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Minimally Invasive Lateral Lumbar Interbody Fusion Shows a Lower Incidence of Radiologic Adjacent Segment Pathology Than Conventional Posterior Lumbar Interbody Fusion. 与传统后路腰椎椎体间融合术相比,微创侧位腰椎椎体间融合术的放射学邻段病理发生率更低。
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-02 DOI: 10.3346/jkms.2026.41.e49
Jaewan Soh, Joonghyun Ahn, Jae Chul Lee, Min Gon Song, Byung-Joon Shin

Background: Radiologic adjacent segment pathology (R-ASP) is a significant consequence following lumbar spinal fusion, potentially resulting from compromised integrity of posterior structures. Few studies have directly compared the incidence of R-ASP between minimally invasive lateral lumbar interbody fusion (LLIF) and conventional posterior lumbar interbody fusion (PLIF). Thus, the objective of this study was to analyze risk factors for R-ASP and compare clinical outcomes between minimally invasive LLIF supplemented with percutaneous pedicle screw fixation and open conventional PLIF.

Methods: This study included 107 patients who underwent one- or two-segment spinal fusion for degenerative lumbar disease. Fifty-one patients underwent minimally invasive LLIF and 56 received conventional PLIF. Factors related to occurrence of R-ASP were investigated by analyzing demographic profiles, radiological results, and clinical outcomes. Correlations between clinical results were determined based on fusion methods and the presence of R-ASP. Patient-related factors, preoperative spinal diagnosis, number of fused segments, and radiologic findings were analyzed. Clinical outcomes were also assessed. Cox regression survival analysis was performed to determine risk factors for R-ASP. Annual incidence and cumulative survival rate of R-ASP were calculated using the life-table method and Kaplan-Meier survival curve.

Results: Cox proportional hazards regression analysis identified three significant risk factors for R-ASP: PLIF over LLIF (P = 0.028; hazard ratio [HR], 2.321; 95% confidence interval [CI], 1.096-4.913), postoperative pelvic incidence-lumbar lordotic angle mismatch ≥ 10° (P = 0.022; HR, 2.280; 95% CI, 1.126-4.617), and preoperative facet arthropathy grade ≥ 2 (P = 0.016; HR, 3.491; 95% CI, 1.266-9.629). The predicted incidence of R-ASP was 48.7% (95% CI, 42.1-55.2%) at 5 years post-fusion and 80.7% (95% CI, 73.0-88.5%) at 8 years. Clinical outcomes showed that the final visual analog scale for lower back pain was significantly lower in patients who underwent LLIF and in patients who did not develop R-ASP.

Conclusion: Minimally invasive fusion techniques that preserve posterior structures might slow the progression of degenerative changes in adjacent segments. To reduce R-ASP, preoperative assessment of facet degeneration and adequate restoration of sagittal balance during surgery are crucial considerations.

背景:放射学邻段病理(R-ASP)是腰椎融合术后的重要后果,可能导致后路结构完整性受损。很少有研究直接比较微创侧位腰椎椎体间融合术(LLIF)和常规后路腰椎椎体间融合术(PLIF)的R-ASP发生率。因此,本研究的目的是分析R-ASP的危险因素,并比较微创LLIF加经皮椎弓根螺钉固定与开放式传统PLIF的临床结果。方法:本研究纳入107例行一节段或两节段腰椎融合术治疗退行性腰椎疾病的患者。51例患者行微创LLIF, 56例接受常规PLIF。通过分析人口统计学资料、放射学结果和临床结果来调查与R-ASP发生相关的因素。根据融合方法确定临床结果与R-ASP存在的相关性。分析患者相关因素、术前脊柱诊断、融合节段数目及影像学表现。临床结果也进行了评估。采用Cox回归生存分析确定R-ASP的危险因素。采用生命表法和Kaplan-Meier生存曲线计算R-ASP的年发病率和累积生存率。结果:Cox比例风险回归分析确定了R-ASP的三个显著危险因素:PLIF超过LLIF (P = 0.028;风险比[HR], 2.321; 95%可信区间[CI], 1.096-4.913),术后骨盆发生率-腰椎前凸角失配≥10°(P = 0.022; HR, 2.280; 95% CI, 1.126-4.617),术前小关节病变等级≥2 (P = 0.016; HR, 3.491; 95% CI, 1.266-9.629)。融合后5年R-ASP的预测发生率为48.7% (95% CI, 42.1-55.2%), 8年为80.7% (95% CI, 73.0-88.5%)。临床结果显示,LLIF患者和未发生R-ASP的患者腰痛的最终视觉模拟量表明显较低。结论:保留后路结构的微创融合技术可能减缓相邻节段退行性改变的进展。为了降低R-ASP,术前评估小关节突变性和术中矢状面平衡的充分恢复是至关重要的考虑因素。
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引用次数: 0
Trends in Sedative-Hypnotic Prescription Among Insomnia Patients: A Nationwide Cohort Study From 2010 to 2022 in Korea. 失眠患者的镇静催眠处方趋势:2010年至2022年韩国全国队列研究
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-02 DOI: 10.3346/jkms.2026.41.e1
Jiyoon Shin, So Yon Jun, Donghyun Won, Minah Kim, Su Young Lee, Mincheol Seo, Aesun Shin, Yu Jin Lee

Background: Global insomnia prevalence increased during the coronavirus disease 2019 (COVID-19) pandemic, driving higher demand for sedative-hypnotics. The objective of this study was to compare sedative-hypnotic prescription patterns in South Korea from 2010 to 2022 and assess the potential impact of the COVID-19 pandemic.

Methods: This population-based cohort study from January 1, 2010, to December 31, 2022, used the Korean National Health Insurance's Health Insurance Sharing Service database of 8,136,437 (60.4% female) unique insomnia patients aged 18 and older. Prescriptions for sedative-hypnotic groups (benzodiazepines, non-benzodiazepines, antidepressants, and antipsychotics), number of patients prescribed sedative-hypnotics, and predicted and observed prescription rates by sex, age, and sedative-hypnotic group were analyzed.

Results: The number of prescriptions per 1,000 population increased across all sedative-hypnotic groups before and during the pandemic. Women and the elderly had higher prescriptions for all sedative-hypnotic groups compared to men and other age groups. Antidepressant prescriptions saw the highest percentage increase (men 38.6%; women 37.1%) in 1st half of 2020 compared to 2019, followed by antipsychotics (men 28.9%; women 25.7%). Antidepressant prescriptions showed the largest increase relative to predicted levels across all age groups from 2020 to 2021, while non-benzodiazepines exhibited the smallest increase (men 5.6%; women 4.5%). In the 18-29 age group, prescriptions for all sedative-hypnotic groups exceeded predicted numbers in 2021.

Conclusion: This study found that sedative-hypnotic prescriptions steadily increased from 2010 to 2022, with the trend becoming more pronounced during the COVID-19 pandemic, when prescription rates tended to exceed predicted levels in Korea. Monitoring the use of sedative-hypnotics for insomnia in women, the elderly, and young adults is essential for potential adverse effects and associated mental problems.

背景:2019冠状病毒病(COVID-19)大流行期间,全球失眠患病率上升,对镇静催眠药的需求增加。本研究的目的是比较2010年至2022年韩国镇静催眠药物的处方模式,并评估COVID-19大流行的潜在影响。方法:这项基于人群的队列研究于2010年1月1日至2022年12月31日,使用韩国国民健康保险的健康保险共享服务数据库,包括8,136,437名18岁及以上的独特失眠患者(60.4%为女性)。分析镇静催眠药物组(苯二氮卓类、非苯二氮卓类、抗抑郁药和抗精神病药)的处方、服用镇静催眠药物的患者人数以及按性别、年龄和镇静催眠药物组预测和观察的处方率。结果:在流感大流行之前和期间,所有镇静催眠组每1000人的处方数量都有所增加。与男性和其他年龄组相比,女性和老年人在所有镇静催眠组中都有更高的处方。与2019年相比,2020年上半年抗抑郁药处方的增幅最高(男性38.6%,女性37.1%),其次是抗精神病药(男性28.9%,女性25.7%)。从2020年到2021年,抗抑郁药处方相对于预测水平的增幅最大,而非苯二氮卓类药物的增幅最小(男性5.6%,女性4.5%)。在18-29岁年龄组中,所有镇静催眠药物组的处方都超过了2021年的预测数量。结论:本研究发现,从2010年到2022年,镇静催眠药物的处方稳步增加,这一趋势在2019冠状病毒病大流行期间更为明显,当时韩国的处方率往往超过预期水平。对女性、老年人和年轻人使用镇静催眠药治疗失眠症的情况进行监测,对潜在的不良反应和相关的精神问题至关重要。
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引用次数: 0
Correlation Between Small Dense Low-Density Lipoprotein and Tissue Perfusion in Diabetic Foot. 小密度低密度脂蛋白与糖尿病足组织灌注的关系
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-02 DOI: 10.3346/jkms.2026.41.e48
Kyu-Il Lee, Ye-Won Choi, Seung-Kyu Han, Seong-Ho Jeong, Eun-Sang Dhong

Background: Small dense low-density lipoprotein (sdLDL) is recognized as a reliable predictor of atherosclerotic vascular diseases and is also associated with the severity of diabetes. Vascular status directly affects tissue perfusion, indicating that sdLDL could serve as a potential marker for tissue perfusion in diabetic feet. However, an alternative possibility exists. In patients with diabetes, discrepancies can occur between vascular status and actual tissue perfusion due to complications related to diabetes such as neuropathy and hematologic changes in red blood cells. In such instances, sdLDL may not consistently correlate with tissue perfusion. Tissue perfusion is a crucial element in managing diabetic foot conditions. Despite acknowledging its importance, no studies to date have explored the relationship between sdLDL levels and tissue perfusion in diabetic feet. This prospective study seeks to explore this correlation.

Methods: Fifty patients with diabetes were enrolled in the study. Tissue perfusion was assessed by measuring the foot's transcutaneous oxygen pressure (TcPO₂). SdLDL levels were determined based on the mean low-density lipoprotein (LDL) particle size, proportion of sdLDL as a percentage of total LDL, and LDL subfraction score. Correlations between TcPO₂ and each variable were evaluated through scatter plots, and correlation coefficients (R) with corresponding P values were calculated. Statistical analyses were conducted for all participants and further stratified into two subgroups based on a TcPO₂ threshold of ≥ 40 mmHg and < 40 mmHg.

Results: In the overall analysis (n = 50), no statistically significant relationships were detected between TcPO₂ and sdLDL size, sdLDL percentage, or LDL subfraction score. Nevertheless, in the TcPO₂ ≥ 40 mmHg subgroup (n = 29), a statistically significant positive correlation was found between mean LDL particle size and TcPO₂ (R = 0.414, P = 0.026). In contrast, statistically significant negative correlations emerged between sdLDL percentage and TcPO₂ (R = -0.415, P = 0.025), as well as between LDL subfraction score and TcPO₂ (R = -0.419, P = 0.024).

Conclusion: This study identified a significant correlation between sdLDL levels and tissue perfusion in diabetic feet with TcPO₂ ≥ 40 mmHg, but no significant correlation in those with TcPO₂ < 40 mmHg.

背景:小密度低密度脂蛋白(sdLDL)被认为是动脉粥样硬化性血管疾病的可靠预测因子,也与糖尿病的严重程度相关。血管状态直接影响组织灌注,提示sdLDL可作为糖尿病足组织灌注的潜在标志物。然而,存在另一种可能性。在糖尿病患者中,由于与糖尿病相关的并发症,如神经病变和红细胞血液学改变,血管状态和实际组织灌注之间可能出现差异。在这种情况下,sdLDL可能与组织灌注不一致。组织灌注是管理糖尿病足疾病的关键因素。尽管承认其重要性,但迄今为止还没有研究探讨sdLDL水平与糖尿病足组织灌注之间的关系。这项前瞻性研究旨在探索这种相关性。方法:50例糖尿病患者入组研究。通过测量足部经皮氧压(TcPO₂)来评估组织灌注。SdLDL水平根据平均低密度脂蛋白(LDL)粒径、SdLDL占总LDL的百分比和LDL亚分数评分来确定。通过散点图评价TcPO₂与各变量的相关性,并计算相应P值的相关系数(R)。对所有参与者进行统计分析,并根据TcPO₂阈值≥40 mmHg和< 40 mmHg进一步分为两个亚组。结果:在总体分析(n = 50)中,TcPO₂与sdLDL大小、sdLDL百分比或LDL亚分数评分之间无统计学意义的关系。然而,在TcPO₂≥40 mmHg亚组(n = 29)中,平均LDL颗粒大小与TcPO₂之间存在统计学上显著的正相关(R = 0.414, P = 0.026)。sdLDL百分比与TcPO₂呈显著负相关(R = -0.415, P = 0.025), LDL亚分数评分与TcPO₂呈显著负相关(R = -0.419, P = 0.024)。结论:本研究发现TcPO₂≥40 mmHg的糖尿病足sdLDL水平与组织灌注有显著相关性,TcPO₂< 40 mmHg的糖尿病足sdLDL水平与组织灌注无显著相关性。
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引用次数: 0
Evaluation of Post-Acute Sequelae of SARS-CoV-2 (PASC) Index and a Recent Long COVID Criteria in Korean Long COVID-19 Cohort. 韩国长冠肺炎队列SARS-CoV-2急性后后遗症(PASC)指数与近期长冠标准的评价
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-02-02 DOI: 10.3346/jkms.2026.41.e54
Kyungsup Kwon, Choi Young Jang, Woori Kim, JuYeon Son, Euijin Chang, Sung-Han Kim

Background: To compare the post-acute sequelae of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) infection (PASC) index and the National Academies of Sciences, Engineering, and Medicine (NASEM) criteria in identifying long coronavirus disease (COVID) among adults with confirmed coronavirus disease 2019.

Methods: A prospective cohort study was conducted from November 2022 to February 2025 at a single tertiary care hospital in Seoul, Korea. Adults aged 18 years or older with confirmed SARS-CoV-2 infection were enrolled, yielding a total of 183 participants. Follow-up assessments took place at 1-, 3-, 6-, and 12-months post-infection. The primary outcome was the prevalence of long COVID at 12 months, measured using the PASC index (≥ 12 points across specified symptoms) and the NASEM criteria (≥ 1 symptom persisting for at least 3 months).

Results: Of 183 participants, 26.2% (48/183) met the PASC index, whereas 47.5% (87/183) fulfilled the NASEM criteria. Of the 48 patients who met the PASC index, 44 (91.7%) also met the NASEM criteria.

Conclusion: The NASEM criteria classified nearly half of participants with long COVID and covered those with PASC index, while the PASC index identified about one quarter. Although the NASEM criteria capture a broader range of persistent symptoms, the PASC index may offer a more stringent threshold, potentially informing targeted research and clinical decision-making.

背景:比较重症急性呼吸综合征-冠状病毒-2 (SARS-CoV-2)感染急性后后遗症(PASC)指数与美国国家科学院、工程院和医学院(NASEM)标准在确诊2019冠状病毒病成人中识别长冠状病毒病(COVID)的效果。方法:一项前瞻性队列研究于2022年11月至2025年2月在韩国首尔的一家三级医院进行。纳入了确诊为SARS-CoV-2感染的18岁或以上的成年人,总共有183名参与者。在感染后1、3、6和12个月进行随访评估。主要终点是12个月时长冠状病毒的患病率,使用PASC指数(指定症状≥12分)和NASEM标准(≥1种症状持续至少3个月)来测量。结果:183名参与者中,26.2%(48/183)符合PASC指数,而47.5%(87/183)符合NASEM标准。在48例符合PASC指数的患者中,44例(91.7%)也符合NASEM标准。结论:NASEM标准对近一半的长COVID患者进行了分类,并覆盖了PASC指数患者,而PASC指数仅识别了约四分之一。虽然NASEM标准涵盖了更广泛的持续性症状,但PASC指数可能提供了更严格的阈值,可能为有针对性的研究和临床决策提供信息。
{"title":"Evaluation of Post-Acute Sequelae of SARS-CoV-2 (PASC) Index and a Recent Long COVID Criteria in Korean Long COVID-19 Cohort.","authors":"Kyungsup Kwon, Choi Young Jang, Woori Kim, JuYeon Son, Euijin Chang, Sung-Han Kim","doi":"10.3346/jkms.2026.41.e54","DOIUrl":"10.3346/jkms.2026.41.e54","url":null,"abstract":"<p><strong>Background: </strong>To compare the post-acute sequelae of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) infection (PASC) index and the National Academies of Sciences, Engineering, and Medicine (NASEM) criteria in identifying long coronavirus disease (COVID) among adults with confirmed coronavirus disease 2019.</p><p><strong>Methods: </strong>A prospective cohort study was conducted from November 2022 to February 2025 at a single tertiary care hospital in Seoul, Korea. Adults aged 18 years or older with confirmed SARS-CoV-2 infection were enrolled, yielding a total of 183 participants. Follow-up assessments took place at 1-, 3-, 6-, and 12-months post-infection. The primary outcome was the prevalence of long COVID at 12 months, measured using the PASC index (≥ 12 points across specified symptoms) and the NASEM criteria (≥ 1 symptom persisting for at least 3 months).</p><p><strong>Results: </strong>Of 183 participants, 26.2% (48/183) met the PASC index, whereas 47.5% (87/183) fulfilled the NASEM criteria. Of the 48 patients who met the PASC index, 44 (91.7%) also met the NASEM criteria.</p><p><strong>Conclusion: </strong>The NASEM criteria classified nearly half of participants with long COVID and covered those with PASC index, while the PASC index identified about one quarter. Although the NASEM criteria capture a broader range of persistent symptoms, the PASC index may offer a more stringent threshold, potentially informing targeted research and clinical decision-making.</p>","PeriodicalId":16249,"journal":{"name":"Journal of Korean Medical Science","volume":"41 5","pages":"e54"},"PeriodicalIF":2.3,"publicationDate":"2026-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12865211/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146112847","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Toward the Implementation of Shared Decision-Making in Korean Clinical Practice: Study Protocol for a Foundational Research Project. 共同决策在韩国临床实践中的实施:一个基础研究项目的研究方案。
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-26 DOI: 10.3346/jkms.2026.41.e38
Min Ji Kim, Sang-Ho Yoo, Kyung-Sook Woo, Heeseung Choi, Eunsuk Chang, Kyungsuk Choi, Young Su Park, Yoongu Kim, Do Hoon Kim, Junhewk Kim, Dong Wook Shin

Shared decision-making (SDM) is an essential component of patient-centered care, yet its implementation in South Korea remains limited due to a persistent physician-centered clinical culture. This project, supported by the Ministry of Health and Welfare, aims to establish a foundation for nationwide SDM implementation by developing a culturally adapted Korean SDM model and creating a framework to support its institutionalization and widespread clinical adoption. This four-year project consists of five interlinked work packages (WPs) organized into two phases, each lasting two years. Using a multi-method approach-comprising nationwide surveys, systematic literature reviews, and psychometric validation studies-we will assess the current landscape (WP1) and develop standardized SDM evaluation tools for primary stakeholders (WP2). A clinical research data management system will be designed and implemented to support data integration and monitoring (WP3). The central component involves developing a Korean SDM conceptual model and corresponding implementation strategies (WP4). Economic evaluations and legal analyses will inform the design of a pilot reimbursement framework to support sustainable system-level integration (WP5). The project is expected to produce the following outcomes: i) an analysis of domestic and international SDM trends; ii) validated SDM assessment tools and guidelines tailored for the Korean context; iii) a standardized and interoperable SDM data management system; iv) a culturally grounded Korean SDM model with evidence-based implementation strategies; and v) policy proposals, including a reimbursement model, to facilitate system-wide adoption. This work will provide the theoretical, empirical, and policy basis required to advance SDM within the Korean healthcare system. By addressing cultural characteristics and structural barriers, the resulting SDM model and policy recommendations are expected to support the sustainable institutionalization of SDM and strengthen patient autonomy and the quality of clinical practice in Korea.

共同决策(SDM)是以患者为中心的护理的重要组成部分,但由于韩国坚持以医生为中心的临床文化,其实施仍然有限。该项目得到了卫生和福利部的支持,旨在通过制定符合韩国文化的可持续发展机制模式,并创建一个框架,支持其制度化和广泛临床采用,为全国实施可持续发展机制奠定基础。这个为期四年的项目包括五个相互关联的工作包,分为两个阶段,每个阶段持续两年。采用多方法方法——包括全国调查、系统文献综述和心理测量验证研究——我们将评估当前形势(WP1),并为主要利益相关者开发标准化的SDM评估工具(WP2)。将设计和实施临床研究数据管理系统,以支持数据整合和监测(WP3)。核心组件包括开发韩国SDM概念模型和相应的实施策略(WP4)。经济评估和法律分析将为试点报销框架的设计提供信息,以支持可持续的系统级整合(WP5)。该项目预计将产生以下成果:i)分析国内和国际SDM趋势;ii)针对韩国情况量身定制的经过验证的SDM评估工具和指南;iii)标准化和可互操作的SDM数据管理系统;4)韩国SDM模式的文化基础和基于证据的实施策略;5)政策建议,包括报销模式,以促进全系统采用。这项工作将提供理论、经验和政策基础,以推动韩国医疗保健系统内的SDM。通过解决文化特征和结构性障碍,由此产生的SDM模型和政策建议有望支持韩国SDM的可持续制度化,并加强患者自主权和临床实践质量。
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引用次数: 0
Study Protocol of a Korean Patient-Centered Shared Decision-Making Model for Management of Severe Knee Osteoarthritis: A Multicenter Pragmatic Clinical Trial (K-SDM-KOA). 韩国以患者为中心的共享决策模型治疗严重膝骨关节炎的研究方案:一项多中心实用临床试验(K-SDM-KOA)
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-26 DOI: 10.3346/jkms.2026.41.e40
Byung Sun Choi, Sujin Seo, Moon Jong Chang, Joong Il Kim, Seong Hwan Kim, Do Weon Lee, Du Hyun Ro, Hyoseon Choi, Hyuk-Soo Han

Severe knee osteoarthritis (KOA) involves complex, preference-sensitive treatment decisions, ranging from non-operative to surgical options. However, despite the preference-sensitive nature of KOA, existing shared decision-making (SDM) processes often lack clarity in effectively incorporating patients' values and preferences into treatment decisions. Moreover, most SDM models have been developed in western contexts, which may limit their applicability in other cultural settings. To address these limitations, a Korean Shared Decision-Making Model for KOA (K-SDM-KOA) has been developed using a culturally adapted, five-step framework that integrates a web-based decision-support platform and age-friendly educational media. The K-SDM-KOA model is designed to support preference-sensitive decision-making through a pragmatic, multicenter cohort framework involving 1,300 patients with Kellgren-Lawrence grade 3-4 across five hospitals. Within this framework, patients receive either standard care or the K-SDM-KOA intervention, which combines pre-consultation preparation (step 1-3) with in-clinic deliberation and decision-making (step 4-5). The primary outcome is patient-perceived SDM measured using the Korean-validated 9-item Shared Decision Making Questionnaire, reported on a 0-100 scale, with higher scores indicating greater SDM. Secondary outcomes include patients' preferred role in decision-making, decisional conflict, decision regret, and knowledge gain related to KOA. Additionally, a nested cohort of 50 patients undergoing contralateral total knee arthroplasty will provide paired analyses of early pain and function (visual analogue scale, Western Ontario and McMaster Universities Osteoarthritis Index, Knee Society Score) at baseline, 3 months, and 12 months. Analyses will follow an intention-to-treat principle and employ linear mixed-effect models and appropriate statistical tests to assess between group differences. This article presents a culturally tailored, technology-supported SDM model designed to enhance decision quality and early patient-reported outcomes in severe KOA. Findings may provide a foundation for future empirical studies and support the broader adoption of structured SDM in Korea's healthcare system.

严重膝骨关节炎(KOA)涉及复杂的,偏好敏感的治疗决策,从非手术到手术选择。然而,尽管KOA具有偏好敏感性,但现有的共同决策(SDM)过程在有效地将患者的价值观和偏好纳入治疗决策方面往往缺乏明确性。此外,大多数SDM模型都是在西方背景下发展起来的,这可能限制了它们在其他文化背景下的适用性。为了解决这些限制,我们开发了韩国KOA共享决策模型(K-SDM-KOA),该模型采用了一种与文化相适应的五步框架,该框架集成了基于网络的决策支持平台和适合年龄的教育媒体。K-SDM-KOA模型旨在通过实用的多中心队列框架支持偏好敏感决策,该框架涉及5家医院的1,300名Kellgren-Lawrence分级3-4患者。在这个框架内,患者接受标准治疗或K-SDM-KOA干预,其中结合了会诊前准备(步骤1-3)和临床审议和决策(步骤4-5)。主要结果是使用韩国验证的9项共享决策问卷测量患者感知的SDM,以0-100的量表报告,得分越高表明SDM越高。次要结局包括患者在决策中的首选角色、决策冲突、决策后悔和与KOA相关的知识获取。此外,50例接受对侧全膝关节置换术的患者将在基线、3个月和12个月时提供早期疼痛和功能的配对分析(视觉模拟量表、西安大略省和麦克马斯特大学骨关节炎指数、膝关节社会评分)。分析将遵循意向治疗原则,采用线性混合效应模型和适当的统计检验来评估组间差异。本文提出了一种文化定制的、技术支持的SDM模型,旨在提高严重KOA的决策质量和早期患者报告的结果。研究结果可能为未来的实证研究提供基础,并支持韩国医疗保健系统更广泛地采用结构化SDM。
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引用次数: 0
Shared Decision-Making for Periodontally Compromised Teeth: Study Protocol for an Ongoing Prospective Multicenter Before-and-After Clinical Trial. 牙周受损牙齿的共同决策:一项正在进行的前瞻性多中心前后临床试验的研究方案。
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-26 DOI: 10.3346/jkms.2026.41.e39
Kyung-A Ko, Ji-Young Jung, Yuan Park, Christina Chi, Hoi-In Jung, Young-Dan Cho, Ji-Young Joo, Sang-Joun Yu, In-Woo Cho, Yong-Gun Kim, Dong-Woon Lee, Young-Taek Kim, Jae-Kwan Lee, Ok-Su Kim, Ji-Youn Hong, Jae-Hong Lee, Jung-Seok Lee

Treatment decisions for teeth with poor periodontal prognosis are often complicated, requiring careful balancing of clinical evidence and patient values. Shared decision-making (SDM) is increasingly recognized as a beneficial approach to align clinical judgment with patient preferences. However, structured SDM implementation in dental settings remains limited. This study was designed to evaluate the effectiveness of a structured SDM protocol compared to usual care decision-making for patients with severe periodontitis and hopeless-prognosis teeth. A multicenter, before-and-after clinical trial will be conducted across 12 dental centers in South Korea. Each center will apply usual care decision-making for the first six months, followed by the SDM intervention for the subsequent six months. The SDM process involves a three-step model: team talk, option talk (aided by web-based decision aids), and decision talk. Eligible participants include patients with stage III or IV periodontitis and at least one hopeless-prognosis tooth. Each patient follows a three-visit schedule. Primary outcome is the rate of tooth preservation decisions. Secondary outcomes include measures related to SDM (SDM-Q-9, SDM-Q-Doc), patient experience (Perceived Involvement in Care Scale [PICS], Decisional Regret Scale [DRS], treatment adherence), and clinical measures (periodontal condition and treatment costs). Data are collected via Research Electronic Data Capture, and statistical analyses include McNemar's test for binary outcomes and repeated-measures analysis of variance for continuous data. This study is expected to provide evidence supporting the integration of structured SDM protocols in dental practice. By evaluating both patient-centered and clinical outcomes, the research aims to advance personalized, participatory approaches in managing severe periodontitis. Trial Registration: Clinical Research Information Service Identifier: KCT0010405.

牙周预后差的牙齿的治疗决策通常是复杂的,需要仔细平衡临床证据和患者的价值。共同决策(SDM)越来越被认为是一种使临床判断与患者偏好保持一致的有益方法。然而,结构化SDM在牙科设置的实施仍然有限。本研究旨在评估与常规护理决策相比,结构化SDM方案对严重牙周炎和预后无望的牙齿患者的有效性。韩国将在全国12个牙科中心进行前后对照的多中心临床试验。每个中心将在前六个月采用常规护理决策,随后六个月采用SDM干预。SDM过程包括一个三步模型:团队对话、选项对话(由基于网络的决策辅助工具辅助)和决策对话。符合条件的参与者包括III期或IV期牙周炎患者和至少一颗预后无望的牙齿。每位患者遵循三次就诊计划。主要结果是决定保留牙齿的比率。次要结局包括与SDM (SDM- q -9、SDM- q - doc)、患者体验(感知参与护理量表[PICS]、决策后悔量表[DRS]、治疗依从性)和临床测量(牙周状况和治疗费用)相关的测量。通过Research Electronic Data Capture收集数据,统计分析包括二元结果的McNemar检验和连续数据的重复测量方差分析。本研究有望为结构化SDM协议在牙科实践中的整合提供证据。通过评估以患者为中心和临床结果,该研究旨在推进个性化,参与性方法管理严重牙周炎。试验注册:临床研究信息服务标识:KCT0010405。
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引用次数: 0
Protocol for DESCIDE-RD: Determining Effectiveness of Shared Decision Making in Drug Therapy Selection for Rheumatic Diseases. deside - rd方案:确定风湿病药物治疗选择共同决策的有效性。
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-26 DOI: 10.3346/jkms.2026.41.e41
Se Rim Choi, Soo-Kyung Cho, Bora Nam, Ha-Rim Park, Soo-Bin Lee, Hye-Rin Ko, Yun Jeong Choi, Eunwoo Nam, Sang Won Lee, Seongjun Yoon, Yoon-Kyoung Sung

The availability of biologic agents and Janus kinase (JAK) inhibitors has expanded therapeutic options for rheumatic diseases, and international guidelines now recommend shared decision-making (SDM) to guide treatment selection. This study will evaluate whether a structured SDM model enhances patients' perceptions of SDM when selecting biologic agents or JAK inhibitors for rheumatoid arthritis (RA) and ankylosing spondylitis (AS), compared to standard care. This open-label, multicentre, stratified cluster-randomised trial will enrol 300 patients with RA or AS. Participants will be assigned in a 1:1:1 ratio to one of three groups: SDM Group I, SDM Group II, or standard care. In the SDM groups, the Three-Talk Model (Team Talk, Option Talk, and Decision Talk) will be implemented. SDM Group I will receive decision aids during Option Talk, while SDM Group II will receive both decision aids and an artificial intelligence-based chatbot. In the standard care group, treatment recommendations will be made at the physician's discretion. The primary outcome will be the Shared Decision-Making Questionnaire score. Secondary outcomes will include changes in the Decisional Conflict Scale, the Health Empowerment Scale, the Leeds Satisfaction Questionnaire, and the EuroQol-5 Dimension. Data will be collected using iCReaT (http://icreat.kr). This study will provide evidence on the effectiveness of structured SDM in selecting biologic agents and JAK inhibitors for RA and AS, with potential implications for improving treatment decisions and patient outcomes. Trial Registration: Clinical Research Information Service Identifier: KCT0011310.

生物制剂和Janus激酶(JAK)抑制剂的可用性扩大了风湿病的治疗选择,国际指南现在推荐共同决策(SDM)来指导治疗选择。本研究将评估在选择生物制剂或JAK抑制剂治疗类风湿关节炎(RA)和强直性脊柱炎(AS)时,与标准治疗相比,结构化SDM模型是否能增强患者对SDM的认知。这项开放标签、多中心、分层集群随机试验将招募300名RA或AS患者。参与者将按1:1:1的比例分配到三个组中的一个:SDM组I、SDM组II或标准治疗组。在SDM组中,将实施三对话模型(团队对话、选项对话和决策对话)。SDM组I将在Option Talk期间获得决策辅助,而SDM组II将同时获得决策辅助和基于人工智能的聊天机器人。在标准治疗组,治疗建议将在医生的判断。主要结果将是共同决策问卷得分。次要结果将包括决策冲突量表、健康赋权量表、利兹满意度问卷和EuroQol-5维度的变化。数据将通过iCReaT (http://icreat.kr)收集。本研究将为结构化SDM在选择治疗RA和AS的生物制剂和JAK抑制剂方面的有效性提供证据,对改善治疗决策和患者预后具有潜在意义。试验注册:临床研究信息服务标识:KCT0011310。
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引用次数: 0
Shared Decision-Making for Determining Treatment Strategies in Low-Risk Thyroid Cancer: Protocol of a Multicenter Cluster-Randomized Trial (MAeSTro-SDM). 确定低风险甲状腺癌治疗策略的共同决策:一项多中心集群随机试验方案(MAeSTro-SDM)。
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-26 DOI: 10.3346/jkms.2026.41.e58
Eun Kyung Lee, Min Joo Kim, Yul Hwangbo, Jae Hoon Moon, Sun Wook Cho, Young Jun Chai, June Young Choi, Yuh-Seog Jung, Kyu Eun Lee, Eun-Jae Chung, Kyungsik Kim, Su-Jin Kim, Woochul Kim, Yoo Hyung Kim, Young Ki Lee, Jinsun Jang, Young Shin Song, Ka Hee Yi, Hyeong Won Yu, Shinje Moon, Kyong Yeun Jung, Hyo-Jeong Kim, Chang Hwan Ryu, Junsun Ryu, Jungirl Seok, Seung Heon Kang, Sangjun Lee, A Jung Chu, Chang Yoon Lee, Ji Ye Lee, Hunjong Lim, Ji-Hoon Kim, Sue K Park, Young Joo Park

Active surveillance (AS) is recommended for low-risk papillary thyroid microcarcinoma (PTMC) in many guidelines. However, while its clinical application requires incorporation of patient values, implementing shared decision-making (SDM) in practice remains challenging. To generate reliable evidence, facilitate the integration of SDM into routine PTMC managements and improve patient satisfaction, this study developed a PTMC-specific SDM model (SM group) and aims to evaluate whether it improves patient-reported outcomes (PROs) compared to usual care (UC group) in patients with low-risk PTMC. This multicenter, parallel-group, cluster-randomized controlled trial will enroll 310 patients with low-risk PTMC across seven academic hospitals in Korea. Participants will be assigned to either the SM group (model) or the UC group (control) through cluster randomization of 26 clinicians, stratified by specialty and AS experience. The SM group will receive structured counseling using a newly developed PTMC-specific SDM model, supported by decision aids such as educational videos, web-based card news, and illustrated leaflets regarding disease-information and patients' values. The UC group will receive standard counseling. The primary outcome is the Decisional Conflict Scale score. Secondary outcomes include satisfaction with decision-making process, decision regret, anxiety, and thyroid-specific quality of life. Data will be collected via the iCReaT v2.0 electronic Case Report Form, supplemented by electronic and paper-based PRO surveys. Assessments will be conducted at baseline, 1-4 weeks, and 6 months after the treatment decision. Trial Registration: ClinicalTrials.gov Identifier: NCT06730893.

在许多指南中,推荐对低风险乳头状甲状腺微癌(PTMC)进行主动监测。然而,尽管其临床应用需要结合患者的价值观,但在实践中实施共同决策(SDM)仍然具有挑战性。为了产生可靠的证据,促进SDM纳入常规PTMC管理,提高患者满意度,本研究建立了PTMC特异性SDM模型(SM组),旨在评估与常规护理(UC组)相比,低风险PTMC患者的SDM是否改善了患者报告的结果(PROs)。这项多中心、平行组、集群随机对照试验将在韩国7家学术医院招募310名低风险PTMC患者。通过对26名临床医生的随机分组,根据专业和AS经验分层,参与者将被分配到SM组(模型)或UC组(对照组)。SM组将使用新开发的针对ptmc的SDM模型接受结构化咨询,并辅以决策辅助,如教育视频、基于网络的卡片新闻以及有关疾病信息和患者价值观的插图传单。UC组将接受标准咨询。主要结果是决策冲突量表得分。次要结局包括对决策过程的满意度、决策后悔、焦虑和甲状腺特异性生活质量。数据将通过iCReaT v2.0电子病例报告表格收集,并辅以电子和纸质PRO调查。评估将在基线、治疗决定后1-4周和6个月进行。试验注册:ClinicalTrials.gov标识符:NCT06730893。
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引用次数: 0
Reliability and Validity of the Korean Version of the Digital Health Literacy Instrument. 韩国版数字健康素养工具的信度和效度。
IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-19 DOI: 10.3346/jkms.2026.41.e42
Jeahyung Lee, Chulwoo Ahn, Jisun Park, Sooyoung Kim, Yerim Kim, Jiwon Park, Jaeyong Shin

Background: As digital transformation accelerates, individuals increasingly engage with digital health services and online medical resources, and digital health literacy (DHL) becomes increasingly important. While the Digital Health Literacy Instrument (DHLI) has been validated internationally, a Korean version applicable across all adult age groups remains limited. This study develops and validates the Korean DHLI, assessing its reliability and validity for broader applicability among Korean adults.

Methods: The DHLI was translated, culturally adapted, and reviewed by expert panels following World Health Organization guidelines. A cross-sectional nationwide web survey was conducted with 524 adults aged 19-69. A follow-up survey was administered to 134 participants after four weeks to assess test-retest reliability. Internal consistency and test-retest reliability were assessed. Construct validity was examined using confirmatory factor analysis (CFA) to determine the most appropriate factor structure in the Korean population. Convergent and discriminant validity were assessed, and hypothesis-testing construct validity was evaluated through correlations with age, health status, and eHealth literacy.

Results: The Korean version of the DHLI (K-DHLI) exhibited excellent psychometric properties. Internal consistency was high (α = 0.91), and test-retest reliability was deemed acceptable (intraclass correlation coefficient = 0.70). CFA demonstrated a 7-factor model, which showed a superior model fit (χ²/degrees of freedom = 2.14, comparative fit index = 0.966, root mean square error of approximation = 0.047) as compared to the 5-factor model. Convergent and discriminant validity were confirmed, with AVE values ranging from 0.7218 to 0.8947 and construct reliability values between 0.8837 and 0.9622. Hypothesis-testing construct validity was supported by hypothesized correlations between K-DHLI scores and age (r = -0.254, P < 0.001), health status (r = 0.252, P < 0.001), and eHealth literacy (r = 0.688, P < 0.001).

Conclusion: The K-DHLI is a reliable and valid instrument for assessing DHL in the Korean population. The findings confirm that the 7-factor structure demonstrates superior model fit and further support its applicability across diverse adult groups. This study provides a standardized instrument for assessing DHL in Korea and facilitates its use in national surveys, clinical screening, and research. It may help identify individuals with limited DHL, thereby supporting targeted interventions to reduce health disparities and improve access to care.

背景:随着数字化转型的加速,个人越来越多地参与数字健康服务和在线医疗资源,数字健康素养(DHL)变得越来越重要。虽然数字健康素养工具(DHLI)已在国际上得到验证,但适用于所有成年年龄组的韩文版本仍然有限。本研究开发并验证了韩国DHLI,评估了其在韩国成年人中更广泛适用性的信度和效度。方法:对DHLI进行翻译,进行文化调整,并由专家小组按照世界卫生组织的指导方针进行审查。在全国范围内对524名年龄在19-69岁之间的成年人进行了一项横断面网络调查。四周后对134名参与者进行了随访调查,以评估重测信度。评估内部一致性和重测信度。运用验证性因子分析(CFA)检验建构效度,以确定最适合韩国人口的因子结构。评估了收敛效度和判别效度,并通过与年龄、健康状况和电子健康素养的相关性来评估假设检验结构效度。结果:韩文DHLI量表(K-DHLI)具有良好的心理测量特性。内部一致性高(α = 0.91),重测信度可接受(类内相关系数= 0.70)。结果表明,7因素模型的拟合效果优于5因素模型(χ²/自由度= 2.14,比较拟合指数= 0.966,近似均方根误差= 0.047)。结果表明,AVE值为0.7218 ~ 0.8947,结构信度值为0.8837 ~ 0.9622。K-DHLI评分与年龄(r = -0.254, P < 0.001)、健康状况(r = 0.252, P < 0.001)和eHealth素养(r = 0.688, P < 0.001)之间的假设相关性支持假设检验结构效度。结论:K-DHLI是一种可靠有效的评估韩国人群DHL的工具。研究结果证实了7因子结构具有良好的模型拟合性,进一步支持了其在不同成人群体中的适用性。本研究为评估韩国DHL提供了一种标准化的工具,并促进了其在国家调查、临床筛查和研究中的使用。它可能有助于确定DHL有限的个人,从而支持有针对性的干预措施,以减少健康差距和改善获得保健的机会。
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引用次数: 0
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Journal of Korean Medical Science
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