Fletcher Simon N, Kennedy Daniel D, Ghosh Indrajit R, Misra Vijay P, Kiff Kevin, Coakley John H, Hinds Charles J
Intensive Care Unit and Department of Neurophysiology, St. Bartholomew's Hospital, West Smithfield, London, UK.
Crit Care Med. 2003 Apr;31(4):1012-6. doi: 10.1097/01.CCM.0000053651.38421.D9.
To establish the prevalence, clinical characteristics, and electrophysiologic features of residual neuromuscular dysfunction after prolonged critical illness.
Prospective follow-up study of survivors of prolonged critical illness.
A university hospital and two district general hospitals in the UK.
The study occurred for a period of 5 yrs. All patients during that time who were in the intensive care unit for >28 days were entered in the study.
At follow-up, length of intensive care unit and hospital stay, duration of mechanical ventilation and admission Acute Physiology and Chronic Health Evaluation II score were recorded from the case notes. A clinical history was obtained, a Barthel Index disability score was calculated, and a full neurologic examination was performed. Nerve conduction studies, needle electromyography, single-fiber electromyography and thermal thresholds were performed. A total of 195 patients were identified. There were 86 survivors, of whom 47 could be contacted and 22 consented to be studied. The median time from intensive care unit discharge to follow-up was 43 months (range, 12-57 months). All gave a clear history of severe weakness and functional impairment after hospital discharge and, in all, recovery was prolonged. Motor or sensory deficits were present on clinical examination in 59% of the patients studied. Common peroneal nerve palsy was present in two patients. A total of 21 of 22 (95%) patients had electromyographic evidence of chronic partial denervation at follow-up, findings indicative of a preceding axonal neuropathy. The single-fiber electromyographic studies were also consistent with a preceding motor neuropathy.
Severe weakness requiring prolonged rehabilitation and abnormal clinical neurologic findings are extremely common in survivors of protracted critical illness. Neurophysiologic evidence of chronic partial denervation of muscle consistent with previous critical illness polyneuropathy is almost invariable and can be found up to 5 yrs after intensive care unit discharge in >90% of these long-stay patients. Evidence of myopathy is unusual. These findings have important implications for the management and rehabilitation of intensive care survivors.
确定长时间危重病后残余神经肌肉功能障碍的患病率、临床特征及电生理特征。
对长时间危重病幸存者进行前瞻性随访研究。
英国一家大学医院和两家地区综合医院。
该研究为期5年。在此期间,所有在重症监护病房住院超过28天的患者均纳入研究。
随访时,从病历中记录重症监护病房住院时间、住院时间、机械通气时间及入院急性生理与慢性健康状况评分II。获取临床病史,计算巴氏指数残疾评分,并进行全面神经系统检查。进行神经传导研究、针极肌电图、单纤维肌电图及热阈值检测。共识别出195例患者。有86名幸存者,其中47名能够取得联系,22名同意接受研究。从重症监护病房出院至随访的中位时间为43个月(范围12 - 57个月)。所有患者均有明确的出院后严重肌无力和功能障碍病史,且恢复均延长。在接受研究的患者中,59%临床检查存在运动或感觉缺陷。两名患者出现腓总神经麻痹。22例患者中有21例(95%)随访时肌电图显示慢性部分失神经,提示先前存在轴索性神经病。单纤维肌电图研究结果也与先前的运动神经病相符。
在长时间危重病幸存者中,严重肌无力需要长期康复治疗且临床神经系统检查异常极为常见。与先前危重病性多发性神经病相符的肌肉慢性部分失神经的神经生理学证据几乎是恒定的,在这些长期住院患者中,超过90%在重症监护病房出院后5年内可检测到。肌病证据不常见。这些发现对重症监护幸存者的管理和康复具有重要意义。