pregnancy Flashcards

1
Q

what is teratogenicity?

A

the ability of a drug to cause foetal abnormalities or congenital malformations

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2
Q

what factors influence teratogenic effects?

A

dose, route, timing, genetics, environmental factors, and other drugs

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3
Q

name 5 known teratogens

A

thalidomide, isotretinoin, valproate, ACEi, NSAIDs

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4
Q

what are the critical phases of human development regarding teratogenic risk?

A

pre-embryonic (0–17 days): all-or-nothing (survival or miscarriage)

embryonic (day 18–55): greatest vulnerability! organ development

foetal (8 weeks–term): functional defects (e.g. hearing loss)

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5
Q

what is the most critical phase for teratogenic risk?

A

embryonic phase (day 18–55) – organ development occurs

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6
Q

what happens if harmful drugs are taken during the pre-embryonic phase?

A

all-or-nothing effect – either full recovery or miscarriage

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7
Q

why should most medications be avoided in the first trimester?

A

because it’s the highest risk period for structural abnormalities

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8
Q

what factors affect a drug’s ability to cross the placenta?

A

molecular weight, ionisation, lipid solubility, protein binding

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9
Q

which drugs cross the placenta easily?

A

lipid-soluble, non-ionised, low-MW drugs like labetalol (for HTN)

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10
Q

which large-molecule drugs do not usually cross the placenta?

A

insulin and heparin

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11
Q

what is the most common mechanism for medicine-related harm in pregnancy?

A

molecules crossing the placenta into foetal circulation (passive diffusion)

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12
Q

what absorption changes occur during pregnancy?

A

intestine: prolonged gastric emptying time; ↓ gastric acid, ↑ pH → affects drug ionisation and absorption
= ionisation and absorption of weak acids impacted
lungs: ↑ cardiac output and tidal volume = ↑ alveolar uptake of inhaled meds (dose reduction needed)

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13
Q

how does pregnancy affect drug distribution?

A

↑ plasma volume and fat stores → ↓ drug concentration

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14
Q

how does plasma volume affect drug levels?

A

plasma volume ↑ → ↑ Vd → ↓ peak serum concentration
(drugs with a large Vd less affected)
also ↑ Vd of drugs distributed in adipose tissue

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15
Q

why are some free drug levels higher in pregnancy?

A

↓ albumin levels → ↓ protein binding due to dilutional
hypoalbuminaemia in late pregnancy; steroid
and placental hormones occupy protein-
binding sites

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16
Q

what happens to hepatic metabolism in pregnancy?

A

↑ hepatic blood flow alters drug metabolism (faster elimination) (↑progesterone = ↑metabolism of some drugs, ↑oestrogen = ↓ clearance)
↑ stroke vol and HR
→ ↑ cardiac output

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17
Q

how is renal elimination affected in pregnancy?

A

↑ GFR and renal flow → faster clearance of some drugs that are excreted unchanged (takes longer to get to steady state concs of drugs)
↑ activity of renal tubular P-gp = ↓ conc of drugs transported by renal system

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18
Q

can medications taken by fathers affect pregnancy?

A

yes - reproductive toxicity from cytotoxics, radiation, or smoking can impact sperm

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19
Q

how long should men wait before conceiving after taking cytotoxics?

A

typically 6–9 months (2–3 spermatogenic cycles depending on the drug)

20
Q

why is shared decision-making important?

A

ensures informed consent and builds trust, especially where data is limited

21
Q

what’s the first step in medicine decision-making in pregnancy?

A

determine if the medicine is essential and if there are non-drug options

22
Q

why is specialist advice crucial for some drugs like valproate?

A

due to high teratogenic risk; must meet Pregnancy Prevention Programme conditions (high risk of neurodevelopmental disorders)
effective contraception needed
even for 3 months after valproate
stopped

23
Q

what are key benefits for breastfeeding?

A

mother: improved mental health - oxytocin release, reduced risk of breast and ovarian cancer, reduced risk of osteoporosis, CVD, and obesity
infant: reduced allergies, improved immunological status, nutritionally complete for first 6 months, reduces risks of SIDS, obesity, CVD in adulthood

24
Q

what are some issues with breastfeeding?

A

mother: pressure - mental health burden, breastfeeding in public - uncomfortable, painful, returning to work is tricky, extra calories needed
infant: premature babies
- deficient in phosphate
- deficient in calories
mothers of very
premature neonates
may cease lactating
before feeding
becomes established

25
how do drugs enter breast milk?
through lipid phase, aqueous phase, and by binding to milk proteins
26
what is the composition of breast milk?
lactose, electrolytes, protein
27
why can large molecules pass through breast milk after the first few days of birth?
there are wide intracellular intracellular gaps in the milk ducts to facilitate passage of immunoglobulins —> to pass on immunity (functional) but also risk of meds into breast milk as large molecules can pass
28
what pharmacokinetic issues affect drug transfer during lactation?
oral bioavailability: if low then baby will not absorb via milk (insulin, LMWH) plasma protein binding: if highly protein bound, less passed via milk (warfarin, ibuprofen) milk : plasma ratio: lower value, smaller amount in milk (iodine - actively transported into milk) fat solubility: lipophilic drugs preferentially dissolve in fat globules of milk - more likely to pass (benzos, amitriptyline) MW: large MW, less likely to pass (heparin; alcohol has LOW MW) absorption from infant gut: may enter into milk but not absorbed by infant's gut (gentamicin, dopamine) 1st pass metabolism: meds undergoing extensive 1st pass less likely to be absorbed by baby (i.e., morphine) neonatal clearance: neonatal kidney/liver function not fully developed → risk of accumulation (i.e., fluoxetine has long half life)
29
what are further considerations?
toxicity of the drug - cytotoxics even in small doses are harmful vs some meds in high doses such as iron are not likely to be harmful relevant infant dose
30
what is the Relative Infant Dose (RID) and what does it mean?
dose received via breast milk <10% = compatible 10–25% = use with caution 25% = contraindicated
31
what is the Relative Infant Dose (RID) threshold considered safe?
<10% is considered compatible with breastfeeding
32
which drugs should be avoided in breastfeeding due to toxicity?
cytotoxics, cocaine, and high RID medications
33
why is drug clearance reduced in breastfeeding neonates?
neonates have immature liver and kidney function
34
how does fat solubility affect drug transfer into milk?
lipophilic drugs (e.g. benzodiazepines, amitriptyline) dissolve in milk fat
35
what factors should be included in information gathering?
gestational age, feeding type, PMHx, DHx, birth method, baby’s age
36
what are reliable resources for pregnancy/lactation medication info?
UKTIS, BNF, LactMed, PMHx/DHx, and specialist consultation
37
what alternatives should be considered before prescribing in pregnancy?
non-pharmacological options, alternative drugs, dose timing
38
when can medicines be timed safely during breastfeeding?
short-acting drugs may be taken after a feed or between feeds
39
why should drugs with long half-lives be avoided in breastfeeding?
they can accumulate and increase risk of neonatal side effects
40
how can breastfeeding be managed around a short medication course?
temporarily interrupt feeding if safe - but avoid if possible
41
what precautions should be taken if a potentially harmful drug must be used?
monitor the infant, use the lowest dose, avoid similar-acting drugs, and choose safer formulations
42
which SSRIs are considered safe in breastfeeding?
sertraline and citalopram
43
why should codeine be avoided in breastfeeding?
risk of ultra-rapid metabolism causing toxicity in the infant (increased s/e such as sedation)
44
is lithium safe in breastfeeding?
no - it’s contraindicated due to high RID and infant risk
45
can Abx be used during breastfeeding?
yes - especially those licensed in children, though temporary lactose intolerance may occur
46
what is the risk of stopping breastfeeding too soon due to meds?
loss of bonding, nutritional benefits, and maternal oxytocin release - may worsen mental health