Drugs in pregnancy Flashcards

1
Q

effect on creatinine clearance

A

increases

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2
Q

effect on protein binding

A

most increase protein binding

hihgly protein bound drugs effected

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3
Q

effect on gastric emptying

A

decreased therefore increased absorption

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4
Q

effect on plasma volume

A

increases by 50%

can get anemia if RBC mass lags behind

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5
Q

effect on skin absorption

A

increased becuase increased vascularity

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6
Q

effect on cardiac output

A

increases 2 fold

if heart cant pull it off get edema in the legs

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7
Q

effect on peripheral resistance

A

decreases

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8
Q

effect on diastolic BP

A

decreases

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9
Q

effect on pulmonary resistance

A

increases

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10
Q

effect on colloid oncotic pressure

A

decreases

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11
Q

change in blood gas

A

increase ppH

decrease CO2

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12
Q

placentas major functions

A
transfer nutrient and oxygen 
remove waste products
synthesize hormones, peptides, steroids
link between the circulations 
barrier to protect from drugs/toxin in the maternal blood
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13
Q

what happens to blood flow through the placenta to maternal side during pregnancy

A

increases

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14
Q

why is metabolism different in the fetus

A

liver enzymes are different

kidney is immature, filtration reduced

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15
Q

what are some adverse drug reactions that occur

A
teratogenesis 
osteoporosis 
uterin stimulation or suppression 
deug dependent infant 
breathing difficulties in neonat 
impaired intellectula or social development
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16
Q

what is the risk of malformations with most teratogens

A

10%

17
Q

Why is it hard to prove a drug is teratogenic

A

incidence of congenital anomalies is low
animal tests not applicable
exposure needs to be prolonged
controlled experiment cant be done in humans
behavioural issues hard to identiy or link

18
Q

requirements to prove a drug is a teratogen

A

must cause specific set of malformations
act only between 4-7 weeks of gestation
incidence should increase with increasing dose and duration of exposure

19
Q

if there is no proof for teratogenicity is the drug safe

A

no

20
Q

shepards principles of teratolofy

A

agent must be rpesent during critical periods of developmetn
acts directly on the embryo
experimental models corroborating the findings

21
Q

preimplantation/presomite period

A

conception to 2 weeks

22
Q

somite period

A

2-4 weeks

23
Q

organ structure formation period

A

4-8 weeks

24
Q

organ function/substructure period

A

8+ weeks

25
Q

what occurs if teratogen exposed during first trimester embryonic period (3-8wks)

A

gross (structural) abnormalities

26
Q

what occurs if teratogen exposed during the fetal period (9-40wks)

A

functional problems
learning deficits
behavioural abnormalities

27
Q

what are two commone types of teratogenic drugs

A

antieliptics
antipsychotics
live vaccines
nsaids

28
Q

problems from diethylstilbesterol

A

vaginal cancer
female children born with vaginal and cervical carcinomas and uterine anomalies
male children abnormal genitalia/sperm

29
Q

thalidomide malformations

A
absence of limbs (phocomlia) 
gongenital heart defects
eye defect
urogenital 
GI 
hearing loss
30
Q

SSRIs in pregnancy

A

disocntinuing high risk because stress bad
treated with low doses appears safe
maybe cardiac malformations

31
Q

what do women think is the teratogenic risk

A

25%