(New) Early Pregnancy Complications R
(New) Early Pregnancy Complications R
(New) Early Pregnancy Complications R
BLEEDING
•urogynaecology
INCIDENCE
Early pregnancy Bleeding (EPB) is the most common complication in early pregnancy.
The incidence of EPB is as high 10 percent
The incidence of second-trimester loss up to 24 weeks gestation is less than 1 percent
The rate of pregnancy Bleeding appears to be further influenced by maternal age and
history of prior pregnancy loss.
Early pregnancy loss
nonviable, intrauterine pregnancy within the first trimester (up to 12+6 weeks from the last menstrual period)
terminology has included "miscarriage," "blighted ovum," "spontaneous abortion," and "missed abortion
Early second-trimester pregnancy loss
is one that occurs after 13+0 and prior to 24+0 weeks of gestation
By convention, pregnancies lost after 24 weeks are typically referred to as stillbirth or fetal death.
Stillbirth or fetal death
Pregnancy loss that occurs at 24 weeks gestation or later, or at a weight of 350 grams or greater, is generally
referred to as a stillbirth or fetal death ,
FIRST TRIMESTER BLEEDING
Although bleeding may be heavy, almost all women remain hemodynamically stable; only
about 1 percent of expectantly managed women require blood transfusion .
Ectopic pregnancy is much less common (prevalence: 2 % of pregnancies), but the most
serious etiology of first trimester bleeding as rupture of the extrauterine pregnancy is a
potentially life-threatening complication; therefore, this diagnosis must be excluded in
every pregnant woman with bleeding
Women may also note a loss or reduction of pregnancy symptoms, such as decreased breast
tenderness and/or nausea and vomiting.
Some women are asymptomatic, and E.P.loss is discovered incidentally or on routine ultrasound
in early pregnancy.
The volume of vaginal bleeding during EPB varies considerably, and women often report passing
clots or tissue.
The pain that occurs with EPB is often crampy in nature and can be mild to severe, especially
during passage of gestational tissue.
The pain can be constant or intermittent and is often associated with vaginal bleeding.
As bleeding and cramping are also symptoms of other early pregnancy complications, including
ectopic and molar pregnancy, pregnant women with vaginal bleeding or pelvic pain should be
evaluated.
Complications of EPB/EBL
Women with hemorrhage typically present with heavy vaginal bleeding combined with
orthostatic vital signs, anemia, and/or tachycardia. The overall risk of this is low,
approximately 1 percent
Infectious complications can occur spontaneously or can follow medical or surgical
interventions
Signs and symptoms include abdominal or pelvic pain, uterine tenderness, purulent
discharge, and/or systemic signs of infection, such as fever, tachycardia, or hypotension.
Some women who have incomplete miscarriage develop an infection in the uterus with retained
products of conception . This is known as a septic miscarriage. Symptoms include fever, chills, flu-
like aches, abdominal pain, vaginal bleeding, and vaginal discharge, which may be thick and may have
a foul odor septic
Women who may be less likely to expect or recognize their pregnancy early in gestation,
such as
adolescents
perimenopausal women
women with irregular menses
might also be at higher risk of later presentation and/or complications.
Types of miscarriage
Complete early pregnancy loss / miscarriage
No further intervention is needed for complete early pregnancy loss if chorionic villi are
identified by pathologic examination of the products of conception.
However, if no villi are identified or no specimens are available for pathologic examination,
then serum hCG levels should be followed serially until the level is undetectable
Inevitable early pregnancy loss
When early pregnancy loss is inevitable, the internal os of the cervix is dilated, vaginal
bleeding is increasing, and painful uterine cramps/contractions are present.
The gestational tissue often can be felt or seen at the internal cervical os; passage of this tissue
typically occurs within a short time.
At a more advanced stage, the membranes may rupture and the fetus may be passed, but
significant amounts of placental tissue can be retained, resulting in an incomplete early
pregnancy loss.
Incomplete early pregnancy loss
This is most common in the late first trimester and early second trimester.
On examination,
the internal cervical os is open
gestational tissue may be observed in the cervical canal
the uterine size is smaller than expected for gestational age, but not well contracted.
The amount of bleeding varies, but can be sufficiently severe to cause hypovolemic
shock.
Painful cramps/contractions are often present.
Ultrasound reveals tissue in the uterus. Medical or surgical evacuation is generally
performed.
Missed miscarriage
A missed abortion refers to in-utero death of the embryo or fetus prior to the 24th week of
gestation, with retention of the pregnancy for a period of time.
Women may notice that symptoms associated with early pregnancy (eg, nausea, breast
tenderness) have abated and they do not "feel pregnant" anymore.
Vaginal bleeding may occur.
The internal cervical os usually remains closed.
Ultrasound reveals an intrauterine gestational sac with or without an embryonic/fetal pole,
but no embryonic/fetal cardiac activity.
Management may be expectant or a medical or surgical intervention to complete process can
be undertaken.
Threatened early pregnancy loss ,diagnostic criteria
Vaginal bleeding
closed cervix
sonographic visualization of an intrauterine pregnancy with detectable fetal
cardiac activity is diagnostic of threatened early pregnancy loss.
Up to 96 percent of pregnancies with both fetal cardiac activity and vaginal bleeding at 7 to
12 weeks of gestation are not lost.
Bleeding in these cases is likely due to disruption of decidual vessels at the maternal-fetal
interface. These separations generally cannot be visualized by ultrasound, but sometimes
appear as a subchorionic hematoma.
Management is expectant.
COMMON ETIOLOGY OF EARLY PREGNANCY LOSS/miscarriage
1-Chromosomal abnormalities
Chromosomal abnormalities are present in up to 70 percent of pregnancy losses before 24 weeks
The use of chromosomal microarray likely increased the ability to identify earlier preclinical
losses that previously were undetected by karyotype.
2-Maternal anatomic anomalies
Anatomic anomalies, such as uterine leiomyomas (fibroids), polyps, adhesions, or septa,based
on their size and position in relation to the developing pregnancy.
the impact of fibroids on pregnancy loss likely varies by other factors, such as distortion of the
uterine cavity and/or blood supply.
3-Trauma
Significant trauma.
The developing embryo is relatively protected within the uterus in early pregnancy, but trauma
that results in direct impact to the uterus can result in E.P.Loss.
This can be due to violent trauma (gunshot wounds, penetrating injuries) or iatrogenic trauma,
as with chorionic villus sampling and amniocentesis.
E.P.LOSS predisposing /risk factors
1. Increasing age
Extremes of age increase the risk of pregnancy loss
with age >35 years being the most significant risk factor because of the strong
association with fetal chromosomal abnormalities
EPL risk does appear to rise with increasing paternal age as well
Obesity – Obesity is more strongly and consistently associated with pregnancy loss than either type
1 or type 2 diabetes.
Diabetes – The effects of type 1 and type 2 diabetes on early pregnancy can be extreme, even
resulting in lethal fetal anomalies or pregnancy loss. Euglycemia in the preconception and
periconception time periods brings this risk back to baseline.
Thyroid disease – Both hyper- and hypothyroidism have been associated with increased risk of
pregnancy loss,
Stress – Both acute and chronic stress can increase the risk of pregnancy loss
Inherited thrombophilias – The effect of inheritable thrombophilias on EPL risk is unclear as the
body of evidence conflicts.
Pregnancy with intrauterine device (IUD) in place the risk of EPL appears to be higher for women
who elect to leave the IUD in place rather than have it removed
4-Medication and substance use
(NSAIDs) aspirin and indomethacin are used for specific obstetric indications (preeclampsia
prevention and treatment of acute preterm labor) while other NSAIDs, including ibuprofen
and diclofenac, may increase EPL risk
7-Subchorionic hematoma
Subchorionic hemorrhage or hematoma is associated with increased risk of EPL, particularly
when it amounts to 25 percent or more of the volume of the gestational sac
women with subchorionic hematoma had double the odds of EPL compared with women
without
DIAGNOSTIC EVALUATION
History
A history of vaginal bleeding and/or crampy pelvic pain in a woman with known pregnancy is suggestive
Women with EPL may also note a reduction in pregnancy-related symptoms that were previously
present.
further evaluation with ultrasound or serial hCG testing is required for definitive diagnosis.
Physical examination
Patients who present with bleeding in pregnancy first undergo a speculum examination to assess the
source and quantity of bleeding.
Signs suggestive of EPL include bleeding coming from the cervix and an open cervical os.
A bimanual examination can also determine whether the cervix is open and whether there is tissue
within the cervical canal..
Lastly, absence of fetal heart tones on handheld Doppler in a pregnancy of 12 weeks or greater should
prompt further evaluation for pregnancy loss,
Imaging
Women whose ultrasound demonstrates an intrauterine pregnancy but no fetal cardiac
activity undergo repeat ultrasound at a future date to assess for interval change
Women with a positive pregnancy test but no intrauterine pregnancy seen on ultrasound
are diagnosed as having a pregnancy of unknown location and followed carefully with
repeat imaging and possibly serial serum hCG levels. These women may have an early
intrauterine pregnancy, an ectopic pregnancy, or a molar pregnancy.
laboratory evaluation
HCG
ULTRASOUND ABDOMINAL /VAGINAL
a dramatic drop in hCG >25 percent over 48 hours in the setting of uterine bleeding is highly
suggestive of EPL and may be especially helpful if ultrasound is not easily available.
By contrast, hCG testing is commonly performed as part of the assessment for pregnancy of
unknown location and is often helpful in excluding ectopic pregnancy..
In normal pregnancies, average hCG levels plateau at approximately 8 to 12 weeks
and then decline
Serum progesterone has been used to assess pregnancy viability, as low serum
progesterone levels are associated with E.P.Loss
An embryo with a crown rump length (CRL) ≥7 mm that does not have cardiac activity.
After a pelvic ultrasound showed a gestational sac without a yolk sac, absence of an
embryo with a heartbeat in ≥2 weeks.
After a pelvic ultrasound showed a gestational sac with a yolk sac, absence of an embryo
with a heartbeat in 2weeks.
Findings that are suspicious for, but not diagnostic of, pregnancy loss include:
CRL <7 mm and no heartbeat.
Absence of embryo with a heartbeat 7 to 13 days after a scan that showed a gestational
sac without a yolk sac.
Absence of embryo with a heartbeat 2weeks after a scan that showed a gestational sac
with a yolk sac.
Absence of embryo ≥6 weeks after last menstrual period.
Enlarged yolk sac (>7 mm).
Physiologic or implantation bleeding
Vaginal bleeding
The volume and pattern of vaginal bleeding vary, and there is no bleeding pattern that is
pathognomonic for ectopic pregnancy.
Bleeding may range from scant brown staining to hemorrhage.
Bleeding is typically intermittent, but may occur as a single episode or continuously.
The vaginal bleeding associated with ectopic pregnancy is typically preceded by amenorrhea.
DIAGNOSTIC EVALUATION OF ECTOPIC PREGNANCY
Multiple gestation
In women with an intrauterine multiple pregnancy, the serum human chorionic
gonadotropin (hCG) level could be higher than 1500 milli-international units/mL and yet
ultrasound examination will not reveal an intrauterine pregnancy (IUP)
Levels of over 9000 international units/L have been described for intrauterine triplet
pregnancies unobserved by transvaginal ultrasound (TVUS)
Heterotopic pregnancy
The investigation for ectopic pregnancy can be terminated, under most circumstances, if a
transvaginal sonogram reveals an IUP.
Heterotopic pregnancy (combined intrauterine and extrauterine pregnancy) is rare, except
among women conceiving through in vitro fertilization (IVF).
The extrauterine pregnancy is usually in the fallopian tube, but can be at another location,
such as the cervix.
Natural history of ectopic pregnancy
If left untreated, an ectopic pregnancy in the fallopian tube can progress to a tubal abortion or tubal
rupture, or it may regress spontaneously.
Rupture
Immunological
genetic
endocrine
infectious
thrombophilic
environmental factors.
1-Uterine factors/cervical
Acquired and congenital uterine abnormalities are responsible for 10 to 50 percent of RPL
Anomalies
Congenital uterine anomalies ;
Pregnancy loss may be related to impaired uterine distention or abnormal implantation due to
decreased vascularity in a septum, increased inflammation, or reduction in sensitivity to steroid
hormones
The septate uterus is the uterine anomaly associated with the poorest reproductive outcome and
the most common uterine abnormality associated with RPL
Leiomyoma
Submucous leiomyomas that protrude into the endometrial cavity can impede normal
implantation as a result of their position, poor endometrial receptivity of the decidua overlying the
myoma, or degeneration with increasing cytokine production
Endometrial polyps
Intrauterine adhesions
Intrauterine adhesions or synechiae lead to pregnancy loss because there is
insufficient endometrium to support fetoplacental growth .The main cause of
intrauterine adhesions is curettage for pregnancy complications.
Cervical insufficiency
Cervical insufficiency is a cause of recurrent mid-trimester, but not early, pregnancy
loss.
Defective endometrial receptivity
Estrogen and progesterone prepare the endometrium for pregnancy Normal
endometrial receptivity allows embryo attachment, implantation, invasion, and
development of the placenta.
These processes are likely to be disturbed when endometrial receptivity is defective
2-Immunologic factors
Antiphospholipid syndrome
Several autoimmune diseases have been linked to poor obstetric outcome,
but antiphospholipid syndrome (APS) is the only immune condition in which
pregnancy loss is a diagnostic criteria for the disease. Five to 15 percent of
patients with RPL may have APS
3-Endocrine factors
Endocrine factors may account for 15 to 60 percent of RPL.
Endocrine factors
Diabetes mellitus
to increased frequencies of miscarriage and congenital malformations
Polycystic ovary syndrome
(PCOS) may be as high as 20 to 40 percent, which is higher than the baseline rate in the general obstetric population (10 to 20
percent)
Thyroid antibodies and disease
Antibodies (thyroid peroxidase or thyroglobulin), including those who are euthyroid increase risk of miscarriage
Poorly controlled thyroid disease (hypo- or hyper-thyroidism) is associated with infertility and pregnancy loss.
Excess thyroid hormone increases the risk of miscarriage independent of maternal metabolic dysfunction
Hyperprolactinemia
Normal circulating levels of prolactin may play an important role in maintaining early pregnancy. Treatment to lower prolactin
concentration was associated with a higher rate of successful pregnancy (86 versus 52 percent). Prolactin levels during early
pregnancy were significantly greater in women who miscarried
Luteal phase defect
Progesterone is required for successful implantation and maintenance of pregnancy; therefore, disorders related to impaired
progesterone production or action are likely to affect pregnancy success Abnormal luteal-phase progesterone production may
occur as the result of medical conditions such as elevated prolactin or abnormal thyroid function; women suspected to have one
of these disorders are evaluated and treated for the underlying condition
4.Genetic factors
Abnormalitiesof chromosome number or structure are the most common cause of sporadic
early pregnancy loss, accounting for at least 50 percent
A significant proportion of RPL may also be associated with structural or numerical
chromosomal abnormalities (eg, aneuploidy, mosaicism, translocation, inversion, deletion,
fragile sites) ,Single-gene, X-linked, or polygenic/multifactorial disorders can also result in
sporadic or recurrent miscarriage.
Aneuploidy
The risk of aneuploidy increases as the number of previous miscarriages increases
5.Thrombophilia and fibrinolytic factors
Thrombosis of spiral arteries and the intervillous space on the maternal side of the
placenta can impair adequate placental perfusion.
resulting in late fetal loss, intrauterine growth restriction, placental abruption, or
preeclampsia.
There is a large and contradictory literature on the association between maternal
inherited thrombophilia and RPL occurring in the first trimester
Early second-trimester pregnancy loss, or fetal death, occurs in approximately 2 to 3 percent of pregnancies
Conventionally, this is defined as fetal death between 13 and 24 weeks, and losses after 24 weeks gestation
are defined as stillbirth, but this cutoff does not have a biological basis
Known and suspected etiologies of second-trimester pregnancy loss include:
Infection, including chorioamnionitis and maternal viral infection
Chronic stressors,
Uterine malformation
Cervical insufficiency
Fetal malformation or syndromes such as anencephaly, trisomies, renal agenesis, or hydrops
Thrombophilias
Abruption
Premature preterm rupture of membranes
Preterm labor
Some surgical instruments