By Claire Bates
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A government review into the PIP breast implant scandal has warned the UK medicine's regulator that it must take decisive action to prevent any similar incidents in the future.
However, it insisted both the MHRA and Department of Health acted 'appropriately' to the health scare at the time, even though conflicting advice caused mass panic among tens of thousands of affected women.

Scare: Implants from the French company Poly Implant Prothse did not contain medical-grade silicone
PIP implants were banned in 2010 in France and the UK after they were found to contain industrial grade silicone gel suitable for mattresses, rather than medical grade, and had an increased risk of rupturing. It is believed this fraudulent practice began before 2001.
The French government recommended removing the implants after finding a rupture rate of five per cent in December 2011. However, the MHRA insisted there was no need for removals as they had found no evidence of health issues or increased rupture rates.
The conflicting advice caused mass anxiety among tens of thousands of women in Britain, with hundreds protesting outside private clinics that refused to remove and replace their implants for free.
In January this year, the Government said anxiety caused by the implants was a sufficient reason to have them taken out. However, Health secretary Andrew Lansley said it was ânot advisable for women to routinely have implants removedâ.
Then in March the Government agreed to perform removals but not replacements for private patients in cases of 'medical need', which included distress.
Now Health Minister Lord Howe has published a report looking at how the MHRA and the Department of Health acted both before and after information about the problems with the implants came to light.
Amazingly, it found both bodies acted 'appropriately' at the time.
However, it said the scandal revealed major flaws in how both bodies communicated with the public as well as how they gathered evidence on medical devices.

Anger: PIP breast implant protesters outside The Harley Medical Group who refused to remove and replace them for free
The report said both the MHRA and Department of Health needed to improve how they provided information on subjects likely to cause 'understandable anxiety' among the public.
'We need to ensure that full, clear and accurate information is made available promptly in a way that is easily accessible and reflects the concerns that weigh so heavily on the lives of individuals who are affected by doubts over the safety of specific medical devices,' it said.
The report, published by the Department of Health today, also found that the Medicines and Healthcare Regulatory Authority (MHRA) had struggled to advise women because of data gathering issues.
'The MHRA was attempting to draw evidence-based conclusions about the performance of a device from data that were incomplete, and which we now know were filtered through a manufacturer that turned out to be fraudulent, while working on the assumption that all parts of the system were acting in good faith,' the report said.
It means even now it is not clear to what extent PIP implants fail more frequently or earlier than expected.
Therefore Lord Howe found the MHRA need to obtain evidence from a wider and more detailed set of sources for higher-risk medical devices, including robust outcomes data from clinicians
WHAT TO DO IF YOU HAVE AN IMPLANT...
Women who have PiP implants and who are concerned are advised to:
- Find out if they have a PIP implant
- Speak to their specialist or GP, if they had them done on the NHS, or clinic if they had them done privately
- Agree what's best. Get advice on whether or not they need further assessment, and discuss appropriate action with their doctor.
The NHS will support removal of PIP implants if, following a clinical assessment, a woman with her doctor decides that it is right to do so.
The NHS will replace the implants if the original operation was done by the NHS. If a clinic that implanted PiP implants no longer exists or refuses to care for their patient, the NHS will remove the implants but not replace.
The report also found that the regulators in all EU countries need to work better together to support early detection of problems, share the information they gather and take appropriate action to protect patients.
It said such changes should uncover problems with medical devices earlier and place the regulators in a better position to take quick and decisive action.
Lord Howe said today: 'This report wonât prevent the distress caused to women who have PiP implants, but it should give them and the public reassurance that we have identified the lessons; that we will take all steps to act on them; and that, should something like this happen again, our systems for dealing with it will be stronger.'
However, he added: 'It must be emphasised that this case was one of deliberate fraud by the PiP manufacturer which purposefully misled European regulators. Regulation alone cannot prevent fraudulent activity such as this. But serious lessons must be learned from this scandal.'
Sir Bruce Keogh - the NHS Medical Director - is currently carrying out a separate review of the wider system of regu lation for cosmetic interventions.
His review will also look at whether a breast implant registry could be put in place in this country, to help monitor any problems that occur and perhaps make it easier to trace people affected if there is ever a problem in the future.
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The MHRA is at fault here. The real scandal is that this is a quango ruled by bonkers political correctness, radical feminists and staffed with just about anyone from around the globe so long as they aren't British. They must be quaking in their boots that the truth will come out. It will. It always does.
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With reference to regulations, I was informed when that all implant patients were registered and given a copy of the implant numbers. What is going on, once again it's in to the case of keep blaming someone else, as usual.
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