Verified Document

Instances When Informed Consent Is Not Required Essay

Healthcare THE PATIENT AND PROVIDER RELATIONSHIP

At any hospital like ABC, informed consent is not needed during emergencies. During emergencies, there lacks time to offer a vivid description of risks involved while physicians act quickly in saving life. Patients do not have an opportunity of suing for absence of informed consent within similar situations even as they did not allow the treatment. Trust remains one of the vital elements that patient-doctor relationships exist. Patients and doctors should believe that other parties are honest and have a willingness in providing necessary information to influence treatment and advice. The medical professional needs to consult the information on patient for potential benefits and risks based on options through availing support to patients and informed choice. It is prudent for caregivers to pay careful attention to processing informed consent and choice in proposing treatment as expensive or way innovative (Maclean, 2009). If patients choose between innovative treatments and evidence-based medicine where no scientific evidence is consulted, there are attempts at presenting patients with balanced and clear summary of scientific information available (Kazmier, 2008).

The second scenario is where there are patients with emotional fragility. If doctors are aware of patients facing distress for refusal of necessary...

For instance, if the brain tumor becomes life threatening, and the removal includes frightening risks such as paralysis, it is appropriate for doctors to remain vague in describing risks. Further, disclosure of too much detail on the necessary procedure makes already frail anxiety about patients where doctors are in a position of withholding some information (Lindh, Pooler & Morris, 2013). Doctors may choose to disclose with reference to the patient's particulars although some instances demonstrate the clear reason as to why the risks should not be disclosed. Informed consent defines permission to apply medical treatment and a requirement to inform of material risks before to treatments. Healthcare professionals must provide the requisite information to patients touching on their consent especially to the treatment and associated risks. Failure to achieve a lead in civil liability causes adverse outcomes of treatment of negligence (Kazmier, 2008).
The third situation relates to the treatment of minors. For instance, visual examination of patient's eyes, mouth, ears or throat through providing first aid and non-prescription drug administration. The painkillers and antihistamine are among recommended dosages. Physicians licensed in medicine, surgery and hospital practice where consent is…

Sources used in this document:
References

Kazmier, J. (2008). Health Care Law. New York: Cengage Learning.

Lindh, W., Pooler, M., & Morris, J. (2013). Delmar's Comprehensive Medical Assisting: Administrative and Clinical Competencies. New York: Cengage Learning.

Maclean, A. (2009). Autonomy, Informed Consent, and Medical Law: A Relational Challenge. New York: Cambridge University Press.
Cite this Document:
Copy Bibliography Citation

Related Documents

Ethics of Informed Consent Ethical Dilemma: Imagine
Words: 1152 Length: 3 Document Type: Essay

Ethics of Informed Consent Ethical Dilemma: Imagine a psychologist treating a minor child depression minor cutting. Because child's parents divorced, obtained consent treat child father, custodial parent. The mother (noncustodial parent) calls involved son's treatment. Ethical dilemma: Treating a child of divorced patients One of the most difficult issues for a therapist regarding the treatment of minors is the question of confidentiality. "An important aspect of treatment is to foster an individual's autonomy,

Consent of Subjects Included in Biomedical Research
Words: 988 Length: 2 Document Type: Research Paper

Consent of Subjects Included in Biomedical Research Informed Consent is the basis of the transfer of information to a subject who is a candidate to participate in a clinical trial. The process of obtaining informed consent is a moral and ethical component of clinical trials conducted under Good Clinical Practices (GCPs). A subject is informed of all aspects of a clinical trial that are determined relevant to their decision to

Consent Analyze the Legal Issues
Words: 994 Length: 3 Document Type: Thesis

Requirements for licensure for psychologists under the American Psychologist Association (APA) set certain educational and ethical standards that govern the profession. Now clinical psychology is, much like medicine and law, a discipline accorded respect in society, and an individual who seeks counseling can feel confident being open and trusting of a licensed therapist. A therapist cannot claim to be a professionally licensed therapist under the law, unless he or she

Proxy Consent in a High
Words: 1394 Length: 5 Document Type: Essay

Mrs. E (Kluge 2005, pp. 191). This does not apply to this situation, however, as Jack's competency for decision making is only temporarily impaired, and he will still be caring for himself by and large for the foreseeable future. Thus, a consideration of his best interests must include a consideration of Jack's psychological, emotional, and religious/philosophical attitudes as well (Kluge 2005, pp. 191). Jill asserts that her husband feels very

Postoperative Vision Loss Elements of
Words: 8700 Length: 30 Document Type: Research Proposal

More times than not, a patient will argue that he did not understand what the physician stated to him; even amidst documented proof the medical professional and the patient did engage in an informed conversation. "The fact that a meeting took place does not necessarily mean that there was a meeting of the minds" (Informed consent…, 2010, ¶ 5). This issue leads some health care providers to assert that

Professional Ethics, State Laws, and
Words: 1809 Length: 5 Document Type: Term Paper

The second category is the expedited category where there is minimal to moderate human contact and low to moderate levels of risk. The last category is the full category where there is moderate to maximum human contact with moderate to high levels of risk. The Saybrook IRB policy specifies how each of these categories is reviewed Saybrook Institutional Review Board, 2012, pp. 7-9() The Saybrook IRB procedure begins with sending

Sign Up for Unlimited Study Help

Our semester plans gives you unlimited, unrestricted access to our entire library of resources —writing tools, guides, example essays, tutorials, class notes, and more.

Get Started Now