Download Free Medical Drugs Used During Pregnancy and Lactation PowerPoint Presentation

Drugs Used During Pregnancy and Lactation PowerPoint Presentation

DOWNLOAD MEDICAL POWERPOINT PRESENTATION

About This Presentation

Description : Check out this medical presentation on Obstetrics & Gynecology, which is titled "Drugs Used During Pregnancy & Lactation", to know about the principles of prescribing drugs during pregnancy, lactation and menstruation. Also know about the physiological changes occurring in pregnancy that affect the pharmacodynamics and pharmacokinetics in mother and important teratogenic drugs with their teratogenicity.

Tags : Obstetrics, Gynecology, Drugs, Pregnancy, Lactation, menstruation, pharmacodynamics, pharmacokinetics

Published on : Jul 12, 2021 | Views : 3633 | Downloads : 6

Shareable Url :

Embed Code :

Comment

Transcript

Slide 1-

Drugs Used During Pregnancy & Lactation Dr Arif Hashmi
Slide 2-

Objectives a. Discuss the principles of prescribing drugs during pregnancy, lactation and menstruation. b. Discuss the physiological changes occurring in pregnancy that affect the pharmacodynamics and pharmacokinetics in mother. c. Define a teratogen and list important teratogenic drugs with their teratogenicity.
Slide 3-

The need to study drugs during pregnancy relates to the physiologic changes that occur with gestation. To accommodate fetal growth and development, and perhaps provide a measure of safety for the woman, pregnancy alters a woman’s underlying physiology. This altered physiology can affect the pharmacokinetics of drugs. Pregnancy – What is different?
Slide 4-

PREGNANCY PHYSIOLOGY AND ITS EFFECTS ON PHARMACOKINETICS Absorption Gastrointestinal motility is decreased but there appears to be no major affect in drug absorption except that reduced gastric emptying delays the appearance in the plasma of orally administered drugs, especially during labor. Absorption from an intramuscular site is likely to be efficient because tissue perfusion is increased due to vasodilatation.
Slide 5-

Total body water increases by up to 8 Litres, creating a larger space within which water soluble drugs may distribute. As a result of haemodilution, plasma albumin (normal 33-55 g/1) declines by some 10 g/1. Thus there is scope for increased free concentration of drugs that bind to albumin. Unbound drug, is free to distribute, metabolized and excreted; e.g. the free (and pharmacologically active) concentration of phenytoin is unaltered, although the total plasma concentration is reduced. Distribution:
Slide 6-

Hepatic metabolism increases, but not the blood flow to liver. So, increased clearance of drugs such as phenytoin and theophylline (elimination rate depends on liver enzyme activity) Drugs that are so rapidly metabolized that their elimination rate depends on their delivery to the liver, i.e. on hepatic blood flow, have unaltered clearance, e.g. pethidine. metabolism
Slide 7-

Renal plasma flow almost doubles So there is rapid loss of drugs that are excreted by kidney e.g. amoxycillin, dose of which should be doubled for systemic infections (but not for urinary tract infections as penicillins are highly concentrated in urine). Elimination:
Slide 8-

PLACENTAL TRANSFER OF DRUGS The placenta is not a perfect barrier to drugs and chemicals administered to mother. Thalidomide tragedy, showed that placenta was capable of transferring drugs ingested by mother to fetus, with potential for great harm. On other hand, placental transfer of drugs administered to mother has been used to treat fetal arrhythmias, congestive heart failure, & other conditions.
Slide 9-

factors affecting placental drug transfer & FetaL tissue Physicochemical properties of drug Rate at which drug crosses placenta & amount of drug reaching the fetus Duration of exposure to drug Distribution characteristics in different fetal tissues Stage of placental & fetal development at time of exposure to the drug Effects of drugs used in combination
Slide 10-

ppt slide no 10 content not found
Slide 11-

TERATOGENESIS A teratogen is a chemical substance that can induce a malformation during development.
Slide 12-

ppt slide no 12 content not found
Slide 13-

Principles of teratology Teratogens act with specificity. A teratogen produces a specific abnormality or constellation of abnormalities. Eg. thalidomide produces phocomelia, and valproic acid produces 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.
Slide 14-

Mechanisms of Teratogenesis Genetic interference, gene mutation, chromosomal breakage, interference with cellular function, enzyme inhibition, and altered membrane characteristics. The response of the developing embryo to these insults is failure of cell–cell interaction crucial for development, interference with cell migration, or mechanical cellular disruption.
Slide 15-

ppt slide no 15 content not found
Slide 16-

ppt slide no 16 content not found
Slide 17-

examples
Slide 18-

PRESCRIBING IN PREGNANCY Prescribing in pregnancy is a balance between the risk of adverse drug effects on the fetus and the risk of leaving maternal disease untreated.
Slide 19-

•minimize prescribing; use ‘tried and tested’ drugs whenever possible in preference to new agents; • use the smallest effective dose; • remember that the fetus is most sensitive in the first trimester; • consider pregnancy in all women of childbearing potential; • discuss the potential risks of taking or withholding therapy with the patient; • seek guidance on the use of drugs in pregnancy in the British National Formulary, Drug Information Services, National Teratology Information Service (NTIS); • warn the patient about the risks of smoking, alcohol, over-the-counter drugs and drugs of abuse.
Slide 20-

DRUG USE DURING LACTATION Most drugs administered to lactating women are detectable in breast milk. Fortunately, the concentration of drugs achieved in breast milk is usually low. Infant would receive in a day is substantially less than what would be considered a “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
Slide 21-

THANK YOU