Paediatrics Flashcards

1
Q

Distribution is affected by:

A

1) Absorption
2) Penetration of biological membrane
3) Perfusion of organs
4) Drugs disposition to distribute
5) Drugs affinity for protein binding

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2
Q

Comment on the Body Composition in Neonates

A

Extracellular fluid volume is higher in neonates, and total body water content is higher in neonates compared to adults

less than 3% of a neonate is fat
30 % of 1 Year olds is fat
less than 18% of adults is fat.

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3
Q

Comment on blood protein content pediatrics and the implications it has on drug binding. Give examples where applicable.

A

Less protein available for drug binding. This means that there is higher competition for binding sites. This leads to displacement of endogenous substances

e.g bilirubin.

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4
Q

what happens if bilirubin gets displaced? and Give examples of what displaces it

A

Bilirubin displacement, particularly in the brain leads to toxicity.

e.g Sulphonamides and Ceftriaxone in neonate.

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5
Q

In terms of oral absorption, how does oral absorption in neonates differ from adults? Comment on gastric pH,

A

Delayed Gastric emptying and transition time

Reduced gastric acid secretion

At birth stomach pH is 7, and this normalises after 2 yrs

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6
Q

what effect does reduced gastric acid secretion have on drugs in paediatrics? Give an example

A

Reduced absorption of drugs that require an acidic environment. E.g Metronidazole

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7
Q

Comment on topical absorption in neonates. Higher or lower and why?

A

Higher. There’s an increased rate and extent of absorption. Due to an immature epidermal barrier, Increased skin hydration and a higher SA to body weight ratio.

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8
Q

what can topical administration lead to in neonate? e.g?

A

Toxicity! e.g Chlorhexidine (burns)

Corticosteroids (cushings syndrome)

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9
Q

Is parenteral absorption a good idea in neonates why not?

A

Smaller veins so hard to administer the drug.

They have less muscle mass so IM is painful and the absorption is unpredictable.

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10
Q

What key enzyme develops slowly in neonates?

A

CYP450

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11
Q

how long does it take to reach phase 1 and phase 2 capacity?

A
  • 6-12 months for phase 1

- 3 years for full capacity in phase 2.

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12
Q

Excretion - is this constant? What does this mean in terms of drugs

A

No wide inter-variation = difficult to predict drug clearance.

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13
Q

State the effects Ceftriaxone, and Metoclopramide has on babies

A

Ceftriaxone - Displaces bilirubin

Metoclopramide can cause EPSEs

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14
Q

What is dosing in children based on?? and how do you calculate BSA (body surface area)

A

Based on weight
Based on age

BSA (body surface area) = square root of Bw * Ht/ 3600

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15
Q

State two key excipients that have adverse effects

A

Benzylalcohol can cause circulatory collapse

Propylene glycol can cause seizures

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