Taly A B, Gupta S K, Vasanth A, Suresh T G, Rao U, Nagaraja D, Swamy H S, Rao S, Subbakrishna D K
Department of Neurology, National Institute of Mental Health & Neuro Sciences (NIMHANS), Bangalore.
J Assoc Physicians India. 1994 Nov;42(11):871-4.
Among the 153 patients fulfilling NINDS criteria for Guillain Barre' Syndrome (GBS) seen over 5.5 yrs, there were 47 (M:F 38.9) critically ill patients (age range 4 to 60 years). Antecedent event was recorded in 25 patients and the peak deficit was attained over a mean period of 9.5 days. Besides severe motor paralysis other salient features were: bulbar paralysis--42, sensory symptoms or signs--21, dysautonomia 31 and requirement for ventilatory assistance 45. CSF protein was raised in 63% cases. All the 17 patients who underwent electromyography had abnormalities of nerve conduction paramentes. Mean stay on the ventilator was 29.6 days and was not influenced by corticosteroid. Complications were frequent: pulmonary and urinary tract infection, dysautonomia, electrolyte disturbances, haemetmesis, bleeding from tracheostomy site and hepatic and renal failure. Mortality in steroids treated group (13/27) and the conservatively managed group (5/20) did not differ significantly. No discriminant factor emerged between survivors and non-survivors. Age and sex of the patients, presence of antecedent event, onset to peak interval and CSF protein level did not predict the need for ventilatory assistance, although these patients at admission had more frequent weakness of facial, bulbar, trunk, neck and proximal muscles of upper limbs and autonomic disturbances. Course of GBS remains unpredictable at the onset of the disease, warrants close supervision and meticulous supportive care and remains a therapeutic challenge.
在5.5年期间诊治的153例符合美国国立神经病学、语言障碍和卒中研究所(NINDS)吉兰-巴雷综合征(GBS)标准的患者中,有47例(男∶女为38.9)病情危重患者(年龄范围4至60岁)。25例患者记录到前驱事件,平均9.5天达到肌无力高峰。除严重运动麻痹外,其他显著特征包括:延髓麻痹42例、感觉症状或体征21例、自主神经功能障碍31例、需要通气支持45例。63%的病例脑脊液蛋白升高。接受肌电图检查的17例患者神经传导参数均有异常。平均呼吸机支持时间为29.6天,不受皮质类固醇影响。并发症常见:肺部和尿路感染、自主神经功能障碍、电解质紊乱、呕血、气管造口部位出血以及肝肾功能衰竭。激素治疗组(13/27)和保守治疗组(5/20)的死亡率无显著差异。幸存者和非幸存者之间未发现鉴别因素。患者的年龄、性别、前驱事件的存在、起病至高峰间隔时间和脑脊液蛋白水平均不能预测是否需要通气支持,尽管这些患者入院时面部、延髓、躯干、颈部和上肢近端肌肉无力及自主神经功能障碍更为常见。GBS病程在疾病发作时仍不可预测,需要密切监测和精心的支持治疗,仍然是一个治疗挑战。