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Multiple Gestation
Supervised by:
Prof. Salah Roshdy
Done by:
Yasser Abdulmohsen Alresiny
426035045
OBJECTIVES:
•   Definition.
•   Incidence and epidemiology.
•   Clinical characteristics.
•   Classification.
•   Diagnosis.
•   Complications.
•   Abnormalities of the twinning process.
•   Management.
DEFINITION:
• Any pregnancy which two or more embryos or
  fetuses present in the uterus at same time.
• It is consider as a complication of pregnancy due
  to ;
 ▫ The mean gestational age of delivery of twins is
   approximately 36w.
 ▫ The perinatal mortality &morbidity increase.
Terminology vs. number
         Singletons  one fetus
          Twins  tow fetuses.
         Triplets three fetuses.
       Quadruplets four fetuses.
       Quintuplets  five fetuses.
        sextuplets  six fetuses.
       Septuplets  seven fetuses.
Mean gestational age of delivery
Number of babies   Weeks of Gestation
    1                40 weeks

     2               36 weeks

     3               33 weeks

     4               29 ½ weeks
Incidence & epidemiology
• The incidence of multiple pregnancy in US is
  approximately 3% (increase annually due to ART ).
• Monozygotic twins ( approx. 4 in 1000 births ).
• Triplet pregnancies ( approx. 1 in 8000 births ).
• Multiple gestation increase morbidity & mortality
  for both the mother & the fetuses.
• The perinatal mortality in the developed countries
  ▫ Twins = 5 – 10 % births.
  ▫ Triplets = 10 – 20 % births.
Clinical characteristics:
Multiple gestation should be suspected when ;
 Uterine size is greater than expected for
  gestational age.
 Multiple FHRs are heard
 Multiple fetal parts are felt.
 hCG & serum alpha-fetoprotein levels are
  elevated for gestational age.
 If the pregnancy is a result of ART.
  Diagnosis is confirmed by US .
DDx of uterus that is greater than
expected for gestational age:
1- Polyhydramnios.
2- Macrosomia.
3- Placental abruption.
4- Gestational trophoplastic disease.
5- Uterine fibroid.
6- Ovarian mass.
Classification

        Dizygotic (>70%)                                   Monozygotic (<30%)



     Dichorionic/Diamniotic
                    Dichorionic/Diamniotic             Monochorionic/Monoamniotic
                             (8%(                                 (1%)


                                    Monochorionic/Diamniotic
                                            (20%)


N.B. : Placentation in higher-order multiples ( triplets, quadruplets…( follows the same
principles, except monochorionic & dichorionic may coexist.
Important notes:
1- Monozygotic twins having same sex & blood
  group.

2- Process of formation of chorion is earlier than
 formation of amnion.

3-Dizygotic twins must be dichorionic/diamniotic.

4- There is no dichorionic/ monoamniotic.
A- Dizygotic twins (fraternal):
Most common represents 2/3 of cases.
Fertilization of more than one egg by more than
 one sperm.
Non identical ,may be of different sex.
Two chorion and two amnion.
Placenta may be separate or fused.
 “each fetus is contained within a complete
 amniotic-chorionic membrane “
Cont
 The incidence of dizygotic twins is higher in ;
1. Certain families .
2. Race ;African Americans .
3. Increases with maternal age, parity, weight and
   height .
4. Ovulation induction.
B- Monzygotic twins:
Constitutes 1/3 of twins
These twins are multiple gestations resulting from
 cleavage of a single, fertilized ovum.
The timing of cleavage determines the
 placentation of the pregnancy.
Constant incidence .
Not affected by heredity.
Not related to induction of ovulation.
Time of        Nature of membranes        %      Perinatal
cleavage                                         mortality

0 - 72 hr       diamniotic,dichorionic     8       8.9%


4 – 8 days    diamniotic,monochorionic    20       25%


9-12days     monoamniotic,monochorionic    1      50-60%



>13 days           Conjoined twin         ----     -----
Placentation in Higher-Order Multiples ;

    The relationship of placentas among triplets,
     quadruplets, and higher-order multiple fetuses
     generally follows the same principles, except that
     monochorionic and dichorionic placentation may
     coexist, and placental anomalies are more frequently
     found in higher-order multiples.
Diagnosis:
• History:
  ▫   Family hx of dizygotic twins.
  ▫   Use of fertility drugs.
  ▫   sensation of excessive fetal movements.
  ▫   Exaggerated symptoms of pregnancy (hyperemesis
      gravidarum ).
• Examination:
  ▫ GPE ( weight gain, Pre-eclampsia signs )
  ▫ Abdominal examination (excessive uterine fundal
    growth, and auscultation of fetal heart rates in separate
    quadrants of the uterus are suggestive but not
    diagnostic).
• Sonographic examination ( diagnostic )
Ultrasound evaluation:
• The diagnosis of multiple gestation requires a
  sonographic examination demonstrating two
  separate fetuses and heart activities.
• The diagnosis can be made as early as 6 weeks of
  gestation.
DETERMINATION OF ZYGOSITY:
 Very important as most of the complications occur in
 monochorionic monozygotic twins.


 By ;
   Ultrasound : genders,numbar of placentas,
   Blood groups.
   HLA.
   DNA analysis.
• During pregnancy by US :

• Very accurate in the first trimester, two sacs,
  presence of thick chorion between amniotic
  membrane .
• Less accurate in the second trimester the
  chorion become thin and fuse with the amniotic
  membrane .
• Different sex indicates dizygotic twins.
• Separate placentas indicates dizygotic twins
After birth ;
• By examination of the MEMBRANE,
  PLACENTA,SEX , BLOOD group .

• Examination of the newborn DNA and HLA may
  be needed in few cases.
DETERMINATION OF ZYGOSITY:
Findings                    Zygosity             Freq.

Different genders           dizygotic            30%

Two placentas,same gender   dizygotic            27%
different blood groups

One placentas               monozygotic          23%

Two placentas,same gender   HLA & DNA analysis   20%
Same blood group
US

  different                  gender                same




dizygotic           Monozygotic                   Number of
  twins               twins                1       placenta




                                                      2
    different         same



                                        same       Blood
                HLA & DNA                          group
                 analysis
                                      different
Septum                Placental type                Twin type

      1- None         Monochorionic/Monoamniotic        monozygotic

   2- Amnion only      Monochorionic/Diamniotic         monozygotic

3- Amnion & chorion     Dichorionic/ diamniotic    Dizygotic or monozygotic

4- No common septum     Dichorionic/ diamniotic           dizigotic




     1                      2                      3                  4
Complications:
• A - Maternal:
  ▫ Antepartum
     Anemia.
     Miscarriage.
     Preeclampsia ( 40% in twins & 60% in triplets ).
     Polyhydramnios ( 5 – 8%).
     PTL ( Twin account for 10% of all PTL & 25% of all preterm
      perinatal deaths ).
     Cervical incompetence.
     Hyperemesis gravidarum.
  ▫ Intrapartum
     CS.
  ▫ Postpartum
     postpartum uterine atony.      b/c of
     post partum Hemorrhage.       Over distended uterus
     postpartum endometritis
Cont..
• B - Fetal:
  ▫   Malpresentation.
  ▫   Umblical cord prolapse.
  ▫   Placenta previa & abruptio placenta.
  ▫   PROM & Prematurity.
  ▫   IUGR .
  ▫   Congenitial anomalies.
  ▫   Increase perinatal morbidity & mortality
Causes of perinatal morbidity and
mortality in twins:
•   Respiratory distress syndrome
•   Birth trauma
•   Cerebral hemorrhage
•   Birth asphyxia
•   Birth anoxia
•   Congenital anomalies
•   Stillbirths
•   Prematurity
Abnormalities of the twinning process:
 •   Conjoined Twins.
 •   Interplacental Vascular Anastomosis.
 •   Twin-Twin Transfusion Syndrome.
 •   Fetal Malformations.
 •   Umbilical Cord Abnormalities.
 •   Discordant Twin Growth.
 •   Locked twins ( delivered by CS ).
 •   Single fetal death
 •   Rupture of membrane in single sac
Locked twins
Conjoined Twins ;
 • Etiology : It result from cleavage of the embryo is
   incomplete because it happen very late (after 13 days,
   when the embryonic disc has completely formed).
 •
 • Incidence : once in 70,000 deliveries.

 • Classification:
   ▫   Thoracopagus (antreior) “most common”.
   ▫   Pygopagus (posterior)
   ▫   Craniopagus (cephalic)
   ▫   Ischiopagus (caudal)

 • Delivery by C.S.
Thoracopagus   Craniopagus
Interplacental Vascular Anastomoses:
• It occurs almost exclusively in monochorionic
  twins at a rate of 90% or more.
• Type:
 ▫ Arterial_artarial(most common).
 ▫ Arterial_venous.
 ▫ Venous_venous.
• Complications:
 ▫   Abortion.
 ▫   Hydramnios.
 ▫   Twin-twin transfusion syndrome (TTTS).
 ▫   Fetal malformations.
Twin-Twin Transfusion Syndrome ;
 • Definition:
   ▫ 15% of monochorionic twins have domensturable
     anastomosis.
   ▫ The presence of unbalanced anastomosis in the placenta
     (typically arterial-venous connections) leads to a syndrome in
     which one twin’s circulation perfuses the other Twin.
 • Complication:
   ▫ Donor : anemic HF, hypovolemia, hypotension, anemia,
     oligohydramnios, growth restriction. ( do intrauterine blood
     trans fusion).
   ▫ Recipient : hypervolemic HF , hypervolemia, hypertension,
     polyhydramnios, thrombosis, hyperviscosity,cardiomegaly,
     polycythemia, hydrops fetalis. ( do repeated amnioreduction).
   ▫ Both: risk of demise & PTL.
Management of TTTs ;
    If not treated death occurs in 80-100% of cases.
    If extreme prematurity prevents immediate delivery,
    Several interventions can be considered in view of the
     high mortality associated with expectant management.
• Repeated amniocentesis from ( recipient) .
• Intrauterine transfusion of the anemic (donor) twin
  is of no benefit in this condition.
• Indomethacin.
• Fetoscopy and laser ablation of communicating
  vessels.
Fetal Malformations:
 • Incidence:
  ▫ Twice as common in twins & 4 times more common
    in triplets than in singleton infants.
  ▫ Monozygotic > Dizygotic.
 • Etiology:
  ▫ Usually result from arterial-arterial anastomosis.
  ▫ Common deformations in twins include limb
    defects, plagiocephaly, facial asymmetry, and
    torticollis.
  ▫ Acardia and twin-reversed arterial perfusion
    (TRAP) “ rare but unique to multiple pregnancy”.
 • Amniocentesis:
  ▫ If U/S shows abnormality.
Acardiac
  Normal        twin
(pump) twin
Umbilical Cord Abnormalities:
• Absence of one umbilical artery occurs in about
  3% to 4% of twins (30% of case absence of one
  artery associated with other congenital
  anomalies”renal agenesis” ).
• Cord entanglement ( esp. in monochorionic
  monoamniotic twins ).
Discordant Twin Growth:
• Definition:
 ▫ Discrepancy of more than 20% in the estimated fetal
   weights.
• Causes:
 ▫   TTTS.
 ▫   Chromosomal or structural anomalies.
 ▫   Discordant viral infection.
 ▫   Interplacental Vascular Anastomoses.
Specific indication C/S in Twins ;
1.   monochorionic monoamniotic twins
2.   Conjoined twins
3.   Non vertex presentation of first twin
4.   Locked twins
5.   Twin-reversed arterial perfusion (TRAP)
6.   Placentation in Higher-Order Multiples
7.   Other obstrictic indication of C/S
Management:
 Antepartum
 • Adequate nutrition.
   ▫ Adequacy of maternal diet is assessed due to the increased
     need for overall calories, iron, vitamins, and folate .
   ▫ The Institute of Medicine (IOM) recommends women with
     twins gain a total of 16.0 to 20.5 kg during the pregnancy.
 • More frequent prenatal visits.
 • Periodic U/S assessment “ every 3-4 weeks from23weeks’
   gestation “ to monitor the growth and detection of
   discordant growth or TTTS.
 • Fetal surveillance:
   ▫ Performance of NST is not indicated before 34 wks unless to
     confirm IUGR or discordant growth.
   ▫ ( avoid CST )
 • Amniocentesis. ( If indicated )
In case of death of one fetus is managed based on the gestational
  age and condition of the surviving fetus.

1- fetal surveillance            weekly measured Until evidence
2- maternal clotting profiles     of fetal lung maturity in the
  surviving fetus is exhibited

Delivery should be considered if :
1) Fetal lung maturity is demonstrated
2) If compromise of the remaining fetus develops
3) If evidence of disseminated intravascular coagulation in the
  mother is present.

In the setting of TTTS, the death of one twin should prompt
  consideration of delivery, particularly after 28 weeks, given the
  high rates of embolic complications in the surviving twin.
Cont..
Intrapartum

• The route of delivery depends on:
 ▫   Presentation of the twins.
 ▫   Gestational age.
 ▫   Presence of maternal or fetal complications.
 ▫   Experience of obstetrician.
 ▫   Availability of anesthesia & neonatal intensive
     care.
Delivery:
 • Vertex/Vertex(43%):
  ▫ Vaginal delivery. (Successful in 70-80%of cases).
  ▫ Surveillance of twin B with real-time U/S.
 • Vertex/Nonvertex(38%):
  ▫ Vaginal delivery ( better ) (in absence of discordant
    growth).
  ▫ Either external cephalic version or podalic version
    with breech extraction may be attempted.
  ▫ CS.
 • Nonvertex Twin A(19%):
  ▫ CS .
Cont.
postpartum
• Active management of PPH:
By giving oxytocin in the 3nd stage of labor just
  after delivery of both fetuses and placentas.
Multiple gestation with more than
two fetuses
 Most frequent cause is iatrogenic from the use of
  ovulation induction agent.
 Prematurity increase as the number of fetuses
  increase .
   1) Multifetal reduction may be offered:
  Reduce the risk to the mother & the remaining
    fetuses.
  Performed only in the setting of dichorionic
    /diamniotic gestation.
  2) Selective termination:
  Termination of one or more fetuses with structural or
    chromosomal anomalies.
Summary:
1- Definition.
2- Incidence why Increased?
3- Types (2).
4- Diagnosis (History, examination & US).
5- Complication( Maternal, fetal & placentation
  process).
6- Management (antepartum, intrapartum &
  postpartum).
References
• The Johns Hopkins manual of gyencology &
  obestetrics.
• Essentials of gyencology & obestetrics by
  Hacker, Moore & Gambone.
• Pictures: From internet.
Thank You

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  • 1. Multiple Gestation Supervised by: Prof. Salah Roshdy Done by: Yasser Abdulmohsen Alresiny 426035045
  • 2. OBJECTIVES: • Definition. • Incidence and epidemiology. • Clinical characteristics. • Classification. • Diagnosis. • Complications. • Abnormalities of the twinning process. • Management.
  • 3. DEFINITION: • Any pregnancy which two or more embryos or fetuses present in the uterus at same time. • It is consider as a complication of pregnancy due to ; ▫ The mean gestational age of delivery of twins is approximately 36w. ▫ The perinatal mortality &morbidity increase.
  • 4. Terminology vs. number Singletons  one fetus Twins  tow fetuses. Triplets three fetuses. Quadruplets four fetuses. Quintuplets  five fetuses. sextuplets  six fetuses. Septuplets  seven fetuses.
  • 5. Mean gestational age of delivery Number of babies Weeks of Gestation 1 40 weeks 2 36 weeks 3 33 weeks 4 29 ½ weeks
  • 6. Incidence & epidemiology • The incidence of multiple pregnancy in US is approximately 3% (increase annually due to ART ). • Monozygotic twins ( approx. 4 in 1000 births ). • Triplet pregnancies ( approx. 1 in 8000 births ). • Multiple gestation increase morbidity & mortality for both the mother & the fetuses. • The perinatal mortality in the developed countries ▫ Twins = 5 – 10 % births. ▫ Triplets = 10 – 20 % births.
  • 7. Clinical characteristics: Multiple gestation should be suspected when ;  Uterine size is greater than expected for gestational age.  Multiple FHRs are heard  Multiple fetal parts are felt.  hCG & serum alpha-fetoprotein levels are elevated for gestational age.  If the pregnancy is a result of ART.  Diagnosis is confirmed by US .
  • 8. DDx of uterus that is greater than expected for gestational age: 1- Polyhydramnios. 2- Macrosomia. 3- Placental abruption. 4- Gestational trophoplastic disease. 5- Uterine fibroid. 6- Ovarian mass.
  • 9. Classification Dizygotic (>70%) Monozygotic (<30%) Dichorionic/Diamniotic Dichorionic/Diamniotic Monochorionic/Monoamniotic (8%( (1%) Monochorionic/Diamniotic (20%) N.B. : Placentation in higher-order multiples ( triplets, quadruplets…( follows the same principles, except monochorionic & dichorionic may coexist.
  • 10. Important notes: 1- Monozygotic twins having same sex & blood group. 2- Process of formation of chorion is earlier than formation of amnion. 3-Dizygotic twins must be dichorionic/diamniotic. 4- There is no dichorionic/ monoamniotic.
  • 11. A- Dizygotic twins (fraternal): Most common represents 2/3 of cases. Fertilization of more than one egg by more than one sperm. Non identical ,may be of different sex. Two chorion and two amnion. Placenta may be separate or fused.  “each fetus is contained within a complete amniotic-chorionic membrane “
  • 12. Cont The incidence of dizygotic twins is higher in ; 1. Certain families . 2. Race ;African Americans . 3. Increases with maternal age, parity, weight and height . 4. Ovulation induction.
  • 13.
  • 14. B- Monzygotic twins: Constitutes 1/3 of twins These twins are multiple gestations resulting from cleavage of a single, fertilized ovum. The timing of cleavage determines the placentation of the pregnancy. Constant incidence . Not affected by heredity. Not related to induction of ovulation.
  • 15. Time of Nature of membranes % Perinatal cleavage mortality 0 - 72 hr diamniotic,dichorionic 8 8.9% 4 – 8 days diamniotic,monochorionic 20 25% 9-12days monoamniotic,monochorionic 1 50-60% >13 days Conjoined twin ---- -----
  • 16.
  • 17.
  • 18. Placentation in Higher-Order Multiples ;  The relationship of placentas among triplets, quadruplets, and higher-order multiple fetuses generally follows the same principles, except that monochorionic and dichorionic placentation may coexist, and placental anomalies are more frequently found in higher-order multiples.
  • 19. Diagnosis: • History: ▫ Family hx of dizygotic twins. ▫ Use of fertility drugs. ▫ sensation of excessive fetal movements. ▫ Exaggerated symptoms of pregnancy (hyperemesis gravidarum ). • Examination: ▫ GPE ( weight gain, Pre-eclampsia signs ) ▫ Abdominal examination (excessive uterine fundal growth, and auscultation of fetal heart rates in separate quadrants of the uterus are suggestive but not diagnostic). • Sonographic examination ( diagnostic )
  • 20. Ultrasound evaluation: • The diagnosis of multiple gestation requires a sonographic examination demonstrating two separate fetuses and heart activities. • The diagnosis can be made as early as 6 weeks of gestation.
  • 21. DETERMINATION OF ZYGOSITY: Very important as most of the complications occur in monochorionic monozygotic twins. By ; Ultrasound : genders,numbar of placentas, Blood groups. HLA. DNA analysis.
  • 22. • During pregnancy by US : • Very accurate in the first trimester, two sacs, presence of thick chorion between amniotic membrane . • Less accurate in the second trimester the chorion become thin and fuse with the amniotic membrane . • Different sex indicates dizygotic twins. • Separate placentas indicates dizygotic twins
  • 23. After birth ; • By examination of the MEMBRANE, PLACENTA,SEX , BLOOD group . • Examination of the newborn DNA and HLA may be needed in few cases.
  • 24. DETERMINATION OF ZYGOSITY: Findings Zygosity Freq. Different genders dizygotic 30% Two placentas,same gender dizygotic 27% different blood groups One placentas monozygotic 23% Two placentas,same gender HLA & DNA analysis 20% Same blood group
  • 25. US different gender same dizygotic Monozygotic Number of twins twins 1 placenta 2 different same same Blood HLA & DNA group analysis different
  • 26. Septum Placental type Twin type 1- None Monochorionic/Monoamniotic monozygotic 2- Amnion only Monochorionic/Diamniotic monozygotic 3- Amnion & chorion Dichorionic/ diamniotic Dizygotic or monozygotic 4- No common septum Dichorionic/ diamniotic dizigotic 1 2 3 4
  • 27.
  • 28. Complications: • A - Maternal: ▫ Antepartum  Anemia.  Miscarriage.  Preeclampsia ( 40% in twins & 60% in triplets ).  Polyhydramnios ( 5 – 8%).  PTL ( Twin account for 10% of all PTL & 25% of all preterm perinatal deaths ).  Cervical incompetence.  Hyperemesis gravidarum. ▫ Intrapartum  CS. ▫ Postpartum  postpartum uterine atony. b/c of  post partum Hemorrhage. Over distended uterus  postpartum endometritis
  • 29. Cont.. • B - Fetal: ▫ Malpresentation. ▫ Umblical cord prolapse. ▫ Placenta previa & abruptio placenta. ▫ PROM & Prematurity. ▫ IUGR . ▫ Congenitial anomalies. ▫ Increase perinatal morbidity & mortality
  • 30. Causes of perinatal morbidity and mortality in twins: • Respiratory distress syndrome • Birth trauma • Cerebral hemorrhage • Birth asphyxia • Birth anoxia • Congenital anomalies • Stillbirths • Prematurity
  • 31. Abnormalities of the twinning process: • Conjoined Twins. • Interplacental Vascular Anastomosis. • Twin-Twin Transfusion Syndrome. • Fetal Malformations. • Umbilical Cord Abnormalities. • Discordant Twin Growth. • Locked twins ( delivered by CS ). • Single fetal death • Rupture of membrane in single sac
  • 33. Conjoined Twins ; • Etiology : It result from cleavage of the embryo is incomplete because it happen very late (after 13 days, when the embryonic disc has completely formed). • • Incidence : once in 70,000 deliveries. • Classification: ▫ Thoracopagus (antreior) “most common”. ▫ Pygopagus (posterior) ▫ Craniopagus (cephalic) ▫ Ischiopagus (caudal) • Delivery by C.S.
  • 34. Thoracopagus Craniopagus
  • 35. Interplacental Vascular Anastomoses: • It occurs almost exclusively in monochorionic twins at a rate of 90% or more. • Type: ▫ Arterial_artarial(most common). ▫ Arterial_venous. ▫ Venous_venous. • Complications: ▫ Abortion. ▫ Hydramnios. ▫ Twin-twin transfusion syndrome (TTTS). ▫ Fetal malformations.
  • 36. Twin-Twin Transfusion Syndrome ; • Definition: ▫ 15% of monochorionic twins have domensturable anastomosis. ▫ The presence of unbalanced anastomosis in the placenta (typically arterial-venous connections) leads to a syndrome in which one twin’s circulation perfuses the other Twin. • Complication: ▫ Donor : anemic HF, hypovolemia, hypotension, anemia, oligohydramnios, growth restriction. ( do intrauterine blood trans fusion). ▫ Recipient : hypervolemic HF , hypervolemia, hypertension, polyhydramnios, thrombosis, hyperviscosity,cardiomegaly, polycythemia, hydrops fetalis. ( do repeated amnioreduction). ▫ Both: risk of demise & PTL.
  • 37. Management of TTTs ;  If not treated death occurs in 80-100% of cases.  If extreme prematurity prevents immediate delivery,  Several interventions can be considered in view of the high mortality associated with expectant management. • Repeated amniocentesis from ( recipient) . • Intrauterine transfusion of the anemic (donor) twin is of no benefit in this condition. • Indomethacin. • Fetoscopy and laser ablation of communicating vessels.
  • 38.
  • 39. Fetal Malformations: • Incidence: ▫ Twice as common in twins & 4 times more common in triplets than in singleton infants. ▫ Monozygotic > Dizygotic. • Etiology: ▫ Usually result from arterial-arterial anastomosis. ▫ Common deformations in twins include limb defects, plagiocephaly, facial asymmetry, and torticollis. ▫ Acardia and twin-reversed arterial perfusion (TRAP) “ rare but unique to multiple pregnancy”. • Amniocentesis: ▫ If U/S shows abnormality.
  • 40. Acardiac Normal twin (pump) twin
  • 41. Umbilical Cord Abnormalities: • Absence of one umbilical artery occurs in about 3% to 4% of twins (30% of case absence of one artery associated with other congenital anomalies”renal agenesis” ). • Cord entanglement ( esp. in monochorionic monoamniotic twins ).
  • 42. Discordant Twin Growth: • Definition: ▫ Discrepancy of more than 20% in the estimated fetal weights. • Causes: ▫ TTTS. ▫ Chromosomal or structural anomalies. ▫ Discordant viral infection. ▫ Interplacental Vascular Anastomoses.
  • 43. Specific indication C/S in Twins ; 1. monochorionic monoamniotic twins 2. Conjoined twins 3. Non vertex presentation of first twin 4. Locked twins 5. Twin-reversed arterial perfusion (TRAP) 6. Placentation in Higher-Order Multiples 7. Other obstrictic indication of C/S
  • 44. Management: Antepartum • Adequate nutrition. ▫ Adequacy of maternal diet is assessed due to the increased need for overall calories, iron, vitamins, and folate . ▫ The Institute of Medicine (IOM) recommends women with twins gain a total of 16.0 to 20.5 kg during the pregnancy. • More frequent prenatal visits. • Periodic U/S assessment “ every 3-4 weeks from23weeks’ gestation “ to monitor the growth and detection of discordant growth or TTTS. • Fetal surveillance: ▫ Performance of NST is not indicated before 34 wks unless to confirm IUGR or discordant growth. ▫ ( avoid CST ) • Amniocentesis. ( If indicated )
  • 45. In case of death of one fetus is managed based on the gestational age and condition of the surviving fetus. 1- fetal surveillance weekly measured Until evidence 2- maternal clotting profiles of fetal lung maturity in the surviving fetus is exhibited Delivery should be considered if : 1) Fetal lung maturity is demonstrated 2) If compromise of the remaining fetus develops 3) If evidence of disseminated intravascular coagulation in the mother is present. In the setting of TTTS, the death of one twin should prompt consideration of delivery, particularly after 28 weeks, given the high rates of embolic complications in the surviving twin.
  • 46. Cont.. Intrapartum • The route of delivery depends on: ▫ Presentation of the twins. ▫ Gestational age. ▫ Presence of maternal or fetal complications. ▫ Experience of obstetrician. ▫ Availability of anesthesia & neonatal intensive care.
  • 47. Delivery: • Vertex/Vertex(43%): ▫ Vaginal delivery. (Successful in 70-80%of cases). ▫ Surveillance of twin B with real-time U/S. • Vertex/Nonvertex(38%): ▫ Vaginal delivery ( better ) (in absence of discordant growth). ▫ Either external cephalic version or podalic version with breech extraction may be attempted. ▫ CS. • Nonvertex Twin A(19%): ▫ CS .
  • 48. Cont. postpartum • Active management of PPH: By giving oxytocin in the 3nd stage of labor just after delivery of both fetuses and placentas.
  • 49. Multiple gestation with more than two fetuses Most frequent cause is iatrogenic from the use of ovulation induction agent. Prematurity increase as the number of fetuses increase . 1) Multifetal reduction may be offered: Reduce the risk to the mother & the remaining fetuses. Performed only in the setting of dichorionic /diamniotic gestation. 2) Selective termination: Termination of one or more fetuses with structural or chromosomal anomalies.
  • 50. Summary: 1- Definition. 2- Incidence why Increased? 3- Types (2). 4- Diagnosis (History, examination & US). 5- Complication( Maternal, fetal & placentation process). 6- Management (antepartum, intrapartum & postpartum).
  • 51. References • The Johns Hopkins manual of gyencology & obestetrics. • Essentials of gyencology & obestetrics by Hacker, Moore & Gambone. • Pictures: From internet.