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Treatment Options for the Comorbidity of Multiple Sclerosis with Other Chronic Inflammatory Diseases. 多发性硬化症合并其他慢性炎症性疾病的治疗方案。
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-08 DOI: 10.3238/arztebl.m2025.0088
Stefan Bittner, Martin A Kriegel, Britta Siegmund, Tania Kümpfel, Robert Sabat

Background: Approximately 280 000 people in Germany suffer from multiple sclerosis (MS), an autoimmune disease of the central nervous system. Of these, approximately 5% have a comorbid chronic inflammatory disease: the more common ones are psoriasis, rheumatoid arthritis (RA), and chronic inflammatory bowel diseases (IBDs, of which the main types are ulcerative colitis and Crohn's disease).

Methods: This narrative review is based on pertinent publications retrieved by a literature search in PubMed, as well as relevant guidelines. All statements in this article reflect a consensus among the authors, who represent different medical disciplines.

Results: As the data from clinical trials to date are limited, judgments about the proposed treatments are a matter of expert opinion. In general, TNFα blockers should not be used in patients with MS, as they can worsen the disease. In patients with MS and psoriasis, dimethyl fumarate is a useful option for mild disease activity. In MS with comorbid RA, azathioprine and leflunomide/teriflunomide are suitable for mild disease activity. For more severe disease activity, anti-CD20 antibodies have been approved for both diseases and should be used. In MS with comorbid IBD, azathioprine is suitable for mild disease activity. Ozanimod has been approved for patients who have MS and comorbid ulcerative colitis with more severe disease activity, especially those who are JCnegative; it shares its mechanism of action (VLA-4 blockade) with natalizumab.

Conclusion: The treatment of patients who have both MS and another chronic inflammatory disease should be interdisciplinary and personalized, and treatments must be planned with due attention to potential adverse effects. Further studies of treatment for this group of patients are needed.

背景:德国大约有28万人患有多发性硬化症(MS),这是一种中枢神经系统的自身免疫性疾病。其中,约5%患有慢性炎症性疾病:较常见的是牛皮癣、类风湿性关节炎(RA)和慢性炎症性肠病(IBDs,其中主要类型是溃疡性结肠炎和克罗恩病)。方法:这篇叙述性综述是基于PubMed文献检索检索到的相关出版物以及相关指南。本文中的所有陈述都反映了代表不同医学学科的作者之间的共识。结果:由于迄今为止临床试验的数据有限,对建议治疗的判断是专家意见的问题。一般来说,TNFα阻滞剂不应用于多发性硬化症患者,因为它们会使疾病恶化。在多发性硬化症和牛皮癣患者,富马酸二甲酯是一个有用的选择轻度疾病活动。对于合并RA的MS,硫唑嘌呤和来氟米特/特氟米特适用于轻度疾病活动。对于更严重的疾病活动,抗cd20抗体已被批准用于这两种疾病,应该使用。对于合并IBD的MS,硫唑嘌呤适用于轻度疾病活动。Ozanimod已被批准用于患有多发性硬化症和合并症溃疡性结肠炎且疾病活动性更严重的患者,特别是jc阴性患者;其作用机制(vla4阻断)与natalizumab相同。结论:多发性硬化症合并其他慢性炎症性疾病患者的治疗应跨学科、个性化,在制定治疗方案时应注意潜在的不良反应。需要进一步研究这类患者的治疗方法。
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引用次数: 0
Media Consumption by Preschool Children: The Risk of Autism and Developmental Disorders. 学龄前儿童的媒体消费:自闭症和发育障碍的风险。
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-08 DOI: 10.3238/arztebl.m2025.0087
Inge Kamp-Becker, Luise Poustka

Background: Autism spectrum disorder (ASD) is a persistent neu - rodevelopmental condition characterized by impaired social communication and the presence of restricted, repetitive patterns of behavior, typically manifesting in early childhood. The rising prevalence of ASD has been discussed in relation to increased media consumption.

Methods: A selective literature search was conducted in the Medline database on the topics of media consumption and mental disorders, particularly autism, in preschool children. Seven systematic reviews and meta-analyses and 36 original studies were included in the analysis.

Results: The findings across studies consistently demonstrated that media consumption in preschool children was associated with deficits in language and cognitive development (adjusted odds ratio [aOR] 1.67-2.28) and was a risk factor for the development of emotional, behavioral, and developmental disorders (aOR: 1.34-3.06). Symptoms consistent with ASD were also found to be associated with increased media consumption (OR 1.97, 95% confidence interval [1.30; 3.00]). However, these observed effects were consistently identified in the context of multiple other risk factors for mental health problems-such as low socioeconomic status, a family history of mental disorders, or parental stress-which mediated these effects, either directly or indirectly. Intervention studies showed that reducing media consumption, combined with an increase in constructive parent-child interactions, led to a reduction in symptom severity.

Conclusion: In the context of additional risk factors, increased media consumption in young children is associated with atypical or delayed development. The extent of developmental disorders can be reduced through targeted support for parents. When risk factors are present, it is therefore essential to educate parents and implement preventive measures to promote the long-term healthy development of children.

背景:自闭症谱系障碍(ASD)是一种持续的神经发育疾病,其特征是社交障碍和存在限制,重复的行为模式,通常在儿童早期表现出来。ASD患病率的上升与媒体消费的增加有关。方法:在Medline数据库中选择性检索学龄前儿童媒体消费与精神障碍,特别是自闭症的相关文献。7项系统综述和荟萃分析以及36项原始研究被纳入分析。结果:所有研究的结果一致表明,学龄前儿童的媒体消费与语言和认知发展缺陷有关(调整优势比[aOR] 1.67-2.28),并且是情感、行为和发育障碍发展的危险因素(aOR: 1.34-3.06)。与ASD一致的症状也被发现与媒体使用增加有关(OR 1.97, 95%可信区间[1.30;3.00])。然而,这些观察到的影响是在精神健康问题的多个其他风险因素的背景下一致确定的,例如低社会经济地位、精神障碍家族史或父母压力,这些因素直接或间接地介导了这些影响。干预研究表明,减少媒体消费,加上增加建设性的亲子互动,导致症状严重程度降低。结论:在其他危险因素的背景下,幼儿媒体消费增加与不典型或发育迟缓有关。通过对父母的有针对性的支持,可以减少发育障碍的程度。因此,在存在风险因素的情况下,必须对父母进行教育并采取预防措施,以促进儿童的长期健康发展。
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引用次数: 0
The Changing Rates of Lower-Limb Amputations in Germany: An Analysis of Data from the Federal Statistical Office, 2005–2023. 德国下肢截肢率的变化:2005-2023年联邦统计局数据分析
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-08 DOI: 10.3238/arztebl.m2025.0104
Christoph Egen, Andrea Bökel, Anika Großhennig, Jennifer Ernst, Christian Sturm, Jörg Schiller
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引用次数: 0
"Insel" in Early Gastric Cancer: A Unique Endoscopic Finding. 早期胃癌的“Insel”:一个独特的内镜发现。
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-08 DOI: 10.3238/arztebl.m2025.0098
Akira Hokama, Yuzuru Kinjo
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引用次数: 0
Vipera berus Bites in Germany From 2012 to 2023: A Retrospective Analysis of Poison Center Databases. 2012年至2023年德国毒蛇叮咬:毒物中心数据库的回顾性分析。
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-08 DOI: 10.3238/arztebl.m2025.0091
Jade Rae, Paul Rahden, Deborah Hosemann, Tim Lüddecke, Jörg Blessmann, Sebastian Matzke, Sophie Kappel, Dagmar Prasa, Rafael Wagner, Raphael Stich, David Steindl, Uwe Stedtler, Benno Kreuels
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引用次数: 0
Pharmacogenetic Testing for DPD Deficiency: Four and a Half Years' Experience in a Large German Laboratory. DPD缺乏症的药物遗传学检测:在德国大型实验室四年半的经验。
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-08 DOI: 10.3238/arztebl.m2025.0092
Thomas Pretzsch, Matthias Schwab, Olga Blau, Bernhard Wörmann, Sebastian Stintzing, Lars Bullinger, Thomas Burmeister
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引用次数: 0
Global Cost of Silencing Science-Editors and Publishers Have a Duty to Resist. 让科学噤声的全球代价——编辑和出版商有义务抵制。
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-08 DOI: 10.3238/arztebl.m2025.0125
Frank Frizelle, Kamran Abbasi, Vivienne Bachelet, Christopher Baethge, Sabine Kleinert, Jin-Hong Yoo, Lilia Zakama
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引用次数: 0
Diseases of the Male Breast: Gynecomastia and Breast Cancer. 男性乳房疾病:男性乳房发育症和乳腺癌。
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-07-25 DOI: 10.3238/arztebl.m2025.0071
Andree Faridi, Bernd Gerber, Steffi Hartmann

Background: Gynecomastia (GM) is the most common abnormality of the male breast; it is benign and usually bilateral. GM is a manifestation of disease and not a diagnosis in itself. An important differential diagnosis of unilateral GM is breast cancer.

Methods: This narrative review is based on pertinent publications from 2010 onward that were retrieved by a PubMed search, with special attention to the guidelines of the AWMF and the European Academy of Andrology (EAA) and the recommendations of the German Society for Gynecology and Obstetrics.

Results: GM can occur physiologically in newborns, during puberty, and in men over age 65. The basic diagnostic evaluation of GM consists of a thorough history and physical examination (especially of the breast area and genitals), breast and testicular sonography, and laboratory testing for total testosterone (tT), estradiol (E2), luteinizing hormone (LH), human chorionic gonadotropin (hCG), and prolactin (PRL) levels. Further tests to be carried out as indicated according to the clinical findings include the determination of follicle-stimulating hormone (FSH), thyroid-stimulating hormone (TSH), fT4, alpha-1-fetoprotein (AFP), dehydroepiandrosterone (DHEA), and free testosterone (fT) levels, liver and kidney function tests, chromosomal analysis, and supplementary imaging procedures. The treatment depends on the underlying disease and the severity of symptoms, ranging from further observation alone to pharmacotherapy and surgery. Approximately 700 men receive a diagnosis of breast cancer each year in Germany. Because breast cancer in men is rare, there are no pertinent studies, and its treatment is analogous to the treatment of breast cancer in women as recommended in the guidelines.

Conclusion: Men should be included in clinical trials of treatment for breast cancer whenever this is fea - sible, so that the evidence base can be enlarged and men can be given access to innovative treatment methods.

背景:男性乳房畸形是男性乳房最常见的畸形;它是良性的,通常是双侧的。转基因是疾病的一种表现,而不是一种诊断。单侧GM的一个重要鉴别诊断是乳腺癌。方法:本叙述性综述基于2010年以来通过PubMed检索检索到的相关出版物,特别关注AWMF和欧洲男科学会(EAA)的指南以及德国妇产科学会的建议。结果:转基因可发生在新生儿、青春期和60岁以上的男性中。定义为腺体组织增生(超声检查≥2 cm);这要与脂肪瘤区别开来,脂肪瘤只是脂肪组织的增加。GM的诊断评估包括详细的病史记录和体格检查(乳房和生殖器),乳房和睾丸超声检查,以及睾酮、雌二醇、LH、FSH、TSH、催乳素、HCG、AFP、肌酐、GOT和GPT水平的实验室检测。治疗取决于潜在疾病和症状的严重程度,从单独的进一步观察到药物治疗和手术。在德国,每年大约有700名男性被诊断为乳腺癌。由于男性乳腺癌很少见,因此没有相关研究,其治疗方法与指南中推荐的女性乳腺癌治疗方法类似。结论:在可行的情况下,应将男性纳入乳腺癌治疗的临床试验,以扩大证据基础,并为男性提供创新的治疗方法。
{"title":"Diseases of the Male Breast: Gynecomastia and Breast Cancer.","authors":"Andree Faridi, Bernd Gerber, Steffi Hartmann","doi":"10.3238/arztebl.m2025.0071","DOIUrl":"10.3238/arztebl.m2025.0071","url":null,"abstract":"<p><strong>Background: </strong>Gynecomastia (GM) is the most common abnormality of the male breast; it is benign and usually bilateral. GM is a manifestation of disease and not a diagnosis in itself. An important differential diagnosis of unilateral GM is breast cancer.</p><p><strong>Methods: </strong>This narrative review is based on pertinent publications from 2010 onward that were retrieved by a PubMed search, with special attention to the guidelines of the AWMF and the European Academy of Andrology (EAA) and the recommendations of the German Society for Gynecology and Obstetrics.</p><p><strong>Results: </strong>GM can occur physiologically in newborns, during puberty, and in men over age 65. The basic diagnostic evaluation of GM consists of a thorough history and physical examination (especially of the breast area and genitals), breast and testicular sonography, and laboratory testing for total testosterone (tT), estradiol (E2), luteinizing hormone (LH), human chorionic gonadotropin (hCG), and prolactin (PRL) levels. Further tests to be carried out as indicated according to the clinical findings include the determination of follicle-stimulating hormone (FSH), thyroid-stimulating hormone (TSH), fT4, alpha-1-fetoprotein (AFP), dehydroepiandrosterone (DHEA), and free testosterone (fT) levels, liver and kidney function tests, chromosomal analysis, and supplementary imaging procedures. The treatment depends on the underlying disease and the severity of symptoms, ranging from further observation alone to pharmacotherapy and surgery. Approximately 700 men receive a diagnosis of breast cancer each year in Germany. Because breast cancer in men is rare, there are no pertinent studies, and its treatment is analogous to the treatment of breast cancer in women as recommended in the guidelines.</p><p><strong>Conclusion: </strong>Men should be included in clinical trials of treatment for breast cancer whenever this is fea - sible, so that the evidence base can be enlarged and men can be given access to innovative treatment methods.</p>","PeriodicalId":11258,"journal":{"name":"Deutsches Arzteblatt international","volume":" Forthcoming","pages":"406-411"},"PeriodicalIF":7.1,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12580830/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143973550","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Material Fatigue With Endoleak After Endovascular Repair of an Abdominal Aortic Aneurysm. 腹主动脉瘤血管内修复术后材料疲劳伴腔内渗漏一例。
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-07-11 DOI: 10.3238/arztebl.m2025.0058
Mikolaj Walensi, Kai Nassenstein, Johannes N Hoffmann
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引用次数: 0
Achievements and Obstacles in the Late Phase of the Global Polio Eradication Initiative. 全球根除脊髓灰质炎行动后期阶段的成就和障碍。
IF 7.1 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-07-11 DOI: 10.3238/arztebl.m2025.0079
Olaf Müller, Guangyu Lu, Peter Meissner, Lorenz von Seidlein, Albrecht Jahn, Oliver Razum

Background: The Global Polio Eradication Initiative (GPEI), founded in 1988, has contributed to a drastic reduction in the number of cases of wild poliovirus (WPV) infection. Progress has stalled for years, however, even though the GPEI has become a very costly global health program. Poliomyelitis is caused by WPV types 1, 2, and 3, as well as by mutated vaccine viruses.

Methods: This review is based on publications retrieved by a selective literature search relating to challenges that currently face the GPEI, with an emphasis on the situation in Germany, e.g., the problem of maintaining the high rate of vaccination coverage.

Results: WPV1 remains endemic in Pakistan and Afghanistan. In addition, outbreaks caused by viral mutants of oral live polio vaccines (OPV) have become a problem in countries with low vac cination coverage, with several thousand cases since 2000. Industrialized countries have also had rare cases of poliomyelitis in recent years, caused by mutated vaccine viruses, which often circulate undetected. Aside from the dysfunctionality of the health care systems of many countries, geopolitical tensions, international and civil wars, mass human migration, hesitancy and skepticism of the population about vaccination, and funding fatigue on the part of donor countries, there are a variety of technical problems confronting the GPEI in its quest for success.

Conclusion: Maintaining high polio vaccination rates may be a more realistic solution to the problem of polio than continuing to pursue the GPEI's objective of putting all polioviruses out of existence. Doctors in Germany can actively contribute to the achievement of both these goals by checking the polio vaccination status of their patients, as recommended by the German Standing Committee on Vaccination (STIKO). This is especially important when doctors care for refugees and asylum-seekers who have arrived in Germany from abroad.

背景:1988年成立的全球根除脊髓灰质炎行动(GPEI)对野生脊髓灰质炎病毒(WPV)感染病例数量的急剧减少作出了贡献。然而,尽管GPEI已成为一项非常昂贵的全球卫生计划,但进展已停滞多年。脊髓灰质炎是由1型、2型和3型野生脊灰病毒以及突变疫苗病毒引起的。方法:本综述基于选择性文献检索检索到的出版物,这些出版物与GPEI目前面临的挑战有关,重点是德国的情况,例如,保持高疫苗接种率的问题。结果:1型野生脊灰仍在巴基斯坦和阿富汗流行。此外,口服脊髓灰质炎活疫苗(OPV)病毒突变引起的疫情在疫苗接种覆盖率低的国家已成为一个问题,自2000年以来已有数千例病例。近年来,工业化国家也出现了罕见的脊髓灰质炎病例,这些病例是由突变的疫苗病毒引起的,这种病毒通常在未被发现的情况下传播。除了许多国家卫生保健系统功能失调、地缘政治紧张局势、国际战争和内战、大规模人口移徙、民众对疫苗接种的犹豫和怀疑以及捐助国的资金疲劳之外,全球根除脊灰行动在寻求成功的过程中还面临各种技术问题。结论:保持较高的脊髓灰质炎疫苗接种率可能是解决脊髓灰质炎问题的更现实的办法,而不是继续追求消灭所有脊髓灰质炎病毒的全球根除脊髓灰质炎行动的目标。德国的医生可以按照德国疫苗接种常设委员会的建议,通过检查患者的脊髓灰质炎疫苗接种情况,积极促进实现这两个目标。当医生照顾从国外抵达德国的难民和寻求庇护者时,这一点尤为重要。
{"title":"Achievements and Obstacles in the Late Phase of the Global Polio Eradication Initiative.","authors":"Olaf Müller, Guangyu Lu, Peter Meissner, Lorenz von Seidlein, Albrecht Jahn, Oliver Razum","doi":"10.3238/arztebl.m2025.0079","DOIUrl":"10.3238/arztebl.m2025.0079","url":null,"abstract":"<p><strong>Background: </strong>The Global Polio Eradication Initiative (GPEI), founded in 1988, has contributed to a drastic reduction in the number of cases of wild poliovirus (WPV) infection. Progress has stalled for years, however, even though the GPEI has become a very costly global health program. Poliomyelitis is caused by WPV types 1, 2, and 3, as well as by mutated vaccine viruses.</p><p><strong>Methods: </strong>This review is based on publications retrieved by a selective literature search relating to challenges that currently face the GPEI, with an emphasis on the situation in Germany, e.g., the problem of maintaining the high rate of vaccination coverage.</p><p><strong>Results: </strong>WPV1 remains endemic in Pakistan and Afghanistan. In addition, outbreaks caused by viral mutants of oral live polio vaccines (OPV) have become a problem in countries with low vac cination coverage, with several thousand cases since 2000. Industrialized countries have also had rare cases of poliomyelitis in recent years, caused by mutated vaccine viruses, which often circulate undetected. Aside from the dysfunctionality of the health care systems of many countries, geopolitical tensions, international and civil wars, mass human migration, hesitancy and skepticism of the population about vaccination, and funding fatigue on the part of donor countries, there are a variety of technical problems confronting the GPEI in its quest for success.</p><p><strong>Conclusion: </strong>Maintaining high polio vaccination rates may be a more realistic solution to the problem of polio than continuing to pursue the GPEI's objective of putting all polioviruses out of existence. Doctors in Germany can actively contribute to the achievement of both these goals by checking the polio vaccination status of their patients, as recommended by the German Standing Committee on Vaccination (STIKO). This is especially important when doctors care for refugees and asylum-seekers who have arrived in Germany from abroad.</p>","PeriodicalId":11258,"journal":{"name":"Deutsches Arzteblatt international","volume":" Forthcoming","pages":"393-398"},"PeriodicalIF":7.1,"publicationDate":"2025-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12571390/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144126376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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