phentermine-topiramate

  • 文章类型: Case Reports
    肥胖是一种全球流行病,在大多数国家患病率稳步上升。面对暴饮暴食和避免身体活动的诱惑,减肥对于患者来说通常是具有挑战性的。因此,临床医生和患者都可能转向使用厌食症。我们报告了一个33岁的女性,没有明显的心脏病史,出现呼吸困难,生产性咳嗽,和胸压持续1个月,被诊断为新发心力衰竭,长期使用苯丁胺后射血分数降低。作者旨在强调芬特明诱发心力衰竭的潜力,即使在一个年轻的,相对健康的人,尤其是在肥胖人口不断增长的情况下。最终,健康的减肥可以通过实施饮食改变和鼓励足够的身体活动来实现,正如世界卫生组织(WHO)所建议的那样。厌食药物可用于短期使用。关于芬特明长期副作用的进一步研究可能会避免处方者和患者滥用该药物。
    Obesity is a global epidemic with steadily increasing prevalence in most countries. Weight loss is generally challenging for patients to tackle in the face of the temptation to overeat and avoid physical activity. Hence, clinicians and patients alike are likely to steer toward the use of anorexigens. We report the case of a 33-year-old female with no significant cardiac history who presented with dyspnea, productive cough, and chest pressure for one month and was diagnosed with new-onset heart failure with a reduced ejection fraction secondary to prolonged phentermine use. The authors aim to highlight phentermine\'s potential for precipitating heart failure, even in a young, relatively healthy person, especially with a growing obese population. Ultimately, healthy weight loss can be achieved by implementing dietary changes and encouraging adequate physical activity, as the World Health Organization (WHO) recommended. Anorectic drugs may be employed for short-term use. Further research concerning the long-term side effects of phentermine may avert the prescriber and patient from abusing this drug.
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  • 文章类型: Journal Article
    肥胖是一种最近定义的疾病,其诊断和治疗继续受到污名化。目前,由于技术进步带来的生活方式的改变以及高热量食品的广泛供应和可负担性,全世界有数百万人患有肥胖症和/或其后遗症。因此,找到适当的预防和治疗方案将导致受影响个体的持续时间和生活质量的大幅改善。在这次审查中,我们在PubMed数据库中搜索了探索FDA目前批准用于治疗肥胖症的5种药物的安全性和有效性的研究.我们只纳入了2012年至2022年间发表的关于成年患者的研究。我们发现了所有分析的药物如奥利司他的证据,苯丁胺/托吡酯,纳曲酮/安非他酮,利拉鲁肽,塞马鲁肽似乎能有效诱导体重减轻,建议司马鲁肽可能具有更好的疗效。然而,制定治疗指南的一个巨大障碍仍然是缺乏监测肥胖药物长期安全性和有效性的长期研究.然而,在有肥胖并发症风险的患者中,减少脂肪量的益处可能超过与这些药物相关的潜在副作用,临床医生应开出他们认为最适合患者具体情况的FDA批准的药物疗法.
    Obesity is a recently defined illness whose diagnosis and treatment continue to be stigmatized. Currently, due to lifestyle changes brought on by technological advancements and the wide availability and affordability of high-calorie foods, millions of people around the world suffer from obesity and/or its sequelae. Finding adequate prevention and treatment options would therefore lead to massive improvements in the duration and quality of life of affected individuals. In this review, we searched the PubMed database for studies exploring the safety and efficacy of the five medications currently approved by the FDA for the treatment of obesity. We included only studies pertaining to adult patients that have been published between 2012 and 2022. We found evidence that all the drugs analyzed such as orlistat, phentermine/topiramate, naltrexone/bupropion, liraglutide, and semaglutide appear to be effective in inducing weight loss, with the suggestion that semaglutide may have superior efficacy. However, a massive obstacle in developing treatment guidelines remains the lack of prolonged studies monitoring the long-term safety and efficacy of obesity medications. Nevertheless, in patients at risk of complications from obesity, the benefits of losing fat mass may outweigh the potential side effects associated with these medications and clinicians should prescribe whichever of the FDA-approved pharmacotherapy they deem most appropriate for the patient\'s specific set of circumstances.
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  • 文章类型: Editorial
    暂无摘要。
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    文章类型: Journal Article
    Objective: The goal of this study was to obtain preliminary data on the usefulness of the combination of phentermine and topiramate extended release (phentermine-topiramate) in binge-eating disorder (BED) associated with obesity or overweight. Design: Ten participants with BED and obesity or overweightness with at least one weight-related complication received phentermine-topiramate in an open-label, prospective, 12-week trial. The primary outcome measure was change in weight. The study was registered under the identifier NCT02659475 at ClinicalTrials.gov. Results: Seven participants completed the study. Phentermine-topiramate treatment was associated with significant reductions in weight, body mass index, binge-eating episode frequency, and measures of global clinical severity, eating disorder psychopathology, and obsessive-compulsive symptoms. Mean daily dose of phentermine-topiramate at endpoint was 6.8 to 41.4mg per day. The most common adverse event (AE) was dysgeusia. There were no serious AEs, and no participants displayed symptoms of medication misuse or withdrawal. Conclusion: Phentermine-topiramate could be helpful for weight loss and reduction of binge-eating symptoms in patients with obesity or overweight in addition to BED. Controlled studies are warranted.
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  • 文章类型: Journal Article
    肥胖症正以惊人的速度在全球蔓延。肥胖的管理是多方面的,包括生活方式的改变作为基石。直到只有奥利司他被批准长期用于肥胖症。2012年,美国食品和药物管理局批准了2012年中期芬特明速释和托吡酯缓释的固定剂量组合,用于治疗患有共病的肥胖患者或超重患者。与安慰剂相比,这种新药的体重减轻时间长达2年。
    Obesity is spreading globally at an alarming speed. The management of obesity is multifaceted and includes lifestyle modifications as the cornerstone. Until only orlistat was approved for long term use in obesity. The US Food and Drug Administration granted approval to a fixed dose mid 2012 combination of phentermine immediate release and topiramate extended release in 2012 for treatment of obese patients or overweight patients with comorbid conditions. The new drug has shown significant weight loss compared with placebo for a period up to 2 years.
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  • 文章类型: Comparative Study
    在过去的几十年中,肥胖在发达国家和发展中国家已成为越来越大的流行病,令人震惊。关于肥胖最令人不安的事实是冠状动脉疾病的易感性增加,充血性心力衰竭和心脏性猝死。目前的抗肥胖药物如奥利司他的适度疗效和几种抗肥胖药物如西布曲明的戒断增加,利莫那班导致了肥胖药物治疗的巨大空白。Lorcaserin和苯丁胺-托吡酯组合(phen-top)是2012年美国FDA批准的两种药物。Lorcaserin,5HT2C激动剂具有中等疗效和可接受的安全性。Phen-top的临床试验显示出合理的疗效,但以致畸性和精神障碍等风险为代价。Cetilistat,据称,一种脂肪酶抑制剂的安全性优于奥利司他,目前正在进行3期临床试验。在临床试验中作用于肠道的其他有希望的抗肥胖分子包括艾塞那肽和利拉鲁肽。作用于单胺能和阿片样物质系统的药物包括安非他酮-纳曲酮和安非他酮-唑尼沙胺。其他已经被探索并在早期临床开发中取得有限成功的新型一流药物包括velneperit,特索芬辛,还有Beloranib.Tesofensine是一种三重单胺再摄取抑制剂,velneperit充当神经肽Y5受体拮抗剂,beloranib是甲硫氨酸氨基肽酶2抑制剂。新的靶标,如组胺H3受体,VEGF,基质金属蛋白酶,沉默酶受体也在研究中。这篇综述试图描述肥胖临床开发中的新分子和新兴分子。
    Obesity has become a growing pandemic of alarming proportions in the developed and developing countries over the last few decades. The most perturbing fact regarding obesity is the increased predisposition for coronary artery disease, congestive heart failure and sudden cardiac death. The modest efficacy of current anti-obesity agents such as orlistat and the increasing withdrawals of several anti-obesity agents such as sibutramine, rimonabant have led to huge gaps in the pharmacotherapy of obesity. Lorcaserin and Phentermine-topiramate combination (phen-top) are two drugs approved by US FDA in 2012. Lorcaserin, a 5HT2C agonist has moderate efficacy with an acceptable safety profile. Clinical trials with Phen-top have shown a reasonable efficacy but at the cost of risks such as teratogenicity and psychiatric disturbances. Cetilistat, a lipase inhibitor is claimed to have superior safety profile to orlistat and is in phase 3 clinical trials. Other promising anti-obesity molecules acting on the gut which are in clinical trials include exenatide and liraglutide. Drugs which act on the monoaminergic and opioid systems include bupropion-naltrexone and bupropion-zonisamide. Other novel first-in-class drugs which have been explored and have limited success in early clinical development include velneperit, tesofensine, and beloranib. Tesofensine is a triple monoamine re-uptake inhibitor, velneperit acts as a neuropeptide Y5 receptor antagonist and beloranib is a methionine amino peptidase 2 inhibitor. Novel targets such as histamine H3 receptor, VEGF, matrix-metalloproteinase, sirtuin receptors are also being investigated. This review is an attempt to describe the new and emerging molecules that are in clinical development for obesity.
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