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W.E.B. DuBois life and role in the history of education Essay

W.E.B. DuBois life and job throughout the entire existence of instruction - Essay Example William Edward Burghardt Du Bois was a compelli...

Monday, October 7, 2019

Human Research Precis Coursework Example | Topics and Well Written Essays - 500 words

Human Research Precis - Coursework Example Notably, the physician must be certain that the treatment option that they recommend is best while still upholding the patient’s rights. If for instance a randomized clinical test is being conducted to compare treatment option A and B, and the physician openly prefers treatment option A, they must inform the patient about their preference but should not force them into buying into their preference. All physicians have an obligation to obtain their patients informed consent to treatment and can attain this by explaining to the patient the benefits and risks of the preferred alternative and alternative option and allow the patient to choose their preferred choice if that is possible. A reasonable alternative is to undertake treatment alternative A or allow the patient to participate in a randomized clinical test comparing the treatment options. Apparently, when a trial is available, enrollment in a haphazard clinical test is a superior therapeutic alternative. Respect for patient’s values is a central purpose of informed consent and physicians must consider it in delivering treatment. Marquis further notes that some patients might prefer participating in a randomized study that will positively contribute to medical progress and development or discovery of aspects that will improve the health of patients in future rather than simply following the unfounded recommendations of physicians. Noteworthy, a physician can recommend a treatment as well as ask the patient whether they are willing to partake a randomized clinical test just to ensure that their consent freely expressed. What’s more, an opportunity to contribute in randomized clinical trials is ethically permissible and morally obligatory. The dilemma of whether to involve patients in randomized clinical tests can be resolved by taking informed consent earnestly. Offering patients a chance to participate in the randomized

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