Based on the BPH curriculum of TU and maternal health program of Nepal. All the drugs have not been discussed and remaining drugs will be discussed in subsequent classes
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Maternal Health Drugs and Programs
1. Drugs Used in
Maternal Health
For BPH 1st Year
Dr. Pravin Prasad
Resident 3rd Year
MD Clinical Pharmacology
Maharajgunj Medical Campus
18th June, 2017 (4th Ashar, 2074) Sunday
2. Maternal Health
Programmes in Nepal
Programmes Drugs/Medicines
Family Planning Hormonal Contraceptives
Antenatal Care Albendazole
Labour and
Delivery
Oxytocics
Postpartum Care Prevention of Post partum
Haemorrhage
Neonatal Care
4. Hormonal Contraception:
Mechanism of Action
Inhibition of
Gonadotrophin
release
Estrogen
decreases FSH
secretion
Progestin
decreases LH
pulse
Ovulation does
not occur
5. Hormonal Contraception:
Mechanism of Action
Thick cervical
mucous (p)
Hostile Endometrium:
Most important in case of
minipills and post coital pills
Uterine and
Tubal
Contractions
Postcoital pills may dislodge a just
implanted blastocyst or may interfere
with fertilization/implantation
6. Hormonal Contraception:
Indications
Birth spacing/Family Planning
Emergency Contraception
Lowers risk of endometrial and ovarian
carcinoma (? Colorectal Ca)
Reduced menstrual blood loss and
anaemia
11. Drugs Used in Antenatal
Care: Anti-helminthics
Albendazole, Mebendazole
Mechanism of Action:
Binds to β-tubulin of susceptible worms
polymerization inhibited intracellular
microtubules gradually lost worm
immobilized and killed.
Blocks glucose uptake by parasite glycogen
storage depleted worm killed
Hatching of nematode eggs and their larvae
are also inhibited
12. Drugs Used in Antenatal
Care: Anti-helminthics
Uses:
Ascariasis
Hookworm
Enterobius, Trichuris (400 mg single oral
dose; 3 day treatment for heavy
trichuriasis)
Tapeworm and strongyloidosis
13. Drugs Used in Antenatal
Care: Anti-helminthics
Side Effects:
Pregnancy Category C
Well tolerated
GI side effects, dizziness
Headache, fever, alopecia, jaundice,
neutropenia on prolonged use.
14. Drugs Used For Induction and
Augmentation of Labour
Posterior Pitutary Hormone: Oxytocin,
Desamino oxytocin
Prostaglandins
Ergot Alkaloids: Ergometrine,
Methylergometrine
Miscellaneous: Ethacridine, Quinine
*Mifepristone
15. Oxytocin
Effects on Uterus:
Increases force and frequency of uterine
contraction
Response of uterus varies
Effects on Breast:
Contracts myoepithelium of mammary
alveoli.
16. Oxytocin
Cardiovascular System (CVS):
Higher Dose: brief fall in blood pressure,
reflex tachycardia, flushing
Kidney:
ADH like action at high doses (pulmonary
edema at high doses of oxytocin with large
amounts of intravenous fluids)
17. Oxytocin
Mechanism of Action:
Oxytocin receptors (GPCR)
On Activation:
Depolarization of muscle fibres and influx
of Ca++ ions
Effective in near term pregnancy
Increase Prostaglandin (PG) synthesis and
release by the endometrium
18. Oxytocin: Uses
Induction of Labour (slow i.v. infusion 5IU in
500 ml glucose or NS; 10milli IU/mL: 0.2-2.0
mL/min)
Uterine Inertia
Postpartum Haemorrhage
Breast Engorgement (inefficient milk ejection
reflex; intra-nasally)
Oxytocin Challenge Test (risky and rarely
performed)
19. Oxytocin: Side effects
Injudicious use: maternal and foetal
soft tissue injury, ruptured uterus,
foetal asphyxia/death
Water intoxication
20. Prostaglandins
Local Hormones
Mechanism of Action:
Change in myometrial cell membrane
permeability and/or alteration of membrane
bound Ca++
Also sensitizes uterus to oxytocin
Promotes myometrial contraction irrespective
of duration of gestation
21. Prostaglandins
Misoprost
Dinoprostone (PGE2): cervical
maturation/ripening; 5 times potent than and
less toxic than PGF2α; costly
Dinoprost tromethammine(PGF2α):
myometrial contractility
22. Prostaglandins: Uses
Induction of abortion: molar pregnancy, tubal
pregnancy
Induction of labour
Poor pre-induction cervical score
Acceleration of labour
Management of atonic postpartum
haemorrhage
Refractive cases
23. Prostaglandins: Side Effects
On systemic use:
Nausea, vomiting, diarrhoea, pyrexia,
bronchospasm
Cervical laceration when used as an
abortifacient
Tachy-systole of uterus during induction
Meconium passage by foetus (Foetal Distress)
Rupture of uterus: Rare
Should not be used in patients with previous
history of Caesarean Section
24. Ergot Alkalodis
Ergometrine and Methylergometrine
Uterus:
Partial agonistic action on 5-HT2 and
alpha adrenergic receptors
Force, frequency and duration of uterine
contraction increased
Dose dependent response
26. Ergot Alkalodis & Oxytocin
Similarity Disparity
Gravid, (near) term
and early puerperal
uterus more sensitive
Polarity of uterus not
maintained
27. Ergot Alkaloids: Uses
Control and Prevent Postpartum
Haemorrhage
After Caesarean Section/Instrumental
Delivery- to prevent uterine atony
To ensure normal involution
28. Ergot Alkaloids: Side Effects
Nausea, vomiting
Rise in blood pressure
Decrease milk secretion if used n higher dose
for many days postpartum
Should be avoided in patients with:
Vascular disease
Presence of sepsis
Liver and Kidney Disease
29. Mifepristone
Anti-progestational, anti-glucorticoid,
antiandrogenic activity
Anti-fertility effects by various mechanisms
Abortifacient effect:
Sensitizes myometrium to PG
Blocks decidualization conceptus
dislodged
hCG production falls decreased
progesterone cervix softens
3rd gen Monophasic pills: Ethinylestradiol 30mcg, progestins (19-nortestosterone- anti-ovulatory) levonorgestrol 60mcg, desogestrel 60, norgestimate- 200, gestodene- 40
Phasic pills- 35 yrs above where breakthrough bleeding is not occurring
Progestin only pills- eliminate estrogen, low efficacy
Emergency pills- levonorgesterol 0.75 mg 2 doses, 12 hrs apart or 1.5 mg single oral dose within 72 hrs; earlier method (Yupze)- levonorgesterol 0.5 mg, ethnylestradiol 0.1 mg, higher nausea and vomiting
Depot medroxyprogesterone acetate (Depo-provera, sangini 3 month injection)
Norplant- levonogesterol 36mg * 6 capsules
Venous thromboembolism: Estrogen
Arterial thromboembolism: Estrogen + Progestin
Genital Carcinoma: (vaginal, cervical, breast) increased risk in predisposed individuals; growth of already existing hormone dependent tumor may be hastened
Venous thromboembolism: Estrogen
Arterial thromboembolism: Estrogen + Progestin
Genital Carcinoma: (vaginal, cervical, breast) increased risk in predisposed individuals; growth of already existing hormone dependent tumor may be hastened
Venous thromboembolism: Estrogen
Arterial thromboembolism: Estrogen + Progestin
Genital Carcinoma: (vaginal, cervical, breast) increased risk in predisposed individuals; growth of already existing hormone dependent tumor may be hastened
Though it is Pregnancy category C, it is given to pregnant women in 2nd trimester because risk of anaemia due to hookworm infestation is high in Nepal and benefit of treating the women for hookworm infestation outweights risk to foetus
Also known as Oxytocics, Abortifacients
PGE1, methyl PGE1 (misoprostol)
PGE2, Dinoprostone
PGF2α ,15-methyl PGF2α(Dinoprost/Carboprost)
Response of uterus varies with:
State of gravidity,
Influence of oestrogens / progesterone
Trimester of Pregnancy
Polarity of uterus
Response of uterus varies with:
State of gravidity,
Influence of oestrogens / progesterone
Trimester of Pregnancy
Polarity of uterus
Effective in near term pregnancy:- Number of oxytocin receptors increases markedly during later part of pregnancy
Induction of labour in postmaturity, prematurely in toxaemia of pregnancy, diabetic mother, erythroblastosis, ruptured membranes, placental insufficiency
Induction of labour in postmaturity, prematurely in toxaemia of pregnancy, diabetic mother, erythroblastosis, ruptured membranes, placental insufficiency
Local Hormones, derived from breakdown of membrane phospholipid (yielding arachidonic acid)
Misoprost: cheap, stable at room temperature, long shelf life, easily administered, less side effects
PGE2 and PGF2α: commonly used clinically
Dinoprostone (PGE2): cervical maturation/ripening (collagenolytic property); 5 times potent than and less toxic than PGF2α; costly
(poor pre-induction cervical score as in Intrauterine Foetal Death, shorter period of gestation, early primigravida: PGE1)
Management of atonic postpartum haemorrhage (Carboprost, 15-methyl PGF2a)
Refractive cases
Low dose phasic response; high dose contracture seen
Low dose phasic response; high dose contracture seen
19-norsteroid with potent anti-progestational and significant antiglucorticoid, antiandrogenic activity
Mechanism of Action:
Follicular phase- attenuation of mid cycle LH surge delayed follicular maturation/ anovulation
Leutal Phase- prevents secretory changes of progesterone
Late phases- blocks progesterone support to endometrium unchecked PG secretion stimulated uterine contractions
Abortifacent actions:
Sensitizes myometrium to PG menstruation
Blocks decidualization conceptus dislodged, hCG production falls secondary leutolysis & decreased endogenous progesterone production cervix softens abortion
Induction of labour- in cases of IUFD, abnormal foetus