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Advance Serenity® | A smoother crossing


Are you treating peripheral artery disease (PAD) in the infrapopliteal or femoropopliteal regions? We are excited to introduce our Advance Serenity 0.018 inch diameter and Advance Serenity 0.014 inch diameter balloon dilatation catheters. Whether targeting the infrapopliteal or femoropopliteal arteries, this next-generation technology provides a smoother crossing of tight lesions.

 

Detailed, close up illustration of an expanded Advance Serenity PTA balloon

Supporting a smoother crossing

Next-gen hydrophilic coating

Provides lubricity to navigate through
diseased vessels with low friction

Laser-formed tipping

Creates trackability and smooth transitions
from wire to tip, allowing it to cross
complex lesions

coaxial shaft design

Balances stiffness and flexibility to deliver
pushability to cross distal lesions

pleated balloon

Facilitates smooth rewrap

What are other physicians saying about Advance Serenity?


Experts talk about treatment trends, product features, and usage

Watch these videos:

Dr Anahita Dua discusses her PAD practice.

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Dr Keith Jones talks about using Advance Serenity.

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Questions and answers with Dr Dua and Dr Jing Li

Dr Dua on navigating tough lesions

How does Advance Serenity fit into your PAD algorithm?
I use [Advance] Serenity balloons for below-the-knee pathology where trackability is essential to reach those tough lesions.

What type of lesion is Advance Serenity best suited for?
Any lesion that is exceptionally tight or calcified is appropriate for this balloon, as I have almost always been able to track a[n] [Advance] Serenity balloon to the location I need to because of the way the tip travels.

How does the laser-formed tip aid in trackability?
I think this is the ticket to why the balloon glides so well and can reach very difficult locations that are tough to traverse with conventional balloons.

Dr Jing Li on treatment trends

What are the particular PAD disease states that Advance Serenity best treats?
I have been using the [Advance] Serenity balloon for our patients with tibial disease. In many patients with diabetes and end-stage renal disease (ESRD), you may not see the typical femoropopliteal distribution of occlusive PAD that had traditionally been treated with bypass surgery. Often in these patients, you lose your outflow vessels first, which speaks to the importance of avoiding injury to the tibial arteries as there often is no open surgical option if endovascular techniques fail. [Advance] Serenity, in my experience, has been particularly helpful in this arterial bed.

How does the laser-formed tip help create a smooth transition to cross complex lesions?
This is a question I have a hard time answering since I have not considered the mechanisms of the balloon because it rarely fails. It is not just a matter of ability to cross, but also minimising trauma to the lumen when crossing, particularly in tibial arteries where there are few technical solutions to dissection or perforation. Although these may not be devastating complications, when the only vessel you can improve upon is affected, this undoubtedly can lead to a worse outcome for the patient.


 

Headshot of Anahita Dua, MD, MS, MBA, FACS, Vascular Surgeon

Anahita Dua, MD, MS, MBA, FACS
Vascular Surgeon
Director of the Vascular Lab
Co-director of the Peripheral Artery Disease Center and Limb Evaluation and Amputation Program (LEAPP)
Massachusetts General Hospital

Headshot of Keith M. Jones, MD, FACS, RPVI, Vascular Surgeon

Keith M. Jones, MD, FACS, RPVI
Vascular Surgeon
Vascular/Endovascular Surgery
Mercy Medical Group
Sacramento, CA

Headshot of Jing Li, MD, RPVI, Attending Vascular Surgeon

Jing Li, MD, RPVI
Attending Vascular Surgeon
Assistant Professor, Weill Cornell Medicine
Site Director of the Program for Advanced Limb Preservation (PALP)
NewYork-Presbyterian/Queens


Dr Anahita Dua is a paid consultant of Cook Medical.

Watch this product animation

Explore how the Advance Serenity® 18 Hydrophilic PTA Balloon Dilation Catheter:

  • Compares to competitors
  • Glides through tortuous anatomy
  • Promotes a smoother crossing with enhanced product features

See the Advance Serenity 18 versus other PTA Balloon Catheters graph featured in this product animation.

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How can the Advance Serenity PTA balloon elevate your patients’ outcomes?


Advance Serenity 18

The Advance Serenity 18 Hydrophilic PTA Balloon Dilatation Catheter is indicated for the percutaneous transluminal angioplasty (PTA) dilation of peripheral vasculature stenosis in the iliac, femoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulas.

Advance Serenity 18 data

The Advance Serenity balloon was evaluated for crossability against leading competitors by measuring the average force (in grams) needed to traverse a synthetic lesion within an anatomical model.
Line graph with title Benchtop Test Crossing 0.9 MM Synthetic Lesion and sub-title Advance Serenity 18 vs other 0.018 inch PTA balloon catheters. The X axis is labeled Distance (cm) and is numbered from 62 to 72 in increments of 2. The Y axis is labeled Group Average Push Force (g) and is numbered from 0.0 to 2000.0 in increments of 200. Six lines plotted on the graph are labeled Balloons A, B, C, D, Cook Advance 18LP, and Advance Serenity 18. The Advance Serenity line plots at the lowest of all the lines, indicating that minimal force is needed for crossing a lesion.

Compared to leading competitors, the Advance Serenity 18 has proven to have excellent crossability using minimal force. With its laser-formed tip design and next-generation hydrophilic coating, the Advance Serenity 18 demonstrated superior crossability within a synthetic lesion. Coaxial shaft design balances stiffness and flexibility to deliver pushability to cross distal lesions. Its pleated balloon design and broad range of diameters enable you to treat the entire limb and may help save time.

Advance Serenity 18 femoropopliteal (above the knee, ATK) size matrix

Catheter platform Over the wire (OTW)
Recommended wire guide diameter 0.018 inch
Sheath compatibility 4, 4.5, 5, 5.5 Fr
Catheter working length 90 cm and 135 cm (all sizes)
Balloon diameters 5-10 mm
Balloon lengths 20-150 mm
Nominal pressure 8 atm (all sizes)
Rated burst pressure 10-16 atm

Advance Serenity 18 Infrapopliteal (below the knee, BTK) size matrix

Catheter platform Over the wire (OTW)
Recommended wire guide diameter 0.018 inch
Sheath compatibility 4 Fr (all sizes)
Catheter working length 150 cm (all sizes)
Balloon diameters 2-4 mm (0.5 mm increments)
Balloon lengths 20-220 mm
Nominal pressure 8 atm (all sizes)
Rated burst pressure 16 atm (all sizes)

Femoropopliteal portfolio


Access

Cross

Treat

Advance Serenity 14

The Advance Serenity 14 Hydrophilic PTA Balloon Dilatation Catheter is indicated for percutaneous transluminal angioplasty (PTA) dilation of peripheral vasculature stenosis in the iliac, femoral, iliofemoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulas.

• All of the balloon sizes are compatible with 4 Fr sheaths.
• Balloon lengths of up to 220 mm allow for the treatment of longer lesions with fewer inflations and deflations.

Advance Serenity 14 data

The Advance Serenity balloon was evaluated for crossability against leading competitors by measuring the average force (in grams) needed to traverse a synthetic lesion within an anatomical model.
Line graph with title Benchtop Test Crossing 0.5 mm Synthetic Lesion and sub-title Advance Serenity 14 vs other 0.014 inch PTA balloon catheters. The X axis is labeled Distance (cm) and is numbered from 62 to 72 in increments of 2. The Y axis is labeled Average Force (g) and is numbered from 0 to 500 in increments of 50. Six lines plotted on the graph are labeled Balloons A, B, C, D, E, Advance 14LP, and Advance Serenity 14. The Advance Serenity line plots mostly at the lowest of all the lines, indicating that minimal force is needed for crossing a lesion.

Compared to leading competitors, the Advance Serenity 14 has proven to have excellent crossability using minimal force. With its laser-formed tip design and next-generation hydrophilic coating, the Advance Serenity 14 demonstrated superior crossability within a synthetic lesion. Coaxial shaft design balances stiffness and flexibility to deliver pushability to cross distal lesions. Its pleated balloon design and broad range of diameters enable you to treat the entire limb and may help save time.

Advance Serenity 14 size matrix

Catheter platform Over the wire (OTW)
Recommended wire guide diameter 0.014 inch
Sheath compatibility 4 Fr (all sizes)
Catheter working length 120-150 cm (all sizes)
Balloon diameters 2-4 mm (0.5 mm increments)
Balloon lengths 20-220 mm
Nominal pressure 6 atm (all sizes)
Rated burst pressure 16 atm (all sizes)

Infrapopliteal portfolio


Antegrade

Access

Cross

Treat

 

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Resources


 

Advance Serenity resources

Advance Serenity® 14 Brochure
Advance Serenity® 18 Brochure

The product information on this website is intended only for physicians and healthcare professionals licensed in the European Union (except France), the United Kingdom, Switzerland, Norway, Iceland, Turkey, and Liechtenstein.

If your region is not listed, visit our Ordering & Returns for more information.
Information provided on this site is not intended to be professional medical advice. Product Instructions for Use (IFU) should be consulted before use of any product.

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Thank You for Your Interest in Cook Medical's Products

The product information on this website is intended only for physicians and healthcare professionals licensed in the European Union (except France), the United Kingdom, Switzerland, Norway, Iceland, Turkey, and Liechtenstein. If you are located in another global region, please click on the regional flag at the very top of the webpage and choose your region from the drop-down options.

If your region is not listed, visit our How to Order section for more information.

Information provided on this site is not intended to be professional medical advice. Product Instructions for Use (IFU) should be consulted before use of any product.

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