Term Paper Assignment Example | Topics and Well Written Essays - 1500 words

Assignment - Term Paper ExampleTo find this, medical professionals have to reckon the role and importance of informed accede, and apply it in their give-and-take and query processes. Informed consent is historic as it helps diligents to make their independent decisions about their treatment, and helps investigate participants to decide independently whether to participate in a research, without being coerced (Carmen and Joffe WEB). This paper discusses the importance of informed consent in medical treatment and research, as intimately as the different ethical issues arising in the course of informed consent in medical treatment and research. The concept of informed consent can be traced to different disciplines, including law, medicine, and philosophy. Consent to treatment is traced to law, while consent to research can be traced to ethical codes and administrative regulations. Informed consent has important moral and mulish influence on the practice of medical treatment. This draws on the principle of autonomy, and the fact that a patient mustiness be availed the opportunity to make their own independent decisions about the treatment offered to them. Similarly, in medical research, the participants ar not coerced to participate. Medical treatment is therapeutic, unlike medical research, which is non-therapeutic, therefore, research participants are expected to participate voluntarily, since the research findings ability not benefit them directly, but the patients in future. This is different from medical treatment, where the treatment benefits the patients directly. Nonetheless, in both(prenominal) cases, it is important to employ informed consent as a sign of respect for the individuals involved (Carmen and Joffe WEB). match to the Evans (WEB), the physician must avail all necessary information concerning the treatment procedure in club for this to be regarded as informed consent. This information will help the patient to make their judgement and dip for a right decision. In medical treatment, the information must include the risks the patient is exposed to by the specific medical procedure, as well as the outcome of the medical procedure and the other alternatives, which cleverness be useful to the patient. In medical research, the participants must be informed about the purpose of the research and its usefulness to the discipline. This information leads to an informed decision by the patients and research participants. In addition, before pronouncing the informed consent, a physician must ensure that he or she understands the concerns of their patient, before starting to act on the patients decision. Physicians should not assume and make decisions for these patients, instead, a physician should take the necessary steps to ensure that those patients, who are poor communicators or those with speaking inabilities get to understand the consent information in golf-club to participate wholly in decision-making concerning their treatment (Caroline 417). This applies to medical research too, where coercion is considered unethical. On the other hand, informed consent in medical research and experimentation is equally important for both the medical investigator and the subject, who might be the patients or other healthy individuals. In some cases, a patient might require an innovative kind of treatment, which goes beyond the normal diagnosis and prescription. Such innovative or experimental treatment