Clinical Use of Bedside Portable Ultra-Low-Field Brain Magnetic Resonance Imaging in Patients on Extracorporeal Membrane Oxygenation: Results From the Multicenter SAFE MRI ECMO Study.

brain injuries critical care extracorporeal membrane oxygenation magnetic resonance imaging

Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
29 Sep 2024
Historique:
medline: 29 9 2024
pubmed: 29 9 2024
entrez: 29 9 2024
Statut: aheadofprint

Résumé

Early detection of acute brain injury (ABI) at the bedside is critical in improving survival for patients with extracorporeal membrane oxygenation (ECMO) support. We aimed to examine the safety of ultra-low-field (ULF; 0.064-T) portable magnetic resonance imaging (pMRI) in patients undergoing ECMO and to investigate the ABI frequency and types with ULF-pMRI. This was a multicenter prospective observational study (SAFE MRI ECMO study [Assessing the Safety and Feasibility of Bedside Portable Low-Field Brain Magnetic Resonance Imaging in Patients on ECMO]; NCT05469139) from 2 tertiary centers (Johns Hopkins, Baltimore, MD and University of Texas-Houston) with specially trained intensive care units. Primary outcomes were safety of ULF-pMRI during ECMO support, defined as completion of ULF-pMRI without significant adverse events. Of 53 eligible patients, 3 were not scanned because of a large head size that did not fit within the head coil. ULF-pMRI was performed in 50 patients (median age, 58 years; 52% male), with 34 patients (68%) on venoarterial ECMO and 16 patients (32%) on venovenous ECMO. Of 34 patients on venoarterial ECMO, 11 (22%) were centrally cannulated and 23 (46%) were peripherally cannulated. In venovenous ECMO, 9 (18%) had single-lumen cannulation and 7 (14%) had double-lumen cannulation. Of 50 patients, adverse events occurred in 3 patients (6%), with 2 minor adverse events (ECMO suction event; transient low ECMO flow) and one serious adverse event (intra-aortic balloon pump malfunction attributable to electrocardiographic artifacts). All images demonstrated discernible intracranial pathologies with good quality. ABI was observed in 22 patients (44%). Ischemic stroke (36%) was the most common type of ABI, followed by intracranial hemorrhage (6%) and hypoxic-ischemic brain injury (4%). Of 18 patients (36%) with both ULF-pMRI and head computed tomography within 24 hours, ABI was observed in 9 patients with a total of 10 events (8 ischemic, 2 hemorrhagic events). Of the 8 ischemic events, pMRI observed all 8, and head computed tomography observed only 4 events. For intracranial hemorrhage, pMRI observed only 1 of them, and head computed tomography observed both (2 events). Our study demonstrates that ULF-pMRI can be performed in patients on ECMO across different ECMO cannulation strategies in specially trained intensive care units. The incidence of ABI was high, seen in 44% of ULF-pMRI studies. ULF-pMRI imaging appears to be more sensitive to ABI, particularly ischemic stroke, compared with head computed tomography.

Sections du résumé

BACKGROUND UNASSIGNED
Early detection of acute brain injury (ABI) at the bedside is critical in improving survival for patients with extracorporeal membrane oxygenation (ECMO) support. We aimed to examine the safety of ultra-low-field (ULF; 0.064-T) portable magnetic resonance imaging (pMRI) in patients undergoing ECMO and to investigate the ABI frequency and types with ULF-pMRI.
METHODS UNASSIGNED
This was a multicenter prospective observational study (SAFE MRI ECMO study [Assessing the Safety and Feasibility of Bedside Portable Low-Field Brain Magnetic Resonance Imaging in Patients on ECMO]; NCT05469139) from 2 tertiary centers (Johns Hopkins, Baltimore, MD and University of Texas-Houston) with specially trained intensive care units. Primary outcomes were safety of ULF-pMRI during ECMO support, defined as completion of ULF-pMRI without significant adverse events.
RESULTS UNASSIGNED
Of 53 eligible patients, 3 were not scanned because of a large head size that did not fit within the head coil. ULF-pMRI was performed in 50 patients (median age, 58 years; 52% male), with 34 patients (68%) on venoarterial ECMO and 16 patients (32%) on venovenous ECMO. Of 34 patients on venoarterial ECMO, 11 (22%) were centrally cannulated and 23 (46%) were peripherally cannulated. In venovenous ECMO, 9 (18%) had single-lumen cannulation and 7 (14%) had double-lumen cannulation. Of 50 patients, adverse events occurred in 3 patients (6%), with 2 minor adverse events (ECMO suction event; transient low ECMO flow) and one serious adverse event (intra-aortic balloon pump malfunction attributable to electrocardiographic artifacts). All images demonstrated discernible intracranial pathologies with good quality. ABI was observed in 22 patients (44%). Ischemic stroke (36%) was the most common type of ABI, followed by intracranial hemorrhage (6%) and hypoxic-ischemic brain injury (4%). Of 18 patients (36%) with both ULF-pMRI and head computed tomography within 24 hours, ABI was observed in 9 patients with a total of 10 events (8 ischemic, 2 hemorrhagic events). Of the 8 ischemic events, pMRI observed all 8, and head computed tomography observed only 4 events. For intracranial hemorrhage, pMRI observed only 1 of them, and head computed tomography observed both (2 events).
CONCLUSIONS UNASSIGNED
Our study demonstrates that ULF-pMRI can be performed in patients on ECMO across different ECMO cannulation strategies in specially trained intensive care units. The incidence of ABI was high, seen in 44% of ULF-pMRI studies. ULF-pMRI imaging appears to be more sensitive to ABI, particularly ischemic stroke, compared with head computed tomography.

Identifiants

pubmed: 39342513
doi: 10.1161/CIRCULATIONAHA.124.069187
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Sung-Min Cho (SM)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).
Departments of Neurology, Neurosurgery, and Anesthesiology and Critical Care Medicine, Neuroscience Critical Care Division, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., J.K.).

Shivalika Khanduja (S)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Christopher Wilcox (C)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Kha Dinh (K)

Divisions of Pulmonary, Critical Care, and Sleep Medicine, University of Texas Health Science Center at Houston. (K.D., B.A.).

Jiah Kim (J)

Departments of Neurology, Neurosurgery, and Anesthesiology and Critical Care Medicine, Neuroscience Critical Care Division, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., J.K.).

Jin Kook Kang (JK)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Ifeanyi David Chinedozi (ID)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Zachary Darby (Z)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Matthew Acton (M)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Hannah Rando (H)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Jessica Briscoe (J)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Errol L Bush (EL)

Department of Surgery, Division of Thoracic Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (E.L.B.).

Haris I Sair (HI)

Department of Radiology and Radiological Science, Division of Neuroradiology, Johns Hopkins University School of Medicine, Baltimore, MD. (H.I.S.).

John Pitts (J)

Hyperfine, Inc, Guilford, CT (J.P., L.R.A.).

Lori R Arlinghaus (LR)

Hyperfine, Inc, Guilford, CT (J.P., L.R.A.).

Audrey-Carelle N Wandji (AN)

Department of Neurosurgery, Division of Neurocritical Care, McGovern School of Medicine, University of Texas Health Science Center at Houston. (A.-C.N.W., E.M., G.T., J.G.-H., H.A.C., A.G.).

Elena Moreno (E)

Department of Neurosurgery, Division of Neurocritical Care, McGovern School of Medicine, University of Texas Health Science Center at Houston. (A.-C.N.W., E.M., G.T., J.G.-H., H.A.C., A.G.).

Glenda Torres (G)

Department of Neurosurgery, Division of Neurocritical Care, McGovern School of Medicine, University of Texas Health Science Center at Houston. (A.-C.N.W., E.M., G.T., J.G.-H., H.A.C., A.G.).

Bindu Akkanti (B)

Divisions of Pulmonary, Critical Care, and Sleep Medicine, University of Texas Health Science Center at Houston. (K.D., B.A.).

Jose Gavito-Higuera (J)

Department of Neurosurgery, Division of Neurocritical Care, McGovern School of Medicine, University of Texas Health Science Center at Houston. (A.-C.N.W., E.M., G.T., J.G.-H., H.A.C., A.G.).

Steven Keller (S)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

HuiMahn A Choi (HA)

Department of Neurosurgery, Division of Neurocritical Care, McGovern School of Medicine, University of Texas Health Science Center at Houston. (A.-C.N.W., E.M., G.T., J.G.-H., H.A.C., A.G.).

Bo Soo Kim (BS)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Aaron Gusdon (A)

Department of Neurosurgery, Division of Neurocritical Care, McGovern School of Medicine, University of Texas Health Science Center at Houston. (A.-C.N.W., E.M., G.T., J.G.-H., H.A.C., A.G.).

Glenn J Whitman (GJ)

Department of Surgery, Division of Cardiac Surgery, Johns Hopkins University School of Medicine, Baltimore, MD. (S.-M.C., S.K., C.W., J.K.K., I.D.C., Z.D., M.A., H.R., J.B., S.K., B.S.K., G.J.W.).

Classifications MeSH