Chapter 36 Pain Management during Pregnancy and Lactation Flashcards
KEY POINTS 1. Pain is frequent during pregnancy and lactation. Many women suffer from pelvic girdle pain and back pain. 2. Physiologic changes during pregnancy may alter drug pharmacokinetics and pharmacodynamics. 3. Most drugs cross the placenta and cross into breast milk. 4. Drug effects on the fetus may be direct or indirect (effect on the mother). 5. Efforts should be made to minimize maternal exposure to drugs during pregnancy and lactation. 6. Possible adverse effects of in utero dr
Diffusion
primarily passive and the drug concentration in the umbilical vein or breast milk depends on the concentration gradient, drug lipid solubility, degree of ionization and protein binding, and the diffusion capacity of the membrane (this may change as pregnancy progresses).
The effects of the drugs on
the fetus or nursing child will depend on
the gestational or postconceptual age, as well as the amount and duration of
drug exposure, and the specific drug
physiologic changes of pregnancy influence
drug absorption, distribution, and elimination
Changes in gastrointestinal function can alter oral drug absorption. Renal elimination is generally increased because of
an increase in glomerular filtration rate. Hepatic metabolism may be increased, unchanged, or decreased, and the increase in total body water may alter drug distribution
and peak concentrations. Protein binding is usually
decreased; however, the free drug concentration may be
unchanged because of increased drug clearance.
The amount of drug that crosses the placenta depends on
maternal cardiac output, fetal cardiac output, placental binding, and placental metabolism, as well as factors that influence passive diffusion across the placenta
Maternal plasma levels of a drug depend on
the site of administration
(e.g., oral, intravascular, or epidural space), the total dose,
the dosing interval, and other drugs that may be co-administered (e.g., epinephrine)
The amount of drug to which
the fetus is exposed also depends on
fetal metabolism (fetal
blood carrying drugs away from the placenta passes first through the fetal liver), fetal protein binding (about half of
maternal protein binding), and the distribution of fetal
cardiac output (fetal distress results in redistribution of
blood flow to the vital organs).
Possible adverse effects on the fetus of in utero drug exposure include
structural malformations, intrauterine fetal death, altered fetal growth, neurobehavioral teratogenicity, acute neonatal intoxication or neonatal abstinence syndromes
A major determinant of the effect of a drug on the
fetus is the
gestational age of the fetus.
The period of classic teratogenesis
corresponds with the critical period of organogenesis and begins approximately 31 days after the first day of the last menstrual period until about 71 days after the last period.
fetal drug exposure at this
time is not risk free.
Fetal development, particularly the central nervous system,
continues into the second and third trimesters, and
indeed after birth.
U.S. Food and Drug Administration Pregnancy Category System - A
Adequate, well-controlled studies in pregnant women have not shown
an increased risk of fetal abnormalities
U.S. Food and Drug Administration Pregnancy Category System- B
Animal studies have revealed no harm to the fetus; however, there are no
adequate and well-controlled studies in pregnant women. Or animal studies
have shown an adverse effect, but adequate and well-controlled studies in
pregnant women have failed to demonstrate a risk to the fetus
U.S. Food and Drug Administration Pregnancy Category System- C
Animal studies have shown adverse fetal effects and there are no adequate
and well-controlled studies in pregnant women. Or no animal studies have
been conducted and there are no adequate and well-controlled studies in
pregnant women.
U.S. Food and Drug Administration Pregnancy Category System- D
Studies, adequate and well controlled or observational, in pregnant women
have demonstrated a risk to the fetus. However, the benefits of therapy may
outweigh the potential risk.
U.S. Food and Drug Administration Pregnancy Category System- X
Studies, adequate and well controlled or observational, in animals and pregnant
women have demonstrated positive evidence of fetal abnormalities. The use of
the product is contraindicated in women who are or may become pregnant.
U.S. Food and Drug Administration Pregnancy Category System- B
Drugs
Acetaminophen; butorphanol, nalbuphine; caffeine; fentanyl,* methadone,* meperidine,*
morphine,* oxycodone,* oxymorphone;* ibuprofen, naproxen, indomethacin;
prednisone, prednisolone
U.S. Food and Drug Administration Pregnancy Category System- C
Drugs
Amitriptyline; aspirin, ketorolac; betamethasone, cortisone; codeine,* propoxyphene,* hydrocodone;* gabapentin; lidocaine; propranolol; sumatriptan; sertraline, fluoxetine; bupropion
U.S. Food and Drug Administration Pregnancy Category System- D
Drugs
Imipramine; carbamazepine; diazepam; paroxetine; phenobarbital; phenytoin,
valproic acid
U.S. Food and Drug Administration Pregnancy Category System- X
Drugs
Ergotamine
Aspirin use during pregnancy may be associated with an
increased risk of
gastroschisis. Pregnant women should not use aspirin (.150 mg/day) regularly.
Ibuprofen and
naproxen during the first trimester
do not appear to be
teratogenic
Prostaglandin inhibitors have been associated with
narrowing of the ductus arteriosus in utero. Aspirin and
other prostaglandin inhibitors may decrease amniotic fluid
volume secondary to decreased fetal urine output, and they may prolong pregnancy and labor.
An increased incidence
of neonatal intracranial hemorrhage has been found in premature infants whose mothers ingested
aspirin near birth. For these reasons, full-dose aspirin and nonsteroidal antiinflammatory
drug (NSAID) therapy should be avoided in the third trimester. If a mild analgesic is indicated during pregnancy, acetaminophen is the drug of choice.