Posts Tagged ‘
synthetic mesh ’
Apr 30th, 2013 |
By Jane Akre
April 30, 2013 ~ Linda K. 0f Teapapers talks about life after mesh removal surgery and the importance of potassium and magnesium level monitoring. She is two weeks past a fascial reconstruction at UCLA’s urology department where they used native tissue (her own) to hold up the urethra in place of a synthetic mesh sling
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Posted in Your Turn |
No Comments »
Tags: bladder sling, fascial reconstruction, fascial reconstruction. urethra, Linda K., magnesium, mesh removal surgery, potassium, synthetic mesh, teapapers, UCLA's urology department
Oct 29th, 2012 |
By Jane Akre
October 29, 2012 ~ The New Zealand Herald reports in a series of articles by Chloe Johnson, on the outcome of mesh surgeries in that country. Specifically Johnson profiles 18-year-old Samantha Wiggins. In “Dance Dreams Crushed by Mesh,” Johnson reports Wiggins always dreamed of being a dancer but after she was implanted with surgical
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Posted in Media Reports |
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Tags: Accident Compensation Corporation, Carmel Berry, Chloe Johnson, complications, FDA, petroleum-based polypropylene mesh., polypropylene mesh implant, polypropylene surgical mesh, prolapsed bladder, synthetic mesh, The new Zealand Herald, umbilical hernia
Sep 19th, 2012 |
By Jane Akre
September 19, 2012 ~ Last January, after a five-fold increase in complications was noted by the U.S. Food and Drug Administration (FDA) concerning synthetic mesh used in women to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI), the FDA ordered mesh makers to find out why. At the time, the unprecedented request was
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Posted in FDA |
1 Comment »
Tags: 510(k), dyspareunia, FDA, fistula, five-fold increase, Food and Drug Administration, infection, least burdensome, mesh erosion, mesh exposure, metal-on-metal hips, mini-slings, neuromuscular, pelvic organ prolapse, pelvic pain, POP, postmarket surveillance, recurrence, revision, section 522, Stress urinary incontinence, SUI, synthetic mesh, transvaginal mesh, urogynecologic surgical mesh, vaginal scarring
Jun 4th, 2012 |
By Jane Akre
June 4, 2012 ~ Breaking news! Bloomberg is reporting (here) that Johnson & Johnson (J&J) has requested the paperwork to stop selling four different types of transvaginal mesh in the face of hundreds of lawsuits. The Ethicon unit of J & J told a federal judge in West Virginia that it has requested the official
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Posted in Legal News |
7 comments
Tags: 510(k), Bloomberg, Ethicon, FDA, Gynecare Prolift, judge Goodwin, product liability lawsuits, Prolift, synthetic mesh, transvaginal mesh
May 25th, 2012 |
By Jane Akre
by Amy Gezon, August 19, 2011 *Editors Note * Amy Gezon allowed me to reprint this story that appeared in Yahoo News. It has many resources and is a great primer on the issues! Thanks Amy!! On July 13, 2011 the United States Food and Drug Administration (FDA) released a second warning against the use
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Posted in Op-Ed |
1 Comment »
Tags: 510(k), American Medical Association, dyspareunia, FDA, Incontinence, Mentor corporation, ObTape, pelvic organ prolapse, ProteGen Sling, Public Health Notification, synthetic mesh, Tension-Free Vaginal Tape, Urodynamics, Urologic diseases
Mar 27th, 2012 |
By Jane Akre
October 1, 2012 is an important day for Beverly Martiniano. It’s her 65th birthday, yes. But it is also the day she qualifies for Medicare allowing her to take the first step to have several synthetic surgical meshes removed from her body that have plagued her life and health for several years. She tells MDND
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Posted in Patient Profiles |
18 comments
Tags: American Medical Systems, bladder prolapse, Deterol, elevate with intepro lite prolapse repair system. AMS, FDA, fentanyl, fibryomyalgia, Incontinence, oxycodone, pain management, percocet, Perigee Vault suspension system, rectum, risk factor, smoking, synthetic mesh, urinary incontinence, urologist, vaginal vault, vicodin
Mar 9th, 2012 |
By Jane Akre
*Editors Note: “Betty” wrote this opinion piece. She is a woman who is represented by a lawyer who does not want her speaking up but she still wants to express herself so is doing so anonymously. Many women and men feel the same way. They want to share their experience so others don’t have to
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Posted in Op-Ed |
2 comments
Tags: complication rate, DePuy, Ethicon, Injuries, pelvic organ prolapse, POP, streee urinary incontinence, SUI, surgical mesh, synthetic mesh, TVT-O, urology today
Nov 28th, 2011 |
By Jane Akre
I’ve been working with a very smart 29-year old web person (who unfortunately has to try to teach this old dog new tricks), but she understands web content and conveying a presence and is amazingly clever in her delivery, in fact, I’m jealous of her youth and brains. So she says what do you want
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Posted in Your Turn |
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Tags: approval, FDA, medical device, synthetic mesh
Oct 4th, 2011 |
By Jane Akre
Where Facts are Few, Experts are Many: The rise of synthetic mesh for the treatment of stress incontinence during an era of bad science.- Amy Gezon The United States Food and Drug Administration convened in Gaithersburg, Maryland on September 9, 2011 to discuss the future of synthetic mesh products used for the treatment of stress
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Posted in Op-Ed |
4 comments
Tags: 510(k), clinical trials, sling, Stress urinary incontinence, SUI, synthetic mesh, synthetic mesh products