Exam 2: Special Pop. & Antibiotics Flashcards
(47 cards)
What are the age groups associated with different pediatric titles?
- 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
What affects pharmacokinetic in all Pediatrics?
- 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)
What is the difference between growth, development, and maturation?
- 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)
How does pediatric body composition affect pharmacokinetics?
- 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)
How is PO absorption affected in pediatrics?
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)
How is IM absorption affected in pediatrics?
-
Neonates: dec muscle mass & activity –> dec blood flow/A
– Infants: > muscle capillaries density –> inc A
How is percutaneous absorption affected in pediatrics?
Neonates and infant
- Skin: dec thickness, inc hydration, dec fat
- MUCH > A than adults –> toxicity
How is rectal absorption affected in pediatrics?
- avoids first pass elimination
- A erratic & incomplete in neonates & infants (feces, frequency, lack sphincter control)
(is still used)
What affects pharmacokinetics in pregnancy?
- 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
How is absorption affected by pregnancy?
- 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
How is pulmonary absorption affected by pregnancy and being an infant or child?
- Pregnancy: inc cardiac & tidal vol (50%) inc blood flow & transfer consider dose reductions
- Infant & children: lower tidal vol & inc RR consider dose inc
How does pregnancy affect drug distribution?
- inc blood vol & inc total body water, body fat Vd: dilutional effect, arterial pH
- Dec: albumin concentration
What affects drug distribution in pediatrics?
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
What is important about metabolism in pediatrics and pregnancy?
- Ped: Ultra-metabolizers die from morphine/opioid metabolites
- Pregnancy: some enzymes induced others inhibited, (200-300% inc lower concentration lamotrigine, antiepileptic)
How is excretion affected in pediatrics and pregnancy?
- 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)
What increases a drug’s ability to cross the placenta?
- Lipid soluble drugs
- Nonionized drugs: heparin ionized so can be used in preg
- Unbound (“free”) drugs
- Lower molecular weight (small)
- P-glycoprotein inhibitors “gandalf”
What is the placental fetal physiology?
- 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
How is pregnancy risk noted for drugs?
- 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
What do we want to know with drugs and lactation?
- 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
What types of drug are preferred or avoided in lactation?
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
How should drugs be selected in pediatrics?
- Risks & benefits
- Long-term effects
- Dosage formulation
- Obesity
– use weight-based dose, UNLESS exceeds recommended adult dose
What are the aspects of weight-based dosing?
- 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
What are the routes of administration for pediatrics?
- 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
How do you prevent pediatric medication errors?
- 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