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Doctors Debate Using Hernia Repair Mesh Or Natural Tissue Hernia Repair

Most patients would probably choose natural tissue hernia repair if they knew the facts about the medical consequences if hernia repair mesh fails

Friday, September 6, 2019 - Hernia repair is one of the more routine and uncomplicated surgeries performed today with over 350,000 hernia procedures performed in the United States every year. The only problem is that the vast majority of hernia repair patients experience hernia recurrence if for some reason the area weakens and the organs once again breakthrough. Hernia recurrences were running at a rate of around 10-12% according to experts who study those sort of things and hernia repair mesh supposed would cut those numbers in half. Ethicon Physiomesh hernia lawsuits are represented by national attorneys with a vast experience and offer a free consultation before filing a claim.

The University of California San Francisco Department of Surgery reports that the need for hernia revisions surgery is higher than what has been previously reported. According to UCSF, "Recurrent hernias greatly increase the complexity of the subsequent repair. If left untreated, severe complications can result such as the intestines being trapped known as an incarcerated hernia, digestive obstruction, or a loss of blood supply to the intestines known as a strangulated hernia. Patients with complex ventral hernias treated at UCSF have a recurrence rate of approximately 18 percent, compared to a 30 to 40 percent recurrence rate nationally." The Center reports that symptoms of a failed hernia repair surgery include a bulge at the site of the previous surgery, pain, and sometimes nausea and vomiting. These can be caused by infection at the surgical site and doctor error in inadequately repairing the hernia initially. Complex hernia repair is more complex and also quite common requiring repairing two or more hernia near the same site simultaneously.

WebMD.com reports that strengthening the hernia surgical site with hernia repair mesh can reduce the percentage of hernia repair patients that require revision surgery. The reduction in hernia revision surgery associated with hernia repair mesh comes at a price, however, as the medical complications of failed hernia repair mesh, far exceed the benefits of having fewer revisions to repair. Hernia repair mesh can become infected causing redness, swelling, and tenderness near the surgical site. Other complications include the device migrating away from the intended site and landing and perforating the bowels causing bleeding, blockages and requiring major invasive surgery to retrieve the faulty medical device.

Synthetic plastic mesh is often used because it is durable, flexible, and less expensive than natural tissue hernia mesh, however, it is becoming apparent that polypropylene hernia repair mesh is incompatible with human tissue and could decay within a few years. Doctors performing hernia repair surgery are having second thoughts when it comes to recommending hernia repair mesh over the natural tissue hernia repair and must weigh the benefits of fewer revision surgeries versus the severity of the medical complications that hernia repair mesh may cause.

Experts think that hernia repair mesh could meet the same disastrous outcome the transvaginal mesh, a supportive mesh device made from the same materials and by the same companies. Johnson & Johnson, one of the leaders in hernia repair mesh, voluntarily removed its Ethicon Physiomesh Hernia repair mesh from the market worldwide when a higher than normal percentage of patients reported that the device had failed and was experiencing pain sufficient to require revision surgery. Surgeons performing hernia mesh removal today are required to send the device in the condition it was retrieved from the patient directly to a Florida medical device holding company to be used as evidence of the condition of the faulty medical device.

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OnderLaw, LLC is a St. Louis personal injury law firm handling serious injury and death claims across the country. Its mission is the pursuit of justice, no matter how complex the case or strenuous the effort. The Onder Law Firm has represented clients throughout the United States in pharmaceutical and medical device litigation such as Pradaxa, Lexapro and Yasmin/Yaz, where the firm's attorneys held significant leadership roles in the litigation, as well as Actos, DePuy, Risperdal and others. The Onder Law Firm has won more than $300 million in four talcum powder ovarian cancer lawsuits in St. Louis. Law firms throughout the nation often seek its experience and expertise on complex litigation.