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Media
Philadelphia Jury Awards $30,000,000.00
In 2006, a Philadelphia jury awarded $30 million the largest verdict seen in the First Judicial District in years - to the family of a 5 month old boy whose severe cognitive and developmental deficiencies were alleged to have resulted from the misadministration of a specific medication.The boy was treated with the medication several years ago while a patient at a well known Philadelphia hospital.
Plaintiff attorneys, Gayle Lewis and associate, Matthew Schelkopf, of the Lewis Law Firm located in Bryn Mawr, handled the case.
According to Ms. Lewis, the plaintiffs stuck to a $50 million dollar demand during the early phases of the litigation, with no official offers from the defense. The demand was later brought down to about $28 million shortly before trial.
The trial lasted approximately 15 business days over the course of three weeks. The 12-member panel reached its verdict after five days of deliberations over the course of one week.
The jury's breakdown on its $30 million verdict called for $5 million in past medical costs, $10 million in future medicals, and $15 million in pain and suffering, Lewis said. The jurors were polled at 10-2 as to the liability finding against the hospital.
The actual jury verdict in this case was the largest reported by The Legal as having been awarded to a med mal plaintiff by a Philadelphia panel in recent years.
According to statistics maintained by the state Supreme Court, there were no medical malpractice verdicts for more than $10 million in Philadelphia county during 2005, and only three in that category in 2004. As a result, it stands as the highest medical malpractice award in Pennsylvania for 2006.
If you believe you have wrongfully injured by a medical provider, please contact the Lewis Law Firm at (877) LAW-9969.
Decoding Disease
AARP Bulletin - June 2008Volume 49 No. 5 - Page 10
By: Barbara Basler
In the last year and a half alone, scientists have discovered more than 100 genetic variations associated with many of the medical conditions that affect older people, including type 2 diabetes, Alzheimer's disease, asthma, osteoporosis, high blood pressure and heart disease.
Indeed, genetic science is moving so swiftly that, experts say, people now in their 60s, 70s and even 80s will see medical breakthroughs that will touch their lives. "What's happened in just this short period of time is dizzying to contemplate," says Francis Collins, M.D., the scientist who directed the international Human Genome Project for the National Institutes of Health - and made news around the world.
Just five years ago Collins' team completed the monumental project - mapping and sequencing all the genetic information encoded in DNA, the "instruction manual" for humans. Using this astonishing guide, researchers can now compare the genes of groups of people who have a particular condition with groups of people who don't, surveying the entire genome to find where the genetic-difference lie. Such a research is vital: Virtually every human ailment, except trauma caused in accidents, has some genetic basis.
The Human Genome Project, experts agree, is a watershed achievement in science. It was Collins, a guitar-playing, motorcycle-riding geneticist, who brought the project in two years early and under budget. In an interview with the AARP Bulletin, the affable 58-year-old talks about the avalanche of information triggered by the genome, particularly in relation to older people.
To see the power and quickness of genomic science, he says, look at age-related macular degeneration, an eye disease that has left nearly 2 million Americans visually impaired. "We've come a huge distance with this disease in the last few years," Collins says. "Using new genomic tools, we've discovered two genes that account for about 60% of the risk - the rest is smoking. But we were surprised. These genes are involved in inflammation, and everybody was thinking macular degeneration was caused by aging in the back of the eye."
Now, doctors are testing for ways to prevent the disease with anti-inflammatory drugs that "have been around for a long time," Collins says. "Even something as simple as aspirin might have value. This is the best insight into this disease we've ever had, and it had completely changed the way we look at it."
Scientists are optimistic that they'll find similar breakthroughs for a host of other conditions. "We knew many common diseases had hereditary links because we knew they tend to run in families," Collins says. Over the years, scientists have pinpointed some 1,700 genes linked to disease, many of them powerful mutation of single genes. Each variation is responsible for a rare disease, such as Huntington's, a degenerative brain disease. "But with the genome we are learning the underlying causes at work in complex diseases like diabetes or high blood pressure,which involve many genes, each with a modest effect," Collinssays. "It's with these more common diseases that we'vehad the recent deluge of discoveries."
A lanky Virginian, Collins earned a doctoratein chemistry at Yale and his M.D. at he University of NorthCarolina. He became a dedicated hunter of disease genesas a faculty member at the University of Michigan. Since1993 he has worked at the epicenter of the genomic revolution,on the leafy NIH campus in Bethesda, Md. The National HumanGenome Research Institute is tucked into a suite of beige-coloredoffices that look more like a dentist's practice than theheadquarters of a world-renowned research center. Fromhere, Collins, who led a team that found the gene for Huntington'sand the gene for cystic fibrosis, oversees 500 scientistson the NIH campus and others at universities.
"Our best hope for curing diseasescomes out of genomics," Collins says, because it pointsto the problem of disease at the molecular level, ratherthan at symptoms or secondary effects. Genomic discoveriesare already pointing the way to new drugs that disruptprocesses at the molecular level and to tests that predictone's risk for a disease. The research is also openingthe way for a new "personalized medicine" thatallows doctors to test a patients to determine which drugswill work most effectively with the patient's genetic makeup.Last year the Food and Drug Administration recommendedgenetic test for patients taking the blood thinner warfarin(also sold as Coumadin, Jantoven, Marevan and Waran) tohelp doctors prescribe the right dosages.
Studies show 40% of those who take thedrug have genetic variations that make them more sensitiveto its effects and so need smaller doses. The genetic testcan identify those at risk for bleeding complications fromthe drug. "Soon, this kind of testing will be happeningfor asthma medications, antidepressants and cholesterol-loweringstatins," Collins says. "We should be able todo better with genetic evaluations of these drugs withinthree to four years.
"And boy, do we need moreof this," says Collins, who in September will begiven the Andrus Award, AARP's highest honor, for hiscontributions to science. "Most of the time yougo to the doctor, and the drug you're given is one wearrived at empirically - we tried something and it seemedto work," he says. "it's one-size-fits-allmedicine, and that's not ideal. Now, with the genome,we have a whole new paradigm. It's very exciting."