Pediatrics Flashcards

1
Q

Define gestational age (GA)

A

Time from conception until birth

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2
Q

Define postnatal age (PA)

A

Chronological age since birth

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3
Q

What is post-conceptual age (PCA)/Corrected Gestational Age (CGA)/ Postmenstrual Age (PMA)?

A
  • Age since conception
  • PCA = GA + PNA
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4
Q

Lucy is an 11 day old neonate that was born at 30 weeks, 2 days gestational age. What is Lucy’s corrected gestational age?

A

31 weeks, 6 days

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5
Q

How old is a premature neonate?

A

< 37 weeks gestational age

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6
Q

How old is a full term neonate?

A

Neonate born 37-41+6/7 weeks gestational age

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7
Q

How old is a neonate?

A
  • Full term neonate up to 28 days PNA
  • Premature neonate whose PCA is <= 42-46 weeks
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8
Q

How old is an infant?

A

1 month to <1 year of age

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9
Q

How old is child/children?

A

1 year to 12 years of age

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10
Q

How old is adolescent?

A

13 years to <18 years of age

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11
Q

How does pH of a child differ from an adult?
How does that affect absorption of acid labile compounds and weak acids?

A

Changes in gastric pH (higher pH earlier in life)
- Absorption of acid labile compounds is increased (e.g., penicilin)
- Absorption of weak acids is decreased (e.g., phenobarbital)

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12
Q

How does absorption differ for neonates? (4)

A
  1. Gastric motility increases with age (normalizes at ~4 months of age)
    - Increased time for gastric emptying and decreased intestinal motility in first months of life
    - Slower drug absorption and longer Tmax in neonates and young infants vs older infants and children
  2. Increased topical absorption in neonates/infants
  3. Reduced skeletal muscle blood flow and inefficient muscular contractions in neonates
  4. Higher density skeletal-muscle capillaries in infants compared to older children
    - Altered absorption in subcutaneous and intra-muscular drug absorption
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13
Q

How does total body water change during the following stages of life:
1. Fetus
2. Preterm neonate
3. Term neonate
4. Adults

A
  1. 94%
  2. 85%
  3. 78%
  4. 60%
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14
Q

How does distribution differ for neonates/infants? (3)

A
  1. Neonates + Infants have very large extracellular and total-
    body fluid
    - Higher Vd of hydrophilic drugs (e.g. gentamicin)
  2. Decreased circulating albumin and alpha-1-acid glycoprotein
    - Increased unbound (free) fraction drug
  3. Higher amount of endogenous products (i.e. unconjugated bilirubin, free fatty acids)
    - Displace drugs from binding sites
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15
Q

What CYP enzymes appear at the following stages of life?
1. First few hours (2)
2. 2. First week (3)
3. First 1-3 months (1)

A
  1. Appear in first few hours: CYP 2D6 and CYP 2E1
  2. First week of life: CYP 2C19, CYP 2C9, CYP 3A4
  3. First 1-3 months of life: CYP 1A2
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16
Q

How do phase II enzymes change with age?

A

Glucoronyltransferase (UGT) increases with age
- Ex// acetaminophen and morphine

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17
Q

How is elimination different for pediatrics? (3)

A
  1. Tubular secretion is immature in neonates/infants
  2. Glomerular filtration increased with age
    - Rapid increase in 1st two weeks of life
    - Reaches adult values at 8-12 months of age
  3. Impacts drugs with primarily renal clearance
    - Ex. Vancomycin, aminoglycosides
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18
Q

What is the best equation to estimate CrCl in pediatrics?

A

Bedside Schwartz uses k = 0.413

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19
Q

What are some considerations when using the Schwartz equation? (3)

A
  1. Remember: this is only an ESTIMATE! Clinical picture and trends remain crucial when evaluating
  2. Validated mostly in chronic kidney disease patients, up to moderate CKD (eGFR 15-75 mL/min)
  3. Study Limitations:
    - Rapidly changing serum creatinine*
    - Infants < 1 year
    - Obesity
    - Malnutrition
    - Muscle wasting
20
Q

What are some dosing considerations for pediatrics? (3)

A
  1. Doses are generally based on body weight
    - CHECK: mg/kg/day or mg/kg/dose
  2. Body Surface Area
    - Chemotherapy and some biologics
    - Mosteller Formula most commonly used
  3. Total daily dose of a medication should not exceed adult
    maximums
    - Caution in overweight children
    - Example: ceftriaxone, amoxicillin
    - Few exceptions: ex// vancomycin or antibiotics used in cystic fibrosis
21
Q

Should maybe know some professional resources for pediatric meds and conditions (4)

A
  1. Pediatric and Neonatal Lexi-Drugs
  2. BC Children’s Online Formulary (pedmed.org)
  3. NeoFax
  4. CHOP or Toronto SickKids Hospital
22
Q

Many dosage forms are not suitable for children. Which ones/why? (5)

A
  1. Capsules
  2. Tablets
    - Can they Swallow?
  3. Syrups
    - Ketogenic Diet?
  4. Suspensions
  5. Solutions
    - Palatability?
    - What is the volume?
23
Q

What are some way to increase palatability for oral meds? (5)

A
  1. Chocolate/strawberry syrup – coats tongue
  2. Peanut butter – coats tongue
  3. Applesauce – masks flavor, provides medium for mixing
  4. Ice cream – cold minimizes flavor, numbs taste buds
  5. Flavoring agent
    - Risk of “ruining” flavor for patient
24
Q

What are some considerations when using the Aliquot method? (3)

A
  1. Final volume must be a volume the child can tolerate
    - E.g. don’t dilute into 50 mLs for a 1-year old child – that’s too much volume!
  2. Is the final volume something that is easily measurable?
    - 2 mLs vs 2.5 mLs vs 2.58 mLs
  3. Is the tablet readily dissolvable in solution?
    - Is the tablet available in chewable?
    - Is it enteric coated or time release?
25
Q

What are some tips for oral administration for peds? (5)

A
  1. Do not administer the liquid straight back into the throat
  2. Slowly introduce the medication to the rear cheek
  3. Always use standardized measuring syringes or cups, NOT
    household table/tea spoons
  4. What if the child throws up after giving the medication?
    - 30 minute rule
    - If the medication is given, child throws up < 30 minutes after administration, can dose again. Do not repeat if dose thrown up a 2nd time
    - If the medication is given, child throws up > 30 minutes after administration, DO NOT repeat the dose.
  5. Taste/flavouring
26
Q

What are some resources for tube administration? (2)

A
  1. Lexicomp under “Administration” section
  2. Handbook of Drug Administration via Enteral Feeding Tubes
27
Q

What are 3 types of parenteral access lines in peds?

A
  1. Peripheral IV
  2. Central IV
    - Peripherally inserted central catheter (PICC)
    - Broviac catheter
    - Umbilical catheter (neonates only)
  3. Intraosseous catheters
28
Q

What are 2 methods to calculating total daily fluid requirements?

A
  1. Formula method
  2. 4/2/1 method
29
Q

Explain the 4/2/1 method

A

To calculate hourly maintenance fluid rate
4 ml/kg/hr each of the first 10kg +
2 ml/kg/hr for next 10 kg +
1 ml/kg/hr for each additional kg above 20

30
Q

What is the empiric fluid selection for child?

A

D5W/NS for all children 1 month CGA to 18 years old
Excluding:
- Renal or Cardiac disease
- Diabetic ketoacidosis
- Severe burns
- Underlying conditions that affect electrolyte regulation

31
Q

For peds, blood pressure assessment requires ___, ___, and _______

A

age, sex, height

32
Q

For peds, HTN is generally classified as what?

A

Either SBP or DBP greater than 95th percentile

33
Q

No need to memorize values, but should know in general if in peds are the following higher or lower compared to adults:
- Blood pressure
- Heart rates
- Resp rates

A
  • BP typically lower
  • HR and RR typically higher
34
Q

What are some ways to take temp in children? (5)

A
  1. Rectal - gold standard but invasive
  2. Axillary
  3. Oral - generally preferred in children who can coordinate
  4. Tympanic
  5. Infrared
35
Q

What is normal temp in children?

A
  1. Standard “normal” is 37.2°C – with variation within a day
    of 0.5°C
    - Morning nadir, late-afternoon/early-evening peak
  2. Neonates and infants have higher temp vs older children
    and adults
    - Higher surface-area to body-weight ratio
    - Higher metabolic rate
36
Q

What antibiotics are relatively contraindicated in less than 8 years old?

A

Tetracycline and derivatives (doxycycline, minocycline)
- Tetracycline chelates with Ca to form tetracycline-Ca complexes which deposit into developing bones and teeth

37
Q

Fluoroquinolones contraindicated in peds why?

A
  1. NOT recommended for use by Health Canada and FDA
  2. Risk of Arthropathy
    - Juvenile Animal data showing adverse effects on cartilage development
    - Appears to be a small absolute risk increase in musculoskeletal adverse events
    - Severe arthropathies (i.e. tendon rupture) necessitates avoiding unless necessary
38
Q

When might fluoroquinolones potentially be used in peds? (2)

A
  1. Potential use when it is reasonable alternative to parenteral therapy
  2. Limited use to when no safe and effective alternative
    exists…
    - Example: multi-drug resistant organisms in cystic fibrosis (e.g. pseudonomas aeruginosa), Extended-spectrum β-lactamase producing (ESBL) organisms, prophylaxis for extended neutropenia in oncology patients
39
Q

Septra (Sulfamethoxazole/Trimethoprim) used in peds?

A

Contraindicated in less than two months of age
- Sulfa antibiotic displaces bilirubin from protein binding sites → hyperbilirubinemia and kernicterus
- Kernictereus – permanent brain damage resulting from hyperbilirubenemia in blood
– Can result in cerebral palsy, hearing loss, problems with vision, growth, and intellectual disabilities

40
Q

High dose amoxicillin/clavulanate in peds? (3)

A
  1. High-dose amoxicillin (90 mg/kg/day) often used to overcome streptococcus pneumoniae resistance
    - Addition of clavulin broadens antimicrobial coverage
    - Clavulinic acid doses greater than ~8 mg/kg/day may be associated with excessive diarrhea
  2. Amoxicillin/Clavulanate available as 4:1 & 7:1 formulation
  3. You may see TWO different amoxicillin prescriptions to achieve high-dose amoxicillin without giving high-dose clavulanate
    - To achieve a 14:1 ratio
41
Q

Acetylsalicylic Acid use in peds? (3)

A
  1. Do NOT use as an anti-pyretic or analgesic in children
  2. Association of Reye Syndrome in patients <18 using ASA, particularly after viral illness (flu, chickenpox)
  3. Acetaminophen and Ibuprofen provide safer analgesics/anti-pyretics
42
Q

ASA use in peds typically not used BUT when might it be used? (3)

A
  1. Often used for cardiac conditions in pediatrics
    - Kawasaki Disease
    - Post-operative Congenital Heart Repair Prophylaxis
    - Rheumatic Fever
  2. Dosing varies, often rounded to convenient dosage for administration
  3. LEXICOMP
43
Q

What are some practice pearls to be aware of for peds? (3)

A
  1. Always ensure you have a weight (and ideally height) prior to assessing ANY medication
  2. Be weary of units: mcg vs ug vs mg
    - E.g. overdoses have happened on multiple occasions with
    clonidine
  3. Check your references, then double-check, then check again if you’re unsure – the biggest mistake you can make is to guess: so don’t do it!
44
Q

What is Kawasaki disease?

A

Acute Systemic Vasculitis of Childhood
- Acute, self-limited febrile illness
- Leads to coronary artery aneurysms in ~25% of untreated cases
- Exact cause unknown
- More common in Japanese and black children, predominantly affecting children <5 years old

45
Q

How is Kawasaki disease diagnosed? (5)

A

Fever > 5 days, and 4+ of the following 5 principal features:
1) Changes to lips and oral cavity
- Strawberry tongue
- Reddened, cracked lips
- Diffuse erythema to oral and pharyngeal mucosa
2) Non-purulent bilateral bulbar conjunctivitis
3) Polymorphous rash (generalized throughout body)
4) Changes in extremities
- Edematous hands/feet, erythematous soles/palms
5) Cervical lymphadenopathy
- > 1.5 cm diameter

46
Q

What are some Kawasaki related complications? (3)

A
  1. Cardiac complications
    - Coronary artery aneurysms
    - Heart Failure
  2. Kawasaki Disease Shock Syndrome (KDSS)
  3. Non-coronary vascular involvement
    - Urinary abnormalities, renal dysfunction, GI abnormalities, CNS involvement less common
47
Q

How is Kawasaki Disease treated? (3)

A
  1. Intravenous Immunoglobulin (IVIG) + Aspirin are mainstay of initial treatment
  2. IVIG 2 g/kg given as single IV infusion (ideally within 10-days of symptom) onset
  3. Administration of low/moderate/high dose ASA