Prescribing in Pregnancy Flashcards

1
Q

is medicine used commonly in pregnancy

A

yes

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2
Q

inherent risks during pregnancy (without medication use)

A
  • miscarriage: 15%
  • congenital anomalies: 2-3% at birth; 5% at 5 years of age
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3
Q

% of birth defects that medication accounts for

A

~1%

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4
Q

for a drug to be classified as teratogen, should meet 4 characteristics:

A
  • cause a PATTERN of birth defects
  • cause defects dependent on time of exposure
  • cause birth defects in a dose dependent manner
  • cause defects in genetically susceptible individuals
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5
Q

what do the 4 characteristics suggest that make for the classification of teratogen

A

=> suggest a biologically plausible mechanism of teratogenicity for a particular drug

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6
Q

define teratogen

A
  • agent or factor that causes malformation of an embryo
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7
Q

[dose response relationship] => teratogenous drug needs to display a dose threshold which means….

A
  • exposures below a certain level do not result in an effect (birth defect)
  • dose not always known
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8
Q

what 2 factors are involved in the Dose Response Relationship (a characteristic in teratogens)

A
  • dose threshold
  • dose response
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9
Q

[dose response relationship] => teratogenous drug needs to display a dose response which means….

A
  • demonstrated increased effect with increasing dose
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10
Q

[time of exposure] when teratogenous drug exposure in 1st trimester, tend result in _____ because….

A
  • malformations
  • because main period of organogenesis in foetus
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11
Q

[time of exposure] when teratogenous drug exposure in 2nd and 3rd trimester, tend result in _____ because….

A
  • growth, neurobehavioural, etc issues
  • because this when growth and maturation of organ systems
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12
Q

[timing of exposure] can same drug, giving at different times in pregnancy, have different risks of same and / or different adverse event/s

A
  • yes
  • drug has periods of varied susceptibility
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13
Q

[timing of exposure] what abnormalities can retinoids (teratogenic) lead to

A

isotretinoin embryopathy
- facial dysmorphia (mental health condition)
- cleft palate
- external ear abnormalities
- eye abnormalities
- cardiovascular abnormalities

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14
Q

[timing of exposure] what is exposure window of retinoids

A

unknown

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15
Q

[timing of exposure] when is exposure window of warfarin

A

week 6-12

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16
Q

[timing of exposure] dose response in warfarin

A

worse effects in exposures >5mg

17
Q

[timing of exposure] what can warfarin (teratogenic) lead to

A

foetal warfarin syndrome
- nasal hyperplasia
- skeletal abnormalities resulting in short limbs and digits

(note: warfarin - anticoagulant to prevent formation blood clots in legs, lungs, heart, brain; can cause serious bleeding)

18
Q

[timing of exposure] what can phenytoin (teratogenic) lead to

A

foetal hydantoin syndrome
- craniofacial dysmorphisms (abnormal body structure)
- digital and nail hyperplasia
- orofacial clefts
- cardiac defects

19
Q

what is phenytoin used for & is it still used during pregnancy

A
  • seizure control
  • important to have adequate seizure control, risk-to-benefit may be necessary to use even though not preferred
20
Q

what considerations can make a drug still used during pregnancy (outside exposure window)

A
  • risk to benefit
    > incl importance of treating condition
    > incl if there other, safer options
21
Q

is the ADEC Categories a reliable resource? why / why not?

A
  • no
    why?
  • simplistic, does not consider: dose, timing, patient, condition, route
  • not regularly updated
  • confusing categories
22
Q

what is an issue with Consumer Medicines Information

A
  • patient have access to info
    (doc not going to rely on for drug info]
  • info can be contradictory or conflict with practice
23
Q

how can you handle patient with conflicting info from Consumer Medicines Information

A
  • communicate discrepancy with patient if they are accessing that sort of information
  • letting patient know about practice guideline use of that drug
24
Q

why is Product Information a less relaible resource

A
  • is company sponsored and so is conservative
25
Q

what resource can you use for information about prescribing a medication in pregnancy if time poor for own research using reliable resources

A

SA Health Medicines Information Service
- accessible to health professionals and consumers

26
Q

use of lithium carbonate for mental health management; what is the risk / benefit analysis

A

usually continued during pregnancy
ie/ condition they have if not treated poses more risk to the pregnancy (bipolar)

27
Q

what is the adverse outcome of lithium carbonate

A

Ebstein’s Anomaly (cardiac defects)

28
Q

is SSRIs (mental health treatment - depression) considered safe during pregnancy and why

A

yes
because relative risk vs absolute risk (of treatments adverse outcomes)

29
Q

Drug Classes to AVOID in pregnancy (contraindicated in pregnancy but remember clinical context dependent)

A
  • ACE-inhibitors (completely avoided; usually used for heart and kidney conditions)
  • angiotensin receptor blockers (completely avoided; usually used for heart conditions or and kidney conditions in diabetics)
  • immunosuppressants and immunomodulators (avoided)
  • anti-epileptics (switch to safer options if can)
  • NSAIDs (tend to be avoided for standard indications like pain)
30
Q

what adverse outcomes from ACE-inhibitors during pregnancy

A
  • severe effects on developing foetal kidney
  • can result in foetal death
31
Q

what adverse outcomes from angiotensin receptor blockers during pregnancy

A
  • can result in foetal death
32
Q

what adverse outcomes immunosuppressants and immunomodulators in pregancny

A
  • severe foetal effects
33
Q

if on immunosuppressants or immunomodulators, what is recommended prior to becoming pregnant

A
  • therapy free intervals
  • so some planning required prior to pregnancy
34
Q

what adverse outcomes associated with anti-epileptics in pregnancy

A
  • increased rates of malformations
  • neurodevelopmental abnormalities
35
Q

what are the considerations when it comes to anti-epileptics in pregnancy

A
  • seizure control is paramount
  • there are safer medication alternatives for treatment of seizure <- pre-pregnancy planning to switch to alternative
  • may not be able to switch: risk-benefit-analysis
36
Q

NSAID exposure window time & adverse effects

A
  • paracetamol (NSAID) exposure after 20 wks gestation
  • renal toxicity in foetus
  • premature closure of ductus arteriosus w/ possible links to persistent pulmonary hypertension of newborn
37
Q

when would NSAIDs used during pregnancy

A

sometimes used therapeutically eg/ after procedure