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INDUCTION OF LABOUR
• 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
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 &macrophages(releases
     inf cytokines_ IL -1B,IL-8 )
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
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
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
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.
When to induce ?
Methods of cx ripening and labour induction
Mechanical dilators
   -Balloon cath
   -Laminaria
   -Osmotic dilators

Stripping of memb

Amniotomy

Pharmacological Preparation
   -PGE2
   -oxytocin
   -Misoprostol(PGE1 analogue)
   -Mifepristone(RU-486)
   -Relaxin
   -NO
Mechanical methods
• Allows slow and controlled dilatation of cx.

• Ideal    cx firm, postr.,long and closed
          severe FGR, oligamnios,
• Method (EASI)
     aseptic precautions foleys catheter
     inflated with 30ml distilled water
     100ml NS extraamniotic space
     spontaneous passage 12hrs

       ARM &pitocin
•
EASI
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
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.
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.
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.
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
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.
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.
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
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.
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.
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
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.
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.
Induction of labour

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ANATOMY AND PHYSIOLOGY OF REPRODUCTIVE SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF REPRODUCTIVE SYSTEM.pptxANATOMY AND PHYSIOLOGY OF REPRODUCTIVE SYSTEM.pptx
ANATOMY AND PHYSIOLOGY OF REPRODUCTIVE SYSTEM.pptx
 

Induction of labour

  • 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 &macrophages(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.
  • 9. Methods of cx ripening and labour induction Mechanical dilators -Balloon cath -Laminaria -Osmotic dilators Stripping of memb Amniotomy Pharmacological Preparation -PGE2 -oxytocin -Misoprostol(PGE1 analogue) -Mifepristone(RU-486) -Relaxin -NO
  • 10. Mechanical methods • Allows slow and controlled dilatation of cx. • Ideal cx firm, postr.,long and closed severe FGR, oligamnios, • Method (EASI) aseptic precautions foleys catheter inflated with 30ml distilled water 100ml NS extraamniotic space spontaneous passage 12hrs ARM &pitocin •
  • 11. EASI
  • 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.