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Essay Available:
Pages:
1 page/β‰ˆ275 words
Sources:
2 Sources
Style:
APA
Subject:
Health, Medicine, Nursing
Type:
Essay
Language:
English (U.S.)
Document:
MS Word
Date:
Total cost:
$ 4.32
Topic:

Informed Consent For Minors or Incapacitated Patients

Essay Instructions:

INFORMED CONSENT, Ethical and Legal Elements of Informed Consent, Special Considerations with Informed Consent, Nursing Role and Responsibilities: Informed Consent. Informed consent provides legal and ethical protection of a patient's right to personal autonomy regarding plans for health care, including the right to refuse interventions and to choose from available alternatives. Information necessary in an informed consent includes: the nature of the concern and prognosis if nothing is done; description of treatment options; and benefits, risks, and consequences of treatment options or nonintervention. Nursing responsibility regarding informed consent includes verifying that the patient is aware of options and the implications of each and advocating for patients to ensure that criteria for autonomous decision making are met in situations where the physician has not attended to these criteria.
For minors or incapacitated patients, how is consent acquired if no blood relative/guardian is present? How is the informed consent process different in an emergency situation versus a planned procedure?
(word count 200 to 300 words or more). You must include a reference page and cover page with your submission. Remember, cover page and reference pages are not included in the word count.

Essay Sample Content Preview:

Informed Consent
Student’s Name
Institutional Affiliation
Course Code and Name
Instructor’s Name
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Informed Consent
Obtaining consent from a subject (patient) before performing any procedure is a critical process that should involve exchange of detailed information and continuous communication. The patient should be in a position to comprehend the nature and effects of the procedure or study (Cocanour, 2017). However, minors or incapacitated patients are not in a position to give consent. In this case, blood relative or guardian comes in handy. However, when the relative or guardian are not present, surrogate consent is sought. All surrogates must be approved by the IRB and the process should be done as a formal evaluation (Cocanour, 2017). Another viable option would be to exclude the minors and incapacitated patients, if the consent is being required for a medical study.
Informed consent...
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