Aquacel Foam Adhesive Sacral Dressing 20 x 16.9 cm Waterproof Silicone Adhesive

Product Overview

The AQUACEL Foam Adhesive Sacral Dressing is an advanced wound management device engineered by ConvaTec specifically for the sacral anatomical region. The dressing integrates Hydrofiber Technology with a multi-layered foam construction to deliver controlled vertical absorption of wound exudate while maintaining an optimal moist wound environment conducive to autolytic debridement and granulation tissue formation. The sacral contour ensures conformability to the complex curvature of the sacrococcygeal area, reducing edge lift and minimising the risk of shear-related complications.

Unlike conventional foam dressings, the AQUACEL Foam Adhesive Sacral variant employs a perforated silicone adhesive border that provides secure fixation without adhering to the wound bed or fragile peri-wound skin. The waterproof polyurethane outer film acts as a bacterial and viral barrier (per EN 13726-2 testing methodology), enabling patients to shower while the dressing remains in situ. This dressing is designed for use under compression bandaging systems and negative pressure wound therapy interfaces where clinically appropriate.

Specifications

Clinical Indications

• Sacral pressure injuries (Category/Stage II through IV) with moderate to heavy exudate, as classified under the NPUAP/EPUAP/PPPIA international pressure injury staging system
• Post-surgical sacral wound management requiring waterproof barrier protection and atraumatic dressing changes
• Chronic sacral wounds including venous and mixed-aetiology ulcers presenting in the sacrococcygeal region
• Fungating or oncological wounds in the sacral area where exudate management and odour containment are clinical priorities
• Wound management under compression therapy or negative pressure wound therapy (NPWT) systems where a conformable secondary dressing is required

Frequently Asked Questions

How does Hydrofiber Technology differ from standard foam absorption?

Hydrofiber Technology absorbs wound exudate vertically into the fibre structure, where it forms a cohesive gel that locks fluid within the dressing matrix. This vertical wicking mechanism reduces lateral spread of exudate across the peri-wound skin, thereby lowering the risk of maceration compared to conventional foam dressings that rely on capillary spread. The mechanism aligns with moist wound healing principles outlined in international wound management guidelines (EWMA, WOCN).

Can this dressing be used on infected sacral wounds?

The AQUACEL Foam Adhesive Sacral Dressing is not an antimicrobial dressing and does not contain silver or PHMB. For wounds with confirmed or suspected infection, clinicians should consider the AQUACEL Ag Foam variant, which incorporates ionic silver for broad-spectrum antimicrobial activity. All dressing selections for infected wounds should be guided by local antimicrobial stewardship protocols and wound culture results.

What is the recommended dressing change frequency?

The dressing may remain in place for up to 7 days, though change intervals should be determined by clinical assessment of exudate saturation, wound progress, and institutional wound care protocols. In heavily exuding acute wounds, more frequent changes (every 1 to 3 days) may be clinically appropriate. The European Wound Management Association (EWMA) recommends individualized dressing change schedules based on wound assessment.

Is this product available for purchase by healthcare facilities in Singapore?

Yes. EMIS (Essential Medical International Supplies Pte Ltd) is an authorised distributor of ConvaTec wound care products in Singapore. Healthcare facilities, home nursing services, and clinic procurement departments can purchase directly through emis.asia with GST-inclusive pricing and delivery across Singapore. Volume pricing is available for institutional orders.

Does this dressing comply with Singapore HSA medical device requirements?

ConvaTec AQUACEL Foam dressings are CE marked under EU MDR 2017/745 as Class IIb medical devices and manufactured under ISO 13485 quality management systems. Products distributed through EMIS comply with the Health Sciences Authority (HSA) Singapore medical device registration framework for Class C/D devices under the Health Products Act.