Exam 2: Special Pop. & Antibiotics Flashcards

(47 cards)

1
Q

What are the age groups associated with different pediatric titles?

A
  • Preterm/premature: <36wk gestational age
  • Neonate: <30d
  • Infant: 1mo-1yr
  • Child: 1-12yr
  • Adolescent 12-18yr
    not little or small adults, less data from trials b/c ethics
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2
Q

What affects pharmacokinetic in all Pediatrics?

A
  • Developing tissues and organs
  • Changing pt body proportions, composition, maturation, & development
  • Body Surface Area: > in peds
  • Short/Long-term effect on growth & development
  • Underlying congenital, chronic, and current disease effect on drug (& vice versa)
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3
Q

What is the difference between growth, development, and maturation?

A
  • Growth: quantitative change in size of body/parts
  • Development: qualitative change in skills or function
  • Maturation: slower, genetically controlled, development independent of environment
    (May not need to know)
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4
Q

How does pediatric body composition affect pharmacokinetics?

A
  • Neonate TBW is high ~75-80%
  • @ 3 months decreases ~65%
  • decrease compensated by increase body fat
  • 2yrs dec body fat, & liver & kidney maximum relative size
    (doubles 5 mo., 1yr - weight 3x, BSA & length 2x, changes water/fat/protein)
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5
Q

How is PO absorption affected in pediatrics?

A

low lipase & no amylase - affect fat soluble
- gut flora > development in breast fed infant
- Gastric pH: alkaline - inc basic drugs, dec acidic drugs
- preterm & full-term neonates: delayed gastric emptying
- neonates & infants: irregular peristalsis (inc. A)
- Young children: greater size duodenum (inc. A)

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6
Q

How is IM absorption affected in pediatrics?

A
  • Neonates: dec muscle mass & activity –> dec blood flow/A
    Infants: > muscle capillaries density –> inc A
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7
Q

How is percutaneous absorption affected in pediatrics?

A

Neonates and infant
- Skin: dec thickness, inc hydration, dec fat
- MUCH > A than adults –> toxicity

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8
Q

How is rectal absorption affected in pediatrics?

A
  • avoids first pass elimination
  • A erratic & incomplete in neonates & infants (feces, frequency, lack sphincter control)
    (is still used)
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9
Q

What affects pharmacokinetics in pregnancy?

A
  • Physiologic changes (CV, GI, renal, hormonal)
  • Placental-fetal unit: drug cross, amount metabolized
  • Fetus distribution & elimination drug by fetus
  • Underlying congenital, chronic, or current disease
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10
Q

How is absorption affected by pregnancy?

A
  • PO: Gastric: inc pH, dec motility, inc emptying (slower)
    inc cardiac output –> intestinal blood flow may cancel out affect: min effect on bioavailability & therapeutic effect
  • Percutaneous: inc by vasodilation, blood flow & water content
  • Musocal
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11
Q

How is pulmonary absorption affected by pregnancy and being an infant or child?

A
  • Pregnancy: inc cardiac & tidal vol (50%) inc blood flow & transfer consider dose reductions
  • Infant & children: lower tidal vol & inc RR consider dose inc
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12
Q

How does pregnancy affect drug distribution?

A
  • inc blood vol & inc total body water, body fat Vd: dilutional effect, arterial pH
  • Dec: albumin concentration
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13
Q

What affects drug distribution in pediatrics?

A

preterm & neonates
- vascular perfusion: respiratory distress syndrome blood from lungs to tissues & organs
- body composition inc TBW, inc Vd of hydrophilic
- tissue-binding characteristics: inc free drug
- physiochemical properties: lipophilic percu drug A
- plasma protein binding: lower a-1 acid glycoprotein –> inc Vd & concentration free drug
- Route of administration; first pass/IV

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14
Q

What is important about metabolism in pediatrics and pregnancy?

A
  • Ped: Ultra-metabolizers die from morphine/opioid metabolites
  • Pregnancy: some enzymes induced others inhibited, (200-300% inc lower concentration lamotrigine, antiepileptic)
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15
Q

How is excretion affected in pediatrics and pregnancy?

A
  • Ped: inc first 2 wks, adult rate 1yr, exceeds 2yrs, immature renal system & dec CO –> dec renal blood flow –> dec renal elimination –> inc drug half-life
    – usually directly proportional to age
  • Preg: inc GFR b/c inc CO dec albumin –> inc renal elimination (Lithium clearance doubled)
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16
Q

What increases a drug’s ability to cross the placenta?

A
  • Lipid soluble drugs
  • Nonionized drugs: heparin ionized so can be used in preg
  • Unbound (“free”) drugs
  • Lower molecular weight (small)
  • P-glycoprotein inhibitors “gandalf”
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17
Q

What is the placental fetal physiology?

A
  • Metabolism: liver enzymes present from 7-8wks but immature
  • Fetal physiology: gestational age at time of drug exposure (ACEI & aspirin more dangerous later)
    – First 14d post conception embryo protected (totipotency SC) after 14 susceptible (first 3 mo most important)
    – olderL TBW dec, fat inc –> inc lipophilic effect
  • Teratogenicity of drugs: cause fetal dysgenesis. Factors: gestational age @ exposure, agent/medication, length exposure
  • Weigh risk vs benefit
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18
Q

How is pregnancy risk noted for drugs?

A
  • No longer used: A, B, C, D, X (after 2018)
  • Now more information needed (after 2001)
    – not apply to approved before 2001 or OTC meds
  • Pregnancy: risk summary, clinical considerations, & data, pregnancy exposure registry
  • Lactation: risk summary, clinical considerations, data: in breast milk & potential effect on infant
  • Reproductive: info for pregnancy testing, contraceptive recommendations, infertility info
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19
Q

What do we want to know with drugs and lactation?

A
  • Does this drug get into the breast milk
  • How does it affect the baby
    1) Absorption into maternal circulation: [plasma] most enter breastmilk passive diffusion
    2) Blood flow to the breast: inc blood flow inc drug in milk
    3) Plasma pH (7.45) & milk pH (7.08) favor higher pH
    4) Mammary tissue composition higher fat in breast tissue, high lipophilic drug in breast milk
    5) Breast milk composition: high affinity protein, fat, water, vitamin, > likely in breastmilk
    6) Drug properties more likely in breast milk if low weight, ionization, protein binding, high lipophilicity
    7) Drug-protein binding in plasma higher then lower in breast milk
    8) Rate of breast milk production: greater –> more diluted
20
Q

What types of drug are preferred or avoided in lactation?

A

Prefer
- Shorter half-lives
- lowest effective dose
- least serious AE
Avoid
- Sustained release (SR)
- High oral bioavailability
Other suggestions
- take dose immediately after breast feeding
- pump and discard milk for short-term illness where risk of drug is thought to outweigh benefits of breastfeeding

21
Q

How should drugs be selected in pediatrics?

A
  • Risks & benefits
  • Long-term effects
  • Dosage formulation
  • Obesity
    – use weight-based dose, UNLESS exceeds recommended adult dose
22
Q

What are the aspects of weight-based dosing?

A
  • Body-weight dosing: most common (mg/kg/d or mg/kg/dose)
  • Body-Surface Area (BSA): reserved for antineoplastic (chemo) agents or critically ill

Conversion factor: 1kg/2.2lb

23
Q

What are the routes of administration for pediatrics?

A
  • Oral: liquid preferred oral syringe (in cheek & gum) or calibrated cup
    (crush & mix sometimes ok, never mix drug w/ baby bottle - drug-nutrient interactions & incomplete dosing)
  • Rectal
  • Parental:
  • Inhaled (Pulm):
    – pMDI: all children need tube spacer
    Valved holding chamber (VHC) + face mask for pt <4yrs old
24
Q

How do you prevent pediatric medication errors?

A
  • Up-to-date allergy profile
  • Weight
  • State specific dosage strengths for formulation
  • Do not abbreviate drug names or pt instructions
  • Avoid abbreviations for dosage units
  • Zero before decimal
  • Avoid zero after decimal
  • Standardize concentrations of high-alert medications
  • Use oral syringes for liquids
  • Create drug order pathways for protocols
  • Collaborate & educate all healthcare members
  • Automated dispensing cabinets, smart infusion pumps, bar coding
25
Why are older adults pharmacologically challenging?
- Physiology - Multiple comorbid conditions - Adherence: cognitive & social issues - Lack of testing - Fastest growing age group (review)
26
How is absorption affected in older adults?
- Oropharyngeal muscle dysmotility & altered swallowing - Dec esophageal peristalsis & lower esophageal sphincter pressure - Dec gastric motility, secretion emptying - Dec Propulsive motility of colon - Impair mucous-bicarbonate barrier (review) - **dec blood flow** - **inc gastric pH** - **dec gastric emptying**
27
How is distribution affected in older adults?
- **Dec lean muscle mass**, **inc fat stores** - **dec** body water content - **dec** serum **albumin** - Inc Vd of lipophilic can --> **inc half-lives** (Diazepam in young adults 20 hrs, elders 70hrs+)
28
How is metabolism affected in older adults?
- **Dec hepatic size & blood flow** - Dec phase one --> dec total body clearance (**dec enzymatic activity**) - Phase II **not** affected
29
How is excretion affected in older adults?
- Dec renal blood flow (GFR dec 1%/yr after 40, & accelerates advanced age) - **dec secretion** - dec lean body mass--> dec creatinine formation + **dec GFR** can make serum creatinine appear normal - **Normal SCr x= normal GFR** - Use Crockcroft-Gault or MDRD
30
What are the pharmacodynamic changes in the older adult?
- Inc CNS effects of drugs - Inc sedative effects of agents - Changes in CV system: orthostatic hypotension b/c loss baroreceptor reflex & change in cerebral blood flow
31
What causes polypharmacy in the older adult?
- Varied symptoms & complaints associated w/ multiple chronic illnesses - Pressure to "prescribe something" - Prescribing cascade: add when unsuccessful - Pt stockpiling meds b/c cost - Pts sharing meds - Poly-providers: multiple specialists, need PCP - Self-prescribe OTC
32
What is important about adverse drug reactions in older adults?
- Any symptom in elderly considered side effect until proven otherwise - Preventable AE: falls, fractures, delirium - Older women > risk b/c receive more Rx & > muscle loss
33
What are common drug-disease interactions in Older adults? (FYI)
**Anticholinergics**, **TCA**, nonaspirin NSAIDs, first-gen calcium channel blockers, opioid analgesics, barbiturates, benzodiazepines, corticosteroids, antipsychotics, sedative hypnotics, digoxin, metoclopramide, aspirin, thioridazine, bupropion, alpha-blockers
34
What lifestyle factors may influence adverse drug reactions?
- **alcohol** & recreational drugs - **Caffeine & nicotine use**
35
What are adherence issues in older adults?
- 40% don't take properly, & take more than 5med/wk - **Cost factors** - **Side effects** - **Physical & mental changes** (vision, arthritis) - **Self-medicating** (& X telling PCP)
36
What are special considerations for long-term care for older adults?
- 50% residence fall annually - Required to receive monthly drug regimen review - **Antipsychotics:** over dx as chem restraint (include muscle reactants, anticholinergics, antihistamines, OTC natural & herbals) -- 14-day limits when PRN - **Anxiolytics**: nonpharmacologic preferred (SSRI > benzos) - **antidepressants**: SSRI > TCAs but drug interactions & SE - **Severe or persistent pain**: tolerance decreases w/ age - **Urinary incontinence, UTIs**: AMS - **Respiratory infections**: spread quickly through facilities - **Constipation**: nonpharmacologic (activity, prune juice, fiber) over meds
37
How can providers reduce psychotic medication use?
- Prevent inappropriate initiation - Taper & discontinue inappropriate - Endure appropriate use/monitoring/documentation - Improve disruptive behaviors w/o psychotropic meds - Encourage more structured & broader approach to manage behaviors (Review)
38
What are nonpharmacologic antianxity treatments?
- Est daily routines in structured environment - Consistent caregiving & hygiene assistance - Avoid overstimulation - Limit social visits - Schedule quiet time w/ rests/naps (Review)
39
What are primary guidelines for safely prescribing to older adults?
- **Beer's criteria: consensus-based document listing potentially inappropriate medications for use in older adults and guidelines for safe prescribing practices** - Choose wisely: "Five things to question" 1) Dementia & Behavioral & Psychological Symptoms of Dementia 2) Screeding & Medication Management 3) Antibiotic use 4) Diabetes management 5) Nutritional management
40
Why should you question Dementia & Behavioral & Psychological Symptoms of Dementia?
- **Avoid** Rx **cholinesterase inhibitors** w/o periodic assessment for cognitive & GI effects: 12 wk trial - Assess use of chemical & physical restraints -- **antipsychotics** limited benefit & serious harm: **limit to pt w/ imminent threat to themselves or others** - Avoid as first choice for BPSD assess underlying cause - Avoid benzos/sedatives as first choice for insomnia, agitation, or delirium -- reserve for alcohol withdrawal/delirium tremens (DTs) or severe generalized anxiety disorder (GAD) - Avoid physical restraints for hospitalized older adults when delirium is identified **proper & thoughtful use**
41
Why should screening and medication management be questioned?
- Consider benefit of screening - what do with information esp when life expectancy is <10 yrs - Hypercholesterolemia no longer major risk factor at older ages - Monthly review LTC residents for unnecessary and underuse of meds **some not beneficial b/c limited effectiveness and/or dangerous AE**
42
Why should antibiotic use be questioned?
- **Do not use antimicrobials for asymptomatic bacteriuria in older adults** - May --> erroneous assumption UTI cause AMS --> fail detect problem - Leads to antibiotic overuse which can cause other problems **X request UA or Rx antibiotics w/o clear indication**
43
What should diabetes management be questioned?
- Basal/bolus insulin therapy over sliding scale insulin (SSI), unless short-term in hospital, because more closely mimics normal physiology - Set reasonable AIc goals, it takes time to have microvascular benefits from tight glycemic control -- **7-7.5%** healthy >65 yo w/ long life expectancy -- **7.5-8%** with moderate comorbidity & lief expectancy <10yrs -- **8-9%** w/ multiple comorbidities & shorter life expectancy
44
Why should nutritional management be questioned?
- **Percutaneous feeding tubes** X prolong/improve QOL in pt w/ advanced dementia -- (fluid overload, diarrhea, abdominal pain. local complications, less human interaction, inc risk aspiration) -- avoid appetite stimulants & high-calorie supplements to treat anorexia/cachexia -- preferred: oral-assisted feedings
45
What are secondary guidelines for safe prescribing to older adults?
- **Explore alternatives to medications** - **Simplify the regimen**: 2 conditions tog, lowest dose - **Edu adults & caregivers**: fear after reading package inserts - **Review medications**: bring & review @ every appointment, esp + specialists & ER
46
What are the methods of therapeutic monitoring?
- Pill boxes: check & count - Open-ended questions: how many days/week do you miss taking meds - Routinely schedule and monitor labs when patients are on meds with narrow therapeutic index - Diuretics & ACEI: periodic renal profile for electrolyte imbalances, renal insufficiency, and/or renal artery stenosis
47
What are the medications with narrow therapeutic ranges?
- Warfarin - Theophyllin - Lithum - Phenetoyn - Gentamycin - Digoxin - Carbamazepine - Valproic acid