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Physician pharmacy, also sometimes referred to as physician dispensing is an outstanding revenue enhancer for physicians, while providing the highest levels of safety and convenience to their patients. A complete turnkey operating system is anchored by state of the art web based dispensing software, which includes the ability to adjudicate claims on a real time basis for your patients with insurance , . . just like the pharmacy! In fact, with today’s technology and availability of repackaged products, and bulk supplies with inexpensive counting machines, there has never been a better time to implement a system that can earn the practice tens of thousands per year in additional income streams.

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Women’s health columns and blogs have been awash recently with frightening reports about the serious dangers associated with the transvaginal placement of surgical mesh to treat pelvic organ prolapse. A July 2011 Safety Communication issued by the FDA, entitled “Serious Complications Associated with Transvaginal Placement of Surgical Mesh in Repair of Pelvic Organ Prolapse”, indicates that the use of vaginal mesh can result in permanent and life-altering side effects. Women attempting to learn more about this topic will find a sea of articles and blog posts, only some of which are factual. Vaginal mesh lawyer sites, health blogs and medical resources all have differing information about transvaginal mesh and its impacts on patients. Read on for the simple facts, distilled from the long version of the FDA’s official warning.

The 2011 safety alert came as a follow-up to a milder warning issued in 2008. Citing the same side effects as were known in 2008, the new report indicates these complications are “not rare”, as previously thought. The three-year period between 2008 and 2010 saw a five-fold increase in the number of reports of vaginal mesh adverse events. Women are teaming up with vaginal mesh attorneys to seek compensation for the side effects they have suffered as a result of the device.

The 2010 FDA report singled out “mesh erosion” or “extrusion” as the foremost complaint against transvaginal mesh. When the mesh erodes, it can either protrude from the vaginal wall or actually break off and become lodged somewhere else in the body. As a result of the use of vaginal mesh, women suffer from excruciating vaginal pain, profuse bleeding, infection, and even damage to pelvic organs. Patients experiencing these symptoms require one or more surgeries to remove the mesh; in one case that has become well-publicized, twelve surgeries have been performed to remove remnants of mesh from a single woman.

Following pelvic organ prolapse repair surgery, the FDA report says you should be sure to continue to attend follow-up doctor’s appointments, inquire with your surgeon as to whether a pelvic sling was used in your surgery, and report any health problems you may be having to your doctor. If you think there is a link between symptoms you are experiencing and pelvic organ prolapse surgery, contact a vaginal mesh attorney for a free consultation to learn about your legal rights. If you’ve had pelvic organ prolapse surgery but have suffered no negative side effects, there is no need to be concerned. Many women do not experience problems related to transvaginal mesh implantation.

If pelvic organ prolapse repair surgery has been recommended to you, be sure to inquire as to the method of repair. The most recent FDA report advised patients and medical professionals to explore all other means of repair before choosing to use transvaginal surgical mesh. The use of transvaginal mesh does not offer any clear advantages over other repair methods, but may pose a significant risk. If you do decide to use transvaginal mesh for pelvic organ prolapse repair, be aware that surgical mesh implantation is permanent and can lead to life-long health problems.

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Read on its own, the FDA’s report on transvaginal mesh used in pelvic organ prolapse surgery makes a reader assume the product is soon to be recalled. From what I’ve heard, pelvic organ prolapse surgery’s failure or success relies far more on the skill of the urogynecologic surgeon than on the method employed or the medical device utilized. Overall, the serious health problems women have encountered after pelvic organ prolapse surgery may be more suggestive of a failure of surgeons and the medical field than of a specific product. Even if the FDA’s report may have pointed out the wrong culprit, it has serves the purpose of bringing attention to the overall high failure rates of pelvic organ prolapse surgery. In the past, patient reports related to pelvic organ prolapse repair surgery failure were less common – perhaps because of the very private nature of the problems that can result. Now, as women see how many others have suffered similar humiliation, pain and suffering, they’ll likely come forward to tell their own stories. What’s more, women have started to seek out surgical mesh lawyers in great numbers in order to pursue justice for these wrongs.

Pelvic organ prolapse is a circumstance that can happen to women after childbirth, after hysterectomy, or during menopause. In simple terms, the condition occurs when the pelvic muscles become damaged or stretched and can no longer support one or more pelvic organs. The organs then prolapse, or sag, into the vaginal cavity – and can even push out of the vagina Many women (up to 50%, some reports say) experience some degree of prolapse during their lives. Most women never experience any symptoms, but those who do may have difficulty with urination and sexual intercourse. Surgery is required to repair the condition in the most extreme cases. It is the use of a vaginal sling made of surgical mesh that has become the focus of transvaginal mesh lawyers and their clients. The 2010 FDA safety alert on this subject blames transvaginal mesh for a wide range of serious and potentially permanent health problems.

Experienced urogynecologic surgeons say that, in many cases, the skill and judgment of the surgeon is the deciding factor in whether a pelvic organ prolapse surgery will succeed or fail. Surgeons that rely on pre-packaged prolapse kits may be more apt to do a shoddy job. The FDA concluded that in many cases, regular stitches are safer than vaginal mesh; this may be because surgeons who are more competent and confident are more likely to trust their skills to make the repair as they see fit, rather than relying on a product developed by a medical device company. In any case, many medical professionals believe that transvaginal surgical mesh is only a part of the problem, and that a surgeon’s abilities will ultimately decide the outcome of a pelvic organ prolapse repair procedure. For now, vaginal mesh lawyers have turned their sights on companies such as Johnson & Johnson, who manufacture and market prolapse repair kits. Medical professionals and patients alike await more information from the FDA this fall after it receives recommendations from a committee on the topic.