Eclypse Adherent Sacral - super absorbent silicone sacral dressing
Summary
Super absorbent sacral dressing with silicone wound contact layer Eclypse Adherent Sacral is a multi-layer sacral wound dressing composed of Silfix soft silicone which adheres only to normal healthy skin, a fabric for rapid absorption of fluid, a super absorbent moisture locking central layer for superior fluid management and a breathable polyethylene protective backing.
Eclypse Adherent Sacral has a very high capacity and uniquely converts all fluid into a moist gel to reduce potential maceration whilst preventing strike-through. [features]
» High capacity exudate management
» Atraumatic dressing technology
» Breathable fluid repellent backing
» Moist wound healing environment
» Moisture locking system
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Eclypse Adherent Sacral - super absorbent silicone sacral dressing
How to Use
[how to use]Apply to wound (white silicone face down, beige side up) allowing a minimum of a 2cm border overlap around the wound area. Do not cut Eclypse Adherent Sacral. Eclypse Adherent Sacral is self adherent but may require additional support with a suitable tape. Eclypse Adherent Sacral must be changed before dressing reaches capacity but depending on wound exudate levels, may be left in place for up to 7 days. |
For all exuding wounds on the sacral area such as pressure ulcers.
[indications]For all exuding wounds on the sacral area such as pressure ulcers |

Eclypse Adherent Sacral - super absorbent silicone sacral dressing
Sizes and Codes
| Product Code | Size | No. in box |
|
CR3986 |
22 x 23 cm | 10 |
| CR3985 | 17 x 19 cm | 10 |
Would you like to try a free sample? Contact us today with the product code.
Eclypse Adherent Sacral - super absorbent silicone sacral dressing
Links
[brochure]
[case study]
Sacral ulcers following cardiac surgery: incidence and risks.
Papantonio CT, Wallop JM, Kolodner KB.
Adv Wound Care. 1994 Mar;7(2):24-36.This study examined the incidence and risk factors that relate to the development of sacral pressure ulcers following elective cardiac surgery. Perioperative variables were assessed using 136 adult patients. Ulcers, including 16 Stage I and 21 Stage II-III, occurred on 27.2% (n = 37) of the patients. Factors such as older age, transfer from another hospital, and a history of diabetes, were associated with ulcer development. These findings may be used to identify patients at risk for pressure ulcers during cardiac surgery.


