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Study questions whether ‘frivolous’ injury lawsuits are really a problem


Insurance companies have been claiming for years that “frivolous” medical malpractice lawsuits are a big problem, driving up health care costs and insurance premiums.

But a recent study by researchers at the Harvard School of Public Health questions whether this is really true.

The researchers reviewed 1,452 claims from five malpractice insurance companies, focusing on surgery, obstetrics, medication and misdiagnosis – four areas that account for about 80 percent of all malpractice claims.

Independent specialist physicians in each of these areas reviewed the claims and the medical records to determine whether the patient had suffered an injury, and, if so, whether the injury was due to a medical error.

According to the study, published in The New England Journal of Medicine, virtually all of the lawsuits involved a real injury. Of these injuries, 80 percent resulted in a significant or major disability and 26 percent resulted in death.

The study found that in about 63 percent of the cases, the injury was related to a medical error. In the rest of the cases, the specialists couldn’t say there was definitely a medical error, but they said many of these cases were “close calls.”

The study also found that the court system does a good job of judging the cases. The vast majority of cases involving an error resulted in compensation, and the vast majority of cases where an error couldn’t be clearly established resulted in no compensation.

In other words, the idea that patients with frivolous claims are winning jackpots in court and driving up medical costs is a myth.

“Some critics have suggested the malpractice system is inundated with

 

groundless lawsuits, and that whether a plaintiff recovers money is like a random ‘lottery,’ virtually unrelated to whether the claim has merit,” said the study’s lead author, David Studdert. “These findings cast doubt on that view by showing most malpractice claims involve medical error and serious injury, and that claims with merit are far more likely to be paid than claims without merit.”

The study also found that any costs associated with meritless claims were relatively minor. According to Harvard professor Michelle Mello, one of the study’s co-authors, what really drives up costs are not meritless claims, but all the roadblocks insurance companies put in the way of genuinely injured people seeking a fair recovery.

“Nearly 80 percent of the administrative costs of the malpractice system are tied to resolving claims that have merit,” Mello found.

In a separate study, Mello determined that fears about liability had very little effect on the number of doctors practicing in a given area, and that “caps” on jury awards and other tort reform measures have not been effective in increasing the number of doctors, reducing insurance premiums, or lowering litigation costs.


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Hospital can be liable for 'independent contractor's' actions


Parents of a newborn delivered at a Florida hospital signed a “consent form” stating that a specialist participating in their child’s birth was an “independent contractor” and was not employed by the hospital.

The couple’s son was born suffering from fetal-maternal hemorrhage and compression of the umbilical vein, which deprived him of oxygen-rich blood. In the hours following his birth, the baby’s breathing became more labored and he required resuscitation.

The baby ultimately developed permanent brain damage, and the parents blamed a neonatologist and the hospital, claiming the resuscitation had not been performed correctly or quickly enough.

The parents asserted the hospital had a contractual obligation to provide proper neonatal care to their newborn son, and to also provide the needed medical and surgical treatments.

 

The hospital countered it wasn’t responsible for the child’s injuries because the specialist was an independent contractor, which the parents had acknowledged when they signed the consent form.

But the Florida Court of Appeal disagreed with the hospital, ruling the case could proceed to trial.

The court said once the hospital contractually agreed to provide medical care it couldn’t avoid liability simply by hiring an independent contractor.

The consent form only indicated the parents acknowledged the medical care was delegated to an independent contractor specialist. While the hospital can’t be liable as an employer, it remained responsible for its obligations under the contract with the parents, the court said.

Because the exact scope of the hospital’s obligations under the contract was unresolved, the court sent the case back to the trial court.


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Versaladder company pays $700,000 for death


The maker of the once-popular folding scaffold called the Versaladder has agreed to pay $700,000 to the widow of a South Carolina man who died when his ladder collapsed.

Frank Socky was replacing rusty screws on a floodlight at his home on Father’s Day when he fell backward onto a concrete walk. Within an hour, he was dead.

 

Since 1990, more than 170 people have been involved in Versaladder collapses. Many of these people have sued, claiming the hinges that extend the scaffolding have failed. So far, the company has paid damages or settled claims with more than 80 people.

The company has stopped making the product, but it is believed that almost a million Versaladders may still be in use.


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Makers of birth control patch continue to be sued


More than 1,000 women have filed lawsuits claiming a contraceptive patch caused serious illnesses and at least one death.

A number of lawsuits were recently filed in California, Colorado, New Jersey, Ohio and Texas.

Some of the lawsuits against Johnson & Johnson and its subsidiary, Ortho-McNeil, which make the patch, include:

• A Texas case alleging that a 22-year-old woman suffered a pulmonary embolism as a result of wearing the Ortho Evra birth control patch for 20 days;

• A number of cases filed in California blaming Ortho Evra for heart attacks, blood clots and deep vein thromboses; and

• A Maryland case involving a 25-year-old woman who died from severe blood clots in her lungs and legs after she

 

started wearing the birth control patch in 2004.

Since its introduction in 2002, over five million women have used the Ortho Evra transdermal contraceptive patch. It’s considered as reliable as oral contraceptives in preventing pregnancy, but is more convenient to use because it doesn’t require women to take a pill each day.

The Food and Drug Administration issued a warning in September 2006 that women using the patch are twice as likely to experience blood clots as those who use a traditional contraceptive pill.

The lawsuits allege the patch delivers a more concentrated level of estrogen than traditional oral contraceptive pills, and that the patch manufacturer failed to warn of the risks associated with using the patch.


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Exhausted interns make more medical mistakes


A study by a Harvard Medical School professor has shown hospital interns who work shifts of 24 hours or longer make more errors because of fatigue – and this could be responsible for thousands of deaths each year.

Interns are more than four times as likely to cause a patient’s death due to a fatigue-related mistake if they work five or more 24-hour shifts a month, the study found.

“We found that for every 100 interns working for a year, they on average made 200 significant medical errors, 20 significant medical errors that caused a preventable injury to their patients, and five serious medical errors that caused the preventable deaths of their patients,” said Dr. Charles Czeisler, who led the study. If these findings are applied to the roughly 100,000 young doctors in the U.S. working such schedules, he said, it would mean that intern fatigue causes tens of thousands of preventable injuries

 

to patients – and thousands of preventable deaths – every year.

The findings were based on a survey of 2,737 interns. A separate study by Dr. Czeisler previously found that interns who work long shifts are twice as likely to cause a car accident after they leave work.

The practice of having interns work extremely long shifts began back in the 1890s, and was intended to allow interns to follow a patient’s complete course of treatment. But these findings suggest that while hospitals still following the practice may think they’re doing a better job of teaching, they’re actually injuring and killing the patients in their care.


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Student injured in golf class can sue for injuries


A 7th grade student was struck in the mouth by a golf club swung by a fellow student during a class in which the teacher had divided the students into groups to practice golf swings.

The student suffered injuries and sued the school and teacher.

The school and teacher successfully had the lawsuit dismissed before it went to trial.

But on appeal, the California Court of Appeal reversed that decision, saying the case should proceed.

People injured during sports activities often cannot sue because the risk of certain injuries is inherent in the sport itself, and people who play the sport

 

voluntarily assume that risk.

But the court emphasized that being struck in the face by a golf club is not an inherent risk of golf.

Requiring golfers to make sure the area around them is clear before they swing the club would not fundamentally alter the game, the court noted.

Similarly, a coach or teacher should ensure that team members or students in a gym class maintain a safe distance from each other while practicing their swings. This would not alter the game, the court added, since it has nothing to do with the mechanics of a golf swing or the fundamental nature of the game.


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Dialysis center could have obligation to warn patient of driving risks


Minutes after a diabetic finished his treatment at a dialysis center, he lost control of his vehicle and collided with another vehicle, injuring its occupants.

They sued the treatment center, alleging it failed to warn the diabetic of the side effects that could result from his dialysis treatment. They claimed the man was experiencing insulin shock or low blood sugar when he left the dialysis center, and the center did not perform the normal post-treatment tests or monitoring prior to releasing the patient.

However, the trial court ruled in favor of the treatment center, saying the center

 

wasn’t legally responsible for injuries to non-patients.

But the South Carolina Supreme Court disagreed. It ruled the treatment center could have legal duty to warn the patient of the risks of driving after dialysis if it knew the man could experience ill effects following the dialysis treatment. The court also found that a car accident following dialysis could be foreseeable.

The case was sent back to trial to determine if the treatment center had a duty to warn based on the facts of the case.


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Maker of migraine medicine hit with $7.4M verdict


A Vermont woman was injected with Phenergen, a drug manufactured by Wyeth designed to combat nausea from migraine headaches.

An injection of the drug was supposed to be in a vein of her arm, but it was accidentally injected into her artery instead, which was severely damaged, causing gangrene. The woman’s hand and forearm were amputated as a result.

She sued Wyeth, alleging the drug label for Phenergen inadequately warned of the dangers of IV injections. A jury ruled in her favor and awarded her $7.4 million.

Wyeth appealed the verdict, arguing Vermont law on failure-to-warn didn’t apply to the woman’s case because the federal Food and Drug Administration had previously approved Phenergen’s label.

But the Vermont Supreme Court upheld the verdict. A federally approved drug label, according to the court, doesn’t necessarily shield a drug maker from liability if an additional warning is required under state law. A label approved by the

 

FDA is only the first step in the process of warning consumers, the court said.

The court also noted the FDA and states share the same purpose of encouraging pharmaceutical companies to alter their labels when they are inadequate to protect consumers.

Consumers are barred from bringing a lawsuit in state court only if a state’s laws would make it impossible for a drug manufacturer to comply with federal labeling requirements, the court held.



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The information in this newsletter is intended solely for your information. It does not constitute legal advice, and it should not be relied on without a discussion of your specific situation with an attorney.

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