Lecture 3 Flashcards

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0
Q

What are the secondary goals of informed consent?

A

limit liability, clarify standards of practice, clarify patient’s responsibility (making a decision consciously)

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1
Q

What is the primary goal of informed consent?

A

Effective communication that honors patient autonomy

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2
Q

What 4 items does the law established in healthcare for obtaining informed consent address?

A
  1. patient’s right to make decisions
  2. Full disclosure of information (risks and benefits)
  3. that the patient full understands the situation (is competent)
  4. Voluntariness (there is no pressure)
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3
Q

What types of things constitute “enough information” for most diagnostic procedures, treatments and prognoses?

A
  • length of treatment
  • time of recovery
  • possible side effects
  • restrictions on ADLs (activities of daily living)
  • other (procedural/treatment) options (their risks and benefits)
  • anticipated results
  • consequences of denying or delaying treatment
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4
Q

When type of exam particularly requires consent?

A

sensitive exams (eg. genital exams)

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5
Q

What does PARQ mean?

A

P - procedure
A - alternatives
R - risks
Q - questions from the patient

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6
Q

What is required if a patient refuses a treatment plan?

A

An informed refusal form - a signed document that goes into the patient’s chart

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7
Q

What is the most well known confidentiality agreement in health care? Why was it created?

A

HIPAA of 1996 - Health Information Portability and Accountability Act
Originally created to safeguard patient health information in faxes and electronic charting (specifically for “individually identifying health information”)

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8
Q

What is the main idea of confidentiality?

A

Keeping a patient’s private (and identifying) information private

  • Keep confidence, build trust, maintain patient’s dignity.
  • -> honor the patient’s expectation that private information shared with the Dr will be kept confidential (professional promise –> duty and fidelity)
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9
Q

Describe “need to know basis”

A

may only share info to other professionals who will further the welfare of the patient

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10
Q

What is “sensitive information”?

A

information that may be harmful to the patient if shared with others
(ex. embarrassing)

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11
Q

What are legal exceptions for privacy of information?

A

Emergency - when keeping/withholding information will harm the patient
Incapacitated patients - healthcare surrogate must be informed
Third party is at serious risk (STI)
Requesting commitment of psychiatrically ill patient
Public at risk (terrorist threat - homeland security)

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12
Q

Describe the lesser know confidentiality act? What is it and what does it do?

A
HITECH Act (Health Information Technology for Economic and Clinical Health Act) of 2009
Widens the scope and enforcement of privacy protections for health electronic records (HER)
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13
Q

Safety and Efficacy (effectiveness) are an extension of what medical ethical principles?

A

beneficence and non-malevolence

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14
Q

What are some issues related to safety/risks?

A

toxicities of medicines, poor quality of medicine (tainted, additives, non-absorbable), compatabilities/incompatibilities with other medicines (drug/drug, drug/herb); accuracy of diagnosis (skill of doctor); correct prescription? (iatrogenic causes of death), appropriateness of prescription/dose for age (children/elderly), psychological/spiritual effects, homeopathy: aggravations, marketing or advice leading to inappropriate treatment
–> how high is the risk for the possible benefit?

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15
Q

Describe the idea of efficacy.

A

Asks: what are the standards of evidence of what works and how does it applly to this particular patient?

  • utilizes evidence based medicine/evidence-informed practice
  • -> hierarchy of evidence
16
Q

What is the gold standard of EBM?

A

RDBPCCT - randomized, double blinded, placebo controlled clinical trial

17
Q

How are some questionable beliefs about efficacy in natural medicine?

A

Charge: natural medicine is not sufficiently studied for safety and efficacy
Charge: alternative medicine’s effectiveness is merely a placebo effect

18
Q

Rebuttal to the charge that natural medicine is not sufficiently studied

A

we have historical writings, testimonials and anecdotal evidence; it simply doesn’t fit into the current western research context

19
Q

What is the rebuttal to the charge the natural medicine functions only due to the placebo effect?

A

The placebo effect is not only restricted to CAM

20
Q

Questions regarding EBM in naturopathic medicine.

A

N = 1 is a difficult study design –> you can’t do it
CAM research - other methods of studies? Ethical rules still apply.
difficulty applying research to the patient at hand
complex treatment plans –> what is THE things that is working?

21
Q

Questions regarding the placebo effect…

A

Does using placebo effect intentionally undermine autonomy?
Does utilizing the placebo effect violate duty of honesty?
Do trust and empathy encourage a placebo effect?

22
Q

Describe broadly the Standards of Care.

A

In medicine, standards of care are those followed by a responsible body of medical opinion.

23
Q

What is a “reasonable standard”?

A

the DUTY of a physician to conduct their practice in accordance with the conduct of a prudent and diligent doctor in the same circumstances
–> Licensure for a profession clarifies this

24
Q

Broadly describe scope of practice

A

What a physician can and can’t do under the licensing law

25
Q

How does scope of practice often vary?

A

scope and formulary varies from jurisdiction (state to state)
special licensure

26
Q

What is a formulary?

A

a list of drugs that can be prescribed within a particular jurisdiction
–> this also applies to taking a patient off of a drug

27
Q

Who do you have to be approved by to prescribe controlled drugs (e.g. opiates and some hormones)?

A

DEA through the Dept of Justice