Department of Anaesthesia, Intensive Care Unit, Watford General Hospital, Vicarage Road, Watford WD18 0HB, UK; Faculty of Medicine, Imperial College, South Kensington Campus, London SW7 2AZ, UK.
Department of Geriatric Medicine, Oslo Delirium Research Group, Oslo University Hospital, Oslo, Norway.
EBioMedicine. 2022 Jun;80:104043. doi: 10.1016/j.ebiom.2022.104043. Epub 2022 May 6.
Delirium predicts poor outcomes, however identifying patients with the worst outcomes is challenging. Plasma neurofilament light protein (NfL) is a sensitive indicator of neuronal damage. We undertook an exploratory observational study to determine the association between plasma NfL and delirium in the critically ill.
MoDUS was a randomised placebo-controlled delirium trial of simvastatin done in an UK adult general ICU. We measured NfL levels in plasma samples using a Single molecule array (Simoa) platform. We explored associations between patient's plasma NfL levels and number of delirium days, and clinical outcomes. The control group for baseline NfL were preoperative patients undergoing major surgery.
The majority of critically ill patients already had a high NfL level on admission. Patients with higher plasma NfL levels at days one and three spent more days in delirium or deep sedation. Patients with zero or one day in delirium or deep sedation had day one mean concentrations of 37.8 pg/ml (SD 32.6) compared with 96.5 pg/ml (SD 106.1)) for patients with two days or more, p-value 0.002 linear mixed effects model. Survivors discharged before 14 days had lower mean plasma NfL concentrations compared to those with longer hospital stays and/or who died within six months. The area under ROC curve for predicting death within six months using day one NfL was 0.81 (0.7,0.9).
Measurement of plasma NfL within three days of admission may be useful to identify those patients with worse clinical outcomes, and as an enrichment strategy for future delirium interventional trials in the critically ill.
Alzheimer's Society UK, UK Dementia Research Institute.
谵妄可预测不良结局,但识别预后最差的患者具有挑战性。神经丝轻链蛋白(NfL)是神经元损伤的敏感标志物。我们进行了一项探索性观察性研究,以确定重症患者血浆 NfL 与谵妄之间的关系。
MoDUS 是一项在英国成人综合 ICU 中进行的辛伐他汀随机安慰剂对照谵妄试验。我们使用单分子阵列(Simoa)平台测量血浆样本中的 NfL 水平。我们探讨了患者血浆 NfL 水平与谵妄天数和临床结局之间的关系。基线 NfL 的对照组为接受大手术的术前患者。
大多数重症患者入院时已经有较高的 NfL 水平。第 1 天和第 3 天血浆 NfL 水平较高的患者谵妄或深度镇静的天数更多。无谵妄或深度镇静 1 天的患者第 1 天的平均浓度为 37.8 pg/ml(SD 32.6),而有 2 天或以上谵妄或深度镇静的患者为 96.5 pg/ml(SD 106.1),p 值为 0.002 线性混合效应模型。在 14 天前出院的幸存者的血浆 NfL 浓度低于住院时间较长和/或在 6 个月内死亡的幸存者。使用第 1 天 NfL 预测 6 个月内死亡的 ROC 曲线下面积为 0.81(0.7,0.9)。
入院后 3 天内测量血浆 NfL 可能有助于识别预后较差的患者,并作为未来重症患者谵妄干预试验的富集策略。
英国阿尔茨海默病协会,英国痴呆症研究协会。