All-metal hip implants, which have been shown to have high failure
rates and cause a host of other health problems, were not linked to
cancer seven years after implantation, new data show.
Concerns have grown in the medical community that the so-called
metal-on-metal hip implants shed metal particles through wear on their
ball-and-socket structure. Many patients who have received the devices
have had elevated levels of cobalt and chromium particles detected in
the bloodstream, leading some doctors to worry about their risk of
developing cancer.
Johnson & Johnson and Stryker Corp have recalled several models
of all-metal implants because of high failure rates - meaning the
patient needed another surgery to fix a problem, such as dislocation -
and set aside billions of dollars to cover patient claims. Neither
company was immediately available to comment. Since the recalls, the use
of all-metal implants, which were sold as being more durable, has
declined sharply.
"Some basic science and some epidemiological studies have suggested
that metal-on-metal hip replacements may be associated with an increased
risk of developing cancer after total hip replacement and specifically
with an increase in malignant melanoma and haematological, prostate, and
renal tract cancers," the UK National Joint Registry (NJR) said in its
annual report, which was released this week at the British Orthopaedic
Association meeting in Manchester, UK.
The NJR, which collects data on joint replacement surgery and
monitors the performance of the implants, said it used UK National
Health Service Hospital Statistics data to test whether metal-on-metal
hip implants are associated with an increased risk of cancer in the
early years after hip replacement, compared with other surfaces, such as
metal-on-polyethelene.
The NJR said it found no association seven years after implantation
but that the devices should continue to be tracked as many cancers can
take longer to manifest themselves.
"Due to the age of the NJR we could only assess the risk for the
first seven years after hip replacement and are happy to report that we
could not identify an increased risk of developing cancer," the NJR
said.
"We must, however, point out that many cancers have prolonged latency
after initial exposure to carcinogens and thus long-term follow up is
needed to provide a definitive answer," it added.
NO U.S. TRACKING MECHANISM
Hundreds of thousands of people have all-metal hip implants. Since
the recall, J&J faces thousands of lawsuits over the failure of its
ASR model, which was pulled from the market, and more lawsuits tied to
its Pinnacle all-metal device, which is still being used.
The United States has no independent registry tracking the
performance of medical devices over time, and health regulators are
still discussing how manufacturers should follow up on complaints over
the all-metal implants.
The U.S. Food and Drug Administration has been monitoring problems
with all-metal hip implants and convened a panel of outside advisers
earlier this year to discuss their safety. The panel concluded there was
little reason for surgeons to use these devices given the risks.
Last year, the FDA ordered implant manufacturers to conduct follow-up
studies in cases in which an implant's failure could have serious
consequences. Companies were ordered to take blood samples from patients
to measure metal ion levels. That analysis has not been completed.
The NJR said its latest analysis continues to support conclusions it
drew last year showing markedly higher failure rate with metal-on-metal
implants.
In addition to J&J and Stryker, makers of all-metal hip implants
include Smith & Nephew, Zimmer Holdings, Wright Medical and Biomet
Inc.
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