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Learning About Your Knee Condition
     Knee Glossary
     General Knee Conditions
     About Cartilage Damage

Treating Damaged Cartilage
      How CARTICEL Can Help
      Talking to Your Doctor

What To Expect
      Pre-Surgery
      Surgery
      Physical Therapy
      Explanation of Benefits
      Frequently Asked Questions

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Medical Professionals
About CARTICEL®

CARTICEL Training and Events
      Introduction to CARTICEL Workshop
      Advanced Concepts in ACI
     CARTICEL Events

Surgery
      Patient Diagnosis & Assessment
     Biopsy
           Pre-Biopsy
           Biopsy Procedure
           Post-Biopsy
      Implant
           Pre-Surgery
           Implant Procedure
      Rehabilitation

Patient Education

Reimbursement Information
      Suggested Billing Codes
      Frequently Asked Reimbursement Questions

Clinical Information
      Case Studies
      About the CARTICEL Registry
      Submit Medical Questions

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This site is intended for United States residents only.
©2005-2008 Genzyme Corporation. All rights reserved. CARTICEL, Carticel Care and Genzyme are registered trademarks of Genzyme Corporation.

Important Safety Information

CARTICEL is for autologous use and is indicated for the repair of symptomatic, cartilage defects of the femoral condyle (medial, lateral or trochlea), caused by acute or repetitive trauma, in patients who have had an inadequate response to a prior arthroscopic or other surgical repair procedure (e.g., debridement, microfracture, drilling/abrasion arthroplasty, or osteochondral allograft/autograft). CARTICEL should only be used in conjunction with debridement, placement of a periosteal flap and rehabilitation. The independent contributions of the autologous cultured chondrocytes and other components of the therapy to outcome are unknown. It is not indicated for the treatment of cartilage damage associated with generalized osteoarthritis. It is not recommended for patients whose knee meniscus has been surgically removed unless the patient has undergone surgical reconstruction prior to or concurrent with CARTICEL implantation.

Pre-existing conditions including meniscal tears, joint instability or malalignment of the joint should be corrected prior to or concurrent with CARTICEL implantation. It should not be used in patients with a known history of hypersensitivity to gentamicin, other aminoglycosides or materials of bovine origin. CARTICEL is not routinely tested for transmissible infectious diseases and may transmit disease to the healthcare provider handling CARTICEL. In addition, it should not be used in patients who have previously had cancer in the bones, cartilage, fat or muscle of the treated limb. Use in children, patients over age 65, or in joints other than the knee has not yet been assessed.

The occurrence of subsequent surgical procedures (SSPs), primarily arthroscopy, following CARTICEL implantation is common. In the Study of the Treatment of Articular Repair (STAR), forty-nine percent (49%) of patients underwent an SSP on the treated knee, irrespective of their relationship to CARTICEL, during the 4-year follow up. The most common serious adverse events (³ 5% of patients), derived from STAR, include arthrofibrosis/joint adhesions, graft overgrowth, chondromalacia or chondrosis, cartilage injury, graft complication, meniscal lesion, graft delamination, and osteoarthritis.

For more information on CARTICEL, please see the Package Insert (PDF).



Terms and Conditions of Use | Privacy Policy | Site Map | This site is intended for United States residents only.
© 2008 Genzyme Corporation. All rights reserved. CARTICEL, Carticel Care and Genzyme are registered trademarks of Genzyme Corporation.