Unit 1: Ch 9, 10 and 11 Flashcards
What happens to excretion during pregnancy?
It is increased
What must be done with drugs to compensate for increased excretion?
Dosage must be increased due to accelerated excretion.
In what situations is it best for a pregnant woman NOT to avoid drug therapy?
When the mother’s illness can do more harm to the fetus than the drugs would. EX: Asthma, Epilepsy, Diabetes.
What happens to metabolism during pregnancy?
Hepatic Metabolism Increases
What happens to drugs that get absorbed in the GI tract during pregnancy?
Tone and motility of the bowel decrease during pregnancy. Drugs traveling this route move at a slower rate increasing the time the drug is able to be absorbed. A reduction in dosage may be needed.
Describe major structural teratogenesis
The most serious defects. 1-3% of babies born with these. May be immediately observable or discovered later if internal. May require surgery.
Describe minor structural teratogenesis
Less serious, don’t necessarily require surgery.
Describe functional teratogenesis
Everything looks normal, but the organ doesn’t function correctly. (eg, mental retardation)
If a fetus encounters a teratogen in the first couple of weeks after conception what will happen?
It is an all or nothing effect – the zygote will either be unharmed or will die.
If a fetus encounters a teratogen in weeks 3-8 what will happen?
Major structural changes may be observed. This is the time when the basic shape of internal organs and other structures is being established. May lead to death or require surgical intervention.
If a fetus encounters a teratogen in weeks 9-38 what will happen?
Minor structural or functional defects may occur.
Likelihood of malformation due to teratogen: If drug exposure was NOT during the period of organ development (organogenesis: weeks 3-8) how much risk of damage is expected?
Minimal
Just because a baby is born with a malformation does that mean there was teratogen exposure?
No
Breastfeeding Moms: Relate to mother that ideally, drugs should not be taken while breastfeeding. But if necessary, instruct the mother to:
1.Dose immediately after breastfeeding 2.Avoid drugs with long half-life 3.Avoid sustained release drugs 4.Choose drugs that tend to be excluded from milk 5.Choose drugs least likely to affect infant 6.Avoid drugs that are known to be hazardous 7.Use lowest effective dose for shortest possible time
Which pediatric age group is the most sensitive to drugs?
Neonates and Infants (the youngest)
Why are neonates and infants the most sensitive age group to drugs?
Their organs are immature and may not be prepared to handle medications.
Why, even when we adjust for weight, are many doses still too high for infants?
Children are not just short adults, they have different bodies and process drugs differently.
How do infants differ in absorption in terms of oral drugs?
Infants have irregular gastric emptying (sometimes really slow, sometimes very accelerated). Infants have changes in gastric pH. When born they are neutral and then become acidic.
How do infants differ in absorption in terms of IM drugs?
Neonates: Slow - because poor blood flow in muscles Infants: fast - absorb IM medications quicker than adults
How do infants differ in absorption in terms of transdermal drugs?
Infants and Neonates: faster Drugs absorption through the skin is more rapid and complete in infants than adults b/c their stratum corneum of skin is thin, and blood flow to skin is greater. Increased risk of toxicity for topical drugs.
How do infants differ in distribution in terms of protein binding?
Distributes easier. Infants have lower levels of albumin which makes protein bound drugs distribute more easily.
How do infants differ in distribution in terms of the BBB?
The Blood Brain Barrier will often not permit the movement of drugs. The BBB is not fully developed in infants, so not as strong of a barrier as in adults.
How do infants differ in terms of metabolism?
Slower. Drug-metabolizing capacity of newborns is low. Neonates especially sensitive to drugs that are primarily eliminated by hepatic metabolism.