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Archive for the ‘Medical Malpractice Verdict’ Category

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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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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Indiana Medical Malpractice Verdict Upheld On Appeal In Failure To Diagnose Colon Cancer Case

Friday, April 27th, 2012

On April 12, 2012, the Court of Appeals of Indiana filed its decision in a medical malpractice case in which the plaintiff alleged that his gastroenterologist failed to timely diagnose his colon cancer. The Court of Appeals upheld the verdict in favor of the plaintiff in the amount of $1.25 million, which had been reduced fom the medical malpractice jury’s original verdict in the amount of $2.5 million pursuant to Indiana’s Medical Malpractice Act.

The Underlying Medical Malpractice Facts

The 35-year-old patient visited a gastroenterologist on April 26, 2004 (the same gastroenterologist who had treated his mother for colon cancer for eight years during the 1990s) with complaints including upper stomach pain, nausea, and occasional vomiting,  rectal bleeding, and diarrhea. The gastroenterologist examined the patient, including a digital rectal exam and a hemoccult test that checks for blood in the stools (which was negative), and had the patient undergo an endoscopy procedure known as an EGD (commonly called “an upper GI”) that showed severe gastritis of the stomach, duodenitis, and a gastric ulcer. However, neither a sigmoidoscopy nor a colonoscopy were ordered at that time.

Exactly one year later (on April 26, 2005), the patient visited the gastroenterologist again and obtained refills for his prescriptions in anticipation of his move to Arizona. The gastroenterologist claimed that no discussion was had at that time regarding the patient’s rectal bleeding.

After the patient’s move to Arizona, he came under the care of an Arizona gastroenterologist, who performed a colonoscopy on the patient on August 31, 2006, which revealed a sizable mass lesion in the sigmoid colon that was surgically removed. However, the patient’s diagnosis was that he had a very advanced Stage Four cancer.

The Defenses To The Medical Malpractice Claim

The Indiana gastroenterologist who was sued for medical malpractice alleged during the jury trial that the patient had failed to tell him about his family’s history of colon cancer. The patient testified during the trial that he told the gastroenterologist about his mother’s history of colon cancer during the initial visit in 2004 and that he had also requested a colonoscopy at that time; nonetheless, the gastroenterologist testified that his since his office notes did not state the family history of cancer, the patient had failed to tell him about his mother’s colon cancer, and without knowing the family history of colon cancer at that time, it was unnecessary to order either a sigmoidoscopy or colonoscopy in 2004.

The medical malpractice defendant further alleged that the patient was contributory negligent for failing to mention his rectal bleeding during the visit in 2005 (the patient testified during the medical malpractice trial that he told the gastroenterologist about his continuing rectal bleeding during the visit in 2005).

The Medical Malpractice Defendant’s Appeal

The Indiana Medical Malpractice Act requires that once a medical malpractice claim is filed, a medical review panel must be convened to consider the evidence to determine if the evidence supports that the medical malpractice defendant(s) failed to meet the applicable standard of care.

In this case, the medical review panel concluded that the evidence did not support that the defendant failed to meet the applicable standard of care. The review panel concluded that because the medical records from the defendant’s office did not state a family history of colon cancer, the patient had failed to tell the defendant about his family’s medical history in 2004 and therefore a sigmoidoscopy or colonoscopy at that time was not required.

The medical malpractice defendant sought to have physicians from the medical review panel testify during the medical malpractice trial as to their conclusions that the defendant did not fail to meet the applicable standard of care and that the patient was contributorily negligent because the patient failed to tell the defendant about his family’s medical history of colon cancer during the visit in 2004 and failed to tell the defendant about continuing rectal bleeding during the visit in 2005, based solely on the absence of such documentation in the defendant’s medical records.

The medical malpractice trial judge refused to permit the defendant’s experts from testifying as stated above because their testimony involved their opinions regarding the credibility (truthfulness) of the patient’s testimony, which is impermissble. The Court of Appeals of Indiana agreed with the trial judge’s decision in this regard, stating in its written opinion in this case, The “ultimate point” of the proffered testimony was that [the patient] was not truthful on the question of whether he had reported a family history of colon cancer and continued rectal bleeding in 2005. See Whedon, 900 N.E.2d at 506. That testimony was directed to [the patient's] credibility as prohibited by Evidence Rule 704(b). Indeed, as our supreme court recently reiterated, “no witness, whether lay or expert, is competent to testify that another witness is or is not telling the truth.”

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If you may be the victim of medical malpractice in Indiana or in another state in the United States, the prompt advice from a medical malpractice attorney in your local area may help you decide how you may want to proceed with the matter.

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 your possible medical malpractice claim for you and represent you in a medical malpractice case, if appropriate.

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Colorado Medical Malpractice Verdict Finally Paid

Saturday, April 21st, 2012

When a 34-year-old woman arrived at a local Fort Collins, Colorado hospital Emergency Department in December, 2006, she complained to the emergency room doctor that she had the worst headache of her life and that she was weak and dizzy. The emergency room doctor diagnosed the woman’s condition as a migraine, he gave the woman pain medication for her headache, and he discharged her to home, despite the woman’s complaints and her dangerously high blood pressure while in the Emergency Department.

The woman was not given a head CT scan while in the Emergency Department that would have found a small bleed in her brain that could have been treated at that time. Unfortunately, the woman became paralyzed on her right side as a result of the alleged medical malpractice.

Her medical malpractice attorneys filed a medical malpractice claim on her behalf that resulted in a verdict in the woman’s favor in the amount of $3.9 million, which was the largest medical malpractice jury verdict in Fort Collins, Colorado to date.

The Colorado medical malpractice insurance carrier for the Emergency Department physician who was sued for medical malpractice recently paid the verdict, despite the fact that the doctor’s medical malpractice insurance policy limit was $1 million (the doctor wanted his medical malpractice insurance company to settle the woman’s claim but it refused to do so, thereby requiring the woman to file her medical malpractice lawsuit and endure the stressful litigation process that resulted in the jury’s $3.9 million verdict in favor of the woman).

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The misdiagnosis of a serious medical condition in hospital emergency departments throughout the United States happen all too often. Sometimes the medical negligence is discovered before the patient’s discharge from the emergency department, before serious and permanent injuries occur. Other times the medical negligence is not discovered unless and until the patient returns to the emergency department with worsening symptoms. And some misdiagnosed or undiagnosed emergency department patients never make it back to the emergency department – they die as a result of the emergency department’s failure to properly diagnose and treatment their dire and deadly medical conditions.

If you or a loved one went to the emergency room and your medical condition was misdiagnosed or not diagnosed and you suffered serious consequences as a result, you may be entitled to compensation for your injuries and losses. It is important to seek the prompt and timely advice of a medical malpractice attorney to investigate your possible medical malpractice claim and to advise you on how to proceed.

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

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Maine Medical Malpractice Verdict For Methadone Overdose

Tuesday, April 17th, 2012

Earlier this month, a medical malpractice jury in Maine deliberated for less than two hours before unanimously awarding a woman compensatory damages in the amount of $1,912,934 for her alleged brain damage caused by her doctor over-prescribing methadone that resulted in her experiencing an episode of slow and shallow breathing during the night which deprived her of oxygen. The woman had been taking the prescribed methadone for only two and half days before she suffered her injuries.

The woman had been living with chronic back pain for which her primary care physician referred her in August, 2006 to a family practice specialist for treatment of her chronic pain. The medical malpractice claim alleged that the woman had been given a prescription for methadone by the family practice specialist at a dose eight times the recommended dosage.

The medical malpractice defendant argued to the medical malpractice jury that the woman had failed to mention to the pharmacist at the time she filled her prescription for methadone that she had pre-existing breathing problems and sleep apnea. The defense also argued that the 40 mg dose prescribed for the woman was within an appropriate range and that the pharmacy’s computerized system for warning of complications, side effects, or other problems with the prescription did not indicate a problem with the dosage prescribed for the woman and that the pharmacist who filled the prescription had called to confirm the prescription and did not indicate any problem with the prescription.

The medical malpractice defendant’s attorney also argued to the jury that the woman never intended to return to her job with the Maine Department of Health and Human Services, where she had worked for 18 years, and therefore her claim for lost wages should not be awarded by the medical malpractice jury. And while the medical malpractice plaintiff claimed her alleged brain damage affected her ability to perform simple tasks and to multitask at work, the medical malpractice defendant argued that the woman’s family did not notice any changes in the woman’s demeanor or behavior during the two and a half days the woman was taking the methadone before the incident.

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Many people associate methadone with its use in treating heroin addicts (opiate addiction). However, methadone is also used to treat moderate to severe pain that has not been relieved by use of non-narcotic pain relievers.

Methadone is a narcotic analgesic that treats pain by changing the way the brain and nervous system responds to pain (methadone is used to treat abusers of opiate drugs by producing similar effects while preventing withdrawal symptoms when the abused drugs are stopped).

The official “warnings” regarding use of methadone include the following: “Methadone may cause slowed breathing and irregular heartbeat, which may be life-threatening. If you experience any of the following symptoms, call your doctor immediately: difficulty breathing; extreme drowsiness; slow, shallow breathing; fast, slow, pounding, or irregular heartbeat; faintness; severe dizziness; or confusion.

The risk that you will experience serious or life-threatening side effects of methadone is greatest when you first start taking methadone, when you switch from another narcotic medication to methadone and when your doctor increases your dose of methadone. Your doctor may start you on a low dose of methadone and gradually increase your dose. Your doctor will monitor you closely during this time.”

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The standard of care requires physicians and other health care providers with the authority to prescribe medications to use that degree of care and skill that similarly situated medical providers would use under similar circumstances. Sometimes a questionable or unusual prescription is flagged by the filling pharmacist when the pharmacy’s computer system provides a warning regarding the information about the prescription entered into the computer system. When that happens, the pharmacist may use his/her knowledge, education, and experience in responding to the computer’s warning, which may range from disregarding the warning as unwarranted to not filling the prescription and speaking with the prescriber regarding the pharmacist’s concerns.

While a pharmacist may also be held responsible for filling a prescription in a manner that violates the pharmacist’s standard of care, the prescribing health care provider remains liable under most circumstances and cannot rely on and expect to be excused of the health care provider’s own negligence by the subsequent negligence of the pharmacist.

If you or loved one have been injured or suffered losses as a result of a prescription medication or an over-the-counter medication, you may be entitled to compensation for your injuries, pain, and other losses. The prompt advice of a medical malpractice attorney may be essential in protecting your legal rights and obtaining fair compensation.

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

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South Carolina Medical Malpractice Verdict For Death After Surgery

Saturday, April 14th, 2012

On March 9, 2012, after a one-week trial before a South Carolina medical malpractice jury, the surviving husband of a woman who died in November, 2007 just three weeks after surgery, received a medical malpractice verdict in his favor in the amount of $2.4 million. The medical malpractice claim alleged that the woman had gynecological surgery during which her bowel was perforated and the perforation was not treated properly or timely, leading to her death.

The medical malpractice defendants claimed that the risk of bowel perforation during the surgery is a known risk and that the diagnosis and treatment of the woman’s bowel perforation were timely and proper. The medical malpractice jury evidently did not agree with the defendants and found against them.

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“Known Risk” Of Treatment Versus Medical Malpractice

One of the most common medical malpractice defenses put forth by medical malpractice defendants is that the “bad outcome” complained of in the medical malpractice claim is a known risk of the treatment that the patient was made aware of and assumed the risk of suffering.

Medical providers are required to obtain “informed consent” from the patient before performing medical procedures, during which the medical provider explains to the patient the proposed medical procedure and all known risks of the procedure and alternatives to the proposed procedure that a reasonable patient would want and expect to know under similar circumstances.

While there is a certain amount of risk associated with all medical treatment, and bad medical outcomes may and do occur without medical negligence being a cause of the bad outcome, it is important to recognize that if substandard medical care was a cause of the bad outcome, then medical malpractice has occurred for which a medical malpractice claim may be made.

As an example of the above, it is a known risk that anyone occupying a motor vehicle being operated on the public roadways is exposed to the risk of becoming involved in a motor vehicle collision. However, if the collision was caused by the negligent operation of a motor vehicle (such as crossing over the double yellow lines separating traffic moving in opposite directions), then the injured occupants of the non-negligent motor vehicle may bring a negligence claim against the negligent driver.

In the medical malpractice lawsuit filed by the surviving husband in South Carolina, while it may be a known risk that the particular gynecological surgery performed on the man’s wife involved a risk of perforating the bowel during surgery, the cause of the perforation may still be due to medical malpractice (that is, the breach of the standard of care by the surgeon).

The South Carolina medical malpractice jury that heard the testimony and considered the evidence during the trial from both the medical malpractice plaintiff and the medical malpractice defendants determined that the medical malpractice defendants breached the standard of care and that the breach was a proximate cause of the woman’s injuries and death (and her surviving spouse’s losses as a result).

If medical malpractice may have been a cause of your injuries and losses, then it may be beneficial to consult with a local medical malpractice attorney to investigate your possible medical malpractice claim for you.

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

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Connecticut Nursing Home Fined $510 For Resident’s Choking Death

Wednesday, April 11th, 2012

Just how much is a Connecticut nursing home resident’s life worth? The answer may be $510, according to the fine imposed on a nursing home by the Connecticut Department of Public Health (DPH) that could have imposed a maximum fine in the amount of $3,000.00, for the choking death of a resident. The DPH also required that the offending nursing home submit a corrective-action plan to address the choking death incident.

According to state investigators, the elderly Connecticut nursing home resident suffered from pulmonary disease and mental illness. The nursing home care plan for the resident required the nursing home staff to cut up the resident’s food in small pieces and to closely monitor the resident to make sure that he ate slowly and took small bites. The staff were also required to cue the resident to chew and swallow his food. The goal of the care plan was to insure that the resident received the proper nutrition while at the same time insuring that he safely chewed and swallowed his food.

On the day of the choking incident in February, 2012, the nursing home staff left the resident unattended as he ate a peanut butter and jelly sandwich. When the staff returned to the resident, he was found unresponsive in a seated position. An ambulance was called and the ambulance report stated that the resident’s airway was completely blocked with peanut butter. The resident choked to death and was declared dead at the hospital from cardiac and respiratory arrest.

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It appears that the nursing home resident had been identified as someone who had a swallowing disorder and/or was at risk for choking while eating that required that close and proper supervision be provided at all times during meals. It is common for some elderly people, people who have dementia, and people with certain physical conditions to require assistance with meals, such as special food preparation (for example, pureeing of food), restrictions on certain foods (such as meats and other foods that may be difficult to chew and/or swallow), and thickening of fluids to help with swallowing. It is quite obvious that people with swallowing disorders may suffer dire consequences, including choking to death, if  there is a lapse in following the required swallowing protocols.

It appears from the investigative report from the Connecticut DPH that the nursing home had identified and addressed the resident’s swallowing/eating issues in his care plan that required close observation, supervision, and cuing while the patient was eating. It is foreseeable that if the care plan requirements are not followed with regard to eating, then the patient can choke to death on the simplest food item in a very short period of time. Choking is a very painful process that takes enough time that most residents would be aware of their dire situation and would suffer severe pain and mental anguish before death.

The Connecticut man’s death is a clear example of the gravest consequences that may result if the simplest but most critical efforts are not consistently made to protect the safety of nursing home residents.

If you or a loved one suffered injuries or death due to nursing home negligence, nursing home neglect, nursing home abuse, nursing home mistakes, or nursing home errors, you may be entitled to compensation for your losses and injuries. The prompt investigation by a medical malpractice attorney may help determine if medical malpractice has occurred.

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

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Michigan Medical Malpractice Verdict For Brain Damage During Surgery

Sunday, April 8th, 2012

On March 30, 2012, a Michigan medical malpractice jury returned a verdict in the amount of $1.23 million in favor of the family of a 66 year old woman who suffered severe brain injury due to lack of oxygen to her brain during surgery in 2008. The medical malpractice lawsuit was filed against an anesthesiologist and a local hospital, but the hospital was dismissed from the medical malpractice case before trial.

Trial had begun on March 21, 2012 and ended with the medical malpractice jury’s finding after three days of deliberations that the anesthesiologist committed medical malpractice and that the medical malpractice was the cause of the woman’s injuries. The damages awarded included $34,274 in economic damages and $1.2 in noneconomic damages (mental suffering, mental anguish, etc.) to the woman’s surviving son.

What Happened During Surgery?

On August 11, 2008, the woman entered the hospital to have surgery to remove her thyroid and parathyroid glands in her neck. Because the surgery involved the administration of general anesthesia that makes it impossible to breath without assistance, the woman needed to be intubated (endotracheal intubation involves the placement of a breathing tube through the mouth or nose into the trachea (the windpipe) to open the airway to provide oxygen, anesthesia, and/or medication, to remove blockages from the airway, to provide protection to a patient’s lungs under certain circumstances, and/or to provide a better view of the patient’s upper airway).

The anesthesiologist allegedly failed to observe that the breathing tube had moved during the surgery, preventing the woman from breathing, and allegedly failed to treat the woman’s dangerously low blood pressure, which resulted in the lack of oxygen to the woman’s brain. The woman never awoke after her surgery — she died eleven days later. Medical testing determined that the woman had suffered a devastating brain injury due to lack of oxygen during her surgery. The woman died from her brain injury, which was confirmed by an autopsy.

Source

When you enter a hospital or outpatient surgical center for elective or necessary surgery and general anesthesia is used, you are totally at the mercy and subject to the training, experience, and competence of the medical personnel who must provide the necessary medical care and medical monitoring to insure that you receive the necessary oxygen and medical care during and after the surgical procedure and that you wake up after the surgery without suffering injuries during the surgery.

While injuries or death may occur during surgery without the cause being medical malpractice, the cause of surgical injuries or death may be due to medical negligence. Because the patient is often unconscious and totally unaware of what is occurring during surgery (especially if general anesthesia is used), the patient and the patient’s family will probably have no idea of what occurred during the surgery that caused the injuries or death. That’s when the assistance of a medical malpractice attorney may be essential to investigate and determine the cause(s) of the surgical patient’s “bad outcome” and to determine if medical malpractice may have occurred.

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