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Archive for the ‘Medical Malpractice Claims’ Category

Pennsylvania Medical Malpractice Cases Level Off After Six Years Of Decline

Tuesday, May 15th, 2012

On May 7, 2012, the Pennsylvania Supreme Court issued a report regarding medical malpractice cases filed during calendar year 2011 as compared to the prior six years. For 2011, there were 1,528 medical malpractice cases filed compared to 1,491 for 2010. In 2009, there were 1,533 medical malpractice cases filed, in 2008 there were 1,602 medical malpractice cases filed , in 2007 there were 1,641 medical malpractice cases filed , in 2006 there were 1,704 medical malpractice cases filed, in 2005 there were 1,711 medical malpractice cases filed, in 2004 there were 1,819 medical malpractice cases filed, in 2003 there were 1,712 medical malpractice cases filed, in 2002 there were 2,904 medical malpractice cases filed, in 2001 there were 2,659 medical malpractice cases filed, and in 2000 there were 2,632 medical malpractice cases filed throughout Pennsylvania.

The year 2011 had the fewest number of jury verdicts when compared to prior years. More than 70% of the jury verdicts in 2011 were defense verdicts. For each of the last six years, including 2011, the number of non-jury verdicts in medical malpractice cases was in the single digits.

The Pennsylvania Supreme Court uses the calendar years 2000 through 2002 as the “base years” for comparing medical malpractice case filings per year. There was a 44.1% decrease in the number of medical malpractice cases filed in Pennsylvania in 2011 when compared to the base years (the medical malpractice case filings for Philadelphia, which is the judicial district with the largest caseload in Pennsylvania, decreased by more than 65%).

The probable explanation for the significant drop in medical malpractice case filings after 2002 (the last of the base years) is that just after the base years, the Pennsylvania Supreme Court made two significant rule changes that had a significant impact on the number of medical malpractice cases filed after the changes. One rule change required that medical malpractice attorneys obtain a certificate of merit from a medical professional that establishes that the medical procedure in the underlying the case fell outside the acceptable professional standard of care. The other rule change required that medical malpractice cases be filed only in the county where the medical malpractice allegedly occurred.

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What do the numbers mean? Well, it does not mean that there is less medical malpractice occurring in Pennsylvania or that physicians and other health care providers in Pennsylvania are now providing a better quality of care when compared to 2002 and in prior years.

What the numbers do mean is that the legal hoops that medical malpractice lawyers must jump through in order to obtain justice for their medical malpractice victims are higher and more numerous since the changes in the rules. While some “frivolous” medical malpractice claims may not have been filed after the changes to the rules, it is much more likely that the changes to the rules have resulted in a much greater number of valid medical malpractice claims not having been filed and medical malpractice victims and their families being left out in the cold. 

Who do the changes to the rules benefit most? The answer is that medical providers who commit medical malpractice that harms their patients will benefit most from the changes to the rules that make it more costly to file valid medical malpractice cases in Pennsylvania.

If you or a family member are the victim of medical malpractice in Pennsylvania or in another state in the United States, you owe it to yourself and your family to contact a medical malpractice attorney to investigate your possible medical malpractice claim for you.  

Click here to visit our website or telephone us toll free at 800-295-3959 to be connected with medical malpractice lawyers in your state who may be able to assist you with your possible medical malpractice claim.

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$50 Million Settlement Paid By Drug Supplier To Nursing Homes

Monday, May 14th, 2012

A company that provides drugs to nursing homes and other long-term care facilities recently settled federal civil claims against it that alleged that the company dispensed drugs to nursing homes without proper prescriptions for the medications. The $50 million settlement involves allegations that the company violated the provisions of the federal Controlled Substances Act that regulates drug distribution in the United States.

The U.S. Drug Enforcement Administration had investigated the company’s practices and procedures and found that the company sometimes dispensed drugs without prescriptions or without properly written prescriptions. Some of the improperly filled medication orders failed to state the name of the drug, the strength of the drug, the quantity of the drug, and/or the dose of the drug. The issue involved how the pharmacy managers communicated with the prescribing doctors at the nursing homes regarding the controlled medications.

The settlement with the federal government recognizes the obligation of pharmacies to receive signed prescriptions containing all of the required contents of prescriptions for controlled substances or to speak directly to the prescribers in emergency situations. The investigation had found that it was not an uncommon practice for pharmacies to dispense medications to nursing homes under the instructions of the nursing home staff who did not have the authority to prescribe controlled substances and without the patients’ doctors being involved in the process.

The federal government’s investigation did not involve allegations that the drugs received from the pharmacies were diverted to people other than the appropriate nursing home residents and the investigation did not involve the nurses or others who gave the medications to the nursing home residents.

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Because many of the residents in nursing homes are taking multiple medications for their medical and other conditions, and all of the nursing home residents who take multiple medications must be closely, carefully, and constantly monitored regarding the effects of their medications, it is imperative that the residents’ physicians are made fully aware of their patients’ medical conditions, changes in their medical conditions, and the medications and other therapies being provided to their patients. Medical mistakes involving the care of nursing home residents and medical errors involving the medications that nursing home residents rely on can result in serious or deadly consequences for the  residents.

Failure to follow procedures and protocols in nursing homes and sloppy record-keeping regarding the care and medications provided to nursing home residents are often cited as the basis for medical malpractice claims brought against nursing homes when residents suffer unanticipated and serious outcomes in nursing homes.

If you or a loved one suffered injury or death as a result of nursing home negligence, the prompt advice from a local medical malpractice attorney may be essential in protecting your legal rights.

Click here to visit our website or call us toll free at 800-295-3959 to be connected with medical malpractice lawyers in your state who may be able to investigate a possible nursing home claim for you and file a medical malpractice case on your behalf, if appropriate.

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Maryland Federal Judge Says Courts Cannot Review Medicare Payment Method

Saturday, May 12th, 2012

On May 9, 2012, a Maryland federal court judge determined that Congress precluded the courts from reviewing the method by which Medicare determines how much doctors get paid by Medicare. Six Georgia physicians had brought a federal lawsuit challenging the method by which the Physician Fee Schedule (PFS) was formulated to determine how much health care providers are paid for various procedures under the Medicare program.

The Plaintiffs’ Allegations

In particular, the physicians challenged the dominating influence that the American Medical Association’s Relative Value Update Committee (RUC) has on the way the “relative value units” (a major component of the fee structure) are calculated. They argued that certain medical specialties are disproportionately represented on the RUC and therefore primary care physicians, like the six physicians in this case, are undercompensated under the PFS. They also argued that there is over-use of unnecessary medical procedures by RUC-favored specialists that results in major harm to the national health care system and negatively affects health care spending due to the over-reliance on RUC in formulating the PFS.

In Simple Terms, What Are The Plaintiffs Claiming?

In short, the argument was that the medical specialists on the Committee have undue influence in determining who gets paid what by Medicare, and that they tend to protect their own specialists’ financial interests at the expense of others, such as primary care physicians.

What Were The Plaintiffs Seeking?

The Plaintiffs wanted the Maryland federal judge to find and declare that Medicare was violating the Federal Advisory Committee Act (FACA) because the RUC’s influence is so dominating in the process that it is actually acting as a Federal Advisory Committee (FAC) and therefore subject to the provisions of FACA, and was violating FACA, the Administrative Procedures Act, and the Patient Protection and Affordable Care Act.

The Judge’s Discussion Of The Relevant Medicare Law And The Plaintiffs’ Claims

The Maryland federal judge stated in his written opinion as follows:

Medicare, Title XVIII of the Social Security Act, is a federal health insurance program for the aged and disabled. This action relates to Part B of Medicare, a voluntary supplemental insurance program that covers payments for physician’s services and other healthcare services…Fees paid to physicians who elect to participate in the program are capped by the annual PFS which sets the fees for hundreds of types of specific services. Payment amounts under the PFS are calculated by multiplying (1) the relative value of a service; (2) the conversion factor for the particular year; and (3) the geographic adjustment factor applicable to the locality in which the service was provided…This case relates to the determination of the first component, the relative value of a service, which is calculated by combining three subcomponents, each of which is measured in terms of relative value units (“RVUs”). The three subcomponents are (1) the work component; (2) the practice expense component; and (3) the malpractice component…

The RVUs are revised each year by CMS. According to the Complaint, RUC has met each year since 1991 to “debate relative values based upon input from surveys distributed to specialty societies.” …RUC then makes recommendations to the Secretary of HHS. Although Plaintiffs acknowledge that the Secretary rejects some of those recommendations,…Plaintiffs assert that most RUC recommendations are routinely adopted into the final PFS.

Accepting as true that RUC plays a major role in the formation of the PFS and also accepting as true that this role unfairly skews the PFS toward certain medical professions and procedures, the Court, nonetheless, finds that Congress has precluded courts from reviewing, not only the final relative values and RVUs, but also the method by which those values and units are generated. Section 1395w-4(i)(1) of Section 42 of the United States Code provides: There shall be no administrative or judicial review under section 1395ff of this title or otherwise of–(A) the determination of the adjusted historical payment basis (as defined in subsection (a)(2)(D)(i) of this section), (B) the determination of relative values and relative value units under subsection (c) of this section, including adjustments under subsections (c)(2)(F), (c)(2)(H), and (c)(2)(I) of this section and section 13515(b) of the Omnibus Budget Reconciliation Act of 1993, (C) the determination of conversion factors under subsection (d) of this section, including without limitation a prospective redetermination of the sustainable growth rates for any or all previous fiscal years, (D) the establishment of geographic adjustment factors under subsection (e) of this section, and (E) the establishment of the system for the coding of physicians’ services under this section.

Therefore, the Maryland federal judge concluded, “the Court finds that Plaintiffs’ claims are barred by 42 U.S.C. § 1395w-4(i)(1). Accordingly, Defendants’ motion to dismiss will be granted.”

You can read the Judge’s Memorandum opinion by clicking here.

We can relate to the primary care physicians’ concern and allegations stated in their federal lawsuit that a small but powerful group of medical specialists were unfairly and with undue influence dictating how much they were being compensated for the services they provided to their patients. In a very similar manner, we are concerned that a small but powerful group (that is, lobbyists for the health care industry) is unfairly and with undue influence dictating how much victims of medical malpractice may receive in compensation for their injuries and losses because of arbitrary caps that many states have placed on the amount of noneconomic damages that they can recover as a result of the lobbyists’ efforts.

If you or a loved one were injured as a result of medical malpractice, you may be entitled to monetary compensation for your injuries and losses. The prompt advice from a local medical malpractice attorney may help you decide if you want to proceed with a medical malpractice claim.

Click here to visit our website or call us toll free at 800-295-3959 to be connected with medical malpractice lawyers in your state who may be willing and able to investigate your possible medical malpractice claim for you and represent you in a medical malpractice case, if appropriate.

Turn to us when you don’t know where to turn.

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Accutane Jury Verdict Upheld

Friday, May 11th, 2012

Accutane (isotretinoin) is a prescription acne medication manufactured by Hoffman-La Roche that was first introduced in the United States in 1982. Accutane was used to treat severe acne (nodular and/or inflammatory acne) that could not be cleared up by using other acne treatments, such as antibiotics. Accutane was removed from the market in 2009 after many lawsuits were filed regarding serious side effects from Accutane.

Side effects of using Accutane may include dryness of the skin and mucous membranes, photophobia, muscle and joint pain, insomnia, lethargy, visual disturbances, hearing deficiencies, headache, nausea, malaise, drowsiness, amnesia, hallucinations, behavioral disorders, seizures, psychosis, schizophrenia, depression, suicide ideation, suicide attempt, and suicide.

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Studies of the generic version of Accutane (isotretinoin) have also linked its use to a serious risk of birth defects and to bowel disorders such as inflammatory bowel diseases, including ulcerative colitis. According to preliminary research evidence presented to the American College of Gastroenterology in January, 2009, the risk of being diagnosed with ulcerative colitis in isotretinoin users was more than four times greater than in the general population, and patients who had filled four or more prescriptions for Accutane had a risk of inflammatory bowel disease that was more than 2.5 times greater than in the general population.

A New Jersey Accutane Lawsuit

A New Jersey woman who had used Accutane for six months in 1998 allegedly developed inflammatory bowel disease (ulcerative colitis) six weeks after she stopped taking Accutane. She alleged in her lawsuit that she would not have taken Accutane had she been made aware of the possible side effects. The jury hearing her case decided that the woman was entitled to $2 million in damages because Hoffman-La Roche failed to adequately warn her about the risks of taking Accutane, including developing ulcerative colitis.  Hoffman-La Roche was dissatisfied with the jury’s verdict and appealed its decision. A judge recently upheld the jury’s verdict.

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Accutane (isotretinoin) is a vitamin A derivative belonging to the retinoid class of medicines, which are used to treat skin conditions. The manner in which Accutane works is not known but it is believed to act on the sebaceous glands that produce oil/wax to reduce sebum excretion, which may indirectly reduce bacterial activity associated with acne and thereby improve acne. To read more from the manufacturer about Accutane, click here.

If you have been injured as a result of taking Accutane or another drug in the United States, you may be entitled to compensation for your losses and injuries. A medical malpractice attorney versed in such claims may be able to assist you with your possible drug claim.

Click here to visit our website or call us toll free at 800-295-3959 to be connected with medical malpractice lawyers in your state who may be able to assist you with a drug claim.

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Maryland Stent Doctor’s License Remains Revoked

Wednesday, May 9th, 2012

A Maryland cardiologist whose license to practice medicine in Maryland had been revoked by the Maryland State Board of Physicians (“Board”) had appealed the Board’s license revocation to the courts, where a judge denied his appeal on May 7, 2012. The Board had revoked the doctor’s medical license in July 2011 after finding that the doctor had engaged in unprofessional conduct, willfully made a false medical report, grossly over utilized health care services, violated the standard of care, and failed to keep adequate medical records with regard to his patients.

Before he got in trouble for implanting stents in cardiac patients without the patients having the need for the stents, the well-known cardiologist practiced in a Baltimore-area hospital beginning in 2008 until the hospital suspended him in July, 2009 for performing the unnecessary stent procedures. The doctor’s tenure at the hospital resulted in the hospital’s cardiology department enjoying national attention. As a result of the stents controversy, the hospital ended up paying the federal government $22 million in November, 2010 in order to to settle a Medicare fraud investigation.

As a result of its own investigation, the hospital sent out letters to 600 of the doctor’s patients in 2010, advising them that their stent procedures done by the doctor may have been unnecessary. Hundreds of the doctor’s former cardiac patients filed medical malpractice cases against the doctor and the hospital as a result.

The hospital’s fortunes declined to such a degree after the scandal that the hospital sought to sell itself to a larger, regional medical system. The medical system recently entered into a letter of intent with the hospital to purchase and incorporate the hospital into its long-list of facilities in the State of Maryland.

Source:  The Daily Record, May 9, 2012.

What’s A Stent?

A stent is a small mesh tube made of metal or fabric (fabric stents are used in larger arteries) implanted in arteries that are too narrow or weak. Stents may or may not be coated with medicine (drug-eluting stents are coated with a slow-release medicine intended to prevent the artery from becoming blocked again). Stents are implanted during a medical procedure known as an angioplasty that restores blood flow through the narrowed or blocked arteries by supporting the inner walls of arteries. Stents may also be used in weak arteries to prevent the arteries from bursting while also increasing blood flow.

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The Risks Of Stents

While stents may help improve the quality of life of patients and extend their lives under appropriate circumstances, angioplasty and stents come with known risks including bleeding at the site where the catheter was inserted, blood vessel damage due to the catheter, irregular heartbeats (arrhythmias), kidney damage due to the dye that is used during the procedure, an allergic reaction to the dye, infection, restenosis (excess tissue growth within the treated portion of the artery that leads to narrowing or blockage of the artery), and blood clots at the stent site that can lead to a heart attack or stroke (approximately 1% to 2% of stent patients develop a blood clot at the stent site, which risk is greatest during the first few months after the stent was placed; this risk is often addressed by the doctor prescribing aspirin and/or anti-clotting medicines for a period of at least one month after a stent procedure; coated stents may increase the risk of developing blood clots but appear to not increase the chance of a heart attack or stroke).

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If you had a bad outcome as a result of angioplasty or suffered a complication with a stent, medical malpractice may be a cause of your injuries and losses. A medical malpractice attorney may help investigate your situation for you to determine if you may have a valid claim for medical malpractice.

Click here to visit our website or telephone us toll free at 800-295-3959 to be connected with medical malpractice lawyers in your state who may be able to assist you with your medical malpractice claim.

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$1.6 BILLION Pharmaceutical Company Payment For Off-Labeling Marketing

Tuesday, May 8th, 2012

The large pharmaceutical company Abbott Laboratories (“Abbott”) has agreed to pay $1.6 billion, the second largest payment by a drug company, to settle an investigation into its drug marketing practices (the largest payment was $2.3 billion that was paid by Pfizer Inc. in 2009). The $1.6 billion includes $700 million in criminal fines and forfeiture and $800 million to settle civil claims brought by states and the federal government.

Additionally, Abbott agreed to pay $100 million to resolve state consumer protection claims, to plead guilty to a misdemeanor violation of  the federal Food, Drug and Cosmetic Act, and to be subjected to court-supervised probation for a five year period.

The settlements, payments, and guilty plea are related to Abbott’s misbranding (improper promotion/marketing) of its drug named Depakote. The only uses of Depakote that are approved by the FDA are for treatment of epilepsy, bipolar disorder, and in the prevention of migraines. One of the known safety risks of Depakote is liver disease. Sales of Depakote reached $1.7 billion in 2007.

According to the U.S. Department of Justice, Abbott promoted Depakote in controlling agitation and aggression in elderly dementia patients as well as in treating schizophrenia, both of which were not approved uses of Depakote by the U.S. Food and Drug Administration. Such improper marketing is often referred to as “off-label” use.

Abbott admitted that the off-label use of Depakote for elderly dementia patients who were agitated or aggressive in nursing homes was actively promoted by a specialized sales force between 1998 and 2006 despite no credible scientific evidence that Depakote was safe and effective for such use (Abbott discontinued a clinical trial of Depakote’s use in treating dementia in 1999 due to adverse effects such as dehydration, anorexia, and drowsiness). Additionally, Abbott also admitted that it paid millions of dollars in rebates to pharmacists who serviced nursing homes based on how much Depakote’s use was increased in the nursing homes that they serviced.

Abbott further admitted that Depakote’s use for treatment of schizophrenia in combination with other drugs was actively promoted between 2001 and 2006 without evidence that it was any more effective than other medications alone in the treatment of schizophrenia (two studies of Depakote’s use in the treatment of schizophrenia that were paid for by Abbott failed to meet their goals, which Abbott did not report to its sales force for two years and which were not published for an additional two years).

The recently announced settlements will result in some ”whistle-blowers” receiving about $84 million as their share of the federal government’s recovery pursuant to the False Claims Act that provides for such incentives. The whistle-blowers had filed four lawsuits in federal court in Virginia regarding Abbott’s improper marketing promotion of off-label uses for Depakote.

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Without the monetary incentives provided under the False Claims Act for whistle-blowers, one must wonder if the illegal activities of a giant pharmaceutical company would have been discovered and punished.

If you have a possible whistle-blower claim against a drug company or other large company in the United States, you may wish to consult with a medical malpractice lawyer or other attorney who is knowledgeable about whistle-blower claims and handles such claims.

Click here to visit our website to be connected with whistle-blower lawyers in your local area who may be able to advise you regarding your whistle-blower responsibilities and possible monetary recovery and to assist you in filing a whistle-blower claim, if appropriate.

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New Jersey Nursing Home Abuse Caught On Video

Saturday, May 5th, 2012

In one of the most disturbing and frightful examples of nursing home violence against a nursing home resident that was caught on video, an 87-year-old paralyzed woman was shown being struck violently and cursed at by the very aides who were supposed to be providing her with necessary care. The video camera was set up in the woman’s room by her daughter and grandson after the grandson noticed unexplained bruising on the woman’s body last year.

The video shows one nursing aide roughly removing the woman’s oxygen mask from her face and then hitting the woman twice on her head for no reason. The nursing aide lost her job, lost her license, and was arrested after the video caught her ruthless and demeaning behavior, but it makes you stop and wonder how many times in the past the elderly woman or other nursing home residents may have been physically abused by the same aide or other nursing home caregivers.

Another employee of the same nursing home who has not been arrested can be heard on the video telling the woman, “Lady, why don’t you die?”  A third nursing home employee was caught on tape roughly handling the woman’s body while changing her bed sheets. Even a supervisor was allegedly heard on the video cursing at the woman.

The nursing home had no comment about what was depicted on the video but is being sued by the woman’s family for medical malpractice and other claims. The woman’s family hopes that by going public with the video of the elderly woman’s abusive treatment that they may help other residents’ families become aware that they must be vigilant in checking up on family members who are in nursing homes.

We urge you to view the clip from the video for yourself.

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Many states in the U.S. still do not allow video cameras to be placed in residents’ rooms due to alleged privacy concerns. We suggest that in many situations, the privacy concerns of nursing home residents and nursing home staff may be outweighed by the concerns regarding the safety and care of the residents. If nursing home employees believe that they will never be caught abusing or neglecting the residents they are assigned to take care of, then callous (or worse) nursing home employees may consider and engage in abusive or neglectful conduct that they would not otherwise engage in if they knew that their actions were being monitored and/or recorded.

In this day and age when almost all telephone calls to businesses are subject to being monitored or recorded, and our movements in public are often being viewed or recorded by public or private video cameras set up outside of businesses, parking garages, state and local governmental offices, and on public street corners so that the police or others may monitor pedestrians or traffic, all in the stated interest of public safety, maybe it is time to change the laws in those states that prohibit cameras in the rooms of nursing home residents so that they have the same hope of being safe that a pedestrian on a public street now enjoys.

If you or a loved one were abused or neglected in a nursing home, you may wish to consult with a local medical malpractice attorney regarding your legal rights and obligations.

Click here to visit our website or call us toll free at 800-295-3959 to be connected with medical malpractice lawyers in your state who may be willing to investigate your possible medical malpractice claim for you and file a medical malpractice claim on your behalf, if appropriate.

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Colorado Medical Malpractice Verdict For Infected Bedsores Leading To Death

Friday, May 4th, 2012

A Colorado medical malpractice jury returned a verdict in the amount of $3.2 million in favor of the family of an 88-year-old-man in a nursing home who died from infected bedsores, one of which was the size of a baseball, that were allegedly not properly treated. The nursing home that is responsible for the medical malpractice verdict is owned by a large out-of-state corporation that has 4,000 nursing home beds in 8 states, including two other nursing homes in Colorado.

The man had become a resident of the nursing home in May, 2009. He had Parkinson’s disease but was able to walk with assistance to the cafeteria in the nursing home and worked as a janitor in the nursing home before he developed a bedsore in September, 2010. After the bedsore developed, the man’s condition deteriorated to the point where he was unable to walk, even with assistance, and he became unresponsive and stayed in his bed. He also stopped eating and drinking.

Apparently the man’s family was not told about the bedsore. It was not until October, 2010 that a nurse’s aide employed by the nursing home told the man’s son about multiple severe bedsores on his father’s buttocks and scrotum that were infected.

Upon discovering the bedsores and their condition, the son wanted his father immediately transferred to the hospital. At first, the nursing home did not want to transfer the man to the hospital for treatment. Once the man was transported to the hospital, he was found to be dehydrated and malnourished (both conditions can lead to the development of bedsores and both conditions can have a negative impact on attempts to successfully treat bedsores). The man’s death was linked by his doctors to his infected bedsores.

After the man’s death, the Colorado Health Department inspected the nursing home and issued citations against the nursing home for 27 deficiencies.

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The development of bedsores in nursing home residents is generally avoidable if proper and timely care is provided to residents. Residents at risk for developing bedsores are often required to be turned and repositioned in their beds at set intervals (often at least every two hours) to help avoid developing bedsores. Pressure relieving devices such as air mattresses for residents’ beds and other devices designed to reduce the pressure points where the body comes in contact with the resident’s bed (such as heals, elbows, buttocks, and the back of the head) are often useful if timely employed.

If bedsores do develop, it is critical that they be diagnosed quickly and promptly and that they be properly treated so that they do not progress to more serious and dangerous stages of development.

If bedsores do develop and cause serious injuries or death to nursing home residents, medical malpractice attorneys often investigate whether there was sufficient staff on all shifts to provide necessary care to the nursing home residents based not only on the number of nursing home residents assigned to each caregiver, but also based on the level of care that each of the assigned residents required from the caregivers. Medical malpractice attorneys also investigate whether the proper care was timely provided to the injured resident.

If appropriate, medical malpractice claims based on the lack of appropriate and timely care owed to nursing home residents may be alleged based on inadequate staffing levels, inadequate training of staff, and/or inadequate care provided by the nursing home’s staff.

If you or a loved one suffered serious injuries or death as a result of nursing home negligence, nursing home neglect, or nursing home abuse, click here to visit our website or telephone us toll free at 800-295-3959 to be connected with medical malpractice lawyers in your state who may be able to investigate your possible medical malpractice claim and represent you in a medical malpractice case, if appropriate.

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Inappropriate Use Of Anti-Psychotic Medications In Nursing Homes

Thursday, May 3rd, 2012

Federal data recently reviewed by a major newspaper pursuant to a Freedom of Information Act request reveals that the inappropriate use of anti-psychotic medications for nursing home residents is rampant. Anti-psychotic medications are typically used in the treatment of severe mental disorders such as schizophrenia and bipolar disorder.

About 185,000 nursing home residents in the United States during 2010 were given anti-psychotic medications when it was inappropriate to do so. More than 1 in 5 U.S. nursing homes used anti-psychotic medications for a significant percentage of residents who did not have psychosis or other serious mental conditions.

The use of anti-psychotic medications in patients with dementia is particularly dangerous, earning FDA black-box warnings regarding potentially fatal side effects. Anti-psychotic medications can cause dizziness, abnormal heart rhythms, a sudden drop in blood pressure, blurred vision, increased risk of deadly infections, cardiovascular complications, and urinary problems.

Nursing homes sometimes give anti-psychotic medications to combative or aggressive residents under the pretext of preventing the residents from harming themselves or others. However, the statistics seem to lend support to the belief that anti-psychotic medications administered to nursing home residents may be used to sedate and control residents who simply need more attention and care from nursing home staff — more care and attention means more time spent with residents, which in turn requires more staff time (and more staff), which means higher costs for nursing home owners.

The newspaper reported that at least 25% of nursing home residents without conditions recommended for anti-psychotic medication use nonetheless received the anti-psychotic medications in 21% of U.S. nursing homes in 2010. There was a direct link between the staffing of the nursing homes and their rate of use of anti-psychotic medications for their residents — the fewer the staff involved with the residents’ direct care, the greater the rate of anti-psychotic medication use for non-recommended conditions. The nursing homes that used anti-psychotic medications for conditions other than psychosis and similar mental conditions tended to have more residents that the nursing home staff identified as having behavioral problems such as wandering, verbal abuse, physical abuse, or being resistant to care, and the nursing homes themselves had a higher percentage of residents whose care was paid for by Medicaid and not by private insurance.

The newspaper reported that 10 nursing homes in California during 2010 administered anti-psychotic medication to all of their residents who were without psychosis or a related mental condition. On the other side of the spectrum, 146 nursing homes in the U.S. did not use anti-psychotic medications for their residents without psychosis or a related mental condition (that is about 1% of the nursing homes in the United States with at least 50 residents).

Source

If your family member or a loved one was mistreated, abused, or neglected in a nursing home in the United States, the assistance of a local medical malpractice attorney may help in investigating a possible medical malpractice claim against the nursing home.

Click here to visit our website or telephone us toll free at 800-295-3959 to be connected with medical malpractice lawyers in your state who may be able to assist you in bringing a medical malpractice claim against the nursing home.

Turn to us when you don’t know where to turn.

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Medical Malpractice Claims Lead To Legal Malpractice Claims

Wednesday, May 2nd, 2012

A Putnam County, West Virginia attorney and his two former law partners are being sued for legal malpractice for the third time in a year for their alleged wrongful handling of medical malpractice claims against the same doctor. In this most recent case filed on April 13, 2012, the three plaintiffs allege that their former attorneys failed to timely file their medical malpractice claims against former osteopathic physician, John King.

The former physician had been sued for medical malpractice in over 100 cases in 2006 for acts of alleged medical malpractice that occurred between November 2002 and June 2003 while the physician practiced at Putnam General Hospital (for more information regarding the former Dr. King and the medical malpractice claims against him, see our blog posting on February 20, 2012).

The most recent legal malpractice claim alleges that the holders of a durable medical power of attorney for the medical malpractice claimant had contacted the lawyers in October 2003 regarding the alleged medical malpractice that occurred earlier in 2003. The lawyers did not file the medical malpractice lawsuit until October 25, 2006, which was after the two-year West Virginia statute of limitations for medical malpractice cases had expired. Their medical malpractice case was dismissed a little over one year later, for failing to file the medical malpractice claim within the two-year statute of limitations. A motion to reconsider the dismissal was denied on March 5, 2010.

The other two legal malpractice lawsuits filed against the attorneys were filed in April and December 2011, respectively. As with the most recent legal malpractice claim, the other two legal malpractice cases allege that their lawyers failed to timely file their medical malpractice lawsuits against the osteopathic physician. Their medical malpractice cases were also filed in October 2006 and were dismissed in November 2007 because they were not filed by the deadline. Both of these cases also had motions to reconsider the dismissals filed which were denied by the court in March 2010.

The lawyers’ law firm was dissolved in 2005, according to records. One of the lawyers has since moved to Florida. The three legal malpractice lawsuits on behalf of the plaintiffs are being handled by the same attorney.

Source

The three legal malpractice cases based on their lawyers’ alleged failures to handle their three medical malpractice claims timely and appropriately must be devastating for the medical malpractice claimants — it appears that they have been victimized twice: once by their trusted physician and then a second time by their trusted lawyers.

If you or a loved one have suffered injuries and losses as a result of possible medical malpractice in West Virginia or in another state in the United States, it is important that you promptly and timely obtain the legal advice of a competent medical malpractice attorney regarding your rights concerning your possible medical malpractice claim.

Click here to visit our website or call us toll free at 800-295-3959 to be connected with local medical malpractice lawyers in your state who may be able to assist you with your medical malpractice claim.

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