Department of Anesthesia and Critical Care Medicine, Section of Neuroanesthesia and Neurocritical Care, University of Brescia at Spedali Civili, Brescia, Italy.
PLoS One. 2013 Sep 30;8(9):e75696. doi: 10.1371/journal.pone.0075696. eCollection 2013.
Degeneration of intraepidermal nerve fibers (IENF) is a hallmark of small fiber neuropathy of different etiology, whose clinical picture is dominated by neuropathic pain. It is unknown if critical illness can affect IENF.
We enrolled 14 adult neurocritical care patients with prolonged intensive care unit (ICU) stay and artificial ventilation (≥ 3 days), and no previous history or risk factors for neuromuscular disease. All patients underwent neurological examination including evaluation of consciousness, sensory functions, muscle strength, nerve conduction study and needle electromyography, autonomic dysfunction using the finger wrinkling test, and skin biopsy for quantification of IENF and sweat gland innervation density during ICU stay and at follow-up visit. Development of infection, sepsis and multiple organ failure was recorded throughout the ICU stay.
Of the 14 patients recruited, 13 (93%) had infections, sepsis or multiple organ failure. All had severe and non-length dependent loss of IENF. Sweat gland innervation was reduced in all except one patient. Of the 7 patients available for follow-up visit, three complained of diffuse sensory loss and burning pain, and another three showed clinical dysautonomia.
Small fiber pathology can develop in the acute phase of critical illness and may explain chronic sensory impairment and pain in neurocritical care survivors. Its impact on long term disability warrants further studies involving also non-neurologic critical care patients.
表皮内神经纤维(IENF)的退化是不同病因引起的小纤维神经病的标志,其临床表现主要为神经性疼痛。目前尚不清楚危重病是否会影响 IENF。
我们招募了 14 名成年神经重症监护病房(ICU)患者,他们的 ICU 住院时间和人工通气时间均较长(≥3 天),且无神经肌肉疾病的既往病史或危险因素。所有患者均接受了神经系统检查,包括意识、感觉功能、肌肉力量、神经传导研究和针极肌电图检查,自主神经功能障碍采用指皱试验进行评估,并在 ICU 住院期间和随访时进行皮肤活检以定量评估 IENF 和汗腺神经支配密度。记录 ICU 住院期间感染、败血症和多器官衰竭的发生情况。
在招募的 14 名患者中,有 13 名(93%)发生了感染、败血症或多器官衰竭。所有患者均出现严重且非长度依赖性的 IENF 丧失。除 1 名患者外,所有患者的汗腺神经支配均减少。在可进行随访的 7 名患者中,有 3 名患者主诉弥漫性感觉丧失和灼痛,另有 3 名患者表现出临床自主神经功能障碍。
小纤维病理学可能在危重病的急性期发展,并可能解释神经重症监护病房幸存者的慢性感觉障碍和疼痛。其对长期残疾的影响需要进一步研究,包括非神经重症监护病房的患者。