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Archive for the ‘Medical Negligence’ 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.

Source

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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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.

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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.

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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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Epidemic Of Drug Babies In The U.S.

Tuesday, May 1st, 2012

Babies born addicted to drugs due to their mothers’ use of illicit drugs during pregnancy is not new. However, an increasing epidemic of babies addicted to prescription medications, especially narcotics such as oxycodone, is particularly alarming.

Many such newborns will be born with neonatal abstinence syndrome (“NAS”), which is the withdrawal process they go through once they are born as a result of no longer being exposed to the drugs their mothers used during pregnancy (narcotic medications such as oxycodone pass through the placental barrier during pregnancy). In 2009, more than 13,000 newborns in the U.S. were born with NAS, a three-fold increase since 2000 (opiate use by pregnant mothers increased five-fold during the same period).

How many babies exposed to opioids during pregnancy go through withdrawal symptoms once they are born? Between 55% and 94%, according to official statistics.

Many NAS babies share common symptoms:  they are easily agitated, cry constantly (many have a distinct, high-pitched cry), they cannot be around sound or light, and they may have muscle tightening and seizures.

Tennessee’s Recent Experience With NAS Newborns

Tennessee ranks among the U.S. states with the greatest overuse of prescription drugs. About one-third of pregnant Tennessee women in state drug treatment programs are addicted to pain medications. In one particular Tennessee hospital, the number of NAS newborns doubled from 2010 to 2011. As a result, this same hospital responded by creating a new wing of private rooms in 2010 that are quieter and darker to help in the treatment of NAS babies.

The Tennessee hospital used to treat NAS babies in a manner similar to the treatment of older addicts — methadone treatment was used to stabilize the newborns who were then discharged to outpatient treatment. Due to safety and effectiveness concerns with the methadone treatment protocol for newborns, the hospital switched to morphine in small doses given every three hours during feeding that is gradually reduced over the following weeks to wean the babies off of the drugs. This newer treatment protocol has reduced the average hospital stay for NAS babies by several days, which now averages 24 days.

And it is not just at the time of birth and for the weeks following birth that NAS babies are at risk. Studies have shown that NAS babies are at an increased risk for learning problems and developmental problems throughout childhood and for behavioral problems as they reach school age.

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If you or a family member have become the victim of medical malpractice in Tennessee or in another state in the U.S., it is important to learn about your legal rights. The advice from a local medical malpractice attorney may help you determine if you can and should proceed with a medical malpractice claim.

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

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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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Massachusetts Hospitals Cited For Turning Away Emergency Room Patients

Wednesday, April 25th, 2012

Within the last six months, three Massachusetts hospitals have been cited for unjustifiably turning away and failing to treat three patients who came to their emergency rooms seeking treatment. One case involved transferring a patient to another hospital while the patient was unstable and in respiratory distress.

Hospital Number One

The patient had arrived at the emergency room with shortness of breath and coughing. The patient had a long-standing serious lung condition that required that he be given oxygen. The patient requested to be transferred to another hospital where he had been treated previously.

An emergency room physician determined that the patient was stable enough to be transferred. However, a subsequent emergency room physician who took over the patient’s care failed to reassess the patient’s condition and whether the patient was stable enough to be transferred, after the patient’s condition deteriorated significantly. The emergency room staff also failed to provide the patient with a breathing tube in case he needed mechanical assistance breathing during the ambulance ride to the other hospital.

Hospital Number Two

In the second case, the patient arrived at the emergency department with a fever and pain from an abscess on the patient’s buttock. The emergency room physician determined that the patient was in poor shape and needed emergency surgery to remove the dead tissue in order to increase the patient’s chance of survival. The on-call surgeon refused to come to the hospital late at night to treat the patient. The patient had to be transferred to another hospital for treatment — the patient’s fate was not disclosed.

Hospital Number Three

In the third case, when the patient arrived at the hospital’s emergency room seeking medical treatment, the staff told the patient that he was banned from that emergency room and a sister-hospital’s emergency room. The patient was not evaluated or treated but was placed in a wheelchair and was escorted by a security guard off of the hospital’s grounds.

The patient sought treatment at another hospital emergency room. The staff of the other emergency room called the first hospital to find out why the patient had not been evaluated and treated. The first hospital arranged for an ambulance to take the patient to its sister-hospital where the patient was admitted.

A federal law, known as the anti patient dumping statute, requires hospitals with emergency rooms to provide people who arrive at their hospitals with medical screening examinations and to stabilize the patients’ emergency medical conditions. Violations of the federal law by hospitals with emergency rooms are subject to severe penalties. In New England alone, there were 11 violations of the law in 2011, 13 violations in 2010, and 7 violations in 2009.

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If you or a loved one have been mistreated in a hospital or subjected to negligent medical care, you may be entitled to compensation for your injuries and losses. The prompt advice from a local medical malpractice attorney may help you to determine if you have a possible medical malpractice claim and to file a medical malpractice claim on your behalf, if appropriate.

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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Surgical Fires

Wednesday, April 18th, 2012

The last place you would expect to suffer burns from a fire would be while lying on a table in an operating room. But that is just what happened to a New York woman who was undergoing a Cesarean-section delivery of her baby on March 12, 2010. While she was under the influence of local anesthesia with her view obstructed by a surgical curtain, the mother-to-be smelled something burning and could see smoke. Her obstetrician who was performing the surgery noticed a flame coming from the woman’s left side and patted the flame to extinguish it, telling his patient that there had been “a little fire” but not to worry.

The woman gave birth to a healthy baby but she suffered a 5 by 7 inches area of third degree burn on her left side where an alcohol-based antiseptic had been used to prepare her for surgery. The antiseptic, known as DuraPrep, was manufactured by the large manufacturing company, 3M Company. One month before the woman’s surgery, 3M Company, at the direction of the FDA, had issued a new warning to hospitals regarding DuraPrep’ s flammability and instructed hospitals on how to prevent fires, which the surgical staff providing care to the woman was unaware of.

The woman has filed a medical malpractice case against her obstetrician and the hospital where her surgery occurred, alleging that they failed to follow the recommendations from 3M Company regarding use of DuraPrep. The woman had to have plastic surgery for her burn injury and the area that was burned constantly feels numb and feels like it will tear open.

The obstetrician had used DuraPrep for 20 years before the woman’s surgery, without any fire incidents. The hospital stopped using DuraPrep for a period of time but reinstated its use with procedures in place to prevent fires.

The fire evidently started when the obstetrician was using an electrical cautery tool that may have caused a spark that ignited the fumes from the DuraPrep that was not allowed to dry prior to the procedure (3M Company instructed that DuraPrep must be allowed to dry completely before being exposed to a flammable source). A fire would also be possible if the DuraPrep soaks into the patient’s gown or into surgical drapes or somehow pools around the patient (the woman’s anesthesiologist testified during a deposition in the medical malpractice case that the anesthesiologist had noticed that the woman’s gown was wet with what could only have been DuraPrep, after the fire).

Of the 50 million surgeries performed each year in the United States, there are only between 400 and 600 surgical fires involving patients, with only 4% of those fires involving skin preparation solutions such as DuraPrep.

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Surgical fires are so rare that when they do occur, an investigation into the incident by a medical malpractice attorney may help determine if the cause of the fire and the resulting injuries to the patient were due to medical malpractice.

If you or a loved one have been injured due to a surgical fire or other medical incident that may have been the result of medical negligence, 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 file a medical malpractice lawsuit on your behalf, if appropriate.

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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.

Source

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.”

Source

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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