静脉注射羧麦芽糖铁作为严重屏气症的抢救治疗:1例报告及文献复习

Q4 Medicine
Hee Jeong Yun, W. Kim, Jon Soo Kim
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引用次数: 0

摘要

儿童期常见的阵发性、行为性、不自主发作,在6至48个月的健康儿童中发生率高达4.6%。它们通常是由情绪刺激引发的,比如愤怒、沮丧、恐惧或受伤。自主神经系统和副交感心肺反射的失调或不稳定可能是BHS的可能证据,但其确切的致病机制尚不完全清楚[2,3]。bhs可分为紫绀或苍白;这些症状持续大约10到60秒,大多会自发消退。bhs的严重并发症是罕见的,但猝死,心脏骤停时间延长和癫痫持续状态的病例已被报道。缺铁性贫血(IDA)被认为是近50%儿童BHS的危险因素。口服补铁在减少屏气发作频率和严重程度方面的有效性是众所周知的[5,6]。在这里,我们描述了一个9个月大的女孩谁经常经历bhs和接受静脉(IV)补铁治疗她的缺氧反复发作。一个9个月大的发育正常的女孩因癫痫样事件来到急诊室(ER)。该事件的特征是剧烈的哭泣,之后她停止哭泣并出现口周紫绀和强直性四肢僵硬并抽搐几分钟。三周前,她有过类似的症状;她在哭泣后停止了呼吸,然后在不知不觉中表现出四肢短暂的抽搐运动和眼球向上倾斜。她是通过自然阴道分娩足月出生的,没有任何围产期问题。她的出生体重是3360克,是母乳喂养的。没有癫痫家族史或类似事件。经检查,生命体征正常,无局灶性神经功能缺损。脑磁共振、脑电图结果正常。除了血红蛋白(Hb)水平为9.4 g/dL和平均红细胞体积为62.4 f l外,实验室检查结果无显著差异。患者被诊断为BHS,并开始经验性口服铁补充剂(5 mg/kg/天的元素铁)。一个月后,她再次来到急诊室,因为她在跌倒时撞到了头部,出现了明确的缺氧发作。在她的过度长时间哭泣停止后,她变成紫绀型伴去饱和,并出现全身性强直-阵挛(GTC)癫痫发作2分钟,pissn 2635-909X•eISSN 2635-9103 Ann Child Neurol [Epub ahead of print] https://doi.org/10.26815/acn.2022.00010
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intravenous Ferric Carboxymaltose as Rescue Therapy in Severe Breath Holding Spells: A Case Report and Literature Review
paroxysmal, behavioral, involuntary episodes frequently seen in childhood, occurring in up to 4.6% of otherwise healthy children aged 6 to 48 months [1]. They are usually triggered by emotional stimuli such as anger, frustration, fear, or injury. Dysregulation or instability of the autonomic nervous system and parasympathetic cardio-respiratory reflexes may represent possible evidence of BHS, but its precise pathogenic mechanisms remain incompletely understood [2,3]. BHSs may be categorized as cyanotic or pallid; the episodes last about 10 to 60 seconds and mostly spontaneously resolve [2]. Serious complications of BHSs are rare, but cases of sudden death, prolonged asystole, and status epilepticus have been reported [4]. Iron deficiency anemia (IDA) has been considered a risk factor for BHS in nearly 50% of children [1]. The effectiveness of oral iron supplementation in reducing the frequency and severity of breath-holding attacks is well-known [5,6]. Here, we describe the case of a 9-month-old girl who frequently experienced BHSs and received intravenous (IV) iron supplementation for her anoxic repetitive seizure attacks. A 9-month-old developmentally normal girl visited the emergency room (ER) with a seizure-like event. The event was characterized by vigorous crying, after which she stopped crying and developed peri-oral cyanosis and tonic stiffening of the limbs and jerking for several minutes. Three weeks previously, she had a similar episode; she stopped being able to breathe after crying and then showed brief convulsive movements of the limbs and upward eyeball deviation without being aware of it. She was born at term via spontaneous vaginal delivery without any perinatal problems. Her birth weight was 3,360 g and she was breastfed. There was no family history of epilepsy or similar events. On examination, vital signs were normal and she had no focal neurologic deficits. Brain magnetic resonance imaging and electroencephalography results were normal. The laboratory findings were unremarkable, except for a hemoglobin (Hb) level of 9.4 g/dL and a mean corpuscular volume of 62.4 f L. The patient was diagnosed with BHS and started on empirical oral iron supplements (5 mg/kg/day of elemental iron). One month later, she re-visited the ER with definite anoxic seizures after having bumped her head while falling. After the cessation of her excessive prolonged crying, she became cyanotic with desaturation and developed generalized tonic-clonic (GTC) seizures for 2 minutes withpISSN 2635-909X • eISSN 2635-9103 Ann Child Neurol [Epub ahead of print] https://doi.org/10.26815/acn.2022.00010
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来源期刊
Annals of Child Neurology
Annals of Child Neurology Medicine-Pediatrics, Perinatology and Child Health
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