Unit of Rehabilitation, Department of Neuroscience, University of Padua, Padua, Italy -
Unit of Severe Brain Injury, Department of Rehabilitation Medicine, Ca' Foncello Regional Hospital, Treviso, Italy.
Eur J Phys Rehabil Med. 2017 Dec;53(6):883-891. doi: 10.23736/S1973-9087.17.04303-9. Epub 2017 May 12.
Cardiac arrest (CA) is a common cause of disability. Multimodal evaluation has improved prognosis but precocious biomarkers are not appropriate in determining long-term functional outcome.
To identify early prognostication markers of long-term functional outcome in post-anoxic coma.
Retrospective assessment of outcomes.
Individuals older than 18 years with post-anoxic coma hospitalized in intensive care units after cardiac arrest (CA) regardless of cause (cardiac or non-cardiac) and location of event (in or out-of-hospital).
Clinical, biological and neurophysiological data were collected within 48 hours from CA. Clinical data included time of no and low flow, CA rhythm, pupillary reflex, Glasgow motor score at admission and hyperthermia. Biological marker was the highest creatinine level. Neurophysiological parameters included EEG pattern and reactivity, Somatosensory Evoked Potential (SSEP), and Middle-Latency (ML) SSEP evoked at low (10 mA) and high (50 mA) intensity stimulation. Level of Cognitive Functioning Scale (LCFS), Disability Rating Scale and recovery from coma (Revised coma Recovery Scale [CRS-R]) were collected at 12 months. A LASSO multiple regression analysis was fitted to data to investigate the best predictors of LCF, DRS and CRS-R. In-sample prediction was obtained to verify the quality of fitting, and accuracy indices (i.e., total error rate) produced.
Presence of short and medium latency SSEPs with low and high stimulation intensity were identified as prognostic predictors of outcome for all the scales. Error rate was 4.5% for CRS and LCF, and 9.1% for DRS.
Middle latency somatosensory evoked potentials associated with short latency somatosensory evoked potentials during the first 48 hours after a cardiac arrest are strong predictors of functional outcome at 12 months from the event. Replication on larger cohorts is needed to support their routine use as prognostic markers.
These markers could inform more appropriate allocation of resources, provide a basis for realistic goal-setting, and help the family to adjust its expectations.
心脏骤停(CA)是导致残疾的常见原因。多模态评估提高了预后,但早期生物标志物并不适合确定长期功能结局。
确定缺氧后昏迷中与长期功能结局相关的早期预后标志物。
结局的回顾性评估。
年龄大于 18 岁的患者,在心脏骤停(CA)后因缺氧而处于昏迷状态,无论 CA 的原因(心源性或非心源性)和事件发生地点(院内或院外)如何,均住院于重症监护病房。
在 CA 后 48 小时内收集临床、生物学和神经生理学数据。临床数据包括无血流和低血流时间、CA 节律、瞳孔反射、入院时格拉斯哥运动评分和发热。生物标志物为最高肌酐水平。神经生理学参数包括脑电图模式和反应性、体感诱发电位(SSEP)以及在低(10 mA)和高(50 mA)强度刺激下诱发的中潜伏期(ML)SSEP。在 12 个月时收集认知功能量表(LCFS)、残疾评定量表和昏迷恢复(修订昏迷恢复量表[CRS-R])。使用 LASSO 多元回归分析对数据进行拟合,以调查对 LCFS、DRS 和 CRS-R 最佳的预测因素。通过内样本来验证拟合的质量,并生成准确性指标(即总错误率)。
发现中潜伏期体感诱发电位在低和高刺激强度下与短潜伏期体感诱发电位同时存在,是所有量表结局的预后预测因子。CRS 和 LCFS 的错误率为 4.5%,DRS 的错误率为 9.1%。
心脏骤停后 48 小时内出现的中潜伏期体感诱发电位与短潜伏期体感诱发电位相关,是事件发生后 12 个月功能结局的有力预测因子。需要在更大的队列中进行复制,以支持将其作为预后标志物的常规使用。
这些标志物可以为更合理地分配资源提供信息,为设定现实目标提供依据,并帮助家庭调整其期望。