Panacryl Sutures
Panacryl Sutures are synthetic, absorbable, sterile surgical sutures composed of a copolymer of 95% lactide and 5% glycolide. The sutures are coated with a copolymer composed of 90% caprolactone and 10% glycolide.
Because of the unique absorption profile of Panacryl, the patient's body may react to this suture as though they were a foreign body. Surgeons should consider its use in specific situations. Because of these unique absorption properties, the sutures are subject to a Class 2 FDA recall. They are currently unavailable on the free market. However, more than 1,061,712 Panacryl sutures were sold before they were pulled from sale.
The following adverse effects are caused by the use of Panacryl Sutures:
- Elevated rate of infection
- "Spitting suture" - the body rejects the suture and pushes it to the surface of the skin
- Suture granulomas - scar tissue forms around the suture and causes a bump under the skin
- Tunneling - the suture inhibits healthy tissue growth, causing tiny tunnels to form around the incision area
- Sutures unable to absorb into the patient's body
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