What is it? How does it work? Evidence Indications
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INADINE®

INADINE® PVP-I Non-Adherent Dressing consists of a low adherent knitted viscose fabric impregnated with a polyethylene glycol (PEG) base containing 10% Povidone Iodine; equivalent to 1.0% available iodine.

INADINE® dressings are designed to protect the wound, even if infected. INADINE® is indicated for the management of ulcerative wounds and may also be used for the prevention of infection in minor burns and minor traumatic skin loss injuries.

View our Iodine White Paper


Click this link to view INADINE® product codes
© Systagenix Wound Management 2011. Brands marked with ® or ™ are trademarks of Systagenix. All other products referenced herein are acknowledged to be trademarks of their respective owners.

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How INADINE® Dressings Work

The Povidone molecule provides an effective release of iodine. The polyethyleneglycol provides a water-soluble environment, which allows the Iodine to reach the bacteria in the wound.

 

Inadine Dressing functionality

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Please click on the table below for the full list if INADINE® references:

For more detailed clincial and in vitro work on the benefits of  INADINE®, please click one of the links below:

 

Systagenix is not responsible for the content of external websites.

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INADINE® Is Indicated For The Prophylaxis and Treatment of Infection.


  • The frequency of dressing changes depends primarily upon the condition of the wound.
  • If large quantities of exudate are produced, daily changes will probably be required; but if the wound is relatively dry, the interval between changes may be extended.
  • Fading of the colour of the dressing indicates the loss of antiseptic efficacy and this is when the INADINE® dressing should be changed.

 

Example of Inadine Indication

 

 

Please refer in full to the Instructions for use leaflet provided in the product packaging.

Click here for references
 
 
 
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Now Playing: WOUNDCHEK™ Protease Status Specimen Collection (Serena's Technique)

Description:
1. Prior to swabbing, cleanse the wound with sterile saline to remove all loose debris, remains of therapeutic agents and necrotic tissue.
2. Ensure that complete hemostasis has been achieved before obtaining the specimen. Do not perform sharp wound debridement prior to sample collection.
3. Moisten wound area to be swabbed with a few (up to five) drops of saline. Care should be taken not to flood the wound with excessive saline.
4. Avoid swabbing areas that contain blood, necrotic material, thick slough or fibrinous tissue.
5. Using a sterile swab provided in the kit, collect the wound fluid sample by pressing the head of the swab flat against the base of the wound and gently rolling it back and forth several times while applying pressure. Continue rolling the swab head until fully coated and discoloured by wound fluid.
6. Test fresh sample swabs as soon as possible after collection. Follow test procedure instructions.

Disclaimer
The product information on this page is not intended for, or to be used by health care professionals or users in the United States

Video footage kindly provided by SerenaGroup

SerenaGroup, 311 Pennsylvania Ave. West, Warren, PA 16365, USA, For more information email: Systagenix.

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WOUNDCHEK™ Protease Status Specimen Collection (Serena's Technique)

Description:
1. Prior to swabbing, cleanse the wound with sterile saline to remove all loose debris, remains of therapeutic agents and necrotic tissue.
2. Ensure that complete hemostasis has been achieved before obtaining the specimen. Do not perform sharp wound debridement prior to sample collection.
3. Moisten wound area to be swabbed with a few (up to five) drops of saline. Care should be taken not to flood the wound with excessive saline.
4. Avoid swabbing areas that contain blood, necrotic material, thick slough or fibrinous tissue.
5. Using a sterile swab provided in the kit, collect the wound fluid sample by pressing the head of the swab flat against the base of the wound and gently rolling it back and forth several times while applying pressure. Continue rolling the swab head until fully coated and discoloured by wound fluid.
6. Test fresh sample swabs as soon as possible after collection. Follow test procedure instructions.

Disclaimer
The product information on this page is not intended for, or to be used by health care professionals or users in the United States