KALTOSTAT® Dressing forms an absorbent gel-fiber matrix on contact with fluid. Maintains a moist wound environment and facilitates atraumatic removal. Aids in the control of minor bleeding. Usable on infected wounds under the care of a health care professional.
KALTOSTAT® Cavity Dressing is an external wound dressing designed to absorb exudate and protect the wound from contamination. KALTOSTAT® Cavity Dressing is indicated as an external wound dressing for the local wound management of exuding cavity wounds such as pressure sores, venous stasis ulcers, arterial ulcers, diabetic ulcers, lacerations, post-surgical wounds, and other external wounds inflicted by trauma.
This dressing is not indicated for dry wounds or third-degree burns and is not intended for use as a surgical swab.
Infection: All wounds can be expected to contain some microorganisms. If, however, true clinical infection (fever, tenderness or redness in the area of the wound) should develop, appropriate steps, as defined by the attending physician, should be taken to address such infection. Regular evaluation and cleansing of an infected wound should be common practice. Use of KALTOSTAT® Cavity Dressing may be continued, provided it is changed on a regular basis (at least daily while infection is present).
Underlying Causes: Some wounds like leg ulcers and pressure sores can be “non-healing” unless steps are taken to correct the underlying pathology. KALTOSTAT® Cavity Dressing is designed for local wound management and can be part of the overall management program for these types of wounds.
Desiccation: KALTOSTAT® Cavity Dressing is designed to create a moist environment that facilitates wound healing. If a KALTOSTAT® Cavity Dressing has initially formed a gel that is allowed to dry out, removal from the wound can be difficult. If the gel dries out, moisten the dried dressing with saline to rehydrate it.
The use of KALTOSTAT® wound dressings is not recommended for infants less than 12 months of age. This device is for single-use only and should not be re-used. Re-use may lead to increased risk of infection or cross contamination. Physical properties of the device may no longer be optimal for intended use.
Gamma sterilized. Sterility is guaranteed unless package is torn or damaged prior to opening. Do not resterilize.
Protect from light; store in a cool dry place.
|Antimicrobial format available|
|Conforms readily to wound||●|
|Intact when saturated||●|
|Moisture vapor permeable|
|Secondary dressing required||●|
|Usable on infected wounds||●|
|Variety of sizes||●|
|Educational Material Available||●|
|Free Samples/Trials Available||●|
|Published Clinical Article Available|
Before applying KALTOSTAT® Cavity Dressing, the wound should be debrided of excessive necrotic tissue and eschar and irrigated with an appropriate non-toxic cleansing solution, such as normal saline. KALTOSTAT® Cavity Dressing should be applied dry into the wound. Do not pack tightly. An appropriate secondary dressing should be used to secure KALTOSTAT Cavity Dressing in place. Change the KALTOSTAT® Cavity Dressing when strikethrough of the secondary dressing occurs or as indicated by good clinical practice. Removal may be assisted by moistening the dressing with sterile saline. Cleanse the wound site, if required, before applying a new dressing. As with any dressing, KALTOSTAT® Cavity Dressing should be removed from the wound and the wound cleansed at appropriate intervals.
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