
Watch On Demand
One year after receiving silicone injections, a 47-year-old woman developed gluteal ulcers that became so severe that she lost her job.
After seeing multiple surgeons and experiencing no improvement, the patient came to Dr. Claire Dillingham, Chief of Plastic Surgery at the Cone Health Medical Group.
Watch this case-specific webinar to hear Dr. Dillingham discuss:
-
- Her approach to grafting the gluteus area
- The role of Cytal® Wound Matrix and MicroMatrix® UBM Particulate
- How she achieved full wound closure
MicroMatrix UBM Particulate
INDICATIONS
MicroMatrix UBM Particulate is intended for the management of wounds including: partial and full-thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, second-degree burns, skin tears), and draining wounds. The device is intended for one-time use.
CONTRAINDICATIONS
1. Patients with known sensitivity or allergy to porcine materials.
2. Third-degree burns.
WARNINGS
1. If active infection is present, treat patient to resolve infection prior to device application.
2. Do not use glass vial if cracked, broken, or otherwise damaged.
3. MicroMatrix UBM Particulate is not indicated for treatment of alopecia.
PRECAUTIONS
Do not tap glass vial with metal objects or handle in a way that may cause glass to break and contaminate wound.
Cytal
INDICATIONS
Cytal Wound Matrix is intended for the management of wounds including: partial and full-thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, second-degree burns, skin tears), and draining wounds. The device is intended for one time use.
CONTRAINDICATIONS
1. Patients with known sensitivity or allergy to porcine materials.
2. Third-degree burns.
WARNINGS
1. Exposure to contaminated or infected field can lead to rapid breakdown of device.
2. If active infection is present, treat patient to resolve infection prior to device application.
3. Do not use if cracked, broken, or otherwise damaged.
PRECAUTIONS
Always use aseptic technique when handling device.
Please fill out the below form to access this premium content:

Watch On Demand
One year after receiving silicone injections, a 47-year-old woman developed gluteal ulcers that became so severe that she lost her job.
After seeing multiple surgeons and experiencing no improvement, the patient came to Dr. Claire Dillingham, Chief of Plastic Surgery at the Cone Health Medical Group.
Watch this case-specific webinar to hear Dr. Dillingham discuss:
-
- Her approach to grafting the gluteus area
- The role of Cytal® Wound Matrix and MicroMatrix® UBM Particulate
- How she achieved full wound closure
Please fill out the below form to access this premium content:
MicroMatrix UBM Particulate
INDICATIONS
MicroMatrix UBM Particulate is intended for the management of wounds including: partial and full-thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, second-degree burns, skin tears), and draining wounds. The device is intended for one-time use.
CONTRAINDICATIONS
1. Patients with known sensitivity or allergy to porcine materials.
2. Third-degree burns.
WARNINGS
1. If active infection is present, treat patient to resolve infection prior to device application.
2. Do not use glass vial if cracked, broken, or otherwise damaged.
3. MicroMatrix UBM Particulate is not indicated for treatment of alopecia.
PRECAUTIONS
Do not tap glass vial with metal objects or handle in a way that may cause glass to break and contaminate wound.
Cytal
INDICATIONS
Cytal Wound Matrix is intended for the management of wounds including: partial and full-thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, second-degree burns, skin tears), and draining wounds. The device is intended for one time use.
CONTRAINDICATIONS
1. Patients with known sensitivity or allergy to porcine materials.
2. Third-degree burns.
WARNINGS
1. Exposure to contaminated or infected field can lead to rapid breakdown of device.
2. If active infection is present, treat patient to resolve infection prior to device application.
3. Do not use if cracked, broken, or otherwise damaged.
PRECAUTIONS
Always use aseptic technique when handling device.