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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
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
Hormonal Contraceptions:
Types
Route Formulation
Oral • Compbined Pills
• Monphasic
• Phased
• Progestin-only pills
• Emergency pills
Injectables • Intramuscular (long acting
progestin only)
Implants • Subcutaenous
• Intra-uterine
Hormonal Contraception:
Mechanism of Action
Inhibition of
Gonadotrophin
release
Estrogen
decreases FSH
secretion
Progestin
decreases LH
pulse
Ovulation does
not occur
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
Hormonal Contraception:
Indications
 Birth spacing/Family Planning
 Emergency Contraception
 Lowers risk of endometrial and ovarian
carcinoma (? Colorectal Ca)
 Reduced menstrual blood loss and
anaemia
Hormonal Contraception:
Indications
 Irregular menstrual cycles
 Premenstural Tensions, Dysmenorrhoea,
Menorrhagia
 Other Benefits:
Endometriosis & Pelvic Inflammatory
Disease
Fibrocystic breast disease & Ovarian
Cyst
Hormonal Contraception:
Adverse Effects
Serious Complications:
Leg vein Thrombosis and Pulmonary
Embolism (E)
Coronary and Cerebral Thrombosis
Rise in Blood Pressure (E+P)
Genital Carcinoma
Benign hepatoma
Gallstones (E)
Hormonal Contraception:
Adverse Effects
Non Serious Side Effects:
 (Frequent, during initial cycles)
Nausea, vomiting
Headache, migraine precipitated
Breakthrough bleeding or spotting (P)
Breast Discomfort
Hormonal Contraception:
Adverse Effects
Side Effects Appearing later:
 Weight gain, acne, increased body hair (older
P)
 Cholasma
 Pruritis vulvae
 Carbohydrate intolerance (older
formulations)
 Mood Swings, abdominal distentions (P)
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
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
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.
Drugs Used For Induction and
Augmentation of Labour
 Posterior Pitutary Hormone: Oxytocin,
Desamino oxytocin
 Prostaglandins
 Ergot Alkaloids: Ergometrine,
Methylergometrine
 Miscellaneous: Ethacridine, Quinine
 *Mifepristone
Oxytocin
 Effects on Uterus:
Increases force and frequency of uterine
contraction
Response of uterus varies
 Effects on Breast:
Contracts myoepithelium of mammary
alveoli.
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)
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
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)
Oxytocin: Side effects
 Injudicious use: maternal and foetal
soft tissue injury, ruptured uterus,
foetal asphyxia/death
 Water intoxication
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
Prostaglandins
 Misoprost
 Dinoprostone (PGE2): cervical
maturation/ripening; 5 times potent than and
less toxic than PGF2α; costly
 Dinoprost tromethammine(PGF2α):
myometrial contractility
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
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
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
Ergot Alkalodis
 CVS:
Weak vasoconstrictors
Can raise blood pressure
 Gastrointestinal Tract:
Increased peristalsis
Ergot Alkalodis & Oxytocin
Similarity Disparity
Gravid, (near) term
and early puerperal
uterus more sensitive
Polarity of uterus not
maintained
Ergot Alkaloids: Uses
 Control and Prevent Postpartum
Haemorrhage
 After Caesarean Section/Instrumental
Delivery- to prevent uterine atony
 To ensure normal involution
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
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
Mifepristone: Uses
 Termination of Pregnancy
 Cervical ripening
 Post-coital contraceptive
 Induction of labour*
 Once-a-month contraceptive
 Cushing Syndrome
Maternal Health Drugs and Programs

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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
  • 3. Hormonal Contraceptions: Types Route Formulation Oral • Compbined Pills • Monphasic • Phased • Progestin-only pills • Emergency pills Injectables • Intramuscular (long acting progestin only) Implants • Subcutaenous • Intra-uterine
  • 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
  • 7. Hormonal Contraception: Indications  Irregular menstrual cycles  Premenstural Tensions, Dysmenorrhoea, Menorrhagia  Other Benefits: Endometriosis & Pelvic Inflammatory Disease Fibrocystic breast disease & Ovarian Cyst
  • 8. Hormonal Contraception: Adverse Effects Serious Complications: Leg vein Thrombosis and Pulmonary Embolism (E) Coronary and Cerebral Thrombosis Rise in Blood Pressure (E+P) Genital Carcinoma Benign hepatoma Gallstones (E)
  • 9. Hormonal Contraception: Adverse Effects Non Serious Side Effects:  (Frequent, during initial cycles) Nausea, vomiting Headache, migraine precipitated Breakthrough bleeding or spotting (P) Breast Discomfort
  • 10. Hormonal Contraception: Adverse Effects Side Effects Appearing later:  Weight gain, acne, increased body hair (older P)  Cholasma  Pruritis vulvae  Carbohydrate intolerance (older formulations)  Mood Swings, abdominal distentions (P)
  • 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
  • 25. Ergot Alkalodis  CVS: Weak vasoconstrictors Can raise blood pressure  Gastrointestinal Tract: Increased peristalsis
  • 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
  • 30. Mifepristone: Uses  Termination of Pregnancy  Cervical ripening  Post-coital contraceptive  Induction of labour*  Once-a-month contraceptive  Cushing Syndrome

Editor's Notes

  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. Also known as Oxytocics, Abortifacients PGE1, methyl PGE1 (misoprostol) PGE2, Dinoprostone PGF2α ,15-methyl PGF2α(Dinoprost/Carboprost)
  7. Response of uterus varies with: State of gravidity, Influence of oestrogens / progesterone Trimester of Pregnancy Polarity of uterus
  8. Response of uterus varies with: State of gravidity, Influence of oestrogens / progesterone Trimester of Pregnancy Polarity of uterus
  9. Effective in near term pregnancy:- Number of oxytocin receptors increases markedly during later part of pregnancy
  10. Induction of labour in postmaturity, prematurely in toxaemia of pregnancy, diabetic mother, erythroblastosis, ruptured membranes, placental insufficiency
  11. Induction of labour in postmaturity, prematurely in toxaemia of pregnancy, diabetic mother, erythroblastosis, ruptured membranes, placental insufficiency
  12. Local Hormones, derived from breakdown of membrane phospholipid (yielding arachidonic acid)
  13. 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
  14. (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
  15. Low dose phasic response; high dose contracture seen
  16. Low dose phasic response; high dose contracture seen
  17. 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
  18. Induction of labour- in cases of IUFD, abnormal foetus