Skip to main content

Table 1 Patient characteristics and adverse events during portable brain MRI scan

From: Assessing the SAfety and FEasibility of bedside portable low-field brain Magnetic Resonance Imaging in patients on ECMO (SAFE-MRI ECMO study): study protocol and first case series experience

 

Age (years)

Sex

BMI

ECMO indication

Cannulation strategy

Neurologic symptoms

MRI time (min)

HCT finding

MRI finding

ABI management

Adverse events*

1

47

Male

30.5

COVID-19 ARDS

Fem-IJ (VV-ECMO)

Coma under sedation

40

Acute left occipital ischemic stroke with hemorrhagic conversion

Acute left occipital ischemic stroke

Anticoagulation held and restarted with serial imaging studies

One self-limited ECMO suction event

2

45

Male

32.5

COVID-19 ARDS

Fem-IJ (VV-ECMO)

Coma under sedation

43

No acute findings

None

Not applicable

None

3

55

Female

27.1

Cardiogenic shock with PE

Fem–Fem (VA-ECMO)

Coma under sedation

34

No acute findings

Acute right basal ganglia ischemic infarct

Anticoagulation held and restarted with serial imaging studies

Frequent ECMO suction events, received intravenous fluids; improved with repositioning patient*

  1. ARDS: Acute respiratory distress syndrome; VV: venovenous; Fem-IJ: femoral–internal jugular; VA: venoarterial; Fem-Fem: femoral–femoral; ECMO: extracorporeal membrane oxygenation; PE: pulmonary embolism; ABI: acute brain injury. *It was noted that the patients torso was positioned in slight extension, bed and MRI were flattened to remove extension with resolution in suction events. *There were no serious adverse events in all patients