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SyncVision Precision guidance system

SyncVision

Precision guidance system

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The SyncVision precision guidance system streamlines lesion assessment, simplifies vessel sizing, and enables precise therapy delivery in conjunction with the existing fluoroscopic image stream.

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Specifications

Power requirements
Power requirements
System input
  • 100V-120V, 50/60Hz, 220-240V, 50/60Hz, 600 VA
Monitor
  • 100-240V, 50/60Hz, 93 VA
Workstation
  • 100-240V, 50/60Hz, 250 VA
Inputs
Inputs
Angiographic system video output
  • Analog or digital
IVUS system
  • Philips Core systems SW version 3.2.2 and above
IVUS catheter
  • Eagle Eye Platinum catheters
ECG signal
  • Contact your local Philips representative for compatibility
Dimensions
Dimensions
Workstation
  • Height: 16.5", 39.6 cm; Width: 6.75", 16.2 cm; Depth: 21.25", 51 cm
Bedside joystick
  • Height: 1.5", 3.7 cm; Width: 4.2", 10.7 cm; Depth: 3", 7.6 cm
Monitor
  • Height: 15-19", 41-56 cm; Width: 15.8", 40.2 cm; Depth: 10", 24.7 cm
Ordering Information
Ordering Information
SyncVision precision guidance system
  • Sync002
  • 1. Costa, Angiolillo DJ, Tannenbaum M, et al. Impact of Stent Deployment Procedural Factors on Long-term Effectiveness and Safety of Sirolimus-Eluting Stents (Final results of the Multicenter Prospective STLLR Trial). Am J Cardiol. 2008; 101(12):1704-1711.
  • 2. Renata Rogacka, Azeem Latib, Antonio Colombo. IVUS-Guided Stent Implantation to Improve Outcome: A Promise Waiting to be Fulfilled. Curr Cardiol Rev. 2009;5(2):78–86.
  • 3. Witzenbichler B, Maehara A, Weisz G, et al. Relationship Between Intravascular Ultrasound Guidance and Clinical Outcomes After Drug-Eluting Stents: The ADAPT-DES Study. Circulation. 2014;129:463-470.
  • 4. 202-0013.53 SRS, Sync-Rx System pg 19,24.
  • 5. Jakabcin J1, Spacek R, Bystron M, et al. Long-term health outcome and mortality evaluation after invasive coronary treatment using drug eluting stents with or without the IVUS guidance. Randomized control trial. HOME DES IVUS. Catheter Cardiovasc Interv. 2010;75(4):578-583.
  • 6. 209-0030.02 Test Rpt, Use Validation, SyncVision. Pg. 9, Section 10.3; pg 14 – results.
  • 7. 505-0100.18, Operator’s Manual. (pg 34).
  • 8. 211-0013.31 Test Protocol, Philips Sync-Rx Wizard phase; 211-9913.07 Verification Protocol, Sync-Rx Co-Registration.
  • 9. Patel, et al. ACCF/SCAI/STS/AATS/AHA/ASNC/HFSA/SCCT 2012 Appropriate use criteria for coronary revascularization focused update: a report of the American College of Cardiology Foundation Appropriate Use Criteria Task Force, Society for Cardiovascular Angiography and Interventions, Society of Thoracic Surgeons, American Association for Thoracic Surgery, American Heart Association, American Society of Nuclear Cardiology, and the Society of Cardiovascular Computed Tomography. J Am Coll Cardiol. 2012;59(9):857-881.
  • 10. Kim SH, Kim YH, Kang SJ, et al. Long-term outcomes of intravascular ultrasound-guided stenting in coronary bifurcation lesions. Am J Cardiol. 2010;106(5):612-618.
  • 11. Patel Y, Depta JP, Novak E, et al. Long-term outcomes with use of intravascular ultrasound for the treatment of coronary bifurcation lesions. Am J Cardiol. 2012;109(7):960-965.
  • 12. Davies JE, et al. Coronary artery physiological stenosis mapping: application of pressure wire technology to measure stenosis significance, length, and predict the outcome of intervention. Abstract presented at PCR 2014
  • 13. An iFR cut-point of 0.89 matches best with an FFR ischemic cut-point of 0.80 with a specificity of 87.8% and sensitivity of 73.0%. (iFR Operator’s Manual 505-0101.23)
  • 14. Fractional Flow Reserve–Guided PCI versus Medical Therapy in Stable Coronary Disease. N Engl J Med. 2012;367(11):991-1001.
  • *Data on file

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