DePuy Hip Replacement Helpline Alaska, Hip Replacement Recall lawyers.
Call the DePuy Hip Replacement Helpline Alaska and speak to a medcal social worker about your DePuy Hip Replacement complications. DePuy Hip Replacement lawyers are filing lawsuits for failed dePuy victims in Anchorage, Juneau and all of Alaska.
The DePuy ASR metal on metal hip was told to be the latest and greatest medical breakthrough in orthopedics. Now it could be one of the greatest medical device failures in history. Members of Congress are even calling for hearings over the dangers that metal on metal hip implants pose to people. Now DePuy Hip Replacement lawyers are filing lawsuits fro victims of failed Depuys across Alaska
Why a total Hip Replacement ?
If your hip was been damaged by arthritis, a fracture, or other conditions, common activities such as walking or getting in and out of a chair may have become painful and difficult. Your hip may be stiff, and it may be hard to put on your shoes and socks. You may even feel uncomfortable while resting.
When medications, changes in your everyday activities, and the use of walking supports do not adequately help your symptoms, you may consider hip replacement surgery. Hip replacement surgery is a safe and effective procedure that can relieve your pain, increase motion, and help you get back to enjoying normal, everyday activities. The DePuy was to be the magic cure for hip pain and improve quality of life. The majority of people effected by this are senior populations who were depending on this to improve their quality of life and not put them back in the hospital for revision surgeries and more pain and rehabilitation.
Bloomberg Businessweek reports that a group of concerned Congressmen have written to the chairpersons of several committees, requesting hearings on the safety of Johnson & Johnson’s DePuy metal-on-metal hip implants and Boston Scientific brain stents.
The DePuy ASR metal-on-metal hip implant, which was approved under the FDA’s 510(k) approval process, in which a device can be cleared for market if it is “substantially equivalent” to devices already on the market, is known to release small metal particles into patients’ bloodstreams, potentially damaging nearby bone and tissue and necessitating painful correctional surgery. The Congressmen note that the FDA has already received over 5,000 complaints since January 2011. However, the United States does not have a registry to track medical device failure and it is possible that the number of failed devices is higher than 5,000 and will continue to rise in the coming years. The high failure rate and lack of a reliable tracking registry led the FDA “to order 20 manufactureres of these devices to submit a plan to the FDA to study how frequently they were failing and to examine the health implications of device failures.”
Toxicity from the DePuy
Cobalt chromium poisoning is yet another medical crisis facing metal hip implant patients.friction from the metal cup and stem rubbing together can cause small dust-like metal particles to break off and spread through your body and bloodstream. In high enough levels, this metal metal chromium cobalt hip recall debris can cause various medical problem
Depuy Hip replacement Helpline Alaska and Depuy Hip replacement lawyers are helping Victims of the Failed Depuy Hip replacement Recall.
A recent report from the British National Joint Registry shows that metal-on-metal hip replacements like the DePuy ASR are failing at much higher rates than other types of artificial hips. Up to 29% of British patients with the DePuy ASR had to get a 2nd hip replacement after only 6 years, according to a New York Times report.
"Up to 29% of British patients with the DePuy ASR had to get a second hip replacement after only 6 years"
"There appears to be a sharp increase in the risk of revision at around 6 years after primary surgery for the metal-on-metal group, although more data is needed to confirm this finding," according to the fall 2011 issue of the Joint Registry newsletter.
Most artificial hips are expected to last about 15 years, but for many patients the DePuy ASR isn't even lasting half that time
What are the DePuy Hip Replacements ?
The ASR XL Acetabular System, which was used to replace the total hip, consisted of three components:
- A femoral stem inserted into the patient’s femur
- A femoral head connected to the stem that fit into the acetabulum
- A single-piece, metal lined cup used to replace the acetabulum
The ASR Hip Resurfacing System consisted of two components:
- A cap that fit over the natural femoral head
- The cup replacing the acetabulum
All of these components in both systems are included in the recall due to the following complications experienced by many patients implanted with one or the other system:
Complications and Symptoms
- Metal flakes in the bloodstream, Cobalt and Chromium levels too high
- Dislocation or Misalignment of the two parts of the implant
- Hip Pain
- Difficulty Walking
- Swelling of the Hip
- Loosening of the Hip Replacement
- Fracture of the bone around the implant
FDA and the DePuy
In August 2010, Johnson & Johnson subsidiary, DePuy Orthopaedics, initiated a DePuy hip Replacement Recall. The Failed DePuy affected around 93,000 people. Foreign artificial joint registries determined that the ASR XL Acetabular System and ASR Hip Resurfacing System both fail at higher-than-normal rates for artificial hips. One reason so many people received the metal-on-metal hip replacements was that DePuy, used the fast track U.S. Food and Drug Administration’s (FDA’s) “510(k) premarket approval process,” (510(k) process). This process allowed the ASR hip replacements for use by Orthopedic surgeons without subjecting them to costlier clinical trials.
If you or a loved one has had complications with your DePuy Hip Replacement contact the Depuy Hip Replacement Helpline Alaska for a DePuy Hip Replacement lawyer.