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3M™ AbThera™ Advance Open Abdomen Dressing

The 3M™ AbThera™ Advance Open Abdomen Dressing actively facilitates drawing wound edges together, directly based upon the technology of 3M™ AbThera™ Therapy.

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Solventum

3M Health Care is now Solventum, a health care company built from a legacy of innovation and dedicated to enabling better, smarter, safer health care to improve lives.
Toll free:(800) 228-3957 Fax:(800) 728-0959 Website: www.solventum.com
Benefits

• Allows rapid access for re-entry
• No sutures required for placement
• Provides separation between the abdominal wall and viscera, protecting abdominal contents
• Allows rapid access for re-entry and does not require sutures for placement
• Perforated foam dressing actively facilitates drawing wound edges together

Indications

The 3M™ AbThera™ Advance Open Abdomen Dressing is indicated for temporary bridging of abdominal wall openings where primary closure is not possible and/or repeat abdominal entries are necessary. Intended use of this system is for use in open abdominal wounds, with exposed viscera, including but not limited to abdominal compartment syndrome. The intended care setting is a closely monitored area within the acute care hospital, such as the ICU. The abdominal dressing will most often be applied in the operating theater.

Contraindications

Contraindicated for use on patients with open abdominal wounds containing non-enteric unexplored fistulas. Protect vital structures with 3M™ AbThera™ Fenestrated Visceral Protective Layer at all times during therapy. Never place exposed foam material directly in contact with exposed bowel, organs, blood vessels, or nerves.

Warnings and Precautions

Key Warnings (for all warnings, refer to Instructions for Use):
-Not for use with instillation therapy.
-Do not substitute, alter or breach the tubing set.
-Monitor closely for bleeding.
-Monitor for intra-abdominal pressure. If IAH/ACS persists, discontinue AbThera Therapy and address underlying
condition as medically indicated.
-3M™ AbThera™ Fenestrated Visceral Protective Layer or 3M™ AbThera™ Visceral Protective Layer should completely cover all exposed viscera and completely separate the viscera from
contact with the abdominal wall.
-Formation of adhesions may reduce the likelihood of fascial reapproximation and increase risk of fistula development,
common complications in patients with exposed viscera.
Key Precautions (for all precautions, refer to the Instructions for Use):
-When using intra-abdominal packing with the AbThera (NPT) System, packing material may be drier than anticipated.
-Monitor fluid output: the volume of exudate in the canister and tubing should be frequently examined.
-Patient size and weight: Use lower negative pressure for elderly/small patients at risk for fluid depletion or
dehydration; monitor fluid output including volume in tubing and canister.

Storage Requirements

Store at room temperature.

How Supplied/Sizing
5 dressings per case.
Patient condition
Product features
cancel Acrylic adhesive drape
cancel Adhesive border dressing
cancel Alternative interface dressing
cancel Antimicrobial
cancel Compatible w/ topicals
cancel Flat drain kit
check_circle Foam interface dressing
cancel Gauze interface dressing
cancel Interface intact when saturated
cancel Kit components available separately
cancel Moisture vapor permeable interface
cancel Round drain kit
cancel Silicone acrylic adhesive drape
cancel Usable on closed wounds
cancel Usable on open wounds
Other features
check_circle Educational Material Available
check_circle Free Samples/Trials Available
check_circle Published Clinical Article Available
Recommended Use

Open Abdomen

Mode of Use/Application

Refer to Instructions for Use.

Removal & Change Frequency

Dressing changes should occur every 24 to 72 hours, or more frequently based upon a continuing evaluation of wound condition and patient presentation. Consider more frequent dressing changes in the presence of infection or abdominal contamination.

Technical Specifications

AbThera™ Visceral Protective Layer (VPL): 665mmx802mm
Encapsulated foam thickness: 10mm
Polyurethane layer thickness: 160 microns
Shelf life: 3 years at room temperature
Sterile, not made with natural rubber latex
Tubing and pad: 4mm lumen for delivery of negative pressure
Dual lumen (one for vacuum/fluid removal, one for pressure sensing)
Antibacterial hydrophobic filters on both lumens
Perforated foam polyurethane

Environmental Conditions
Storage temperature range: -20°F-140°F(-29°C-60°C)
Operating temperature range: 50°F-100°F (10°C-38°C)
Altitude range for optimum performance: 0 to 8,000ft (0 to 2438m)

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