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Patient perspectives on barriers to optimal asthma control in Danish respiratory specialist practice. 患者对丹麦呼吸专科实践中最佳哮喘控制障碍的看法。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-15 DOI: 10.61409/A03250213
Jørgen Vestbo, Frida Paustian, Lars Frølund, Inge Vestbo, Stig Brøndum, Charlotte Ulrik, Marie Broholm-Holst

Introduction: Although well-documented asthma treatments are available, many patients with asthma remain symptomatic, even when managed by respiratory specialists. We aimed to describe barriers to optimal asthma management in Danish respiratory specialist practice.

Methods: This was a qualitative study of 20 patients (mean age 37.6 years, six 40+ years; 17 women) with asthma from two specialist practices, with interviews conducted by phone.

Results: Many patients were unaware of the timeline for their course of treatment or what it entailed to be a patient in a pulmonary clinic, including being uncertain about how many consultations they were entitled to, the agenda of the next appointment and what the exact goals of the treatment were. Patients expressed doubts regarding the dosage and effectiveness of their medication. Some questioned whether they were taking their medication correctly and whether it was acceptable to take additional doses. Patients reported that they occasionally forgot to take their medication because they had not established a consistent routine for it.

Conclusions: Barriers were often quite practical and simple, and can most likely be broken down by focusing on simple behavioural aspects rather than by providing more information.

Funding: This study was funded by Fonden for Faglig Udvikling i Speciallægepraksis, Danske Regioner.

Trial registration: Not relevant.

虽然有充分的证据证明哮喘治疗是可用的,但许多哮喘患者仍然有症状,即使由呼吸系统专家管理。我们的目的是描述丹麦呼吸专科实践中最佳哮喘管理的障碍。方法:对来自两家专科医院的20例哮喘患者(平均年龄37.6岁,6例40岁以上,17例女性)进行定性研究,采用电话访谈方式。结果:许多患者不知道他们疗程的时间表,也不知道作为肺病门诊患者需要做什么,包括不确定他们有权进行多少次咨询,下次预约的日程以及治疗的确切目标是什么。病人对药物的剂量和疗效表示怀疑。一些人质疑他们是否正确服用了药物,是否可以接受额外的剂量。患者报告说,他们偶尔会忘记服药,因为他们没有建立一个一致的常规。结论:障碍通常是非常实际和简单的,并且很可能通过专注于简单的行为方面而不是提供更多信息而被打破。资助:本研究由Fonden为丹麦地区的Faglig Udvikling提供资助。试验注册:不相关。
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引用次数: 0
Reliability of ultrasound measurement of glenohumeral instability. 超声测量肩关节不稳定性的可靠性。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-15 DOI: 10.61409/A11240835
Catarina Malmberg, Kristine Rask Andreasen, Jesper Bencke, Birgitte Hougs Kjær, Per Hölmihc, Kristoffer Weisskirchner Barfod

Introduction: Ultrasound (US) is an accessible and non-invasive method for assessing pathology in the musculoskeletal system. Its application may include assessment of glenohumeral (GH) instability. Whereas GH instability is typically assessed in symptomatic patients, US measurements of anterior-posterior (AP) GH translation have shown good to excellent reliability in healthy populations. The aim of this study was to test the intra- and interrater reliability of measurements of AP GH translation in a clinical setting.

Methods: Two clinicians performed measures of AP GH translation in patients with anterior shoulder instability. Measurements were conducted from both an anterior and a posterior view. The primary outcome was the intraclass correlation coefficient (ICC(2,1)).

Results: Twenty-three patients were included. The intrarater ICCs ranged from 0.70 to 0.76. The interrater ICCs ranged from 0.20 to 0.49. The most reliable test was a simulated "Load and Shift" test. The minimal detectable changes ranged from 2.16 to 3.42 mm for the same rater, and from 2.71 to 4.78 mm between raters.

Conclusions: When performed in a clinical setting by raters with limited US experience, the US measurements of AP GH translation in patients with anterior shoulder instability demonstrated moderate to good intrarater reliability and poor interrater reliability. These findings suggest that while US may have potential for clinical use, its reliability may be limited when performed by novice raters.

Funding: Amager and Hvidovre Hospitals Forskningspulje.

Trial registration:

Clinicaltrials: gov (ID: NCT05250388).

简介:超声(US)是一种易于获取和非侵入性的方法来评估病理在肌肉骨骼系统。其应用可包括肩关节不稳定性的评估。虽然生长激素不稳定性通常是在有症状的患者中评估,但美国测量的前后(AP)生长激素翻译在健康人群中显示出良好到极好的可靠性。本研究的目的是测试在临床环境中测量AP - GH翻译的内部和内部可靠性。方法:两名临床医生对前肩不稳患者进行了AP - GH转化的测量。测量从前面和后面的观点进行。主要结局为类内相关系数(ICC(2,1))。结果:纳入23例患者。内部icc范围为0.70 ~ 0.76。解释器icc范围为0.20 ~ 0.49。最可靠的测试是模拟的“负载和位移”测试。最小可检测变化范围从2.16到3.42毫米,在相同的评级和评级之间从2.71到4.78毫米。结论:当由美国经验有限的评分员在临床环境中进行评估时,美国对前肩不稳患者的AP - GH翻译的测量显示出中度至良好的椎间可靠性和较差的椎间可靠性。这些发现表明,虽然US可能具有临床应用的潜力,但当由新手评分时,其可靠性可能受到限制。资助:管理和Hvidovre医院Forskningspulje。试验注册:Clinicaltrials: gov (ID: NCT05250388)。
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引用次数: 0
Fatal poisoning among people who use drugs in Denmark in 2022. 2022年丹麦,吸毒人群中毒致死。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-15 DOI: 10.61409/A03250147
Charlotte Uggerhøj Andersen, Simon Kjær Hermansen, Kristine Boisen Olsen, Kristian Linnet, Kirsten Wiese Simonsen

Introduction: The patterns of drug use and causes of fatal poisonings among persons who use drugs (PWUD) have been reported every fifth year since 1991 by the Danish Departments of Forensic Medicine. The present study aimed to describe these patterns in 2022.

Methods: All fatal poisonings among PWUD undergoing legal autopsy at the three Departments of Forensic Medicine in Denmark in 2022 were included in the study.

Results: The number of fatal poisonings among PWUD was 199. The median age was 42 years and 23% were female. Heroin/morphine and methadone were the most frequent main intoxicants, responsible for 22% and 37% of the poisonings, respectively. However, the proportion of deaths caused by other opioids and central stimulants has increased compared to previous years. Oxycodone deaths increased tenfold to 6% from 0.6% in 2017. Cocaine and amphetamine caused 11% and 4.5% of fatal poisonings, respectively. Methadone remained the most frequently detected drug, followed by cocaine, tetrahydrocannabinol, clonazepam and heroin/morphine, detected in 52%, 45%, 37%, 35% and 26% of cases, respectively. Tramadol and oxycodone were most frequently detected among PWUD aged 15-25 years.

Conclusions: Our findings indicate an increasing diversity of opioids causing fatal poisonings in PWUD and a rising detection rate and proportion of deaths linked to central stimulants.

Funding: None.

Trial registration: Not relevant.

导言:自1991年以来,丹麦法医部门每五年报告一次吸毒者的吸毒模式和致命中毒原因。本研究旨在描述2022年的这些模式。方法:以2022年在丹麦三个法医学部门进行合法尸检的puwud中发生的所有致命中毒为研究对象。结果:PWUD致死性中毒199例。中位年龄为42岁,23%为女性。海洛因/吗啡和美沙酮是最常见的主要毒物,分别占中毒病例的22%和37%。然而,与前几年相比,其他阿片类药物和中枢兴奋剂造成的死亡比例有所增加。羟考酮死亡率从2017年的0.6%上升至6%,增长了10倍。可卡因和安非他明分别造成11%和4.5%的致命中毒。美沙酮仍然是最常检出的药物,其次是可卡因、四氢大麻酚、氯硝西泮和海洛因/吗啡,分别在52%、45%、37%、35%和26%的病例中检出。曲马多和羟考酮在15-25岁的PWUD中检出最多。结论:我们的研究结果表明,导致PWUD致命中毒的阿片类药物越来越多样化,与中枢兴奋剂相关的检出率和死亡比例也在上升。资金:没有。试验注册:不相关。
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引用次数: 0
Aetiology of pneumonia in patients in the intensive care unit treated with chlordiazepoxide. 重症监护病房用氯二氮环氧化物治疗患者肺炎的病因学分析。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-15 DOI: 10.61409/A03250157
Andreas Faarbaek, Helena Roed Otte, Henrik Calum, Nanna Reiter, Rune Gärtner

Introduction: Research on pneumonia in patients undergoing treatment for alcohol withdrawal symptoms (AWS) is sparse. This study describes the microbiological aetiology in this patient group within an intensive care unit (ICU).

Methods: We conducted a retrospective, observational study at Copenhagen University Hospital, Bispebjerg, Denmark. Patients admitted to the ICU between 1 June 2017 and 31 December 2020 who had received at least 200 mg of chlordiazepoxide for AWS within the preceding days were identified through electronic health records. Admissions presenting with clinical symptoms of pneumonia were included in the study.

Results: A total of 76 patients with 88 admissions met the inclusion criteria. We identified 58 bacterial species, with the most common being Staphylococcus aureus (n = 14; 24%), Haemophilus influenzae (n = 12; 21%) and Streptococcus pneumoniae (n = 11; 19%). In the overall ICU population, excluding our cohort study, 516 bacterial samples from the lower airways were identified. The prevalence rate in the study period for S. aureus was 25.6% (n = 132), for H. influenzae 8.3% (n = 43) and for S. pneumoniae 8.5% (n = 44).

Conclusions: Pneumonia was prevalent in patients with AWS in the ICU, and it had a predominantly bacterial aetiology. The most frequently isolated bacteria were S. aureus, H. influenzae and S. pneumoniae. Notably, the prevalence of S. aureus in our study cohort was similar to that in the overall ICU population at the study site.

Funding: None.

Trial registration: The study was approved by the Hospital Board of Directors as a quality study.

前言:对酒精戒断症状(AWS)治疗患者肺炎的研究较少。本研究描述了重症监护病房(ICU)内该患者组的微生物病因学。方法:我们在丹麦比斯贝尔格哥本哈根大学医院进行了一项回顾性观察性研究。通过电子健康记录确定2017年6月1日至2020年12月31日期间入住ICU的患者,这些患者在前几天内接受了至少200毫克氯二氮环氧化物治疗AWS。以肺炎临床症状入院者纳入研究。结果:共有76例患者88例入院,符合纳入标准。我们鉴定出58种细菌,其中最常见的是金黄色葡萄球菌(n = 14; 24%)、流感嗜血杆菌(n = 12; 21%)和肺炎链球菌(n = 11; 19%)。在整个ICU人群中,不包括我们的队列研究,从下气道鉴定了516个细菌样本。研究期间,金黄色葡萄球菌患病率为25.6% (n = 132),流感嗜血杆菌患病率为8.3% (n = 43),肺炎链球菌患病率为8.5% (n = 44)。结论:肺炎在ICU的AWS患者中普遍存在,其主要是细菌性病因。最常见的分离细菌是金黄色葡萄球菌、流感嗜血杆菌和肺炎链球菌。值得注意的是,我们的研究队列中金黄色葡萄球菌的患病率与研究现场ICU总体人群的患病率相似。资金:没有。试验注册:该研究被医院董事会批准为质量研究。
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引用次数: 0
Risk-stratified breast cancer screening - a protocol for a non-blinded randomised trial. 风险分层乳腺癌筛查——一项非盲法随机试验方案。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-15 DOI: 10.61409/A03250154
Line Hjøllund Pedersen, Janne Bigaard, Pia Rørbæk Kamstrup, Berit Andersen, Ilse Vejborg, Antonis C Antoniou, Stig Egil Bojesen

Introduction: Breast cancer accounts for 14% of all cancer-related deaths among women. Women aged 50-69 years are offered biennial mammography, which reduces breast cancer-specific mortality. Simulations suggest that risk-stratified screening detects more early-stage cancers while lowering the number of unnecessary recalls, assessments and biopsies in low-risk women. This trial will investigate whether multifactorial risk-stratified screening, including polygenic score, is feasible, acceptable, cost-efficient and safe.

Methods: A minimum of 962 consenting women aged 50-67 years will be randomised 1:1 into a control group receiving standard screening or an intervention group offered screening intervals based on individual risk. Risk factor data collection, communication and follow-up will occur online using a tool co-designed with women in the target group. The primary outcome will be the proportion of low-risk women who, within 800 days of their baseline mammogram, will refrain from their legally ensured two-year mammogram interval. Secondary outcomes include quality of life, anxiety and breast cancer worry, measured at baseline and repeated three times during follow-up. In addition, health economy analyses will be conducted.

Conclusions: The findings will inform the development of large-scale risk-stratified screening trials.

Funding: Novo Nordisk Foundation, grant no. NNF21OC0070842. ACA is supported by Cancer Research UK grants: PPRPGM-Nov20100002 and SEBCD3-2024/100001.

Trial registration:

Clinicaltrials: gov Identifier: NCT06060938. Registration date: 11092023.

导言:乳腺癌占女性所有癌症相关死亡的14%。50-69岁的妇女每两年接受一次乳房x光检查,可降低乳腺癌特异性死亡率。模拟结果表明,风险分层筛查可以发现更多的早期癌症,同时减少低风险女性不必要的召回、评估和活检次数。该试验将探讨包括多基因评分在内的多因素风险分层筛查是否可行、可接受、成本效益和安全。方法:至少962名年龄在50-67岁之间的同意女性将以1:1的比例随机分配到接受标准筛查的对照组或根据个体风险提供筛查间隔的干预组。风险因素数据的收集、交流和随访将使用与目标群体中的妇女共同设计的工具在线进行。主要结果将是在基线乳房x光检查后800天内不按法律规定的两年乳房x光检查间隔进行检查的低风险妇女的比例。次要结果包括生活质量、焦虑和对乳腺癌的担忧,在基线时测量,并在随访期间重复三次。此外,还将进行健康经济分析。结论:这些发现将为开展大规模风险分层筛查试验提供信息。资助:诺和诺德基金会,批准号:NNF21OC0070842。ACA由英国癌症研究中心资助:PPRPGM-Nov20100002和SEBCD3-2024/100001。试验注册:Clinicaltrials: gov标识符:NCT06060938。报名日期:11092023。
{"title":"Risk-stratified breast cancer screening - a protocol for a non-blinded randomised trial.","authors":"Line Hjøllund Pedersen, Janne Bigaard, Pia Rørbæk Kamstrup, Berit Andersen, Ilse Vejborg, Antonis C Antoniou, Stig Egil Bojesen","doi":"10.61409/A03250154","DOIUrl":"10.61409/A03250154","url":null,"abstract":"<p><strong>Introduction: </strong>Breast cancer accounts for 14% of all cancer-related deaths among women. Women aged 50-69 years are offered biennial mammography, which reduces breast cancer-specific mortality. Simulations suggest that risk-stratified screening detects more early-stage cancers while lowering the number of unnecessary recalls, assessments and biopsies in low-risk women. This trial will investigate whether multifactorial risk-stratified screening, including polygenic score, is feasible, acceptable, cost-efficient and safe.</p><p><strong>Methods: </strong>A minimum of 962 consenting women aged 50-67 years will be randomised 1:1 into a control group receiving standard screening or an intervention group offered screening intervals based on individual risk. Risk factor data collection, communication and follow-up will occur online using a tool co-designed with women in the target group. The primary outcome will be the proportion of low-risk women who, within 800 days of their baseline mammogram, will refrain from their legally ensured two-year mammogram interval. Secondary outcomes include quality of life, anxiety and breast cancer worry, measured at baseline and repeated three times during follow-up. In addition, health economy analyses will be conducted.</p><p><strong>Conclusions: </strong>The findings will inform the development of large-scale risk-stratified screening trials.</p><p><strong>Funding: </strong>Novo Nordisk Foundation, grant no. NNF21OC0070842. ACA is supported by Cancer Research UK grants: PPRPGM-Nov20100002 and SEBCD3-2024/100001.</p><p><strong>Trial registration: </strong></p><p><strong>Clinicaltrials: </strong>gov Identifier: NCT06060938. Registration date: 11092023.</p>","PeriodicalId":11119,"journal":{"name":"Danish medical journal","volume":"72 11","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145354081","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Feasibility of a decentralised trial of sleep apnoea screening in patients with atrial fibrillation. 心房颤动患者睡眠呼吸暂停筛查分散试验的可行性。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-10-02 DOI: 10.61409/A12240892
Mads Hashiba, Ali Al-Alak, Sebastian Kinnberg Nielsen, Lars Kayser, Nina Nouhravesh, Mariam Elmegaard, Mohamed El-Chouli, Signe Risom, Rune Asger Vestergaard Frandsen, Poul Jennum, Morten Lamberts

Introduction: Atrial fibrillation (AF) prevalence is projected to double in the coming decades, necessitating innovative management strategies. This study evaluated the feasibility of a decentralised clinical trial for home-based sleep apnoea (SA) screening, activity tracking and heart rhythm monitoring in patients with AF.

Methods: This prospective cohort study enrolled patients with AF without known SA. Participants underwent a 12-week study using three home-monitoring systems: NightOwl for SA evaluation, FibriCheck for heart rhythm monitoring and SENS Motion for activity tracking. Patients completed questionnaires assessing AF-related quality of life, symptom severity, sleep quality and eHealth literacy at baseline and 12 weeks.

Results: The study included 18 patients with AF with a median age of 68.0 (interquartile range: 60.0-71.5) years, 11 (61%) women and 15 (83%) with paroxysmal AF. The study demonstrated high feasibility of remote monitoring, with data completeness rates of 83.3% for SA home evaluations, 97.6% for questionnaires, 91.7% for activity tracking and 88.8% for heart rhythm measurements. A drop-out rate of only 5.6% was recorded.

Conclusions: The study reports the feasibility of a decentralised digital platform for comprehensive AF patient monitoring. High patient engagement and data completeness suggest that digital health technologies can effectively integrate into clinical trials for patients with AF.

Funding: The Danish Heart Foundation (2023-12410) and Helsefonden (20-B-0269).

Trial registration: NCT06188247.

导言:房颤(AF)患病率预计在未来几十年翻一番,需要创新的管理策略。本研究评估了一项分散临床试验对房颤患者进行家庭睡眠呼吸暂停(SA)筛查、活动跟踪和心律监测的可行性。方法:这项前瞻性队列研究纳入了房颤患者,但不知道SA。参与者使用三种家庭监测系统进行了为期12周的研究:用于SA评估的NightOwl,用于心律监测的FibriCheck和用于活动跟踪的SENS Motion。患者在基线和12周完成评估af相关生活质量、症状严重程度、睡眠质量和电子健康素养的问卷调查。结果:本研究纳入18例房颤患者,中位年龄为68.0岁(四分位间距:60.0-71.5岁),女性11例(61%),阵发性房颤15例(83%)。研究显示远程监测的可行性高,SA家庭评估的数据完整性率为83.3%,问卷调查的数据完整性率为97.6%,活动跟踪的数据完整性率为91.7%,心律测量的数据完整性率为88.8%。辍学率仅为5.6%。结论:该研究报告了一种用于房颤患者综合监测的分散数字平台的可行性。高患者参与度和数据完整性表明,数字健康技术可以有效地整合到af患者的临床试验中。资助:丹麦心脏基金会(2023-12410)和Helsefonden (20-B-0269)。试验报名:NCT06188247。
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引用次数: 0
Real-world efficacy of tucatinib in Danish human epidermal growth factor receptor 2-positive metastatic breast cancer. 图卡替尼治疗丹麦人表皮生长因子受体2阳性转移性乳腺癌的实际疗效。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-18 DOI: 10.61409/A11240821
Laurits Sebastian Dahl, Ann Søegaard Knoop, Maj-Britt Jensen, Eva Harder, Jeanette Dupont Rønlev, Tobias Berg

Introduction: Tucatinib in combination with trastuzumab and capecitabine is approved for the treatment of metastatic human epidermal growth factor receptor 2 (HER2) positive breast cancer in third-line and later based on the results of the HER2CLIMB trial. In this short report, we evaluate the extent and efficacy of tucatinib treatment among Danish patients.

Methods: This is a retrospective study that includes all known Danish patients who initiated tucatinib prior to June 1, 2024. We utilised the nationwide clinical database of the Danish Breast Cancer.

Results: In total, 38 patients were treated. Nineteen (50%) of the patients had central nervous system (CNS) metastases, and 21 (55%) had visceral disease. Median progression-free survival was 8.7 months (95% CI: 6.2; 13.3) and median overall survival was 22.4 months (95% CI: 13.1; N/A). Nine patients exhibited a performance status of 2-3 (n = 5) or uncontrollable CNS metastases (n = 4), not meeting the inclusion criteria applied in the HER2CLIMB trial.

Conclusions: Our results align with data presented from the HER2CLIMB trial. Considerably fewer patients than initially expected have been treated in Denmark.

Funding: None.

Trial registration: Approved by the Capital Regions Research Overview (P-2024-175774) and the Centre for Health Research (R-24065900).

基于HER2CLIMB试验的结果,图卡替尼联合曲妥珠单抗和卡培他滨被批准用于三线及后期转移性人表皮生长因子受体2 (HER2)阳性乳腺癌的治疗。在这篇简短的报告中,我们评估了图卡替尼治疗丹麦患者的程度和疗效。方法:这是一项回顾性研究,包括所有已知的在2024年6月1日之前开始使用图卡替尼的丹麦患者。我们使用了丹麦乳腺癌的全国临床数据库。结果:共治疗38例。19例(50%)患者有中枢神经系统(CNS)转移,21例(55%)有内脏疾病。中位无进展生存期为8.7个月(95% CI: 6.2; 13.3),中位总生存期为22.4个月(95% CI: 13.1;无)。9例患者表现为2-3 (n = 5)或不可控的中枢神经系统转移(n = 4),不符合HER2CLIMB试验的纳入标准。结论:我们的结果与HER2CLIMB试验的数据一致。在丹麦接受治疗的患者比最初预期的要少得多。资金:没有。试验注册:由首都地区研究概况(P-2024-175774)和卫生研究中心(R-24065900)批准。
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引用次数: 0
Danish cardiologists' attitude towards clinical AI support: a survey study. 丹麦心脏病专家对临床人工智能支持的态度:一项调查研究。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A01250019
Søren A Rand, Anna Kirstine Ringgaard, Anders Christian Riis-Jensen, Henning Bundgaard, Iben Mundbjerg Gjødsbøl, Johan Skov Bundgaard

Introduction: AI represents a conceptual change in medicine, and AI-based tools are rapidly being developed and implemented in clinical medicine. This study aimed to evaluate how clinicians at selected Danish cardiology departments perceive the role of AI in clinical decision-making.

Methods: We conducted a ten-item anonymous survey among clinicians in Danish cardiology departments to evaluate physicians' attitudes towards AI support in clinical decision-making for ischaemic heart disease. Key focus areas included perceived impact on patient outcomes, safety, workflow and clinician training. Responses were measured on a five-point Likert scale (1 = strongly disagree, 5 = strongly agree), with 4 or 5 collectively categorised as agreement. Participants were stratified by seniority (less-than 10 years versus ≥ 10 years).

Results: A total of 60 Danish clinicians at cardiology departments participated. The highest level of agreement was observed for AI optimism/expectations (68%, mean: 3.7), willingness to invest time in training (65%, mean: 3.8) and interest in AI use (63%, mean: 3.6). Although nosignificant, junior clinicians showed greater enthusiasm for training and adoption, whereas concerns about trust, safety and time-saving potential persisted across seniority.

Conclusions: Danish cardiologists generally expressed moderate to high expectations, interest and willingness towards AI support in clinical decision-making. However, the study revealed concerns about accuracy, patient safety and whether AI will ultimately save clinicians' time.

Funding: This project was supported by NordForsk (PM-Heart grant number 90580), Novo Nordisk Foundation (grant no. NNF14CC0001, NNF17OC0027594 and NNF22OC0079382), Innovation Fund Denmark (BigTempHealth grant no. 5153-00002B, case no. 8114-00033B and 8114-00034B), Rigshospitalets Forskningspulje and Rigshospitalets Forskningspulje Rammebevilling (#A11336). The funders had no role in the design or interpretation of the study.

Trial registration: Not relevant.

导论:人工智能代表了医学概念的变化,基于人工智能的工具正在迅速开发并在临床医学中实施。本研究旨在评估选定的丹麦心脏病科临床医生如何看待人工智能在临床决策中的作用。方法:我们对丹麦心脏病科临床医生进行了一项十项匿名调查,以评估医生对人工智能支持缺血性心脏病临床决策的态度。重点领域包括对患者预后、安全性、工作流程和临床医生培训的感知影响。回答采用李克特5分量表(1 =非常不同意,5 =非常同意)进行测量,4或5分为同意。参与者按工龄分层(少于10年vs≥10年)。结果:共有60名丹麦心内科临床医生参与。对人工智能的乐观/期望(68%,平均值:3.7)、愿意投入时间进行培训(65%,平均值:3.8)和对人工智能使用的兴趣(63%,平均值:3.6)的认同程度最高。虽然不显著,但初级临床医生对培训和采用表现出更大的热情,而对信任、安全性和节省时间潜力的担忧持续存在。结论:丹麦心脏病专家普遍对人工智能在临床决策中的支持表现出中等到较高的期望、兴趣和意愿。然而,该研究揭示了对准确性、患者安全以及人工智能最终是否会节省临床医生时间的担忧。项目资助:诺和诺德基金会(批准号:90580),诺和诺德基金会(批准号:90580)。NNF14CC0001, NNF17OC0027594和NNF22OC0079382),丹麦创新基金(BigTempHealth资助号:5153-00002B,箱号8114-00033B和8114-00034B), Rigshospitalets Forskningspulje和Rigshospitalets Forskningspulje rammebeviling (#A11336)。资助者在研究的设计或解释中没有任何作用。试验注册:不相关。
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引用次数: 0
Adaptation and interobserver agreement in a Danish translation of the Clinical Frailty Scale Questionnaire. 临床虚弱量表问卷丹麦语翻译中的适应和观察者间的一致。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A08240549
Line Houkjær, Stig Brorson

Introduction: The Clinical Frailty Scale (CFS) assesses frailty in older adults. Although the scale has been translated into Danish, the accompanying questionnaire and classification tree have not. The questionnaire includes seven questions about basic and instrumental activities of daily living, chronic conditions, self-rated health, energy level and physical activity, guiding the respondent to a CFS level through the classification tree. This study translated and cross-culturally adapted the CFS questionnaire and classification tree into Danish and assessed the interobserver agreement in a hospital setting.

Methods: The Danish version of the CFS short questionnaire and classification tree was developed in five stages: forward translations, synthesis, back-translation, review by a committee panel and pre-testing, followed by comprehension interviews and an interobserver agreement study.

Results: The back-translations closely matched the original. Minor discrepancies in contextual and idiomatic expressions were resolved through committee review. Pre-test confirmed comprehension, requiring no further changes. The kappa for interobserver agreement was 0.78.

Conclusions: The CFS questionnaire and classification tree were translated and cross-culturally adapted into Danish and are attached to this paper. The interobserver agreement achieved is considered acceptable for applying the CFS in emergency and orthopaedic departments.

Funding: None.

Trial registration: Not relevant.

简介:临床虚弱量表(CFS)评估老年人的虚弱。虽然量表已翻译成丹麦语,但随附的问卷和分类树尚未翻译。问卷包括日常生活基本活动和工具活动、慢性病、自评健康、能量水平和身体活动等七个问题,通过分类树引导被调查者达到CFS水平。本研究将CFS问卷和分类树翻译成丹麦语并进行跨文化改编,并在医院环境中评估了观察者之间的一致性。方法:丹麦版的CFS短问卷和分类树分为五个阶段:前译、综合、后译、委员会小组审查和预测试,随后是理解访谈和观察者间协议研究。结果:反译与原文吻合较好。通过委员会审查,解决了上下文和习语表达上的小差异。预先测试确认理解,不需要进一步更改。观察者间一致性kappa为0.78。结论:将CFS问卷和分类树翻译成丹麦语并进行跨文化改编,并附在本文中。观察员间达成的协议被认为可以接受在急诊科和骨科应用CFS。资金:没有。试验注册:不相关。
{"title":"Adaptation and interobserver agreement in a Danish translation of the Clinical Frailty Scale Questionnaire.","authors":"Line Houkjær, Stig Brorson","doi":"10.61409/A08240549","DOIUrl":"https://doi.org/10.61409/A08240549","url":null,"abstract":"<p><strong>Introduction: </strong>The Clinical Frailty Scale (CFS) assesses frailty in older adults. Although the scale has been translated into Danish, the accompanying questionnaire and classification tree have not. The questionnaire includes seven questions about basic and instrumental activities of daily living, chronic conditions, self-rated health, energy level and physical activity, guiding the respondent to a CFS level through the classification tree. This study translated and cross-culturally adapted the CFS questionnaire and classification tree into Danish and assessed the interobserver agreement in a hospital setting.</p><p><strong>Methods: </strong>The Danish version of the CFS short questionnaire and classification tree was developed in five stages: forward translations, synthesis, back-translation, review by a committee panel and pre-testing, followed by comprehension interviews and an interobserver agreement study.</p><p><strong>Results: </strong>The back-translations closely matched the original. Minor discrepancies in contextual and idiomatic expressions were resolved through committee review. Pre-test confirmed comprehension, requiring no further changes. The kappa for interobserver agreement was 0.78.</p><p><strong>Conclusions: </strong>The CFS questionnaire and classification tree were translated and cross-culturally adapted into Danish and are attached to this paper. The interobserver agreement achieved is considered acceptable for applying the CFS in emergency and orthopaedic departments.</p><p><strong>Funding: </strong>None.</p><p><strong>Trial registration: </strong>Not relevant.</p>","PeriodicalId":11119,"journal":{"name":"Danish medical journal","volume":"72 10","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145257663","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Surgical treatment of breast fibroadenomas. 乳腺纤维腺瘤的外科治疗。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A03250179
Cecilie Jansen, Nethe Eichen, Niels Kroman, Tove Tvedskov

Introduction: Fibroadenoma is a benign tumour with a prevalence of 9-22% and the third most common palpable breast tumour. Management is primarily conservative, but treatment varies due to a lack of national guidelines. We aimed to estimate the proportion of women diagnosed with fibroadenoma who underwent surgical excision in Denmark between 2011 and 2014, including regional differences in age, tumour size and year of surgery.

Methods: In this nationwide registry-based cohort study, we identified all patients who underwent surgical excision of a fibroadenoma from 1 January 2011 to 31 December 2014, using the Danish National Register of Pathology. This registry provided information on age and region. Operation rates were calculated using population data from Statistics Denmark.

Results: We identified 1,843 patients. The mean size of surgically removed fibroadenomas was 25.5 mm, and the mean age at surgery was 37 years. Patients > 50 years had a significantly higher proportion of small fibroadenomas (less-than 20 mm) removed than younger patients (p less-than 0.01). The overall operation rate was 20.6 per 100,000 women per year, highest in the 18-25-year age group (56.8 per 100,000 per year). Significant regional variation was found (p less-than 0.01), with the North Denmark Region having the highest operation rate (43.6 per 100,000 per year).

Conclusions: Despite conservative management being recommended in Denmark during the study period, many fibroadenomas were surgically removed, and considerable regional variations were recorded. National guidelines are needed to ensure uniform, evidence-based treatment and reduce overtreatment.

Funding: None.

Trial registration: nr. SABN 3-3013-1306/1.

纤维腺瘤是一种良性肿瘤,发病率为9-22%,是第三常见的乳腺可触及肿瘤。治疗主要是保守的,但由于缺乏国家指导方针,治疗方法各不相同。我们的目的是估计2011年至2014年间丹麦诊断为纤维腺瘤的女性接受手术切除的比例,包括年龄、肿瘤大小和手术年份的地区差异。方法:在这项全国范围内基于登记的队列研究中,我们使用丹麦国家病理登记册,确定了2011年1月1日至2014年12月31日期间接受纤维腺瘤手术切除的所有患者。该登记处提供了有关年龄和地区的信息。使用丹麦统计局的人口数据计算手术率。结果:我们确定了1843例患者。手术切除纤维腺瘤的平均大小为25.5 mm,平均手术年龄为37岁。50岁以下患者的小纤维腺瘤(小于20 mm)切除比例明显高于年轻患者(p < 0.01)。总手术率为每年每10万名妇女20.6例,在18-25岁年龄组中最高(每年每10万名妇女56.8例)。发现显著的地区差异(p < 0.01),北丹麦地区的手术率最高(每年每10万人中有43.6例)。结论:尽管在研究期间丹麦推荐保守治疗,但许多纤维腺瘤是手术切除的,并且记录了相当大的区域差异。需要制定国家指南,以确保统一的循证治疗并减少过度治疗。资金:没有。试验注册:编号:SABN 3-3013-1306/1。
{"title":"Surgical treatment of breast fibroadenomas.","authors":"Cecilie Jansen, Nethe Eichen, Niels Kroman, Tove Tvedskov","doi":"10.61409/A03250179","DOIUrl":"https://doi.org/10.61409/A03250179","url":null,"abstract":"<p><strong>Introduction: </strong>Fibroadenoma is a benign tumour with a prevalence of 9-22% and the third most common palpable breast tumour. Management is primarily conservative, but treatment varies due to a lack of national guidelines. We aimed to estimate the proportion of women diagnosed with fibroadenoma who underwent surgical excision in Denmark between 2011 and 2014, including regional differences in age, tumour size and year of surgery.</p><p><strong>Methods: </strong>In this nationwide registry-based cohort study, we identified all patients who underwent surgical excision of a fibroadenoma from 1 January 2011 to 31 December 2014, using the Danish National Register of Pathology. This registry provided information on age and region. Operation rates were calculated using population data from Statistics Denmark.</p><p><strong>Results: </strong>We identified 1,843 patients. The mean size of surgically removed fibroadenomas was 25.5 mm, and the mean age at surgery was 37 years. Patients > 50 years had a significantly higher proportion of small fibroadenomas (less-than 20 mm) removed than younger patients (p less-than 0.01). The overall operation rate was 20.6 per 100,000 women per year, highest in the 18-25-year age group (56.8 per 100,000 per year). Significant regional variation was found (p less-than 0.01), with the North Denmark Region having the highest operation rate (43.6 per 100,000 per year).</p><p><strong>Conclusions: </strong>Despite conservative management being recommended in Denmark during the study period, many fibroadenomas were surgically removed, and considerable regional variations were recorded. National guidelines are needed to ensure uniform, evidence-based treatment and reduce overtreatment.</p><p><strong>Funding: </strong>None.</p><p><strong>Trial registration: </strong>nr. SABN 3-3013-1306/1.</p>","PeriodicalId":11119,"journal":{"name":"Danish medical journal","volume":"72 10","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145257723","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Danish medical journal
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