We are IntechOpen,
the world’s leading publisher of
Open Access books
Built by scientists, for scientists
6,100
Open access books available
150,000
International authors and editors
185M
Downloads
Our authors are among the
154
Countries delivered to
TOP 1%
most cited scientists
12.2%
Contributors from top 500 universities
Selection of our books indexed in the Book Citation Index
in Web of Science™ Core Collection (BKCI)
Interested in publishing with us?
Contact book.department@intechopen.com
Numbers displayed above are based on latest data collected.
For more information visit www.intechopen.com
Chapter
Multiple Pregnancy
Mandefro Yilma Asfaw
Abstract
Multiple pregnancies mean when the woman carries more than one fetus at a time.
Multiple pregnancy, multiple gestation, and multifetal pregnancy are synonyms.
These can be twins, triplets, quadruplets, or more. These types of pregnancy have
become one of the most common high-risk pregnancies encountered by obstetri-
cians. It is associated with an increased risk of both maternal and perinatal morbidity
and mortality. The incidence of multiple pregnancies has risen significantly over the
last four decades, primarily due to increased use of ovulation induction drugs. The
symptoms and signs of multiple pregnancies include excessive nausea and vomiting,
larger uterus than expected for the date of pregnancy, and excessive weight gain. The
aim of this chapter is to discuss the occurrence, causes, epidemiology, maternal and
perinatal morbidity and mortality, antepartum, and intrapartum management of
multiple pregnancies.
Keywords: multiple pregnancy, chorionicity, zygosity, antenatal care, morbidity,
mortality
1. Introduction
Multiple pregnancies are the presence of more than one fetus at a time.
Simultaneous development of two fetuses, three fetuses, and four fetuses is called as
twins, triplets, quadruplets, respectively, and so on. These types of pregnancies may
result from two or more fertilization or from single fertilization followed by cleavage of
the zygote or combination of both [1]. Such pregnancies are associated with increased
maternal and perinatal morbidity and mortality compared to that singleton gestations.
They can cause almost every potential complication of pregnancy except post-term
delivery and macrosomia [2, 3]. Twins’ pregnancy is the most common variety of
multiple pregnancies and the rate of occurrence of multiple pregnancies decreases with
an increased number of fetuses [4]. The rate and the number of both twin and higher-
order multi-fetal births have increased dramatically over the last four decades, mainly
due to ovulation induction and early detection by ultrasound [1, 5]. According to
Hellin’s rules, the mathematical frequency of multiple births is 1 in 80 (n−1) pregnancies,
1
Multiple Pregnancy - New Insights
where n is the number of fetuses [4]. For example, twins 1 in 80 pregnancies, triplets 1
in 6400, quadruplets 1 in 512,000, etc. [4, 5].
2. Zygosity and chorionicty
Zygosity refers to the genetic makeup of the twin pregnancy while chorionicty
indicates the placenta’s membrane status [4]. Early determination of chorionicity is
essential because it is a major factor in determining obstetrical risks, management,
and outcomes [2, 3].
Twins can be either monozygotic or dizygotic.
• Dizygotic (DZ) or fraternal twins result from fertilization of two ova by two
sperms during a single ovarian cycle.
• Monozygotic (MZ) or identical twins are the result of fertilization of a single
ovum by single sperm and followed by splitting of the zygote. Chorionicity will
depend on the timing of the division of the embryo. The following possibilities
may occur:
I. If the division takes place within 72 hours after fertilization, the resulting
embryos will have two separate placenta, chorions, and amnions, that is, a
thick four-layered intervening membrane. It accounts for 25 to 30% of MZ
twins.
II. If the division takes place between the 4th and 8th days of fertilization when
the chorion is already formed, monochorionic, diamniotic twins will evolve
with a thin two-layer dividing membrane. It accounts 70–75% of MZ twins.
III. If the division occurs between 8th and 12th days of fertilization, the result will
be a monochorionic and monoamniotic twin. It accounts 1–2% of MZ twins.
IV. If the division occurs after 13th day of fertilization, the result will be a
monochorionic, monoamniotic, and conjoined twins. It is a rare type of MZ
and occurs in less than 1%.
The following table shows the relationship between the timing of division and the
nature of membranes in twin pregnancy.
Time of cleavage Nature of membranes
0–72 hours Dichorionic, diamniotic
4–8 days Monochorionic, diamniotic
9–12 days Monochorionic, monoamniotic
After 13 days Monochorionic, monoamniotic (conjoined twins)
The following figures show placentation in twin pregnancies [2].
2
Multiple Pregnancy
DOI: http://dx.doi.org/10.5772/intechopen.104836
3. Rates and causes of monozygotic and dizygotic twinning
Dizygotic twins occur in about 1% to 1.5% and monozygotic twins 1 in 250 preg-
nancies among natural conception [2]. The rates of spontaneous DZ twinning are
influenced by maternal age, family history, and race [2, 3, 6]. The frequency of MZ
twinning is constant in all populations studied at about 1 in 250 births [3].
The risk for DZ twinning increases with maternal age, peaking at 37 years of age.
Maternal family history also increases the chance of spontaneous DZ twinning, while
paternal family history contributes little or nothing to this risk [2, 7]. The frequency
of multiple pregnancies varies significantly among different races and ethnic groups.
Women of African descent have higher rates of DZ twinning than white women,
who in turn have higher rates than women of Asian descent [2]. In Japan, 1 in 250
3
Multiple Pregnancy - New Insights
newborns is a twin, whereas in Nigeria, 1 in 11 babies is a result of a twin gestation
[2, 6]. Ovulation induction increases the occurrence of multiple pregnancies, includ-
ing both dizygotic and monozygotic [4, 7].
4. Superfecundation and superfetation
Superfecundation is the fertilization of two different ova released in the same
cycle, by separate acts of coitus within a short period of time. Sexual intercourse may
not necessary with the same man [1, 4].
Superfetation is the fertilization of two ova released in different menstrual cycles.
The implantation and development of one fetus over another fetus are theoretically
possible until the uterine cavity is obliterated by 12 weeks of pregnancy. In other
words, superfetation requires ovulation and fertilization during the course of an
established pregnancy [1, 4].
5. Diagnosis of multiple pregnancies
5.1 Clinical evaluation
With multiple fetuses, a woman may experience excessive nausea and vomiting
during the first trimester. The uterine size is typically larger than expected during the
second and third trimesters.
In general, it is difficult to diagnose twins by palpation of fetal parts before the
third trimester. In obese women, presence of hydramnios and overlapping fetuses are
factors that make it difficult to identify twins by abdominal palpation. Palpating two
or more fetal heads and or fetal poles supports a diagnosis of multiple pregnancies.
Identification of two fetal heartbeats suggests that their rates are clearly distinct
from each other and from that of the mother suggests twin pregnancy.
6. Sonography
Routine prenatal ultrasound scan has proved important for early detection of multiple
pregnancies. Before the advent of routine prenatal ultrasound, many twins were not diag-
nosed until late in gestation or delivery [2]. Separate gestational sacs with individual yolk
sacs can be visualized as early as 5 weeks from the first day of the last menstrual period,
and embryos with cardiac activity can usually be seen by 6 weeks by transvaginal ultra-
sound [2]. Prenatal sonography in multiple pregnancies is useful for the following [6]:
• Confirming a diagnosis of multiple gestations
• Determining chorionicty
• Detecting fetal anomalies
• Evaluating fetal growth
• For fetal well-being
4
Multiple Pregnancy
DOI: http://dx.doi.org/10.5772/intechopen.104836
7. Determination of chorionicity
Accurate determination of chorionicity early in pregnancy is essential to optimal
obstetrics care [4]. It is a major determinant of pregnancy outcome and its determina-
tion is easiest and most reliable when assessed in the first trimester [2].
• The presence of two separate gestational sacs, each containing the fetus, and a
thick dividing membrane strongly suggests dichorionic diamniotic pregnancy.
• When there is one gestational sac and a thin dividing membrane (< 2 mm)
suggests monochorionic diamniotic pregnancy.
• A single gestational sac that contains two fetuses without dividing membrane
suggests monochorionic monoamniotic pregnancy.
Examination of the base of the intertwin membrane is also useful for the determi-
nation of chorionicity.
• The twin peak sign appears as a triangular projection of placental tissue extend-
ing a short distance between the layers of the dividing membrane, suggesting
dichorionic pregnancy.
• The T sign is the right-angle relationship between the membranes and placenta
and no apparent extension of the placenta between the dividing membranes
suggests monochorionic pregnancy.
The determination of chorionicity and amnionicity in the second and third
trimesters can be made based on sex of fetuses, number of placentas, and thickness of
the dividing membrane.
• For instance, different gender, two separate placentas, and thick dividing
membrane strongly suggest dichorionic pregnancy.
After delivery, a careful visual examination of the placenta and membranes serves
to establish zygosity and chorionicity in approximately two-thirds of cases [4].
8. Maternal adaptation to multiple pregnancies
The degree of maternal physiologic changes during pregnancy is exaggerated
with multiple gestations. The levels of maternal hormones related to pregnancy are
higher in multiple gestations than in singleton. Compared to singleton pregnan-
cies, multiple pregnancies are associated with an increased risk of the following
conditions.
• Nausea and vomiting
• Weight
• Blood volume
5
Multiple Pregnancy - New Insights
• Cardiac output
• Glomerular filtration rate
• Tidal volume
• Mechanical distress
9. Maternal morbidity and mortality related to multiple pregnancies
Rates of essentially every obstetrical complication are elevated with multiple
pregnancies with the exception of macrosomia and post-term pregnancy. In general,
these complications rise proportionally with increasing the number of fetuses.
• Hyperemesis gravidarum
• Spontaneous abortion
• Anemia
• Hypertensive disorder of pregnancy
• Abruption placentae
• Placenta previa
• Gestational diabetics
• Polyhydramnios
• Thromboembolism
• Postpartum hemorrhage
• Cesarean delivery
10. Perinatal morbidity and mortality related to multiple pregnancies
Babies who are products of multiple gestations have higher rates of:
• Low birth weight
• Preterm birth
• Malpresentation
• Premature rupture of membranes
6
Multiple Pregnancy
DOI: http://dx.doi.org/10.5772/intechopen.104836
• Umbilical cord prolapse
• Intrauterine growth restriction
• Congenital anomalies
• Neonatal and infant death and cerebral palsy
11. Fetal complications unique to multiple pregnancies
11.1 “Vanishing twin”
It refers to the loss of one member of a twin or other higher-order gestations early
in pregnancy. This is typically either asymptomatic or associated with spotting or
mild bleeding [2, 7]. It is responsible for lower frequency of twin or higher-order
multiple gestations during the second trimester than the first trimester. For instance,
if two gestational sacs are confirmed by the first-trimester ultrasound, the chance
of delivering twins is 63% for women younger than 30 years and 52% for women
30 years or older [2]. Monochorionic twin gestations are at higher risk for a vanishing
twin than dichorionic twins. Vanishing twin is even more common in higher-order
pregnancies [2, 7]. This condition can be diagnosed with serial ultrasound with the
loss of one or more fetus/fetuses.
11.2 Twin-twin transfusion syndrome (TTTS)
TTTS is exclusively a complication of monochorionic multiple pregnancies that
occur in 10–15% of monochorionic diamniotic gestations [2, 5, 7]. This syndrome is
characterized by unbalanced anastomoses in the placenta which leads to under perfu-
sion of the donor twin and over perfusion of the recipient. The donor twin develops
oligohydramnios and intrauterine growth restriction; the recipient experiences
volume overloads which result in polyhydramnios [1–3].
TTTS can be present at any gestational age. The earlier the onset is associated
with a poorer prognosis. If untreated, the mortality rates range from 80–100%
[2, 7]. Both twins are at risk of demise from circulatory derangement, and the
pregnancy is predisposed further for preterm delivery due to uterine overdistention
with hydramnios [2].
There are three types of possible vascular anastomosis in the monochorionic
placenta [1, 2, 5,]. Arteriovenous (AV), arterioarterial (AA), and venovenous (VV).
11.3 Diagnosis and staging
The two classic criteria required for antenatal diagnosis of TTTS are monochori-
onic diamniotic twin gestation and oligohydramnios in one amniotic sac and polyhy-
dramnios in the other sac [1].
Once identified, TTTS is typically staged by the quintero staging system:
• Stage I- oligohydramnios, polyhydramnios sequence. Donor twin bladder is
visible.
7
Multiple Pregnancy - New Insights
• Stage II- oligohydramnios, polyhydramnios sequence. The donor twin bladder is
not visible and the doppler scan is normal.
• Stage III- oligohydramnios, polyhydramnios sequence. Donor twin bladder is not
visible and doppler scans are abnormal.
• Stage IV- ascites or frank hydrops in either twin.
• Stage V- one or both fetuses have died.
When TTTS diagnosed management, it depends on gestational at diagnosis and
the severity of clinical findings. There are five management options available [2]:
• Expectant management
• Septostomy
• Serial amnioreduction
• Selective termination/cord occlusion
• Fetoscopic laser photocoagulation
Generally, expectant management is not recommended in stage II or greater TTTS
and selective termination is only offered in extreme cases of advanced TTTS [2].
11.4 Conjoined twins
This is a very rare event of MZ twinning resulting when the division occurs after
the embryonic disc has completely formed, that is, after 13 days. It occurs with a
frequency of about 1 in 50,000 pregnancies. Most conjoined twins are female, with a
reported female-to-male ratio of 2:1 or 3:1 [2].
Conjoined twins are classified according to the anatomic location of the incom-
plete splinting [3]. The most common location is the chest (thoracopagus), followed
by the anterior abdominal wall (omphalopagus), the buttocks (pygopagus), the
ischium (ischiopagus), and the head (cephalopagus) [2, 3].
Conjoined twins can be diagnosed by ultrasound as early as the first trimester
based on visualization of monoamnionicity and a bifid fetal pole [2].
The pregnancy termination should be offered when the diagnosis is confirmed before
the age of viability. The prognosis for survival and successful separation depends on the
degree of organ and vascular sharing between the two fetuses. For a better outcome,
women with conjoined twins should be cared for by a multidisciplinary team [1, 2].
11.5 Intrauterine death of one fetus
Intrauterine death of one fetus in a multiple gestation can occur at any gestation.
This condition is more common during the first trimester and has no or little effect
on the prognosis of the surviving fetus or fetuses. After the death of one twin in a
monochorionic gestation, approximately 15% of the remaining fetus also dies, while
approximately 3% of remaining fetus dies in a dichorionic gestation [2].
8
Multiple Pregnancy
DOI: http://dx.doi.org/10.5772/intechopen.104836
The risk for significant neurologic morbidity is increased after intrauterine
death of one fetus in a monochorioic, but not in a dichorionic gestation. The surviv-
ing twin runs the risk of cerebral palsy, microcephaly, renal cortical necrosis, and
disseminated intravascular coagulation. The DIC is due to thromboplastin liberated
from the dead twin that crosses via placental anastomosis to the living twin. In such
cases, the maternal coagulation profile should be followed once a week to identify
possible coagulation abnormalities. The dead fetus is reabsorbed if the death occurs
prior to 12 weeks gestation, while the fetus shrinks and becomes dehydrated beyond
this time [1, 2].
11.6 Twin reversed arterial perfusion (TRAP)
The TRAP sequence is also known as acardiac twinning and occurs only in
monochorionic pregnancies. It is characterized by an acardiac-perfused twin having
blood supply from a normal cotwin via arterio-arterial or vein-to-vein connection. In
majority, the cotwin dies due to high output failure. The arterial pressure of the donor
twin is high, the recipient twin receives the used blood from the donor. The perfused
twin is often chromosomally abnormal and an extremely malformed fetus with either
no heart at all or only rudimentary cardiac tissue [1, 2].
The management of TRAP is controversial. The options for management are [2, 4]:
• Expectant management
• Delivery
• Occlusion of the acardiac twin’s umbilical cord by bipolar cord coagulation or
laser ablation.
11.7 Twin anemia polycythemia sequence (TAPS)
This is a form of chronic fetofetal transfusion that is characterized by significant
hemoglobin differences between donor and recipient twins without discrepan-
cies in amniotic fluid volumes. The spontaneous form complicates from 3–5% of
monochorionic pregnancies and it occurs in up to 13% of pregnancies after laser
photocoagulation.
It is diagnosed antenatally by middle cerebral artery peak systolic velocity of more
than 1.5 multiples of median (MoM) in the donor and less than 1.0 MoM in the recipi-
ent twin [1].
The options for management include expectant management and intrauterine
transfusions both intraperitoneal and intravenous.
11.8 Complete hydatidiform mole with coexisting normal fetus
One of the fetuses is either complete or partial molar pregnancy, whereas the
cotwin is normal fetus. The prevalence rates range from 1 in 22,000 to 100,000
pregnancies [1].
The diagnosis is usually made in the first half of pregnancy and using similar
diagnostic modalities.
The possible complications are persistent and heavy bleeding, preeclampsia,
preterm delivery, and persistent trophoblastic disease.
9
Multiple Pregnancy - New Insights
Optimal management is not known for this twin gestation. The possible options of
management are termination at the time of diagnosis, and observation and pregnancy
progression [1].
12. Antepartum management of multiple pregnancies
Gestational age at delivery and the adequacy of fetal growth are two important
factors that most influence pregnancy outcomes [2].
The care provider should understand and advise on the following issues during
antenatal care:
• Increased dietary supplement is needed for increased energy supply to the extent
of 300 Kcal/day above that needed in a singleton pregnancy. Dietary supplemen-
tation includes both macronutrients and micronutrients [4].
• Increased rest at home and early cessation of work.
• Interval of antenatal contact should be more frequent.
• Multiple gestations are an increased risk for uteroplacental insufficiency. So,
fetal surveillance is mandatory. It should be started at 28 weeks for triplets and
higher-order pregnancies, while at 32 and 34 weeks for monochorionic twins
and dichorionic twins, respectively [1, 2, 4]. The non-stress test and biophysical
profile can be used and the interpretation is similar to singleton pregnancy.
• Fetal growth is monitored by ultrasound every 4 to 6 weeks beginning at
24 weeks. Twins grow at the same rate as singletons until 30 to 32 weeks gesta-
tion, after which their growth velocity slows compared with singletons. Institute
of Medicine recommends women with twins and normal body mass index gain a
total of 37–54 lb. weight during the pregnancy [2].
• Assess the risk for preterm birth using a transvaginal cervical length of 20 mm or
less between 20- and 24-weeks’ gestation and fetal fibronectin sampling [2].
• Routine use of tocolytic agents to prevent preterm delivery has no significant ben-
efit. However, short-term use of these agents for acute tocolysis in preterm labor
is helpful to gain time for administration of corticosteroids and allow transport to
a tertiary care facility. Tocolytic use in multiple gestations needs careful monitor-
ing of maternal condition as these women are at higher risk for cardiovascular
complications due to exaggerated maternal cardiovascular adaptations [1, 2].
• As the numbers of fetuses increases, the prognosis of multiple pregnancies gets
poorer. Now a day, there is a practice of selective fetal reduction to improve the
outcome of the remaining fetus or fetuses.
13. Timing of delivery in multiple pregnancies
The timing of delivery depends on maternal and fetal complications. The available
data suggest that nadir perinatal complications occur at earlier gestational ages in
10
Multiple Pregnancy
DOI: http://dx.doi.org/10.5772/intechopen.104836
multiple gestations compared with singletons [2]. There is an increased risk in twin
pregnancies that extend past 38 to 39 weeks gestation. Allowing a dichorionic twin
gestation to go beyond 38 weeks requires convincing evidence of normal fetal growth,
reassuring fetal condition as well as a woman’s desire to extend the pregnancy. It is not
advisable to prolong twin pregnancy past 39 weeks because of clear risk without any
known benefit.
The ACOG, NICHD, and SMFM recommend the delivery of uncomplicated
dichorionic twins at 38 weeks and uncomplicated monochorionic twins between 34
and 37 weeks [2].
Based on experts’ opinions, it is reasonable to offer delivery of uncomplicated
triples anytime between 35 and 36 weeks.
14. Mode of delivery in multiple pregnancies
Mode of delivery for patients with multiple gestations depends on the gestational
age, estimated weight of the fetuses, number of fetuses, presentation of fetuses,
presence or absence of complications, etc.
I. Mode of delivery in diamniotic twins
• Both twins are vertex presentation, vaginal delivery in the absence of
obstetric indications for cesarean delivery.
• Twin A vertex and twin B non-vertex presentation, vaginal delivery is pos-
sible if the estimated fetal weight is 1500 g–3500 g
• Twin A non-vertex cesarean delivery is indicated.
II. Monoamniotic twins–cesarean delivery
III. Triplet and higher-order gestation–cesarean delivery
15. Intrapartum management of twin vaginal delivery
Twin pregnancy is considered high risk and needs careful preparation and multi-
disciplinary cooperation among obstetrics, anesthesia, nursing, and neonatology.
Both fetuses should be monitored continuously. Use of analgesic drugs is to
be limited as the babies are small and rapid delivery may occur. The third stage of
labor should be managed actively as these women are at high risk for postpartum
hemorrhage.
Abbreviations
ACOG American College of Obstetricians and Gynecologist
DIC Disseminated intravascular coagulation
DZ Dizygotic
MZ Monozygotic
11
Multiple Pregnancy - New Insights
MoM Multiples of the median
NICHD The national institute of child health and human development
SMFM Society for maternal-fetal medicine
TAPS Twin anemia polycythemia sequence
TTTS Twin-twin transfusion syndrome
TRAP Twin reversed arterial perfusion
Author details
Mandefro Yilma Asfaw
Hawassa University, Ethiopia
*Address all correspondence to: ymande23@gmail.com
© 2022 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of
the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided
the original work is properly cited.
12
Multiple Pregnancy
DOI: http://dx.doi.org/10.5772/intechopen.104836
References
[1] Cunningham, Leveno, Bloom, Dashe,
Hoffman, Casey, Sheffield. Multifetal
Pregnancy. In: Cunningham FG,
Leveno KJ, Bloom SL, Spong CY,
Dashe JS, Hoffman BL, Casey BM,
Sheffield JS, editors. Williams Obstetrics.
24th ed. 2014. pp. 891-920
[2] Newman RB and Unal ER. Multiple
gestations. In: Gabbe, Niebly, Simpson,
Landon, Galan, Jauniaux, Driscoll,
Berghella, Grobman, editors. Obstetrics
Normal And Problem Pregnancies. 7th
ed. 2017. pp. 706-733
[3] Moore TR. Multifetal gestation and
malpresentation. In: Hacker, Moore,
Gambone, editors. Essentials of
Obstetrics and Gynecology. 4th ed. 2007.
pp. 183-188
[4] Dutta DC. Multiple pregnancy,
amniotic fluid disorders,
abnormalities of placenta and cord. In:
Konar H, editors. DC Dutta’s Textbook
of Obstetrics including Perinatology and
Contraception. 8th ed. 2015. pp. 233-245
[5] Bush MC and Pernoll ML. Multiple
gestation. In: Dechrney AH, Nathan L,
Laufer N and Roman AS, editors. Current
Diagnosis and Treatment –Obstetrics and
Gynecology. 11th ed. 2013. pp. 301-309
[6] Benirschke K. Multiple gestation:
The biology of twinning. In: Creasy RK,
Resnik R, Iams JD, Lockwood CJ,
Moore TR, Greene MF, editors. Creasy
and Resnik’s Maternal-Fetal Medicine.
7th ed. 2014. pp. 53-65
[7] Newman RB and Rittenberg C.
Multiple gestation. In: Gibbs RS,
Karlan BY, Haney AF, Nygaard IE,
editors. Danforth’s Obstetrics and
Gynecology. 10th ed. 2008.
pp. 221-244
13