Autonomy and Consent in Health Care Medical consent forms play a crucial role relating to treatment in the medical field. Consent can be defined as understanding the procedure and agreeing to it (Soper, 2016). The consent form serves two purposes to inform the patient of the upcoming procedure and to protect the hospital by outlining potential risks and complications. However, the vast majority of citizens are not versed in medical jargon and this can affect how well they understand what is going on. It is up to medical professionals to properly inform patients on what their medical options are and the risks associated with various treatments. This paper will discuss: whether a basic consent form properly informs patients of their rights, …show more content…
Autonomy and self determination are ethical cornerstones that recognize the patient as a competent individual and give them the right to choose their treatment options (Paola, Walker, & Nixon, 2010). As a health care professional it is your job to properly inform them of what treatment options are available and once they have decided on a course of action they are given a consent form to sign. The consent form is used to show that the patient fully understands and consents to the medical treatment they have selected. Using a standard laparoscopic cholecystectomy consent form as a frame of reference it does a pretty good job of conveying patient rights. It outlines multiple treatment options, risks/benefits of the procedure, and information for both pre and post operation. While the consent form offers alternative procedures and necessary information for the operation it seems somewhat biased towards the operation. The bulk of the consent form only deals with the surgery while other options are only briefly introduced. This may pressure the patient towards a certain treatment option and infringing upon their autonomy. Overall the consent form adequately presents patient right but it does so in a somewhat biased …show more content…
Improving the ways to inform patients is something that must occur to ensure safety for the patient. One way to do this is through supplemental information. Consent forms are information dense and daunting so a physician should walk them through all of it to make sure that they fully understand and then provide them with pamphlets or additional notes to simplify and highlight the most important parts (Gyomber, Lawrentschuk, Wong, Parker, & Bolton, 2009). Another way to better inform patients is to provide people who specialize in informing vulnerable population. This includes uneducated, elderly, special needs, and those with language barriers. A physician may be able to simplify information but at times it may take a communication expert to further simplify or translate the information for a patient. Another related way to improve informed consent would be for physicians to briefly probe the patient for information on the procedure to ensure that they fully understand what us being done and can accurately make a decision (Vucemilo & Borovecki, 2015) Lastly another way to improve patient understanding is to require multiple friends/family members signatures. By forcing more people to read the document and be presented with the information it makes it more likely that the
The process of consent should apply not only to surgical procedures but all clinical procedures and examinations which involve any form of touching. This must not mean more forms: it means more communication. As part of the process of obtaining consent, except when they have indicated otherwise, patients should be given sufficient information about what is to take place, the risks, uncertainties, and possible negative consequences of the proposed treatment, about any alternatives and about the likely outcome, to enable them to make a choice about how to proceed.”5
According to the Oxford Dictionary consent is defined as ‘giving permission for something to happen or agreeing to do something’. They define confidentiality as ‘entrusted with private information and if something is intended to be kept secret or in confidence’ (Soanes and Hawker, 2005). As a healthcare professional consent and confidentiality are in place as protective vices, by gaining consent and keeping a patients confidentiality it protects both the patient and the healthcare professional. There are three types of consent: Verbal consent, consent in writing and implied consent. Depending on the situation each type of consent may not be acceptable. For example if a procedure is putting a patient at risk, is complex or invasive for example an operation, written consent is
According to sense two, legal or institutional effectiveness takes precedence. In other words, a subject’s consent is limited to the scope of the rules of the institution. Faden and Beauchamp illustrate that even if a patient autonomously gives her consent, it does not follow that effective consent is given if the requirements of the institution are not met. Consequently, the authors propose that sense one and sense two should both contribute in defining informed consent. Using Jay Katz’s argument, Faden and Beauchamp argue that sense two should satisfy sense one for there to be some type of balance between the two.
Informed consent is the basis for all legal and moral aspects of a patient’s autonomy. Implied consent is when you and your physician interact in which the consent is assumed, such as in a physical exam by your doctor. Written consent is a more extensive form in which it mostly applies when there is testing or experiments involved over a period of time. The long process is making sure the patient properly understands the risk and benefits that could possible happen during and after the treatment. As a physician, he must respect the patient’s autonomy. For a patient to be an autonomous agent, he must have legitimate moral values. The patient has all the rights to his medical health and conditions that arise. When considering informed
The Doctor and Patient relationship aspect of Medicine has changed drastically in the last twenty years. It has evolved from paternalism (the doctor makes the decision for the patient) to shared decision making where the patient is considered an equal partner in his/her own health related decisions. Informed consent is the cornerstone for this view. When a patient or a research subject makes an autonomous decision after understanding, the risks and benefits involved with the decision is Informed consent. Complete Informed consent covers the following components: competency, disclosure, comprehension and voluntary. Competency refers to the requirement for the individual to be of legal age and be mentally competent to understand the process.
Patient informed consent refers to the situation where the patient is fully informed on the consequences of their health care decision after which the patient gives the decision. For there to be informed consent, there are five elements that must be discussed. The first is the nature of the patient's decision then the applicable alternatives to the proposed intervention. Third are the risks, benefits and uncertainties associated with each of the alternatives. Fourth is the assessment of the patient's understanding and last is the acceptance of the intervention or an alternative by the patient. Before the patient's consent is considered to be valid, the patient's competency to make the decision must be addressed. The criteria for evaluating the patient's competency is clearly stated in section 3 of the 2005 Mental Capacity Act which states that provided the person is able to understand, retain and use information provided and to communicate their decision in any way such as talking or sign language, they are competent to make a decision. If a patient is treated against their refusal to consent, it amounts to the tort of battery or can also be considered the crime of assault. In addition to this, laws that touch on human rights reinforce the importance of the protection of the physical integrity of the individual in terms of their right to respect of their private life. Therefore, refusal of medical treatment is a human right.
Every patient has a right to decide on their own course of treatment and freely consent to that treatment. In order to make an educated decision they must be provided with the proper information to make an informed choice (Opinion 8.08 - Informed Consent, 2006). It is the physician’s legal and ethical obligation to provide this information when making their recommendation on treatment. The choices given must be in accordance with good medical practice (Opinion 8.08 - Informed Consent, 2006). The informed consent is the legal policy, either written or verbal, that gives full disclosure of all the information including potential risks that is applicable to the patient’s condition and treatment being offered (Kazmier, 2008).
Dimond (2009) and NHS choices (2016) explained consent as the process involving a person giving their approval to accept or refuse a treatment or interventions, after receiving detailed information from a health care professional about the risk or benefits of the procedure. In order for consent to be deemed valid, it needs to be given voluntarily without any influence or pressure from either a family member or clinician. In addition, the capacity of the person is important when giving consent and the ability to process the given information and make a decision. Tingle &Cribb (2014) agree, emphasizing that the autonomy of the person giving
Obtaining an informed consent is a vital part of current health care. This document lists out several key pieces of information for both the patient, Provider, and the ancillary staff that also access the document during the procedure process. However, obtaining informed consent has not always been the practice norm and in research, informed consent carries different specifications.
However, Franklins claims that consent form should be the responsibility of just the doctor is flawed. Although doctors should not “act as if informed consent is a piece of paper with somebody’s name on it” it should not be only the doctor that is trying to be informed about the process Debroah (261). Franklin does not consider that the doctors already have a great number of patients they have to see. In addition to their job of keeping you healthy they have to check to see and if their patient is a poor reader, and if they understand the text and seeing that not all adults read at the same
It is best demonstrated when patients signs for proposed treatment once they feel fully informed and completely understand what a treatment or procedure entails. The idea of informed consent is based on the principle of autonomy and respect of self-determination. In this paper I am going to present different perspectives of informed consent by different institutions that why it is important to treatment procedure.
When a patient needs to have a medical procedure performed, they must first consent to the procedure. Before accepting or rejecting the treatment, the practitioner is required to give the patient information pertaining to the risks and benefits of the procedure, as well as available alternatives. Additionally, the patient must be mentally competent enough to make an informed decision, and not be manipulated or coerced into a decision.
Delivery of excellent healthcare involves a multitude of dynamics including an extremely straightforward requirement of a patient’s permission for treatment or procedure. Informed consent, a patient’s authorization, consist of communiqué between healthcare provider or physician and the healthcare consumer, providing sufficient information allowing the patient to make a knowledgeable decision regarding healthcare treatment
Nursing is an all encompassing profession in which practitioners are not only proficient in technical medical functionality, they also have the obligation to remain compassionate and respectful of patients and as such are expected to adhere to pre established codes of ethics. Of these ethics, autonomy is of extreme importance as it offers patients a sense of personal authority during a time where they may feel as if their lives, or at the very least their health, is no longer under their control. Autonomy in the context of nursing allocates the patient and often their family with the final word on the course of treatment. The concept of patient autonomy is a highly variable subject in all fields of health care. It is a universal concept that varies widely in its meaning and interpretation. Autonomy in its simplest form can be defined as a state of independence or self governing (Atkins, 2006). Patient autonomy can also be defined as the ability to make once own decisions, based on one’s sound judgment. It is defined by the American Nurses Association (ANA, 2011) as the "agreement to respect another 's right to self determine a course of action; support of independent decision making." This seemingly straight forward ethical concept is rife with difficulties when one considers potential disagreements that may arise even when informed consent is provided, particularly among children or vulnerable people. Relevant research and
Consent can be quite tricky, a legal minefield for healthcare teams, this is due to the patients who will give or refuse to give private information about themselves who is legally competent but