What is Strattice?
What kind of treatment is the Strattice consent form for?
The Strattice consent form pertains to surgical treatment involving the use of Strattice, a bioprosthetic acellular dermal matrix for soft tissue reconstruction.
- Intended for breast reconstruction, hernia repair, and other surgical applications.
- Strattice provides supportive tissue for improved healing and aesthetic results.
- Patients may expect enhanced structural integrity and reduced scarring.
- Used in conjunction with implants or as standalone support in surgery.
As with any surgical procedure, there are potential risks, including infection or complications from anaesthesia.

- It is a legal and ethical requirement in the UK
- Confirms you understand the treatment and possible side effects
- Helps set realistic expectations and ensures safe practice
- Builds trust between you and your practitioner
- Your signed confirmation of informed consent
Potential side effects of Strattice treatments
Strattice treatments may result in various side effects that patients should be aware of.
- Infection
- Seroma formation
- Wound healing complications
- Allergic reactions
- Changes in sensation
Rare side effects may include graft rejection or chronic pain.
Who is the ideal candidate for this treatment?
The ideal candidate for Strattice treatment is an individual seeking soft tissue reinforcement without contraindications.
- Non-pregnant individuals
- No known allergies to materials used
- Absence of active infections
- No severe autoimmune conditions
Consult a healthcare professional for personalised advice.
Aftercare advice for best results
Proper aftercare for Strattice is essential for optimal healing and results.
- Keep the area clean and dry.
- Avoid strenuous activities and heavy lifting.
- Follow your surgeon's instructions on dressing changes.
- Attend all follow-up appointments.
Always monitor for signs of infection or unusual discomfort.
How to fill the consent form?
To complete the consent form, carefully read each section outlining the treatment, potential risks, and expected outcomes. Ensure you understand all information before proceeding. Fill in personal details accurately and confirm agreement by ticking the required boxes. The form must be signed digitally to confirm your informed consent.
