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Validity of a thyrotoxicosis diagnosis code among women of fertile age. 育龄妇女甲状腺毒症诊断代码的有效性。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A04250296
Nanna Maria Uldall Torp, Signe Kirkegaard, Karoline Schack, Stine Linding Andersen

Introduction: Graves' disease (GD) is the leading cause of hyperthyroidism in women of fertile age. Register-based studies rely on diagnostic codes; this study examined the validity of diagnosed thyrotoxicosis among women of fertile age in the Danish National Hospital Register (DNHR).

Methods: All women in the North Denmark Region aged 18-45 years with a diagnosis of thyrotoxicosis (Tenth International Classification of Diseases: E05.0-05.9) in the DNHR from 2017-2018 were identified and medical records reviewed.

Results: Among 263 women included, thyrotoxicosis was confirmed in 249 cases with a positive predictive value (PPV) of 94.7% (95% confidence interval (CI): 91.2-97.1%) for the diagnostic group (E05.0-05.9). Autoimmune hypothyroidism was the leading cause of misclassification. GD was the aetiology in 150 women, resulting in a PPV for GD of 57.0% (95% CI: 50.8-63.1%) in the diagnostic group (E05.0-05.9), increasing to 83.6% (95% CI: 76.4-89.3%) when restricted to women who were prescribed an antithyroid drug (ATD). The PPV for GD was highest when the specific diagnosis (DE05.0) was considered (PPV 91.1% (95% CI: 84.7-95.5%); however, 42 women with GD (28.0%) were first given a diagnosis of unspecified thyrotoxicosis (E05.9).

Conclusions: The validity of thyrotoxicosis identified in the DNHR among women of fertile age was high. Results emphasise the importance of how subtypes of thyrotoxicosis are defined and show that the combined use of diagnoses and prescriptions of ATD is warranted to define GD.

Funding: Novo Nordisk Foundation (grant no: NNF20OC0059465).

Trial registration: Not relevant.

格雷夫斯病(GD)是育龄妇女甲状腺功能亢进的主要原因。基于登记册的研究依赖于诊断代码;本研究检查了丹麦国家医院登记(DNHR)中诊断的育龄妇女甲状腺毒症的有效性。方法:对2017-2018年DNHR中诊断为甲状腺毒症(第十种国际疾病分类:E05.0-05.9)的北丹麦地区所有年龄在18-45岁的女性进行识别并回顾医疗记录。结果:在纳入的263例妇女中,诊断组(E05.0-05.9)确诊甲状腺毒症249例,阳性预测值(PPV)为94.7%(95%置信区间(CI): 91.2-97.1%)。自身免疫性甲状腺功能减退是误分类的主要原因。在150名妇女中,GD是病因,导致诊断组(E05.0-05.9) GD的PPV为57.0% (95% CI: 50.8-63.1%),当仅限于服用抗甲状腺药物(ATD)的妇女时,PPV增加到83.6% (95% CI: 76.4-89.3%)。当考虑特异性诊断(DE05.0)时,GD的PPV最高(PPV为91.1% (95% CI: 84.7 ~ 95.5%);然而,42名患有GD的女性(28.0%)首次被诊断为未明确的甲状腺毒症(E05.9)。结论:DNHR对育龄妇女甲状腺毒症诊断的有效性较高。结果强调了如何定义甲状腺毒症亚型的重要性,并表明ATD的诊断和处方的联合使用是有理由定义GD的。资助:诺和诺德基金会(批准号:NNF20OC0059465)。试验注册:不相关。
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引用次数: 0
Delirium prevalence and screening in the Danish healthcare system. 丹麦卫生保健系统中谵妄的患病率和筛查。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A01250038
Marie O Collet, Martin Shultz, Eva Laerkner, Charlotte Bjerg Sand Riis, Laura Krone Larsen, Kristine Mildahl Kjærgaard, Christina Emme, Iben Tousgaard, Bianca Bech, Anne-Dorte Krapper, Linette Thorn, Anne Højager Nielsen, Pernille Reck Miller, Camilla Grube Segers, Marie Damgaard Winther, Susanne Fischer, Sally Jakobsen, Tina Tang Fredenslund, Cecilie Fuglsbjerg, Helle Svenningsen

Introduction: Delirium is an acute and severe syndrome, commonly occurring in elderly hospitalised or terminal patients, causing cognitive and psychotic symptoms due to somatic illness or medication. This study aimed to investigate the prevalence of delirium across hospitals and nursing homes in Denmark.

Methods: This Danish cohort study, part of a global survey on March 15, 2023, examined delirium prevalence in hospitals and nursing homes. Data was collected on delirium screening practices, prevalence and staff experience.

Results: Of 69 recruited hospitals and nursing homes, 66 participated, and 63 provided complete data for analysis. Participants included 79.4% nurses and 14.3% researchers. Delirium prevalence was 13.6% at 8 a.m. (general ward 9.7%, intensive care unit (ICU) 29.7%, emergency department 40.0% and nursing home 8.9%) and 13.9% at 8 p.m. (general ward 12.0%, ICU 19.8%, emergency department 27.2% and nursing home 10.8%) on March 15, 2023. The Confusion Assessment Method (CAM) was used by 23.8% of participants, and the confusion-assessment method for the ICU (CAM-ICU) was used by 28.6% of participants and was the most frequently used screening tool.

Conclusions: On March 15, 2023, delirium prevalence in Denmark was 13.6% at 8 a.m. and 13.9% at 8 p.m. across 63 hospital departments and nursing homes. The CAM, brief CAM, and CAM-ICU were the most used assessment tools.

Funding: There was no funding allocated to this study.

Trial registration: The study was registered in the German Registry for Clinical Trials (DRKS00030002).

谵妄是一种急性重症综合征,常见于老年住院患者或终末期患者,由躯体疾病或药物引起认知和精神症状。本研究旨在调查丹麦医院和疗养院谵妄的患病率。方法:这项丹麦队列研究是2023年3月15日全球调查的一部分,研究了医院和养老院谵妄的患病率。收集有关谵妄筛查做法、患病率和工作人员经验的数据。结果:69家医院和养老院中,66家参与其中,63家提供完整数据供分析。其中79.4%为护士,14.3%为研究人员。上午8时谵妄患病率为13.6%。(普通病房9.7%,重症监护病房(ICU) 29.7%,急诊科40.0%,疗养院8.9%),晚上8点13.9%。(普通病房12.0%,ICU 19.8%,急诊科27.2%,养老院10.8%)。23.8%的参与者使用混淆评估法(CAM), 28.6%的参与者使用ICU混淆评估法(CAM-ICU),是最常用的筛查工具。结论:2023年3月15日,丹麦63个医院部门和疗养院的谵妄患病率在上午8点为13.6%,在晚上8点为13.9%。CAM、brief CAM和CAM- icu是最常用的评估工具。经费:本研究未获拨款。试验注册:该研究已在德国临床试验注册中心(DRKS00030002)注册。
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引用次数: 0
General practitioners' experiences of a data-driven quality development process. 全科医生在数据驱动的质量发展过程中的经验。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A12240912
Louise Hansen, Sarah Sofie Elmer Brandborg, Ulla Bjerre-Christensen, Trine Kjeldgaard Møller, Natasja Bjerre

Introduction: Research shows that structured data use can optimise treatment in general practice clinics. This qualitative feasibility study evaluated a one-year intervention (DataSam) to assess whether increased use of population data can enhance type 2 diabetes treatment and workflows in general practice clinics.

Methods: Audio-recordings of visits from 12 clinics at baseline, six and 12 months and end-of-intervention semi-structured interviews (n = 14) explored data use, workflow changes and implementation challenges. The data analysis was inspired by qualitative content analysis.

Results: Clinics were positive about project activities and how structured data use enhanced management and patient overview while optimising treatment and prescribing practices. Most clinics experienced workflow improvements, such as nurses taking on more responsibilities and heightened staff skills, knowledge, job satisfaction and confidence in data-driven decision-making, medications and guidelines. However, approximately half of the clinics faced some implementation challenges, including technical issues and time constraints. Furthermore, some raised concerns about overtreatment, data misuse and de-prioritisation of other diagnoses.

Conclusions: DataSam emphasises the potential of population data to optimise patient care, though further attention to implementation is needed.

Funding: This study received an internal grant from Steno Diabetes. Centre Copenhagen.

Trial registration: Registered as "not required approval" with the Regional Ethics Committee of the Capital Region (F-22073139).

研究表明,结构化数据的使用可以优化全科诊所的治疗。本定性可行性研究评估了一项为期一年的干预(DataSam),以评估增加人口数据的使用是否可以增强全科诊所的2型糖尿病治疗和工作流程。方法:12家诊所在基线、6个月和12个月的就诊录音和干预结束时的半结构化访谈(n = 14),探讨数据使用、工作流程变化和实施挑战。数据分析受到定性内容分析的启发。结果:诊所对项目活动以及结构化数据如何使用增强管理和患者概况,同时优化治疗和处方实践持积极态度。大多数诊所都经历了工作流程的改进,例如护士承担了更多的责任,提高了员工的技能、知识、工作满意度和对数据驱动决策、药物和指南的信心。然而,大约一半的诊所面临一些执行方面的挑战,包括技术问题和时间限制。此外,一些人提出了对过度治疗、数据滥用和其他诊断不优先的担忧。结论:DataSam强调了人口数据优化患者护理的潜力,尽管需要进一步关注实施。资助:本研究获得了Steno Diabetes公司的内部资助。哥本哈根会议中心。试验注册:在首都大区伦理委员会注册为“无需审批”(F-22073139)。
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引用次数: 0
A survey of emergency physicians' prescription of piperacillin/tazobactam. 急诊医师哌拉西林/他唑巴坦处方调查。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A11240794
Sofie Damgaard Mortensen, Sanne Schjødt, Marianne Lisby

Introduction: Piperacillin/tazobactam (Pip/Taz) is a broad-spectrum antibiotic, often prescribed in emergency departments (EDs). Excessive use of broad-spectrum antibiotics may lead to the rise of antimicrobial resistance, a concerning health issue. We investigated physicians' adherence to regional guidelines and their considerations when prescribing Pip/Taz in the ED.

Methods: In this cross-sectional survey, a ten-item survey questionnaire was administered to ED physicians in five EDs from 10 January to 7 February 2024.

Results: A total of 261 physicians employed in the ED were invited to participate in the survey. Among these, 144 physicians completed the survey, yielding a response rate of 55.2%. Based on the results, 25% were unaware of the regional guidelines on the prescription of Pip/Taz. In addition, over the past month, 25% had prescribed Pip/Taz in situations where regional guidelines recommended a narrow-spectrum antibiotic, primarily because of concerns regarding the patient's condition (74.3%); 30.6% of those who deviated from guidelines were consultants.

Conclusions: This study found that a fourth of physicians in EDs were unaware of regional guidelines for prescribing Pip/Taz. Moreover, one in every four physicians purposely deviated from the recommended type of antibiotics, mainly because of concerns about the patient's clinical condition.

Funding: None.

Trial registration: Not relevant.

简介:哌拉西林/他唑巴坦(Pip/Taz)是一种广谱抗生素,常用于急诊科(EDs)。过度使用广谱抗生素可能导致抗菌素耐药性上升,这是一个令人关切的健康问题。我们调查了医生对地区指南的依从性以及他们在ED处方Pip/Taz时的考虑。方法:在这项横断面调查中,从2024年1月10日至2月7日,对5个ED医生进行了一份10项调查问卷。结果:共有261名在急诊科工作的医生参与了调查。其中144名医生完成了调查,回复率为55.2%。根据结果,25%的人不知道Pip/Taz处方的区域指南。此外,在过去一个月里,25%的医生在区域指南建议使用窄谱抗生素的情况下开了Pip/Taz,主要是因为担心患者的病情(74.3%);30.6%偏离指南的是咨询师。结论:本研究发现急诊科四分之一的医生不知道开具Pip/Taz处方的地区指南。此外,四分之一的医生故意偏离推荐的抗生素类型,主要是因为担心患者的临床状况。资金:没有。试验注册:不相关。
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引用次数: 0
Symptom profiles in long COVID compared to functional somatic disorder and the general population. 与功能性躯体疾病和普通人群相比,长冠状病毒的症状概况。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A09240627
Jane Agergaard, Lisbeth Frostholm, Per Fink, Thomas Meinertz Dantoft, Berit Schiøttz-Christensen, Marie Weinreich Petersen

Introduction: Long COVID, characterised by persistent symptoms following COVID-19, affects about 10% of individuals recovering from SARS-CoV-2. The overlap of symptoms described in long COVID and functional somatic disorder (FSD) raises questions about shared pathophysiology. This report compares the prevalence and profiles of physical symptoms among patients with long COVID, patients with FSD and the general population.

Methods: Data from a cohort of patients with long COVID referred for diagnostics, a cohort of patients seen in a regional clinic for FSD and individuals from the general population were used. Questionnaires, including the bodily distress syndrome checklist, were used to assess physical symptoms.

Results: A total of 436 patients with long COVID, 264 patients with FSD and 9,656 individuals from the general population were included. A lower prevalence of symptoms was observed in patients with long COVID than in patients with FSD. However, the prevalence of symptoms in patients with long COVID remained higher than in the general population. In patients with long COVID, dominant symptoms were from the general symptoms (GS) cluster (concentration difficulties, fatigue, headache, memory problems) and muscle pain. Additionally, 11% met the criteria for multi-organ FSD, exhibiting a similar symptom profile to patients with FSD.

Conclusions: A total of 11% of long COVID patients had a symptom profile similar to that of patients with multi-organ FSD. GS, including fatigue and muscle pain, were common. These findings highlight the need for prospective studies to identify patients with similar symptoms, pathogenesis and treatment options.

Funding: None.

Trial registration: Not relevant.

长冠状病毒的特征是在COVID-19之后持续出现症状,约10%的SARS-CoV-2患者会受到影响。长冠状病毒病和功能性躯体疾病(FSD)中描述的症状重叠引发了对共同病理生理学的质疑。本报告比较了长冠状病毒感染者、FSD患者和一般人群中身体症状的患病率和概况。方法:数据来自转诊的长COVID患者队列、在FSD区域诊所就诊的患者队列和普通人群。问卷,包括身体痛苦综合征检查表,被用来评估身体症状。结果:共纳入长冠肺炎患者436例,FSD患者264例,普通人群9656例。长COVID患者的症状发生率低于FSD患者。然而,长期感染新冠肺炎的患者出现症状的比例仍高于普通人群。在长冠状病毒感染者中,主要症状为一般症状(GS)类(注意力集中困难、疲劳、头痛、记忆问题)和肌肉疼痛。此外,11%符合多器官FSD的标准,表现出与FSD患者相似的症状特征。结论:11%的长冠患者的症状特征与多器官FSD患者相似。包括疲劳和肌肉疼痛在内的GS很常见。这些发现强调了前瞻性研究的必要性,以确定具有相似症状、发病机制和治疗方案的患者。资金:没有。试验注册:不相关。
{"title":"Symptom profiles in long COVID compared to functional somatic disorder and the general population.","authors":"Jane Agergaard, Lisbeth Frostholm, Per Fink, Thomas Meinertz Dantoft, Berit Schiøttz-Christensen, Marie Weinreich Petersen","doi":"10.61409/A09240627","DOIUrl":"https://doi.org/10.61409/A09240627","url":null,"abstract":"<p><strong>Introduction: </strong>Long COVID, characterised by persistent symptoms following COVID-19, affects about 10% of individuals recovering from SARS-CoV-2. The overlap of symptoms described in long COVID and functional somatic disorder (FSD) raises questions about shared pathophysiology. This report compares the prevalence and profiles of physical symptoms among patients with long COVID, patients with FSD and the general population.</p><p><strong>Methods: </strong>Data from a cohort of patients with long COVID referred for diagnostics, a cohort of patients seen in a regional clinic for FSD and individuals from the general population were used. Questionnaires, including the bodily distress syndrome checklist, were used to assess physical symptoms.</p><p><strong>Results: </strong>A total of 436 patients with long COVID, 264 patients with FSD and 9,656 individuals from the general population were included. A lower prevalence of symptoms was observed in patients with long COVID than in patients with FSD. However, the prevalence of symptoms in patients with long COVID remained higher than in the general population. In patients with long COVID, dominant symptoms were from the general symptoms (GS) cluster (concentration difficulties, fatigue, headache, memory problems) and muscle pain. Additionally, 11% met the criteria for multi-organ FSD, exhibiting a similar symptom profile to patients with FSD.</p><p><strong>Conclusions: </strong>A total of 11% of long COVID patients had a symptom profile similar to that of patients with multi-organ FSD. GS, including fatigue and muscle pain, were common. These findings highlight the need for prospective studies to identify patients with similar symptoms, pathogenesis and treatment options.</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":"145257715","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
The Danish version of the Dizziness Handicap Inventory - translation and validation. 丹麦版眩晕障碍量表-翻译与验证。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A12240910
Helle Elisabeth Agger-Nielsen, Signe Fiil Bønløkke, Hanne Owen, Therese Ovesen

Introduction: The Dizziness Handicap Inventory (DHI) is a widely used patient-reported outcome measure assessing the impact of dizziness on daily life. A Danish version (DHI-DK) was developed to facilitate its use in Danish-speaking populations.

Methods: The DHI was translated into Danish following standard cross-cultural adaptation procedures. The psychometric properties of the DHI-DK were evaluated in a sample of 100 patients with dizziness. Internal consistency was assessed using Cronbach's alpha, test-retest reliability with intraclass correlation coefficients (ICCs), and construct validity through correlations with the visual analogue scale (VAS).

Results: The DHI-DK demonstrated high internal consistency (Cronbach's alpha = 0.88) and excellent test-retest reliability (ICC = 0.95). A strong correlation was observed between DHI-DK and VAS scores (r = 0.60, p less-than 0.001), supporting construct validity.

Conclusions: The DHI-DK is a reliable and valid instrument for assessing the self-perceived handicap due to dizziness in Danish-speaking patients. It is suitable for use in both clinical practice and research settings.

Funding: This study received no external funding.

Trial registration: Not relevant.

头晕障碍量表(DHI)是一种广泛使用的患者报告的结果测量方法,用于评估头晕对日常生活的影响。为了方便在讲丹麦语的人群中使用,开发了丹麦语版本(DHI-DK)。方法:按照标准的跨文化适应程序将DHI翻译成丹麦语。在100例眩晕患者的样本中评估了DHI-DK的心理测量特性。采用Cronbach’s alpha评估内部一致性,采用类内相关系数(ICCs)进行重测信度评估,并通过视觉模拟量表(VAS)进行结构效度评估。结果:DHI-DK具有较高的内部一致性(Cronbach’s alpha = 0.88)和良好的重测信度(ICC = 0.95)。DHI-DK与VAS评分之间存在很强的相关性(r = 0.60, p < 0.001),支持结构效度。结论:DHI-DK是评估丹麦语患者自我感觉障碍的一种可靠、有效的工具。它适用于临床实践和研究设置。经费:本研究未获得外部资助。试验注册:不相关。
{"title":"The Danish version of the Dizziness Handicap Inventory - translation and validation.","authors":"Helle Elisabeth Agger-Nielsen, Signe Fiil Bønløkke, Hanne Owen, Therese Ovesen","doi":"10.61409/A12240910","DOIUrl":"https://doi.org/10.61409/A12240910","url":null,"abstract":"<p><strong>Introduction: </strong>The Dizziness Handicap Inventory (DHI) is a widely used patient-reported outcome measure assessing the impact of dizziness on daily life. A Danish version (DHI-DK) was developed to facilitate its use in Danish-speaking populations.</p><p><strong>Methods: </strong>The DHI was translated into Danish following standard cross-cultural adaptation procedures. The psychometric properties of the DHI-DK were evaluated in a sample of 100 patients with dizziness. Internal consistency was assessed using Cronbach's alpha, test-retest reliability with intraclass correlation coefficients (ICCs), and construct validity through correlations with the visual analogue scale (VAS).</p><p><strong>Results: </strong>The DHI-DK demonstrated high internal consistency (Cronbach's alpha = 0.88) and excellent test-retest reliability (ICC = 0.95). A strong correlation was observed between DHI-DK and VAS scores (r = 0.60, p less-than 0.001), supporting construct validity.</p><p><strong>Conclusions: </strong>The DHI-DK is a reliable and valid instrument for assessing the self-perceived handicap due to dizziness in Danish-speaking patients. It is suitable for use in both clinical practice and research settings.</p><p><strong>Funding: </strong>This study received no external funding.</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":"145257718","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
Re-referrals to a Danish regional spine centre. 转介到丹麦地区脊柱中心。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A12240871
Anders Hansen, Casper Nim, Dorthe Ziegler, Jakob Blaabjerg Espesen, Natalie Hong Siu Chang, Søren O'Neill, Steen Harsted

Introduction: In Denmark, general practitioners are the primary providers, referring patients to specialised spine care. Re-referral may indicate unresolved spinal pain, but can also reflect inefficiencies in patient management. This study determined the rate of re-referrals to a Danish regional spine centre within 500 days of the initial visit and identified patient-specific factors associated with re-referrals.

Methods: A cohort study of patients at the Spine Centre of Southern Denmark was conducted from January 2019 to December 2023. Re-referrals were defined as visits between 50 and 500 days after the initial consultation. Factors investigated included referral diagnoses, patient-reported outcomes and clinical services initiated. Multivariable logistic regression identified associations with re-referral.

Results: Among 30,872 patients, re-referrals were observed in 10.3% (n = 3,095). Previous back surgery (OR = 1.23), pain medication (OR = 1.37), MRI referrals (OR = 1.6), provision of rehabilitation plans (OR = 1.26), extremity pain (OR = 1.02) and loneliness (OR = 1.02) were associated with increased odds of re-referrals. In contrast, non-specific spinal pain diagnosis reduced the likelihood (OR = 0.83). Model discrimination was limited (Tjur's coefficient of discrimination (D) = 0.017), indicating weak predictive performance.

Conclusions: Re-referrals were common. Certain clinical factors were associated with re-referrals to a spine centre. Still, their predictive value was limited, making it difficult to recommend strategies to reduce re-referrals from general practice.

Funding: None.

Trial registration: Not relevant.

简介:在丹麦,全科医生是主要提供者,将患者转介到专门的脊柱护理。重新转诊可能表明未解决的脊柱疼痛,但也可以反映病人管理效率低下。本研究确定了首次就诊后500天内丹麦地区脊柱中心的转诊率,并确定了与转诊相关的患者特异性因素。方法:2019年1月至2023年12月,对丹麦南部脊柱中心的患者进行了一项队列研究。重新转介的定义是在初次咨询后50至500天内的访问。调查的因素包括转诊诊断、患者报告的结果和开始的临床服务。多变量逻辑回归确定了与再转诊的关联。结果:在30,872例患者中,10.3% (n = 3,095)观察到再转诊。既往背部手术(OR = 1.23)、止痛药(OR = 1.37)、MRI转诊(OR = 1.6)、提供康复计划(OR = 1.26)、肢体疼痛(OR = 1.02)和孤独感(OR = 1.02)与再转诊的几率增加相关。相比之下,非特异性脊柱疼痛诊断降低了可能性(OR = 0.83)。模型判别有限(Tjur判别系数(D) = 0.017),预测性能较弱。结论:转诊是常见的。某些临床因素与再转诊到脊柱中心有关。尽管如此,他们的预测价值是有限的,这使得很难推荐减少转诊的策略。资金:没有。试验注册:不相关。
{"title":"Re-referrals to a Danish regional spine centre.","authors":"Anders Hansen, Casper Nim, Dorthe Ziegler, Jakob Blaabjerg Espesen, Natalie Hong Siu Chang, Søren O'Neill, Steen Harsted","doi":"10.61409/A12240871","DOIUrl":"https://doi.org/10.61409/A12240871","url":null,"abstract":"<p><strong>Introduction: </strong>In Denmark, general practitioners are the primary providers, referring patients to specialised spine care. Re-referral may indicate unresolved spinal pain, but can also reflect inefficiencies in patient management. This study determined the rate of re-referrals to a Danish regional spine centre within 500 days of the initial visit and identified patient-specific factors associated with re-referrals.</p><p><strong>Methods: </strong>A cohort study of patients at the Spine Centre of Southern Denmark was conducted from January 2019 to December 2023. Re-referrals were defined as visits between 50 and 500 days after the initial consultation. Factors investigated included referral diagnoses, patient-reported outcomes and clinical services initiated. Multivariable logistic regression identified associations with re-referral.</p><p><strong>Results: </strong>Among 30,872 patients, re-referrals were observed in 10.3% (n = 3,095). Previous back surgery (OR = 1.23), pain medication (OR = 1.37), MRI referrals (OR = 1.6), provision of rehabilitation plans (OR = 1.26), extremity pain (OR = 1.02) and loneliness (OR = 1.02) were associated with increased odds of re-referrals. In contrast, non-specific spinal pain diagnosis reduced the likelihood (OR = 0.83). Model discrimination was limited (Tjur's coefficient of discrimination (D) = 0.017), indicating weak predictive performance.</p><p><strong>Conclusions: </strong>Re-referrals were common. Certain clinical factors were associated with re-referrals to a spine centre. Still, their predictive value was limited, making it difficult to recommend strategies to reduce re-referrals from general practice.</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":"145257755","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
Sepsis research is hampered by the lack of a clear definition of suspected infection. 脓毒症的研究由于缺乏对疑似感染的明确定义而受到阻碍。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A03250219
Lana Chafranska, Rune Husås Sørensen, Osama Bin Abdullah, Thomas Andersen Schmidt, Finn Erland Nielsen

Introduction: A prevalent approach in sepsis research is pairing obtained cultures with antibiotic treatment to identify suspected infections. However, cultures are insensitive and nonspecific. Therefore, the present study aimed to examine the proportion of patients with infections admitted to an emergency department (ED) with and without having cultures obtained and to estimate 28-day mortality and prognostic factors of mortality according to culture status.

Methods: We conducted a secondary analysis of prospectively collected data from adult ED patients with suspected or documented infections (1 October 2017 - 31 March 2018). Patients receiving both cultures and antibiotics were compared to those treated solely with antibiotics. Logistic regression analyses assessed mortality differences.

Results: Among 2,055 patients, 1,441 (70.1%) had at least one culture obtained in addition to antibiotic treatment. Among patients without cultures, 163 (26.6%) had a Sequential Organ Failure Assessment score (SOFA) ≥ 2 on admission, compared to 528 (36.6%) among patients with cultures obtained (difference: 5.7-14.3). The 28-day mortality was 7.3% and 7.7%, respectively (difference: -2.1-2.9). Age, SOFA and the Charlson Comorbidity Index were the most important prognostic factors in both groups.

Conclusions: Defining suspected infections using cultures and antibiotics may introduce bias in sepsis research. Data sources relying on these criteria should be validated to examine their applicability.

Funding: The Region Zealand Health Research Foundation and the Naestved, Slagelse and Ringsted Hospital Research Fund.

Trial registration: Not relevant.

简介:在败血症研究中,一种流行的方法是将获得的培养物与抗生素治疗配对,以确定疑似感染。然而,文化是不敏感和非特异性的。因此,本研究的目的是检查急诊科(ED)接受和未接受培养的感染患者的比例,并根据培养情况估计28天死亡率和死亡率的预后因素。方法:我们对疑似或记录感染的成年ED患者(2017年10月1日至2018年3月31日)前瞻性收集的数据进行了二次分析。同时接受培养和抗生素治疗的患者与仅接受抗生素治疗的患者进行比较。Logistic回归分析评估了死亡率差异。结果:在2055例患者中,1441例(70.1%)在抗生素治疗之外至少进行了一次培养。在未接受培养的患者中,163例(26.6%)患者入院时序贯器官衰竭评估评分(SOFA)≥2,而接受培养的患者中有528例(36.6%)(差异:5.7-14.3)。28天死亡率分别为7.3%和7.7%(差异为-2.1 ~ 2.9)。年龄、SOFA和Charlson合并症指数是两组患者最重要的预后因素。结论:使用培养物和抗生素来定义疑似感染可能会在败血症研究中引入偏见。应验证依赖这些标准的数据源,以检查其适用性。资助:新西兰地区卫生研究基金会和Naestved、Slagelse和Ringsted医院研究基金。试验注册:不相关。
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引用次数: 0
No post-infusion reactions after infliximab or vedolizumab. 注射英夫利昔单抗或维多单抗后无反应。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-09-09 DOI: 10.61409/A03250206
Lars Koch Hansen, Karina Winther Andersen, Sara Emmerich Jensen, Michael Dam Jensen

Introduction: Biologic therapies like infliximab and vedolizumab effectively treat inflammatory bowel disease (IBD), but post-infusion observation consumes considerable clinical resources. This study evaluated whether post-infusion observation periods may be safely reduced or eliminated.

Methods: A retrospective analysis included all IBD patients receiving infliximab or vedolizumab from January 2019 to December 2020 at Sygehus Lillebaelt, Denmark. Data included infusion counts, observation duration, timing and severity of reactions.

Results: Among 380 patients receiving 3,847 infusions, 43 reactions (1.1%) occurred exclusively during infusions, mostly within the first 15 minutes. No reactions were reported after infusion had concluded.

Conclusions: Routine post-infusion observation after infliximab and vedolizumab appears unnecessary. Reducing or eliminating this practice may optimise clinical resources without compromising patient safety.

Funding: None.

Trial registration: Not relevant.

英夫利昔单抗、维多单抗等生物疗法治疗炎症性肠病(IBD)有效,但输注后观察耗费大量临床资源。本研究评估输注后的观察期是否可以安全减少或消除。方法:回顾性分析包括2019年1月至2020年12月在丹麦Sygehus Lillebaelt接受英夫利昔单抗或维多单抗治疗的所有IBD患者。数据包括输注计数、观察时间、反应时间和严重程度。结果:380例接受3847次输液的患者中,43例(1.1%)反应完全发生在输液过程中,且多发生在前15分钟。输注结束后无反应报告。结论:英夫利昔单抗和维多单抗治疗后无需常规输液后观察。减少或消除这种做法可以在不损害患者安全的情况下优化临床资源。资金:没有。试验注册:不相关。
{"title":"No post-infusion reactions after infliximab or vedolizumab.","authors":"Lars Koch Hansen, Karina Winther Andersen, Sara Emmerich Jensen, Michael Dam Jensen","doi":"10.61409/A03250206","DOIUrl":"https://doi.org/10.61409/A03250206","url":null,"abstract":"<p><strong>Introduction: </strong>Biologic therapies like infliximab and vedolizumab effectively treat inflammatory bowel disease (IBD), but post-infusion observation consumes considerable clinical resources. This study evaluated whether post-infusion observation periods may be safely reduced or eliminated.</p><p><strong>Methods: </strong>A retrospective analysis included all IBD patients receiving infliximab or vedolizumab from January 2019 to December 2020 at Sygehus Lillebaelt, Denmark. Data included infusion counts, observation duration, timing and severity of reactions.</p><p><strong>Results: </strong>Among 380 patients receiving 3,847 infusions, 43 reactions (1.1%) occurred exclusively during infusions, mostly within the first 15 minutes. No reactions were reported after infusion had concluded.</p><p><strong>Conclusions: </strong>Routine post-infusion observation after infliximab and vedolizumab appears unnecessary. Reducing or eliminating this practice may optimise clinical resources without compromising patient safety.</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":"145257689","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
Rental shoes are not a source of tinea pedis. 租来的鞋子并不是足癣的根源。
IF 1.2 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-26 DOI: 10.61409/A03250148
Tanja Roehmer Wriedt, Kristoffer Nagy Skaastrup, Adeline Held Everland, Karen Marie Thyssen Astvad, Maiken Cavling Arendrup, Viktoria Sigsgaard, Gregor Borut Ernst Jemec, Ditte Marie Lindhardt Saunte

Introduction: Tinea pedis is a common disease that affects up to 70% of adults during a lifetime. Most cases are caused by Trichophyton species. Worldwide, terbinafine resistance among dermatophytes is rising, which is concerning as terbinafine is the first-line treatment. Due to concerns regarding potential epidemics, this study was conducted to investigate whether rental climbing and bowling shoes are a source of societal spread.

Methods: A sampling was conducted on 103 pairs of rental climbing shoes and 102 pairs of bowling shoes across four climbing clubs and four bowling clubs, utilising a previously published swabbing technique and culturing. Positive cultures were identified by microscopy and internal transcribed spacer sequencing. Additionally, a questionnaire was completed regarding shoe material and disinfection method.

Results: No dermatophytes were detected on any of the rental shoes. All bowling clubs and one climbing club employed fungicidal cleaning methods.

Conclusion: Rental climbing and bowling shoes are unlikely to present an immediate risk for the societal transmission of dermatophytes.

Funding: The Royal Hofbundtmager Age Bang Foundation is acknowledged for funding the laboratory work (number 9622-3439).

Trial registration: The local committee of research ethics (Region Zealand, Denmark, EMN-2021-01399) waived ethical approval.

简介:足癣是一种常见病,在一生中影响高达70%的成年人。大多数病例是由毛癣菌引起的。在世界范围内,特比萘芬对皮肤真菌的耐药性正在上升,这是令人担忧的,因为特比萘芬是一线治疗药物。出于对潜在流行病的担忧,本研究旨在调查租赁攀岩鞋和保龄球鞋是否是社会传播的来源。方法:采用先前发表的拭子技术和培养方法,对4个攀岩俱乐部和4个保龄球俱乐部的103双租赁攀岩鞋和102双保龄球鞋进行抽样。通过显微镜和内部转录间隔序列鉴定阳性培养物。并对鞋材和消毒方法进行问卷调查。结果:所有租鞋均未检出皮癣。所有的保龄球俱乐部和一个攀岩俱乐部都采用了杀真菌的清洁方法。结论:租攀岩鞋和保龄球鞋不太可能对皮肤癣菌的社会传播产生直接的风险。资助:皇家hofbundtmanager Age Bang基金会为实验室工作提供资金(编号9622-3439)。试验注册:当地研究伦理委员会(新西兰地区,丹麦,EMN-2021-01399)放弃伦理批准。
{"title":"Rental shoes are not a source of tinea pedis.","authors":"Tanja Roehmer Wriedt, Kristoffer Nagy Skaastrup, Adeline Held Everland, Karen Marie Thyssen Astvad, Maiken Cavling Arendrup, Viktoria Sigsgaard, Gregor Borut Ernst Jemec, Ditte Marie Lindhardt Saunte","doi":"10.61409/A03250148","DOIUrl":"https://doi.org/10.61409/A03250148","url":null,"abstract":"<p><strong>Introduction: </strong>Tinea pedis is a common disease that affects up to 70% of adults during a lifetime. Most cases are caused by Trichophyton species. Worldwide, terbinafine resistance among dermatophytes is rising, which is concerning as terbinafine is the first-line treatment. Due to concerns regarding potential epidemics, this study was conducted to investigate whether rental climbing and bowling shoes are a source of societal spread.</p><p><strong>Methods: </strong>A sampling was conducted on 103 pairs of rental climbing shoes and 102 pairs of bowling shoes across four climbing clubs and four bowling clubs, utilising a previously published swabbing technique and culturing. Positive cultures were identified by microscopy and internal transcribed spacer sequencing. Additionally, a questionnaire was completed regarding shoe material and disinfection method.</p><p><strong>Results: </strong>No dermatophytes were detected on any of the rental shoes. All bowling clubs and one climbing club employed fungicidal cleaning methods.</p><p><strong>Conclusion: </strong>Rental climbing and bowling shoes are unlikely to present an immediate risk for the societal transmission of dermatophytes.</p><p><strong>Funding: </strong>The Royal Hofbundtmager Age Bang Foundation is acknowledged for funding the laboratory work (number 9622-3439).</p><p><strong>Trial registration: </strong>The local committee of research ethics (Region Zealand, Denmark, EMN-2021-01399) waived ethical approval.</p>","PeriodicalId":11119,"journal":{"name":"Danish medical journal","volume":"72 9","pages":""},"PeriodicalIF":1.2,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145029201","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}
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Danish medical journal
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