Justia Lawyer Rating for Robert D. Kreisman

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The use of medications to induce labor has become increasingly common over the last 50 years. Pitocin is one of the most well-known medications given to mothers to try and speed labor along. However, this drug does not come without its risks, which can include uterine rupture, more intense contractions, and fetal stress.

The Cook County birth injury lawsuit of Louis Montes, a minor, et al. v. West Suburban Hospital Medical Center, Inc., 05 L 14157, involves the use of Pitocin during a 2005 delivery. The baby’s mother was given Pitocin in order to promote labor. However, she was given too much of the drug, which led to a hyperstimulated uterus and to fetal distress.

A review of the fetal heart tracings taken during this period clearly demonstrate that the baby was in distress. However, the West Suburban Medical Center nurses failed to alert the obstetrician of the baby’s fetal distress. Because he was not aware of the problem, the doctor did not order a timely c-section to avoid injury to the baby.

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A Cook County medical malpractice lawsuit was critical of a Naperville hospital for its failure to appropriately monitor the vital signs of an expectant mother. As a result of the poor monitoring by the Cook County hospital, the mother not only lost her baby, but had to undergo future surgery herself. Sabine C. Miller v. Edward Hospital, et al., 05 L 1192.

In November 2004, 30 year-old Sabine Miller was brought by ambulance to Edward Hospital. She was 14 weeks pregnant and had developed severe abdominal pain and vomiting. Upon her arrival, the Naperville hospital immediately began evaluating Miller to determine whether her baby was the cause of her severe pain.

The Emergency Department was able to rule out any problems with the fetus and Miller’s pregnancy. However, in order to determine what was the cause of Miller’s abdominal pain, the staff elected to admit her for further testing and observation. Up to this point, there were no violations in the standard of care administered by the Edward Hospital staff. It was not until Miller was admitted to the hospital’s postpartum unit that the medical negligence occurred.

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A $1 million jury verdict award was entered against a Cook County surgeon and his surgical center for their negligence during an eye surgery. The surgical error left the 24 year-old plaintiff, Cindy Zaleski, with a permanent eye injury. Cindy Zaleski v. Elmhurst Eye Surgery Center, et al., No. 08 L 7387.

In 2006, Ms. Zaleski presented to the Kovach Eye Institute in order to undergo a procedure to correct her nearsightedness. Dr. Kevin Kovach recommended Zaleski undergo a phakic intraocular lens implant procedure, which involved implanting a corrective lens behind the eye’s cornea. This type of procedure is typically performed on patients whose nearsightedness too severe to undergo a standard LASIK procedure.

Zaleski required the eye surgery for both her right and left eyes. And while the right eye procedure was uneventful, she was left with permanently distorted and blurred vision in her left eye. The Cook County medical malpractice alleged that her vision loss was a direct result of Dr. Kovach’s surgical negligence.

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Over the years, medical advances have led to countless innovative inventions that have saved many lives. However, not every medical innovation lives up to its expectations. The recall of DuPuy’s metal-on-metal hip joint is a perfect example of a medical device that failed to delivery as promised.

The first artificial hip joint was developed in the 1960s and was made of a metal ball placed in a plastic cup, which were meant to replicate the thigh bone and hip socket, respectively. Then, metal-on-metal hip implant devices were developed in response to studies showing that metal and plastic hip devices were leading to bone loss in some patients.

The medical community believed the medical device changes made to metal-on-metal hip implants would revolutionize the future of artificial hips. Not only would the newer design lead to less bone loss in patients, but by replacing plastic with metal, the belief was that the new medical device would last longer than the original metal and plastic version. Medical professionals viewed metal-on-metal hip devices as the final solution to hip implant patients’ problems.

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A Cook County wrongful death lawsuit involving the death of a 45 year-old woman was settled by the decedent’s estate for $1.35 million. The Illinois lawsuit dealt with claims of medical negligence on behalf of the defendant surgeon and the hospital where he as employed. Jerry Markbreit for the Estate of Betsy Markbreit v. Jose Velasco, M.D., et al., 07 L 8703.

The Illinois surgical malpractice began in 2004, when Ms. Markbreit was admitted to Rush North Shore Medical Center to have a benign growth on her thyroid gland. Prior testing had indicated that the benign growth was limited to the right side of Ms. Markbriet’s thyroid gland, a finding that was confirmed on the surgical report. Yet the surgeon, Dr. Jose Velasco, elected to perform a total thyroidectomy on the decedent.

The Cook County medical malpractice claim was critical of the surgeon’s decision to perform a total thyroidectomy. Ms. Markbreit had only been scheduled for a partial thyroidectomy and given the fact that her benign growth was isolated to one side of her thyroid gland there was no medical reason to perform a total thyroidectomy. This lack of medical necessity was significant because the plaintiff’s wrongful death lawsuit traced all of Ms. Markbreit’s subsequent medical problems and eventual death back to the unnecessary total thyroidectomy.

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Johnson & Johnson has announced that it will be dropping one of its medical devices from production – by the end of 2011, the company will cease manufacturing its drug-coated heart stents. The company explains its decision was due its decreasing market share in the heart stent category; Johnson & Johnson is looking to funnel the newly freed funds into developing other medical products.

Johnson & Johnson’s drug-coated heart stents were manufactured in conjunction with Cordis, its subsidiary. Cordis’s Cypher stent was the first drug-coated heart stent approved by the FDA. However, by the end of this year, it will no longer be manufactured. Likewise, Cordis will halt its research and development of a new stent, the Nevo stent.

The sale of drug-coated heart stents represents a $4 billion market, which previously had been divided between Johnson & Johnson/Cordis, Boston Scientific, Medtronic, and Abbott Laboratories. However, Cordis’s portion of that market has been decreasing. In 2006, Cordis made $2.6 billion globally from the sale of drug-coated stents, whereas last year it only made $627 million.

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The Illinois Supreme Court ruled as to the statute of limitations regarding the Illinois lawsuit of Kristen Kaufmann v. Roger A. Schroeder, M.D., Jersey Community Hospital, a municipal corporation, et al., No. 109738. While the plaintiff argued that she had filed her claim well within the two year statute, the Illinois Supreme Court held that she had failed to meet the actual one year statute of limitations. The deciding factor of whether or not it was a one or two year statute dealt with whether or not Kaufmann’s claim was considered an Illinois medical malpractice lawsuit.

The facts surrounding Kaufmann involved allegations that the plaintiff woke up after being sedated to find her physician licking her breasts. The complaint also contended that not only had her OB-GYN, Dr. Roger Schroeder, committed sexual assault against Kaufmann, but that he had unnecessarily sedated her in order to do so.

Kaufmann had presented to Jersey Community Hospital under Dr. Schroeder’s care for treatment of an urinary tract infection and was told that she needed to be sedated for the procedure; she later discovered that this was not true. As a result of Dr. Schroeder’s actions, Kaufmann filed a complaint not only against the doctor, but also against Jersey Community Hospital, the hospital employing him.

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Medicine is a healing profession; as patients we look to our physicians to cure our ailments and relieve our pain. However, in order to heal us, doctors must first diagnose the problem – a quick and speedy diagnosis is often the key to a successful recovery. Likewise, when there is an unnecessary delay in diagnosis, oftentimes the outcome is not very favorable for the patient.

Take for instance the case of 76 year-old Shirley Cyborski, who died as a result of the failure to diagnose her colon cancer for over a year. The medical lawsuit resulting out of this misdiagnosis of cancer, Estate of Shirley Cyborski v. Advocate Health and Hospitals Corp., et al, No. 08 L 6447, was recently settled for $2.05 million.

In 2006, Shirley presented to Advocate South Suburban Hospital for a barium enema examination. This exam is typically performed when a patient experiences a change in bowel habits, has abdominal pain or rectal bleeding, or if there is a suspicion that the patient has diverticulitis or polyps. An x-ray of Shirley’s colon was taken at the time of the barium enema exam, which showed a mass in her colon. However, the colon mass was not reported and therefore her cancer went undiagnosed.

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France’s Agence Francaise De Securite Sanitaire Des Produits De Sante (AFSSAPS) banned the use of Actors, a drug prescribed to control diabetes, due to concerns that it increases the risk of bladder cancer amongst patients taking the drug. Actors manufactured by Japan’s Takeda Pharmaceutical and is one of the pharmaceutical company’s top-selling drugs. The French medical board’s decision has caused Germany to follow suit in banning the diabetes drug, with reports that the UK might soon follow.

The French drug suspension not only affects Actos, but also applies to Competact, a similar prescription drug that combines Actos with metformin. Both drugs were suspended because they contained the active ingredient Pioglitazone, which has been linked to the increase risk of bladder cancer. This risk was documented in a study of antidiabetic patients taking antidiabetic medicines that was conducted by the Caisse National d’Assurance Maladie between 2006 and 2009.

The sale of Actos was approved in Europe in 2000, with Competact being approved in 2006. Since that time, an estimated 230,000 patients use Actos in France alone. In 2010, Europe accounted for Y29.5 billion, or about 7.5%, of Actos Y387.9 billion in global sales. The banning of Actos in Europe could drastically affect the fate of the Japan-based pharmaceutical company and exposes it to potential pharmaceutical liability lawsuits.

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When undergoing a major surgery, as patients we tend to focus on the risks associated with the surgery itself: will the doctor cut something he shouldn’t, will I have a bad reaction to anesthesia, or will my body reject the new heart. However, in some instances the period following the surgery can be just as risky as the surgery itself.

Take for example The Estate of Shamiran David v. Rush North Shore Medical Center, et al., 07 L 8444, an Illinois wrongful death lawsuit involving the death of fifty-nine year-old Shamiran David. Mrs. David presented to Rush North Shore Medical Center in July 2005 for an aortic valve replacement and coronary artery bypass surgery. While the complex surgery went well, Mrs. David’s post-operative care was mismanaged, leading to her death less than six months later.

Following her heart surgery, Mrs. David was placed on Coumadin therapy, which is the common procedure following a mechanical aortic valve replacement. Coumadin is a drug that works to decrease your blood’s clotting ability in order to prevent blood clots from forming. However, it is important for patients taking Coumadin to be on the right dosage. If too much Coumadin is given, a patient is at increased risk for bleeding; however, if too little is given, then the patient is at risk for getting blood clots.

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