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一例普瑞巴林中毒病例。

A case of pregabalin intoxication.

作者信息

Miljevic C, Crnobaric C, Nikolic S, Lecic-Tosevski D

机构信息

Institute of Mental Health, Belgrade.

出版信息

Psychiatriki. 2012 Apr-Jun;23(2):162-5.

PMID:22796916
Abstract

Pregabalin, or S-(+)-3-isobutylgaba, is a lipophilic analogue of GABA. Although pregabalin is structurally related to GABA, it is inactive at GABA receptors and does not appear to mimic GABA physiologically. Pregabalin is a potent ligand for the alpha-2-delta subunit of voltage-gated calcium channels in the central nervous system. It is currently being licensed for epilepsy, neuropathic pain, and generalized anxiety disorder. There are few case reports that have demonstrated safety of pregabalin in case of intoxication. We report here a case of pregabalin toxicity with a moderate pregabalin concentration that was successfully managed with conservative treatment only. The case report describes a 54-year-old man who was treated with pregabalin for generalized anxiety disorder. After having experienced a significant stress on a job the patient ingested huge amount of pregabalin (4,2 r) together with bromazepam (21 mg) and chlorimipramine (125 mg). On presentation he was conscious and alert with a stable condition of cardiovascular and respiratory systems. The serum pregabalin concentration was 20.8 mg/L but the patient did not have any signs of toxicity. Thanks to his good and stable somatic condition the patient was managed with supportive treatment only. Although anecdotal, our case report points toward safety of pregabalin following deliberate self-poisoning. Our observation is in accordance with the recent international literature underlining that pregabalin was listed as the drug ingested in only 1% of fatalities, usually in combination with other drugs.

摘要

普瑞巴林,即S-(+)-3-异丁基γ-氨基丁酸,是γ-氨基丁酸(GABA)的亲脂性类似物。尽管普瑞巴林在结构上与GABA相关,但它在GABA受体上无活性,且在生理上似乎不会模拟GABA的作用。普瑞巴林是中枢神经系统电压门控钙通道α-2-δ亚基的强效配体。它目前已获批准用于治疗癫痫、神经性疼痛和广泛性焦虑症。很少有病例报告证明普瑞巴林在中毒情况下的安全性。我们在此报告一例普瑞巴林中毒病例,其普瑞巴林浓度适中,仅通过保守治疗就成功治愈。该病例报告描述了一名54岁男性,因广泛性焦虑症接受普瑞巴林治疗。在工作中经历重大压力后,该患者摄入了大量普瑞巴林(4200毫克)以及溴西泮(21毫克)和氯米帕明(125毫克)。就诊时,他意识清醒,心血管和呼吸系统状况稳定。血清普瑞巴林浓度为20.8毫克/升,但患者没有任何中毒迹象。由于其良好且稳定的身体状况,该患者仅接受了支持性治疗。尽管只是个案,但我们的病例报告表明普瑞巴林在蓄意自我中毒后是安全的。我们的观察结果与最近的国际文献一致,该文献强调普瑞巴林仅在1%的死亡病例中被列为摄入药物,通常是与其他药物联合使用。

相似文献

1
A case of pregabalin intoxication.一例普瑞巴林中毒病例。
Psychiatriki. 2012 Apr-Jun;23(2):162-5.
2
Pregabalin: a novel gamma-aminobutyric acid analogue in the treatment of neuropathic pain, partial-onset seizures, and anxiety disorders.普瑞巴林:一种新型γ-氨基丁酸类似物,用于治疗神经性疼痛、部分性发作及焦虑症。
Clin Ther. 2007 Jan;29(1):26-48. doi: 10.1016/j.clinthera.2007.01.013.
3
[Pregabalin--a neuromodulator for the treatment of neuropathic pain, generalized anxiety disorders and fibromyalgia syndrome].[普瑞巴林——一种用于治疗神经性疼痛、广泛性焦虑症和纤维肌痛综合征的神经调节剂]
Med Monatsschr Pharm. 2007 Nov;30(11):396-400.
4
[Pregabalin: new therapeutic contributions of calcium channel alpha2delta protein ligands on epilepsy and neuropathic pain].[普瑞巴林:钙通道α2δ蛋白配体对癫痫和神经性疼痛的新治疗作用]
Rev Neurol. 2006;42(4):223-37.
5
Treatment of pregabalin toxicity by hemodialysis in a patient with kidney failure.一名肾衰竭患者通过血液透析治疗普瑞巴林中毒。
Am J Kidney Dis. 2009 Dec;54(6):1127-30. doi: 10.1053/j.ajkd.2009.04.014. Epub 2009 Jun 3.
6
Pregabalin for the treatment of painful neuropathy.普瑞巴林用于治疗疼痛性神经病变。
Expert Rev Neurother. 2006 Nov;6(11):1629-35. doi: 10.1586/14737175.6.11.1629.
7
Intensive monitoring of pregabalin: results from an observational, Web-based, prospective cohort study in the Netherlands using patients as a source of information.对普瑞巴林的强化监测:一项基于网络的前瞻性荷兰队列研究结果,该研究利用患者作为信息来源。
Drug Saf. 2011 Mar 1;34(3):221-31. doi: 10.2165/11585030-000000000-00000.
8
Pregabalin is increasingly prescribed for neuropathic pain, generalised anxiety disorder and epilepsy but many patients discontinue treatment.普瑞巴林越来越多地被用于治疗神经性疼痛、广泛性焦虑障碍和癫痫,但许多患者会中断治疗。
Int J Clin Pract. 2014 Jan;68(1):104-10. doi: 10.1111/ijcp.12182. Epub 2013 Jul 1.
9
[Pregabalin (Lyrica)].[普瑞巴林(乐瑞卡)]
Masui. 2013 Jul;62(7):808-13.
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[Pregabalin (Lyrica) and neuropathic pain syndromes].[普瑞巴林(乐瑞卡)与神经性疼痛综合征]
Rev Med Brux. 2006 Sep-Oct;27(5):445-50.

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Drugs. 2017 Mar;77(4):403-426. doi: 10.1007/s40265-017-0700-x.