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Twins
John R. Martinelli
NBIMC Ob/Gyn
October 28, 2013
Stats
• 1% of all pregnancies.
• 97% of multiple pregnancies are twin pregnancies.
• Double the chance to have twins if conception is within one month
after stopping OCP.
• Increased with ART (1970’s).

• Increased perinatal mortality & morbidity.
Stats
Hellin’s Law
•
•
•
•

Twin 1 : 89
Triplets 1 : 892
Quadruplets 1 : 893
Quintuplets 1 : 894

• Frequency: Highest – Black
Lowest – Asian
• Increased with maternal age and parity.
• ART
Zygotes – Chorions - Amnions
• Zygosity = Type of Conception
• Chorionicity = # of Placenta’s
• Amnionicity = # of Amniotic Sacs
Monozygotic
• Also known as identical twins.
• No genetic predisposition.
• Fertilization of single ovum.
• Same sex.
• Identical – including HLA genes.
Monozygotic
Dizygotic
Zygotes – Chorions - Amnions
• 2/3:

Dizygotic -> Dichorionic, Diamniotic
• 1/3:
Monozygotic -> Monochorionic, Diamniotic (75%)
-> Dichorionic, Diamniotic (25%)
-> Monochorionic, Monoamniotic (1%)
Timing of Split
Monoamniotic
monochorionic

Diamniotic
monochorionic

Diamniotic
dichorionic

9 – 12 days

4 – 8 days

0 – 3 days

<1%

75 %

25 %

After amnion and
chorion are formed

After chorion formed
Before amnion
formed

Before amnion and
chorion formed

3, 9, 12, Split after 13 days  Conjoined Twins
Timing of Split
Diagnosis of Twins
• History

Ovulation inducing drugs?
• Symptoms
Magnified symptoms.
Nausea, vomiting, abnormal bleeding, excessive weight gain,
pressure symptoms, dyspnea, dyspepsia.
• Signs
Anemia, edema, HTN, abnormal weight gain.
Uterus larger than date.
Multiple fetal poles.
FHS.
Ultrasound.
Prenatal Screening
• Biochemical screening for aneuploidy not recommended.
• Quad Screen?

• MSAFP
• NT
Prenatal Screening
Genetic Testing
• Age 32 consider invasive testing.
• Amniocentesis/CVS uncertain risk with twin gestation.
• Age 32 same Down’s Syndrome risk as singleton age 35.
Assessment
• Zygosity
DNA Fingerprinting
Amniocentesis
Chorionic Villus Sampling
Cordocentesis
• Chorionicity/Amnionicity
Ultrasound @ 10 – 14 weeks
Placenta(s) and Amniotic Sac(s)
Lamba Sign
T Sign
Cervical Assessment
• Transvaginal US cervical assessment in the prenatal period has not
been determined due to lack of controlled studies.
• Good evidence that premature cervical change by digital
examination predicts preterm birth in twins.
Home Uterine Monitoring
• No reduction in the incidence of preterm labor, advanced cervical
dilation at presentation, or preterm birth in well-controlled
randomized clinical trials.
• Moderate evidence against home uterine activity monitoring in
multiple gestation.
Pre-Term Labor
Bedrest?

• Randomized controlled trials and a meta-analysis of hospital bedrest
in twin pregnancies have shown no reduction in preterm birth or
perinatal death.
• In uncomplicated twin pregnancies, hospital rest may result in
increased risk of preterm birth and maternal psychosocial stress.
• In women with twin pregnancy at high risk for preterm birth
because of premature cervical change, there is no evidence that
hospital bedrest will reduce the rate of preterm birth.
• There is insufficient evidence to support prophylactic activity
restriction or work leave in multiple gestation.
Pre-Term Labor
Tocolytics?
• Most randomized controlled trials have failed to show any benefit of
prophylactic oral or intravenous tocolytic therapy in multiple
gestation.

• There is moderate evidence against prophylactic tocolysis in the
management of multiple gestation, but it may be indicated on other
grounds.
Pre-Term Labor
Cervical Cerclage?

• Prophylactic cervical cerclage has not been shown to be effective in
preventing preterm birth in twin pregnancy in observational or
controlled trials.
• There is moderate evidence against routine prophylactic cervical
cerclage in multiple gestation.
• Cerclage may be indicated for the treatment of incompetent cervix
or other specific circumstances.
Pre-Term Labor
Cervicovaginal Fibronectin
• High NPV
• PPV for delivery before 37 weeks is 60 percent for patients in
preterm labor, 45 percent in asymptomatic high-risk women, and 30
percent in asymptomatic low-risk women.
• No interventional trials.
Mortality & Morbidity
• Twins = High-risk pregnancy.
• Fetal mortality rate for twins is 4x the mortality rate for single births.
• Neonatal mortality rate for twins is 5x the mortality rate for single
births.
• Increased prevalence of low birth weight infants secondary to
prematurity and IUGR.
Mortality & Morbidity
• Gestational HTN 3x greater risk – with earlier onset and increased
severity compared to single birth.
• Anemia 2X greater risk compared to single birth.
• Congenital Birth Defects 2X greater risk of neural tube defects,
gastrointestinal, and heart anomalies.
Mortality & Morbidity
•

Vascular anastomosis of twins

•

Single intrauterine demise

•

Discordant twins

•

Cord entanglement

•

Conjoined twins
Vascular Anastomosis
• Only monochorionic twins.
• Approximately 100% of monochorionic twin placentas have vascular
anastomoses.
• Variations in the number, size, and direction.
Vascular Anastomosis
TTTS
Twin-Twin Transfusion Syndrome

• TTTS results in hypoperfusion of the donor twin with hyperperfusion
of the recipient twin.
• Donor twin becomes hypovolemic and oliguric/anuric.
• Oligohydraminos develops in the amniotic sac of the donor twin.
• Oligohydraminos can result in “Stuck-Twin” phenomenon with the
twin fixed against the uterine wall.
TTTS: Stuck-Twin
TTTS
• Hydrops fetalis in either twin.

• Donor twin secondary to anemia and/or high-output heart failure.
• Recipient twin secondary to hypervolemia.

• Recipient twin risk of hypertension, hypertrophic cardiomegaly,
disseminated intravascular coagulation, and hyperbilirubinemia
after birth.
TTTS
• 60-100% fetal or neonatal mortality rate.
• Associated with premature delivery.
• Death of one twin is associated with neurologic sequelae in 25% of
surviving twins.
TRAPS
Twin Reverse Arterial Perfusion Syndrome
•
•

1% of monochorionic
.
Arterio-arterial anastomosis.

•

55% mortality in pump twin secondary to polyhydramnios and/or
high-output cardiac failure.

•

Acardiac twin receives blood supply via “pump” twin.

•

Results in absent/rudimentary development upper body structures.

•

Invasive treatment dependent on fetal progress of pump twin.
TRAPS
Vascular Anastamosis Tx
•

Amniotic septostomy

•

Laser ablation

•

Selective fetocide

•

Serial amnioreduction
Single Fetal Demise
• 2-6% of twins pregnancies.
• Up to 25% in MC twin pregnancy.
• Increased perinatal morbidity and mortality of the surviving co-twin.
Related to blood loss of surviving twin.
19% perinatal death
24% having serious long-term sequelae
Discordant Fetal Growth
• Secondary to different genetic growth potentials, structural anomaly
of one fetus, or irregular placental implantation.
• Aneuploidy, congenital anomaly, or viral syndrome affecting only
one fetus must also be considered when discordant growth is
identified.
• Risk increased if weight discordance exceeds 25%.
• Discordance is an indicator for an increased risk of IUGR, morbidity,
and mortality for the smaller twin.
Cord Entanglement
• 70% of MCMA twins.

• Major cause for sudden intra-uterine fetal demise.
• Ultrasound diagnostic.
• Close fetal surveillance from 24 weeks onward.
• Prophylactic delivery via caesarean section at 32 to 34 weeks.
Cord Entaglement
Conjoined Twins
• 1: 55,000 pregnancies
• Monoamniotic.
• Prenatal diagnosis in first trimester.

• Types:
Anterior (thoracopagus)
Posterior (pygopagus)
Cephalic (craniopagus)
Caudal (ischiopagus)
Conjoined Twins
Presentation
• 40% Vertex/Vertex
• 35% Vertex/Non-vertex
• 25% Non-vertex twin A
C-Section
Elective/Scheduled
First twin non-cephalic
Conjoined twin
Monoamniotic twin
Placenta previa
IUGR of dichorionic twin
Congenital abnormality
Emergency
Fetal distress
Cord prolapse of 1st twin
Non progress of labor
Collision of both twins
2nd twin transverse after delivery of 1st twin
THANK YOU!

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Twins

  • 1. Twins John R. Martinelli NBIMC Ob/Gyn October 28, 2013
  • 2. Stats • 1% of all pregnancies. • 97% of multiple pregnancies are twin pregnancies. • Double the chance to have twins if conception is within one month after stopping OCP. • Increased with ART (1970’s). • Increased perinatal mortality & morbidity.
  • 3. Stats Hellin’s Law • • • • Twin 1 : 89 Triplets 1 : 892 Quadruplets 1 : 893 Quintuplets 1 : 894 • Frequency: Highest – Black Lowest – Asian • Increased with maternal age and parity. • ART
  • 4. Zygotes – Chorions - Amnions • Zygosity = Type of Conception • Chorionicity = # of Placenta’s • Amnionicity = # of Amniotic Sacs
  • 5. Monozygotic • Also known as identical twins. • No genetic predisposition. • Fertilization of single ovum. • Same sex. • Identical – including HLA genes.
  • 8. Zygotes – Chorions - Amnions • 2/3: Dizygotic -> Dichorionic, Diamniotic • 1/3: Monozygotic -> Monochorionic, Diamniotic (75%) -> Dichorionic, Diamniotic (25%) -> Monochorionic, Monoamniotic (1%)
  • 9. Timing of Split Monoamniotic monochorionic Diamniotic monochorionic Diamniotic dichorionic 9 – 12 days 4 – 8 days 0 – 3 days <1% 75 % 25 % After amnion and chorion are formed After chorion formed Before amnion formed Before amnion and chorion formed 3, 9, 12, Split after 13 days  Conjoined Twins
  • 11. Diagnosis of Twins • History Ovulation inducing drugs? • Symptoms Magnified symptoms. Nausea, vomiting, abnormal bleeding, excessive weight gain, pressure symptoms, dyspnea, dyspepsia. • Signs Anemia, edema, HTN, abnormal weight gain. Uterus larger than date. Multiple fetal poles. FHS. Ultrasound.
  • 12. Prenatal Screening • Biochemical screening for aneuploidy not recommended. • Quad Screen? • MSAFP • NT
  • 13. Prenatal Screening Genetic Testing • Age 32 consider invasive testing. • Amniocentesis/CVS uncertain risk with twin gestation. • Age 32 same Down’s Syndrome risk as singleton age 35.
  • 14. Assessment • Zygosity DNA Fingerprinting Amniocentesis Chorionic Villus Sampling Cordocentesis • Chorionicity/Amnionicity Ultrasound @ 10 – 14 weeks Placenta(s) and Amniotic Sac(s)
  • 17. Cervical Assessment • Transvaginal US cervical assessment in the prenatal period has not been determined due to lack of controlled studies. • Good evidence that premature cervical change by digital examination predicts preterm birth in twins.
  • 18. Home Uterine Monitoring • No reduction in the incidence of preterm labor, advanced cervical dilation at presentation, or preterm birth in well-controlled randomized clinical trials. • Moderate evidence against home uterine activity monitoring in multiple gestation.
  • 19. Pre-Term Labor Bedrest? • Randomized controlled trials and a meta-analysis of hospital bedrest in twin pregnancies have shown no reduction in preterm birth or perinatal death. • In uncomplicated twin pregnancies, hospital rest may result in increased risk of preterm birth and maternal psychosocial stress. • In women with twin pregnancy at high risk for preterm birth because of premature cervical change, there is no evidence that hospital bedrest will reduce the rate of preterm birth. • There is insufficient evidence to support prophylactic activity restriction or work leave in multiple gestation.
  • 20. Pre-Term Labor Tocolytics? • Most randomized controlled trials have failed to show any benefit of prophylactic oral or intravenous tocolytic therapy in multiple gestation. • There is moderate evidence against prophylactic tocolysis in the management of multiple gestation, but it may be indicated on other grounds.
  • 21. Pre-Term Labor Cervical Cerclage? • Prophylactic cervical cerclage has not been shown to be effective in preventing preterm birth in twin pregnancy in observational or controlled trials. • There is moderate evidence against routine prophylactic cervical cerclage in multiple gestation. • Cerclage may be indicated for the treatment of incompetent cervix or other specific circumstances.
  • 22. Pre-Term Labor Cervicovaginal Fibronectin • High NPV • PPV for delivery before 37 weeks is 60 percent for patients in preterm labor, 45 percent in asymptomatic high-risk women, and 30 percent in asymptomatic low-risk women. • No interventional trials.
  • 23. Mortality & Morbidity • Twins = High-risk pregnancy. • Fetal mortality rate for twins is 4x the mortality rate for single births. • Neonatal mortality rate for twins is 5x the mortality rate for single births. • Increased prevalence of low birth weight infants secondary to prematurity and IUGR.
  • 24. Mortality & Morbidity • Gestational HTN 3x greater risk – with earlier onset and increased severity compared to single birth. • Anemia 2X greater risk compared to single birth. • Congenital Birth Defects 2X greater risk of neural tube defects, gastrointestinal, and heart anomalies.
  • 25. Mortality & Morbidity • Vascular anastomosis of twins • Single intrauterine demise • Discordant twins • Cord entanglement • Conjoined twins
  • 26. Vascular Anastomosis • Only monochorionic twins. • Approximately 100% of monochorionic twin placentas have vascular anastomoses. • Variations in the number, size, and direction.
  • 28. TTTS Twin-Twin Transfusion Syndrome • TTTS results in hypoperfusion of the donor twin with hyperperfusion of the recipient twin. • Donor twin becomes hypovolemic and oliguric/anuric. • Oligohydraminos develops in the amniotic sac of the donor twin. • Oligohydraminos can result in “Stuck-Twin” phenomenon with the twin fixed against the uterine wall.
  • 30. TTTS • Hydrops fetalis in either twin. • Donor twin secondary to anemia and/or high-output heart failure. • Recipient twin secondary to hypervolemia. • Recipient twin risk of hypertension, hypertrophic cardiomegaly, disseminated intravascular coagulation, and hyperbilirubinemia after birth.
  • 31. TTTS • 60-100% fetal or neonatal mortality rate. • Associated with premature delivery. • Death of one twin is associated with neurologic sequelae in 25% of surviving twins.
  • 32. TRAPS Twin Reverse Arterial Perfusion Syndrome • • 1% of monochorionic . Arterio-arterial anastomosis. • 55% mortality in pump twin secondary to polyhydramnios and/or high-output cardiac failure. • Acardiac twin receives blood supply via “pump” twin. • Results in absent/rudimentary development upper body structures. • Invasive treatment dependent on fetal progress of pump twin.
  • 33. TRAPS
  • 34. Vascular Anastamosis Tx • Amniotic septostomy • Laser ablation • Selective fetocide • Serial amnioreduction
  • 35. Single Fetal Demise • 2-6% of twins pregnancies. • Up to 25% in MC twin pregnancy. • Increased perinatal morbidity and mortality of the surviving co-twin. Related to blood loss of surviving twin. 19% perinatal death 24% having serious long-term sequelae
  • 36. Discordant Fetal Growth • Secondary to different genetic growth potentials, structural anomaly of one fetus, or irregular placental implantation. • Aneuploidy, congenital anomaly, or viral syndrome affecting only one fetus must also be considered when discordant growth is identified. • Risk increased if weight discordance exceeds 25%. • Discordance is an indicator for an increased risk of IUGR, morbidity, and mortality for the smaller twin.
  • 37. Cord Entanglement • 70% of MCMA twins. • Major cause for sudden intra-uterine fetal demise. • Ultrasound diagnostic. • Close fetal surveillance from 24 weeks onward. • Prophylactic delivery via caesarean section at 32 to 34 weeks.
  • 39. Conjoined Twins • 1: 55,000 pregnancies • Monoamniotic. • Prenatal diagnosis in first trimester. • Types: Anterior (thoracopagus) Posterior (pygopagus) Cephalic (craniopagus) Caudal (ischiopagus)
  • 41. Presentation • 40% Vertex/Vertex • 35% Vertex/Non-vertex • 25% Non-vertex twin A
  • 42. C-Section Elective/Scheduled First twin non-cephalic Conjoined twin Monoamniotic twin Placenta previa IUGR of dichorionic twin Congenital abnormality Emergency Fetal distress Cord prolapse of 1st twin Non progress of labor Collision of both twins 2nd twin transverse after delivery of 1st twin