Semaglutide

司马鲁肽
  • 文章类型: Editorial
    胰高血糖素样肽受体激动剂(GLP-1RA)用于治疗2型糖尿病,最近,它们在促进减肥方面的有效性引起了人们的注意。它们与几种胃肠道不良反应有关,包括恶心和呕吐。推测这些副作用是由于残留的胃内容物增加。考虑到潜在的误吸风险,并基于有限的数据,美国麻醉医师协会于2023年更新了GLP-1RA患者术前管理指南.其中包括在镇静前强制停止GLP-1RA的持续时间,以及如果在手术前没有适当地服用这些药物,则使用“全胃”预防措施。这导致了更多的挑战,例如延长等待时间,更高的成本,增加患者的风险。在这篇社论中,我们回顾了当前的社会指导方针,临床实践,以及未来关于GLP-1RA在接受内镜手术的患者中使用的方向。
    Glucagon-like peptide receptor agonists (GLP-1RA) are used to treat type 2 diabetes mellitus and, more recently, have garnered attention for their effectiveness in promoting weight loss. They have been associated with several gastrointestinal adverse effects, including nausea and vomiting. These side effects are presumed to be due to increased residual gastric contents. Given the potential risk of aspiration and based on limited data, the American Society of Anesthesiologists updated the guidelines concerning the preoperative management of patients on GLP-1RA in 2023. They included the duration of mandated cessation of GLP-1RA before sedation and usage of \"full stomach\" precautions if these medications were not appropriately held before the procedure. This has led to additional challenges, such as extended waiting time, higher costs, and increased risk for patients. In this editorial, we review the current societal guidelines, clinical practice, and future directions regarding the usage of GLP-1RA in patients undergoing an endoscopic procedure.
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  • 文章类型: Letter
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  • 文章类型: Journal Article
    目的:本指南(GL)旨在为超重或肥胖与代谢并发症相关且对生活方式改变有抵抗力的成年患者的管理提供临床实践参考。
    方法:外科医生,内分泌学家,胃肠病学家,心理学家,药理学家,全科医生,营养学家,一名护士和一名患者代表充当多学科小组。本总账是根据建议评估等级制定的,开发和评估(等级)方法。由一个方法学组进行系统评价和网络荟萃分析。对于每个问题,小组确定了潜在的相关结果,然后对它们对治疗选择的影响进行评级。在对证据的系统评价中,仅考虑了分类为“关键”和“重要”的结果。那些被归类为“关键”的被认为是临床实践建议。通过多数票达成了关于建议的方向(赞成或反对)和强度(有力或有条件)的共识。
    结果:本GL为BMI>27kg/m2和<40kg/m2与体重相关的代谢合并症相关的成年患者人群的临床管理提供了药物和手术治疗的建议。抵制生活方式的改变。小组:建议及时实施治疗干预措施,除了饮食和体力活动;建议使用semaglutide2.4毫克/周,并建议利拉鲁肽3毫克/天的肥胖或超重患者也受糖尿病或糖尿病前期影响;建议semaglutide2.4毫克/周的肥胖或超重患者也受非酒精性脂肪肝影响;建议semagluttide2.4毫克/周作为超重或超重患者的高甘油三酯降低的患者的一剂情绪化饮食;建议手术干预(袖状胃切除术,Roux-en-Y胃旁路术,对于BMI≥35kg/m2的患者,适合进行代谢手术的患者,或代谢性胃旁路术/单次吻合胃旁路术/胃微型旁路术;并建议尽可能进行胃束带术,虽然效果较差,手术替代方案。
    结论:当前的GL针对所有在医院工作的肥胖患者的医生,领土服务或私人执业-以及全科医生和患者。建议还应考虑患者的偏好以及可用的资源和专业知识。
    OBJECTIVE: This guideline (GL) is aimed at providing a clinical practice reference for the management of adult patients with overweight or obesity associated with metabolic complications who are resistant to lifestyle modification.
    METHODS: Surgeons, endocrinologists, gastroenterologists, psychologists, pharmacologists, a general practitioner, a nutritionist, a nurse and a patients\' representative acted as multi-disciplinary panel. This GL has been developed following the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach. A systematic review and network meta-analysis was performed by a methodologic group. For each question, the panel identified potentially relevant outcomes, which were then rated for their impact on therapeutic choices. Only outcomes classified as \"critical\" and \"important\" were considered in the systematic review of evidence. Those classified as \"critical\" were considered for clinical practice recommendations. Consensus on the direction (for or against) and strength (strong or conditional) of recommendations was reached through a majority vote.
    RESULTS: The present GL provides recommendations about the role of both pharmacological and surgical treatment for the clinical management of the adult patient population with BMI > 27 kg/m2 and < 40 kg/m2 associated with weight-related metabolic comorbidities, resistant to lifestyle changes. The panel: suggests the timely implementation of therapeutic interventions in addition to diet and physical activity; recommends the use of semaglutide 2.4 mg/week and suggests liraglutide 3 mg/day in patients with obesity or overweight also affected by diabetes or pre-diabetes; recommends semaglutide 2.4 mg/week in patients with obesity or overweight also affected by non-alcoholic fatty liver disease; recommends semaglutide 2.4 mg/week as first-line drug in patients with obesity or overweight that require a larger weight loss to reduce comorbidities; suggests the use of orlistat in patients with obesity or overweight also affected by hypertriglyceridemia that assume high-calorie and high-fat diet; suggests the use of naltrexone/bupropion combination in patients with obesity or overweight, with emotional eating; recommends surgical intervention (sleeve gastrectomy, Roux-en-Y gastric bypass, or metabolic gastric bypass/gastric bypass with single anastomosis/gastric mini bypass in patients with BMI ≥ 35 kg/m2 who are suitable for metabolic surgery; and suggests gastric banding as a possible, though less effective, surgical alternative.
    CONCLUSIONS: The present GL is directed to all physicians addressing people with obesity-working in hospitals, territorial services or private practice-and to general practitioners and patients. The recommendations should also consider the patient\'s preferences and the available resources and expertise.
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  • 文章类型: Editorial
    非酒精性脂肪性肝病(NAFLD)是一种非常普遍的疾病和未满足的临床需求,我们最近提出将其更名为脂肪肝(FLD),以简化和准确。具有特定的子分类。它通常与代谢合并症有关,包括肥胖,2型糖尿病(T2D),高血压,和高脂血症。由于迄今为止没有联邦和药物管理局(FDA)批准的治疗方法,最近的指南推荐生活方式干预,减肥手术,和药物治疗,即胰高血糖素样肽-1受体激动剂(GLP-1RA),过氧化物酶体增殖物激活受体-γ(PPAR-γ)激动剂,和SGLT-2抑制剂用于其治疗。一种治疗T2D的新药物,泰西帕肽,一个双GIP/GLP-1RA,在指南发布一周后才获得FDA的批准,和正在进行的临床试验表明,不仅对T2D,而且对体重和脂肪变性都有希望的结果。此外,我们意识到在FLD的保护下存在不同的子组,因此,需要更精确的治疗建议,以实现针对这些亚组的个性化医疗和治疗的目标.由于代谢领域进展非常快,并且在可预见的未来,几种分子在发展中很可能在NAFLD治疗中显示出益处,指南需要经常更新。这种快速的变化促使我们提出,准则应作为生活在线文件存在于专业协会的网站上,以便它们继续被更新,并反映出这一医学领域和其他医学领域的快速进展。
    Non-Alcoholic Fatty Liver Disease (NAFLD) is a highly prevalent disease and unmet clinical need that we have recently proposed to be renamed for simplicity and accuracy as Fatty Liver Disease (FLD), with specific subclassifications. It has been commonly associated with metabolic comorbidities, including obesity, type 2 diabetes (T2D), hypertension, and hyperlipidemia. Since no Federal and Drug Administration (FDA) approved treatments exist to date, recent guidelines recommend lifestyle interventions, bariatric surgery, and pharmacotherapy, i.e. glucagon-like peptide-1 receptor agonists (GLP-1RA), peroxisome proliferator-activated receptor-γ (PPAR-γ) agonists, and SGLT-2 inhibitors for its treatment. A new and novel medication for the treatment of T2D, tirzepatide, a dual GIP/GLP-1RA, was approved by the FDA only one week after guidelines were published, and ongoing clinical trials demonstrate promising results not only for T2D but also for body weight and steatosis. Moreover, we realize that distinct subgroups exist under the umbrella of FLD and, thus, more precise therapeutic recommendations would be needed towards the goal of personalized medicine and therapeutics for these subgroups. As the metabolism field is moving forward very fast and as several molecules in development will most likely demonstrate benefits in NAFLD treatment in the foreseeable future, guidelines will need to be frequently updated. This rapid pace of change prompts us to propose that guidelines should exist as living online documents on the websites of professional societies, so that they continue being updated following and reflecting the rapid progress in this and other fields of medicine.
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