Week 3 Reverse Flashcards

1
Q

Renally cleared metabolites may accumulate in renal dysfunction, increasing the risk of toxicity.

A

Active Metabolites

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2
Q

Often requires increased dosages or shorter intervals between doses for effective treatment.

A

Adolescent Metabolism

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3
Q

More common in the Older Adult due to polypharmacy and age-related changes in drug processing.

A

Adverse Drug Event (ADE) by Age

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4
Q

Leads to altered drug responses, necessitating careful monitoring and dosage adjustments.

A

Age-Related Physiologic Decline

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5
Q

Lower levels can increase the free drug concentration, particularly for highly protein-bound drugs.

A

Albumin

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6
Q

Impairment can lead to drug accumulation and potential toxicity.

A

Biliary Excretion

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7
Q

High levels can cause jaundice, and drugs that displace bilirubin (like ceftriaxone) are used cautiously in neonates.

A

Bilirubin Levels in Neonates

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8
Q

Infants have higher water content, which impacts hydrophilic drug distribution and dosing.

A

Body Composition in Infants

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9
Q

Alters the volume of distribution for lipophilic drugs, like diazepam, increasing their half-life.

A

Body Fat impact on Lipophilic drugs

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10
Q

Lipophilic nature of drugs should be considered when prescribing to breastfeeding mothers to avoid drug-related adverse effects in infants. Must monitor infant for clinical adverse effects.

A

Breast Milk Transfer

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11
Q

Anticholinergics and sedatives are known to worsen cognitive function in Older Adult patients.

A

Anticholinergics and Cognitive Impairment

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12
Q

Requires careful management to avoid adverse drug interactions and liver toxicity.

A

Complex Medication Regimens

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13
Q

Essential for minimizing polypharmacy and reducing adverse effects in chronic disease management.

A

Deprescribing

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14
Q

Crucial for determining safe and effective dosing strategies for pediatric patients.

A

Developmental Pharmacology

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15
Q

Older Adult patients are at higher risk, particularly with drugs that have narrow therapeutic indices.

A

Drug Injury

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16
Q

Factors like lipid solubility and protein binding affect the degree of transfer and potential infant exposure.

A

Drug Transfer in Breast Milk

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17
Q

Important to consider in Older Adult patients with multiple chronic diseases.

A

Drug–Disease Interaction

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18
Q

Medication use during this period is common and must be carefully considered due to potential teratogenic effects.

A

First Trimester

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19
Q

Affects medication adherence and necessitates adjustments in drug regimens to account for limitations.

A

Functional Decline

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20
Q

Higher in infants, leading to changes in drug absorption and bioavailability compared to adults.

A

Gastric pH in Infants

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21
Q

Enzyme-specific variations can increase or decrease drug clearance, affecting therapeutic levels.

A

Hepatic Clearance

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22
Q

Higher doses may be needed in infants to achieve therapeutic levels.

A

Hydrophilic Drugs in Infants

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23
Q

Influenced by gastric pH, which changes with age, especially in infants.

A

Ionization and Age

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24
Q

Often preferred in pediatrics due to ease of administration compared to tablets or capsules.

A

Liquid Oral Formulation

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25
Critical in Older Adult patients to avoid drug duplication, omissions, and interactions.
Medication Reconciliation
26
Common in the Older Adult, as altered pharmacokinetics can increase the risk of toxicity.
Narrow Therapeutic Index Older Adults
27
Drugs with a narrow index require precise dosing, particularly in renal impairment.
Narrow Therapeutic Index Renal Impairment
28
Requires careful monitoring and dose adjustments due to immature liver and kidney function.
Neonatal Drug Metabolism
29
Necessary due to differences in drug processing compared to adults.
Pediatric Dose Adjustments
30
Altered due to changes in receptor sensitivity, leading to differences in therapeutic outcomes and side effects.
Pharmacodynamics in Geriatrics
31
Can vary significantly due to changes in receptor sensitivity and physiological adaptations.
Pharmacodynamics in Pregnancy
32
Affected by factors like decreased hepatic and renal function, impacting drug absorption, distribution, metabolism, and excretion.
Pharmacokinetics in Geriatrics
33
Requires age-specific adjustments due to developmental differences across neonates, infants, children, and adolescents.
Pharmacokinetics in Pediatrics
34
Includes changes in absorption, distribution, metabolism, and excretion due to physiological adjustments.
Pharmacokinetics in Pregnancy
35
Critical for adjusting medication regimens to prevent toxicity in patients with reduced kidney function.
Pharmacokinetics in Renal Impairment
36
Immature at birth, affecting drug breakdown and leading to potential toxicities in young children.
Phase 1 and Phase 2 Enzymes in Neonates and Children
37
Pregnancy affects these pathways variably, impacting drug levels and effectiveness.
Phase 1 and Phase 2 Metabolism in Pregnancy
38
Older Adult patients may experience altered metabolism, increasing the likelihood of drug accumulation and toxicity.
Phase 1 and Phase 2 Metabolism in Older Adults
39
Lower levels in neonates can increase the risk of drug displacement, leading to conditions like jaundice.
Plasma Binding Proteins in Neonates
40
Decreases in pregnancy, leading to higher free drug concentrations.
Plasma Protein Binding in Pregnancy
41
Decreased in liver disease, leading to higher free drug concentrations and potential toxicity.
Plasma Protein Binding in Liver Disease
42
Increases the risk of adverse drug effects, especially in Older Adult patients with multiple chronic conditions.
Polypharmacy
43
Can lead to unnecessary polypharmacy and increase the risk of adverse drug reactions.
Prescribing Cascade
44
In the Older Adult, often complicated by polypharmacy and the use of PIMs.
Prescribing Patterns
45
Liver dysfunction can impact the activation of prodrugs, affecting their efficacy.
Prodrug
46
Pediatric patients with immature liver function may struggle to activate prodrugs, reducing efficacy.
Prodrugs in Children
47
Lower protein levels in pediatrics lead to a higher free drug fraction, impacting drug effects.
Protein Binding in Pediatrics
48
Can affect the levels of drugs in the body, particularly in patients with altered renal function.
Reabsorption and Renal Function
49
Decreased in patients with renal impairment, necessitating dose adjustments.
Renal Clearance in Renal Impairment
50
Matures over time; neonates have lower renal clearance, affecting dosing for drugs primarily excreted by kidneys.
Renal Clearance in Neonates
51
Decreased levels in liver disease can affect drug binding and distribution.
Serum Albumin in Liver Disease
52
Used in the Child-Pugh score to assess liver function and potential drug clearance impact.
Serum Bilirubin and Drug Clearance
53
Drugs like warfarin and ACE Inhibitors are known teratogens and should be avoided during pregnancy.
Teratogenic
54
Especially important for drugs metabolized by the liver with narrow therapeutic indices.
Therapeutic Drug Monitoring
55
Can vary widely across life stages, with higher variability in pediatrics.
Therapeutic Response
56
Affects the volume of distribution for hydrophilic drugs, requiring dose adjustments in Older Adult patients.
Total Body Water in Older Adults
57
Impacts the dosing of hydrophilic drugs, as lower body water alters their volume of distribution; requires dose adjustments based on age.
Total Body Water and Hydrophilic Drugs
58
Increases in pregnancy due to higher total body water and fat, requiring dosing adjustments.
Volume of Distribution (VD) in Pregnancy
59
Higher VD in infants due to body water content affects dosing for hydrophilic drugs.
Volume of Distribution (VD) in Infants
60
Practical but does not account for developmental differences in drug absorption, distribution, and metabolism.
Weight-Based Dosing