pelvic vaginal mesh stress urinary incontinence Polypropylene vaginal mesh

BD withdraws surgical mesh products for SUI and POP

A spokesperson said: “BD has decided to discontinue the manufacture and sale of pelvic organ prolapse and stress urinary incontinence products in all remaining markets worldwide. While thousands of women over many years have benefited from the safe use of these products, we have decided to stop production of these devices to focus on other strategic priorities rather than continue to invest in clinical data to support additional EU requirements.” The government website says there is no need for implanted devices to be removed and no additional follow-up is required for patients implanted with such devices but anyone who has any concerns about their implanted device should contact their GP. Read more.

Source: Medical Plastics News, March 7, 2019

London Researchers Examine Psychological Fallout of Incontinence Surgery Complications

London researchers are zeroing in on the potential psychological effects of complications from women’s incontinence surgery, uncovering an increased risk of depression and self-harm after the corrective surgery. Researchers at the Western University branch of Toronto-based Institute for Clinical Evaluative Sciences and Lawson Health Research Institute — the research arm of the London Health Sciences Centre and St. Joseph’s Health Care London — examined patient outcomes after pelvic mesh implants from January 2004 to December 2012. Using 12 years of data from Ontario’s public health-care system, researchers studied the files of 57,611 women who underwent the midurethral mesh sling procedure during the study period. Of those, 1,586 went under the knife again to correct a complication from the mesh. Read more.

Source: The London Free Press, January 9, 2019

New Vaginal Mesh Material Could Help Thousands of Women Affected By Life Changing Complications

Scientists from the University of Sheffield have developed a material that could be used as an alternative to the current vaginal mesh material, polypropylene, used to treat pelvic organ prolapse and stress urinary incontinence. The use of these current meshes, in particular surgical procedures, has led to severe complications for millions of women across the world and is now banned in Australia. The research conducted by the University of Sheffield, published today in the journal Neurourology and Urodynamics, provides evidence which supports the use of a softer and more elastic material better suited for use in the pelvic floor and one that releases oestrogen into the surrounding pelvic tissue to form new blood vessels and ultimately speed up the healing process. Read more.

Source: EurekAlert, February 13, 2018

surgeons perform pelvic organ prolapse surgery

New Zealand’s Medsafe regulatory body removes pelvic mesh products from market

New Zealand’s regulatory body Medsafe has taken steps to remove a number of surgical mesh products from the country, according to a release posted today. The agency said the product’s removal was the outcome of a recent regulatory action on surgical mesh products, specifically those designed for treating pelvic organ prolapse via transvaginal implantation and one mini-sling product designed to treat stress urinary incontinence. Medsafe said that last December it requested safety information from four surgical mesh suppliers in New Zealand, following action taken by Australia’s TGA as it looked to review meshes used for urogynaecological use. The earlier TGA’s investigation ended in regulatory actions to remove the devices from the market, MedSafe said, and similarly resulted in their removal from New Zealand’s market. Read more.

Source: +Mass Device, January 31, 2018

Vaginal Mesh Operations Should Be Banned, Says NICE

The health watchdog NICE is to recommend that vaginal mesh operations should be banned from treating organ prolapse in England, the BBC’s Victoria Derbyshire show has learned. Draft guidelines from NICE say the implants should only be used for research – and not routine operations. Some implants can cut into the vagina and women have been left in permanent pain, unable to walk, work or have sex. One expert said it is highly likely the NHS will take up the recommendation. However, the organisation is not compelled to act on findings it receives from NICE. Both NHS England and NICE declined to comment. Read more.

Source: BBC News, November 27, 2017

Women Damaged by Surgical Mesh to Treat Incontinence Are Furious at Report

Women damaged by surgical mesh used to treat post-childbirth incontinence have reacted with fury to a Government report investigating the problem. At least 7,800 women say they’ve suffered lacerations and nerve damage because the mesh has broken into tiny fragments. The report, which is unpublished but has been seen by Good Health, is the result of a three-year investigation by NHS England. It confirms that many more women have complained of injuries than previously suggested and calls for a helpline to support victims. But it did not look at the safety of the mesh and rejects calls for a ban. Instead, it says hospitals should ensure that surgeons be trained to implant it; at the moment any gynaecologist can perform the procedure. Read more.

Source: Daily Mail, July 25, 2017

My Transvaginal Mesh Surgery

My Story – Submitted by: Mary

I am a 53-year old woman who had a hysterectomy for cervical cancer at 27 and chronic bronchitis in my 40’s. This caused my incontinence and I was told I would get relief if I had the transvaginal mesh implanted. I had the surgery in 2009, both bladder and rectal repairs.

Since then, I have had nothing but problems. The mesh is eroding out of my vagina, my bladder has fallen again, I cannot empty my bladder totally, have the urge to urinate often and I leak constantly. I also can’t be intimate with my husband without pain. That is not even close to being the worst of it.Continue reading→