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Drug use in obs & gyne practice

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    Progesterone inhibit contraction of smooth muscles in various regions in the GIT resulting in reduced gastric motility and reduced drug availability after oral use.

    Skin: vasodilation, increased tissue perfusion and increased absorption of IM drugs.

    Increased total body water: hemodilution, large space for distribution of water soluble drugs, free concentration of drugs bound to albumin.

    Increased hepatic metabolism (not blood flow): the dose of drugs metabolized in the liver such as phenytoin, aminophylline should therefore be adjusted (reduce dose but increase dosing interval).

    Increased renal plasma flow: increased excretion e.g. amoxicillin- an advantage in the treatment of UTIs.

    Placental transfer: both risk and benefit.

    A teratogen is any chemical substance that can induce abnormal development in the fetus.

    fig. I. Malformations due to maternal ingestion of thalidomide.

    Principles of teratology

    Teratogens act with specificity. A teratogen produces a specific abnormality or constellation of abnormalities e.g. thalidomide produces phocomelia, and valproic acid produced neural tube defects.

    Teratogens demonstrate a dose-effect relationship.

    Teratogens must reach the developing conceptus in sufficient amounts to cause their effects.

    The effect that a teratogenic agent has on a developing fetus depends upon the stage during development when the fetus is exposed.

    fig. II. Critical periods of fetal development.
    fig. III. Risk categories of drugs in pregnancy.
    fig. IV. Human teratogenic drugs.

    Consider pregnancy in all women of childbearing potential.

    Do a risk/benefit evaluation.

    Minimize prescribing- use ‘tried and tested’ drugs in preference to new agents.

    Use the smallest effective dose.

    Remember the fetus is most sensitive in the first trimester.

    Discuss the potential risks of taking or withholding therapy with the patient.

    Seek guidance on the use of drugs in pregnancy- seniors, formulary.

    Antimalarial- most are safe in pregnancy

    Antibiotics- antibiotics such as metronidazole (hepatic failure), chloramphenicol (gray baby syndrome), aminoglycosides (ototoxicity) and tetracyclines (teeth discoloration and liver failure) are contraindicated in pregnancy.

    Tocolytic- nifedipine, magnesium sulfate are commonly used.

    Antiemetic- promethazine, metoclopramide are commonly used.

    Fetal lung maturity- dexamethasone, betamethasone are commonly used.

    Induction of labor- oxytocin, prostaglandins, mifepristone are commonly used.

    Uterotonics- oxytocin, prostaglandins are commonly used.

    Cigarette smoking is the most common form of substance abuse in pregnancy, it is linked to-

    • Decreased fertility
    • Spontaneous abortion
    • Placenta previa
    • Placental abruption
    • Ectopic pregnancy
    • Preterm premature rupture of membranes (PPROM).
    • Pre-eclampsia

    Most drugs used during lactation are detectable in breast milk but in low concentration.

    Daily infant exposure is substantially less than the ‘therapeutic dose’.

    If the nursing mother must take medications and the drug is a relatively safe one, she should optimally take it 30—60 minutes after nursing and 3—4 hours before the next feeding.

    Caution- sedative-hypnotics, lithium, tetracyclines.

    Antibiotics

    Hormones: estrogen/progestogen

    GnRH agonists/antagonist

    Cytotoxic drugs

    Prostaglandin analogues

    Antiprogestogen – mifepristone

    Ovulation induction- clomiphene citrate


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