NUR 641E Midterm Study Guide, Exams of Nursing

NUR 641E Midterm Study GuideNUR 641E Midterm Study Guide

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2025/2026

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NUR 641E Midterm Study Guide
1.
Prodrug:
An inactive drug dosage form that is converted to an active metabolite by various biochemical reactions once it is inside the body.
-Cytochrome
P450
-Ex.
Aspirin,
psilocybin,
heroin
2.
Bioavailability:
the rate at and the extent to which a nutrient is absorbed and used
-Attected
by
route
of
administration
and
drug
dosage
-Drug
clearance
(rate
drug
leaves
circulation)
-Steady
state
concentration
-Attected by chemical stability, solubility, and first pass
3.
Steady
state
(of
a
drug):
stable
level
of
drug
in
the
body,
occurs
in
5
half
lives
of
the
drug
-rate of drug being added to system is equal to amount being eliminated from system
4.
Pharmacokinetics:
The process by which drugs are absorbed, distributed within the body, metabolized, and excreted.
-what
the
body
does
to
the
drug
5.
First
pass:
the
fact
that
a
medication
in
the
GI
tract
passes
through
the
liver
before
entering
other
organs
6.
does
not:
bioequivalence does/does not attect bioavailability
7.
Bioequivalence:
relative
therapeutic
ettectiveness
of
chemically
equivalent
drugs.
8.
Bioavailability (is affected by): -chemical
instability
-
solubility
-first
pass
metabolism
pf3
pf4
pf5
pf8
pf9
pfa
pfd
pfe

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NUR 641E Midterm Study Guide

1. Prodrug: An inactive drug dosage form that is converted to an active metabolite by various biochemical reactions once it is inside the body.

-Cytochrome P -Ex. Aspirin, psilocybin, heroin

2. Bioavailability: the rate at and the extent to which a nutrient is absorbed and used

-Attected by route of administration and drug dosage -Drug clearance (rate drug leaves circulation) -Steady state concentration -Attected by chemical stability, solubility, and first pass

3. Steady state (of a drug): stable level of drug in the body, occurs in 5 half lives of the drug

-rate of drug being added to system is equal to amount being eliminated from system

4. Pharmacokinetics: The process by which drugs are absorbed, distributed within the body, metabolized, and excreted.

-what the body does to the drug

5. First pass: the fact that a medication in the GI tract passes through the liver before entering other organs

6. does not: bioequivalence does/does not attect bioavailability

7. Bioequivalence: relative therapeutic ettectiveness of chemically equivalent drugs.

8. Bioavailability (is affected by): -chemical instability

  • solubility -first pass metabolism

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9. Cytochrome P450: -enzymes that function to metabolize potentially toxic compounds, including drugs and products of endogenous metabolism such as

bilirubin, principally in the liver. -genetics influence presence of enzymes -attects metabolism of warfarin, antidepressants, antiepileptics, and statins. -the levels of these drugs are higher when taken with certain drugs that are inhibitors (ex. warfarin with omeprazole) because there is competition for enzyme metabolism. -inducers lead to decreased plasma concentration of drug.

10. cytochrome p450 inducer: An inducer increases the metabolism of a substrate resulting in a decreased level or ettect of the

substrate

11. cytochrome p450 inhibitor: An inhibitor decreases the metabolism of a substrate resulting in an increased level or ettect of the

substrate.

12. Clopidogrel: prodrug that must be activated by hepatic CYP2C19 metabolism; individuals who are poor metabolizers may not form the active

metabolite and have reduced antiplatelet response

13. half-life (determines): how often a drug is administered

14. 4-5: steady state is reached in - times the half-life

15. Warfarin (MOA): -Vitamin K antagonist

-Factors II, VII, IX, X -takes several days to take ettect -monitor INR

16. Vitamin K: warfarin antidote

17. Heparin (MOA): -rapid anticoagulation by binding with antithrombin III and inhibits factors IXa, Xa, XIIa, and XIII

-aPTT monitoring (low dose SQ does not require monitoring)

4 / 14 -enteric, extended-release

26. enteric-coated: -protects the drug from stomach acid

-delivers to less acidic intestine -useful for drugs that are acid labile or irritating to stomach (ex. omeprazole, aspirin)

27. extended-release: -control drug release

-maintain therapeutic range over longer period -good for drugs with short half-life (i.e. morphine with half-life of 2-4 hours)

28. aPTT: activated partial thromboplastin time

29. 30-40 seconds: Normal activated partial thromboplastin time (APTT)

30. 1.5-2.5: therapeutic aPTT is x more than normal aPTT

31. low dose heparin: -5000 units BID

-does not require aPTT monitoring

32. INR: international normalized ratio

33. 2-3 (INR): therapeutic INR for warfarin

34. <1.1: normal INR

35. Dabigatran (Pradaxa): -direct thrombin inhibitor

  • anticoagulant -blood factor IIa inhibitor

36. idarucizumab: antidote for dabigatran

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37. factor xa inhibitors: apixaban, edoxaban, rivarozaban, fondaparinux

38. apixiban (MOA): -Factor Xa inhibitor

  • Eliquis

39. Edoxaban (MOA): -Factor Xa inhibitor

  • Savaysa

40. Rivaroxaban (MOA): -factor Xa inhibitor

  • Xarelto

41. Fondaparinux (MOA): -factor Xa inhibitor

  • Arixtra

42. Pulmonary Embolism: -usually a clot from the leg that blocks the pulmonary vasculature

-attects right ventricle d/t backing up of blood

7 / 14 -congregate settings such as homeless shelters are high risk, including for employees -increased in the mid 90s d/t AIDS but have decreased since 2000s

51. isoniazid (INH): - antiTB

  • take daily for 6-12 months and most likely with other meds too -worked if 3 neg. sputum cultures, no temp.
  • Liver toxicity (hepato) check liver fxn --> JAUNDICE
  • Don't take with alcohol (liver fxn remember?)
  • Take on empty stomach

52. polypharmacy (side effects): - hallucinations

-appetite alterations -tiredness, decreased alertness, AMS -weakness, falls

  • dizziness -skin rashes -anxiety, excitability

53. vertical transmission: when a parasite is transmitted from a parent to its ottspring

54. horizontal transmission: disease is spread through a population from one infected individual to another

55. empiric antimicrobial therapy: 1) site of infection and organism most likely to be colonizing the site

2) prior knowledge of bacteria known to colonize the person

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3) local bacteria resistance patterns of organisms that are available at the hospital

56. (antibiotics that) inhibit cell wall integrity: - penicillins

  • ampicillin
  • cephalosporins
  • carbapenems

57. (antibiotics that) inhibit bacterial protein synthesis: - aminoglycoside

  • tetracyclines
  • fluoroquinolones

58. Fluoroquinolones: use is reserved for pneumonias or exasperations of chronic bronchitis to decrease the potential for development of further

development

59. endotoxic bacteria: -gram negative bacteria that stain red or pink

-stuck to outside of cell and released when the bacteria die

  • LPS

60. exotoxic bacteria: -gram positive bacteria that stain purple

-released from bacteria

61. invasion period: -when immune and inflammatory responses are initiated

62. pneumonia: -infection of lower respiratory tract

-sixth leading cause of death in U.S. -CAP, HCAP, HAP, VAP -HAP has 20-50% mortality

10 / 14 hormonal signals -Millions of distinct B cells develop and "home" to specific sites in the lymph nodes, spleen, and GALT -Come into contact with antigens throughout life -Have immunoglobulin as surface receptors for antigens

68. (types of) T cells: Helper T cells (CD4+): stimulates cytotoxic t cells, B cells, and macrophages to develop immune response

Cytotoxic T cells (CD8+): simulates cell apopotosis Memory T cells: antigen specific t cells that retain a memory of prior infections

69. ABO (compatibility): O is universal donor; AB universal receiver

70. respiratory acidosis (causes): • Depression of the respiratory center.

(1) Head injuries.

(2) Oversedation with sedatives and/or narcotics.

  • Conditions attecting pulmonary function.

(1) COPD

(2) Pneumonia.

(3) Atelectasis.

  • Conditions that interfere with chest wall excursion.

(1) Thoracic trauma: flail chest.

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(2) Diseases attecting innervation of thoracic muscle (Guillain-Barré syndrome, myasthenia gravis, polio).

(3) Mechanical hypoventilation.

71. cytokines (cause fever): These proinflammatory cytokines reach the CNS where, through induction of central mediators such as prostaglandins

(PGs), they are able to increase the temperature set point and cause fever -hypothalamus regulates temperature

72. Asthma: -chronic inflammatory disorder of the bronchial mucosa that causes bronchial hyper-responsive- ness, constriction of the airways, and

variable airflow obstruction that is reversible -chest constriction, expiratory wheezing, dyspnea, nonproductive coughing, prolonged expiration, tachycardia, an tachypnea, pulsus paradoxus, respiratory alkalosis, hypoxemia

73. pulsus paradoxus: beats have weaker amplitude with respiratory inspiration, stronger with expiration

74. increased (RR): - Fever

  • Asthma
  • Dehydration
  • COPD
  • Hyperventilation
  • Lung conditions
  • Infections
  • Newborns
  • Acidosis
  • Overdoses

13 / 14 promotes a higher blood volume and pressure -promotes potassium excretion -acts on late distal tubule and collecting duct of kidney

83. loop diuretics (MOA): Act on ascending loop of Henle, inhibit sodium-potassium-chloride transporter; decrease renal vascular resistance

84. thiazide diuretics (MOA): Decrease sodium reabsorption at distal convoluted tubule; net loss of sodium and potassium

85. potassium sparing diuretics (MOA): Aldosterone antagonist in the distal convoluted tubule

86. atrial netriuretic peptide: acts acutely to reduce plasma volume by at least 3 mechanisms: increased renal excretion of salt and water,

vasodilation, and increased vascular permeability.

87. edema (oncotoic pressure): Edema occurs when there is a decrease in plasma oncotic pressure, an increase in hydrostatic pressure, an increase in

capillary permeability, or a combination of these factors. Edema also can be present when lymphatic flow is obstructed.

88. angiotensin: a peptide hormone that constricts blood vessels, causes the retention of sodium and water, and produces thirst and a salt appetite

89. amiodarone (pharmacokinetics): Onset: 2-3 days (oral) Within minutes (IV)

Peak Ettect: 3-7 days (oral) Duration: varies Half-life: 40-55 days

90. heart failure (patients): have more than just heart failure. look for underlying angina, HTN...

91. digoxin (and electrolytes): hypomagnesemia, hypercalcemia, and hypokalemia

92. hyperkalemia (renal failure): renal failure results in elevated potassium levels because the body cannot clear the excess potassium from

the blood stream through the kidneys like it normally does.

93. hyperkalemia (addison's disease): deficiency of aldosterone will result in decreased excretion of potassium

94. hypercalcemia (treatment): -calcitonin, pamidronate (nitrogen containing biphosphonate

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95. compensatory hyperplasia: an adaptive mechanism that enables certain organs to regenerate; occurs significantly in epidermal and intestinal

epithelia, hepatocytes, bone marrow cells, fibroblasts, and some bone, cartilage, and smooth muscle.

96. naproxen: NSAID said for use in CAD patient

97. NSAIDs (MOA): Reversibly inhibit COX-1 & COX-2 Block

prostaglandin synthesis

98. COX 2 inhibitor (MOA): Inhibits COX-2, but does not inhibit COX- 1

99. NSAID alternative: COX 2 inhibitors; given with risk of GI bleed (indicated by darkening stool and epigastric pain)

100. diphenhydramine (side effects): Cardiovascular: tachycardia, hypotension, palpitations Neurological: drowsiness, seizures

Respiratory: mucus plugs, wheezing

101. lortadine: lack of sedation and impairment of performance, longer duration of action, and absence of anticholinergic side ettects.

102. dimenhydrinate (onset of action): within 15 minutes; lasts 3-6 hours

103. (patients with history of kidney stones should) avoid: calcium

104. tendon rupture:

Fluoroquinolones have a black box warning for or tendonitis. There is an increased risk in elderly patients.

105. Pseudomembranous colitis: Clindamycin, ampicillin, cephalosporins (C. ditt)

106. chronic pain: episode of pain that lasts for 6 months or longer; may be intermittent or continuous. NOT cancer pain