Evidence map›Paper›PMID 40663295›Full record

ArticleArchives of osteoporosis2025

Comparative outcomes of denosumab and zoledronic acid discontinuation in hip fracture surgery: a nationwide database study.

Seok Ha Hong, Yeon Ju Yu, Seung Beom Han

Abstract readComparative Study
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In one paragraph

Article in Archives of osteoporosis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Seok Ha HongDepartment of Orthopedic Surgery, College of Medicine, Korea University Anam Hospital, 73, Inchon-Ro, Seongbuk-Gu, Seoul, 02841, Republic of Korea.ORCID 0009-0003-3114-6045
Yeon Ju YuDepartment of Biostatistics, College of Medicine, Korea University, Seoul, Republic of Korea.ORCID 0009-0007-1589-1239
Seung Beom HanDepartment of Orthopedic Surgery, College of Medicine, Korea University Anam Hospital, 73, Inchon-Ro, Seongbuk-Gu, Seoul, 02841, Republic of Korea. oshan@korea.ac.kr.ORCID 0000-0003-1880-4229

Funding

Korea Medical Device Development Fund RS-2020-KD000038
6 · The paper itself

Abstract

In hip fracture patients with poor medication adherence, DMAB discontinuation significantly increased the risk of subsequent vertebral and rib fractures. Additionally, higher CCI scores were associated with an increased risk of these fractures. These findings underscore the importance of maintaining treatment adherence to minimize fracture risk in this vulnerable population. PURPOSE: To assess the risk of major osteoporotic fractures and periprosthetic fractures in hip fracture patients who discontinued denosumab (DMAB) or zoledronic acid (ZOL).

methodsData from the South Korean National Health Insurance Review and Assessment Service were analyzed, focusing on patients aged ≥ 60 years who underwent hip fracture surgery and initiated DMAB or ZOL treatment. Among 20,180 patients, 1737 discontinued DMAB, and 3720 discontinued ZOL. After 1:1 propensity score matching, 3240 patients were included in the final analysis. The DMAB group was stratified into three subgroups based on the cumulative DMAB duration after hip fracture surgery: 1-2, 2-3, and > 3 Y. Discontinuation was defined as a 270-day gap for DMAB or 540-day gap for ZOL last injections. Subsequent osteoporotic fractures after discontinuation were evaluated.

resultsDMAB discontinuation significantly increased the risk of subsequent vertebral fractures (hazard ratio [HR] = 1.81; 95% confidence interval [CI], 1.28-2.56, P = 0.01) and rib fractures (HR = 2.04; 95% CI, 1.27-3.23, P = 0.004) compared to ZOL discontinuation. Higher Charlson Comorbidity Index (CCI) scores were also significantly associated with an increased risk of subsequent vertebral (HR 1.05, 95% CI 1.03-1.09, P = 0.02) and rib fractures (HR 1.12, 95% CI 1.06-1.19, P < 0.01). Although the incidence of hip fractures was lower in DMAB discontinuation group (1 case) than in the ZOL discontinuation group (10 cases), this difference did not reach statistical significance. No significant difference was observed in the risk of other nonvertebral fractures (humerus, wrist, ankle) and periprosthetic fracture between the two groups.

conclusionThis nationwide study, the first to use real-world data, highlighted the significant increase in the risk of vertebral and rib fracture associated with DMAB discontinuation in patients with poor adherence and higher comorbidity burden. Optimizing medication adherence is crucial to minimize the fracture risk in this vulnerable population. LEVEL OF EVIDENCE: Level III, Prognostic.

Indexed as

Bone Density Conservation AgentsDenosumabHip FracturesOsteoporotic FracturesZoledronic AcidAgedAged, 80 and overDatabases, FactualFemaleHumansMaleMiddle AgedRepublic of KoreaSpinal FracturesBone Density Conservation AgentsDenosumabZoledronic AcidAnti-osteoporotic medicationsDenosumab discontinuationHip fracturesNationwide cohort studyOsteoporotic fractures

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.