General Information about Medical Malpractice/Negligence
Medical Malpractice occurs when a physician fails to properly treat a medical condition and the negligent act or omission is the cause of additional or aggravated injury to the patient. Obviously the physician cannot be responsible for the original underlying medical problem. This negligence could cause a case against the doctor if his/her actions differ from generally accepted standards of practice, or it may be against the hospital for improper care. These include problems with nursing care, medications or sanitation. Local, state and/or federal agencies, which operate such hospital facilities, may also be held liable.
Medical malpractice laws are designed to protect a patients' rights to seek compensation if they are injured due to negligence. Medical malpractice cases are by their very nature, complex, expensive to pursue and have a high risk of no recovery. If you believe you have a medical malpractice claim, it is essential to seek advice from our experienced medical malpractice attorney who may assist in determining the validity of your claim and the details that need to be proven to see if it is worth pursuing.
Variations in Medical Malpractice Cases
Negligence of Physicians, Hospitals and Others
The negligence in medical malpractice cases may occur in a variety of situations including but not limited to a delay or failure in diagnosing a disease; injury to the patient; a health care professional's deviation from the applicable standard of care; a health care professional who has made the correct diagnosis, may thereafter commit medical malpractice by failing to properly treat the disease or injury.
Several criteria must be established to prove medical malpractice. First and foremost is establishing the standard of care the health care professional should have provided. Some errors in judgment may result in additional injury to a patient, yet not all medical errors are understood to be negligible.
To be legally at fault, the patient must be able to prove that the health care provider's actions fell below the standard of medical care established. Expert testimony to confirm the standard required relating to the patient and the professional failed to work within the established standard. In rare cases, expert testimony is not required when it is obvious to the average person that the standard was violated.
Expert witnesses must be qualified by the Court, based on the prospective experts qualifications and the standards set from legal precedent. To be qualified as an expert in a medical malpractice case, a person must have a sufficient knowledge, education, training or experience regarding the specific issue before the court to qualify the expert to give a reliable opinion on a relevant issue. The qualifications of the expert are not the deciding factors as to whether the individual will be qualified, although they are certainly important considerations. Expert testimony is not qualified "just because somebody with a diploma says it is so" (United States v. Ingham, 42 M.J. 218, 226 [A.C.M.R. 1995]).
It is possible that the cause of the injury may not be established, but the injury could not have occurred unless there was medical negligence. A legal doctrine known as res ipsa loquitur, permits a jury to infer the health care professional's negligent conduct in these types of medical malpractice. Additional items must also be proven such as the doctor and physician relationship, the action or lack of action that was the source of the medical malpractice, or the "causation" is also an essential factor.
Misuse of Medications and Medical Devices
A health care professional may be held responsible for the negligent prescription of a medication or medical device if he/she ignored the manufacturer's instructions, or prescribed the wrong medication and/or dosage, which resulted in an injury to the patient. In some cases the pharmaceutical manufacturer may be held responsible where a drug caused a patient injury, but only if the manufacturer neglected to warn of potential side effects or dangers of the drug. A prescribing physician, because of advanced knowledge and the adequate information from the manufacturer, is in the best position to determine whether a particular drug or device is appropriate for a patient. When using a medical device, it is incumbent upon the doctor to disclose to the patient the risks attached to the use of this device. Failure to give such informed consent may, in some states, give cause to a claim for malpractice against the doctor.
Emergency Situations vs. Informed Consent
In many situations, failure to obtain a patient's informed consent prior to a procedure or treatment is a form of medical negligence. This means a health care professional must inform a patient of all the potential benefits, risks, and alternatives involved in any medical procedure, surgical procedure or any other course of treatment, and must obtain the patient's written consent to proceed. Informed consent may be either express or implied. Express consent is given in writing or verbally. If written, it should include the name of the health care provider who discussed the proposed treatment with the patient, time and location where the consent form was signed. Consent not given by a patient verbally or in writing, but is understood from the surrounding circumstances of the procedure or treatment at issue, is known as implied consent.
In some emergency situations, opportunity does not allow time to obtain a patient's informed consent or the patient may be unconscious and unable to communicate. If an emergency involves risk to a patient's life or the patient is unable to communicate, consent may be implied with the understanding that the patient would have consented to such emergency treatment. The process of obtaining informed consent for a competent adult may seem relatively easy. However, in situations pertaining to mentally disabled individuals or children, the ability of the health care professional to obtain informed consent becomes more difficult. In such instances, serious questions may arise concerning who is able to give informed consent for these individuals. In many situations, a mentally disabled person has an appointed guardian who is authorized to make medical decisions and give informed consent for that individual. Health care providers need to be sure when they obtain informed consent for incompetent individuals, that they have obtained it from the correct person or persons.
In most circumstances, parents can give informed consent for treatment of their minor children. However, some states allow young adults under eighteen to participate more actively in their medical care and treatment, including the process of informed consent. Most states focus on mature minors adequately ready to understand the nature and consequences of treatment. In those states, such young adults may be able to provide consent without parental consent. Some states have passed specific laws allowing minors to consent, without a parents' knowledge and/or consent, to health care treatments pertaining to mental health, sexual activity and substance abuse.
A consent form does not release a health care professional from the applicable standard of care in performing a procedure, and you were injured as a result, you may still recover against him/her. Patients are entitled to complete information on all treatments and/or procedures to which they are subjected. A health care professional who fails to provide such information may be held accountable.
Not all situations require that informed consent be given. For example, although listening to a heartbeat through a stethoscope may be considered a "treatment" or "procedure," to some people (especially those who are uncomfortable in physician's offices), it's rare that a physician and patient would have a lengthy discussion about the benefits and risks of listening to a heartbeat using that device.
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