ISRN.OBGYN2012-843245

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    International Scholarly Research NetworkISRN Obstetrics and GynecologyVolume 2012, Article ID 843245,8pagesdoi:10.5402/2012/843245

    Review ArticleTo Compare theMethods of Pregnancy Termination forFetal Abnormality in the First and SecondTrimesters

    H.S.Wong

    Australian Womens Ultrasound Centre, Brisbane, QLD 4109, Australia

    Correspondence should be addressed to H. S. Wong,[email protected]

    Received 20 January 2012; Accepted 10 February 2012

    Academic Editors: N. A. Ginsberg, F. M. Reis, and C. von Kaisenberg

    Copyright 2012 H. S. Wong. This is an open access article distributed under the Creative Commons Attribution License, whichpermits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

    Fetal abnormality is a major cause of termination of pregnancy and preservation of the fetus is important for confirmation ofthe diagnosis. Various regimes have been reported for termination of pregnancy for fetal abnormality in the first and the secondtrimesters. In this paper, we compare those regimes that allow preservation of the fetus, in terms of the efficacy in expulsion of thefetus, the factors and the side effects.

    1. IntroductionFetal abnormality is known to be a major cause of perinatalmortality. Termination of pregnancy for fetal abnormalitiessignificantly decreases perinatal mortality resulting frombirth defects [1,2]. Fetal morphological anomalies (withoutchromosomal anomalies) and chromosomal anomalies formthe main ground for termination of pregnancy in 39%and 35% of cases respectively in a study by Guillem et al.[3] and 47% and 33%, respectively, in another study byRamalho et al. [4]. For morphological anomalies identifiedby ultrasound with no evidence for abnormal karyotype, itis estimated that autopsy adds information that leads to arefinement of the risk of recurrence in 27% and revision

    to a higher risk of 1 in 4 in 8% of cases [5]. In anotherstudy, complete correlation between ultrasound findingsand pathological examination is found in only 61.1% ofautopsies. This highlights the importance of pathologicalexamination for confirmation [4]. When surgical termina-tion is employed for fetal abnormality, an intact fetus isnot obtained. Pathological examination of fetal parts by useof radiography, gross dissection, microscopic examination,and/or cell culture for karyotyping or biochemical analysismay detect a major abnormality in 92%, and in 46%a specific diagnosis was obtained only from pathologicexamination [6]. As there is a trend for prenatal diagnosisto take place earlier in pregnancy, largely as a result of first

    trimester ultrasound screening [7], more pregnancies areexpected to be terminated in the first trimester. Preservationof the whole fetus is possible with medical termination inthe first trimester [811] although pathological examinationis usually technically more difficult in these specimens [12].In this paper, we compare the methods and outcome fortermination of pregnancy for fetal abnormality in the firstand second trimesters, respectively, especially those thatpotentially allow preservation of the fetus for pathologicalexamination.

    2.Method andMaterials

    Medline was searched for induced abortion (MeSH) andprenatal diagnosis, and also for induced abortion (MeSH)for fetal abnormality. The first search resulted in 604 hitsand the second 29 hits. The papers in English languagewere reviewed for any description and outcome analysis ontermination of pregnancy for fetal abnormality in the firstand second trimesters. Further search was performed byhand from related or cited articles.

    3. Results

    3.1. Termination in the Second Trimester for Fetal Abnormality.Kanhai and Keirse studied the use of low dose sulprostonein termination of pregnancy for fetal abnormality between

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    2 ISRN Obstetrics and Gynecology

    16 and 35 weeks in 32 pregnancies [13]. In 31 pregnancies,intravenous infusion of 0.5 mg sulprostone per minute wasgiven for 60 minutes followed by 1 mcg per minute untilthe fetus was expelled. All patients delivered vaginally. 84%delivered within 36 hours. The median induction-expulsioninterval was 23 hours. In one patient, 0.5 mg of endocervical

    prostaglandin E2 was given followed by infusion of upto 2 mcg sulprostone per minute. This patient deliveredvaginally after 74 hours. Induction-expulsion intervals werenot associated with gestational age. Manual removal ofplacenta was required in 28% of cases. Median blood losswas 100 mLs. 9% patients lost more than 1000 mLs. Six outof 32 patients (18%) did not require analgesic and 6 patients(18%) experience gastrointestinal side effects.

    Hinshaw et al. studied the use of 600 mg mifepris-tone priming followed by misoprostol 3648 hours later(800 mcg vaginally then 400 mcg orally 3-hourly, maximum4 doses) in 20 cases of mid-trimester termination for fetalabnormality [14]. All patients aborted within 15 hours.The median induction-to-abortion interval was shorter forparous women compared with nulliparous women (5.5versus 11.25 hours). Medical termination of pregnancy wascomplete in 95% with only one patient requiring uterineevacuation. Intramuscular opiates were administered in 12(60%) and 2 other required nonnarcotic analgesics alone(10%). The remaining 30% did not require analgesia. Tenwomen (50%) developed nausea and 8 (40%) had vomiting.Four patients (20%) noted diarrhoea. There was no case ofinfection and 9 (45%) developed prostaglandin-associatedpyrexia (

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    ISRN Obstetrics and Gynecology 3

    Table1:Comparisonofthemethodsfortermina

    tionofpregnancyforfetalabnormalityin

    thefirstandsecondtrimester.

    Study

    Methodsof

    terminationof

    pregnancy

    No.o

    f

    patients

    Gestational

    age(weeks)

    Median/

    meanGA

    (weeks)

    Typeofstudy

    Patients

    characteristic

    Medianduration

    (hours)

    Duration>

    24h(%)

    Bloodloss(mLs)

    Incomplete

    abortion

    (%)

    Analges

    ia

    required

    Sideeffects

    Kanhai

    andKeirse

    [13]

    SulprostoneIV

    0.5mg/minfor

    60minthen

    1mcg/min

    31/32

    1635

    Caseseries

    23hours,

    Notrelatedto

    gestationalage

    Median100mLs,

    9%>

    1000mLs

    28%

    82%

    18%GI

    Hinshaw

    etal.[

    14]

    Mifepristone

    600mgpothen

    misoprostolafter

    3648hours,

    800mcgPVthen

    400mcgpoq3h,

    max4doses

    20

    Caseseries

    5.5

    hours

    multiparous,

    11.25hours

    nulliparous

    5%

    70%

    Upto50%GI

    Dickinson

    andEvans

    [15]

    MisoprostolPV

    400mcgq6h,or

    28

    1426

    19.6

    Randomized

    clinicaltrial

    14.5

    14.3

    %

    NP

    42.9

    %

    75%

    Adjunctive

    methods

    requiredin0%,

    Misoprostolpo

    400mcgq3h,or

    29

    19.4

    25.5

    55.2

    %

    34.5

    %

    69%

    20.7

    %,and

    Misoprostol600

    mcgPVthen

    200mcgpoq3h

    27

    20.5

    (mean)

    16.4

    Parityand

    previousCShave

    noeffects

    25.9

    %

    30.8

    %

    77.8

    %

    3.7%after48h

    GIsideeffects

    higherwithoral

    misoprostol

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    4 ISRN Obstetrics and Gynecology

    Table1:Continued.

    Study

    Methodsof

    terminationof

    pregnancy

    No.of

    patients

    Gestational

    age(weeks)

    Median/

    meanGA

    (weeks)

    Typeof

    study

    Patients

    char

    acteristic

    Medianduration

    (hours)

    Duratio

    n>

    24h(%)

    Bloodloss

    (mLs)

    Incomplete

    abortion

    (%)

    Analgesia

    required

    Sideeffects

    Dickinson

    [16]

    Misoprostolin6

    differentregimes,

    mostcommonly

    400mcgq6h

    720

    1428

    19.4

    Cohort

    Prev

    iousCS

    (101

    )versus

    unscarred

    uterus(619)

    16.6

    17.8%

    7.9%>

    500mLs

    41.6%

    adjunct

    methods

    requiredin

    somepatients

    19.3

    14.5

    23.9%

    5.6%>

    500mLs

    34.4%

    Nocaseof

    uterinerupture

    Dickinson

    etal.[

    17]

    Misoprostol

    400mcgq6h

    (max48h)versus

    189

    1424

    19.6

    Cohort

    Multiparous

    in60.3%and

    15.5

    (16.8nullip14.1

    multip)

    21.7%

    150mLs

    24.9%

    66.1%

    Durationof

    hospitalisa-

    tion31.5

    h

    versus27.2

    h

    Mifepriston

    200mgpothen

    199

    19.1

    57.8

    %

    8.6

    (11nullip6.9

    multip)

    8.5

    %

    100mLs

    25.6%

    74.9%

    Misoprostol

    800mcgPV

    2448hourslater

    then400mcgpo

    q6h(max5

    doses/day,4

    8h)

    20.9

    %had

    1previous

    CS

    Nulliparityand

    advancinggestation

    increase

    induction-abortion

    interval

    About

    10%

    500mLsin

    both

    groups

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    ISRN Obstetrics and Gynecology 5

    Table1:Continued.

    Study

    Methodsof

    termination

    ofpregnancy

    No.o

    f

    patients

    Ges

    tational

    age(we

    eks)

    Median/

    meanGA

    (weeks)

    Typeofstudy

    Patients

    characteristic

    Median

    duration

    (hours)

    Duration>

    24h(%)

    Bloodloss(mLs)

    Incomplete

    abortion

    (%)

    Analgesia

    required

    Sideeffects

    16.1overall

    100mLswhen

    placentanot

    retained

    31.1%

    overall,

    Dickinson

    and

    Doherty

    [18]

    Misoprostol

    PV400mcg

    q6h

    1066

    13

    28

    19.5

    Cohort,

    excludingthe

    patientsin

    publication

    dated2003

    Multiparous

    in6

    0.2%

    15.4%with

    1previous

    CSStra

    tified

    accordingto

    typesoffetal

    ano

    maly

    19nullip

    14.3multip

    23%

    53.2%at