伴有潜在脑电图异常的幼儿多潘立酮相关急性肌张力障碍

K. Tang, Fauzana A. Mokhti, J. Fong, Hunainah Khairul Anwar
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引用次数: 2

摘要

多潘立酮是儿童呕吐和胃食管反流的首选治疗方法。众所周知,与甲氧氯普胺相比,它的副作用较小,很少与锥体外系副作用相关。我们报告一个病例急性肌张力障碍在一个4岁的女孩,发生后给予两剂多潘立酮。她最初因持续呕吐到急诊室就诊,并给予多潘立酮糖浆、雷尼替丁和口服补液盐治疗。最后一次口服多潘立酮后约24小时,患者出现5次异常运动,即双侧上肢和下肢僵硬,眼睛盯着一个方向,不眨眼。每次发作持续时间不超过10 s,患者未发生意识丧失。无头部外伤史或任何神经系统疾病家族史记录。病人入院检查以排除癫痫。在病房里,她又出现了两次短暂的类似症状,没有任何治疗就自行消退了。在3天的住院期间,没有发现类似事件再次发生。计算机断层扫描证实无急性颅内出血或局灶性脑损伤。在随后的临床随访中,脑电图显示由于慢波活动增加而出现一些异常记录,但家长不同意进行磁共振成像。患者在一年两次的随访中保持良好,没有任何癫痫发作或肌张力障碍发作。尽管多潘立酮的产品说明书并未提及潜在脑异常或癫痫患者使用的预防措施,但应仔细评估涉及中枢神经系统的罕见不良事件。国际儿科临床杂志,2020;9(2):55-58 doi: https://doi.org/10.14740/ijcp364
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Domperidone-Related Acute Dystonia in a Young Child With Underlying Abnormal Electroencephalogram
Domperidone is the preferred treatment for vomiting and gastroesophageal reflux in pediatric population. It is known to have lesser side effects compared to metoclopramide and is rarely associated with extrapyramidal side effects. We report a case of acute dystonia in a 4-year-old girl that occurred after given two doses of domperidone. She initially presented to the emergency department for persistent vomiting and treated with syrup domperidone, ranitidine and oral rehydration salts. Approximately 24 h after last dose of oral domperidone, she developed five episodes of abnormal movement, i.e. stiffness over bilateral upper and lower limbs with eye staring to one direction without blinking. Each episode lasted for less than 10 s and patient did not lose consciousness. No history of head trauma or any family history of neurological diseases was documented. Patient was admitted for workup to rule out seizure. In ward, she developed another two brief episodes of similar presentations which resolved spontaneously without any treatment. No re-occurrence of similar episodes throughout the 3 days of hospitalization was noted. Computed tomography scan of brain confirmed no acute intracranial bleed or focal brain lesion. Electroencephalogram done during subsequent clinic follow-up noted some abnormal records due to increase in slow delta activity, but parents did not consent for magnetic resonance imaging. Patient remained well on biannual follow-up without any seizure or dystonia episode. Rare adverse event involving the central nervous system should be carefully evaluated although product label for domperidone did not mention precaution of use in patients with underlying cerebral abnormalities or epilepsy. Int J Clin Pediatr. 2020;9(2):55-58 doi: https://doi.org/10.14740/ijcp364
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