Chicago Medical Malpractice Attorney Blog

As surgical techniques become more advanced, more Americans are undergoing minor surgical procedures. And while many times these surgical procedures result in seemingly miraculous results, with the prior symptoms disappearing completely, some may also result in unanticipated side effects. A recent Cook County lawsuit serves as an example of some of the negative potential outcomes that can result from surgical negligence.

The Cook County lawsuit was filed against Gottlieb Memorial Hospital following a 2007 vaginal prolapse reconstruction surgery performed at its hospital. The surgeon, Dr. Robert Lai of Midwest Urology Associates, Ltd., was also named in the medical malpractice lawsuit. The lawsuit alleged that the negligent post-operative care the plaintiff received resulted in permanent nerve damage.

The 50-some year-old plaintiff had presented to Dr. Lai for a reconstruction surgery that was meant to correct her incontinence, constipation, and vaginal prolapse. The surgery was performed and seemed to have been a success. However, as the plaintiff prepared for her discharge from the hospital the day after the surgery, she began to experience weakness, pain, and tingling in her leg and buttock.

Continue reading "$1.5 Million Jury Verdict for Postop Nerve Damage in Vaginal Prolapse Reconstruction Surgery" »

In Illinois, the statute of limitations governing civil cases, e.g. medical malpractice, product liability, and personal injury cases, is typically two years. However, the Illinois Appellate Court recently revisited exactly when that two-year statute begins in its analysis of the "discovery rule" as it relates to Mitsias v. I-Flow, 2011 Ill.App. (1st) 101126 (Sept. 23, 2011).

The discovery rule refers to the general rule that the statute begins when a plaintiff knew or should have know about the cause for his injury. The injury in question in Mitsias deals with both a medical malpractice claim and a later product liability lawsuit involving the plaintiff's shoulder surgery. In 2001, Mitsias underwent a shoulder surgery during which a "pain pump" was implanted. However, Mitsias later developed glenohumeral chondrolysis, or destruction of cartilage in her shoulder and joint.

In 2003, Mitsias filed a medical malpractice lawsuit against the surgeon who implanted the pain pump. However, during the course of the medical malpractice proceedings, Mitsias discovered that the source of her shoulder injury might not be a simple case of medical malpractice, but also have a product liability component. Consequently, Mitsias filed a second complaint against the manufacturers of the pain pump alleging that its defects caused her shoulder injury.

Continue reading "Illinois Appellate Court Clarifies Discovery Rule - Mitsias v. I-Flow" »

A recent report by the National Joint Registry for England and Wales brings more bad news for patients who have received DePuy metal-on-metal hip replacements. According to the report, the DePuy metal-on-metal device has failed in over one-third of the British patients who'd received it. While the study does not reflect the failure rates for U.S. patients, it does report on data that we do not collect in the U.S. and therefore can be a useful indicator of potential failure rates in the U.S.

Metal-on-metal artificial hips were designed to last longer than their plastic counterparts, yet the medical advances in this case might have done more harm than good. The British report clearly shows that these all metal hip devices are failing at a much faster rate than artificial hips composed of alternate materials, including a combination of metal and plastic. And while the British report is not the first of its kind, its findings collaborates earlier studies which demonstrated that all metal hips are not as durable as the other options.

The main theory on why the metal-on-metal hip devices fail at a faster rate centers on the fact that every component is made of metal. While it would seem that metal would be more durable than plastic, in reality the all metal construction has led to other unexpected problems. As the metal hip socket rubs against the metal hip joint, the movement seems to release tiny particles of the various metals. This debris is released into the surrounding hip cavity and not only causes crippling injuries to the person, but also diminishes the effectiveness of the metal artificial hip. Therefore, it is the design defect of the all metal construction that is leading to the increased failure rate of metal-on-metal hip devices.

Continue reading "More Bad News for DePuy All-Metal Hip Replacements - British Registry Reports Increased Failure Rates" »

In recent years there has been a lot of debate over the effectiveness of the Food and Drug Administrations' medical device review system, i.e., the 501(k) process. Its critics say that the review system is not comprehensive enough and allows for the approval of unsafe medical devices. However, its advocates argue that a quick and easy approval process is necessary to ensure American patients can take advantage of the most advanced medical products available; a more involved review system would only mean more red tape for medical device companies.

In an attempt to find ways to improve its much-debated medical device review system, the FDA sought the advice of a panel of doctors and researchers from the Institute of Medicine (IOM). Over the years, the IOM has made numerous recommendations for improving government programs. However, in the case of the 501(k) process, the IOM's recommendations were perhaps more severe than the FDA had anticipated. Rather than suggesting various ways the program could be changed, the IOM instead recommended that it be abandoned all together.

In support of its recommendation, the IOM panel stated that the 501(k) approval process was "flawed" and "does not really assess safety and effectiveness." In order to obtain approval under the 501(k) process>, a medical device manufacturer must show that its medical device is similar to a device that is already on the market. The approval process was created in the 1970s to allow the FDA to quickly grant approval to those products shown to be similar to those already on the market. However, while it was meant as a temporary method to help grandfather in devices that were already in widespread use, the 501(k) process has become the standard for medical device approval.

Continue reading "FDA Rejects Recommendations to Abandon Flawed Medical Device Review System" »

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.

Continue reading "Medical Advances Not Always What They're Cracked Up to Be" »

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.

Continue reading "Johnson & Johnson to Stop Manufacturing Drug-Coated Heart Stents" »

A recent New York Times article reported that a new study indicated that in recent years the Food and Drug Administration (FDA) has not rigorously studied or tested many of its approved medical devices before clearing them for sale. The study specifically assessed many medical devices which have been the subject of major recalls over the past few years, such as mechanical ventilators, hospital infusion pumps, and external heart defibrillators.

Diana Zuckerman and Paul Brown, both with The National Research Center for Women and Families, headed up the study along with cardiologist Steven Nissen, M.D. of the Cleveland Clinic. The study, published in The Archives of Internal Medicine, focused on those medical devices that have since been labeled as high risk for recalls between 2005 and 2009. It found that most, if not all, of the medical devices were cleared for public use by the FDA without being first being tested. The FDA and a trade group representing medical device manufacturers called The Archives of Internal Medicine study flawed.

Continue reading "Majority of Recalled Medical Devices Were Untested According to New Study in Archives of Internal Medicine" »

Radiation therapy is a common treatment for a large range of cancers and has been responsible for saving, or at least extending, many peoples' lives. However, the basic premise of radiation therapy involves targeting and killing cancerous cells in one's body. And while properly administered radiation therapy can save lives, when hospitals and doctors administer too much radiation it can result in negative effects for the treating patient.

Overdoses of radiation is becoming more and more widespread amongst cancer patients. A recent report of Evanston's Northshore University HealthSystem, a Chicago-area hospital, provided one such example. A 50 year-old mother of three was administered dangerously high doses of radiation when the hospital staff made radiology errors involving the administration of her radiation doses. The young Illinois resident went from an active, vibrant person pre-radiation to a virtual invalid post-radiation and now resides in an Illinois nursing home.

This woman was just one of three oncology patients who received an overdose of radiation at Evanston Hospital. All three instances of the radiation errors were allegedly the result of faulty linear particle accelerators. These accelerators are used to focus the radiation on the cancerous cells and are commonly used for stereotactic radiosurgery (SRS).

Continue reading "Evanston Hospital Over-Radiation Leads to Severe Brain Damage: The Hidden Dangers of Stereotactic Radiosurgery (SRS)" »

Federal preemption of medical device liability lawsuits has been a volatile issue in recent years, with the courts typically preempting product liability lawsuits citing violations of individual state safety standards. However, in Bausch v. Stryker Corporation, et al., No. 09-3434, the issue was whether a product defect claim citing federal safety standard violations was also preempted by that product having federal approval. While a Chicago federal district court had dismissed Ms. Bausch's claim, that decision was recently overturned by the United States Court of Appeals for the Seventh Circuit. That Court of Appeals decision permitted Mr. Bausch to pursue his claim in federal court.

The case facts of the Bausch medical device lawsuit involve a hip replacement 56 year-old Margaret Bausch underwent, during which she received a Trident brand ceramic-on-ceramic hip replacement system manufactured by Stryker Corporation. The prosthetic hip device ended up failing and required an additional surgery to have it removed.

The specific type of prosthetic hip Ms. Bausch received was approved for sale in the U.S. by the Food and Drug Administration (FDA), but was later recalled due to a failure to comply with federal standards. In her Chicago medical device lawsuit, Bausch's attorneys cited Stryker's failure to comply with federal standards during the manufacturing process of its prosthetic hip devices.

Continue reading "Chicago Prosthetic Hip Replacement Case Not Preempted According to Court of Appeals - Bausch v. Stryker Corp." »

Medicine is an area where new advances are being made on a regular basis that lead to better care and treatment for patients. However, this means that in some cases, patients who received older forms of treatment develop unforeseen complications, particularly in the area of Illinois defective medical devices. Consider the case of patients receiving metal-on-metal hip replacements. Once considered the norm, these types of hip replacements are now leading to an increase in problems for patients.

A recent editorial in The Journal of Arthroplasty, a medical journal for orthopedic surgeons, urge doctors to use metal-on-metal devices only with “great caution, if at all.” This comes on the heels of reports that metal-on-metal hip replacement procedures create tiny particles of debris that can damage soft tissue and bone.

Recent studies that estimated that anywhere from one to three percent of hip implant recipients could be affected by the problem, however, given the large number of people who have received metal devices the number could actually be dealing with thousands of patients in the United States who have been affected by defective medical devices.

Continue reading "Chicago Hospital Study Finds New Hip Replacement Procedures Required For Metal-On-Metal Devices" »