anti-inflammatory agents

抗炎药
  • 文章类型: Journal Article
    头皮脂溢性皮炎(SSD)是一种慢性和复发性炎症性皮肤病。目前的SSD治疗主要包括抗真菌剂和抗炎剂的局部应用。审查有关SSD的信息,并为皮肤科医生提供管理成人SSD的实用建议。材料和方法:在2023年9月至12月之间,一个皮肤病学和头发和头皮疾病的国际专家组开会讨论有关SD的公开数据,SSD,头皮屑,和管理选项。共分析了PubMed提供的131份手稿,讨论并用于目前的共识。每个作者都被要求根据文献和他们自己的经验完成一个表格,列出目前使用的治疗SSD的方法。作者证实了他们的使用和治疗方案,并评论了当地治疗例外。然后,他们就处方实践达成一致,并提出了一般治疗方法。目前,不存在用于管理中度和重度形式的SSD的批准疗法,并且需要有效和安全地治疗该疾病的经过调整和批准的药物。我们提出了一种处理算法,可以处理SSD的所有严重程度等级。该算法可以用局部治疗规范来完成。尽管缺乏批准的治疗方法来管理中等形式的SSD,提出了一种治疗算法,可以帮助处方者更有效地管理SSD。
    Seborrheic Dermatitis of the scalp (SSD) is a chronic and relapsing inflammatory skin condition. Current SSD treatments mainly consist of topical applications of anti-fungals and anti-inflammatory agents. to review information about SSD and to provide dermatologists with practical recommendations for managing adult SSD. Material and methods: Between September and December 2023, an international group of experts in dermatology and hair and scalp disorders met to discuss published data about SD, SSD, dandruff, and management options. A total of 131 manuscripts available from PubMed were analysed, discussed and used for the present consensus. Each author was asked to complete a table listing currently used treatments to treat SSD according to the literature and to their own experience. The authors confirmed their use and regimen and commented on local treatment exceptions. They then agreed on prescription practices and proposed a general treatment approach. Currently, approved therapies to manage moderate and severe forms of SSD do not exist and there is a need for adapted and approved medications that treat efficiently and safely the disease. We propose a treatment algorithm that allows for the treatment of all severity grades of SSD. This algorithm may be completed with local treatment specifications. Despite the lack of approved therapies to manage moderate forms of SSD, a treatment algorithm is proposed and may help prescribers to manage SSD more efficiently.
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  • 文章类型: English Abstract
    重症患者COVID-19相关性肺曲霉病(CAPA)的发病率和死亡率较高。尽管COVID-19相关毛霉菌病(CAPM)相对罕见,其严重程度和经常延迟诊断或误诊导致其高死亡率。危重患者CAPA和CAPM的诊断和治疗具有挑战性。早期诊断和标准化治疗是获得良好结果的两个最重要因素。因此,组织了一个由中国胸科学会和中国胸科医师协会重症监护小组专家组成的工作组,根据目前的医学证据和临床实践,以提高危重患者CAPA和CAPM的临床治疗能力。工作组根据文献和临床实践经验起草了初步文本。经过两轮讨论,最后提出了16项建议,将推荐强度分为推荐,建议和不推荐。-胸部图像和支气管镜的利用1.胸部CT,而不是胸部X光,建议可能的CAPA或CAPM患者为支气管镜检查提供诊断证据和定位以获取微生物标本。不能仅根据胸部CT的阳性体征来诊断CAPA。对于可能患有CAPM.2的患者,建议使用胸部造影CT或肺动脉CT(CTPA)。在可能的CAPA或CAPM的情况下,建议尽快进行支气管镜检查和收集BALF以进行微生物学检查。·微生物检验的选择策略3.显微镜检查,文化,曲霉菌的GM检测和PCR。BALF的建议用于可能的CAPA患者。对于可能的CAPM,建议对BALF进行真菌染色和培养。建议在重症患者和可能的CAPM中选择适当的标本进行分子生物学检测。-诊断判决书4.建议将修订的ECMM/ISHAM共识声明作为CAPA的诊断标准,并建议将Delphi共识声明作为CAPM的诊断标准。-抗真菌治疗的适当时间5。对于患有严重COVID-19的患者,尤其是具有CAPA6危险因素的患者,建议使用两性霉素B或其脂质体进行CAPA的预防性治疗。对于可能的CAPA,建议尽快开始经验性抗曲霉治疗,并同时获得曲霉菌的微生物证据。严重COVID-19患者不推荐CAPM预防性治疗。建议尽早开始对可能的CAPM进行经验性治疗,和微生物证据应同时获得。-抗真菌剂的临床应用9.建议伏立康唑或伊沙康康唑作为CAPA的初始治疗。两性霉素B脂质体被建议作为CAPM的初始治疗。对于肾功能不全或两性霉素B脂质体不耐受/不可用的患者,可选择使用艾沙康唑或泊沙康唑。在患有气管支气管炎的CAPA患者中,除全身抗真菌药物外,还建议吸入抗真菌药物。11.联合治疗不推荐作为CAPA的初始治疗,但可以用作挽救治疗策略。建议使用三唑或两性霉素B与卡泊芬净或米卡芬净组合;而不建议使用两性霉素B与三唑组合。对于有广泛病变的CAPM患者,快速进展或一般情况差,建议将两性霉素B脂质体与伊沙康康唑或泊沙康唑联合使用。-反应评估和治疗持续时间12.建议根据临床症状/体征全面评估治疗反应,患者的影像学和微生物学检查。CAPA可以结合血清GM.13的动态变化进行评估。CAPA的推荐治疗持续时间为至少6-12周。CAPM建议至少3-6个月的总课程,应根据4-6周静脉治疗的反应考虑序贯治疗。-如何调整抗炎治疗14.在严重COVID-19合并可能或可能的丝状真菌感染的患者中,建议停止或适当减少抗炎治疗,考虑到疾病过程中感染和炎症的严重程度。在这些患者中不建议使用基于糖皮质激素的巴利替尼和/或托珠单抗的组合。-如何治疗潜在的疾病15.在糖尿病患者中,建议严格控制血糖。长期使用糖皮质激素和/或免疫抑制剂的患者,建议降低免疫抑制的强度。建议使用粒细胞集落刺激因子来改善由于各种原因导致的粒细胞缺乏患者的循环粒细胞水平。-什么时候应该考虑手术16。在CAPA患者中,不建议手术,除非大血管,心包,或者涉及胸壁,或者患者有反复或大咯血。对于CAPM患者,建议诊断后早期手术切除病灶。手术是严重COVID-19患者的高风险手术,建议多学科团队对此进行讨论。
    经验证COVID-中医中医中医中医中医中医中医中医中医(CAPA)的康复病症,中医中医中医中医高,中医中医中医中医中医中医中医中医中医高。而中医中医中医中医中医嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯嗯
    The incidence and mortality of COVID-19 associated pulmonary aspergillosis (CAPA) are high in critically ill patients. Although COVID-19 associated mucormycosis (CAPM) is relatively rare, its severity and often a delayed diagnosis or misdiagnosis lead to its high mortality. The diagnosis and treatment of CAPA and CAPM in critically ill patients are challenging. Early diagnosis and a standardized therapy are the two most important factors for a good outcome. Therefore, a working group of experts from Chinese Thoracic Society and Chinese Association of Chest Physicians Critical Care Group was organized to develop this consensus based on the current medical evidence and clinical practice, in order to improve the ability of clinical treatment for critically ill patients with CAPA and CAPM. The working group drafted a preliminary text based on the literature and clinical practice experience. Following two rounds of discussion, 16 final recommendations were made, with the recommendation strength divided into recommend, suggest and not recommend.-Utilization of chest images and bronchoscopy1. Chest CT, rather than chest X-ray, is recommended for possible CAPA or CAPM patients to provide diagnostic evidence and localization for bronchoscopy to obtain microbiological specimens. A diagnosis of CAPA could not be made on the basis of positive signs on chest CT alone. Chest contrast CT or pulmonary artery CT (CTPA) is recommended in patients with probable CAPM.2. In the case of possible CAPA or CAPM, it is recommended that bronchoscopy and BALF collection for microbiological examinations be pereformed as soon as possible.-The selection strategies of microbiological examinations3. Microscopic examination, culture, GM testing and PCR for aspergillus Spp. of BALF are recommended in patients with probable CAPA. Fungal staining and culture of BALF are suggested for possible CAPM. Selected appropriate specimens for molecular biological detection are suggested in critically ill patients and possible CAPM.-Diagnostic critieria4. The revised ECMM/ISHAM consensus statement is recommended as the diagnostic criteria for CAPA and the Delphi consensus statement is recommended as the diagnostic criteria for CAPM.-Appropriate time for antifungal therapy5. Prophylactic therapy of CAPA with amphotericin B or its liposomes is suggested for patients with severe COVID-19, especially those with risk factors for CAPA.6. It is recommended to start the empirical anti-Aspergillus therapy as soon as possible for possible CAPA, and obtain the microbiological evidence for aspergillosis at the same time.7. Prophylactic therapy for CAPM is not recommended for severe COVID-19 patients.8. Early initiation of empirical therapy for possible CAPM is recommended, and microbiological evidence should be obtained at the same time.-Clinical applications for antifungal agents9.Voriconazole or isavuconazole are recommended as initial treatment for CAPA. Amphotericin B liposomes are suggested as the initial treatment for CAPM. Isavuconazole or posaconazole may be an option in patients with renal insufficiency or amphotericin B liposome intolerance/unavailability.10. In CAPA patients with tracheobronchitis, antifungal drug inhalation is recommended in addition to systemic antifungal medication.11. Combination therapy is not recommended as initial therapy for CAPA, but may be used as a salvage therapy strategy. Triazole or amphotericin B in combination with caspofungin or micafungin is recommended; whereas amphotericin B in combination with triazole is not recommended. For CAPM patients with extensive lesions, rapid progression or poor general condition, a combination of amphotericin B liposome with isavuconazole or posaconazole is suggested.-Response assessment and treatment duration12. It is recommended that treatment response be assessed comprehensively according to the clinical symptoms/signs, imaging and microbiological examination of patients. CAPA can be evaluated in combination with the dynamic change in serum GM.13. The recommended treatment duration of CAPA is at least 6-12 weeks. A total course of at least 3-6 months is suggested for CAPM, and the sequential treatment should be considered according to the response to 4-6 weeks of intravenous therapy.-How to adjust the anti-inflammatory therapy14. In patients with severe COVID-19 combined with possible or probable filamentous fungal infection, it is suggested that of anti-inflammatory therapy be stopped or reduced appropriately, taking into account of the severity of the infection and inflammation of the disease course. The combination of baritinib and/or tozzizumab based on glucocorticoids is not suggested in these patients.-How to treat the underlying diseases15. In patients with diabetes, strict glycaemic control is suggested. In patients with long-term use of glucocorticoids and/or immunosuppressants, it is suggested to reduce the intensity of immunosuppression. Granulocyte colony-stimulating factor is suggested to use to improve the circulating granulocyte levels in patients with granulocyte deficiency due to various causes.-When an operation should be considered16. In patients with CAPA, surgery is not recommended unless large blood vessels, pericardium, or chest wall are involved, or the patient has recurrent or massive hemoptysis. For CAPM patients, early surgical removal of lesions after diagnosis is recommended. Surgery is a high-risk procedure in patients with severe COVID-19, and a multidisciplinary team discuss is suggested.
    重症COVID-19相关肺曲霉病(CAPA)的发病率及病死率均较高。而新型冠状病毒感染相关肺毛霉病(CAPM)虽然相对少见,但疾病本身的严重性加之误诊及诊断延误也导致其病死率居高不下。目前,重症CAPA及CAPM的诊断及治疗均面临巨大挑战。如何早期诊断并规范治疗是救治成功的关键。因此,中国医师协会呼吸医师分会危重症学组与中华医学会呼吸病学分会危重症学组发起并组织相关领域专家,基于目前的循证医学证据及临床实践经验,撰写本共识,以期提高重症CAPA及CAPM患者的临床救治。工作组结合文献及临床实践经验,形成共识的初步文本。经两次讨论会,最终确定16条核心推荐意见并给出推荐强度,分为推荐、建议及不推荐。.
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  • 文章类型: Journal Article
    治疗孕妇或哺乳期妇女的特应性皮炎(AD),在女性和男性与AD渴望成为父母是困难的,以不确定性为特征,作为决定全身抗炎治疗的证据是有限的.这个项目绘制了皮肤科医生的共识,欧洲西北部的产科医生和患者为生育年龄的男性和女性进行全身性抗炎治疗以管理AD提供实用建议。21个人(16名皮肤科医生,两名产科医生和三名患者)参加了两轮Delphi过程。就32项声明达成了充分共识,对四项声明部分达成共识,对四项声明未达成共识。环孢菌素A是孕前妇女长期全身性AD治疗的首选药物,在怀孕期间和母乳喂养时,短期强的松龙用于耀斑管理。在第二选择系统的概念前或怀孕期间没有达成共识,尽管在母乳喂养期间,dupilumab和硫唑嘌呤被认为是合适的。如果女性提供良好的疾病控制,并且其在怀孕期间的益处超过其风险,则讨论继续使用现有的全身性AD药物可能是适当的。Janus激酶(JAK)抑制剂,女性在孕前应避免使用甲氨蝶呤和霉酚酸酯,怀孕和母乳喂养,建议使用特定药物清除期。男性先入为主:环孢素A,硫唑嘌呤,dupilumab和皮质类固醇是合适的;甲氨蝶呤和霉酚酸酯在受孕前需要3个月的洗脱;JAK抑制剂没有达成共识.患者和临床医生对妊娠中使用的适当(和不适当)AD治疗的教育至关重要。倡导并概述了用于AD患者跨学科管理的共享护理框架。这一共识为以前护理AD患者的临床医生提供了跨学科的临床指导,怀孕期间和之后。虽然全身性AD药物在该患者组中使用并不常见,本文中的考虑因素可能有助于重度难治性AD患者。
    Treating atopic dermatitis (AD) in pregnant or breastfeeding women, and in women and men with AD aspiring to be parents is difficult and characterized by uncertainty, as evidence to inform decision-making on systemic anti-inflammatory treatment is limited. This project mapped consensus across dermatologists, obstetricians and patients in Northwestern Europe to build practical advice for managing AD with systemic anti-inflammatory treatment in men and women of reproductive age. Twenty-one individuals (sixteen dermatologists, two obstetricians and three patients) participated in a two-round Delphi process. Full consensus was reached on 32 statements, partial consensus on four statements and no consensus on four statements. Cyclosporine A was the first-choice long-term systemic AD treatment for women preconception, during pregnancy and when breastfeeding, with short-course prednisolone for flare management. No consensus was reached on second-choice systemics preconception or during pregnancy, although during breastfeeding dupilumab and azathioprine were deemed suitable. It may be appropriate to discuss continuing an existing systemic AD medication with a woman if it provides good disease control and its benefits in pregnancy outweigh its risks. Janus kinase (JAK) inhibitors, methotrexate and mycophenolate mofetil should be avoided by women during preconception, pregnancy and breastfeeding, with medication-specific washout periods advised. For men preconception: cyclosporine A, azathioprine, dupilumab and corticosteroids are appropriate; a 3-month washout prior to conception is desirable for methotrexate and mycophenolate mofetil; there was no consensus on JAK inhibitors. Patient and clinician education on appropriate (and inappropriate) AD treatments for use in pregnancy is vital. A shared-care framework for interdisciplinary management of AD patients is advocated and outlined. This consensus provides interdisciplinary clinical guidance to clinicians who care for patients with AD before, during and after pregnancy. While systemic AD medications are used uncommonly in this patient group, considerations in this article may help patients with severe refractory AD.
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  • 文章类型: Journal Article
    目的:制定涵盖评估的临床实践指南,管理,回到患有肩袖疾病的成年人的工作中。设计:临床实践指南。方法:使用系统评价,对文献的评价,以及获得关键利益相关者共识的迭代方法,在魁北克省(加拿大)的医疗保健系统和工作环境的背景下,制定了临床建议和算法.结果:建议(n=73)和临床决策算法(n=3)被开发以匹配目标。初步评估应包括患者的病史,主观评价,和体检。诊断成像仅在特定情况下是必要的。对乙酰氨基酚,非甾体抗炎药,注射疗法可能在短期内有助于减轻疼痛。临床医生应制定积极和面向任务的康复计划(锻炼和教育),以减少患有肩袖疾病的成年人的疼痛和残疾。肩峰下减压不推荐用于治疗肩袖肌腱病。手术适用于选定的全厚度肩袖撕裂患者。应及早制定复工计划,与工人和其他利益相关者合作,必须结合多种策略来促进重返工作岗位。结论:制定本临床实践指南是为了协助为患有肩袖疾病的成年人提供医疗保健的多学科临床医生团队。CPG指导诊断和治疗的临床决策,并计划成功重返工作岗位。J正交运动物理学2022;52(10):647-664。Epub:2022年7月27日。doi:10.2519/jospt.202.11306。
    OBJECTIVE: To develop a clinical practice guideline covering the assessment, management, and return to work of adults with rotator cuff disorders. DESIGN: Clinical practice guideline. METHODS: Using systematic reviews, appraisal of the literature, and an iterative approach to obtain consensus from key stakeholders, clinical recommendations and algorithms were developed in the context of the health care system and work environment of the province of Quebec (Canada). RESULTS: Recommendations (n = 73) and clinical decision algorithms (n = 3) were developed to match the objectives. The initial assessment should include the patient\'s history, a subjective assessment, and a physical examination. Diagnostic imaging is only necessary in select circumstances. Acetaminophen, nonsteroidal anti-inflammatory drugs, and injection therapies may be useful to reduce pain in the short term. Clinicians should prescribe an active and task-oriented rehabilitation program (exercises and education) to reduce pain and disability in adults with rotator cuff disorders. Subacromial decompression is not recommended to treat rotator cuff tendinopathy. Surgery is appropriate for selected patients with a full-thickness rotator cuff tear. A return-to-work plan should be developed early, in collaboration with the worker and other stakeholders, and must combine multiple strategies to promote return to work. CONCLUSION: This clinical practice guideline was developed to assist the multidisciplinary team of clinicians who provide health care for adults with a rotator cuff disorder. The CPG guides clinical decisionmaking for diagnosis and treatment, and planning for successful return to work. J Orthop Sports Phys Ther 2022;52(10):647-664. Epub: 27 July 2022. doi:10.2519/jospt.2022.11306.
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  • 文章类型: Journal Article
    特应性皮炎(又称特应性湿疹)是一种常见于儿童的慢性复发性炎症性皮肤病,在过去的几十年中,包括台湾在内的许多国家的患病率越来越高。儿科特应性皮炎的管理可能具有挑战性,特别是随着近年来新型全身和局部抗炎药物的出现,治疗选择范围不断扩大.台湾儿科变态反应学院,哮喘和免疫学(TAPAAI)制定了台湾儿童特应性皮炎的诊断和管理指南,它提供了其流行病学的简要概述,临床特征和诊断,机制,治疗,和教育。本指南的内容整合了最近的国家和国际特应性皮炎诊断和治疗指南的原则,最新的研究结果,以及台湾经验丰富的儿科过敏专家的专家意见。出于实际目的,本指南提供了小儿特应性皮炎的简化且易于使用的诊断标准和严重程度分级.还提出了一种逐步处理算法,以加快理性,成本效益高,和循证管理战略。这个准则,根据台湾儿科过敏专家目前的最佳证据和现实经验开发,旨在促进实践,医生对小儿特应性皮炎的最新管理。
    Atopic dermatitis (also known as atopic eczema) is a chronic relapsing inflammatory skin disease commonly seen in children, with increasing prevalence over the past few decades in many countries including Taiwan. The management of pediatric atopic dermatitis can be challenging, particularly as treatment options are expanding with the emergence of novel systemic and topical anti-inflammatory medications in recent years. The Taiwan Academy of Pediatric Allergy, Asthma and Immunology (TAPAAI) has developed the Taiwan guidelines for the diagnosis and management of pediatric atopic dermatitis, which provides a concise overview of its epidemiology, clinical characteristics and diagnosis, mechanisms, treatments, and education. The contents of this guideline integrate the principles of recent national and international guidelines for the diagnosis and management of atopic dermatitis, latest research findings, and expert opinions of experienced pediatric allergy specialists in Taiwan. For practical purposes, this guideline presents simplified and easy-to-use diagnostic criteria and severity grading for pediatric atopic dermatitis. A stepwise treatment algorithm is also proposed to expedite rational, cost-effective, and evidence-based management strategy. This guideline, developed based on current best evidence and real-world experience of pediatric allergy experts in Taiwan, is intended to facilitate practical, up-to-date management of pediatric atopic dermatitis among physicians.
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  • 文章类型: Journal Article
    膝关节骨性关节炎(非关节成形术)的治疗循证临床实践指南基于对成人(17岁及以上)膝关节骨性关节炎非关节成形术治疗的已发表研究的系统评价。本临床实践指南的目的是评估当前与治疗相关的最佳证据。本指南的范围包括对有症状的膝骨关节炎的非药物和药物干预措施,包括侵入性小于膝关节置换术的外科手术。它没有为类风湿关节炎患者提供建议,其他关节的关节炎,或其他炎症。本指南包含29条建议,以帮助所有合格且经过适当培训的医疗保健专业人员参与膝关节骨关节炎的非关节成形术管理,并为患者提供信息。此外,工作组强调需要更好地研究关节内皮质类固醇,透明质酸,和富含血小板的血浆详细说明骨关节炎的特征,包括亚组分析和骨关节病严重程度分层,与对照受试者的临床相关结果进行偏倚和成本效益分析。比较轻度至中度膝骨关节炎和MRI证实半月板撕裂的患者的结果的研究,这些患者在经过保守治疗后未能改善(非甾体类抗炎药,类固醇注射,和物理治疗)与那些没有经过专门保守治疗的半月板部分切除术的人相比。仍需要前瞻性随机试验或前瞻性队列研究来确定特定亚组和人群中单独口服非甾体类抗炎药的疗效,以定制全身药物,以帮助提高疗效并降低不良反应的风险。
    Management of Osteoarthritis of the Knee (nonarthroplasty) Evidence-Based Clinical Practice Guideline is based on a systematic review of published studies for the nonarthroplasty treatment of osteoarthritis of the knee in adults (ages 17 years and older). The purpose of this clinical practice guideline is to evaluate current best evidence associated with treatment. The scope of this guideline contains nonpharmacologic and pharmacologic interventions for symptomatic osteoarthritis of the knee, including surgical procedures less invasive than knee arthroplasty. It does not provide recommendations for patients with rheumatoid arthritis, arthritis of other joints, or other imflammatory athropathies. This guideline contains 29 recommendations to assist all qualified and appropriately trained healthcare professionals involved in the nonarthroplasty management of osteoarthritis of the knee and provide information for patients. In addition, the work group highlighted the need for better research into intra-articular corticosteroid, hyaluronic acid, and platelet-rich plasma detailing osteoarthritis characterization, including subgroup analyses and osteoarthrosis severity stratification, and clinically relevant outcomes with control subjects for bias and cost-effectiveness analysis. Studies comparing outcomes in patients with mild-to-moderate knee osteoarthritis and an MRI confirmed meniscal tear who have undergone partial meniscectomy after failing to improve with a course of conservative treatment (nonsteroidal anti-inflammatory drugs, steroid injection, and physical therapy) versus those who have undergone partial meniscectomy without a dedicated course of conservative treatment. Prospective randomized trials or prospective cohort studies are still needed to establish efficacy of individual oral nonsteroidal anti-inflammatory drugs within specific subgroups and populations to tailor systemic medications to help increase efficacy and decrease the risk of adverse effects.
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  • 文章类型: Case Reports
    OBJECTIVE: Case report based presentation of the current German interdisciplinary guideline on the diagnosis and management of juvenile idiopathic arthritis-associated (JIA) uveitis.
    METHODS: Guideline of the German Society of Ophthalmology, the Society of Paediatric and Adolescent Rheumatology, the German Society of Rheumatology, the Professional Association of German Ophthalmologists, with the participation of patient representatives. Recent primary publications were critically graduated for evidence and recommendations; the methodology included consensus building through Delphi rounds and external peer review. The outcomes are presented with typical case studies.
    RESULTS: Once JIA is first diagnosed, periodic ophthalmological check-ups should promptly be instituted ensuring that uveitis is diagnosed before irreversible sequelae become manifest. High-quality patient care can be provided depending on the severity of each uveitis case. At present, anti-inflammatory treatment relies on corticosteroids, conventional synthetic (cs), biological (b) and other disease-modifying anti-rheumatic drugs (DMARDs).
    CONCLUSIONS: Timely diagnosis and state-of-the-art guideline-based management can significantly improve the long-term outcome of JIA-associated uveitis.
    UNASSIGNED: Darstellung der aktuellen deutschsprachigen interdisziplinären Leitlinie zur Diagnostik und Therapie der JIA-assoziierten Uveitis (JIA: juvenile idiopathische Arthritis) anhand von Kasuistiken.
    METHODS: Leitlinie der Deutschen Ophthalmologischen Gesellschaft, der Gesellschaft für Kinder- und Jugendrheumatologie, der Deutschen Gesellschaft für Rheumatologie, des Berufsverbandes der Augenärzte Deutschlands unter Beteiligung von Patientenvertretern. Die unlängst publizierte Primärliteratur wurde kritisch bewertet hinsichtlich Evidenz und Empfehlungen; methodisch wurden Konsensfindung mittels Delphi-Runden und eine externe Begutachtung einbezogen. Die Ergebnisse werden anhand von typischen Fallbeispielen erläutert.
    UNASSIGNED: Bei JIA-Erstdiagnose sollten regelmäßige augenärztliche Kontrollen erfolgen mit dem Ziel, dass die Uveitis vor Manifestation irreversibler Folgeschäden diagnostiziert wird. Entsprechend dem individuellen Schweregrad der Uveitis kann eine qualitativ hochwertige Versorgung der Patienten erzielt werden. Zur antientzündlichen Therapie finden aktuell Kortikosteroide, konventionell synthetische (cs) und biologische (b) und andere Disease-modifying anti-rheumatic Drugs (DMARDs) Verwendung.
    UNASSIGNED: Frühzeitige Diagnose und aktuelle leitliniengerechte Therapie können die Langzeitprognose der JIA-assoziierten Uveitis wesentlich verbessern.
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  • 文章类型: Journal Article
    Hospitalised patients with coronavirus disease 2019 (COVID-19) have a high mortality rate. There are an increasing number of published randomised controlled trials for anti-inflammatory, anti-viral and other treatments. The European Respiratory Society Living Guidelines for the Management of Hospitalised Adults with COVID-19 were published recently, providing recommendations on appropriate pharmacotherapy.Patient, Intervention, Comparator and Outcomes questions for key interventions were identified by an international panel and systematic reviews were conducted to identify randomised controlled trials meeting the inclusion criteria. The importance of end-points were rated, and mortality was identified as the key \"critical\" outcome for all interventions. Random-effects meta-analysis was used to pool studies and provide effect estimates for the impact of treatments on mortality.Corticosteroids, hydroxychloroquine, azithromycin, remdesivir, anti-interleukin (IL)-6 monoclonal antibodies, colchicine, lopinavir/ritonavir and interferon-β have been reviewed.Our results found further evidence in support of the use of corticosteroids, particularly dexamethasone, and anti-IL-6 receptor monoclonal antibody therapy. These data support the need to identify additional therapies with beneficial effects on mortality.
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  • 文章类型: Consensus Development Conference
    炎症性肠病(IBD)患者发生血栓事件的风险增加。IBD的疗法有可能调节这种风险。本循证指南的目的是总结现有证据并提供有关流行病学方面的实用建议。IBD患者静脉和动脉血栓事件的预防和药物相关风险。2020年5月举行了一次虚拟会议,来自12个国家的14名国际IBD专家和3名血栓形成专家参加了会议。拟议的声明以匿名方式进行了表决。协议被定义为至少75%的参与者投票“完全同意”或“大多数同意”。对于每个语句,根据苏格兰校际指南网络(SIGN)分级系统对证据水平进行分级.达成了19项声明的共识。IBD患者静脉和动脉血栓事件的风险增加。IBD患者因任何原因住院期间需要预防血栓。疾病活动是IBD患者的一个可改变的危险因素,医生应致力于实现深度缓解以降低风险。应限制接触类固醇。抗肿瘤坏死因子药物可能与降低血栓形成事件的风险有关。
    Patients with inflammatory bowel disease (IBD) are at increased risk of thrombotic events. Therapies for IBD have the potential to modulate this risk. The aims of this Evidence-Based Guideline were to summarize available evidence and to provide practical recommendations regarding epidemiological aspects, prevention and drug-related risks of venous and arterial thrombotic events in patients with IBD. A virtual meeting took place in May 2020 involving 14 international IBD experts and 3 thrombosis experts from 12 countries. Proposed statements were voted upon in an anonymous manner. Agreement was defined as at least 75% of participants voting as \'fully agree\' or \'mostly agree\' with each statement. For each statement, the level of evidence was graded according to the Scottish Intercollegiate Guidelines Network (SIGN) grading system. Consensus was reached for 19 statements. Patients with IBD harbour an increased risk of venous and arterial thrombotic events. Thromboprophylaxis is indicated during hospitalization of any cause in patients with IBD. Disease activity is a modifiable risk factor in patients with IBD, and physicians should aim to achieve deep remission to reduce the risk. Exposure to steroids should be limited. Antitumour necrosis factor agents might be associated with a reduced risk of thrombotic events.
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  • 文章类型: Consensus Development Conference
    The pandemic caused by the SARS-CoV-2 virus declared by the WHO in March 11th 2020, affects a small number of pediatric patients, who mostly present mild respiratory compromise and favorable evolution. However began to be observed in previously healthy children, an increase in cases defined as \"Multisystemic Inflammatory Syndrome\" (MIS-C) or \"Kawasaki-like\" post-COVID 19 (KLC) that evolve to shock and require hospitalization in the Pediatric Intensive Care Unit. MIS-C and KL-C are characterized by fever; signs of inflammation, gastrointestinal symptoms, and cardiovascular dysfunction, associated with sever forms of presentation with higher incidence of hypotension and/or shock. In the laboratory, markers of inflammation, hypercoagulability and myocardial damage are observed. Firstline drug treatment consists of intravenous immunoglobulin plus oral acetylsalicylic acid. A multidisciplinary approach is recommended for an accurate diagnosis and an early and effective treatment, in order to reduce morbidity and mortality.
    La pandemia ocasionada por el nuevo coronavirus (SARS-CoV-2), declarada por la Organización Mundial de la Salud OMS) en marzo de 2020, afecta a un reducido número de pacientes pediátricos, quienes presentan, en su mayoría, compromiso respiratorio leve y evolución favorable. Sin embargo, en niños previamente sanos, comenzó a observarse un aumento de casos definidos como síndrome inflamatorio multisistémico (SIM-C) o similar a Kawasaki (Kawasaki-like) asociado a la enfermedad por el nuevo coronavirus (COVID-19) (KL-C) que evolucionan al shock y requieren internación en la unidad de cuidados intensivos. Los cuadros de SIM-C y los KL-C se caracterizan por fiebre, signos de inflamación, síntomas gastrointestinales y disfunción cardiovascular; las formas graves de presentación tienen mayor incidencia de hipotensión y/o shock. En el laboratorio se observan marcadores de inflamación, hipercoagulabilidad y daño miocárdico. El tratamiento farmacológico de primera línea consiste en la administración de inmunoglobulina por vía intravenosa más ácido acetilsalicílico por vía oral. Se recomienda un abordaje multidisciplinario para un diagnóstico certero y un tratamiento temprano y eficaz para disminuir la morbimortalidad.
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