2. • Induction of labour involves the use of some
methods to initiate uterine contractions before the
spontaneous onset of labour
• Includes Ripening of cervix.
onset of uterine contractions
• Purpose Achieve vaginal delivery
To avoid operative delivery by cs
3. RIPENING OF CX
• Normal physiological process that precedes
ut.contractions & includes highly complex biochemical
process
• Remodelling of cx occurs towards term
* dissociation of collagen bundles
* increase in water content of cx
* invaded by neutrophils ¯ophages(releases
inf cytokines_ IL -1B,IL-8 )
4. MODIFIED BISHOP SCORE
Factor Score
0 1 2
Dilatation <1.5 1.5-3 >3
Effacement(cm) 1.5> intermediat 0.5or less
e
Station -2 or higher -1 0 or
lower
Consistency Firm intermediat Soft
e
Position Posterior Mid Anterior
5. Prerequisites for IOL
Maternal & fetal risk –benefit analysis
should be assessed before
IOL
Informed consent
Maternal pelvis assessed
Fetal wt. & presentation
Confirm lung maturity
cx status assessed ---success of induction
& outcome
6. Contraindications to cx ripening
Absolute CI
• Special caution
•pl. preavia
•Vasa preavia – Previous LSCS
• Active genital herpes – Multiple preg.
•Invasive ca cx. – Polyhydramnios
•Previous ut. Surgery – Mat. Heart ds
Classical cs – Severe HTN.
Previous metroplasty
Myomectomy---cavity
opened
7. ELECTIVE INDUCTION
• Induction of labour in the absence of
maternal or fetal indication.
• Convenience of pt. and obstetrician.
• Not encouraged.
• Unripe cx. prolonged labour
failed induction.
12. Stripping of membranes
Release of endogenous PG
Risk ascending infection
bleeding from pl .preavia
accidental rom
Advantage - makes spontaneous onset of
labour more likely.
Reduces the need for formal IOL
When? 39 wks
13. Amniotomy
• ARM is commonly used along with oxytocin infusion
• Shortens the induction –delivery interval
• Ideally ARM done - cx. is favorable
• Spontaneous labour - do only in the active phase
• Delay ARM - occipitoposterior position.
• Oxytocin infusion can be started if ut. Contractions do
not ensue in 2-4 hrs.
14. PROSTAGLANDINS
ONLY When cervix is unripe.
• Action------- dissolution of collagen bundles
increases tissue water content
stimulates myometrium
PG-E2 (dinoprostone)
Preparation and dosages
0.5mg intracervical
2.5mg intravaginal
Kept refrigerated
Brought to room temp. b/f admn.
Contraindications fever
allergy to PG
abn. Vaginal bleed.
15. Mode of admn
• Studies show that intravaginal route is
more superior to IC route (RCOG)
• Rcog(2008) does not recommend other
routes like;
• Oral ,extraamniotic, intracervical PG
Intracervical preparation should not be used for
Intravaginal application.
16. Additional dosage?
• Pv exam done after 6hrs –no cx response
rpt. dose admn.
• Maximum recommended cumulative dose
is 2 doses*24hrs.
• Recommended interval before
administering oxytocin( after PG-E2 )is 6-
12 hrs
17. MISOPROSTOL
• More effective than PG-E2 in producing cx ripening
• Not approved by FDA for IOL at term.
• Advantage inexpensive
easy to store
stable at room temp.
• Risk high incidence of ut. Hyperstimulation
thick meconium
• Low dose regime--25microgm of PGE1
incidence of tachysystole < by 50%
RCOG 2008: PGE1 should only be offered as a method of IOL in IUD
or in the context of a clinical trial.
18. Complications of prostaglandins
• Systemic side effects: nausea,vomiting,diarrhoea,fever
• Ut. Hyperstimulation
» Defined as tachysystole or hypersystole ass. with
nonreassuring FHR pattern.
» tachysystole—def. as 6>more ut. Contractions in 10
mts.
» Hyper systole--- def. as single contraction of at least
2mts duration.
19. Oxytocin
Mechanism of action
binds to OTR in the myometrial cell wall and
increase intracellular ca conc.
increase plasma PG conc.
Dosage
oxytocin is started as a low dose in normal saline(5U in
500ml NS) and the rate is doubled every 30 mts.
4 drops/mt=2.5mu/mt
max dose is 40mu/mt (60 drops/mt)
ARM before oxytocin
20. Guidelines for oxytocin infusion
• A written protocol for oxytocin admn. should
be available in the labour room.
• Unfavorable cx. ---oxytocin should not be
used as a primary method of IOL.
• All medical personnel who administer
oxytocin should be able to identify and
manage oxytocin complications.
• Once the intensity of contractions increases
oxytocin rate should be reduced or stopped.
• Partogram
• CTG monitoring.
21. Complications
Ut. Hyperstimulation
Mgt stop ,left lateral position ,
O2 inhalation ,iv fluids
terbutaline 250 microgm sc
Water intoxication
• Large dose of oxytocin given for prolonged period
• Sodium poor iv fluids are used
• Hyponatremia-----confusion, convulsions coma death.
22. Rupture uterus
multi ,prev.cs ,
malpresentations
overdistented ut.
Cl.presentation nonspecific and variable
most imp. Warning sign is FHR variation
sudden tearing pain
pp may spontaneously lose station
p/a- abn .uterine contour
shock and referred pain to shoulder---late
23. RCOG recommendations in Special
circumstances
Previous cs
PGE2 & oxytocin is safe in pts .who are candidates for VBAC
.
PGE1 contraindicated.
IUGR - severe FGR with fetal compromise- IOL is not recommended
PPROM-
<34 wks-expectant mgt.
>34wks---intravaginal PGE2
IUD
labour induced with oral mifepristone (200mgdaily *2days) foll. by vaginal PGE2 or PGE1
IUD with previous cs - dosage of PG should be reduced.
24. Summary
• Stripping of membranes at 39 wks.
• ARM only in active phase of labour.
delay ARM op position.
• Foleys catheter long rigid cx, IUGR
• PG ONLY when cx is unripe.
• Misoprostol low dose regime - 25 microgm 6th hrly.
• Oxytocin start as low dose in NS.
do ARM before oxytocin.
• Avoid cocktail regimen.