SyncVision
Precision guidance system
SyncVision
Precision guidance system
The SyncVision precision guidance system is suitable with IntraSight and Core Integrated interventional platforms and streamlines lesion assessment, simplifies vessel sizing and enables precise therapy delivery all while integrating seamlessly in daily workflows in interventional suites of choice.
Features
iFR Scout pullback
The iFR Scout pullback shows the most significant gradient in the mid-vessel lesion with diffuse proximal disease.
Angio+ device inflation
SyncVision Angio+ device inflation provides enhanced visualization of balloon to observe proper inflation. Successful cardiovascular treatment relies on proper balloon inflation, and enhanced imaging can help determine successful inflation functioning.⁸
Fractional Flow Reserve measurement
Various clinical studies demonstrate that physiologic lesion assessment by FFR to guide routine PCI is superior to current angiography guided treatment. This measured ratio represents the potential decrease in coronary flow distal to the coronary stenosis.¹⁴
Specifications
- 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
- Angiographic system video output
- Analog or digital
- IVUS system
- CORE system with IVUS version 3.4 and FFR 2.5.1 and IntraSight 5
- IVUS catheter
- Eagle Eye Platinum catheters
- Pressure Guidewire
- Verrata Plus
- OmniWire
- 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
- SyncVision precision guidance system
- Sync002
Related products
- The IntraSight Interventional Applications Workspace is where imaging, physiology, co-registration* and software all come together to clearly identify coronary and peripheral artery disease, and allow for more optimized treatment plans. IntraSight is built on a new foundational platform designed to meet the evolving needs of your lab today and tomorrow.
- OmniWire combines a unique solid core workhorse design with iFR proven outcomes and iFR Co-registration compatibility, making it easy to use physiology throughout complex cases.¹,²,³ New Nitinol distal core increases durability and shape recovery. Unique solid core improves torque and pushability. Integrated conductive bands for greater signal reliability.
- The Eagle Eye Platinum ST digital IVUS catheter offers a 2.5 mm tip-to-imaging distance designed to assess more of the vessel than standard catheters by providing a closer visualization of highly stenosed lesions and distal anatomy. The short tip catheter fits through all 5F guides and has all features of our top-selling Eagle Eye Platinum model, including plug-and-play simplicity, three radiopaque markers, GlyDx hydrophilic coating, and SyncVision compatibility.*
- For over 20 years Philips has led the way in physiology, putting patients first through continuous innovation. Experience our 10ᵗʰ generation physiology wire: Verrata Plus.
Disclaimer
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
Product availability is subject to country regulatory clearance. Please contact your local sales representative to check the availability in your country.