A voice for women's health

Medical Devices

Medical Devices - How Safe Are They?


April 2012

Recent events continue to highlight the fact that neither the government or the Ministry of Health or any other government agency has done any-thing about ensuring that medical devices used in New Zealand are fit for purpose, have undergone clinical trials and are safe. This despite the fact that several major scandals have made the headlines in the media both here and internationally over the past six months.
 

The Gynaecological Mesh

In the October 2011 issue of the AWHC newsletter, an article on the problems associated with the use of the gynaecological mesh revealed how medical devices can avoid having to undergo clinical trials before they are marketed and sold as the best thing since sliced bread.1
 

French Breast Implants

In February 2012 the AWHC newsletter featured an article on how French breast implants manufactured by Poly Implant Prothese, a French company founded by French entrepreneur Jean-Claude Mas, had been found to contain a substandard, industrial grade silicone, a fact that only came to light after doctors began reporting an abnormal number of rips and leaks in the implants.
 

Hip Replacement Joints

The latest medical device to dominate headlines around the world are two models of metal-on-metal hip joint replacements. The first of these was the DePuy hip implant; the second is the Mitch THR hip implant.2 The Ministry of Health and Medsafe remained quiet until confronted by several major exposes in the New Zealand Herald in 2011 that led to light bulbs going on in the heads of a number of New Zealanders who had had a hip replacement. But nothing appeared on the Medsafe website.

As New Zealand patients struggled to get information an article appeared in the February 2012 issue of the British Medical Journal by investigations editor Deborah Cohen. It began:

“Hundreds of thousands of patients around the world may have been exposed to toxic substances after being implanted with poorly regulated and potentially dangerous hip devices, a BMJ/BBC Newsnight investigation reveals this week. Despite the fact that these risks have been known and well documented for decades, patients have been kept in the dark about their participation in what has effectively been a large uncontrolled experiment.”3

The metal-on-metal hip replacement implants arrived on the scene in 1997. The head at the top and the lining of the cup it fits into are made of cobalt-chromium alloy rather than ceramic or polyethylene. Of course they were marketed as the latest advance in hip replacement and were specifically targeted at younger patients who needed a hip that would last their life-time.

 

DNA Damage (Genotoxicity)

As the BMJ paper points out, multiple studies and research organisations have warned about the carcinogenic potential of metal-on-metal hips. That cobalt and chromium ions lead to genotoxic changes, (changes that are damaging to DNA and therefore capable of causing mutations or cancer), both in laboratory settings and in animals was described in scientific journals over 30 years ago.3

It will come as no surprise to learn that the manufacturers were aware of the potential for genotoxicity. A DePuy internal memo from July 2005 says: “In addition to inducing potential changes in immune function, there has been concern for some time that wear debris may be carcinogenic. The mechanism is not known and only 24 local malignancies have been reported in patients with joint replacements. Also worrying is the possibility of distant effects. One study suggested a threefold risk of lymphoma and leukaemia 10 years after joint replacement. The metal to metal total hip appears to be quite promising and in the laboratory the data is (sic) definitely in its favour. However, the ultimate test is the long term human experience.”

Rather than advising regulators and patients of their concerns, companies tweaked the design of these devices.

And so the experiment continued, but outside the USA. While the DePuy ASR products were approved by the Australian Therapeutic Goods Administration in October 2003, they were not cleared by the US Food and Drug Administration until January 2008. However, the failure rates for total hip replacements were soon found to be higher than they should be, and concerns began to be raised. In December 2009 DePuy withdrew the ASR products from both the Australian and New Zealand markets.

In August 2010 DePuy contacted Medsafe proposing to distribute a recall notice to all ASR trained surgeons in New Zealand. Medsafe did not list the recall on its website, and nor did it provide any information to patients about the problems associated with metal-on-metal hip replacements. When the Herald asked the Minister of Health about Medsafe’s failure to list the ASR recall on its website when other recalls were listed, Tony Ryall is reported as replying “As part of the new joint agreement with Australia, which comes into effect July 1, I would expect such recalls to be listed on the joint website. The fact that it hasn’t reflects Medsafe’s past practice and this will be changing.”4

The rebuke from the Minister was clearly enough to make Medsafe spring into immediate action. Two and a half months out from the 1 July 2012 deadline, a comprehensive timeline of events and documents leading up to the recall of ASR hip replacements can now be found on their website.5 It tells a by now very familiar and extremely depressing story.

Despite the existence of the Code of Consumers’ Rights, New Zealand consumers remain uninformed and unaware that they have been part of yet another disastrous experiment.

The need for change is now urgent and the AWHC has written to the Minister of Health asking for statistical information on the number of New Zealanders who have had the three devices referred to in this article implanted in them.

 

Informed Consent

The lack of informed consent about the safety of medical devices also needs to be addressed. As far as the risks associated with ASR hip joints are concerned, when problems began to surface and various committees in the UK met to discuss the issues, the concerns were not made public and no alert was put out to surgeons or patients. Another disturbing aspect to this was mentioned in the BMJ article, which referred to the fact that there were special risks for women of childbearing age because metal ions had been detected in umbilical cord and placental blood.

Neither the European nor the American regulators picked up the high levels of metal ions produced by the modified hip replacement devices when they came onto the market. This was no doubt because they did not insist on any post-approval studies that would follow-up patients implanted with devices capable of producing toxic debris. The only follow-up data came from ad-hoc studies by individual research teams.

 

BMJ Conclusion

The BMJ paper ended with the following conclusion:
“After a series of failures, device regulation is in need of radical change. For its part, the FDA has decided to place all hip implants into a high risk category – fast track entry will be forbidden.

In Europe there is little doubt the current system is not fit for purpose and talks are underway about how to improve it. As Professor Freemantle asks: “Why is it that people are afforded different levels of protection depending on whether they have a heart attack, diabetes, or a hip replacement in their old age? The methods of device regulation seem to be more from the 1950s than the 21st century.”3

Professor Freemantle’s question is a very good question, and is one that needs an answer from both the Minister of Health and the Health and Disability Commissioner.

The AWHC intends to write and ask them both for such an answer (see below).

 

References
  1. AWHC, 2011: The Gynaecological Mesh
  2. Recall sparks hunt for hip patients, New Zealand Herald, 14 April 2012.
  3. Deborah Cohen, 2012: How safe are metal-on-metal hip implants? BMJ 2012; 344.
  4. Why weren’t we told? New Zealand Herald. 17 March 2012.
  5. Medsafe: Metal-on-Metal Hip Implants Timeline


Update on the Use of Medical Devices in NZ

May 2012

The AWHC has now received a response from Stewart Jessamine, the Group Manager of Medsafe, to its Official Information Act request for information on the use of three types of medical devices – the gynaecological mesh, PIP breast implants, and DePuy ASR hip joints.

 

Gynaecological Mesh

The letter the AWHC received advised that the Ministry of Health/ Medsafe does not collect specific information on gynaecological meshes and is therefore unable to say how many women have had these implanted. There are a variety of surgical mesh products on the Web Assisted Notification of Devices (WAND) database.
 

PIP Breast Implants

There have been no notifications of PIP breast implants to the WAND database since it was established in 2004. “As notification to the WAND database is a legislative requirement for any medical devices intended for marketing in New Zealand it is believed that there have been no commercial importation of these devices into New Zealand since 2004 and the Australian supplier of the product confirmed this.”

Following publicity about the implants one woman did contact Medsafe and advise them that she had a PIP breast implant from a New Zealand-based surgeon in 2000. A second woman has now also come forward.
However since the letter was written, the NZ Association of Plastic Surgeons has revealed that some of these breast implants were imported privately and implanted.

 

DePuy ASR Hip Implants

The letter states that DePuy supplied a total of 525 ASR hip systems in New Zealand between 2004 and 2010, and that these were implanted into approximately 400 patients.

According to the letter, Medsafe has been active in ensuring that DePuy provided appropriate patient manage-ment information to surgeons who had used its product. The information was reviewed and approved by Medsafe and included a requirement to contact the patients affected.

There is however no mention of any monitoring by Medsafe to ensure that surgeons did contact their patients.

 

WAND Database

The WAND database is not publicly available as it was developed solely for use by the regulator for identifying those responsible for supplying medical devices in New Zealand. Medsafe claims it cannot make this information generally available.

As reported in previous articles in the AWHC newsletter, New Zealand has no pre-market assessment for medical devices. The letter claims that “all three devices had been approved for use by reputable overseas regulators using best-practice assessment processes. Procurement processes operated by New Zealand healthcare organisations also provide a level of scrutiny that provides some measure of protection against unacceptable products.”

It is now painfully obvious that these measures failed to protect New Zealand patients from faulty products.
Recent events continue to highlight the fact that neither the government or the Ministry of Health or any other government agency has done any-thing about ensuring that medical devices used in New Zealand are fit for purpose, have undergone clinical trials and are safe. This despite the fact that several major scandals have made the headlines in the media both here and internationally over the past six months.

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