Discovery NMCT 670 Pro Data Sheet
Discovery NMCT 670 Pro Data Sheet
Cardiac Morphing
Siting Requirements
Optional software providing the following performance:
Minimum Room Size
• Delivers enhanced perfusion image quality for Gated SPECT data • Exam Room Size: 20’8” x 12’1” (6.3 m x 3.7 m)
• Overcomes non-uniform blurring of the myocardium due to • Control Room Size: 9’ x 14’ (2.74 m x 4.27 m)
cardiac motion, enhancing the visual clarity of the images • With single desktop table: 15’5” x 8’11” (4.7 m x 2.4 m)
• Based on elastic summation of tomograms representing all bins in These values meet minimum clearance requirements under U.S.
a cardiac cycle – rescaled to match end-diastolic LV size Federal Regulations and National Standards: 29 CFR 1910 (OSHA),
NFPA 70E (Standard for Electrical Safety in the Workplace) and NFPA
Quantitation 101 (Life Safety Code). Specific room requirements may also need to
comply with local and regulatory requirements.
Advanced quantitation and CT AC enhancement options include:
• Dosimetry Toolkit optional application enabling quantification
of changes in radiopharmaceutical absorption at multiple body
Power Requirements
organs over time through analysis of SPECT or planar WB studies Power conditioning is incorporated into the primary power supply of
and a hybrid SPECT/CT scan. The results may help in radiotherapy the system. The system can operate on line voltage based on local
treatment planning. The quantification algorithm includes: conditions and codes.
– Aligning multiple planar WB and/or SPECT studies to each other 380-480 VAC nominal, 3 phase Delta or Wye, 50/60 Hz. Power
and to a registered hybrid SPECT/CT scan of the same patient consumption is 90 kVA peak, 22 kvA average.
– Delineating organ VOIs through CT segmentation
– Applying the VOIs for organ uptake quantification in a series
of NM scans acquired over time resulting in calculated residual Operating Conditions
time per organ Maximum
Parameter Maximum Minimum
• Q.Metrix‡ option, employing SPECT and CT segmentation Change Rate
tools for quantifying radiopharmaceutical uptake using patient
26° C 18° C 3° C/hr
demographics information and the same methods that are Temperature
(79° F) (64° F) (5° F/hr)
currently used to calculate SUV for PET images to quantify the
60% 30%
following parameters: Humidity non-condensing non-condensing 5 % / hr
– Radiotracer uptake in Bq/ml relative relative
– % of injected dose
– Total uptake assessment in segmented organs/lesions Cooling Requirements
• Q.AC‡ option, for maintaining AC quality at low CT dose. Its
• The cooling requirements do not include cooling for the room
unique CT reconstruction and processing algorithms provide
lighting, personnel or non-NM/CT equipment present. Cooling
SPECT attenuation correction that maintains quantitative SPECT
requirements are listed by subsystem to allow planning for each
measurements accuracy even at very low CT dose.
room of the NM/CT suite.
• WideView‡ option for reduced CT clipping artifacts, enabling
• Cooling requirements are given for minimum, recommended and
CT attenuation correction of SPECT scans throughout the entire
growth allowance scenarios.
reconstructed SPECT field-of-view.
• The minimum cooling figures assume patient throughput of 3
patients per hour and 75 scan rotations per patient
• The recommended cooling requirements assume patient.
throughput limited by the tube-cooling algorithm.
• The suite cooling can be sized for future developments by using
the growth allowance figures. This cooling will accommodate more Regulatory Compliance
patients per hour and/or potential future system enhancements.
This product is designed to comply with applicable safety
standards. The Discovery NM/CT 670 Pro system is CE marked
Minimum Allowance (± 10%)
and it complies with the requirements of IEC 60601-1 and relevant
Subsystem Watts BTU/hr collateral, UL 60601-1, Safety Standards for Medical Electrical
Equipment.
Gantry 7,700 26,300 GE Healthcare has been certified to be ISO-9001 and ISO-13485
compliant.
Table 500 1,700
NM Detector Scan Radius Minimum: 3.9” (10 cm) radius/7.8” (20 cm) diameter
(With LEHR Collimators) Maximum: 13.8” (35 cm) radius/27.6” (70 cm) diameter
NM GANTRY Externally mounted dual detectors Patient friendly; ease and speed of patient positioning
Emergency Stop buttons Stops all system motions upon emergency for patient safety
Motorized radial detector movement in 90° Highly flexible patient positioning for cardiac imaging; COR stability
position and reproducibility
Free geometry capability of various 0°, 90° High throughput configurations for cardiac SPECT and whole body
and 180° configurations imaging, as well as providing flexibility of a single-head camera
Flexible detectors positioning including
upright standing or seated patients and High clinical utility including “single-head positioning flexibility”
hospital bed scanning
Rapid transition between the various
Technologist productivity; ease and speed of study set-up
gantry geometries
SUBSYSTEM KEY FEATURE USER/PATIENT BENEFIT
Graphical user interface with Xeleris
Facilitates ease of use
workstation
Standard high-end Windows PC running a
May enhance productivity with multi-window, multi-tasking system
real-time multi-tasking interface
NM ACQUISITION
Parallel operations allow simultaneous acquisition and display to
STATION Linux operating system
help enhance productivity
Fully-integrated PECT/CT workflow Workflow productivity for streamlined imaging procedures including
solution with Ignite camera/patient setup, acquisition, processing and archiving
Networks to Xeleris Processing & Review Non-proprietary communication protocols; open system
DICOM Networks to DICOM-compliant systems Communicates with 3rd party DICOM-compliant workstations
CONNECTIVITY DICOM Modality Worklist Streamlines patient admittance and scheduling
Intrinsic Count Rate Maximum @ 20% Window ≥ 400 kcps 400 kcps
§
Per NEMA NU-1 2007.
Evolution for Bone SPECT Performance Specifications
SPECIFICATION PARAMETER RANGE Full time Half time
Extended** 320/330
I-123/
Low Energy 0.3 (I-123) (Tc-99m) 144/148 (Tc-99m)
ELEGP H2506TD Kr-81 54x 40 10.3/10.6 hex 2.5 0.4 40 62/136
General 2.3 (Kr-81) 224/245 101/110 (I-123)
Studies
Purpose (I-123)
Medium Ga-67/
144/150 65/67
Energy General MEGP H2506TC In-111 54 x 40 2.0 (Ga-67) 9.4/9.8 hex 3.0 1.05 58 103/227
(Ga-67) (Ga-67)
Purpose studies
High Energy
I-131 97/165 43/73
General HEGP H2506TE 54 x 40 2.0 (I-131) 12.0/12.5 hex 4.0 1.8 66 131/289
studies (I-131) (I-131)
Purpose
**L-mode SPECT (90° detectors geometry) is effective with low energy collimators (LEUHR, LEHR, and ELEGP)
Notes:
• Recommended brain scan radius is 14-16 cm
• Focal distance from collimator surface is 350 mm
• Effective collimator thickness is 57 mm
The floor plan of minimum room layout above (6.30 m x 3.70 m / 20’8” x 12’1”) meets the following egress and service clearance
requirements under U.S. Federal Regulations and National Standards:
• 29 CFR 1910 (OSHA), NFPA 70E (Standard for Electrical Safety in the Workspace)
• NFPA 101 (Life Safety Code)
Specific room layouts may be subject to additional local and regulatory requirements. For non-U.S. installations, specific installations are
subject to country, local and regulatory requirements. For more information, please contact your local GE representative.
*Trademark of General Electric Company
**Only LEHR, LEUHR and ELEGP collimators can be used for SPECT at 90° geometry
***See Optima CT540 Data Sheet for more detail
§ (1) ASiR is licensed for use with a GE x-ray tube. Use of a third party x-ray tube will require an additional license.
(2) In clinical practice, the use of ASiR may reduce CT patient dose depending on the clinical task, patient size, anatomical
location and clinical practice. A consultation with a radiologist and a physicist should be made to determine the
appropriate dose to obtain diagnostic image quality for the particular clinical task.
(3) Evolution Disclaimer and tags:
• In clinical practice, Evolution options (Evolution for Bone, Evolution for Cardiac, Evolution for Bone Planar) and Evolution
Toolkit are recommended for use following consultation of a NM physician, physicist and/or application specialist to
determine the appropriate dose or scan time reduction to obtain diagnostic image quality for a particular clinical task,
depending on the protocol adopted by the clinical site.
• Evolution claims are supported by simulation of count statistics using default factory protocols and imaging of Tc-99m
based radiotracers with LEHR collimator on anthropomorphic phantom or realistic NCAT – SIMSET phantom followed by
quantitative and qualitative images comparison.
• Evolution Toolkit claims are supported by simulation of full count statistics using lesion simulation phantom images based
on various radiotracers and collimators and by showing that SPECT image quality reconstructed with Evolution Toolkit
provides equivalent clinical information but has better signal-to-noise, contrast and lesion resolution compared to the
images reconstructed with FBP/OSEM.
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