Health Science 20 Final Exam Review PDF
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This document is a review of health science, focusing on health and ethics, different types of medicines, patient rights, clinical trials, and application of key terms to medical scenarios. It appears to be a final exam review for a health science course.
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Health Science 20 Final Exam Review Health and Ethics Multiple Choice Section 1. Know the meaning of the following terms and be able to recognize/explain examples of each: a. Beneficence: acting in the best interest of the person Provide benefit Advocating for a patient’s needs b....
Health Science 20 Final Exam Review Health and Ethics Multiple Choice Section 1. Know the meaning of the following terms and be able to recognize/explain examples of each: a. Beneficence: acting in the best interest of the person Provide benefit Advocating for a patient’s needs b. Nonmaleficence: the obligation to do no harm Hippocratic Oath Stopping a medication known to be harmful c. Informed consent: the person must understand what they’re consenting to, and the risks and benefits of the action When a patients advised by an EMT of the risks associated with refusing care, ensuring the patient’s decision is well informed d. Justice: treating all persons with fairness, equality, and impartiality, compatible with the legal statutes Patients diagnosed with cancer are entitled to a range of treatments e. Autonomy: the ability to self-govern Healthcare professionals cannot impose treatments or interventions on patients without their informed consent 2. Be able to describe and provide examples of: a. Western (conventional) Medicine: focuses on treating symptoms Emphasis on disease and treatment technology Scientifically based, treatments proven effective through scienific research Ex: Drugs, radiation, surgery, vaccines, physical therapy, diagnostic testing b. Alternative Medicine: refers to using a non-mainstream approach in place of conventional (western) medicine (replacement for Western medicine) Ex: acupuncture, homeopathy, and herbal remedies c. Complementary Medicine: generally refers to using a non-mainstream approach together with conventional medicine (alongside Western medicine) Ex: someone might use acupuncture to help manage pain while still receiving traditional medical care 3. Patient's Rights in Canada fall into 4 main categories. Know what each of these terms mean. a. Disclosure: the right ot be fully informed of: Their medical condition Treatment options availabe and risks associated with those options Qualifications of their healthcare provider b. Privacy: the right to privacy with regards to: Communicating with health professionals = required to keep all information confidential Healthcare records = access to records is restricted to public health services specially for treatment c. Access: access to and copies of all personal health records The right to a second opinion with regards to diagnosis and treatment d. Consent: the right to accept or reject medical interventions (verbally or written) for consent to be considered valid: Must be voluntary Patient must be legally competent to consent = must be a “mature minor” (SK~16) and mentally stable Patient must be properly informed = healthcare provider must tell you about the nature and consequences of the treatment before you consent it 4. Know the terms associated with clinical trial studies: single blind study: the groups being studied, including the control, are NOT aware of the group in which they are placed; only researchers know double blind study: neither the patients nor the researchers know who is getting a placebo and who is getting treatment randomized trial: a type of expereimental study where people are randomly assigned to either a control or intervention group epidemiological studies: studies on how human populations, which attempt to link human health effects (e.g. cancer) to a cause (e.g. exposure to a sepcific chemical) independent variable: (the cause) is systematically manipulated in a controlled experiment dependent variable: (the effect) is measured in a controlled experiment control group: not given the treatment (placebo) experimental group: given the treatment Placebo: “I Will Please” in Latin; an inactive substance or procedure used as a control the placebo effect: the measurable, observable, or perceived improvement in a health condition that is not attributable to an actual medicine treatment the nocebo effect: “I Will Harm”; when an inactive treatment causes harm because we believe that it will 5. Be able to apply the terms: informed consent, autonomy, beneficence, nonmaleficence & justice to several case studies/medical scenarios