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在危重症患者床边使用便携式低场磁共振成像评估脑损伤

Assessment of Brain Injury Using Portable, Low-Field Magnetic Resonance Imaging at the Bedside of Critically Ill Patients.

作者信息

Sheth Kevin N, Mazurek Mercy H, Yuen Matthew M, Cahn Bradley A, Shah Jill T, Ward Adrienne, Kim Jennifer A, Gilmore Emily J, Falcone Guido J, Petersen Nils, Gobeske Kevin T, Kaddouh Firas, Hwang David Y, Schindler Joseph, Sansing Lauren, Matouk Charles, Rothberg Jonathan, Sze Gordon, Siner Jonathan, Rosen Matthew S, Spudich Serena, Kimberly W Taylor

机构信息

Department of Neurology, Yale University School of Medicine, New Haven, Connecticut.

Neuroscience Intensive Care Unit, Yale New Haven Hospital, New Haven, Connecticut.

出版信息

JAMA Neurol. 2020 Sep 8;78(1):41-7. doi: 10.1001/jamaneurol.2020.3263.

Abstract

IMPORTANCE

Neuroimaging is a key step in the clinical evaluation of brain injury. Conventional magnetic resonance imaging (MRI) systems operate at high-strength magnetic fields (1.5-3 T) that require strict, access-controlled environments. Limited access to timely neuroimaging remains a key structural barrier to effectively monitor the occurrence and progression of neurological injury in intensive care settings. Recent advances in low-field MRI technology have allowed for the acquisition of clinically meaningful imaging outside of radiology suites and in the presence of ferromagnetic materials at the bedside.

OBJECTIVE

To perform an assessment of brain injury in critically ill patients in intensive care unit settings, using a portable, low-field MRI device at the bedside.

DESIGN, SETTING, AND PARTICIPANTS: This was a prospective, single-center cohort study of 50 patients admitted to the neuroscience or coronavirus disease 2019 (COVID-19) intensive care units at Yale New Haven Hospital in New Haven, Connecticut, from October 30, 2019, to May 20, 2020. Patients were eligible if they presented with neurological injury or alteration, no contraindications for conventional MRI, and a body habitus not exceeding the scanner's 30-cm vertical opening. Diagnosis of COVID-19 was determined by positive severe acute respiratory syndrome coronavirus 2 polymerase chain reaction nasopharyngeal swab result.

EXPOSURES

Portable MRI in an intensive care unit room.

MAIN OUTCOMES AND MEASURES

Demographic, clinical, radiological, and treatment data were collected and analyzed. Brain imaging findings are described.

RESULTS

Point-of-care MRI examinations were performed on 50 patients (16 women [32%]; mean [SD] age, 59 [12] years [range, 20-89 years]). Patients presented with ischemic stroke (n = 9), hemorrhagic stroke (n = 12), subarachnoid hemorrhage (n = 2), traumatic brain injury (n = 3), brain tumor (n = 4), and COVID-19 with altered mental status (n = 20). Examinations were acquired at a median of 5 (range, 0-37) days after intensive care unit admission. Diagnostic-grade T1-weighted, T2-weighted, T2 fluid-attenuated inversion recovery, and diffusion-weighted imaging sequences were obtained for 37, 48, 45, and 32 patients, respectively. Neuroimaging findings were detected in 29 of 30 patients who did not have COVID-19 (97%), and 8 of 20 patients with COVID-19 (40%) demonstrated abnormalities. There were no adverse events or complications during deployment of the portable MRI or scanning in an intensive care unit room.

CONCLUSIONS AND RELEVANCE

This single-center series of patients with critical illness in an intensive care setting demonstrated the feasibility of low-field, portable MRI. These findings demonstrate the potential role of portable MRI to obtain neuroimaging in complex clinical care settings.

摘要

重要性

神经影像学检查是脑损伤临床评估的关键步骤。传统的磁共振成像(MRI)系统在高强度磁场(1.5 - 3T)下运行,需要严格的、有门禁控制的环境。在重症监护环境中,及时进行神经影像学检查的机会有限,这仍然是有效监测神经损伤发生和进展的关键结构性障碍。低场MRI技术的最新进展使得在放射科以外的地方以及床边存在铁磁性材料的情况下也能获取具有临床意义的影像。

目的

使用床边便携式低场MRI设备对重症监护病房中的重症患者进行脑损伤评估。

设计、地点和参与者:这是一项前瞻性、单中心队列研究,研究对象为2019年10月30日至2020年5月20日期间入住康涅狄格州纽黑文市耶鲁纽黑文医院神经科学或2019冠状病毒病(COVID - 19)重症监护病房的50例患者。如果患者出现神经损伤或改变、无传统MRI检查的禁忌证且体型不超过扫描仪30厘米的垂直开口,则符合入选标准。COVID - 19的诊断通过严重急性呼吸综合征冠状病毒2聚合酶链反应鼻咽拭子检测结果呈阳性来确定。

暴露因素

在重症监护病房内使用便携式MRI。

主要结局和测量指标

收集并分析人口统计学、临床、放射学和治疗数据。描述脑成像结果。

结果

对50例患者(16名女性[32%];平均[标准差]年龄59[12]岁[范围20 - 89岁])进行了床旁即时MRI检查。患者的疾病包括缺血性卒中(n = 9)、出血性卒中(n = 12)、蛛网膜下腔出血(n = 2)、创伤性脑损伤(n = 3)、脑肿瘤(n = 4)以及伴有精神状态改变的COVID - 19(n = 20)。检查在入住重症监护病房后的中位时间为5天(范围0 - 37天)进行。分别为37例、48例、45例和32例患者获得了诊断级别的T1加权、T2加权、T2液体衰减反转恢复和扩散加权成像序列。在30例非COVID - 19患者中有29例(97%)检测到神经影像学异常,20例COVID - 19患者中有8例(40%)显示异常。在重症监护病房内使用便携式MRI或进行扫描期间未发生不良事件或并发症。

结论和意义

在重症监护环境中对这单中心系列重症患者的研究证明了低场便携式MRI的可行性。这些发现表明便携式MRI在复杂临床护理环境中获取神经影像学检查结果方面具有潜在作用。

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