drugs in extremes of age - children and neonates

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  • Created by: Rscottqub
  • Created on: 07-01-20 14:44
neonate
<37 weeks but also 0-27 days
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infant/toddle
28days-23 months
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children
2-11years
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adolescent
12-18years
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AMDE most dramatic changes
within 1st month of life
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types of absorption
oral absorption. IM absorption. percutaneous ab. rectal absorption
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2 factors contributing to oral absorption
1. gastric acid secretion 2. gastric emptying
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gastric acid secretion
is decreased at birth --> pH 6-8 . 2-3 years --> 1.5-3.5 .
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what does this mean
acidic drugs will now be ionised and less absorption . higher dose required
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2. gastric emptying
slow and delayed - decreased rate of absorption.
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pancreatic function is
decreased, so less enzymes
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IM absorption
unpredictable due to - decreased blood flow, decreased muscle mass
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if give IM injection
can be painful if high volumes are used - risk muscle damage
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arterial pressure is
high during 1st 4 weeks of life
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so this means
increased IM absorption and muscle perfusion (why babies get injections after 4 weeks? risk damge to muscle)
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Bilirubin
toxic yellow metabolite of RBCs
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what happens to bilirubin once formed
binds to albumin and taken to liver , at liver converted in to conjugated bilirubin and then is eventaully excreted in the urine
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changes in body composition will affect
distribution of drugs - most dramatic changes in body comp - 1st year of life
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the distribution of a drug
will affect its efficacy
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levels of plasma protein in 1st 6 months
low levels of both albumin and a1 glycoproteins
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level of bilirubin in 1st 6 months
high
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decreased plasma proteins means
more free drug - lower dose required
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BBB in neonates
may be functionally incomplete
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kernicterus
bilirubin brain dysfunction
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jaundice
xs bilirubin in the blood
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classed as kernicterus when
bilirubin is found in the brain
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high levels of bilirubin can lead to
deafness, cerebral palsy , mental retardation
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hepatic blood flow
is reduced , as get older a greater proportion of cardiac output is distributed to the liver
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is the liver fully developed at birth
NO
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Phase 1 met at birth
reduction - fully functional.. demethylation - partial oxidation, hydrolysis - develop over 6 months
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CYP enzymes present at birth
yes but in low conc - diff cyp enzymes arise at diff ages
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phase II met at birth
acetylation and glucoronidation - increase over 2 months - adult levels by 3 years
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Glucoronidation
Hb--> bilirubin . then at liver conjugated with glucoronic acid . but in neonates glucoronic acid levels are lower --> jandice
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chloramphenicol and gray baby syndrome
lack of enzyme glucoryl transferase to metabolise - toxcity
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renal clearance
is reduced . reduced GFR at birth , adult levels by 3-5 months
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can we use NSAIDS in neonates
no due to GFR
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Other cards in this set

Card 2

Front

infant/toddle

Back

28days-23 months

Card 3

Front

children

Back

Preview of the front of card 3

Card 4

Front

adolescent

Back

Preview of the front of card 4

Card 5

Front

AMDE most dramatic changes

Back

Preview of the front of card 5
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