W04: Pharmacology in Pregnancy; Pharmacology in Breast Feeding Flashcards

1
Q

Explain pharmacokinetics in pregnancy

A

pharmacokinetics = passage of drugs throughout the body

  • oral route compromised dt N/V
  • ⇩gastric emptying and gut motility
  • ⇧abs of inhaled drugs dt ⇧CO and ⇩tidal vol.
  • altered distribution dt ⇧plasma volume and ⇧ fat change
  • ⇧plasma dilutation = ⇧plasma proteins = ⇧free drug circulating
  • oestrogen and progesrone levels = altered drug metabolism
    = differing [drg] will affect pharmacodynamics
  • ⇧ GFR = ⇧ Excretion
  • may require higher drug conc for renally cleared drugs e.g gentamicin, digoxin
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2
Q

Outline the main concerns regarding the use of medication in pregnancy

A

risks must outweight benefits
* drugs should be avoided
* e.g consider risks such as epilepsy and effect of uncontrolled epilepsy on baby

  • placenta is not a barroer (apart from high molecular weight such as aspirin and heparin) THUS drugs can travel across and affect unborn baby
  • TERATOGENS = malformation, prevent implantation, abortion etc.
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3
Q

Outline the main concern regarding the use of medication in breast feeding

A

Some medicines can pass from women through breastmilk to their baby. Only small amounts of the medicine usually reach the baby and most medicines can be used while breastfeeding. For some medicines, this may mean the baby should be monitored more often to make sure they are not harmed by the medicine whilst they are breastfed.

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4
Q

Describe where to find information about risks with specific drugs in pregnancy/ breast feeding

A

BNF
gov.uk pregnancy prevention programme: valporate

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5
Q

Explain the principles of prescribing for these patients

A

CONSIDERATIONS FOR WOMEN OF CHILD-BEARING AGE

  • always consider possibility of pregnancy
  • warn of risks
  • advice tratment options prior to stopping meds
  • contraception discussion
  • certain drugs have pregnancy prevention programmes
  • AVOID ALL DRUGS IN FIRST TRIMESTER
    • drugs given after first 2 mos of preg more likely to cause abruption to growth or interefere with essential development
  • consider dose changes and therapeutic monitoring
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6
Q

Phenytoin levels in pregnancy

A

Are increased dt metabolism being induced

  • anti-seizure medication. It is useful for the prevention of tonic-clonic seizures and focal seizures, but not absence seizures.
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7
Q

Theophylline levels in pregnancy

A

Increased dt metabolism inhibited = more free drug in circ.

  • theophylline used in asthma
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8
Q

Explain pharmacodynamics in pregnancy

A

Body’s response to drug.
* altered site of action/receptor response, efficacy, adverse effects

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9
Q

Fetal pharmacokinetics

A

Altered ADME

DISTRIBUTION
* diff. circulation, less protein binding = more free drug
* little fat thus less destirbution
* more blood flow to brain

EXCRETION
* excr. into amniotic fluid and swallowed and re-circulated = thus risk of accumulation in amniotic fluid

METABOLISM
* less enzyme activity which increases with gestation

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10
Q

Considerations of prescribing valporate in women and girls of childbearing age

A

Must meet pregnancy prevention programme dt teratogenic medicines

  • epilepsy
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11
Q

Significance of prescribing Trimethoprim in pregnancy

A
  • safe in 2nd or 3rd trimesters but
    AVOID IN ALL TRIMESTERS FOR THOSE WITH FOLATE DEF., LOW DIETARY FOLATE, OR TAKING FOLATE ANTAGONISTS
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12
Q

Mgmt of UTI in pregnancy

A

First trimester
> NITROFURANTOIN
> CEFALEXIN

2nd and 3rd Trimester
> NITROFURANTOIN
!avoid during labour and 36w+

> TRIMETHROPRIM

3rd Trimester after 36w
> TRIMETHOPRIM
> CEFALEXIN: req uterine culture seven days to check therapeutic effect

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12
Q

Mgmt of UTI in pregnancy

A

First trimester
> NITROFURANTOIN
> CEFALEXIN

2nd and 3rd Trimester
> NITROFURANTOIN
!avoid during labour and 36w+

> TRIMETHROPRIM

3rd Trimester after 36w
> TRIMETHOPRIM
> CEFALEXIN: req uterine culture seven days to check therapeutic effect

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13
Q

Understand the pharmacological properties during lactation

A

Almost all drugs cross into breastmilk but multiple factors affect this:

*maternal factors: dose, ADME
* drug characteristics: pH ionisation, lipid solubility, protein binding, molecular weight
* breast physiology: vol of milk and yield

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14
Q

Outline the risks of taking certain medication while breastfeeding; consider neonatal monitoring

A

monitoring if possibility of harm to baby?

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15
Q

Demonstrate the ability to use relevant information resources to determine the risk of using specific drugs while breastfeeding

A

BNF
UK Tetrology service
Summary of Product Characteristics
Patient information leaflet

16
Q

Explain the principles of prescribing for women while breastfeeding

A
  • preference for durgs that are highly protein bound
  • avoid long half lives
  • delay treatment?
  • pump out affected milk and dump?
  • question OTC and herbal medicines
  • in general if safe in paediatrics and neonates, likely to be safe in breastfeeding

avoid:
- cytotoxics
- imm suppr.
- anti convulsants
- drugs of abuse
- amioda9rone (Vent tachy. etc.)
- lithium (mood)
- radio-iodine

17
Q

Diazepam in breastfeeding

A

risk of accumulation and sedation

18
Q

Barbituates in breastfeeding

A

risk of lethargy, sedation, and poor suck reflexes

19
Q

Drugs affecting lactation

A

> CABERGOLINE inhibition of lactation

> METOCLOPRAMIDE enhances lactation

20
Q

Importance of non-pharma approaches

A

> hot/cold treatment for pain
exercise for pain
physio for pain

20
Q

Importance of non-pharma approaches

A

> hot/cold treatment for pain
exercise for pain
physio for pain