Jumpstart® Composite Antimicrobial Wound Dressing
JumpStart® Composite Antimicrobial Wound Dressings provide broad-spectrum antimicrobial efficacy and an optimal environment for wound healing. Indicated for a broad variety of superficial and full-thickness wounds.
• Broad-spectrum antimicrobial efficacy, including against multi-drug resistant and biofilm-forming bacteria
• Conforms to wound site
• Waterproof, high performance bandage
JumpStart® Composite Antimicrobial Wound Dressing is intended for the management of wounds to provide a moist wound environment and is indicated for partial and full-thickness wounds such as surgical incisions, pressure ulcers, venous ulcers, diabetic ulcers, first- and second-degree burns, donor and recipient graft sites, etc.
JumpStart® dressings should not be used on individuals with sensitivity or allergy to silver, zinc or other dressing components.
Frequent or prolonged use of this product may result, in rare occasions, in temporary discoloration of the skin.
Caution: Federal law restricts this device to sale by or on the order of a physician.
Single use; do not use if the pouch is open or damaged.
For external use only.
Do not apply JumpStart® dressing in conjunction with topical agents such as antimicrobial ointments, enzymatic debriders, antibiotic creams or ointments, silver- or zinc-containing creams, oxidizing agents, or petroleum-based products.
The use of adhesive dressings on fragile or sensitive skin may pose a risk of skin damage upon removal of the dressing. To mitigate this risk, a skin prep may be applied on the wound perimeter prior to dressing application.
The patient should stop using the dressing and consult a physician if allergy, irritation, increased pain, maceration or any irregular skin discoloration occurs.
JumpStart® dressings are not intended to be used on wounds with uncontrolled bleeding.
Remove JumpStart® dressing during energy-based procedures (such as radiofrequencies, ultrasound, radiation, etc.) where the dressing may interfere with delivery.
Avoid contact with electrodes or conductive gels during electronic measurements (e.g., EEG or ECG).
JumpStart® dressings may be used on infected wounds being clinically managed, as an adjunct to the local clinical protocol.
The safety of daily JumpStart® dressing use for longer than 28 days has not been studied.
Adverse effects/reactions include, but are not limited to allergic reaction to silver or zinc, dressing may adhere to wound site if dry.
Store the dressing in dry conditions at room temperature. Protect from light.
0.9mg/cm sq of elemental silver, 0.3mg/cm sq of elemental zinc
|Absorptive dressing format|
|Alginate dressing format|
|Antimicrobial effects up to 3 days|
|Antimicrobial effects up to 48 hours|
|Antimicrobial effects up to 7 days||●|
|Collagen dressing format|
|Composite dressing format||●|
|Contact layer dressing format|
|Foam dressing format|
|Gauze or non-woven dressing format|
|Gelling fiber dressing format|
|Hydrogel (amorphous) dressing format|
|Hydrogel (impregnated) dressing format|
|Hydrogel (sheet) dressing format|
|Impermeable to outside contaminants|
|Impregnated dressing format|
|Moisture vapor permeable|
|Secondary dressing required||●|
|Super absorbent polymers|
|Sustained release formula|
|Transparent film dressing format|
|Wound filler dressing format|
|Educational Material Available||●|
|Free Samples/Trials Available||●|
|Published Clinical Article Available||●|
Moderate/Highly Exudating Wounds
Non/Minimally Exudating Wounds
NOTE: If dressing a joint, apply the dressing while the joint is in slight flexion.
1. Cleanse the wound area with an appropriate wound cleanser according to local clinical protocol.
2. For optimal adhesion results, apply skin prep to the area surrounding the wound (skin prep not included).
3. Peel back the dressing liner to expose the dotted pad, leaving the edges in place.
4. Moisten the dotted JumpStart® pad with sterile saline, water or a thin, even layer of water-based hydrogel (not included).
5. Position the dressing over the wound site, with the dotted pad over the wound. Gently press the dressing against the skin, to ensure contact with the wound surface.
6. Remove the remaining liner and smooth the adhesive down over the skin.
Change the dressing according to institution protocol, as needed (when the dressing becomes soiled, or after seven days of use).
Arthrex, Inc. is a global medical device company and leader in new product development with a corporate mission of helping surgeons treat their patients better.