Pharmacology Flashcards

1
Q

Common reasons pregnant women are on medication?

A
  • Hypertension
  • Migraine
  • Asthma
  • Epilepsy
  • Long term anticoagulant therapy
  • Mental health disorders
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2
Q

What are the four basic kinetic processes?

A
  • Absorption
  • Distribution
  • Metabolism and elimination
  • Excretion
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3
Q

Absorption changes: Oral? intramuscular route? Inhalation?

A

Oral:

  • Morning sickness causes difficulties (nausea/vomming)
  • Increased gastric emptying and gut motility: may affect single doses

Intramuscular:

  • Blood flow may be increased, so absorption may also increase using this route

Inhalation:

  • Increased cardiac output and decreased tidal volume may cause increased absorption of inhaled drugs
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4
Q

Distribution changes in pregnancy?

A
  • Increased plasma volume and fat will effect distribution [increased volume of distribution]
  • Greater dilution of plasma will decrease relative amount of plasma proteins [greater fraction of free drug]
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5
Q

What are the metabolism changes during pregnancy?

A
  • Oestrogen and progesterones can induce or inhibit liver P450 enzymes, increasing or reducing metabolism
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6
Q

What is the effect on the excretion during pregnancy?

A
  • GFR is increased in pregnancy meaning there is an increased excretion of drugs
  • This can reduce the plasma concentration, and can necessitate an increase in dose of renally cleared drugs
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7
Q

What does the placental transfer of medication depend upon?

A
  • Molecular weight (smaller sizes will cross more easily)
  • Polarity (non-polar cross more readily)
  • Lipid solubility (lipid soluble drugs will cross)
  • Placenta may also metabolise some drugs
  • Safest to assume all drugs will cross placenta
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8
Q

Fetal pharmacokinetics: how does distribution differ?

A
  • Circulation is different
  • Less protein binding than adults therefore more ‘free’ drug is available
  • Little fat so this effects distribution
  • Relatively more blood flow to the brain
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9
Q

Fetal pharmacokinetics: how does metabolism differ?

A
  • Less enzyme activity, though increases with gestation
  • Different isoenzymes to adults
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10
Q

Fetal pharmacokinetics: hows does excretion differ?

A
  • Excretion is into amniotic fluid – this is swallowed and can allow recirculation
  • Drugs and metabolites can accumulate in amniotic fluid
  • Placenta not functioning at delivery so can be issues with excretory function
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11
Q

What trimester does teratogenicity have importance?

A

First trimester

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12
Q

At which trimester(s) does Fetotoxicity have effect?

A

2nd and 3rd

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13
Q

What are some mechanisms of teratogenicity?

A
  • Folate Antagonism
  • Neural Crest Cell Disruption
  • Endocrine Disruption: Sex Hormones
  • Oxidative Stress
  • Vascular Disruption
  • Specific Receptor- or Enzyme-mediated Teratogenesis
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14
Q

What is folate antagonism and what are the effects on the fetus?

A
  • Key process in DNA formation and new cell production
  • The drugs will either block the conversion of folate to THF by binding irreversibly to the enzyme or block other enzymes in the pathway
  • This results in neural tube defects, oro-facial or limb defects
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15
Q

Which drugs can cause neural crest cell distribution issues? and effect on fetus?

A
  • Retinoid drugs (isotretinoin)

Problems:

  • Aortic arch anomilies
  • Ventricular septal defects
  • Craniofacial abnormalities
  • Oesophageal atresia
  • Pharyngeal gland abnormalities
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16
Q

What are some issues caused by fetotoxicity?

A
  • Growth retardation
  • Structural malformations
  • Fetal death
  • Functional impairment
  • Carcinogenesis

Example

  • ACE inhibitors/ARBs – renal dysfunction and growth retardation
17
Q

Give some examples of known teratogens and their fetal effects.

A
  • Anticonvulsants: Valproate is associated with neural tube defects, as is carbamazepine and phenytoin
  • Antiocoagulents: Warfarin is associated with haemorrhage in the fetus, as well as multiple malformations in the CNS and skeletal system
  • Antihypertensive agents: ACE inhibitors cause renal damage and may restrict normal growth patterns in the unborn child
  • NSAIDS: Premature closure of the ductus arteriosus
  • Bevs: Fetal alcohol syndrome/effects
18
Q

What are some drugs to avoid during breastfeeding?

A
  • Cytotoxics
  • Immunosuppressants
  • Anti-convulsants (not all)
  • Drugs of abuse
  • Amiodarone
  • Lithium
  • Radio-iodine
19
Q

What are some general guidelines for prescribing during pregnancy?

A
  • Try non-pharma treatment first
  • Use drug with best safety record
  • Use lowest effective dose
  • Avoid first 10 weeks of pregnancy if possible
  • Consider stopping or reducing dose before delivery
20
Q

General principles for prescribing during breastfeeding?

A
  • Avoid unecessary drug use
  • If licensed and safe in paediatric use (esp under 2 years), a drug is likely to be safe in breast feeding
  • Choose drugs with pharmacokinetic properties that reduce infant exposure (eg highly protein bound)