Artificial Meniscus Offers Patients Real Relief

February 18, 2016 Brigham and Women's Hospital

The artificial meniscus stays in place – even when squatting – without being attached to bones or any other surrounding tissue.

The artificial meniscus stays in place without being attached to bones or any other surrounding tissue.

Brigham and Women’s Hospital (BWH) orthopedic surgeon Dr. Andreas Gomoll recently became the first physician in New England to perform a new type of knee surgery that replaces a patient’s damaged meniscus with an artificial implant made from synthetic polymers (plastics). The procedure is being offered to certain patients as part of a clinical trial studying the experimental device’s effectiveness at relieving pain and restoring function in the knee.

The artificial meniscus is inserted into a patient’s knee through a small incision (two to three inches). Because of its special design, featuring a thick rim and a thinner center, the device stays in place – even when squatting – without being attached to bones or any other surrounding tissue. Over time, the implant molds itself to the patient, creating a secure, comfortable shock absorber for the knee. This design is a significant advance from a similar approach that uses a metal device, which, due to its hardness, doesn’t provide shock absorption or mold itself to the patient’s anatomy.

Patients wear a knee brace for approximately one week after the procedure, but they can put their entire weight on the knee during this time. After removing the brace, the pain and swelling continue to diminish, and within four to six weeks, the knee is functional for daily activities. Recovering the full range of motion, however, may take up to three months.

Who is a candidate for an artificial meniscus implant?

For the majority of patients with meniscus damage, arthroscopic surgery to clean out the torn tissue leads to satisfactory outcomes. However, in some patients with significant meniscus damage, arthroscopy doesn’t provide a sufficient remedy. Without a healthy meniscus to act as a shock absorber and protect cartilage, these patients continue to experience pain and are at risk of developing arthritis more quickly.

There are a few treatment options for these patients. These include meniscus implantation from an organ donor or an osteotomy, which involves cutting the shin (tibia) bone. However, these procedures are more complex and require a longer recovery.

“We’ve been looking for something that’s a bridge for those patients,” says Dr. Gomoll. “They don’t have a meniscus, they don’t like the current treatment options, and they’re not candidates yet for joint replacement. For them, this artificial meniscus implant would be a great option.”

Meniscus implant outcomes

Although this latest meniscus implant is relatively new in the United States, several generations of the device have been tested in Europe and Israel. This has led to significant improvements in design and material composition, and according to Dr. Gomoll, there haven’t been any reported tears or dislocations for the current generation of the implant.

The VENUS Clinical Study (Verifying the Effectiveness of the NUsurface® System) is currently recruiting participants. For those who are interested in participating at BWH, please contact Amy Phan at  

– Chris P.

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