苏弗雷克桑和伦博雷克桑的短期有效性和安全性:一项回顾性研究
Koki Mori1, Michio Kimura1, Eiseki Usami1
1Pharmacy, Ogaki Municipal Hospital, Ogaki, JPN.
Cureus
|November 8, 2024
概括
伦博雷克桑在治疗失眠的最初几天里,比苏沃雷克桑更有效地改善了睡眠时间. 虽然这两种素受体对抗剂 (ORA) 都比二zepines更安全,但lemborexant对睡眠持续时间的早期影响更强.
科学领域:
- 药理学 药理学是指药理学的学科.
- 睡眠医学 睡眠医学
- 临床研究 临床研究
背景情况:
- 长期使用二二类药物对失眠治疗有风险.
- 素受体对抗剂 (ORA) 为治疗失眠提供了更安全的替代方案.
- 比较新的ORAs,如suvorexant和lemborexant对于临床实践至关重要.
研究的目的:
- 为了比较suvorexant和lemborexant在治疗失眠方面的疗效和安全性.
- 评估早期睡眠时间作为主要疗效终点.
- 评估跌倒发生率作为一个关键的安全结果.
主要方法:
- 一项回顾性研究包括了105名新处方suvorexant或lemborexant的患者.
- 排除标准包括同时服用睡眠药物或抗精神病药物.
- 主要终点:睡眠时间 (前3天);次要终点:跌倒发生率.
主要成果:
- 与基线相比,lemborexant在所有三天都显著增加了睡眠时间;suvorexant在第二天和第三天显著增加了睡眠时间.
- 伦博雷克桑在第一天的睡眠时间显著增加 (5.93±1.90小时) 与苏博雷克桑 (5.10±1.84小时) 相比.
- 在两组中,跌倒发病率都很低 (0%为suvorexant,5.3%为lemborexant),没有统计学上显著的差异.
结论:
- 与suvorexant相比,Lemborexant在治疗的第一天对睡眠时间产生了更强大的影响.
- 这种增强的疗效可能归因于勒博雷克桑特对素2受体的强烈抑制.
- 这两种ORA都代表了对二类药物治疗失眠的可行的替代品,而勒博雷克桑特显示出更强的初始睡眠诱导.
相关概念视频
Sedatives and Hypnotics Drugs: Miscellaneous Agents
146
Sedatives and hypnotics encompass a wide range of substances, each with its unique mechanism of action, uses, and potential adverse effects.
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
146
Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein
253
Antiepileptic drugs, such as levetiracetam (Keppra) and brivaracetam (Briviact), have emerged as crucial tools in managing epilepsy. These medications exert their therapeutic effects by targeting the synaptic vesicle protein SV2A, a transmembrane glycoprotein primarily found in the brain.
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
253
Antidepressant Drugs: MAOIs and Other Agents
195
Atypical antidepressants, including bupropion (Wellbutrin), mirtazapine (Remeron), nefazodone (Serzone), trazodone (Desyrel), and vilazodone (Viibryd), offer unique mechanisms of action. Bupropion weakly inhibits dopamine and norepinephrine reuptake, aiding depression treatment and smoking cessation, with a low risk of sexual dysfunction. Mirtazapine enhances serotonin and norepinephrine neurotransmission, leading to sedation, increased appetite, and weight gain. As a result, it helps treat...
195
Antiepileptic Drugs: Potassium Channel Activators
147
Ezocgabine or retigabine, an antiepileptic drug of remarkable efficacy, has revolutionized the management of seizures. It is a potassium channel activator, explicitly targeting the family of Q subtype potassium channels. It enhances the transmembrane potassium currents, regulating neuronal excitability. This action stabilizes the resting membrane potential, a pivotal factor in mitigating the hyperexcitability that characterizes epilepsy.
Ezogabine has gained approval as an adjunctive treatment...
Ezogabine has gained approval as an adjunctive treatment...
147
Anxiolytic Drugs: Benzodiazepines and Buspirone
525
Benzodiazepines are a class of anxiolytic drugs known for their rapid efficacy and high therapeutic-to-lethal dose ratio, but with a potential risk of drug dependence. These drugs are lipophilic, allowing for rapid absorption after oral administration, eventually reaching the central nervous system (CNS). Once in the CNS, benzodiazepines bind to the allosteric site of the GABAA receptor. This binding enhances the inhibitory effects of the neurotransmitter GABA. By doing so, they prevent...
525
Skeletal Muscle Relaxants: Adverse Effects
337
Skeletal muscle relaxants are widely used for muscle paralysis and relieving pain following any muscle injury or stiffness. However, depending on the drug type, they can have adverse effects that range from mild to severe. Usually, nondepolarizing neuromuscular blockers have minimal side effects. For example, drugs like d-tubocurarine, cisatracurium, and rocuronium cause hypotension, whereas drugs like baclofen, when stopped abruptly, can lead to the recurrence of spastic conditions.
Unlike...
Unlike...
337


