Therapeutics- Prescribing in Special Groups- Pregnant Women Flashcards

1
Q

In general should medications for chronic disorders be stopped during pregnancy?

A

No it is usually better not to stop

Risk from untreated disease is usually greater as it can adversely effect the pregnancy

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2
Q

Are OTC drugs safe to use in pregnancy?

A

Yes, generally any adverse effects would cause the drug to not be available OTS

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3
Q

How does ECF change during pregnancy?

A

ECF increases and therefore the renal clearance of renally cleared drugs increases

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4
Q

How does drug absorption change?

A

Nausea and vomiting can occur during pregnancy which can reduce absorption of oral drugs. GI transit time also increases which delays absorption

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5
Q

How does absorption from IM injections change?

A

Blood flow increases and so absorption increases

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6
Q

How does absorption from inhaled medications change?

A

Blood flow increases (ECF increases) and so absorption increases

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7
Q

When are foetuses most sensitive to teratogens?

A

During the first trimester as this is when the development of major organs is occuring

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8
Q

What is a teratogen?

A

A substance, organism, physical agent or deficiency state capable of inducing abnormal structure or function

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9
Q

What percentage of prescribed drugs are known teratogens?

A

1%

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10
Q

How many congenital malformations are due to drugs?

A

2-3%

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11
Q

What is the all or nothing effect during the pre-embryonic phase?

A

This is in the first 14 days

Insult at this stage either leads to spontaneous recovery or loss

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12
Q

What effect could teratogenic drugs have during the first or second trimester?

A

Affect growth
Affect functional development
Toxic effect on tissues- Fetotoxicity

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13
Q

What are some drugs to be avoided in pregnancy?

A
ACEi
ARBs
Quinolone antibiotics
Tetracyclines
Warfarin
Sodium Valproate
Androgens
Opiates
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14
Q

What changes occur to maternal drug concentration in pregnancy?

A

As ECF increases and renal clearance decreases the concentration will be reduced compared to a non-pregnant woman with the same dose
Foetal and placental metabolism also affect drug concentrations

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15
Q

Till what age is it advised to exclusively breast feed?

A

6 months

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16
Q

Why are neonates most at risks with drugs that can be excreted in the breast milk?

A

They have immature excretory functions and so there is a risk of drug accumulation

17
Q

What characteristics would make a drug less likely to enter the breast milk?

A

High molecular weight
Low lipid solubility
High protein binding in the plasma
Lower pH- breast milk has a lower pH than plasma and so acidic drugs (e.g. amoxicillin) will be less likely to enter the breast milk

18
Q

Which drugs should be avoided in breastfeeding?

A

Amiodarone
Antithyroid drugs- can cause neonatal goitre and hypo-thyroidism
Benzodiazepines- enter the breast milk
Lithium salts- Present in breast milk and risk of toxicity
Radioactive iodine
Statins- high concentration in breast milk
Sulphonamides

19
Q

How might certain drugs affect lactation?

A

Dopamine prevents prolactin release and so dopamine agonists can reduce prolactin release
This decreases milk production

20
Q

Give an example of a dopamine agonist/antagonst

A

Agonist- cabergoline

Antagonist- Domperidone

21
Q

What are the age categorisations?

A
Premature baby- less than 36 weeks
Newborm/Neonate- Up to 27 days old
Infant- 28 days to 23 months old
Child- 2 years to 11 years
Adolescent- 12 years to 16 years
22
Q

How is oral absorption different in children?

A

Absorption is affected by slower gastric emptying which takes 6-8 months to reach adult levels

23
Q

How is the uptake of IM drugs altered in children?

A

Neonates have a low muscle mass and there is variability in blood flow to muscles making IM absorption unpredictable

24
Q

How is percutaneous drug absorption different in children?

A

Percutaneous absorption is increased as the stratum corneum is thinner in children and there is increased skin hydration

25
Q

How is the distribution of water soluble drugs different in children?

A

Children have a much higher % of body water and so there is a greater volume of distribution for water soluble drugs. This decreases as children age. This causes lower concentration of the drug so higher doses may be required (e.g. Gentamicin)

26
Q

How is the binding of drugs to plasma proteins altered in children?

A

Neonates have less plasma proteins and so binding is reduced. This can cause increases in the free and active form of the drug

27
Q

Why might sulphonamides cause jaundice?

A

They can displace bilirubin from albumin and this increase in bilirubin causes jaundice

28
Q

How is excretion different in neonates compared to adults?

A

Neonates have reduced ability to excrete drugs. Renal function is not fully developed and so the elimination of renally cleared drugs is reduced, drugs cleared by the kidney’s can therefore accumulate (e.g. gentamicin)

29
Q

What measurements may be used when deciding doses for children?

A

Age banding- low therapeutic index drugs (parcetemol, amoxicillin)
Weight- many drugs
Surface Area- for small therapeutic index drugs

30
Q

Over what age are children classed as adults for dosing purposes?

A

12 years

31
Q

What colour should syringes be for orally given drugs?

A

Purple

These syringes are not compatible with IV lines, this prevents incorrect administration of the drug

32
Q

What is the intraosseous route? When might it be used?

A

This is delivery of drugs into the bone marrow
It is used in paediatric emergency situations
The bone marrow is highly vascular

33
Q

Which drugs should be avoided in children?

A

Tetracyclines- Cause yellow discolouration of teeth (Not given to children under 12)
Aspirin- Risk of Reye’s Sndrome (Should not be given to children under 16)
Cloramphenicol- Grey Baby Syndrome in neonates