首页> 外文期刊>The annals of pharmacotherapy >Intrathecal ziconotide for refractory chronic pain.
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Intrathecal ziconotide for refractory chronic pain.

机译:鞘内注射齐考诺肽治疗顽固性慢性疼痛。

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OBJECTIVE: To describe the pharmacology, efficacy, and safety of ziconotide for treatment of severe chronic pain in patients who are candidates for intrathecal therapy. DATA SOURCES: A PubMed/MEDLINE search (1966-June 2006) was conducted using the terms ziconotide, Prialt, and SNX-111. Manufacturer-provided data, the Food and Drug Administration medical review of ziconotide, and abstracts presented at American Pain Society meetings (2001-2006) were also reviewed. STUDY SELECTION AND DATA EXTRACTION: Human studies evaluating the efficacy and safety of ziconotide for the treatment of chronic pain were considered. Animal data were excluded. DATA SYNTHESIS: Ziconotide is the first and only neuronal-type (N-type) calcium-channel blocker. Ziconotide must be administered intrathecally via continuous infusion. A programmable implanted variable-rate microinfusion device, or an external microinfusion device and catheter must be utilized. In double-blind, placebo-controlled studies, ziconotide significantly improved patient perception of pain from baseline to the end of the study periods, which ranged from 11 to 21 days. Patients enrolled in clinical trials were intolerant of or refractory to other treatment modalities. There have been no studies that directly compared ziconotide with other intrathecal or systemic analgesics. Key ziconotide-related adverse events are neuropsychiatric, including depression, cognitive impairment, and hallucinations; depressed levels of consciousness; and elevation of creatine kinase levels. Ziconotide is also associated with a risk of meningitis due to possible contamination of the microinfusion device. CONCLUSIONS: Ziconotide is a therapeutic option for treatment of severe chronic pain in patients who have exhausted all other agents, including intrathecal morphine, and for whom the potential benefit outweighs the risks of serious neuropsychiatric adverse effects and of having an implanted device. Further studies are needed to determine the comparative efficacy of ziconotide and other pain therapies.
机译:目的:描述齐考诺肽治疗鞘内注射候选患者的严重慢性疼痛的药理学,疗效和安全性。数据来源:使用术语ziconotide,Prialt和SNX-111进行了PubMed / MEDLINE搜索(1966年6月至2006年6月)。还审查了制造商提供的数据,食品和药物管理局对ziconotide的医学评论以及在美国疼痛学会会议(2001-2006年)上发表的摘要。研究选择和数据提取:考虑了评估齐考诺肽治疗慢性疼痛的有效性和安全性的人类研究。排除动物数据。数据合成:Ziconotide是第一个也是唯一的神经元型(N型)钙通道阻滞剂。 Ziconotide必须通过连续输注在鞘内给药。必须使用可编程的植入式可变速率微输注设备,或外部微输注设备和导管。在双盲,安慰剂对照研究中,齐考诺肽从基线到研究结束(从11天到21天不等)显着改善了患者对疼痛的感知。参加临床试验的患者对其他治疗方式不耐受或不耐受。尚无直接将齐考诺肽与其他鞘内或全身镇痛药进行比较的研究。与Ziconotide相关的主要不良事件是神经精神病,包括抑郁症,认知障碍和幻觉。意识水平低落;和肌酸激酶水平升高。由于微输注装置的可能污染,齐考诺肽还具有脑膜炎的风险。结论:齐考诺肽是一种治疗严重慢性疼痛的治疗方法,该患者已经用尽了所有其他药物,包括鞘内吗啡,并且其潜在获益超过了严重的神经精神不良反应和植入装置的风险。需要进一步的研究来确定齐考诺肽和其他止痛药的比较疗效。

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