Depuy Hip Recall Lafayette

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Depuy Hip Recall Lafayette:Research Links Metal-on-Metal Hp Replacement Systems to Mental Health Issues

Study Links Metal-on-Metal Hip Replacement Systems to Mental Medical Issues
The authors of a first-of-its-kind study encouraged doctors treating patients who have had hip replacement surgery involving a metal-on-metal joint system to monitor the patients’ neuropsychiatric condition due to potential heavy metals making their way into the bloodstream.
In accordance with the research, the existence of these pollutants can lead to psychological troubles for instance depressive disorders and dementia like signs and symptoms.
The study, authored by the National Center for Biotechnology Information and underneath the umbrella of the National Institutes of Health chronicles patients in the United Kingdom who experienced the surgery and received a metal-on-metal hip replacement system, like DePuy Orthopaedic’s Pinnacle system, that has since been recalled.
Thus far, the producer of the Pinnacle system, has been found to blame for hundreds of millions of dollars in damages to patients who experienced complications after their implantation. The Pinnacle system was discovered to have both design and production problems, resulting in the failure. DePuy Orthopaedics is a subsidiary of Johnson & Johnson. Metal-on-metal hip replacement systems use a metal ball and joint, rather than a plastic or ceramic joint. However, these systems failed at a higher than normal rate, requiring revision surgery or surgeries and causing other difficulties, such as soreness at the implantation site. Another problem has been the heavy metal particles that could cause bleeding at the implant site or leech into the patient’s bloodstream. This condition is known as “metallosis.”
Metal-on-metal hip replacement systems use cobalt and chromium, each of which might cause a variety of health concerns.
The NIH study discovered that the cobalt and chromium shavings were having mental health consequences on the patients: “We present the first case series suggestive of clinically significant depressed mood and neurocognitive impairment following MoM hip failure with concomitant chromium and cobalt toxicity.”
The case study established that a few of the mental health problems could have stemmed from worry about the hip replacement system failure and potential ramifications. However, the researchers concluded that there was more at play: “Neurocognitive abnormalities however might be mediated by either static brain damage a result of chromium and cobalt toxicity or could symbolize a dynamic process, that is an early onset dementia created by metallosis. If the latter is the case it might have major, as yet unrecognised, implications for public health and wellbeing.”
The researchers concluded that metal-on-metal hip replacement systems need to be removed even if they have not yet broken: “Other than revision surgery there is no effective adsorption or chelation therapy for chromium and cobalt, and if such therapies could be safely developed, it may avoid the need for further surgery. In the meantime, to protect neurocognitive function implant removal conceivably need to be as quickly as possible after toxicity is discovered.”
Although the research workers noted the potential impact on product liability cases continuing and in the future, they commented that patient health is far more significant than commercial worries: “There are additionally potential public health implications for the care needed by many thousands of patients who have potentially suffered MoM related cobalt and chrome toxicity, should progressive cognitive decline be found in this group and the associated requirements for dementia care. This has some relevance to product liability litigation worldwide. However we believe that any commercial factors should be set aside in the interest of public safety and the bioethical principle of social justice.”
The study centered on patients in the UK who experienced hip replacement systems with a metal-on-metal ball and joint. The researchers narrowed down their patient list to 10 patients whose systems had failed. They found that prior to revision surgery, nine of the 10 were experiencing unsafe levels of chromium and cobalt in their blood.
All nine of the patients met clinical standards for depressive disorders at a “moderately severe” level.
Seven of the nine exhibited short-term memory loss.
Other mental difficulties seen in the patients included confusion, problems with tests of focus and word finding difficulties.
--authored by Rick Fahr.


DePuy Pinnacle Metal-on-Metal Hip Replacement System Found at Fault in Texas Lawsuit

DePuy Pinnacle Metal-on-Metal Hip Replacement System Found at Fault in Texas Lawsuit Johnson & Johnson has been ordered to pay out nearly a quarter-billion dollars to six victims in a so-called “bellwether” lawsuit. The case, in a Texas federal court, pitted the defendants against the company for Johnson & Johnson’s faulty DePuy Orthopaedics’ Pinnacle metal-on-metal hip replacement system. DePuy Orthopaedics is a subsidiary of Johnson & Johnson. Reported by a Reuters story on the case, jurors granted the victims $247 million in damages. Metal-on-metal hip replacement systems use a metallic ball and joint system, as opposed to other hip replacement systems who make use of ceramic components. The metal-on-metal systems fail at a much higher rate than other types of systems. The failures cause joint pain and internal bleeding in the hip area and can lead to metallosis, an issue that occurs when metals get into the blood stream. Most metal-on-metal system failures lead to remedial surgery. Hip replacement surgeries have grown in recent years, with upward of 300,000 such surgeries being performed in the United States every year. The condition generally known as osteoarthritis is a biggest cause of hip failure. According to the Reuters story, jurors found that DePuy’s Pinnacle system had a faulty design. Jurors also determined that the companies neglected to warn consumers about the risks of such systems. The story noted that nearly 10,000 lawsuits have already been filed in the United States against Johnson & Johnson for use of the DePuy Pinnacle hip replacement system. The combined trial is another in a series of “bellwether” trials regarding the DePuy Pinnacle metal-on-metal hip replacement system. The purpose of the trials is to help the trial judge determine if similar cases should go forward and provide the defendants an understanding of their future liability. The Texas suit was the fourth “bellwether” trial in connection with DePuy Pinnacle system. The defendants won one trial, but plaintiffs have won the last three - two in Texas and one in California. To date, Johnson & Johnson has been ordered to pay hundreds of millions of dollars in damages to victims of the defective hip replacement systems. --authored by Rick Fahr.

MOM Link to Dementia/Heart Disease

Metal Hip

Metal-on-metal hip replacement systems have been known to cause various problems — including painful revision surgeries and the accompanying physical rehabilitation — but researchers have recently discovered a potentially new and devastating side effects — a link between metal-on-metal hip replacement systems and dementia and heart disease. According to a story published by the Daily Mail in London, Great Britain’s Medicines and Healthcare products Regulatory AgencyBritain’s Medicines and Healthcare products Regulatory Agency recently notified the public that patients who have had metal-on-metal hip replacement systems implanted will be “called in” for X-rays and blood testing to determine if the heavy metals in the systems are causing any “adverse reactions.” The medical personnel will be trying to determine chromium and cobalt levels in the patient’s blood. Those two heavy metals have been linked to both dementia and heart disease. Metal-on-metal hip replacement systems, such as Johnson & Johnson’s DePuy Orthopaedics Pinnacle system, use a metallic ball joint to replace the hip. Other systems use ceramics, plastics or other materials. The problems associated with metal-on-metal hip replacement systems stem from wear on the joint. That wear may cause the system to fail entirely at much higher rates than hip replacement systems made of other materials, which leads to surgery to fix the system. Additionally, the metal shavings can lead to irritation at the implant site and to the metals entering the blood system, a condition known as metallosis . Hip replacement surgeries have become popular in the United States, with surgeons performing upward of 300,000 such operations each year. Several thousand lawsuits have been filed against Johnson & Johnson for its metal-on-metal hip replacement system failures. DePuy’s Pinnacle system has had a particularly long string of issues, starting with its design and production. Testimony in trials in the United States and abroad has revealed that the Pinnacle systems were not correctly manufactured and that a design flaw led to a higher-than-normal failure rate. Johnson & Johnson no longer sells the Pinnacle system, but tens of thousands of people have had it implanted. Regarding the Great Britain cases, the Daily Mail story quoted Dr. Neil McGuire, clinical director of medical devices for the regulatory agency as saying that prudence mandates checking the overall health of patients to ensure that the hip replacements aren’t causing other problems. “We’re always balancing depriving people of the benefits of these devices versus protecting people from harm,” he told the newspaper. “We don't want to set a lot of hares running if there's nothing to find. It may be at the end of it we say, ‘There's nothing to see here folks.’ --authored by Rick Fahr.


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