Tag: Baltimore medical malpractice attorneys

Vacuum-Assisted Delivery And Birth Injury

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Sometimes, during the labor and delivery process, the baby needs a little help getting through the birth canal. Approximately 1 out of 20 vaginal deliveries in the United States result in some form of assistance being required. Prolonged labor can be dangerous to the baby as well as extremely painful and exhausting to the mother. Two common forms of assisted delivery, used by medical providers to when labor is stalled, are vacuum extraction and forceps delivery.

Vacuum extraction involves placing a small round cup on the baby’s head, which attaches to a vacuum pump creating suction to help guide the baby out of the birth canal. If performed incorrectly, suction during vacuum extraction can cause permanent and even life-threatening injuries, including: massive bleeding (hemorrhage and hypovolemic shock) beneath the scalp or within the brain (intracranial hemorrhage and encephalopathy); brain damage; skull fracture; and, retinal hemorrhage. Forceps delivery (another assisted delivery method), can also cause skull fractures, skull bleeding, and bruising on the baby’s head and face. These injuries have been known to cause permanent brain damage, neurological injuries and more specifically, cerebral palsy (CP).

In the hands of an inexperienced or untrained physician, a vacuum-assisted or forceps-assisted delivery can cause you and your child serious and permanent injuries. The cost of care for a child with cerebral palsy, or any birth injury, is very high. If your child’s birth injury was caused by a complication during vacuum-assisted or forceps-assisted delivery, contact The Yost Legal Group today at 1-800-YOST-LAW (800-403-7259). When you call, you will speak with an experienced Baltimore Medical Malpractice attorney absolutely FREE.

We handle all cases on a contingency fee basis. This means you will never pay an attorney’s fee up front, and you owe us nothing unless we win your case. The attorneys at Yost Legal Group are experienced, caring professionals ready to investigate your claim with compassion and determination. Call us today to receive a free, confidential consultation about your possible case. A The Yost Legal Group, there is no fee or expense unless you recover.

 

Paralysis Caused By Spinal Surgery

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An ideal outcome in spinal surgery is dependent of the coordination of efforts by the surgeon, anesthesiologist, and neurophysiologist. Because patients are under general anesthesia during surgery, techniques for examining the nervous system for potential injuries can be somewhat limited. Intraoperative spinal cord monitoring (IOM) allows the surgeon to record the electrical signals transferred along the spinal cord and use this recording to prevent neural irritation or spinal cord injury during surgery.

Electrodes are placed on the patient’s body to monitor and record nerve signal responses throughout the spinal surgical procedure. The most common forms of spinal cord monitoring during surgery are EMG (electromyography), SEP (somatosensory evoked potentials) and MEP (motor evoked potentials). Ideally, this is done in an efficient manner without interrupting the flow of the operation and producing unnecessary interruptions.

The monitoring personnel must be able to detect and understand the source of any variables in spinal cord signals in order to deal with them appropriately. An intra-operative disruption or complete loss of spinal cord electrical signals in the appropriate monitoring channels (either SEP sensors, MEP sensors, or both) is clearly an indication of significant disturbance of spinal cord function. If this is not recognized and sensation is not restored during the spinal surgery, severe spinal cord and/or spinal nerve root injury, up to and including partial or total paralysis, may occur.

If you or a loved one has suffered permanent neurological injury and/or paralysis due to a complication during spinal surgery, contact The Yost Legal Group today at 1-800-YOST-LAW (800-403-7259). When you call, you will speak with an experienced Baltimore Medical Malpractice attorney absolutely FREE.

The attorneys at Yost Legal Group are experienced, caring professionals ready to investigate your claim with compassion and determination. Call us today to receive a free, confidential consultation about your possible case. At The Yost Legal Group, there is no fee or expense unless you recover.

 

Abdominal Injury During Laparoscopy

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Laparoscopy is one of the most common abdominal surgical procedures performed around the world. It is a minimally invasive surgery, which a surgeon performs by making several small incisions, each one about ½” in size, through which surgical instruments are inserted. Minimizing the size of the surgical incision greatly reduces the patient’s post-operative healing time, decreases the patient’s risk of developing a post-operative hernia, and minimizes surgical scars.

Unfortunately, the very small size of the laparoscopic incisions limits the surgeon’s view while entering the patient’s abdomen.  This limited view during insertion of sharp surgical instruments can cause serious injury to the patient.  If the surgeon is negligent in placing surgical tools too deep into the patient’s abdominal cavity, blood vessels or bowel are damaged and the patient can suffer life-threatening injuries such as internal bleeding (hemorrhage from a lacerated artery or vein) or sepsis (infection spread from a perforated or lacerated small intestine or bowel).

Vascular injury (injury to blood vessels) and bowel injury are the most common injuries suffered by patients having laparoscopic surgery and very often occur just as the abdomen is being entered and before the intended surgical procedure begins.  Major injury can occur when the Veress needle (a special needle used inflate the abdomen) or a trocar (a sharply pointed metal tube through which surgical tools are passed in and out of the abdomen) is negligently inserted into an artery, vein, colon, small intestine, ureter or other internal organ.

Additionally, a medical mistake can occur when the weight of a patient is not taken into consideration before surgery. In thinner patients, the distance between the anterior abdominal wall (where there are layers of abdominal muscle and tendons) and the retroperitoneal vascular structures (the major blood vessels located just behind the abdominal wall) is incredibly small. The distance between the abdominal wall and the thin patient’s aorta, iliac artery, and other great vessels may be as little as two centimeters. The distal aorta and right common iliac artery are particularly prone to injury and can be cut or damaged by negligent trocar placement at the beginning of the laparoscopic procedure.

Before laparoscopy is performed on a patient, the patient must be properly evaluated, including a full clinical history and thorough clinical examination. If you would like to discuss your potential claim arising from an injury during laparoscopy, the attorneys at Yost Legal Group are experienced professionals ready to investigate your claim with compassion and determination.

Call The Yost Legal Group today at 1-800-YOST-LAW (967-8529) for a FREE, confidential, no-obligation consultation.

At The Yost Legal Group, you will never pay an attorney’s fee unless we achieve a recovery for you. We don’t get paid until you do

PREVENTABLE MEDICAL MISTAKES IN HOSPITALS

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Hospital-acquired conditions, also known as “never events”, are particularly awful medical mistakes that should not ever occur. Some examples of these preventable errors include:

  • Operating on the wrong place on the patient’s body
  • Discharging a newborn to the wrong parents
  • Leaving a foreign object, such as a scalpel or sponge, inside the body
  • Mismatched blood transfusion
  • Causing an air embolism during treatment of a patient

Unfortunately, not all medical mistakes are avoidable at all times. In 1999, the Institute of Medicine (IOM) reported medical errors account for as many as 98,000 deaths per year. A more recent study specific to surgical errors conducted in 2013, found that more than 4,000 surgical “never events” occur annually in the United States.

Due to the fact that these events are preventable, health care organizations are attempting to get rid of them completely and health insurance providers, including Medicare and Medicaid, are no longer paying for costs related to hospital-acquired conditions (HACs). Also, many of these “never events” are being openly reported by the public. All of these strategies aim to inspire hospitals and medical professionals to accelerate the progress of patient safety.

Never events within hospitals can point to a major safety problem within an organization. It has been reported these error rates are much higher in the U.S. than in other developed countries such as United Kingdom, Germany, Canada, New Zealand and Australia. Some states, such as Minnesota (the first state to pass a statute that required obligatory reporting), have enacted legislation requiring reporting of hospital-acquired conditions but not all states are required to do so. It has been up for debate whether or not required reporting of HACs has affected how frequently they occur.

As the term “never events” indicates, these events should under no circumstance be occurring however, they continue to occur. If you or a loved one feel you are the victim of a medical mistake contact The Yost Legal Group today at 1-800-YOST-LAW (800-403-7259). When you call, you will speak with an experienced Baltimore Medical Malpractice attorney absolutely FREE.

The attorneys at Yost Legal Group are experienced, caring professionals ready to investigate your claim with compassion and determination. Call us today to receive a free, confidential consultation about your possible case.

At The Yost Legal Group, we will investigate every detail of your situation at no cost to you, and fight hard to ensure that your rights are protected.

We handle all cases on a contingency fee basis. This means you will never pay an attorney’s fee up front, and you owe us nothing unless we win your case.

 

Stryker Rejuvenate and ABG II Modular Hip System Recall

Posted on by YostLaw

Thousands of Americans receive hip replacements every year due to sports injuries, falls, aging and a host of other reasons. The goal of a hip replacement surgery is to return to your active lifestyle as quickly as possible. There are many different hip replacement medical devices on the market, from plastic implants to metal on metal implants.

Over the past decade, there have been a number of recalls on many of the top, name brand, metal on metal hip implant devises. It is the FDA’s duty to be the guardhouse for safe products, but sometimes defective products are passed through the system due to inadequate testing, manipulated reporting and of course, from human error.

Stryker is letting patients know that they should undergo a hip revision surgery to replace their metal on metal hip device for another model. Stryker will cover the cost of the revision surgery, but there is more to having a revision surgery then the procedure alone. There is prep time, the surgery itself, the recovery time and the hopes that the revision surgery will go well and not create any further medical problems.

Unfortunately, sometimes, medical devices and pharmaceutical drugs get fast tracked through the system, meaning the FDA approves them for market use, before enough research and testing has been conducted.

This is what happened with many metal on metal hip implant devices. The FDA approved them all, but as they were used, more and more adverse reaction reports were being sent to the FDA, so an investigation began. Usually this takes years for a medical device or prescription drug to be recalled off the market. And while the FDA waits, innocent patients continue to be harmed.

Over two years ago, on July 6, 2012 Stryker issued a voluntary recall of its Rejuvenate and ABG II modular-neck hip stems due to the increased potential for neck-body dissociation and increasing amounts of metal debris generated and deposited by the device.

Long-term toxicity of metal particles is not well known, but doctors have expressed concerns about metal exposure and there are numerous reports showing significant effects on organs. Metal toxicity has been linked to serious illnesses and is a very real concern for patients.

The modular interface of the Rejuvenate and ABG II creates corrosion, causing an inflammatory response, which results in a local reaction, such as metallosis, eventually affecting the entire body. Many patients have suffered a range of adverse reactions, such as:

  • Osteolysis (bone dissolution)
  • Synovitis (inflammation of the synovial membrane)
  • Pseudo-tumors
  • Fluid in the joint
  • Tissue and bone necrosis
  • Hypersensitivity to metal

Adverse reactions that affect the entire body include:

  • Decreased total lymphocyte cells, which defends against tumors and virally infected cells
  • Decreased CD8+T cells, which fight intracellular pathogens and malignancies
  • DNA changes
  • Chromosomal aberrations

If you have a Stryker Rejuvenate or Stryker ABG II implant and require a revision surgery call The Yost Legal Group at 1-800-YOST-LAW (1-800-967-8529). We’ll speak with you for free to discuss your situation and help you to understand your rights.

If we take your case we will do so on a no win/no fee or expense basis only. That means you do not pay a fee or expense unless you recover.

Call now for a free confidential consultation.

The Yost Legal Group, Experienced Lawyers Dedicated to Protecting your Rights.

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