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Drugs in Pregnant FK Warmadewa

Date post: 02-Jun-2018
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    http://rds.yahoo.com/_ylt=A0S0201422JICzgBBQyJzbkF;_ylu=X3oDMTByZjdvaWd2BHBvcwMxOQRzZWMDc3IEdnRpZANJMDgyXzEwNA--/SIG=1m48r0214/EXP=1214524664/**http%3A//images.search.yahoo.com/images/view%3Fback=http%253A%252F%252Fimages.search.yahoo.com%252Fsearch%252Fimages%253F_adv_prop%253Dimage%2526fr%253Dyfp-t-501%2526va%253Dpregnancy%252Bfunny%2526sz%253Dall%26w=333%26h=500%26imgurl=static.flickr.com%252F2321%252F2460925544_2a47d03bc4.jpg%26rurl=http%253A%252F%252Fwww.flickr.com%252Fphotos%252Fwishshaper%252F2460925544%252F%26size=115.4kB%26name=C%2527s%2Bbelly%2Bafter%2BHenna%26p=pregnancy%2Bfunny%26type=JPG%26oid=c48a64a197fa2378%26fusr=wishshaper%26tit=C%2527s%2Bbelly%2Bafter%2BHenna%26hurl=http%253A%252F%252Fwww.flickr.com%252Fphotos%252Fwishshaper%252F%26no=19%26sigr=11jgvclal%26sigi=11g8q7apo%26sigb=1330u1rr6%26sigh=118lvb08i&tt=3699
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    http://upload.wikimedia.org/wikipedia/commons/b/b5/Pregnancy_26_weeks.jpg
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    Teratogens

    A substance, organism, physical agents ordeficiency state capable of inducing abnormalstructure or function such as:

    Gross structural abnormalities

    Functional deficiencies

    Intrauterine growth restriction

    Behavioral aberrations

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    Drug Transfer to the Fetus Placental transfer may occur by:

    Passive diffusion

    Facilitated diffusion

    Active transport

    Placental surface area

    Placental metabolism

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    Drug Passage into Breast Milk

    Diffusion from maternal plasma into milk

    Higher maternal plasma levels mean higher

    breast milk concentrations Equilibrium will be established with most

    drugs between milk and plasma

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    STADIUM EMBRIOGENESISWeek II- late week VIII

    Most sensitive stadiumOrgan development

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    STADIUM FETOGENESIS

    Late week VIII

    Growth and development stadium

    Histogenesis CNS

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    DRUGS GIVEN AFTER THE

    FIRST TRIMESTER

    1. Heparin

    - Vertebral compression fractures- Osteoporosis

    2. Warfarin

    - Bleeding into the fetal brain

    3. Anticonvulsants- Neonatal coagulation defect

    - Sedation

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    4. Cloramphenical

    - Gray baby syndrome

    - Cardiovascular collapse

    5. Tetracycline

    - Tooth discoloration- Enamel hypoplasia

    - Bone dysplasia

    6. Aminoglycosides

    - Fetal ototoxicity

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    7. Sulfonamide- Neonatal jaundice

    - Hemolytic anemia

    8. Ciprofloxacin

    - Fetal cartilage damage

    9. -Blockers

    - Intrauterine growth retardation,

    hypoglycemia, hypotension,bradycardia, death

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    PHARMACOKINETICS

    1. Molecular Size

    - 250-500 can cross easily

    - 500-1000 cross with moredifficulty

    - Greater than 1000 cross very

    poorly

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    2. Lipid solubility- Lipophilic drugs readily cross placenta(thiopental)

    3. Ionization- Highly ionized cross the placentaslowly (succinylcholine,tubocurarrine)

    - anionized is highly lipid soluble

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    4. Protein binding

    Only unbound drug is capable ofcrossing the placenta

    Drugs with low protein binding reachhigher concentrations in the fetus thanmom

    Ex: Ampicillin, digoxin

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    2. Therapeutic drugs actions in the fetus- Corticosteroid lung maturation

    - Phenobarbital Jaundice is lower

    3. Predictable toxic drugs action in the fetus

    - Chronic use of opioids

    - ACE-inhibitor

    - Diethylstilbestrol

    4. Teratogenic drugs actions

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    DRUGS IN THE FIRST

    TRIMESTER

    1. AnticonvulsantsPoor growth, nail hypoplasia, microcephaly,cleft lip or palate

    2. Phenytoin

    - Craniofacial- Limb

    - Growth deficiencies

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    3. Sodium valproate- CNS

    4. Carbamazepine

    - Craniofacial

    - Fingernail

    5. Sex hormone

    - Cardiac defects

    - Multiple anomalies

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    Drug classification for pregnancy

    Category AControlled studies in pregnant women fail to

    demonstrate a risk to the fetus in the first trimesterwith no evidence of risk in later trimester.

    EX: Paracetamol

    Category B

    Presumed safety based on animal studies, with no

    controlled studies in pregnant, or animal studies haveshown an adverse effect that was not confirmed incontrolled studies in women in the first trimester andthere is no evidence of a risk in later trimesters

    EX: Penicilline

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    Category C

    Studies in women and animals are not available orstudies in animals have revealed adverse effects on thefetus and there are no controlled studies in women.Drugs should be given only if the potential benefitsjustify the potential risk of the fetus

    EX: Corticosteroid, Vitamin D, Vitamin B12

    Category DThere is positive evidence of human fetal risk (unsafe),

    however in some cases such as a life-threatening illness

    the potential risk may be justified if there are no otheralternatives

    EX: Warfarin, Fenitoin, Sodium Valproat, Diazepam,obat kanker

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    Penicillins Category B in pregnancy

    Crossthe placenta easily and rapidly

    Concentrations equal maternal levels

    Lactation

    Crosses in low concentrations

    Compatible with breastfeeding

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    Aminoglycosides

    (amikacin, gentamicin, tobramycin) Pregnancy Category C

    Rapidly cross placenta

    Enter amniotic fluid through fetal circulation

    Lactation

    Compatible with breastfeeding Not absorbed through GI tract

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    Sulfonamides

    Pregnancy Category C

    Readily cross the placenta

    Concerns of use at term

    Lactation

    Excreted into breastmilk in low levels Use should be avoided in premature infants

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    Tetracyclines

    (doxycycline, minocycline, tetracycline) Pregnancy Category D

    Can cause problems with teeth and bone and

    other defects/effects Have been linked to maternal liver toxicity

    Lactation

    Compatible with breastfeeding

    Serum levels in infants undetectable

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