lecture 1 Flashcards

(23 cards)

1
Q

controlled substances - schedule 1

A

abuse potential - high
medical use - none
dependency potential - severe physical and psychological
Ex - heroin

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2
Q

controlled substances - schedule II

A

abuse potential - high
medical use - accepted
dependency potential - severe physical and psychological
Ex - fentanyl

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3
Q

controlled substances - schedule III

A

abuse potential - less than 2
medical use - accepted
dependency potential - moderate to low physical and psychological
Ex - anabolic steroids, acetaminophen w/codiene

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4
Q

controlled substances - schedule IV

A

abuse potential - less than 3
medical use - accepted
dependency potential - less
Ex - alprazolom, zolpidem, tramadol

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5
Q

controlled substances - schedule V

A

abuse potential - less than 4
medical use - accepted
dependency potential - less
Ex - cough medicine w/ <200mg of codiene

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6
Q

controlled substances count

A

counted by two nurses at the start of each shift, must be equal. must sign out a controlled substance for administration

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7
Q

drug polymorphism

A

the effects of a patient’s age, gender, size, body composition, and other characteristics on the pharmacokinetics of drugs

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8
Q

How do the rights of medication administration guide safe nursing practice? How can you prevent medication errors?

A

o Provide a structured framework for that ensures that meds are given safely, accurately, and legally. Doing the 7 rights of med admin helps prevent wrong patient, wrong medication, and wrong dose errors.
o Performing the three safety checks
Taking the drug out
Alongside MAR
before opening the package and administering
Using two patient identifiers
Using BCMA, MAR, CPO
Do not administer if you didn’t draw up or prepare the medication yourself
Question a medication order when in doubt or when verbalized
Never assume
Do not use list of abbreviations; use tall man letters
Listen to concerns of the patient

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9
Q

what is pharmacokinetics

A

the process of what the body does to the drug; how meds move through the body. Absorption  Distribution  Metabolism  Excretion

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10
Q

absorption

A

: movement of the drug from admin site to the bloodstream
 Bioavailability - extent of drug absorption to be used by the body
 First-pass effect – oral medications have to make it past the liver
 Route – enteral (GI – oral), parenteral (injections), topical (transdermal and inhalation)

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11
Q

distribution

A

: movement of the drug from admin site to the bloodstream
 Bioavailability - extent of drug absorption to be used by the body
 First-pass effect – oral medications have to make it past the liver
 Route – enteral (GI – oral), parenteral (injections), topical (transdermal and inhalation)

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12
Q

metabolism

A

chemically altering a substance so it can be excreted from the body after it has produced an action.
 Most common site is the liver
 Also kidneys, GI tract, skin, plasma, and the lungs
 Co-existing conditions can affect metabolism.
 Ex: CV dysfunction or renal insufficiency can decrease a drug’s metabolism

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13
Q

excretion

A

 Often in kidneys, lungs, skin and GI tract.
 Half-live – time required for 50% of the drug to be removed
 Ex: administer 40 mg, half-life is 2 hours
 In two hours, you can expect half of that initial dose to be in the body
 Usually take around 5 half-lives for the medication to be removed.

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14
Q

pharmacokinetics: older adult considerations

A

high use of medications, polypharmacy: multiple medications, noncompliance/nonadherence, increased incidence of chronic illnesses, sensory and motor deficits, decreased renal and hepatic function, higher risk for toxicity, and altered protein binding. May require lower doses and Beers list screening

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15
Q

pharmacokinetics: pregnant patients

A

drugs cross the placenta by diffusion. Must consider risk-to-benefit ration. FDA has a labeling rule for pregnancy and breastfeeding, must know how it affects these patients

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16
Q

pharmacokinetics: pediatric and neonatal patients

A

skin is thin and permeable, stomach lacks acid to kill bacteria, lungs have weaker mucous barriers, body temperature less regulated, easily dehydrated, live and kidney are immature. Use weight-based dosages and KIDs list

17
Q

how do different routes of administration affect onset of action, effectiveness, and patient safety?

A

o IV: fastest onset, highest bioavailability, highest toxicity risk
o Oral: slower onset, affected by food, GI absorption, and first-pass metabolism.
o IM/Subcutaneous: moderate onset, influenced by muscle mass and circulation
o Topical/Inhalation: localized or rapid effects with reduced systemic exposure

18
Q

what is the first-pass effect, and how does it influence the effectiveness of certain medications

A

o Oral medications are metabolized by the liver before reaching systemic circulation, reducing bioavailability.
 May need higher doses

19
Q

legal responsibilities for safe med admin and nursing decision-making

A

nurses are legally accountable for knowing medication actions, side effects, contraindications, and administration practices.
 Controlled substances are controlled by the DEA, and must be counted by two nurses at the start of each shift (1 coming in, one leaving)

20
Q

ethical responsibilities for safe med admin and nursing decision-making

A

: practicing autonomy (patient choose for themselves), beneficence (promoting the best outcome, protecting from mistreatment), nonmalefiecense (avoiding harm), and justice (treating fairly)

21
Q

professional responsibilities for safe med admin and nursing decision-making

A

accurate documentation, patient education, and timely reporting for errors

22
Q

how can drug interactions affect med effectiveness

A

can increase therapeutic effects, cause toxicity, and reduce medication effectiveness. Can interact with medical conditions, food, drugs, and supplements
 Meds from the same class – augmented effects of those medications.
 Meds from different classes – can be positive or cause adverse effects. Continuously monitor.
 Cardiac meds interact with many herbal remedies
 Most frequent drug-food interactions are with grapefruits because they are metabolized in the same pathway – liver.
 Other frequent foods are dairy, vitamin K, tyramine, and alcohol

23
Q

drug interactions - monitor

A

for therapeutic actions, adverse and side effects. Look at black box warnings which are from the FDA meaning serious adverse effects were reported. Check lab results (serum drug levels, prothrombin time or partial thrombin time, electrolytes, and cardiac monitoring), ensure right med and dose, patient adherence, detect toxicity, and prevent client harm. Check the therapeutic index (link/ratio between the therapeutic and toxic medication concentrations). Also, check for tolerance, dependance, and withdrawal