Intraoperative MRI with a Rotating, Tiltable Surgical Table: A Time–Use Study and Clinical Results in 122 Patients
Jonathan S. Lewin1,2,
Sherif Gamal Nour1,
Mariana L. Meyers1,
Andrew K. Metzger3,4,
Robert J. Maciunas3,
Michael Wendt1,5,
Jeffrey L. Duerk1,
Arnulf Oppelt5 and
Warren R. Selman3
1 Department of Radiology, University Hospitals of Cleveland/Case Western
Reserve University, Cleveland, OH 44106.
2 Present address: Department of Radiology, Johns Hopkins University, Outpatient
Center, 601 N Caroline St., Rm. 4210, Baltimore, MD 21287.
3 Department of Neurosurgery, University Hospitals of Cleveland/Case Western
Reserve University, Cleveland, OH.
4 Present address: New Mexico Neurosurgery, Albuquerque, NM.
5 Siemens Medical Engineering Group, Erlangen, Germany.

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Fig. 2A —Overview of setup of operating room equipped with open
low-field MRI unit. Photographs show prototype surgical table that permits
wide range of spatial freedom. Table can be rotated back and forth between
imaging (A) and operating (B) positions. It also allows height
adjustment and tilting to both Trendelenburg and reverse Trendelenburg
positions. Color codes are marked on floor to define different zones of fringe
field strength. Arrow in A indicates in-room LCD monitor that allows
tableside imager control and image viewing.
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Fig. 2B —Overview of setup of operating room equipped with open
low-field MRI unit. Photographs show prototype surgical table that permits
wide range of spatial freedom. Table can be rotated back and forth between
imaging (A) and operating (B) positions. It also allows height
adjustment and tilting to both Trendelenburg and reverse Trendelenburg
positions. Color codes are marked on floor to define different zones of fringe
field strength. Arrow in A indicates in-room LCD monitor that allows
tableside imager control and image viewing.
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Fig. 2C —Overview of setup of operating room equipped with open
low-field MRI unit. Photograph shows MR–surgical table has been rotated
to bring patient's head in operating position where surgeons can implement
their conventional surgical approaches. Standard operating microscopes,
electrocautery instruments, and fiberoptic headlamps were used.
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Fig. 2D —Overview of setup of operating room equipped with open
low-field MRI unit. Photograph shows patient repositioned into scanner for
intraoperative imaging. Any MR-incompatible instruments are removed from
surgical field. Prototype sterilizable solenoidal coil with surgical pin head
fixation (Heidelberg Neurosurgical Research Group) is placed around patient's
head, and table is moved into draped scanner for imaging. Time necessary to
position patient's head at magnet isocenter and tune system ranges from 30 to
90 seconds.
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Fig. 3A —Gadolinium-enhanced 2D FLASH images (TR/TE, 418/9; flip
angle, 90°; number of signals averaged, 2; acquisition time, 3 minutes 36
seconds) in 60-year-old woman with glioblastoma multiforme. Coronal (A)
and axial (B) images obtained during resection of right frontal lobe
glioblastoma multiforme. Area of focal nodular enhancement (arrow,
A) is noted at base of resection bed that is consistent with incomplete
tumor resection. Contrast level (arrow, B) within operative
bed denotes blood pooling within area of resection.
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Fig. 3B —Gadolinium-enhanced 2D FLASH images (TR/TE, 418/9; flip
angle, 90°; number of signals averaged, 2; acquisition time, 3 minutes 36
seconds) in 60-year-old woman with glioblastoma multiforme. Coronal (A)
and axial (B) images obtained during resection of right frontal lobe
glioblastoma multiforme. Area of focal nodular enhancement (arrow,
A) is noted at base of resection bed that is consistent with incomplete
tumor resection. Contrast level (arrow, B) within operative
bed denotes blood pooling within area of resection.
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Fig. 4A —Gadolinium-enhanced 2D FLASH images (flip angle, 90°;
number of signals averaged, 2) in 71-year-old woman during resection of
temporal lobe glioblastoma. Axial (A) (TR/TE, 418/9; acquisition time,
3 minutes 36 seconds) and coronal (B) (330/9; acquisition time, 2
minutes 30 seconds) images obtained after craniotomy show faintly enhancing
partially ill-defined lesion (arrowheads) involving left-sided mesial
temporal lobe and extending superiorly into inferior aspect of ipsilateral
lentiform nucleus. Adjacent edema is responsible for mass effect exerted on
left lateral ventricle, sylvian fissure, and overlying cortical sulci.
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Fig. 4B —Gadolinium-enhanced 2D FLASH images (flip angle, 90°;
number of signals averaged, 2) in 71-year-old woman during resection of
temporal lobe glioblastoma. Axial (A) (TR/TE, 418/9; acquisition time,
3 minutes 36 seconds) and coronal (B) (330/9; acquisition time, 2
minutes 30 seconds) images obtained after craniotomy show faintly enhancing
partially ill-defined lesion (arrowheads) involving left-sided mesial
temporal lobe and extending superiorly into inferior aspect of ipsilateral
lentiform nucleus. Adjacent edema is responsible for mass effect exerted on
left lateral ventricle, sylvian fissure, and overlying cortical sulci.
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Fig. 4C —Gadolinium-enhanced 2D FLASH images (flip angle, 90°;
number of signals averaged, 2) in 71-year-old woman during resection of
temporal lobe glioblastoma. Axial (C) (418/9; acquisition time, 3
minutes 36 seconds) and coronal (B) (330/9; acquisition time, 2 minutes
30 seconds) images obtained after resection show minimal residual enhancement
along deep aspect of resection bed and small nodule (arrows)
medially, denoting residual neoplastic tissue. Further resection was
subsequently performed based on these intraoperative imaging findings.
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Fig. 4D —Gadolinium-enhanced 2D FLASH images (flip angle, 90°;
number of signals averaged, 2) in 71-year-old woman during resection of
temporal lobe glioblastoma. Axial (C) (418/9; acquisition time, 3
minutes 36 seconds) and coronal (B) (330/9; acquisition time, 2 minutes
30 seconds) images obtained after resection show minimal residual enhancement
along deep aspect of resection bed and small nodule (arrows)
medially, denoting residual neoplastic tissue. Further resection was
subsequently performed based on these intraoperative imaging findings.
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Fig. 5A —Axial gadolinium-enhanced 2D FLASH images (TR/TE, 418/9; flip
angle, 90°; number of signals averaged, 2; acquisition time, 3 minutes 36
seconds) obtained during resection of glioblastoma multiforme in 66-year-old
woman. Image obtained after patient has undergone left craniotomy shows
complex cystic neoplastic lesion with predominant marginal enhancement
involving left temporal lobe and left operculum.
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Fig. 5B —Axial gadolinium-enhanced 2D FLASH images (TR/TE, 418/9; flip
angle, 90°; number of signals averaged, 2; acquisition time, 3 minutes 36
seconds) obtained during resection of glioblastoma multiforme in 66-year-old
woman. Image obtained after resection at location corresponding to A
shows complete resection of enhancing component of glioblastoma multiforme.
Intraoperative edema has caused effacement of left lateral ventricle and
basilar cisterns.
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Fig. 6A —Coronal gadolinium-enhanced 2D FLASH images (TR/TE, 418/9;
flip angle, 90°; number of signals averaged, 2; acquisition time, 3
minutes 36 seconds) in 39-year-old man with left frontal gemistocytic
anaplastic astrocytoma (World Health Organization grade II). Image shows left
frontoparietal craniotomy exposing partially cystic, partially solid
neoplastic mass that involves underlying left frontoparietal lobe and extends
deeply to involve body of corpus callosum. Vasogenic edema is seen compressing
left lateral ventricle and effacing ipsilateral cortical sulci and sylvian
fissure.
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Fig. 6B —Coronal gadolinium-enhanced 2D FLASH images (TR/TE, 418/9;
flip angle, 90°; number of signals averaged, 2; acquisition time, 3
minutes 36 seconds) in 39-year-old man with left frontal gemistocytic
anaplastic astrocytoma (World Health Organization grade II). Image obtained
intraoperatively after tumor resection shows residual rind of enhancement
(arrowheads) surrounding margins of resection bed, reflecting
incomplete tumor resection.
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Copyright © 2007 by the American Roentgen Ray Society.