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INDUCTION OF LABOUR
Moderator:
Asst Prof. Dr. B.K. Borah
Speaker:
Dr. Nancy Anitha
What is Induction of Labour?
• Induction of labor is the artificial
initiation of labour mechanism prior
to its spontaneous onset.
Mechanism of initiation of labor
Mechanism (continued)
Endocrinology of labor
Time, place & preparation
• Time of induction: Preferably early morning
• Place of induction: where facility for
intervention and fetal monitoring is available
• Preparation of Patient : Enema may be given
to patients prior to induction
Indications of Induction of
labor
Indications for induction of
labor
Contraindications of induction of
labor
• Contracted pelvis and CPD
• Malpresentations
• Previous classical caesarean section &
hysterotomy
• Uteroplacental factors: unexplained
vaginal bleeding,vasa previa,placenta
previa
• Cord presentation,cord prolapse
• Active genital herpes infection,HIV
• Pelvic tumor
Factors to assess prior to
induction
Maternal
 To confirm the
indication
 Exclude the
contraindicatn
 Assess Bishop
score
 Assess pelvic
adequacy
Fetal
 Ensure fetal
gestn age
 Ensure fetal
presentation
 Confirm fetal
well being
Modified Bishop’s Score
Favourable score->6 Best score-8
hygroscopic dilators, osmotic dilators (Laminaria japonicum), Foley
catheters, double balloon devices, and extraamniotic saline infusion.
• Misoprostol (a prostaglandin E1 analogue) has several potential
advantages: it is stable at room temperature, it is relatively
inexpensive and it can be given via several routes (oral, vaginal,
sublingual, buccal). These properties make misoprostol an ideal
agent for induction of labour, particularly in settings where the
use of prostaglandin E2 is not possible owing to lack of
availability, facilities for storage, or financial constraints.
• Since the use of a powerful uterotonic such as misoprostol can
lead to adverse maternal and perinatal effects, it is important
to review the effectiveness and the side-effects of misoprostol
use in cervical priming and induction of labour. This commentary
evaluates three Cochrane reviews that sought to determine the
effectiveness and safety of misoprostol administered orally (3),
buccally (sublingually) (4), or vaginally (5) for third-trimester
cervical ripening and induction of labour.
Membrane sweeping
• Its possible only if the
cervix has ripened to allow
the passage of one finger.
• Insertion of a gloved
finger through the cervix
and it’s rotation against
the wall of the uterus.
• Its strips off the chorionic
membrane from the
underlying decidua
releases PGS
• Placenta previa should be
excluded, Accidental
amniotomy is a
disadvantage.
Amniotomy
• AROMstretching of the cervix & separation
of the membranes  release of Prostaglandins
• Depends on the state of the cervix and station
of the presenting part
• ADV:High success rate and chance to see the
amniotic fluid
• DIS: cannot be applied in an unfavourable
cervix, possibility of cord prolapse
Amniotomy
CONTRAINDICATIONS:
1.IUD
2.HIV
HAZARDS:
1.Cord prolapse
2.Amnionitis
3.Amniotic fluid
embolism
4. Abruptio placentae
Prostaglandins
• Chemistry:PG is a carboxylic
acid synthetised from
arachidonic acid.
• Source: menstrual fluid,
endometrium, decidua and
amniotic membrane
TYPES
• PGE1 -amnion
• PGE2-amnion
• PGF2-decidua and myometrium
• PGI2-myometrium
Mechanism of action
• It causes change in the
myometrial cell memb
permeablity and alteration
in the membrane bound
calcium
• It also sensitises the
mometrium to the oxytocin
• PGE2 has its collagenolytic
activityalter the ground
substance of cervixcx
ripening
Prostaglandins
PGE1
Misoprostol
PGE2
Dinoprostone
(Cerviprime)
How to give Misoprostol?
• Dose of 25 micro gram every 4hrly to a
maximum of 6 doses can be given
intravaginally
• Dose of 50micro gram every 3hrs to a
maximum of 6 doses can be given orally
• Dose of 25micro gram every 2hrs can
be given orally
• Other routes of administration:
1.Buccal
2.rectal
3.sublingual
Oral Vs vaginal Misoprostol
ORAL
• Less effective
when compared
to vaginal PG
• Chance of fetal
distress is less
VAGINAL
• More effective when
compared to oral
route
• Chance of fetal
distress is more
Dinoprostone
• Vaginal gel 0.5mg can be given
intracervically.
• It can be repeated after 6 hrs for 3 – 4
doses if required
• Vaginal tab 3 mg can be given in
the posterior fornix followed by
3mg after 6-8 hrs to a maximum
dose of 6mg
• Vaginal pessary releasing
dinoprostone 10mg over 24hrs.It
is removed when cx ripening is
adequate
Misoprostol Vs Dinoprostone
• Cheap & cost
effective
• Stable at room temp
• Easy to administer
• Costly
• Need refrigeration
Advantages Disadvantages
• Misoprostol is Cheap
and has long half life
• It is stable at room
temp
• Induction-delivery
interval is short
• Failure of induction is
less
• Powerful oxytoxic
effect irrespective
of gestation
• Side eff: Vomiting,
diarrhoea
• Bronchospasm
• Hyerstimulation of
uterus
• Tachysystole
• Fetal distress
• Rupture uterus
Contraindications of PGs
• Bronchial asthma
• Pulmonary disease
• Previous uterine scar is
relatively
contraindicated
Oxytocin
• It’s a nanopeptide
synthetised in the supra
optic and paraventricular
nuclei of the hypothalamus.
• Half life of 3-4 mins and
duration of action 20 mins
• Oxytocin is used very
commonly to achieve
induction of labour.
• The objective is to produce
uterine contractions that
effectively produce cervical
change and descent of the
presenting part.
Mode of Action
1.It acts throgh the receptor and voltage
gated calcium channelmyometrial
contraction
2.It stimulates amniotic and decidual PG
production
Preparations
• Available in ampoules containing 5IU/ml
• Buccal tab containing 50IU/ml
• Nasal solution containing 40units/ml
Routes of administration:
• 1.I.V infusion
• Intra muscular
• Buccal tablets
• Nasal spray
How to give?
Maximum dose of oxytocin 5IU in 500ml of
fluid at the rate of 40drops /min
Oxytocin Surgical Infusion Pump
Oxytocin (syntocinon) should be used
with extreme caution in multiparous
women.
 Oxytocin (syntocinon) should not be
started for six hours following
administration of vaginal prostaglandins
 If a trial of labour is judged safe
then Oxytocin may be used.
 Oxytocin should be used with caution
with a previous uterine scar.
 Oxytocin should always be used in
conjunction with the partogram once in
established labour.
F
A
C
T
S
Advantages
• Cheaper and effective
• Easy titrable
Disadv:
.Needs refrigeration
.Effectiveness less with:
1. less Bishop score
2.IUD
3.lesser weeks of
pregnancy
Hazards of oxytocin
• Uterine hyperstimulation:
(Normal:3 contractions in 10 mins
each lasting for 45secs)
(>5 contractions in 10mins each
lasting for 1min)
• Water intoxication:It due to
anti diuretic action(30-
40IU/ml).Manifested by
hyponatremia,confusion,coma
and CCF
• Fetal distress
• Uterine rupture
• Hypotension
When to interrupt?
• When there is hyperstimulation of
uterus
• Fetal distress
• Signs of water intoxication.(Occurs
with the max dose of 100 IU in the
interval of less than 24hrs .clinically
Manifested after 24hrs)
Oxytocin Vs Misoprostol
• Safe,cheap and
effective
• Unstable at room
temp
• Easily titrable
• Chance of fetal
distress is less
• More effective near
term
• Less effective with
less Bishop score
and in IUD
• Tablet form is
cheap& effective
• Stable at room
temp,PGE1-unstable
• Not titrable
• Chance of fetal
distress is more
• Effective
irrespective of
gestation
Failed Induction Of Labor
• If Amniotomy is still
impossible after a
maximum no. of doses of
Prostaglandins have been
given or
• If the cervix remains
uneffaced and <3cm
dilated after an
Amniotomy has been
performed &
• Oxytocin has been
running for 6-8hrs with
regular contractions
• Possible Causes
1. Placental Sulfatase
deficiency
2. Lack of Essential
Cytokines
Complications of IOL
• Uterine
Hyperstimulation
• Uterine rupture
• Maternal Upset
• Iatrogenic Fetal
Prematurity
• Fetal Distress
• Failed induction
CONCLUSION
during Induction of Labor,
B enefits should be weighed,
R isks should be assessed,
A lternatives should be considered,
N ecessity of intervention adjudged
&
D ecision should be taken
accordingly
BUT,
INJUDICIOUS USE of Labor Inducing agents should
be avoided
THANK YOU

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Induction of labour

  • 1. INDUCTION OF LABOUR Moderator: Asst Prof. Dr. B.K. Borah Speaker: Dr. Nancy Anitha
  • 2. What is Induction of Labour? • Induction of labor is the artificial initiation of labour mechanism prior to its spontaneous onset.
  • 6. Time, place & preparation • Time of induction: Preferably early morning • Place of induction: where facility for intervention and fetal monitoring is available • Preparation of Patient : Enema may be given to patients prior to induction
  • 9. Contraindications of induction of labor • Contracted pelvis and CPD • Malpresentations • Previous classical caesarean section & hysterotomy • Uteroplacental factors: unexplained vaginal bleeding,vasa previa,placenta previa • Cord presentation,cord prolapse • Active genital herpes infection,HIV • Pelvic tumor
  • 10. Factors to assess prior to induction Maternal  To confirm the indication  Exclude the contraindicatn  Assess Bishop score  Assess pelvic adequacy Fetal  Ensure fetal gestn age  Ensure fetal presentation  Confirm fetal well being
  • 11.
  • 12. Modified Bishop’s Score Favourable score->6 Best score-8
  • 13. hygroscopic dilators, osmotic dilators (Laminaria japonicum), Foley catheters, double balloon devices, and extraamniotic saline infusion.
  • 14. • Misoprostol (a prostaglandin E1 analogue) has several potential advantages: it is stable at room temperature, it is relatively inexpensive and it can be given via several routes (oral, vaginal, sublingual, buccal). These properties make misoprostol an ideal agent for induction of labour, particularly in settings where the use of prostaglandin E2 is not possible owing to lack of availability, facilities for storage, or financial constraints. • Since the use of a powerful uterotonic such as misoprostol can lead to adverse maternal and perinatal effects, it is important to review the effectiveness and the side-effects of misoprostol use in cervical priming and induction of labour. This commentary evaluates three Cochrane reviews that sought to determine the effectiveness and safety of misoprostol administered orally (3), buccally (sublingually) (4), or vaginally (5) for third-trimester cervical ripening and induction of labour.
  • 15. Membrane sweeping • Its possible only if the cervix has ripened to allow the passage of one finger. • Insertion of a gloved finger through the cervix and it’s rotation against the wall of the uterus. • Its strips off the chorionic membrane from the underlying decidua releases PGS • Placenta previa should be excluded, Accidental amniotomy is a disadvantage.
  • 16. Amniotomy • AROMstretching of the cervix & separation of the membranes  release of Prostaglandins • Depends on the state of the cervix and station of the presenting part • ADV:High success rate and chance to see the amniotic fluid • DIS: cannot be applied in an unfavourable cervix, possibility of cord prolapse
  • 18. Prostaglandins • Chemistry:PG is a carboxylic acid synthetised from arachidonic acid. • Source: menstrual fluid, endometrium, decidua and amniotic membrane TYPES • PGE1 -amnion • PGE2-amnion • PGF2-decidua and myometrium • PGI2-myometrium
  • 19. Mechanism of action • It causes change in the myometrial cell memb permeablity and alteration in the membrane bound calcium • It also sensitises the mometrium to the oxytocin • PGE2 has its collagenolytic activityalter the ground substance of cervixcx ripening
  • 21. How to give Misoprostol? • Dose of 25 micro gram every 4hrly to a maximum of 6 doses can be given intravaginally • Dose of 50micro gram every 3hrs to a maximum of 6 doses can be given orally • Dose of 25micro gram every 2hrs can be given orally • Other routes of administration: 1.Buccal 2.rectal 3.sublingual
  • 22. Oral Vs vaginal Misoprostol ORAL • Less effective when compared to vaginal PG • Chance of fetal distress is less VAGINAL • More effective when compared to oral route • Chance of fetal distress is more
  • 23. Dinoprostone • Vaginal gel 0.5mg can be given intracervically. • It can be repeated after 6 hrs for 3 – 4 doses if required • Vaginal tab 3 mg can be given in the posterior fornix followed by 3mg after 6-8 hrs to a maximum dose of 6mg • Vaginal pessary releasing dinoprostone 10mg over 24hrs.It is removed when cx ripening is adequate
  • 24. Misoprostol Vs Dinoprostone • Cheap & cost effective • Stable at room temp • Easy to administer • Costly • Need refrigeration
  • 25. Advantages Disadvantages • Misoprostol is Cheap and has long half life • It is stable at room temp • Induction-delivery interval is short • Failure of induction is less • Powerful oxytoxic effect irrespective of gestation • Side eff: Vomiting, diarrhoea • Bronchospasm • Hyerstimulation of uterus • Tachysystole • Fetal distress • Rupture uterus
  • 26. Contraindications of PGs • Bronchial asthma • Pulmonary disease • Previous uterine scar is relatively contraindicated
  • 27. Oxytocin • It’s a nanopeptide synthetised in the supra optic and paraventricular nuclei of the hypothalamus. • Half life of 3-4 mins and duration of action 20 mins • Oxytocin is used very commonly to achieve induction of labour. • The objective is to produce uterine contractions that effectively produce cervical change and descent of the presenting part.
  • 28. Mode of Action 1.It acts throgh the receptor and voltage gated calcium channelmyometrial contraction 2.It stimulates amniotic and decidual PG production Preparations • Available in ampoules containing 5IU/ml • Buccal tab containing 50IU/ml • Nasal solution containing 40units/ml Routes of administration: • 1.I.V infusion • Intra muscular • Buccal tablets • Nasal spray
  • 29. How to give? Maximum dose of oxytocin 5IU in 500ml of fluid at the rate of 40drops /min
  • 31. Oxytocin (syntocinon) should be used with extreme caution in multiparous women.  Oxytocin (syntocinon) should not be started for six hours following administration of vaginal prostaglandins  If a trial of labour is judged safe then Oxytocin may be used.  Oxytocin should be used with caution with a previous uterine scar.  Oxytocin should always be used in conjunction with the partogram once in established labour. F A C T S
  • 32. Advantages • Cheaper and effective • Easy titrable Disadv: .Needs refrigeration .Effectiveness less with: 1. less Bishop score 2.IUD 3.lesser weeks of pregnancy
  • 33. Hazards of oxytocin • Uterine hyperstimulation: (Normal:3 contractions in 10 mins each lasting for 45secs) (>5 contractions in 10mins each lasting for 1min) • Water intoxication:It due to anti diuretic action(30- 40IU/ml).Manifested by hyponatremia,confusion,coma and CCF • Fetal distress • Uterine rupture • Hypotension
  • 34. When to interrupt? • When there is hyperstimulation of uterus • Fetal distress • Signs of water intoxication.(Occurs with the max dose of 100 IU in the interval of less than 24hrs .clinically Manifested after 24hrs)
  • 35. Oxytocin Vs Misoprostol • Safe,cheap and effective • Unstable at room temp • Easily titrable • Chance of fetal distress is less • More effective near term • Less effective with less Bishop score and in IUD • Tablet form is cheap& effective • Stable at room temp,PGE1-unstable • Not titrable • Chance of fetal distress is more • Effective irrespective of gestation
  • 36. Failed Induction Of Labor • If Amniotomy is still impossible after a maximum no. of doses of Prostaglandins have been given or • If the cervix remains uneffaced and <3cm dilated after an Amniotomy has been performed & • Oxytocin has been running for 6-8hrs with regular contractions • Possible Causes 1. Placental Sulfatase deficiency 2. Lack of Essential Cytokines
  • 37. Complications of IOL • Uterine Hyperstimulation • Uterine rupture • Maternal Upset • Iatrogenic Fetal Prematurity • Fetal Distress • Failed induction
  • 38. CONCLUSION during Induction of Labor, B enefits should be weighed, R isks should be assessed, A lternatives should be considered, N ecessity of intervention adjudged & D ecision should be taken accordingly BUT, INJUDICIOUS USE of Labor Inducing agents should be avoided