Archive

Posts Tagged ‘Medical Malpractice’

Las Vegas Latinos Preyed Upon By Unlicensed Nevada Physicians

April 13th, 2012 No comments

Elena Caro desperately wanted a shapelier figure. The 42-year old woman had researched plastic surgery solutions in Southern Nevada, but had decided using a licensed practitioner would be too costly. Then she heard about two Columbian plastic surgeons travelling to Las Vegas. They were providing the surgery she wanted significantly cheaper than American doctors, so she booked an appointment and headed over to the tile retailer they were working out of to get her implants. She was injected with 200ccs of a silicone gel 6 times by Ruben Dario Matallan-Galvas and Carmen Oflidia Torres-Sanchez. Then, it is alleged that Ms. Caro began to have an allergic reaction to the anesthesia. She was later found in distress by passers-by on Las Vegas Blvd, who called an ambulance. She was rushed to N. Vista Hospital and later died from the reaction. Ms. Carmen Oflidia Torres-Sanchez and Mr. Ruben Dario Matallan-Galvas were arrested at McCarran airport and are being sued by Elena Caro’s family for medical malpractice and wrongful death.

This incident has shed a light on the Las Vegas Latino community’s reliance on unlicensed medical professionals. Due to cultural and economic forces, many Las Vegas Latinos receive a significant amount of their medical care from unlicensed physicians and herbalists who work out of homes and beauty salons. While many of the transactions for herbal remedies are legal, much of the remaining medical care is not. One of the prevailing reasons is the high cost of licensed medical care in Nevada. Another is the limited number of Spanish speaking medical professionals practicing in Southern Nevada. This has led to many Latinos suffering serious injury and even wrongful death from unlicensed medical care in Las Vegas. If you or a loved one was seriously injured or killed from an unlicensed physician in Las Vegas, contact Benson and Bingham for a free legal consultation.

The attorneys at Benson and Bingham pride ourselves on the relationships we build with our clients. While we cannot promise a successful outcome to your case, we believe our client/attorney relationships are one of the reasons we secured over $24,000,000 for our clients in 2010 and 2011. Our staff includes many Spanish speaking legal professionals.

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS

Las Vegas DUI Lands Man in Hospital, Woman in Jail

December 28th, 2011 No comments

Yesterday, a 65-year old Las Vegas woman, Diana Chambers, was arrested on suspicion of Las Vegas DUI charges after striking a Nevada man, Shannon Newland, and his vehicle as he was filling the car with gasoline. The man is currently at University Medical Center being treated. If you have missed work, lost property or incurred medical costs due to a Nevada traffic accident, contact us today.

The accident, which occurred on Cheyenne Avenue near US95 has put Mr. Newland in critical but stable condition. While he is doing well and expected to recover, the Southern Nevada resident faces a difficult couple of months. He will likely miss significant work and need compensation for his damaged automobile and hospital costs. Ms. Chambers is currently being held in a Clark County jail and it is unknown how much insurance she carries.

Benson and Bingham are one of Southern Nevada’s premiere injury recovery firms. Our Nevada licensed attorneys pride ourselves on customer satisfaction and we work closely with our clients to ensure the best possible outcome for their case. Go to Bensonbingham.com today to start your case.

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS

Loose regulations allow hip replacement manufacturers to put Nevada seniors at risk

In our conversations about healthcare in the United States, we tend to focus on access to care: Who should be insured? At what personal cost? What medical services should be provided? One thing we tend to take for granted is the quality and safety of these medical interventions, but this is an assumption we make at our own peril. A new wave of Nevada product liability lawsuits is focusing on major medical devices that appear to have been rushed to market, to the detriment of hundreds of users.

This August will mark one year since DePuy Orthopedics — a division of health-and-beauty giant Johnson & Johnson — issued a massive product recall for thousands of its ASR artificial hip implants. Synthetic hip implants are designed to simulate the hip socket that holds the ball of the femur bone in place while permitting it to rotate. As a person ages out of middle age and begins considering options such as transitioning to a Nevada assisted care facility, the hip joints are often among the first to wear out and make movement difficult or painful. The ASR device attracted thousands of eager users by promising an industry-leading 15-year lifespan, but hundreds of elderly patients endured painful implant surgeries only for these devices to fail or need replacement within five years.

Failure rates for the ASR were two to three times higher than is common for these devices (sometimes known as “critical implants”), with approximately one out of every six requiring replacement or secondary surgery. The most common problem is the product’s tendency to shed tiny particles of metal that intoxicate surrounding muscle and bone tissues and leave large dead areas in the upper thigh. To be clear, investigations have determined that these symptoms were not related to unsound installation or other medical malpractice — the devices themselves were defective. Patients were treated with bad medicine.

Critics blame a flawed regulatory system for this latest round of Nevada medical device injuries. Unlike in the pharmaceutical industry — where patent laws prevent copycat products and approval by the Food and Drug Administration requires clinical trials — medical device manufacturers can circumvent the toughest scrutiny and testing by incorporating new technologies into older, proven designs to take advantage of a fast-track  loophole. Observers say the FDA should end this workaround and create an orthopedic registry that could better track medical device failures. Other countries have successfully implemented these reforms to make patients safer without limiting new, helpful, and safe developments in medical technology.

If a loved one received an ASR hip implant and now suffers from increased pain, seek medical attention to determine if the device may be degrading within the person’s body or otherwise failing. If you discover that this is the case, contact us for a free consultation about seeking compensation for the medical device injury.

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS

For Clark County Malpractice Attorneys, Detail is Vital

November 3rd, 2010 No comments

When a loved one becomes the victim of medical malpractice, the shock and emotion of the experience can be blinding. In the least tragic cases, a medical condition can be worsened or a new ailment can arise; cases involving surgical errors can be devastating and irreversible.

At times like this, it is important that you act quickly to find a medical malpractice attorney you can trust. Here in Nevada, victims have only one year to file a claim — it is hard to understand how little time that really is until you are preparing a case.

The tiniest details can derail a case, too: for Clark County malpractice victims (as in many places), the use of a medical expert must be accompanied by all the requisite affidavits and paperwork. In some cases, an expert medical opinion is central to the claim, and failure to properly file can result in the loss of a winnable case.

Don’t wind up on the losing side when tragedy strikes — contact the Las Vegas medical malpractice lawyers at Benson and Bingham today for a free consultation.

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS

Haunting Story of Surgery Complications Raises Questions About Medical Malpractice at Las Vegas Hospital

November 1st, 2010 No comments

It is a story the Southern Nevada medical community won’t soon forget: a 70-year-old woman spent a week doubled over in pain after a routine gall bladder surgery before dying of peritonitis, an infection of the stomach lining. Today, the family has turned to Las Vegas medical malpractice attorneys for answers.

The infection is thought to have been caused by a leak from her gall bladder into her abdomen. Doctors think that a clamp was somehow misused and created a small leak, which began filling her abdomen with bile. Laparoscopic gall bladder surgery is a routine outpatient surgery, and experts say that this Las Vegas woman’s death from the procedure can only be described as a “freak accident.” However, medical experts also say that the Nevada grandmother of 14 complained about exceptional pain as her condition worsened but doctors declined to run tests that could have discovered the dangerous mistake. The doctors’ failure to diagnose the woman’s condition resulted in a wrongful death.

This family is devastated, and nothing can restore to them the life of the vibrant and involved woman they lost so abruptly. The family has filed a medical malpractice lawsuit, in part motivated by a desire to prevent other Clark County families from suffering medical tragedy.

If you or a loved one have been affected by the failure of a medical professional, call us today for a free consultation at one of our two Las Vegas medical malpractice law offices located downtown and in Summerlin.

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS

TAKEN AVANDIA FOR DIABETES?

June 29th, 2010 No comments

If you have suffered a heart attack or stroke and have taken Avandia for Diabetes, then Call the law firm of Benson & Bingham today.  702-382-9797.  Rosiglitazone is used along with a diet and exercise program and sometimes with one or more other medications to treat type 2 diabetes (condition in which the body does not use insulin normally and, therefore, cannot control the amount of sugar in the blood).  Rosiglitazone is in a class of medications called thiazolidinediones. It works by increasing the body’s sensitivity to insulin, a natural substance that helps control blood sugar levels. Rosiglitazone is not used to treat type 1 diabetes (condition in which the body does not produce insulin and, therefore, cannot control the amount of sugar in the blood) or diabetic ketoacidosis (a serious condition that may occur if high blood sugar is not treated).  Rosiglitazone comes as a tablet to take by mouth. It is usually taken once or twice daily with or without meals. Rosiglitazone should be consumed at about the same time(s) every day.  Your doctor may have increased your dose of rosiglitazone after 8-12 weeks, based on your body’s response to the medication.  Rosiglitazone claims to help control type 2 diabetes but does not cure it.  Usually it takes 2 weeks for your blood sugar to decrease, and 2-3 months or longer for you to feel the full benefit of rosiglitazone.  If you need an Avandia Lawyer call the experts at Benson & Bingham today.

U.S. News and World Report Claims there is no real problem with Avandia.  “Our observational study does not suggest a significant cardiovascular hazard and may suggest a beneficial effect on ischemic cardiovascular events associated with treatment with rosiglitazone among patients with type 2 diabetes and established coronary artery disease,” said Dr. Richard Bach, an associate professor of medicine at Washington University School of Medicine in St. Louis.

The FDA is on record that the drug is NOT SAFE.  It is a matter of time before the drug is pulled off the shelf. FDA previously communicated to the public about the possible association between rosiglitazone and increased cardiovascular risk in a 2007 safety alert. The agency also sought advice from external experts at the July 30th 2007 joint meeting of the FDA Endocrinologic and Metabolic Drugs and Drug Safety and Risk Management Advisory Committees. The RECORD study data represent the only new information from a completed randomized, controlled clinical trial of rosiglitazone received by FDA since the 2007 announcements. The RECORD study was designed to evaluate the cardiovascular safety of rosiglitazone, which is consistent with FDA’s December 2008 Guidance for Industry recommending that manufacturers of new treatments for diabetes carefully design their clinical trials to include an evaluation of cardiovascular safety. The RECORD study will be evaluated in the context of this recent Guidance.

* Rosiglitazone is sold as a single-ingredient product under the brand name Avandia. It is also available in combination with other diabetes medications, metformin under the brand name Avandamet or glimepiride under the brand name Avandaryl.

FDA recommends that patients currently using rosiglitazone:  Not stop taking their medication without talking with their healthcare professional. Discuss any questions or concerns they have about rosiglitazone with their healthcare professional. Read the Medication Guide that comes with each rosiglitazone prescription to better understand the risks and benefits of their medication. Report any side effects with rosiglitazone to FDA’s MedWatch program.

Similar to Vioxx, drugs that cause an increase in heart attacks will have serious legal contention if the Plaintiff has other risk factors like obesity, hypertension, high cholesterol, or other issues that may alone cause a heart attack.   Those who have diabetes and smoke will also have trouble fighting the makers of Avandia.   The biggest risk factor will likely be obesity.  Given that fatter humans are likely to have diabetes and therefore develop Type II diabetes, it will be hard to conclusively understand whether the heart issues are from the underlying weight issue or the drug.   Studies will continue to give us valuable research to help juries understand the true risks of this drug.  To help you fight for your rights, Call the Avandia and other dangerous drug recall attorneys at Benson & Bingham today who are taking new cases today.  Don’t delay!  702-382-9797

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS

Nevada’s $500,000,000.00 Punitive Damage Award: Fair or Absurd?

May 10th, 2010 No comments

Recently, A Nevada Jury awarded $500 Million in punitive damages to a couple infected with Hepatitis from an Endoscopy center.  It is well known the facility and its doctors, primarily Dr. Desai, reused Propofol vials (an anesthestic) on patients mixing the syringes and needles between patients cross contaminating.  It is well known the Doctors did not have the money to compensate the victims who have genetically linked their disease to the outbreak at the facility.   The jury awarded $5.1 Million in compensatory and then awarded the 1/2 billion dollar sum to punish the maker of the drug.  The convincing argument was the 50ml vials should not have been sold to centers that had minimal use for such large doses of medication.

This lawsuit was based on the Strict Products Liability Cause of Action that is a very strong action, if the Plaintiff’s can prove the product failed in its warnings, was defectively designed, or was mis-manufactured in some fashion.  The key here was the defectively designed containers that “encouraged” multi uses for business/profit reasons–allegedly.  The vials do have qualified uses in drip systems and other longer sleep patient procedures.  So, in essence, the company was punished by the jury (in this case Teva and Baxter Pharmaceuticals) for this “encouragement” in that they knew doctors may be reusing the vials and they helped in some fashion by making such a “large” dosage.  Whether or not personal injury lawyers are correct in their allegations, the jury believed the arguments and found not only that these companies were liable, but that they should be punished for their bad behavior.  Given that the combined annual revenue of these companies exceeds $13 billion, even the $500,000,000 is a slap on the wrist–but it would get any accountant’s attention.   So, one must contemplate whether the underlying case was justified.    To understand how a jury gets to this, one must understand that Negligence is not a bar to strict products liability.

The law is founded on the assumption that manufacturers need to make safe products–very safe products, or face severe ramifications for bad design, bad warnings, or bad product.  If a product is misused this is a defense to products liability.  And, arguably the doctors misused the “single” dose vials.  The jury did not believe this argument because they were not allowed to hear it!    The jury was barred from hearing testimony that doctors misused the vials given that this “negligence” was not a factor in the products liability action.  While this author did not sit through the trial and hear all the relevant testimony, the point is clear that the case was tried as a products case, and the jury found that the manufacturer was liable for creating an unreasonably dangerous product.     The absurd response comes from those who compare this scenario to that of a car driver who car drives 100 mph but yet the roads only allow for 55mph.  Should we sue the car manufacturer for the drivers error when he crashes doing 100mph?  Another comparison is one to cough syrup.  It comes in 10 oz bottles.  The consumer is “warned” to only take 2 tablespoons (one ounce).  If a consumer drinks the whole bottle, should we then sue Robitussan or Vick’s Cough syrup because the consumer did not follow the instructions?  Well, the crazier thing here, is not only was warning not obeyed, it was a doctor who did not obey it…

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS

Personal Injury Law Set to Change in Medical Mal-practice Cases.

March 27th, 2010 1 comment

Many states, such as Nevada, have imposed egregiously unfair limits on pain and suffering damages in Medical malpractice cases.  These cases often have horrible damages leaving the victims unfairly compensated for bad medicine.  Nevada currently has a cap of $350,000 for pain and suffering.   Two states in 2010 have now repealed their respective States’ laws on caps.  The first this year was Illinois and now Georgia (who has a cap similar to Nevada $350,000.)

These States’ Supreme Courts banned such limitation based on the Separation of Powers Doctrine Embodied in the US Constitution.  The crux of the argument is that the legislature can’t impose rules on those duties fundamentally outlined for the judiciary—here reducing verdicts.   The principle behind the Courts’ rulings is likely to be challenged.   Can a legislature make laws that affect the judiciary?  It really depends on your legal philosophy.  In some respects, it seems like a conflict of interest to have a Court decide whether they have the power over the legislature to interpret a law—in other respects, it does make sense that our Separation of Powers doctrine was implemented to serve the very issue of fairness over the legislature.  With the new health insurance reform, time will tell how this may impact our Medical mal-practice laws.  What do you think?

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS

NRS 41A.071 Affidavits of Medical Experts: A complaint must now also include and Affidavit for Medical Corporations

February 15th, 2010 1 comment

Nevada’s strict rule requiring an affidavit for medical mal-practice complaints is now even stricter.  The NV Supreme court declared that expert affidavits for the mal-practice of doctors now also applies to those corporations (e.g Hospitals and their nurses) for their respective negligent conduct.   The rule simply adds harshness to the already cut-throat rule that an affidavit must be supplied to any complaint or it is automatically dismissed.  Thus, if your assistant fails to apply a staple–the case is over.  Very ridiculous, but this is medical tort reform just as the doctors wanted it.  Way to go Nevada legislature!

Fierle v. Perez, 125 Nev. Adv. Op. No. 36 (Nov 19, 2009)1 MEDICAL MALPRACTICE, PROFESSIONAL NEGLIGENCE AND NRS 41A.071’S

EXPERT AFFIDAVIT REQUIREMENT

Summary

An appeal from the First Judicial District Court’s dismissal of medical malpractice and professional negligence claims against a physician, his professional medical corporation and several staff members for failure to attach an expert affidavit to their initial complaint.

Disposition/Outcome

District court’s judgment affirmed with regards to claims that required an affidavit, reversed and remanded with regards to claim that qualified under res ipsa loquitor exceptions.

Facts and Procedural History

Patricia Fierle (“Fierle”) was diagnosed in July 2005 with breast cancer and subsequently underwent a mastectomy. To facilitate ongoing chemotherapy, a catheter was inserted into her chest, the tip of which was meant to terminate in her subclavian vein. Chemotherapy drugs were to be injected into the vein through this catheter.

After the surgery, Fierle became a patient of Dr. Perez and his staff, including Melissa Mitchell (“Mitchell”), a registered nurse, and nurse practitioners Charmaine Cruet and Linda Lesperance. On Fierle’s third visit to Dr. Perez’ office, Mitchell administered chemotherapy. However, rather than in fusing in to the catheter, the medication infused into her tissue. This caused a subcutaneous burn known as an “extravasation.” According to Fierle, her complaints of discomfort at the time were not met with any treatment or attention.

The next day, after one of Dr. Perez’ nurses noticed redness and swelling on Fierle’s chest, she was referred to a radiologist. His tests revealed that the tip of the catheter was not in the vein, but coiled in her tissue. She then sought treatment from another doctor who referred her to Dr. Miercort. His opinion was that “negligent extravasation” had occurred and he referred her to U.C. Davis Medical Center. There, she was diagnosed with “severe extravasation of chemotherapy over the right shoulder and subclavian region.”

Mr. and Mrs. Fierle filed a complaint in district court on September 14, 2006. They claimed Mitchell was negligent in her administration of chemotherapy, Dr. Perez, Cruet and Lesperance were negligent in their training of Mitchell, loss of consortium and “Willful Failure to Provide Treatment and Constructive Fraud” against Dr. Perez and his professional medical corporation Jorge Perez M.D., Ltd. They later amended their complaint to include an affidavit from Dr. Miercort.

Dr. Perez, Jorge Perez M.D., Ltd., and Mitchell moved for dismissal of the Fierles’ complaint, citing failure to include an expert affidavit with the original complaint as required by

1 By Mark HesiakNRS 41A.071.2 They also moved to strike the amended complaint, relying on Nevada precedent that said a complaint filed under NRS 41A.071 without the expert affidavit is void ab initio and shall be dismissed.3 These motions were joined by Cruet and Lesperance. The district court granted both motions, finding that the complaints did not qualify for NRS 41A.100(1)(c)’s res ipsa loquitor exception. The Fierles’ motions under NRCP 52(b), 59(e) and 60(b) were also later denied. This appeal followed.

Discussion

Standard of Review

The district court’s dismissal was based on its interpretation of statutes. The Nevada Supreme Court reviews a district court’s statutory interpretation de novo.4

NRS 41A.071 applies to professional medical corporations

Under NRS 41A.071, an action for medical or dental malpractice must be accompanied by an affidavit from a medical expert who practices a type of medicine similar to that which forms the basis of the malpractice claim.5 NRS 41A.009 contains the following definition for medical malpractice: “the failure of a physician, hospital or employee of a hospital, in rendering services, to use reasonable care, skill or knowledge ordinarily used under similar circumstances.”6 The appellants argued that no affidavit is required under these statutes in a suit against a professional medical corporation.

While the definition of medical malpractice does not explicitly include professional medical corporations, the Court held that NRS 41A.071 requires expert affidavits be attached to any non res ipsa loquitor malpractice claim against such a corporation. “Professional Corporation” is defined in NRS Chapter 89, and under NRS 89.060 and 89.220, no statute can alter the personal liability of a physician in a medical malpractice claim.7 Harmonizing Chapters 41A and 89, the Court determined that the affidavit requirement applies to claims against professional medical corporations as well as physicians.

NRS 41A.071 applies to professional negligence claims

The Fierles’ also argued that the definition of medical malpractice only covers claims against Dr. Perez’. Therefore, the claims against the other respondents would be for professional negligence and would not require an affidavit as 41A.071 only addresses malpractice claims. The Court looked to resolve the ambiguity by looking to the intent of the initiatives passed in 2004 as NRS 41A.015 and 41A.017, which provided protections for professional negligence for providers of health care.

2 NEV. REV. STAT § 41A.017 (2007). 3 Washoe Med. Ctr. v. Dist. Court, 122 Nev. 1298, 1300, 148 P.3d 790, 792 (2006). 4 Beazer Homes Nevada, Inc. v. Dist. Court, 120 Nev.575, 579, 97 P.3d 1132, 1135 (2004); Keife v. Logan, 119 Nev. 372, 374, 75 P.3d 357, 359 (2003). 5 NEV. REV. STAT § 41A.017 (2007). 6 Id. § 41A.009 (2007). 7 Id. §§ 89.060, 89.220 (2007).

First, the Court noted that the definition of professional negligence in the statute is basically the same as medical malpractice. The intent of the statute was to give other providers of health care the same protection doctors received from the legislature in 2002.8 The Court also reasoned that a malpractice claim against a doctor is the same as a professional negligence claim. To make one of these claims subject to the affidavit requirement and not the other would defeat the intent of the legislature and the citizens of Nevada. It would provide a way around the requirement by calling a claim professional negligence instead of malpractice. Therefore, NRS 41A.071’s affidavit requirement extends to non-res ipsa loquitor professional negligence claims against providers of health care, whether doctors, nurses or nurse practicioners.

Claims based on res ipsa loquitor are not subject to the affidavit requirement

NRS 41A.100 provides res ipsa loquitor exceptions to the affidavit requirement in malpractice or professional negligence claims.9 The Court found its recent decision in Szydel v. Markman conclusive on the issue at hand.10 In Szydel, the court concluded that that the expert affidavit requirement does not apply when the malpractice action is based solely on the res ipsa loquitor doctrine.11 The Syzdel court further concluded that when a plaintiff files a res ipsa loquitor claim in conjunction with other medical malpractice claims that are not based upon the res ipsa loquitor doctrine, those other claims are still subject to the expert affidavit requirements of NRS 41A.071.12

Here, the negligent extravasation claim would fall under one of the listed exceptions. If a “provider of health care” causes a patient to suffer “an unintended burn caused by heat, radiation or chemicals… in the course of medical care,” or any of the other exceptions listed in the statute, no expert testimony or affidavit is required to establish negligence.13 Therefore, the Court allowed the claim against Mitchell to continue as she administered the medication.

A claim amended to include an affidavit will not relate back to the initial filing even if some of the claims do not require the affidavit

The appellants next argued that because some of their initial complaint did not require an affidavit, the amended filing could relate back and cure the initial deficiency. Here, the court followed precedent and determined that all claims under NRS 41A.071 that do not include an affidavit are void ab initio, and must be dismissed.14 The Court applied this rule even to situations where some claims survive because of lack of an affidavit requirement.

Conclusion

The Court concluded that, because under NRS Chapter 89, the establishment of a professional entity cannot alter the personal liability of a participant, NRS 41A.071’s affidavit

8 See 2004 General Election Sample Ballot, p. 12. 9 NEV. REV. STAT § 41A.100(1)(c) (2007). 10 Szydel v. Markman, 121 Nev. 453, 117 P.3d 200 (2005). 11 Id. at 454, 117 P.3d at 201. 12 Id. at 460, 117 P.3d at 205. 13 NEV. REV. STAT § 41A.100(1)(c) (2007); see also Szydel, 121 Nev. at 454, 117 P.3d at 201. 14 Washoe Med. Ctr., 122 Nev. at 1300, 148 P.3d at 792.

requirement applies to claims against professional medical corporations as well as individuals. The Court further concluded that the requirement extends to professional negligence claims against all providers of health care, nurse practitioners, nurses and doctors alike. However, the Court concluded that any claim that falls under the res ipsa loquitor exceptions listed in NRS 41A.100 may be filed without an affidavit as no expert testimony is needed to establish negligence. Finally, the Court concluded that a complaint filed containing some claims subject to the affidavit requirement and some that do not fall under 41A.071 cannot be cured by filing an amended complaint that includes the affidavits. Thus, all claims subject to NRS 41A.071 that are filed without the affidavits are void ab initio and must be dismissed. In accordance with these conclusions, the Court reversed in part and affirmed in part the district court’s order and remanded the case for further proceedings consistent with the opinion.

Concurrence in Part, Dissent in Part (Pickering, J.)

Justice Pickering agreed with the result the majority reached, but not with its reasoning. While medical malpractice is encompassed in the term “professional negligence,” the opposite is not true. As the amendments in 2004 did not change the words “medical malpractice” in 41A.071 to “professional negligence,” the requirement should not be extended to claims of professional negligence. However, in this case, Justice Pickering found the injection to be a part of the rendering of medical services by a physician as defined in the malpractice statute, regardless of the fact that it was a nurse who physically gave the drugs. Therefore, this action would be one for medical malpractice and require an affidavit.

Justice Pickering also believes that both the nurse and the physician with the duty to supervise are subject to the res ipsa loquitor exception. The injection was given by the nurse under the doctor’s supervision, and therefore the remand should be for Dr. Perez and Mitchell for the negligent extravasation.

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS

Attorney Fee Cap Amendment Fails: Good News for Victims

December 6th, 2009 No comments

The John Ensign Amendment Fails!  Sunday, December 06, 2009  The Ensign Amendment, which would have capped attorneys’ fees in medical malpractice cases, failed by a vote of 66-32.   It is hard to believe that a person representing Nevada would be so quick to jump on the bandwagon in favor of high priced medicine instead of helping innocent and helpless medical malpractice victims.  Some people might think (at first glance) this amendment would help give more to the victims as the fees are capped.  What people don’t understand is that essentially this would have been not only hard, but nearly impossible to find an attorney willing to take on such cases.

Why would an attorney want to risk a huge investment just in litigation costs for a meager award of attorney fees–they won’t.   If you are an injured medical malpractice victim, go try and find an attorney now in Nevada–we currently have caps of 15% attorney fees over $500,000 and the victim is capped at $350,000 for non-economic damages;  plain and simple, this is already a problem… just imagine what Ensign’s bill would have done.

Share and Enjoy

  • Facebook
  • Twitter
  • Delicious
  • LinkedIn
  • StumbleUpon
  • Add to favorites
  • Email
  • RSS