ILUMIEN™ System – Know which
lesion to treat and how to treat it.

ILUMIEN™ PCI Optimization System

This device is commercially available for use in the United States.

Illuminating the Future of PCI Optimization

ILUMIEN

The ILUMIEN PCI Optimization System provides the physician unprecedented physiological and anatomical insight to improve diagnostic therapy and optimize PCI.

With Knowledge Comes Clarity

Knowing which lesion to treat and how to treat it is key to optimizing interventional treatment strategies. The ILUMIEN system is the first to combine the functional modality of fractional flow reserve (FFR) and the anatomical modality of optical coherence tomography (OCT) to provide the physician insight to help diagnose and treat coronary artery disease — and optimize percutaneous coronary intervention (PCI).

Mobile Integration™

The ease of use of an integrated system with the flexibility and cost efficiency of a mobile unit.

Fast

  • Wireless FFR set-up in one or multiple labs
  • Move between FFR and OCT modalities with one touch

Easy

  • Quick and easy movement between multiple labs
  • Easy on-screen guide simplifies ILUMIEN FFR and OCT procedures with a new, seamless user interface

Flexible

  • Integrated case storage and easy patient ID retrieval
  • Accommodates future updates and technology

ILUMIEN Cath Lab Illustration

 ILUMIEN System

ILUMIEN™ PCI Optimization System

 ILUMIEN System

Specifications

Size (mm) Maximum
Frame Rate (fps)
Nominal
Pullback Speed
Lines per
Frame
Scan
Diameter (mm)
Axial
Resolution (μm)
1430 (h) x 471 (w) x 683 (d) 100 20 mm/sec 500 10 15

 Contents (1 unit per box)

  • OCT Imaging Engine
  • Application Software Package
  • Drive-motor and Optical Controller
  • ILUMIEN Custom Computer
  • Operator's Monitor – High Resolution LCD17"
  • Physician's Monitor – High Resolution LCD 19"
  • Integrated Mobile Console
  • Keyboard and Mouse
  • Accessory Tools
  • Operator's Manual

Reorder Information

Reorder Number

Description

900-700-00 ILUMIEN  PCI Optimization System

 

C7 Dragonfly™ Intravascular Imaging Catheter

DragonFly Imaging Catheter

Specifications

Usable
Length (cm)

Intracoronary Usable
Length
(cm)

Outer Diameter
(distal)
Wire Lumen 
(in)
Coating
135 28 2.7 F 0.014 Hydrophilic

Kit Contents (1 unit per box)

  • C7 Dragonfly Intravascular Imaging Catheter
  • Sterile DOC cover
  • Sterile 3 ml syringe

 Reorder Information

 Reorder Number   

 Description

 100-100-KT  C7 Dragonfly Imaging Catheter

 

PressureWire™ Aeris™

PressureWire Aeris

Pressure Specifications

 Pressure Range  Pressure Accuracy  Frequency Response
 -30 to +300 mmHg

 ±1  mmHg plus ±1% of reading (over the pressure range - 30 mmHg to 50 mmHg)

± 3% of reading (over the range 50 mmHg to 300 mmHg)

 DC to 25 Hz

Wireless Transmission Specifications

Radio Range Battery Time Transmitter Frequency Range Radio Type Radio Power Total Signal Time Delay
2 m (15–20 m in free line of sight)  3 hours  2.4000–2.4835 GHz (ISM band) Frequency hopping spread spectrum (FHSS) 1 mW peak, 70 μW average  <10 ms

Reorder Information

Reorder Number

Description

12056 PressureWire Aeris, 175 cm
12356 PressureWire Aeris, 300 cm

 

Wi-Box™

Wi-Box

Specifications

Power Input External Power Supply Input Transducer Impedance Accuracy
2.4 to 8 VDC (for 2.4 to 4 VDC,
use Wi-Box External Power Supply)
100 to 240 VAC, 50-60 Hz > 270 Ω ±1 mmHg or ±1% of reading,
whichever greatest

Resolution Bandwidth Weight Dimensions
≤ 0.2 mmHg 0-50 Hz 0-25 Hz 108 x 87 x 33 mm

Radio Specifications

Frequency Range Type Range External Power Supply AO IN, AO OUT
2.4000-2.4835 GHz (ISM-band) Frequency-hopping spread spectrum (FHSS) 0–4 m Electrical safety Class II Galvanically connected
CF, Defibrillation Proof

Rerorder Information

Reorder Number

Description

C12783 Wi-Box

 *Cables (for initial installation) are available separately. Please refer to your St. Jude Medical product catalog.

NOTE: One Wi-Box is needed for each cath lab where ILUMIEN is used.

FFR Physiological Assessment

Know What to Treat

FFR allows more accurate identification of hemodynamically significant stenoses, reducing rates of death, myocardial infarction and repeat revascularization1.

  • FFR-guided PCI significantly reduces mortality and results in reduced procedural and healthcare costs, without prolonging the cath lab procedure compared to angiography alone1
  • Recognize lesions that can cause ischemia
  • Determine if blood flow is sufficiently restored after balloon or stent deployment

In addition, Wi-Box™ provides a wireless connection to ILUMIEN, and is permanently installed between the AO-transducer and hemodynamic recording system. FFR is always available - all labs - anytime.

 

OCT Anatomical Assessment

Know How to Treat

The ILUMIEN system incorporates the most advanced OCT technology for enhanced anatomical assessment and PCI optimization.

  • Optimize stent implantation, strut coverage, neointimal response and follow-up2-3
  • Evaluate stent placement, expansion and apposition
  • Differentiate and classify plaque4
  • Evaluate lumen area quickly, with accurate automated measurements

The ILUMIEN system has 10 times better resolution and is 20 times faster than IVUS (acquires full vessel segment pull-back in under 5 seconds)5-9.

 

Image Samples

Malapposed stent struts with early
tissue coverage

Two edge dissections

Mallapposed Struts Edge Dissection

Circumferential calcium

White thrombus at side branch

Circumfrential Calcium Thrombus at Sidebranch

Golden Image

The familiar gold color and Golden Image™ of OCT are available exclusively with the St. Jude Medical ILUMIEN™ and C7-XR™ systems.

 

References

  1. Tonino PA, De Bruyne B, Pijls NH, et al. Fractional flow reserve versus angiography for guiding percutaneous coronary intervention. FAME study. N Engl J Med. 2009;360(3):213-24.
  2. Murata A, Wallace-Bradley D, Tellez A, et al. Accuracy of optical coherence tomography in the evaluation of neointimal coverage after stent implantation. JACC Cardiovasc Imaging. 2010;3(1):76-84.
  3. Santos MC, Lin T, Barlis P. In-stent restenosis associated with stent malapposition: Seven year optical coherence tomography findings. Int J Cardiol. 2011;147(1):149-51.
  4. Prati F, Regar E, Mintz GS, et al. Expert review document on methodology, terminology, and clinical applications of optical coherence tomography: Physical principles, methodology of image acquisition, and clinical application for assessment of coronary arteries and atherosclerosis. Eur Heart J. 2010;31(4):401-15. 
  5. Nissen SE, Yock P. Intravascular unlrasound: Novel pathophysiological insights and current clinical applications. Circulation. 2001;103(4);604-16.
  6. Dijkstra J, Koning G, Reiber JH. Quantitative measurements in IVUS images. Int J Card Imaging. 1999;15(6):513-22.
  7. St. Jude Medical. Data on File.
  8. Volcano Corporation, R-100 Instructions for Use.
  9. Boston Scientific Corporation, Galaxy Instructions for Use.

FAME STUDY1

One-year Outcomes

The PressureWire sensor was the exclusive FFR technology used in the FAME Study. Compared to angiography only procedures, the FAME one-year study results showed that FFR:

  • Reduces composite rates of death, myocardial infarction, re-PCI, and CABG at one year by 28%
  • Reduces mortality and myocardial infarction at one year by 34%
  • Is cost-saving and does not prolong procedure time
  • Decreases amount of contrast agent used
  • Results in similar, if not better, functional status 

Supported by ACC/AHA/SCAI Guidelines2 

  • The AHA/ACC/SCAI guidelines are Class II A, Level of Evidence A, for determining whether PCI of a specific coronary lesion is warranted. Additionally, FFR was recently awarded the highest level of evidence, Class I, Level of Evidence A by European Society of Cardiology (ESC) and European Association for Cardio-Thoracis Surgery (EACTS)3

     

References

  1. Tonino PA, De Bruyne B, Pijls NH, et al. Fractional flow reserve versus angiography for guiding percutaneous coronary intervention. N Engl J Med. 2009;360(3):213-224.
  2. Kushner FG, Hand M, Smith SC Jr. King SM 3rd, et al: 2009 focused updates: ACC/AHA guidelines for the management of patients with ST-elevation myocardial infarction (updating the 2004 guideline and 2007 focused update) and ACC/AHA/SCAI guidelines on percutaneous coronary intervention (updating the 2005 guidelines and 2007 focused update) a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2009 Dec 1;54(23):P2205-41.
  3. European (ESC/EACTS) guidelines 2010: Wijns, et al., Eur Heart J 2010; first published online August 29, 2010.

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