Pryers now act for over 200 hip patients

January 27th, 2012

Pryers Solicitors of York now act for over 200 patients who have suffered the premature failure of their metal-on-metal hip replacements and resurfacings.  Claims for compensation are being brought against DePuy International Ltd, the UK distributor of the ASR and ASR XL hip products.

The team, headed by Richard Starkie, has been strengthened by the recruitment of two more solicitors, Lucy Macklin-Smith and Lindsay Perryman, who join Aftar Waris and Jamie Paddock.

The ASR hip was introduced in July 2003 and used extensively in a few areas of the UK, particularly York, North Tees, Surrey, Rotherham, Merseyside and Cardiff.  By 2007, a number of surgeons raised concerns that they were experiencing a higher than expected failure rate with the ASR.  DePuy’s response was that this was a problem with surgical technique, rather than a problem with the product.  However, as concerns grew, DePuy withdrew the product form the Australian market in December 2009 and from the rest of the world in August 2010.

hip_replacement

Since then, hospitals have been recalling patients for tests, including blood tests; ultrasound and MRI scans; and aspirations of fluid from the hip.  Hundreds of people have been found to be suffering from excessive wear of the components, which can lead to damage to the soft tissues around the joint and even to the bone.  Revision surgery is then required, with a lengthy recovery period.  Patients frequently fail to make a full recovery and many require further surgery after revision.

Although, at the time of the product recall in August 2010, DePuy put the 5 year failure rate at 12-13%, some surgeons now estimate the 6 year failure rate as being as high as 49%.  If that is correct, it is likely that several thousand people in the UK alone will require further surgery.

hip_replacement_2

Over the last 18 months, Pryers have worked with some of the world’s leading biomechanical engineers, biotribologists, metallurgists, metrologists, surgeons, toxicologists, epidemiologists, histopathologists and microbiologists.

We have been one of the leading law firms in the investigation of these claims and in the discussions with DePuy.

We have carried out extensive work the following: -

  • the precise nature of the design defect;
  • the testing procedures and how they failed;
  • the manufacturer’s delay in recalling the product;
  • establishing causation in individual cases and excluding other potential causes of joint failure;
  • determining prognosis after an ASR failure;
  • establishing causation of cobalt and chromium toxicity;
  • and the long-term health risks posed by exposure to these metals.

We have also been instrumental in establishing and co-ordinating a patient support group for the North of England, called Altogether ASR, which has had several meetings and will shortly be launching a website.  The group’s next meeting will be in March 2012.  Please contact Pryers for details.

If you or a relative has suffered the premature failure of a metal-on-metal hip replacement or resurfacing, particularly the DePuy ASR, please contact Pryers Solicitors on 0800 316 0166 or by email at hips@pryers.co.uk.

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Pryers expands team dealing with defective hips

December 1st, 2011

new-recruitsPryers Solicitors of York now act for over 200 patients who have suffered the premature failure of their metal-on-metal hip replacements and resurfacings. Claims for compensation are being brought against DePuy International Ltd, the UK distributor of the ASR and ASR XL hip products.

The team, headed by Richard Starkie, has been strengthened by the recruitment of two more solicitors, Lucy Macklin-Smith and Lindsay Perryman.

The ASR hip was introduced in July 2003 and used extensively in a few areas of the UK, particularly York, North Tees, Surrey, Rotherham, Merseyside and Cardiff. By 2007, a number of surgeons raised concerns that they were experiencing a higher than expected failure rate with the ASR. DePuy’s response was that this was a problem with surgical technique, rather than a problem with the product. However, as concerns grew, DePuy withdrew the product form the Australian market in December 2009 and from the rest of the world in August 2010.

Since then, hospitals have been recalling patients for tests, including blood tests; ultrasound and MRI scans; and aspirations of fluid from the hip. Hundreds of people have been found to be suffering from excessive wear of the components, which can lead to damage to the soft tissues around the joint and even to the bone. Revision surgery is then required, with a lengthy recovery period. Patients frequently fail to make a full recovery and many require further surgery after revision.

Although, at the time of the product recall in August 2010, DePuy put the 5 year failure rate at 12-13%, some surgeons now estimate the 6 year failure rate as being as high as 49%. If that is correct, it is likely that several thousand people in the UK alone will require further surgery.

If you or a relative has suffered the premature failure of a metal-on-metal hip replacement or resurfacing, particularly the DePuy ASR, please contact Pryers Solicitors on 0800 316 0166 or by email at hips@pryers.co.uk.

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DePuy ASR Hip Replacement Implants Recall

November 9th, 2010


Pryers Solicitors have been instructed by a number of patients to bring claims for compensation in relation to the failure of De Puy ASR hip implants, which have been recalled by the manufacturer.

Since the product was launched in 2003, over 10,000 people in the UK have been fitted with a De Puy ASR hip implant, either during hip replacement or hip resurfacing.

Towards the end of 2009, experts in Australia became concerned that a large number of ASR hips were failing prematurely, often requiring further surgery.  Earlier this year, the UK Medicines and Healthcare Products Regulatory Authority (MHRA) issued a notice about the ASR hip, saying that there may be a problem.  They began their own investigations.  In September 2010, the manufacturer, De Puy, decided that the products should no longer be used; that unused stock should be returned to the manufacturer; and patients who had received an ASR device should be checked by their surgeons and, if they showed symptoms of failure of the device, revision surgery should be considered.

While the revision rate is still relatively low, at about 12 or 13% within five years, this is more than twice the rate that would be expected from other hip products.  It is therefore expected that a very large number of patients will have hip pain and will require additional surgery due to the defect in the particular hip used.   In many cases, such patients will be entitled to compensation from De Puy.

Pryers represent a number of people, from all over the UK, who have had problems with the De Puy ASR hip and who have required further surgery for revision, or are expected to require revision in the future.  Claims for compensation will be brought against the manufacturer under the Consumer Protection Act, which requires manufacturers to pay compensation for injuries and financial losses caused by defective products.  Most cases will be conducted on a “no win no fee” basis.

If you have been fitted with a De Puy ASR prosthesis, whether as a replacement or resurfacing,  and are having hip pain or other hip symptoms, please contact Richard Greensit, a specialist medical solicitor at Pryers.

Richard can be contacted on 01904 556600 or at richard.starkie@pryers-solicitors.co.uk.

Update: Please see related post: DePuy ASR Hip Replacement Products

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