A Case of Status Epilepticus Caused by Intravenous Tramadol

Q4 Medicine
S. Y. Kim, Young Eun Kim, Kook Won Kim, Sungwon Byun
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引用次数: 1

Abstract

Tramadol is a recently developed, centrally acting synthetic analgesic agent. The pharmacological mechanism of tramadol has not yet been fully elucidated, but unlike standard opioid analgesics, tramadol alleviates pain by modulating norepinephrine secretion and inhibiting serotonin reuptake [1]. The potency of tramadol is between 10% and 25% of that of morphine at the μ-opioid receptor, so it is considered a “weak opioid.” For this reason, it is regarded as relatively safe. Tramadol has been commonly used for postoperative pain treatment in children who have mild to moderate pain. The recommended dose for the intravenous (IV) route for children is 2 mg/kg every 4 to 6 hours, which is best for analgesic action with minimal side effects [2]. However, tramadol has some unique properties compared to other standard opioid medications that are attributable to its mechanism of inhibiting monoamine reuptake. Examples of the adverse effects of tramadol include respiratory depression, seizure, tachycardia, hypertension, serotonin syndrome, and manic syndrome [3]. Seizures have been noted as a concerning side effect of tramadol since its market approval in the United States in 1995, based on post-marketing reports to the U.S. Food and Drug Administration (FDA). Between 1997 and 2017, 30,730 tramadol-related cases had been reported to the FDA's Adverse Event Reporting System, and seizures accounted for 7% of the cases [4]. The FDA issued a black-box warning in 2017, banning the use of tramadol in children and adolescents under the age of 12, and in those aged 12 to 18 with underlying diseases, due to its potential to cause serious respiratory side effects and death [5]. Despite the FDA’s warning, tramadol continues to be given, which is worrisome. Here, we present a case of tramadol-induced status epilepticus in a 15-year-old girl with no past history of seizures. A 15-year-old girl (height, 159 cm; weight, 47 kg) presented to the emergency department due to abdominal pain. She had normal developmental milestones and her past medical history was unremarkable. She had undergone laparoscopic left ovarian cystectomy (pathology: functional cyst) 23 days earlier. A clinical examination revealed normal hemodynamic variables, and there was no sign of dehydration, or fever. On physical examination, widespread abdominal tenderness without rebound tenderness was found, while other physical examination and lab test results were normal. Abdominopelvic computed tomography (CT) showed paralytic small bowel ileus. She was referred to the gynecology department for conservative management. The patient was given 30 mg of IV ketorolac tromethamine (Trolac, Whanin Pharm Co., Seoul, Korea) and 100 mg of IV tramadol (Tandol, AJU Pharm Co., Seoul, Korea). Since the pain persisted, IV tramadol was
曲马多静脉注射致癫痫状态1例
曲马多是最近开发的一种集中作用的合成镇痛剂。曲马多的药理机制尚未完全阐明,但与标准的阿片类止痛药不同,曲马多通过调节去甲肾上腺素分泌和抑制血清素再摄取来减轻疼痛[1]。曲马多在μ-阿片受体上的效力是吗啡的10%至25%,因此被认为是“弱阿片”。因此,它被认为是相对安全的。曲马多通常用于轻度至中度疼痛儿童的术后疼痛治疗。儿童静脉注射(IV)途径的推荐剂量为每4至6小时2 mg/kg,这对镇痛作用最好,副作用最小[2]。然而,与其他标准阿片类药物相比,曲马多具有一些独特的特性,这归因于其抑制单胺再摄取的机制。曲马多的不良反应包括呼吸抑制、癫痫发作、心动过速、高血压、血清素综合征和躁狂综合征[3]。根据提交给美国食品药品监督管理局(FDA)的上市后报告,曲马多自1995年在美国上市以来,缉获一直被认为是一种令人担忧的副作用。1997年至2017年间,美国食品药品监督管理局的不良事件报告系统报告了30730例曲马多相关病例,癫痫发作占病例的7%[4]。美国食品药品监督管理局在2017年发布了一项黑匣子警告,禁止12岁以下的儿童和青少年以及12至18岁患有潜在疾病的人使用曲马多,因为它可能会导致严重的呼吸道副作用和死亡[5]。尽管美国食品药品监督管理局发出警告,曲马多仍在继续使用,这令人担忧。在此,我们报告一例曲马多诱导的15岁女孩癫痫持续状态,该女孩既往无癫痫病史。一名15岁女孩(身高159厘米,体重47公斤)因腹痛被送往急诊科。她有正常的发育里程碑,过去的病史并不明显。23天前,她接受了腹腔镜左卵巢囊肿切除术(病理学:功能性囊肿)。临床检查显示血流动力学变量正常,没有脱水或发烧的迹象。体格检查发现腹部广泛压痛,无反弹性压痛,其他体格检查和实验室检查结果正常。腹部计算机断层扫描(CT)显示麻痹性小肠梗阻。她被转诊到妇科进行保守治疗。给患者静脉注射30 mg酮咯酸氨丁三醇(Trolac,Whanin Pharm Co.,Seoul,Korea)和100 mg曲马多(Tandol,AJU Pharm Co.)。由于疼痛持续,静脉注射曲马多
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来源期刊
Annals of Child Neurology
Annals of Child Neurology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.50
自引率
0.00%
发文量
35
审稿时长
8 weeks
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