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首页> 外文期刊>Journal of Nepal Paediatric Society >Guillain Barre Syndrome: Major Cause of Acute Flaccid Paralysis in Children and Adolescents of Nepal
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Guillain Barre Syndrome: Major Cause of Acute Flaccid Paralysis in Children and Adolescents of Nepal

机译:格林巴利综合征:尼泊尔儿童和青少年急性弛缓性麻痹的主要原因

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Introduction . Guillain Barre Syndrome (GBS) is a post infectious polyneuropathy involving mainly motor but sometimes sensory and autonomic nerves. It is an acquired disease of the peripheral nerves that is characterized by rapidly progressing paralysis, areflexia and albumino-cytological dissociation in CSF. Methodology : Prospective, descriptive, observational, hospital based study was carried out to find out the clinico-epidemiological features of GBS including existing treatment modalities and its outcome. All cases fulfilled the criteria for AFP (Acute flaccid Paralysis) surveillance was included. Cases were reviewed for full medical history and examinations. To confirm the diagnosis, necessary investigations were carried out and combined with clinical symptoms. Results : Thirty patients were included in the study during study period. Among them 90% were diagnosed as GBS, 7.4% patients of GBS were associated with hypokalemic paralysis, 7.4% diagnosed as transverse myelitis and 3.7% diagnosed as idiopathic neuropathy. Different types of GBS were classified as AIDP (Acute inflammatory demyelinating polyneuropathy) 62.96%, AMAN (Acute motor axonal neuropathy) - 25.52%, AMASAN (Acute motor and sensory axonal neuropathy) - 3.3% and MFS (Miller fisher's syndrome) - 6.6% according to NCV result. Male female ratio is 1.7:1.0. There was 14.8% patients had relapse within 5 year. Associated diseases were URTI, pneumonia, sore throat and diarrhea. Facial Nerve palsy was commonest cranial nerve involvement.Sixty percentage of patients presented with sensory symptoms. There was transient bowel and bladder involvement in 20% of the cases. 69.2% patients became bed ridden at the nadir. There was albumin-cytological dissociation in 80% case. Majority of patients improved with supportive treatment alone, 19.5% patient required ventilator support among them 40% died. 7.4% of cases expired during treatment. Half of the patients fully recovered within 3 months. Conclusion: GBS is the commonest cause of AFP, AIDP being commonest subtype in our setting. We have to improve our existing treatment facilities and extend to different centers to detect and treat GBS. Most of the patients improve with supportive treatment alone. Ventilator support indicates grave prognosis. Key words : GBS (Gullein Barre Syndrome); AFP (Acute flaccid Paralysis); AIDP (Acute inflammatory demyelinating polyneuropathy; AMAN (Acute motor axonal neuropathy); AMASAN (Acute motor and sensory axonal neuropathy); MFS (Miller fisher's syndrome). DOI: 10.3126/jnps.v31i2.4065 J Nep Paedtr Soc 2010;31(2):93-97.
机译:介绍 。格林巴利综合征(GBS)是一种感染后多发性神经病,主要涉及运动神经,有时还包括感觉神经和自主神经。它是一种后天性周围神经疾病,其特征是脑脊液中快速进展的麻痹,反射消失和白蛋白细胞学解离。方法:进行前瞻性,描述性,观察性,医院为基础的研究,以发现GBS的临床流行病学特征,包括现有的治疗方式及其结果。所有病例均符合AFP(急性弛缓性麻痹)监测标准。对病例进行了全面的病史检查和检查。为了确认诊断,进行了必要的研究,并结合了临床症状。结果:30名患者在研究期间被纳入研究。其中90%被诊断为GBS,7.4%患者患有低钾性瘫痪,7.4%被诊断为横贯性脊髓炎,3.7%被诊断为特发性神经病。不同类型的GBS分为AIDP(急性炎症性脱髓鞘性多发性神经病)62.96%,AMAN(急性运动轴索神经病)-25.52%,AMASAN(急性运动和感觉轴索神经病)-3.3%和MFS(米勒费雪综合症)-6.6%。根据NCV结果。男女比例为1.7:1.0。 5年内有14.8%的患者复发。相关疾病包括尿道感染,肺炎,喉咙痛和腹泻。面神经麻痹是最常见的颅神经受累.60%的患者出现感觉症状。 20%的病例有短暂的肠和膀胱受累。 69.2%的患者在最低点卧床休息。 80%病例有白蛋白细胞学解离。大多数患者仅通过支持治疗即可改善,需要呼吸机支持的患者占19.5%,其中40%死亡。 7.4%的病例在治疗期间死亡。一半的患者在3个月内完全康复。结论:GBS是导致AFP的最常见原因,而AIDP是本研究中最常见的亚型。我们必须改善现有的治疗设施,并扩展到不同的中心来检测和治疗GBS。大多数患者仅靠支持治疗即可改善。呼吸机支持可指示严重的预后。关键词:GBS(格林巴利综合征); AFP(急性弛缓性麻痹); AIDP(急性炎症性脱髓鞘性多发性神经病; AMAN(急性运动轴突神经病); AMASAN(急性运动和感觉轴突神经病); MFS(米勒费雪综合征)。DOI:10.3126 / jnps.v31i2.4065 J Nep Paedtr Soc 2010; 31(2 ):93-97。

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