guidelines for vaginal birth after previous caesarean birth

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  • 8/14/2019 Guidelines for Vaginal Birth After Previous Caesarean Birth

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    GUIDELINES FORGUIDELINES FOR

    VAGINAL BIRTH AFTERVAGINAL BIRTH AFTERPREVIOUSPREVIOUS

    CAESAREAN BIRTHCAESAREAN BIRTHDr .Ashraf Fouda

    Egypt - Damietta GeneralHospital

    E. mail :

    [email protected]

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    S.O.G.C.(Society ofObstetricians &Gynecologists ofCanada)

    CLINICAL PRACTICE GUIDELINESThis document with articles publishedfromJanuary 1995 to February 2004,

    obtained by searching the MEDLINEdatabase using the key words

    vaginal birth after C.S.

    SOURCE:

    July 2004

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    BACKGROUND

    The most frequentindications for C.S are

    previous C.S., dystocia,malpresentation, and non-

    reassuring fetal status.The rate of birth by C.S.

    and the rate of VBAC tend

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    Schell first reportedVBAC in 1923,

    describing the successfulvaginal delivery of

    infants in mothers withprevious Caesarean

    deliveries.

    BACKGROUND

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    A trial of labour afterC.S. should be

    considered in womenwho present for

    prenatal care with ahistory of previous

    BACKGROUND

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    In certain situations, TOLafter C.S. will be

    contraindicated and arepeat C.S. will advised,

    But in most cases,successful vaginal birth can

    be achieved safely for both

    BACKGROUND

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    Women and their

    health-care providerswill need to discuss

    the risks and benefitsof VBAC when

    planning the birth.

    BACKGROUND

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    The data obtained is limited by 3

    important factors:

    First, there are no randomized trials ofTOL versus elective repeat C.S. (ERCS);

    Second, adverse maternal or perinataloutcomes are rare and large studypopulations are necessary to observe a

    significant difference in maternal andperinatal outcomes; and,

    Finally, the womans choice to attempt a

    TOL after C.S. is heavily influenced by

    BACKGROUND

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    TRIAL OF LABOUR VERSUS ELECTIVE

    REPEAT CAESAREAN SECTION

    The success rate of trial oflabour after Caesarean rangesbetween 50% and85%.

    In a study examining 1776women undergoing TOL after

    Caesarean, the overall

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    Predictors of successful VBACinclude nonrecurring

    indication for Caesareanbirth, such as: Malpresentation , Gestational hypertension and

    a

    Previous vaginal delivery

    TRIAL OF LABOUR VERSUS ELECTIVE

    REPEAT CAESAREAN SECTION

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    When the previous C.S. was for:

    2. Dystocia,

    3. Failure to progress, or

    4. Cephalopelvic disproportion,

    Some studies found the rates ofsuccessful VBAC comparable,

    while others reported or

    lower-than-expected rates.

    TRIAL OF LABOUR VERSUS ELECTIVE

    REPEAT CAESAREAN SECTION

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    In 1996, McMahon et al. published areport ofmaternal morbidity in TOLcompared to ERCS from 1986 to 1992.

    In an examination of3249 womenundergoingTOL and 2889 womenwho delivered by ERCS, the risk of

    major complications (hysterectomy,uterine rupture, and operative injury)was almost doubled in the TOL group

    TRIAL OF LABOUR VERSUS ELECTIVE

    REPEAT CAESAREAN SECTION

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    Complications like puerperalfever, transfusion and abdominalwound infection were

    comparable.When comparing those who had

    a successful TOL to those whorequired a repeat Caesareansection after failed TOL, the risks

    were greater of operative injury

    TRIAL OF LABOUR VERSUS ELECTIVE

    REPEAT CAESAREAN SECTION

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    In 1999, Rageth et al. reviewed 17613TOL and 11 433 ERCS deliveries.

    The rates ofhysterectomy ,febrile

    morbidity and thromboemboliccomplications were less in the TOLgroup than in the ERCS group.

    There is less blood loss with asuccessful VBAC and a shorterhospital stay with more rapid

    recovery and return to full activity.

    TRIAL OF LABOUR VERSUS ELECTIVE

    REPEAT CAESAREAN SECTION

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    Rosen et al. also reported that therisk of febrile morbidity is lower in

    women who attempt a TOL afterCaesarean and is lowest in thosewho succeed ,compared to ERCS,

    But is increased in those whoattempt a TOL and ultimatelydeliver by Caesarean section.

    TRIAL OF LABOUR VERSUS

    ELECTIVE REPEAT CAESAREAN

    SECTION

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    An examination of 16 938women who had undergone aCaesarean delivery found

    that previous C.S. isassociated with an increasedrisk of:

    Ectopic pregnancy, Placenta previa , and

    Abruptio placenta

    TRIAL OF LABOUR VERSUS ELECTIVE

    REPEAT CAESAREAN SECTION

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    A repeat Caesarean

    section has beenassociated with anincreased risk of :

    Placenta previa and Placenta accreta

    in subse uent

    TRIAL OF LABOUR VERSUS

    ELECTIVE REPEAT CAESAREAN

    SECTION

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    A meta-analysis

    published in 2000demonstrated that the

    overall risk ofperinataldeath is increased in

    those attempting a TOL .

    TRIAL OF LABOUR VERSUS

    ELECTIVE REPEAT CAESAREAN

    SECTION

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    The risks of perinatalmortality and severe

    morbidity are directly relatedto uterine rupture .

    If uterine rupture occurs,the risk of perinatal mortality

    and severe morbidity are

    TRIAL OF LABOUR VERSUS ELECTIVE

    REPEAT CAESAREAN SECTION

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    The risk of suspectedneonatal sepsis is greater

    in those attempting a TOLbut appears to be confined

    to the group of TOL whofail and require a repeat

    Caesarean section .

    TRIAL OF LABOUR VERSUS

    ELECTIVE REPEAT CAESAREAN

    SECTION

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    If an ERCS is chosen,

    the risk ofrespiratoryproblems in the newbornis increased comparedto those who have a

    successful VBAC.

    TRIAL OF LABOUR VERSUS

    ELECTIVE REPEAT CAESAREAN

    SECTION

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    CONTRAINDICATIONS TO VAGINAL

    BIRTH AFTER CAESAREAN SECTION

    1. Previous classical or invertedT uterine scar.

    2. Previous hysterotomy ormyomectomy entering theuterine cavity.

    3. Previous uterine rupture.

    4. The presence of a

    contraindication to labour, such

    PLANNING A TRIAL OF LABOUR

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    PLANNING A TRIAL OF LABOUR

    AFTER

    CAESAREAN SECTION

    The woman and her

    health-care provider mustdecide together whetheran appropriate situationexists for considering aTOL after Caesarean.

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    DOCUMENTATION OF PREVIOUS

    UTERINE INCISION

    Documentation of the

    location and type ofuterine incision

    used during theprevious C.S. is ideal.

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    In most cases, this informationcan be obtained by reviewing theoperative record from theprevious surgery.

    Other information in this record,

    such as the indication for theCaesarean section and theopinion of the previous surgeon,

    DOCUMENTATION OF PREVIOUS

    UTERINE INCISION

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    The fact that the record has beenreviewed and that no

    contraindications to a TOL afterCaesarean are present should bedocumented clearly on the

    prenatal record.If the record is not available, the

    scar is considered unknown.

    DOCUMENTATION OF PREVIOUS

    UTERINE INCISION

    FACILITIES AND

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    FACILITIES AND

    RESOURCES

    A trial of labour after Caesareanis always associated with a risk ofuterine rupture, however small.

    For this reason, a TOL afterCaesarean should only be

    considered in a hospital whereprovisions for performing animmediate Caesarean section are

    available.

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    Facilities providing VBACshould have a policy in

    place to manage suchladies so that all resources

    are mobilized promptly ifan intrapartum emergencyoccurs.

    FACILITIES AND

    RESOURCES

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    Women who live in areaswhere local hospitals cannot

    offer immediate C.S. shouldbe offered the opportunity for

    transfer to a facility where

    this service is available, inorder to permit a TOL after

    Caesarean.

    FACILITIES AND

    RESOURCES

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    The members of the teamwho could be called urgently

    in the case of an intrapartumcomplication (anaesthesia,

    pediatric, and obstetric

    services) should be notifiedthat the woman is in hospital

    and in labour and their

    FACILITIES AND RESOURCES

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    MATERNAL MONITORING

    The woman planning a TOL afterCaesarean should have appropriatemonitoring in labour.

    Progress of labour should beassessed frequently as there is someevidence that prolonged labour isassociated with an increased risk offailure and uterine rupture.

    Epidural analgesia is not

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    FETAL MONITORING

    Continuous electronic fetalmonitoring in labour isrecommended for all womenattempting a TOL after Caesarean.

    The most reliable first sign of uterine

    rupture is a non-reassuring fetalheart tracing.

    This may be sudden in onset and

    may not be related to contractions.

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    POSTPARTUM

    EVALUATION

    Routine digital

    exploration of theCaesarean section scarpostpartum is notnecessary, except when

    signs or symptoms

    su est uterine ru ture

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    UTERINE RUPTURE

    Defined as completeseparation of the

    myometrium with or withoutextrusion of the fetal parts

    into the maternal peritoneal

    cavity requiring emergencyCaesarean delivery or

    postpartum laparotomy.

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    It is an uncommoncomplication of VBAC,

    but is associated withsignificant maternal and

    perinatal morbidity andmortality.

    UTERINE RUPTURE

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    The most common

    sign or symptom ofuterine rupture is

    non-reassuring fetal heart

    rate monitoring

    UTERINE RUPTURE

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    Other clinical signs include :

    2. Cessation of contractions,

    3. Loss of the presenting part onvaginal examination,

    4. Abdominal pain,

    5. Vaginal bleeding,6. Hematuria, or

    7. Maternal cardiovascular

    instability.

    UTERINE RUPTURE

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    The type and

    location of theprevious uterineincision helps to

    determine the risk ofuterine rupture.

    UTERINE RUPTURE

    UTERINE RUPTURE INCIDENCE

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    0.2% to 1.5% in a woman whoattempts labour after a transverselower-uterine-segment incision and

    1% to 1.6% after a vertical incisionin the lower uterine segment.

    4% to 9% with a classical or T

    incision; and for this reason, a TOLafter Caesarean is contraindicatedin these situations.

    UTERINE RUPTURE INCIDENCE

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    The relative risk of: uterine rupture, maternal morbidity, and perinatal mortality or severe

    morbidity

    is increased in thoseundergoing a TOL afterCaesarean compared to ERCS,

    but that the absolute risk

    UTERINE RUPTURE

    UTERINE RUPTURE

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    The treatment ofsuspected uterine ruptureis immediate laparotomy

    after maternal stabilizationand anaesthesia.

    Once the fetus isdelivered, maternal

    hemorrhage must be

    UTERINE RUPTURE

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    In 1996, Rozenberg et al.examined

    ultrasonographicmeasurement of the lower

    uterine segmentsmyometrial thickness 36to 38 weeks gestation as

    a predictor of uterine

    UTERINE RUPTURE

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    If the lower segmentthickness was less than 3.5

    mm, the risk of uterinerupture or dehiscence was

    11.8%; and themeasurement was greaterthan 3.5 mm, the risk of

    UTERINE RUPTURE

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    In a follow-up open study,Rozenberg et al. found

    that the use of the lower-uterine-segment

    measurement helpedclinicians select women fora TOL after Caesarean.

    UTERINE RUPTURE

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    OXYTOCICS AND

    TRIAL OF LABOUR AFTERCAESAREAN SECTION

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    Zelop et al. supported

    the same conclusionabout the risk of uterinerupture with

    augmentation in a 1999study .

    AUGMENTATION

    AUGMENTATION

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    Goetzl et al. examined therelationship between the dose ofoxytocin used and the risk of

    uterine rupture in womenundergoing a TOL afterCaesarean.

    No significant association wasdetected between exposure to

    oxytocin and the risk of uterine

    AUGMENTATION

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    Careful surveillance of the womanfor progress of labour is required,especially when the diagnosis ofdystocia is being considered.

    There are insufficient studies

    examining the use of other agents toaugment labour, such asprostaglandins, and their safety in a

    TOL after Caesarean.

    AUGMENTATION

    INDUCTION

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    INDUCTION

    In 2000, Ravasia et al. reviewed the risk

    of uterine rupture in women undergoingan induction TOL after Caesarean.

    In 575 women with a previous

    Caesarean section, labour was inducedwith:

    3. Prostaglandin E2 gel ,

    4. Intracervical foley catheter , or5. Amniotomy and/or oxytocin .

    Outcomes were compared to those

    women undergoing a TOL with

    INDUCTION

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    The risk of uterine rupture wasnot increased in those who

    underwent either

    amniotomy/oxytocin or foleycatheter induction,

    but was significantly increasedin those who underwent aprostaglandin E2 induction .

    INDUCTION

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    INDUCTION

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    In 2003, Delaney and Young reported

    the examination of3746 women with aprior Caesarean delivery who underwenteither induced or spontaneous labour.

    They found that induced labour wasassociated with a greater risk of :

    Early postpartum hemorrhage(7.3% vs. 5.0%),

    Caesarean delivery(37.5% vs. 24.2%), and

    Admission to a neonatal intensive care

    unit (13.3% vs. 9.4%).

    INDUCTION

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    There was a trendtowards a higher rate ofuterine rupture, but this

    was not statistically

    significant (0.7% vs.0.3%).

    INDUCTION

    INDUCTION

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    In another retrospective studyof560 women, the rate ofuterine rupture in women

    whose labour was inducedwith :

    Oxytocin was 2%,with

    Prostaglandin was 2 9%

    INDUCTION

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    Up to 2001, there was conflictingdata on the risk of induction of

    labour with prostaglandin E2.Several other smaller studies

    reported that it appeared to besafe, effective, and notassociated with an increased risk

    of uterine rupture.

    INDUCTION

    INDUCTION

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    In the largest study published todate, conducted by Lydon-Rochelle et al., the incidence ofuterine rupture was reviewed

    retrospectively in 20 095women with a previous C.S. andreported as follows:

    Elective repeat C.S. (no labour)0.16%;

    Spontaneous labour 0.52% ; Labour induced without

    INDUCTION

    INDUCTION

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    The possibility that the use of oxytocinand/or prostaglandin for induction oflabour in women considering a TOL afterCaesarean may be associated with an

    increased risk of uterine rupture and itssequelae must be discussed with thepatient.

    The absolute risks of uterine rupture arelow, but the relative risks (especially withthe use of prostaglandin E2 compared to

    spontaneous labour) are greater.

    INDUCTION

    MISOPROSTOL

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    MISOPROSTOL

    Misoprostol has been proposed as an

    effective and economical agent forcervical ripening and induction.

    In 1998, Sciscione et al. reported a case

    of uterine rupture in a woman with 2previous Caesarean sections aftermisoprostol was administered as a

    cervical ripening agent.A number of small series reported a risk

    of uterine rupture from 0% to 11.7% withmisoprostol in women undergoing a TOL

    MISOPROSTOL

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    Blanchette et al. compared

    prostaglandin E2 to misoprostol inwomen undergoing induction TOLafter Caesarean and found them tobe equally effective,

    But misoprostol was associated with

    a higher incidence of uterine rupture(18.8% compared to no ruptures inthe prostaglandin E2 group).

    The numbers in all of these studies

    MISOPROSTOL

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    Until further randomizedstudies are completed,

    misoprostol should bediscouraged as a method

    of induction or cervicalripening in women withprevious Caesarean

    MISOPROSTOL

    CERVICAL PREPARATION

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    CERVICAL PREPARATION

    In situations where delivery is indicated

    and the cervix is unfavourable, a TOLafter Caesarean can be considered.

    In a cohort study published in 2002,

    Ben-Aroya et al. compared womenundergoing a trial of labour afterCaesarean section in 3 situations:

    Spontaneous labour (n=1432), Prostaglandin cervical ripening (n=55),

    and

    Cervical ripening by foley catheter

    CERVICAL PREPARATION

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    There was a significantly higherrate of dystocia (30.4% vs.11.6%) and repeat Caesarean

    sectionin the second stage(49.1% vs. 35.2%) in the foleycatheter group compared to the

    control group.There was no difference in the

    rate of uterine rupture fetal

    CERVICAL PREPARATION

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    In a Canadian study published in2004, Bujold et al. compared therate of uterine rupture in 1807women who presented inspontaneous labour,

    417 induced with amniotomy withor without oxytocin, and

    255 induced with transcervical

    foley catheter.

    CERVICAL PREPARATION

    CERVICAL PREPARATION

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    The rate of successful vaginal birthwas :

    78% in the spontaneous group,

    77.9% in the amniotomy group, and 55.7% in the transcervical foley

    group .

    However, the rates of uterinerupture did not differ significantly:

    1.1%, 1.2%, and 1.6%,

    CERVICAL PREPARATION

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    These data support theuse of the foley catheter

    for cervical ripening ofan unfavourable cervix

    in women undergoing aTOL after Caesarean.

    CERVICAL PREPARATION

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    SPECIAL

    CIRCUMSTANCES

    MORE THAN ONE PREVIOUS LOW

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    .TRANSVERSE C.S

    Several authors have assessedthe rate ofsuccessful VBAC andrisk ofuterine rupture in women

    with more than one previous lowtransverse Caesarean section.

    All indicated success ratesbetween 62% and 89%, anduterine rupture rates between

    MORE THAN ONE PREVIOUS LOW

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    Unfortunately, the use ofprostaglandins or oxytocin forinduction or augmentation was not

    considered.Caughey et al. reported a uterine

    rupture rate of 3.7% versus 0.8% in aretrospective review of 134 womenundergoing labour after 2 previous

    Caesarean sections.

    MORE THAN ONE PREVIOUS LOW

    .TRANSVERSE C.S

    MORE THAN ONE PREVIOUS LOW

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    In the largest study, Miller et al.demonstrated :

    A VBAC success rate of 75.3% in1827 women with 2 or moreprevious low transverse

    Caesarean sections withA uterine rupture rate of 1.7%

    vs. 0.6% in the ERCS group.

    TRANSVERSE

    CAESAREAN SECTION

    MULTIPLE PREGNANCY

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    MULTIPLE PREGNANCY

    Seven studies have examined atotal of 233 women attemptingVBAC in multiple pregnancy.

    All support a trial of VBAC inmultiple pregnancy as being safeand effective,

    With success rates of69% to84%, and without increased

    maternal or fetal morbidity or

    MULTIPLE PREGNANCY

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    In one study, uterine dehiscence wasnoted in 1 woman on manualexploration after successful vaginaldelivery of both twins, and notreatment was required.

    Each of these studies examined a

    small number of women, however;and greater numbers would berequired to detect rare outcomes

    such as uterine rupture and maternal

    MULTIPLE PREGNANCY

    BREECH PRESENTATION

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    BREECH PRESENTATION

    A large multicentre trial by Hannahet al. demonstrated that a plannedCaesarean birth is associated withbetter perinatal and neonataloutcomes in breech presentation atterm.

    This recommendation has beenadopted by the SOGC and wouldtherefore preclude a planned TOL

    after Caesarean in women

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    External cephalic

    version is notcontraindicated in a

    woman with aprevious Caesarean

    BREECH PRESENTATION

    DIABETES MELLITUS

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    Coleman et al. examined 156women with GDM and planned

    TOL after Caesarean and

    compared them to non-GDMwomen attempting TOL afterCaesarean.

    They reported that the successrate for VBAC of 64.1% in women

    with GDM was lower than the

    DIABETES MELLITUS

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    A retrospective study of TOL afterCaesarean in women with pre-gestational or gestationaldiabetes found similar results.

    Based on these studies,

    diabetes mellitus should not beconsidered a contraindication toTOL after Caesarean.

    DIABETES MELLITUS

    MACROSOMIA

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    In a study examining the

    outcome of365 women whounderwent a TOL after

    Caesarean, giving birth toneonates weighing more than4000 g, Zelop et al.

    demonstrated asuccess rate of 60%, withno increase in maternal or fetal

    MACROSOMIA

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    In 2003, Elkousy et al. reported an

    examination of9960 women with aprevious C.S. planning a trial oflabour further stratified by neonatalbirth weights and birth history.

    His results indicate that the

    likelihood of successful VBACdecreases with increasing birthweight and is lowest in those who

    have never had a successful vaginal

    MACROSOMIA

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    Based on these results,suspected macrosomia is

    not a contraindication to aTOL after Caesarean,although it may be

    associated with a lowerchance of success.

    MACROSOMIA

    INTERDELIVERY INTERVAL

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    INTERDELIVERY INTERVAL

    Four studies haveexamined the

    relationship betweenthe inter-delivery

    interval and the rate ofsuccessful VBAC and

    uterine rupture

    INTERDELIVERY INTERVAL

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    Esposito et al. examined 23 cases ofuterine rupture and compared themto 127 controls.

    There was an increased risk ofuterine rupture with a shortinterpregnancy interval

    (

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    Shipp et al. reviewed 311 womenwho underwent a TOL afterCaesarean less than 18 months after

    their Caesarean section andcompared them to 2098 women whounderwent a TOL after Caesarean

    after more than 18 months.The shorter interval was associated

    with a 3-fold increase in the

    risk of uterine rupture (2 25% vs

    INTERDELIVERY INTERVAL

    INTERDELIVERY INTERVAL

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    In 2002, Bujold et al.reported an observational

    study of 1527 womenundergoing a planned TOL

    after Caesarean atdifferent intervals from the

    index Caesarean delivery

    INTERDELIVERY INTERVAL

    INTERDELIVERY INTERVAL

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    The rates of uterine rupturewere as follows:

    36 months, 1%.

    INTERDELIVERY INTERVAL

    POSTDATISM

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    OS S

    Three studies have examinedpostdatism and TOL afterCaesarean.

    Success rates for VBACafter 40 weeks were

    reported from 65% to 73%and were comparable to

    success rates for women

    POSTDATISM

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    Zelop et al. reported that therisk of uterine rupture in a

    TOL after Caesarean after 40

    weeks was not significantlyincreased when compared to

    those who delivered before 40weeks, whether inspontaneous labour or after

    ONE- VERSUS TWO-LAYER CLOSUREOF LOW TRANSVERSE

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    OF LOW TRANSVERSE

    CAESAREAN SECTION

    In 1992, Hauth et al. published datacomparing :

    Operative time, Endometritis,Transfusion, and Placement of extra hemostatic

    sutures in women undergoinguterine closure in 1 layer comparedto 2 layers.

    ONE- VERSUS TWO-LAYER CLOSUREOF LOW TRANSVERSE

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    The only significant difference was inoperative time:

    44 minutes with 1-layer

    compared to 48minutes with 2-layer closure.

    Similar findings were published byOhel et al. in 1996.

    The trend shifted in many centres

    towards single-layer closure

    OF LOW TRANSVERSE

    CAESAREAN SECTION

    ONE- VERSUS TWO-LAYER CLOSURE OFLOW

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    In 1997, Chapman et al. publisheda review of 145 women whounderwent a TOL after Caesarean

    after being randomized to either 1-layer or 2-layer closure in theprevious Caesarean section.

    They reported no significantdifference in the outcome of the

    next pregnancy

    LOW

    TRANSVERSE CAESAREAN SECTION

    - -LOW

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    In a 2002 review of 2142 womenwho underwent a TOL afterCaesarean, Bujold et al. noted that

    a 1-layer interlocking closure wasassociated with an increased risk ofuterine rupture when compared to a

    2-layer closure (3.1% vs.0.5%).

    Further study in this area is

    TRANSVERSE CAESAREAN SECTION

    UNKNOWN SCAR

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    All records available or obtainable

    describing the womans previous C.S.should be reviewed.

    If unavailable, information about thecircumstances of the C.S. will helpdetermine the likelihood of a verticaluterine incision.

    The majority of unknown scars willbe lower transverse incisions (92%)

    and therefore at low risk for uterine

    UNKNOWN SCAR

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    If the history suggests a reasonablelikelihood of a classical incision, itwould be prudent to recommend arepeat C.S. ,

    But in settings where the history

    indicates a high likelihood of lowertransverse uterine incision and thewoman wishes to proceed after

    counselling a TOL after

    UNKNOWN SCAR

    OTHER FACTORS

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    Factors such as :

    2. Maternal obesity,

    3. The presence of postpartum fever afterCaesarean section,

    4. Type of suture material,

    5. Mllerian duct anomalies, and

    6. Maternal age andTheir relationship to the risk of uterine

    rupture have been examined in small

    studies, but definitive conclusions

    :Recommendations:Recommendations

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    :Recommendations

    Provided there are noProvided there are nocontraindications, a womancontraindications, a woman

    with one previous transversewith one previous transverse

    L.S.C.S. should be offered aL.S.C.S. should be offered a

    trial of labour after C.S. withtrial of labour after C.S. with

    appropriate discussion ofappropriate discussion ofmaternal and perinatal risksmaternal and perinatal risks

    and benefitsand benefits.)II-2B()II-2B(

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    :Recommendations:Recommendations

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    The intention of a womanThe intention of a woman

    undergoing a TOL after C.S.undergoing a TOL after C.S.

    should be clearly stated andshould be clearly stated anddocumentation of the previousdocumentation of the previous

    uterine scar should be clearlyuterine scar should be clearly

    marked on the prenatalmarked on the prenatalrecord.record.

    :Recommendations:Recommendations

    )II-2B()II-2B(

    :Recommendations:Recommendations

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    For a safe labour afterFor a safe labour after

    C.S. , the woman shouldC.S. , the woman should

    deliver in a hospitaldeliver in a hospitalwhere an immediatewhere an immediate C.S.C.S.

    is available.is available.

    :Recommendations:Recommendations

    )II-2A()II-2A(

    :Recommendations:Recommendations

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    The woman and her health-The woman and her health-care provider must be awarecare provider must be aware

    of the hospital resources andof the hospital resources andthe availability of obstetric,the availability of obstetric,

    anaesthesia, pediatric, andanaesthesia, pediatric, and

    operating-room staff.operating-room staff.

    :Recommendations:Recommendations

    )II-2A()II-2A(

    :Recommendations:Recommendations

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    Each hospital should have aEach hospital should have awritten policy in placewritten policy in place

    regarding the notificationregarding the notificationand/or consultation for theand/or consultation for the

    physicians responsible for aphysicians responsible for a

    possible immediatepossible immediate C.S.C.S.

    :Recommendations:Recommendations

    )III B()III B(

    :Recommendations:Recommendations

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    Continuous electronicContinuous electronic

    fetal monitoring offetal monitoring of

    women attempting awomen attempting aTOL afterTOL after C.S.C.S. isis

    recommended.recommended.

    :Recommendations:Recommendations

    )II-2A()II-2A(

    :Recommendations:Recommendations

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    Suspected uterine ruptureSuspected uterine rupturerequires urgent attentionrequires urgent attention

    and expedited laparotomyand expedited laparotomyin order to attempt toin order to attempt to

    decrease maternal anddecrease maternal and

    perinatal morbidity andperinatal morbidity and

    mortality.mortality.

    :Recommendations:Recommendations

    )II-2A()II-2A(

    :Recommendations:Recommendations

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    OxytocinOxytocinaugmentation is notaugmentation is not

    contraindicated incontraindicated inwomen undergoing awomen undergoing a

    TOL afterTOL after C.S.C.S.

    :Recommendations:Recommendations

    )II-2A()II-2A(

    :Recommendations:Recommendations

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    Medical induction of labourMedical induction of labourwith oxytocin may bewith oxytocin may be

    associated with anassociated with anincreased risk of uterineincreased risk of uterine

    rupture and should be usedrupture and should be used

    carefully after appropriatecarefully after appropriate

    counselling.counselling.

    :Recommendations:Recommendations

    )II-2B()II-2B(

    :Recommendations:Recommendations

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    Medical induction of labourMedical induction of labourwith prostaglandin E2with prostaglandin E2

    (dinoprostone) is associated(dinoprostone) is associatedwith an increased risk ofwith an increased risk of

    uterine rupture and should notuterine rupture and should not

    be used except in rarebe used except in rarecircumstances aftercircumstances after

    appropriate counselling.appropriate counselling.

    :Recommendations:Recommendations

    )II-2B()II-2B(

    :Recommendations:Recommendations

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    Prostaglandin E1Prostaglandin E1(misoprostol) is associated(misoprostol) is associated

    with a high risk of uterinewith a high risk of uterinerupture and should not berupture and should not be

    used as part of a TOL afterused as part of a TOL after

    C.S.C.S.

    :Recommendations:Recommendations

    )II-2A()II-2A(

    :Recommendations:Recommendations

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    A foleys catheterA foleys cathetermay be used safely tomay be used safely to

    ripen the cervix in aripen the cervix in awoman planning awoman planning a

    TOL afterTOL after C.S.C.S.

    :Recommendations:Recommendations

    )II-2A()II-2A(

    :Recommendations:Recommendations

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    The available data suggestThe available data suggestthat a trial of labour inthat a trial of labour in

    women with more than onewomen with more than oneprevious C.S.previous C.S.is likely to beis likely to besuccessful but is associatedsuccessful but is associated

    with a higher risk of uterinewith a higher risk of uterinerupture.rupture.

    :Recommendations:Recommendations

    )II-2B()II-2B(

    :Recommendations:Recommendations

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    Multiple gestation isMultiple gestation is

    not a contraindicationnot a contraindicationto a TOL afterto a TOL after

    Caesarean.Caesarean.

    :Recommendations:Recommendations

    )II-2B()II-2B(

    :Recommendations:Recommendations

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    Diabetes mellitusDiabetes mellitusis not ais not a

    contraindication tocontraindication toTOL after C.S.TOL after C.S.

    :Recommendations:Recommendations

    (II-2B)(II-2B)

    :Recommendations:Recommendations

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    Suspected fetalSuspected fetal

    macrosomia is not amacrosomia is not a

    contraindication to acontraindication to a

    TOL after Caesarean.TOL after Caesarean.

    :Recommendations:Recommendations

    (II-2B)(II-2B)

    :Recommendations:Recommendations

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    Women deliveringWomen deliveringwithin 18 to 24within 18 to 24

    months of a C.S. shouldmonths of a C.S. shouldbe counseled about anbe counseled about an

    increased risk of uterineincreased risk of uterinerupture in labour.rupture in labour.

    :Recommendations:Recommendations

    (II-2B)(II-2B)

    :Recommendations:Recommendations

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    Postdatism is notPostdatism is not

    aacontraindication tocontraindication to

    a TOL aftera TOL after

    CaesareanCaesarean

    :Recommendations:Recommendations

    (II-2B)(II-2B)

    :Recommendations:Recommendations

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    Every effort should beEvery effort should bemade to obtain themade to obtain the

    previous Caesarean sectionprevious Caesarean sectionoperative report tooperative report to

    determine the type ofdetermine the type ofuterine incision used.uterine incision used.

    (II-2B)(II-2B)

    :Recommendations:Recommendations

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    In situations where the scar isIn situations where the scar is

    unknown, informationunknown, informationconcerning the circumstances ofconcerning the circumstances of

    the previous delivery is helpful inthe previous delivery is helpful indetermining the likelihood of adetermining the likelihood of a

    low transverse incision.low transverse incision.

    If the likelihood of a lowerIf the likelihood of a lowertransverse incision is high, TOLtransverse incision is high, TOL

    after Caesarean can be offeredafter Caesarean can be offered.

    (II 2B)(II 2B)

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