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RECURRENT MISCARRIAGE GUIDELINES

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Title: RECURRENT MISCARRIAGE GUIDELINES


1
RECURRENT MISCARRIAGEGUIDELINES
  • MAJ DR AMINA AKBAR
  • MBBS, MCPS, FCPS

2
DEFINITION
  • A recurrent miscarriage is defined as 3 or more
    consecutive, spontaneous pregnancy losses, under
    20 week gestation from the last menstrual period

3
  • Primary recurrent pregnancy loss" refers to
    couples that have never had a live birth
  • While "secondary RPL" refers to those who have
    had repetitive losses following a successful
    pregnancy

4
TERMINOLOGY
  • The medical term ' abortion' should be replaced
    with the term 'miscarriage'
  • Other names Recurrent Pregnancy Loss (RPL),
  • Habitual Abortions ,
  • Habitual Miscarriages,
  • Recurrent Abortions ,
  • Recurrent Miscarriages.

5
INCIDENCE
  • 1015 of all clinically recognized pregnancies
    end in a miscarriage
  • Recurrent miscarriage affects 0.5-2 of all women
    -- Hence, only a proportion of women presenting
    with recurrent miscarriage will have a persistent
    underlying cause for their pregnancy losses

6
RISK FACTORS
  • Advanced maternal age adversely affects ovarian
    function, giving rise to a decline in the number
    of good quality oocytes, resulting in
    chromosomally abnormal conceptions that rarely
    develop further
  • Previous number of miscarriages

7
POSSIBLE CAUSES
  • Recurrent miscarriage is a heterogeneous
    condition that has many possible causes more
    than one contributory factor may underlie the
    recurrent pregnancy losses
  • Each may have had a different cause

8
Recurrent Miscarriage
Explained
Un-explained
Genetic factors
Infective agents
Endocrine
Enviromental factors
Anatomical factors
Immune factors
Inhereted Thrombophilic defect
Bacterial Vaginosis
Body
Cervix
C I
APS
Uterine anomalies
Paternal karyotyping
Cytogenetic Of miscarriage
9
GENETIC FACTORS
10
  • All couples with a history of recurrent
    miscarriage should have peripheral blood
    karyotyping performed. The finding of an abnormal
    parental karyotype should prompt referral to a
    clinical geneticist.
  • 35 of couples with recurrent miscarriage, one
    of the partners carries a balanced structural
    chromosomal anomaly
  • 510 chance of a pregnancy with an unbalanced
    translocation.

11
FETAL CHROMOSOMAL ABNORMALITIES
  • This may be due to abnormalities in the egg,
    sperm or both. The  most common chromosomal
    defects are-
  • Trisomy
  • Monosomy
  • Polyploidy

12
  • Chromosome Testing on Fetal (Miscarriage) Tissue
  • This can only be done right at the time of
    miscarriage.
  • It is an analysis of the genetic makeup of the
    fetus.
  • It can indicate genetic problems that lead to
    RPL.
  • Many miscarriages are caused by chromosomal
    abnormalities that are unlikely to repeat. To
    know if the problem is likely to recur, it is
    necessary to study the genetics of both parents
    as well.

13
  • Karyotyping of Parents
  • Chromosome analysis of blood of both parents.
  • It can show if there is a potential problem with
    one of the parents that leads to miscarriage, but
    often has to be done in conjunction with fetal
    testing to provide answers.

14
ANATOMICAL FACTORS
15
CONGENITAL ANOMALIES
  • An abnormal or irregularly shaped uterus.
  • Sometimes the uterus has an extra wall down its
    centre, which makes it look as if it is divided
    into
  • two (bicornuate or septate uterus)
  • a septate uterus Where as a partial septum
    increases the risk to 60-75 a total septum
    carries a risk for loss of up to 90.
  • Today a relatively simple surgical procedure
    can remove a uterine septum
  • or it may have only developed one half
    (unicornuate uterus).

16
  • The reported prevalence of uterine anomalies in
    recurrent miscarriage populations range between
    1.8 and 37.6.
  • The prevalence of uterine malformations appears
    to be higher in women with late miscarriages
    compared with women who suffer early miscarriages
  • Untreated uterine anomalies has a term delivery
    rate of only 66.
  • Open uterine surgery is associated with
    postoperative infertility and carries a
    significant risk of uterine scar rupture during
    pregnancy. Therefore treatment of uterine
    anomalies in women with recurrant miscarriage
    remains controversial.

17
FIBROIDS
  • If fibroids are detected on the inside of the
    uterus (termed submucous fibroids) and distort
    the uterine lining, they are a significant cause
    of reproductive problems and should be removed.
    It is less clear whether fibroids in the wall of
    the uterus cause reproductive problems

18
All women with recurrent miscarriage should have
a pelvic ultrasound to assess uterine anatomy and
morphology
  • Two dimensional pelvic ultrasound assessment of
    the uterine cavity with (or without)
    Sonohysterography

19
HYSTEROSALPINGOGRAPHY
  • The routine use of hysterosalpingography as a
    screening test for uterine anomalies in women
    with recurrent miscarriage is questionable.
  • It is associated with patient discomfort,
  • carries a risk of pelvic infection and radiation
    exposure
  • and is no more sensitive than the non-invasive
    two dimensional pelvic ultrasound assessment of
    the uterine cavity with (or without)
    Sonohysterography when performed by skilled and
    experienced personnel.

20
HYSTEROSCOPY
  • This investigation, performed under general
    anaesthetic, examines the inside of the uterus
    with a thin
  • telescope (3-5 mm in diameter) . By inserting
    this telescope through the cervix and into the
    uterus,
  • the doctor can see the shape of the uterus and
    examine its lining.

21
CERVICAL WEAKNESS
22
  • Diagnosis of cervical incompetence is based on
    history of late miscarriage preceded by
    spontaneous rupture of memb or painless cervical
    dilatation. Vaginal USG is helpful in assessing
    early features of cervical incompetence. Cervical
    cerclage is associated with potential hazards
    associated with surgery and risk of uterine
    contractions.

23
ENDOCRINE FACTORS
24
Routine screening for occult diabetes and thyroid
disease with oral glucose tolerance and thyroid
function tests in asymptomatic women presenting
with recurrent miscarriage is uninformative
  • Well-controlled diabetes mellitus is not a risk
    factor for recurrent miscarriage, nor is treated
    thyroid dysfunction

25
There is insufficient evidence to evaluate the
effect of progesterone supplementation in
pregnancy to prevent a miscarriage
26
There is insufficient evidence to evaluate the
effect of human chorionic gonadotrophin (hCG) in
pregnancy to prevent miscarriage.
  • Early pregnancy hCG supplementation failed to
    show any benefit in pregnancy outcome

27
IMMUNE FACTORS
  • One in ten women with recurrent miscarriages show
    evidence of auto immune factors on investigation
  • As much as 40 percent of unexplained infertility
    may be the result of immune problems.
    Unfortunately for couples with immunological
    problems, their chances of recurrent loss
    increase with each successive pregnancy.

28
ANTITHYROID ANTIBODIES
  • Routine screening for thyroid antibodies in women
    with recurrent miscarriage is not recommended.

29
ANTIPHOSPHOLIPID SYNDROME
  • To diagnose APS it is mandatory that the patient
    should have two positive tests at least six weeks
    apart for either lupus anticoagulant or
    anticardiolipin (aCL) antibodies of IgG and/or
    IgM class present in medium or high titre.
  • Adverse pregnancy outcomes include
  • Three or more consecutive miscarriages before
    ten weeks of gestation
  • One or more morphologically normal fetal deaths
    after the tenth week of gestation and
  • One or more preterm births before the 34th week
    of gestation due to severe pre-eclampsia,
    eclampsia or placental insufficiency.

30
  • In women with a history of recurrent miscarriage
    and aPL, future live birth rate is significantly
    improved when a combination therapy of aspirin
    plus heparin is prescribed.
  • Pregnancies associated with aPL treated with
    aspirin and heparin remain at high risk of
    complications during all three trimesters.

31
INHERITED THROMBOPHILIC DEFECTS
32
  • Inherited thrombophilic defects,
  • Including activated protein C resistance (most
    commonly due to factor V Leiden gene mutation),
    deficiencies of protein C/S and antithrombin III,
    hyperhomocysteinaemia and prothrombin gene
    mutation,
  • Are established causes of systemic thrombosis

33
INFECTIVE AGENTS
34
  • Screening for and treatment of bacterial
    vaginosis in early pregnancy among high risk
    women with a previous history of second-trimester
    miscarriage or spontaneous preterm labour may
    reduce the risk of recurrent late loss and
    preterm birth.

35
ENVIRONMENTAL FACTORS
36
  • Exposture to noxious or toxic substances are
    known to be associated with recurrent miscarriage
    ( cigarretes,alcohol and caffeine ,anaestetic
    gases,petrolium products )

37
UNEXPLAINED RECURRENT MISCARRIAGE
  • In about half the women in the research studies,
    no cause could be found, so no specific treatment
    could be given.
  • However, this group responded very well to a
    programme which removed as many stress factors as
    possible from their lives, resulting in an 80
    success rate with the subsequent pregnancy

38
PSYCHOLOGICAL SUPPORT
  • The value of psychological support in improving
    pregnancy outcome has not been tested in the form
    of a randomised controlled trial. However, data
    from several non-randomised studies8688 have
    suggested that attendance at a dedicated early
    pregnancy clinic has a beneficial effect,
    although the mechanism is unclear
  • All professionals should be aware of the
    psychological sequelae associated with
    miscarriage and should provide support and
    follow-up, as well as access to formal
    counselling when necessary.

39
THANK YOU
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