Bernstein Liebhard LLP reports on the increase in revision hip procedures. In 2010, revision procedures represented 11.3 percent of all hip replacements, while the number increased to 12.5 percent in 2011.
New York, NY (PRWEB) September 28, 2012
The high revision surgery rates attributed to the recalled DePuy ASR hip implant were a notable finding in the recently released Australian Orthopaedic Association National Joint Replacement Registry’s (“AOANJRR”) 2012 annual report. Bernstein Liebhard LLP reports on the increase in revision hip procedures. In 2010, revision procedures represented 11.3 percent of all hip replacements, while the number increased to 12.5 percent in 2011. According to the report summary, “The major reason for this increase was the high number of revisions being undertaken for the ASR, in particular the ASR XL used in primary total conventional hip replacement. Last year there were 573 revision procedures reported for this prosthesis, this accounted for almost all of the increase in revision hip procedures.” There were 38,022 hip replacements reported to the registry in 2011.
The AOANJRR raised concerns about the DePuy ASR hip implant even before DePuy Orthopaedics issued the worldwide recall. DePuy removed the ASR hip from the Australian market in 2009 after receiving reports from the AOANJRR about higher than anticipated revision rates, and a decline in use of the device in Australia. “This decline was the reason the company gave for removing the ASR from the Australian market, well ahead of the subsequent worldwide withdrawal in 2010.”
Registry Report Finds High Failure Rates Of Metal-On-Metal Hip Replacements
The AOANJRR report also found that metal-on-metal bearing surfaces in total hip replacements, especially those with large femoral heads of 32mm and above, have higher failure rates than other bearing surfaces. “This increased rate of revision is evident in most metal on metal prostheses. This has been identified by the Registry for a number of years and the use of large head metal on metal bearings has now almost completely ceased in Australia.”
The findings from the AOANJRR report highlight the problems associated with the recalled DePuy ASR hip implants and other metal-on-metal hip replacement devices. Since the DePuy ASR hip recall, Bernstein Liebhard LLP has carefully monitored developments and reports on the safety of metal hip implants. The Firm is representing clients who were implanted with the recalled devices in In re: DePuy Orthopaedics, Inc. ASR Hip Implant Products Liability Litigation (“MDL No. 2197”), which is currently underway in the U.S. District Court for the Northern District of Ohio. The first federal DePuy ASR hip recall lawsuit trial is scheduled to begin on May 6, 2013 with the second trial set for July 8, 2013.
DePuy ASR hip recall lawsuits continue to be filed by Bernstein Liebhard LLP, a nationwide law firm representing clients who have been injured by dangerous drugs and defective medical devices. Those who experienced complications or underwent revision surgery as a result of a defective metal-on-metal hip implant may be entitled to compensation for medical expenses, pain and suffering, lost wages and other injuries. Learn more by watching this DePuy ASR hip recall video, or by visiting our website, http://www.consumerinjurylawyers.com/DePuy/. Or, contact a hip replacement lawyer today for a free case review: (877) 779-1414.
About Bernstein Liebhard LLP
Bernstein Liebhard LLP is a New York-based law firm exclusively representing injured persons in complex individual and class action lawsuits nationwide since 1993, including those who have been harmed by dangerous drugs, defective medical devices and consumer products. The firm has been named by The National Law Journal to the “Plaintiffs’ Hot List,” recognizing the top plaintiffs’ firms in the country, for the past nine consecutive years. Only two firms in the country have been selected for the Hot List nine years in a row.
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