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Sycosis Barbae Treated With Bimekizumab Bimekizumab治疗Barbae Sycosis
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-10-10 DOI: 10.1111/ajd.14608
Matiar Madanchi, Riccardo Curatolo, Lorenzo S. Pelloni, Hazem A. Juratli

Sycosis barbae (SB) is a chronic, potentially scarring alopecia that primarily affects the beard. We report a unique case of refractory SB in a 31-year-old male successfully treated with bimekizumab, a dual inhibitor of interleukin (IL)-17A and IL-17F. Significant clinical improvement was observed after the second injection, with complete remission achieved after 4 months, highlighting the potential of this novel therapeutic approach for SB.

秃发(SB)是一种慢性、潜在的瘢痕性脱发,主要影响胡须。我们报告一个独特的难治性SB病例,在31岁男性成功治疗比美珠单抗,白细胞介素(IL)-17A和IL- 17f的双重抑制剂。第二次注射后观察到显著的临床改善,4个月后完全缓解,突出了这种新型治疗SB的潜力。
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引用次数: 0
Linear Subepidermal Calcified Nodule With Somatic FGFR3 Mutation 线状表皮下钙化结节伴体细胞FGFR3突变。
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-10-10 DOI: 10.1111/ajd.14607
Italo Francesco Aromolo, Michela Brena, Valerio Pedrelli, Gianluca Tadini
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引用次数: 0
Association of Cognitive Flexibility With Negative Emotional States and Quality of Life in Patients With Hidradenitis Suppurativa: A Cross-Sectional Study 化脓性汗腺炎患者认知灵活性与负性情绪状态和生活质量的关联:一项横断面研究。
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-10-01 DOI: 10.1111/ajd.14606
Jacqueline Jiang, Susan Rossell, Diana Norris, Mei Tam, Rachael Davenport, Diana Courtney, Helen Saunders
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引用次数: 0
Systemic Treatment of Moderate to Severe Alopecia Areata in Adults: Updated Australian Expert Consensus Statement 成人中度至重度斑秃的全身治疗:更新的澳大利亚专家共识声明。
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-09-30 DOI: 10.1111/ajd.14597
Daniella Kushnir-Grinbaum, Laita Bokhari, John Frewen, Anthony Moussa, Daranporn Triwongwaranat, Ragini Ghiya, Flavia Rodrigues Dias, Shin Shen Yong, Bevin Bhoyrul, Zeyad Dabbagh, Ahmed Kazmi, Adam Daunton, Jane Li, Leona Yip, Vivian Lai, Katherine York, William Cranwell, Dmitri Wall, Samantha Eisman, Rodney Sinclair

Over 5000 patients are newly diagnosed with Alopecia areata (AA) in Australia each year. AA severity varies from a single small patch to complete loss of scalp hair, body hair including eyelashes and eyebrows. Approximately 40% of affected individuals experience only a single patch and achieve spontaneous, complete and durable remission within 6 months (acute AA). A further 27% develop additional patches but still attain complete remission within 12 months (chronic AA). Chronic persistent AA (CPAA) is defined by an episode duration of > 12 months and occurs in approximately 33% of patients. Without systemic treatment, 55% of individuals with CPAA will have persistent multifocal relapsing and remitting disease, 30% will progress to alopecia totalis (AT) and 15% will ultimately develop alopecia universalis (AU). The physical disfigurement, unpredictable course, social isolation and rejection contribute to the psychological distress attributable to AA. A wide range of topical, intralesional and systemic agents used to treat AA were evaluated in the 2018 Australian expert consensus statement. In 2020, the international Alopecia Areata Consensus of Experts (ACE) publication stated that if reimbursed, Janus Kinase inhibitors (JAKi's) would be an ideal systemic treatment for adults with AA. TGA approval of baricitinib in 2023 and ritlecitinib in 2024 for severe AA is the first step on the pathway for these systemic medications to be reimbursed on the Australian Government Pharmaceutical Benefits Scheme (PBS). Reimbursement would significantly transform the Australian therapeutic landscape for AA. The purpose of this 2025 Update on the Australian Expert Consensus Statement on the treatment of chronic, moderate to severe AA is to augment the 2018 treatment algorithm to include these TGA-approved medications and to address indications for initiation, continuation and dose titration of systemic JAKi treatment, appropriate choice of agent, satisfactory outcome measures and to provide guidance on when to discontinue successful or unsuccessful treatment.

在澳大利亚,每年有超过5000名新诊断为斑秃(AA)的患者。AA的严重程度从单个小斑块到头皮、体毛(包括睫毛和眉毛)完全脱落不等。大约40%的受影响个体只经历一次贴片,并在6个月内实现自发、完全和持久的缓解(急性AA)。另外27%的患者使用了额外的贴片,但仍在12个月内获得完全缓解(慢性AA)。慢性持续性AA (CPAA)的定义是发作持续时间为10 ~ 12个月,发生在约33%的患者中。如果不进行系统治疗,55%的CPAA患者会出现持续的多灶性复发和缓解性疾病,30%会发展为全发性脱发(AT), 15%最终发展为全发性脱发(AU)。躯体毁容、过程不可预测、社会孤立和排斥是嗜酒者心理困扰的主要原因。2018年澳大利亚专家共识声明对用于治疗AA的广泛局部、局部和全身药物进行了评估。2020年,国际斑秃专家共识(ACE)出版物指出,如果得到补偿,Janus激酶抑制剂(JAKi)将是成人斑秃患者理想的全身治疗方法。TGA将于2023年批准baricitinib, 2024年批准ritlecitinib治疗严重AA,这是这些全体性药物在澳大利亚政府药物福利计划(PBS)中获得报销的第一步。报销将显著改变澳大利亚AA的治疗格局。澳大利亚专家共识声明2025年更新的目的是增加2018年的治疗算法,纳入这些tga批准的药物,并解决系统JAKi治疗的起始、持续和剂量滴定的适应症,药物的适当选择,满意的结果测量,并提供何时停止成功或不成功治疗的指导。
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引用次数: 0
Yellow Nested Melanoma: Line-Field Confocal Optical Coherence Tomography and Literature Review 黄色巢状黑色素瘤:线场共聚焦光学相干断层扫描和文献综述。
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-09-26 DOI: 10.1111/ajd.14604
Luca Bettolini, Vincenzo Maione, Andrea Carugno, Zeno Fratton, Enzo Errichetti, Mariachiara Arisi, Nicola Zerbinati, Iacopo Ghini, Stefano Bighetti

Nested melanoma, a relatively new subtype of melanoma first reported in 2012, is characterised by neoplastic cells organised into nests. We present a unique case of yellow nested melanoma, detailing its clinical, dermoscopic, RCM, and, for the first time to our knowledge, LC-OCT features. Alongside a comprehensive review of the literature, our findings challenge the traditional associations with advanced age and sun-damaged skin, advocating for the term ‘nested melanoma’ to better reflect its characteristics.

巢状黑色素瘤是2012年首次报道的一种相对较新的黑色素瘤亚型,其特征是肿瘤细胞组织成巢状。我们报告了一个独特的黄色巢状黑色素瘤病例,详细介绍了其临床,皮肤镜,RCM,以及我们所知的第一次LC-OCT特征。在对文献进行全面回顾的同时,我们的研究结果挑战了老年和晒伤皮肤之间的传统联系,提倡使用“嵌套黑色素瘤”一词来更好地反映其特征。
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引用次数: 0
The Association Between Type 2 Diabetes Mellitus and Melanoma Prognosis in Patients With High-Risk Primaries 高危原发患者2型糖尿病与黑色素瘤预后的关系
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-09-24 DOI: 10.1111/ajd.14605
Hansa Sharma, Maria Celia B. Hughes, Danielle Gavanescu, B. Mark Smithers, Kiarash Khosrotehrani, Lena von Schuckmann
<p>Melanoma is a potentially aggressive skin cancer, and the determinants of its prognosis are yet to be fully understood [<span>1</span>]. Several studies have found type 2 diabetes mellitus (T2DM), a chronic metabolic disorder, to be linked to an increased risk of melanoma onset, thicker and/or ulcerated tumours, and an increased risk of recurrence, though some studies have shown conflicting results [<span>2-4</span>].</p><p>Our prospective cohort study recruited 700 eligible patients aged over 16 with newly diagnosed T1b–T4b (using AJCC 8th edition) cutaneous melanoma from various public and private healthcare facilities in Queensland, Australia between 2010 and 2014. We defined ‘high-risk’ melanoma as T1b and above, > 0.8 mm or < 0.8 mm with ulceration. Patients found with macroscopic lymph node metastasis or distant metastatic disease within 30 days of diagnosis were excluded. Further details of the study have been published previously [<span>4</span>]. This study was approved by the respective ethics committees.</p><p>A baseline questionnaire collected information on participants' age, sex, body mass index (BMI) [<span>5</span>], diabetes status, smoking status, statin usage in the preceding 5 years, and socioeconomic status (SES; calculated using the Socio-Economic Index for Areas [SEIFA] [<span>6</span>]). Tumour thickness and ulceration were extracted from the participants' histopathology reports. Recurrence data was obtained during follow-up, from hospital records and from the Queensland Cancer Registry. Multiple recurrences within 30 days were considered one event and assigned the earliest date of recurrence. Follow-up times were calculated as the number of months from the date of diagnosis to the date of first recurrence, death, last communication/withdrawal, or 84 months, whichever came first.</p><p>Tumour thickness was grouped as thinner (≤ 2.0 mm) and thicker (> 2.0 mm). Patient's socioeconomic status was categorised as lower (deciles 1–6) or higher (deciles 7–10), using the Index of Relative Socio-Economic Advantage and Disadvantage (IRSAD) [<span>6</span>]. Univariable chi-squared tests (<i>p</i> < 0.05) were used to describe patient and tumour characteristics with diabetes status. We used logistic regression and Cox proportional hazards to associate diabetes status with tumour thickness and 7-year recurrence, respectively. We adjusted for age, sex, presence of ulceration, smoking status, statin use, and tumour thickness (where relevant). Sub-group analyses were conducted using SES and BMI. Adherence to proportionality was verified using a Kolmogorov-type supremum test. Participants who were recurrence-free and alive (<i>n</i> = 460), died without having a recurrence (<i>n</i> = 44), or were lost to follow-up (<i>n</i> = 17) by 7 years were censored. All analyses were performed using SAS version 9.4 (SAS Institute Inc., Cary, NC).</p><p>Of the 700 study participants, 94 (13%) had a diagnosis of T2DM at the time of mel
黑色素瘤是一种潜在的侵袭性皮肤癌,其预后的决定因素尚不完全清楚。一些研究发现,2型糖尿病(T2DM)是一种慢性代谢紊乱,与黑色素瘤发病风险增加、肿瘤变厚和/或溃疡以及复发风险增加有关,尽管一些研究得出了相互矛盾的结果[2-4]。我们的前瞻性队列研究招募了700名16岁以上新诊断为T1b-T4b(使用AJCC第8版)皮肤黑色素瘤的符合条件的患者,这些患者来自2010年至2014年澳大利亚昆士兰州的各种公共和私人医疗机构。我们将“高风险”黑色素瘤定义为T1b及以上,&gt; 0.8 mm或&lt; 0.8 mm伴有溃疡。排除诊断30天内发现肉眼淋巴结转移或远处转移的患者。该研究的进一步细节已于2010年发表。本研究得到了各自伦理委员会的批准。基线问卷收集了参与者的年龄、性别、体重指数(BMI)[6]、糖尿病状况、吸烟状况、过去5年他汀类药物使用情况和社会经济地位(SES;使用地区社会经济指数[SEIFA][6]计算)。从参与者的组织病理学报告中提取肿瘤厚度和溃疡。在随访期间,从医院记录和昆士兰癌症登记处获得复发数据。30天内多次复发视为一个事件,并确定最早复发日期。随访时间计算为从诊断之日至首次复发、死亡、最后一次通信/停药之日的月数,或84个月,以先到者为准。肿瘤厚度分为较薄(≤2.0 mm)和较厚(&gt; 2.0 mm)。使用相对社会经济优势和劣势指数(IRSAD)[6],将患者的社会经济地位分为较低(1-6分位数)或较高(7-10分位数)。单变量卡方检验(p &lt; 0.05)用于描述糖尿病患者和肿瘤特征。我们使用logistic回归和Cox比例风险分别将糖尿病状况与肿瘤厚度和7年复发率联系起来。我们调整了年龄、性别、溃疡、吸烟状况、他汀类药物使用和肿瘤厚度(如相关)。采用SES和BMI进行亚组分析。使用kolmogorov型最大检验验证了对比例性的依从性。筛选无复发存活(n = 460)、无复发死亡(n = 44)或随访7年未随访(n = 17)的参与者。所有分析均使用SAS 9.4版(SAS Institute Inc., Cary, NC)进行。在700名研究参与者中,94名(13%)在黑色素瘤诊断时已诊断为2型糖尿病。T2DM患者多为男性(67%),肥胖(30 kg/m2) BMI(59%),使用他汀类药物(63%),SES较低(60%)(表1)。我们发现T2DM患者和非T2DM患者诊断时患较厚黑色素瘤的可能性无显著差异(校正优势比[OR] 0.66, 95%可信区间[CI] 0.40-1.09, p = 0.10)。我们发现,较低社会经济地位的T2DM患者与非糖尿病患者相比,患较厚黑色素瘤的可能性显著降低(OR 0.49, 95% CI 0.25-0.94, p = 0.03)(表2)。假设社会经济地位较低的2型糖尿病患者比没有社会经济地位的患者更容易获得医疗保健,这一结果可能是由于在糖尿病相关的健康检查中发现了机会性病变。此外,这一结果可能是由于我们的研究中未捕获的其他健康行为或药物使用。来自大规模人群队列的进一步证据可能有助于澄清这些结果。我们发现T2DM与黑色素瘤诊断后7年复发之间没有总体上的显著关联(校正风险比[HR] 1.27, 95% CI 0.83-1.94, p = 0.27)。然而,BMI分层显示,与非糖尿病患者相比,肥胖T2DM患者在7年内复发的风险显著增加(HR 1.96, 95% CI 1.02-3.74, p = 0.04),这表明这些共病可能由于炎症增加或慢性炎症而产生潜在的叠加效应(表3)。本研究的局限性在于T2DM的诊断是自我报告的(通过医疗记录证实)。鉴于黑色素瘤和2型糖尿病的异质性,其他未被探索的临床病理因素可能促成了这些关联。我们得出结论,T2DM可能不是肿瘤厚度或复发的独立危险因素,但与BMI一起起作用。与非糖尿病患者相比,社会经济地位较低的2型糖尿病患者在诊断时更有可能有较薄的黑色素瘤。 此外,与肥胖的非糖尿病患者相比,肥胖的T2DM患者在诊断后7年内复发的风险更高。由昆士兰大学审核和批准,ID#15895。南方地铁医院和卫生服务以及QIMR伯格霍夫医学研究所伦理委员会。作者没有什么可报告的。作者声明无利益冲突。支持本研究结果的数据可根据通讯作者的合理要求提供。
{"title":"The Association Between Type 2 Diabetes Mellitus and Melanoma Prognosis in Patients With High-Risk Primaries","authors":"Hansa Sharma,&nbsp;Maria Celia B. Hughes,&nbsp;Danielle Gavanescu,&nbsp;B. Mark Smithers,&nbsp;Kiarash Khosrotehrani,&nbsp;Lena von Schuckmann","doi":"10.1111/ajd.14605","DOIUrl":"10.1111/ajd.14605","url":null,"abstract":"&lt;p&gt;Melanoma is a potentially aggressive skin cancer, and the determinants of its prognosis are yet to be fully understood [&lt;span&gt;1&lt;/span&gt;]. Several studies have found type 2 diabetes mellitus (T2DM), a chronic metabolic disorder, to be linked to an increased risk of melanoma onset, thicker and/or ulcerated tumours, and an increased risk of recurrence, though some studies have shown conflicting results [&lt;span&gt;2-4&lt;/span&gt;].&lt;/p&gt;&lt;p&gt;Our prospective cohort study recruited 700 eligible patients aged over 16 with newly diagnosed T1b–T4b (using AJCC 8th edition) cutaneous melanoma from various public and private healthcare facilities in Queensland, Australia between 2010 and 2014. We defined ‘high-risk’ melanoma as T1b and above, &gt; 0.8 mm or &lt; 0.8 mm with ulceration. Patients found with macroscopic lymph node metastasis or distant metastatic disease within 30 days of diagnosis were excluded. Further details of the study have been published previously [&lt;span&gt;4&lt;/span&gt;]. This study was approved by the respective ethics committees.&lt;/p&gt;&lt;p&gt;A baseline questionnaire collected information on participants' age, sex, body mass index (BMI) [&lt;span&gt;5&lt;/span&gt;], diabetes status, smoking status, statin usage in the preceding 5 years, and socioeconomic status (SES; calculated using the Socio-Economic Index for Areas [SEIFA] [&lt;span&gt;6&lt;/span&gt;]). Tumour thickness and ulceration were extracted from the participants' histopathology reports. Recurrence data was obtained during follow-up, from hospital records and from the Queensland Cancer Registry. Multiple recurrences within 30 days were considered one event and assigned the earliest date of recurrence. Follow-up times were calculated as the number of months from the date of diagnosis to the date of first recurrence, death, last communication/withdrawal, or 84 months, whichever came first.&lt;/p&gt;&lt;p&gt;Tumour thickness was grouped as thinner (≤ 2.0 mm) and thicker (&gt; 2.0 mm). Patient's socioeconomic status was categorised as lower (deciles 1–6) or higher (deciles 7–10), using the Index of Relative Socio-Economic Advantage and Disadvantage (IRSAD) [&lt;span&gt;6&lt;/span&gt;]. Univariable chi-squared tests (&lt;i&gt;p&lt;/i&gt; &lt; 0.05) were used to describe patient and tumour characteristics with diabetes status. We used logistic regression and Cox proportional hazards to associate diabetes status with tumour thickness and 7-year recurrence, respectively. We adjusted for age, sex, presence of ulceration, smoking status, statin use, and tumour thickness (where relevant). Sub-group analyses were conducted using SES and BMI. Adherence to proportionality was verified using a Kolmogorov-type supremum test. Participants who were recurrence-free and alive (&lt;i&gt;n&lt;/i&gt; = 460), died without having a recurrence (&lt;i&gt;n&lt;/i&gt; = 44), or were lost to follow-up (&lt;i&gt;n&lt;/i&gt; = 17) by 7 years were censored. All analyses were performed using SAS version 9.4 (SAS Institute Inc., Cary, NC).&lt;/p&gt;&lt;p&gt;Of the 700 study participants, 94 (13%) had a diagnosis of T2DM at the time of mel","PeriodicalId":8638,"journal":{"name":"Australasian Journal of Dermatology","volume":"66 8","pages":"e572-e575"},"PeriodicalIF":1.8,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ajd.14605","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145129976","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Comment on: An Online Questionnaire Improves Outcomes for Children With Atopic Eczema 评论:一份在线问卷改善了特应性湿疹患儿的治疗效果。
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-09-19 DOI: 10.1111/ajd.14602
Deryn L. Thompson
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引用次数: 0
Biologic-Induced Paradoxical Psoriatic Alopecia: A Systematic Review 生物诱导的矛盾型银屑病脱发:系统综述。
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-09-12 DOI: 10.1111/ajd.14600
Yaron Gu, Deshan F. Sebaratnam, Mani Makhija, Joshua Farrell

A systemic review was completed of primary research articles reporting patient outcomes in paradoxical psoriatic alopecia in association with biologic therapy. Our search strategy identified 96 patients from 45 studies in addition to our own case. Our review indicates a higher prevalence of paradoxical psoriatic alopecia in younger female patients, most commonly secondary to TNF-alpha inhibitors. Unlike alopecia secondary to psoriasis vulgaris, a mixed inflammatory infiltrate featuring lymphocytes, plasma cells and eosinophils was observed. Remission was observed in most patients, including approximately a third of whom continued biologic therapy.

Trial Registration: PROSPERO registration number: CRD42023471174

一项系统综述完成了主要研究文章,报告了与生物治疗相关的矛盾银屑病性脱发的患者结局。除了我们自己的病例外,我们的搜索策略从45项研究中确定了96名患者。我们的回顾表明,在年轻女性患者中,悖论性银屑病脱发的患病率较高,最常见的继发于tnf - α抑制剂。与寻常型银屑病继发性脱发不同,观察到淋巴细胞、浆细胞和嗜酸性粒细胞混合炎症浸润。在大多数患者中观察到缓解,包括大约三分之一的患者继续进行生物治疗。试验注册:PROSPERO注册号:CRD42023471174。
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引用次数: 0
Practice Guidelines for Teledermatology in Australia: 2025 Update 澳大利亚远程皮肤科实践指南:2025年更新。
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-09-12 DOI: 10.1111/ajd.14599
Liam J. Caffery, Monica L. Taylor, Lisa M. Abbott, Monika Janda, Pascale Guitera, Victoria Mar, Haley Bennett, Chris Arnold, Stephen Shumack, Tony Caccetta, Robert Miller, H. Peter Soyer

In 2020, [the Australasian College of Dermatologists] released its first teledermatology practice guidelines for Australia, with a commitment to regular updates. This article presents the revised guidelines, aimed at educating dermatologists on the benefits and limitations of telehealth, while promoting safer, higher-quality patient care. The updated guidelines harmonise with the Medical Board of Australia's 2023 telehealth guidelines. They address the growing use of telephone consultations—boosted by Medicare subsidies introduced during the COVID-19 pandemic. The latest guidelines provide recommendations on the appropriate choice of modality (telephone versus video) for teleconsultation. They also include updated guidance on clinical image acquisition. The guidelines are divided into two parts: (1) core recommendations and (2) supporting notes for practical application. Topics covered include teledermatology modalities, patient selection and consent, imaging standards, quality and safety, privacy and security, communication, and documentation, including image retention.

2020年,[澳大利亚皮肤科医师学院]发布了澳大利亚第一个远程皮肤科实践指南,并承诺定期更新。本文提出了修订后的指导方针,旨在教育皮肤科医生远程医疗的好处和局限性,同时促进更安全,更高质量的患者护理。更新后的指南与澳大利亚医学委员会2023年远程保健指南保持一致。它们解决了在COVID-19大流行期间引入的医疗保险补贴推动下越来越多地使用电话咨询的问题。最新的指导方针就远程咨询的适当选择方式(电话还是视频)提供了建议。它们还包括关于临床图像采集的最新指导。指南分为两个部分:(1)核心建议和(2)实际应用的支持性说明。涉及的主题包括远程皮肤医学模式、患者选择和同意、成像标准、质量和安全、隐私和安全、通信和文档,包括图像保留。
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引用次数: 0
Too Much and Too Little Medicine Are Two Sides of the Same Coin 药物过多和药物过少是一枚硬币的两面。
IF 1.8 4区 医学 Q2 DERMATOLOGY Pub Date : 2025-09-08 DOI: 10.1111/ajd.14598
Eugene Tan
<p>The <i>Choosing Wisely</i> campaign highlights the harm of ‘Too Much Medicine’—overdiagnosis and unnecessary interventions. While much has been written about this topic, less attention has been paid to its counterpart—‘Too Little Medicine’. Two examples from the UK exemplify this; where effective treatments are restricted leading to undertreatment.</p><p>Isotretinoin has been linked to psychiatric and sexual side effects, resulting in usage restrictions [<span>1</span>]. Topical steroid withdrawal (TSW) is recognised as a distinct entity linked to prolonged use of topical steroids, prompting mandatory potency labelling and warnings [<span>2</span>]. Our college has issued statements contradicting these views. High-quality studies do not support a causal link between isotretinoin and psychiatric or sexual dysfunction [<span>3</span>]. Similarly, topical steroids are safe and effective, but ‘steroid phobia’ triggers eczema flares in children [<span>4</span>]. These conflicting conclusions cannot both be correct.</p><p>Here, the COVID-19 pandemic offers valuable insights. Policy responses varied widely—from strict lockdowns to minimal ones and from extensive use of drugs to minimal use of antivirals. What lessons can we draw in hindsight?</p><p>First, adhering to evidence-based medicine (EBM) increases the probability of getting things right [<span>5</span>]. Numerous studies confirmed that even during a pandemic, rigorous clinical trials—including randomised controlled trials—are not only feasible but also essential [<span>6</span>]. Quality matters! More information does not mean more truth—of the quarter of a million articles on COVID-19, many were of poor quality, and over 500 have been retracted [<span>7</span>].</p><p>Second, the GRADE framework ensures decisions consider benefits, harms, patient values, costs and feasibility [<span>5</span>]. For instance, mandated school closures affected 1.5 billion children globally, yet may not have been necessary to control viral spread [<span>8</span>]. Little attention was given to the negative effects—social isolation, mental health issues and lost education—which could have generational consequences [<span>8</span>].</p><p>It is concerning that policy makers did not grade the quality of evidence nor apply GRADE when evaluating isotretinoin or TSW [<span>1, 2</span>]. A myopic view of risk overlooks the harms of withholding effective treatment.</p><p>At best, isotretinoin restrictions will result in fewer patients receiving effective treatment. At worst, patients may suffer irreversible scarring and serious psychiatric illness, including depression and suicide. Similarly, the cautionary labelling of topical steroids may not improve eczema treatment but at worst, it may increase the risk of misdiagnosis. TSW is not a formally accepted diagnosis, with symptoms that overlap with many conditions. In the worst-case scenario, misdiagnosing cutaneous T-cell lymphoma—that can resemble eczema and is similar
“明智选择”运动强调了“过度用药”的危害——过度诊断和不必要的干预。虽然有很多关于这个话题的文章,但很少有人关注它的对应物——“太少的药”。来自英国的两个例子说明了这一点;有效的治疗受到限制,导致治疗不足。异维甲酸与精神和性方面的副作用有关,因此限制了其使用。局部类固醇停用(TSW)被认为是与长期使用局部类固醇相关的一个独特实体,促使强制性效力标签和警告[2]。我们学院发表了反驳这些观点的声明。高质量的研究并不支持异维甲酸与精神或性功能障碍之间的因果关系。同样,局部类固醇是安全有效的,但“类固醇恐惧症”会引发儿童湿疹。这些相互矛盾的结论不可能都是正确的。在这方面,COVID-19大流行提供了宝贵的见解。政策反应各不相同——从严格的封锁到最低限度的封锁,从广泛使用药物到最低限度地使用抗病毒药物。事后我们能得出什么教训?首先,坚持循证医学(EBM)增加了把事情做好的可能性。大量研究证实,即使在大流行期间,严格的临床试验——包括随机对照试验——不仅是可行的,而且是必不可少的。质量问题!更多的信息并不意味着更多的真相——在25万篇关于COVID-19的文章中,许多文章质量很差,500多篇文章被撤回。其次,GRADE框架确保决策考虑益处、危害、患者价值、成本和可行性。例如,强制关闭学校影响了全球15亿儿童,但对于控制病毒传播可能没有必要。很少有人注意到负面影响——社会孤立、心理健康问题和失去教育——这些可能会对几代人产生影响。值得关注的是,政策制定者在评估异维a酸或TSW时没有对证据质量进行分级,也没有应用grade[1,2]。对风险的短视忽视了拒绝有效治疗的危害。在最好的情况下,异维a酸限制将导致更少的患者接受有效治疗。在最坏的情况下,患者可能会遭受不可逆转的疤痕和严重的精神疾病,包括抑郁症和自杀。同样,局部类固醇的警示标签可能不会改善湿疹的治疗,但在最坏的情况下,它可能会增加误诊的风险。TSW不是一种正式接受的诊断,其症状与许多疾病重叠。在最坏的情况下,误诊皮肤t细胞淋巴瘤(类似湿疹,对局部类固醇同样无反应)可能会导致严重的、潜在的危及生命的后果。我们如何减轻这种情况?我们必须要求决策者在做出任何公共卫生决策时遵循循证医学和GRADE的框架。绝对的知识在认识论上是不可达到的,错误是不可避免的。然而,通过坚持grade——系统地评估证据质量,权衡结果的相对重要性,平衡获益与风险,整合患者价值、偏好和资源考虑——我们可以大大降低错误的可能性及其后果的影响[10]。在大流行期间,许多公共政策缺乏这种系统方法,令人担心在异维甲酸和局部类固醇方面可能出现类似的失误。期望政策制定者接受循证医学培训是不合理的,但期望他们不顾政治压力遵守既定框架并非不合理。如果EBM超出了他们的专业范围,他们应该与受过这方面培训的人接触。这一框架确保了透明度,减少了混乱,提高了公众的信任。药物过多和药物过少是同一枚硬币的两面,都反映了对循证医学的漠视。历史上没有一个社会因为人民要求太多高质量的证据而遭受苦难。患者发表同意书:不适用。人工智能(AI)工具的使用:作者声明在撰写本文时没有使用生成式AI或AI辅助技术。作者没有什么可报道的。作者声明无利益冲突。数据共享不适用于本文,因为在当前研究期间没有生成或分析数据集。
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Australasian Journal of Dermatology
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