & editing: Park K. All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Use of Large Language Models, AI and Machine Learning Tools: None declared.
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Conflict of interest: The authors state no conflict of interest.
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Research funding: None declared.
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Data availability: The raw claims datasets generated and/or analyzed in this study are not publicly available because of the ethical restrictions imposed by the HIRA. All data used in this study were obtained from HIRA research data (M20241030002).
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Supplementary Material
This article contains supplementary material (https://doi.org/10.1515/cclm-2025-0641).
© 2025 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Editorial
- Advancing diagnostic stewardship through claims-based utilization analysis: toward a system-wide vision of diagnostic excellence
- Review
- Biomarkers in body fluids and their detection techniques for human intestinal permeability assessment
- Mini Review
- Challenges of using natriuretic peptides to screen for the risk of developing heart failure in patients with diabetes: a report from the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Committee on Clinical Applications of Cardiac Bio-Markers (C-CB)
- Opinion Papers
- Reference intervals in value-based laboratory medicine: a shift from single-point measurements to metabolic variation-based models
- Overview of laboratory diagnostics for immediate management of patients presenting to the emergency department with acute bleeding
- What Matters Most: an Age-Friendly approach to pathology and laboratory medicine
- No fault or negligence after an adverse analytical finding due to a contaminated supplement: mission impossible. Two examples involving trimetazidine
- General Clinical Chemistry and Laboratory Medicine
- Utilization analysis of laboratory tests using health insurance claims data: advancing nationwide diagnostic stewardship monitoring systems
- Evaluating large language models as clinical laboratory test recommenders in primary and emergency care: a crucial step in clinical decision making
- A novel corrective model based on red blood cells indices and haemolysis index enables accurate unhaemolysed potassium determination in haemolysed samples – Hemokalc project
- Validation of (self-collected) capillary blood using a topper collection system as alternative for venous sampling for 15 common clinical chemistry analytes
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- An assessment of molecular diagnosis of tuberculosis and multi-drug resistant tuberculosis testing and quality assessment: findings of an international survey
- Letters to the Editor
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- Is successfulness of platelet clump disaggregation by vortexing influenced by platelet measurement methods?
- Oligoclonal banding analysis: assessing plasma use and time interval requirements for paired CSF and blood
Articles in the same Issue
- Frontmatter
- Editorial
- Advancing diagnostic stewardship through claims-based utilization analysis: toward a system-wide vision of diagnostic excellence
- Review
- Biomarkers in body fluids and their detection techniques for human intestinal permeability assessment
- Mini Review
- Challenges of using natriuretic peptides to screen for the risk of developing heart failure in patients with diabetes: a report from the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Committee on Clinical Applications of Cardiac Bio-Markers (C-CB)
- Opinion Papers
- Reference intervals in value-based laboratory medicine: a shift from single-point measurements to metabolic variation-based models
- Overview of laboratory diagnostics for immediate management of patients presenting to the emergency department with acute bleeding
- What Matters Most: an Age-Friendly approach to pathology and laboratory medicine
- No fault or negligence after an adverse analytical finding due to a contaminated supplement: mission impossible. Two examples involving trimetazidine
- General Clinical Chemistry and Laboratory Medicine
- Utilization analysis of laboratory tests using health insurance claims data: advancing nationwide diagnostic stewardship monitoring systems
- Evaluating large language models as clinical laboratory test recommenders in primary and emergency care: a crucial step in clinical decision making
- A novel corrective model based on red blood cells indices and haemolysis index enables accurate unhaemolysed potassium determination in haemolysed samples – Hemokalc project
- Validation of (self-collected) capillary blood using a topper collection system as alternative for venous sampling for 15 common clinical chemistry analytes
- Acoustophoresis-based blood sampling and plasma separation for potentially minimizing sampling-related blood loss
- Clinical validation of a liquid chromatography single quadrupole mass spectrometry (LC-MS) method using Waters Kairos™ Amino Acid Kit reagents
- Robustness of steroidomics-based machine learning for diagnosis of primary aldosteronism: a laboratory medicine perspective
- Investigation of the possible cause of over-estimation of human aldosterone in plasma, using a unique, non-synthetic human aldosterone-free matrix
- Performance of afternoon (16:00 h) serum cortisol for the diagnosis of Cushing’s syndrome
- MAGLUMI® Tacrolimus (CLIA) assay: analytical performances and comparison with LC-MS/MS and ARCHITECT Tacrolimus (CMIA) assay
- Assessment of 2023 ACR/EULAR antiphospholipid syndrome classification criteria in a Spanish cohort
- Comprehensive evaluation of antiphospholipid antibody testing methodologies in APS diagnosis: performance comparisons across assay systems and clinical subtypes
- Candidate Reference Measurement Procedures and Materials
- Exploring commutable materials for serum folate measurement: challenges in cross-method harmonization
- Reference Values and Biological Variations
- Reference ranges for ionized calcium in plasma in Danish children aged 0 days to 3 years using laboratory registry data
- A step forward in pediatric hemophagocytic lymphohistiocytosis and autoimmune disease: pediatric reference interval for serum soluble IL-2 receptor and soluble CD163
- Cancer Diagnostics
- Cellular expression of PD-1, PD-L1 and CTLA-4 in patients with JAK2V617F mutated myeloproliferative disorders
- Diabetes
- Serum N-glycans as independent predictors of the incidence of type 2 diabetes: a prospective investigation in the AEGIS cohort
- Infectious Diseases
- An assessment of molecular diagnosis of tuberculosis and multi-drug resistant tuberculosis testing and quality assessment: findings of an international survey
- Letters to the Editor
- Targeting low-value laboratory care
- Is time a significant factor in the release of potassium from lithium heparin plasma and serum?
- External quality assessment in resource-constrained laboratories: a survey of practices and perceptions in Nepal
- Is successfulness of platelet clump disaggregation by vortexing influenced by platelet measurement methods?
- Oligoclonal banding analysis: assessing plasma use and time interval requirements for paired CSF and blood