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Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality
Authors: Charles J Lockwood, MD, MHCM, Karen Russo-Stieglitz, MD
Section Editors: Deborah Levine, MD, Vincenzo Berghella, MD
Deputy Editor: Vanessa A Barss, MD, FACOG
All topics are updated as new evidence becomes available and our peer review process is complete.
Literature review current through: May 2018. | This topic last updated: Aug 04, 2017.
INTRODUCTION — Placenta previa refers to the presence of placental tissue that extends over the internal
cervical os. Sequelae include the potential for severe bleeding and preterm birth, as well as the need for
cesarean delivery.
Placenta previa should be suspected in any pregnant woman beyond 20 weeks of gestation who presents with
vaginal bleeding. For women who have not had a second-trimester ultrasound examination, bleeding after 20
weeks of gestation should prompt sonographic determination of placental location before digital vaginal
examination is performed because palpation of the placenta can cause severe hemorrhage.
This topic will discuss the epidemiology, clinical features, diagnosis, morbidity, and mortality of placenta previa.
The natural history of placenta, risk of bleeding, and management are reviewed separately. (See "Placenta
previa: Management".)
EPIDEMIOLOGY
Prevalence — In systematic reviews, the pooled prevalence of placenta previa is about 4 per 1000 births, but
varies worldwide [1,2]. The prevalence is several-fold higher around 20 weeks of gestation (as high as 2
percent), but most previas identified early in pregnancy resolve before delivery. (See 'Natural history' below.)
Risk factors — Major risk factors for placenta previa include [3-15]:
Other risk factors, some of which are interdependent, include:
®
Previous placenta previa – Placenta previa recurs in 4 to 8 percent of subsequent pregnancies [16].●
Previous cesarean delivery – In two systematic reviews, previous cesarean delivery was found to increase
the risk for placenta previa by 47 percent [17] and 60 percent [3]. The risk increases with an increasing
number of cesarean deliveries [18-20]. Prelabor cesarean delivery may increase previa risk in a subsequent
delivery more than previous intrapartum cesarean or vaginal delivery [13].
●
Multiple gestation – The prevalence of placenta previa was 40 percent higher among twin births than
among singleton births (3.9 and 2.8 per 1000 births, respectively) in one study [5]. In another study,
dichorionic twin pregnancies were more likely to have a placenta previa than monochorionic twin
pregnancies (odds ratio [OR] 3.3) or singleton pregnancies (OR 1.5) [21].
●
Increasing parity●
Increasing maternal age●
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PATHOGENESIS — The pathogenesis of placenta previa is unknown. One hypothesis is that the presence of
areas of suboptimally vascularized decidua in the upper uterine cavity due to previous surgery or multiple
pregnancies promotes implantation of trophoblast in, or unidirectional growth of, trophoblast toward the lower
uterine cavity [1,3,22]. Another hypothesis is that a particularly large placental surface area, as in multiple
gestation, increases the probability that the placenta will encroach upon/cover the cervical os.
PATHOPHYSIOLOGY OF BLEEDING — Placental bleeding is the major adverse sequelae of placenta previa. It
is thought to occur when uterine contractions or gradual changes in the cervix and lower uterine segment apply
shearing forces to the inelastic placental attachment site, resulting in partial detachment. Vaginal examination or
coitus can also disrupt this site and cause bleeding. Bleeding is primarily maternal blood from the intervillous
space, but fetal bleeding can occur if fetal vessels in the terminal villi are disrupted.
CLINICAL PRESENTATION AND COURSE
Asymptomatic finding on midtrimester ultrasound examination — The most common presentation of
placenta previa is as a finding on routine ultrasound examination at about 16 to 20 weeks of gestation for
assessment of gestational age, fetal anatomic survey, or prenatal diagnosis. One to 6 percent of pregnant
women are found to have sonographic evidence of a placenta previa on these examinations. (See
'Ultrasonography' below.)
Natural history — Approximately 90 percent of placenta previas identified on ultrasound examination before
20 weeks of gestation resolve before delivery [23]. Two theories have been proposed to account for this
phenomenon:
In either case, the placental edge overlying the cervix atrophies.
Predicting presence at delivery — Findings that suggest that a placenta previa will persist until delivery
include lack of resolution by the third trimester and extension over the os by more than 25 mm.
In a retrospective cohort study of 714 women with placenta previa, singleton gestation, and a liveborn infant ≥25
weeks of gestation, when the most recent ultrasound showed placenta previa at [24]:
Infertility treatment●
Previous abortion●
Previous uterine surgical procedure●
Maternal smoking●
Maternal cocaine use●
Male fetus●
Non-white race●
The lower uterine segment lengthens from 0.5 cm at 20 weeks of gestation to more than 5 cm at term [16].
This development of the lower uterine segment relocates the stationary lower edge of the placenta away
from the internal os.
●
Progressive unidirectional growth of trophoblastic tissue toward the fundus results in upward migration of the
placenta away from the cervix. This phenomenon has been termed "trophotropism."
●
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The more the placenta extends over the internal os, the more likely it is to persist until delivery. Although
available data are insufficient to make precise predictions, pooled data suggest that when the placenta extends
at least 14 to 15 mm but <25 mm over the cervical os at 18 to 23 weeks of gestation, then the probability of
placenta previa at delivery is about 20 percent; extension ≥25 mm is associated with a 40 to 100 percent
probability of placenta previa at delivery [25-29].
Low-lying placentas and placentas formerly called partial previa are most likely to resolve (eg, only 6 to 7 percent
of those diagnosed at 15 to 19 weeks and 39 to 63 percent of those diagnosed at 32 to 35 weeks were present
at delivery). Anterior placenta previas are more likely to resolve than posterior placenta previa [30].
Recommendations for follow-up sonography to determine resolution are discussed separately. (See "Placenta
previa: Management", section on 'Monitoring placental position'.)
Bleeding — In the second half of pregnancy, the most common symptom of placenta previa is relatively painless
vaginal bleeding, which occurs in up to 90 percent of persistent cases [31]. Ten to 20 percent of women present
with uterine contractions, pain, and bleeding, similar to the presentation of abruptio placenta [32,33]. (See
"Placental abruption: Pathophysiology, clinical features, diagnosis, and consequences".)
In approximately one-third of pregnancies with persistent previa, the initial bleeding episode occurs prior to 30
weeks of gestation; this group is more likely to require blood transfusions and is at greater risk of preterm
delivery and perinatal mortality than women whose bleeding begins later in gestation [32-35]. An additional one-
third of patients becomes symptomatic between 30 and 36 weeks, while most of the remaining patients have
their first bleed after 36 weeks [32,33]. About 10 percent of women reach term without bleeding. The number of
antepartum bleeding episodes and need for blood transfusion have been identified as independent predictors for
emergency cesarean delivery [36].
Antepartum bleeding from any cause is a risk factor for preterm labor and preterm premature rupture of
membranes. (See "Pathogenesis of spontaneous preterm birth", section on 'Decidual hemorrhage' and "Preterm
prelabor rupture of membranes", section on 'Risk factors'.)
DIAGNOSIS — The diagnosis of placenta previa is based on sonography and requires the identification of
echogenic homogeneous placental tissue over the internal cervical os.
Placenta previa should be suspected in any woman beyond 20 weeks of gestation who presents with vaginal
bleeding. For women who have not had a second- or third-trimester ultrasound examination, antepartum
bleeding should prompt sonographic determination of placental location before digital vaginal examination is
performed because palpation of the placenta can cause severe hemorrhage.
15 to 19 weeks – 20 percent were present at delivery if no prior cesarean delivery, and 41 percent if a prior
cesarean delivery
●
20 to 23 weeks – 45 percent were present at delivery if no prior cesarean delivery, and 73 percent if a prior
cesarean delivery
●
24 to 27 weeks – 56 percent were present at delivery if no prior cesarean delivery, and 84 percent if a prior
cesarean delivery
●
28 to 31 weeks – 88 to 89 percent were present at delivery whether or not there was a prior cesarean
delivery
●
32 to 35 weeks – 89 to 90 percent were present at delivery whether or not there was a prior cesarean
delivery
●
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Diagnostic criteria — The diagnosis of placenta previa is based on identification of placental tissue extending
over the internal cervical os on a second or third trimester imaging study (image 1), preferably transvaginal
ultrasound [37]. The distance (millimeters) that the placenta extends over the internal cervical os should be
described in the diagnostic report.
Of note, when the placental edge is <2 cm from, but not over, the internal os, the placenta is labeled "low-lying"
(image 2). The distance (millimeters) between the internal cervical os and the inferior edge of the placenta
should be described in the diagnostic report [38]. (See 'Morbidity of low-lying placenta' below.)
The historic terms "marginal" and "partial" for characterizing a placenta previa are no longer used, as they
referred to information gathered on a digital vaginal examination, which should be avoided and is not needed
given the superiority of ultrasound diagnosis.
Ultrasonography
Transabdominal — Transabdominal sonographic assessment of placental location is one of the standard
components of the basic obstetrical ultrasound examination, and thus can be considered a screening test for
placenta previa.
Screening performance — If the placenta-cervix distance is ≤2 cm on transabdominal ultrasound, we
perform transvaginal sonography to better define placental position and make the diagnosis. The overall false
positive rate of transabdominal ultrasound for diagnosis of placenta previa is up to 25 percent, and varies by
study design [39,40]. In a planned secondary analysis of a prospective cohort study of women with singleton
gestations undergoing both transabdominal and transvaginal cervical length measurement during the second
trimester anatomic survey, a transabdominal placenta-cervix distance threshold of 4.2 cm had sensitivity 93.3
percent, specificity 76.7 percent, negative predictive value 99.8 percent, and screen-positive rate 25.0 percent for
detection of previa [41]. A threshold of 2.8 cm yielded a sensitivity 86.7 percent, specificity 90.5 percent, negative
predictive value 99.6 percent, and screen-positive rate of 11.4 percent. Thus, a threshold of 2.8 cm maximizes
specificity while a threshold of 4.2 cm maximizes sensitivity.
Technique and pitfalls — Sagittal, parasagittal, and transverse sonographic views should be obtained
with the patient's bladder partially full.
Specific points that should be appreciated when performing transabdominal sonographic examination for
placenta previa include:
An over-distended bladder can compress the anterior lower uterine segment against the posterior lower
uterine segment to give the appearance of a previa (image 3). The diagnosis of placenta previa should not
be made without confirming placental position after the patient has emptied her bladder. Care should be
taken to not make the diagnosis of placenta previa when the lower uterine segment is contracting, which
commonly occurs after a woman empties her bladder, and obscures the relationship between the placental
edge and the cervical os.
●
A previa can be missed near term if the fetal head is low in the pelvis since acoustic shadowing from or
compression of placental tissue by the fetal skull may obscure the placental location. In these cases, the
cervix may be better visualized by placing the patient in Trendelenburg position and/or gently pushing the
fetal head cephalad with an abdominal hand or the transducer.
●
The sonographic diagnosis of a central placenta previa is readily made since the placenta is centered over
the cervix and placental tissue is imaged anterior and posterior to the cervix. Complete noncentral previas,
particularly when lateral, are more difficult to confirm. Transverse views at and above the internal cervical os
should facilitate an accurate diagnosis.
●
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Transvaginal — Transvaginal ultrasound (TVS) can be performed safely in patients with placenta previa
since the optimal position of the vaginal probe for visualization of the internal os is 2 to 3 cm away from the
cervix, and the angle between the cervix and vaginal probe is sufficient to prevent the probe from inadvertently
slipping into the cervical canal [42].
Performance — TVS generally provides a clearer image of the relationship between the edge of the
placenta and the internal cervical os than transabdominal ultrasound. Randomized trials and prospective
comparative studies have established the superior performance of TVS over transabdominal sonography for
diagnosis of placenta previa [43-45]. In one study of 100 suspected cases, sensitivity, specificity, and positive
and negative predictive values of TVS for diagnosis of placenta previa at cesarean were 87.5, 98.8, 93.3, 97.6
percent, respectively [46].
Use of color Doppler is employed in the cases of suspected morbidly adherent placentation (eg, accreta) or
umbilical cord in the lower uterine segment, to rule out a vasa previa. (See "Clinical features and diagnosis of
placenta accreta spectrum (placenta accreta, increta, and percreta)" and "Velamentous umbilical cord insertion
and vasa previa".)
Characteristics predictive of bleeding — Although the magnitude of bleeding risk may differ according to
the following characteristics, all patients with placentas over or in close proximity to the cervical os are at risk of
significant antepartum, intrapartum, and postpartum bleeding.
Characteristics that appear to be predictive of antepartum bleeding include:
Other ultrasound techniques — Translabial (transperineal) ultrasound imaging is an alternative technique
that provides excellent images of the cervix and placenta [58]. The use of three-dimensional ultrasound may also
improve accuracy [59].
Magnetic resonance imaging — Magnetic resonance imaging (MRI) is well-suited to the assessment of
placental-cervical relationships because of the differing magnetic resonance characteristics of the two tissues.
However, it is not used for diagnosis of placenta previa because of its high cost, limited availability, and the well-
established safety and accuracy of transvaginal sonography [38]. MRI is most useful for diagnosis of complicated
placenta previa, such as previa-accreta and previa-percreta [60]. (See "Clinical features and diagnosis of
placenta accreta spectrum (placenta accreta, increta, and percreta)", section on 'Magnetic resonance imaging'.)
ASSOCIATED FINDINGS
A posterior placenta previa may be more difficult to visualize than an anterior placenta previa, even on
transvaginal ultrasound.
●
Bleeding can result in formation of a hematoma under and/or proximate to the placenta, which can obscure
the relationship between the placental edge and the cervical os.
●
Extension over the internal os rather than lying proximate to it [47-50].●
Thick (>1 cm) placental edge and/or angle between the basal and chorionic plates greater than 45 degrees
[51,52].
●
Echo-free space in the placental edge over the internal os [53].●
Cervical length ≤3 cm [52,54,55].●
Decrease in cervical length in the third trimester [56,57].●
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Placenta previa-accreta — When placenta previa is diagnosed, the possibility of placenta previa-accreta (or
more) should be considered. In a prospective study including 723 women with placenta previa undergoing
cesarean delivery, the frequency of placenta accreta increased with an increasing number of cesarean deliveries
as follows [61]:
In another large series, composite maternal morbidity in women with placenta previa and zero, one, two, or three
prior cesarean deliveries was 15, 23, 59, and 83 percent, respectively, and almost all of the excess composite
maternal morbidity in women with a prior cesarean was related to complications associated with placenta
accreta, such as peripartum hysterectomy [62]. (See "Clinical features and diagnosis of placenta accreta
spectrum (placenta accreta, increta, and percreta)", section on 'Prenatal diagnosis'.)
Other associated findings
MORBIDITY AND MORTALITY
Maternal — Maternal morbidity from placenta previa is primarily related to antepartum and/or postpartum
hemorrhage [77]. In systematic reviews, 52 percent of women with placenta previa had antepartum bleeding
(95% CI 42.7 to 60.6 percent) [31] and 22 percent had postpartum hemorrhage (95% CI 15.8 to 28.7 percent)
[78]. Because of antepartum and/or postpartum bleeding, women with placenta previa are more likely to receive
blood transfusions (12 versus 0.8 percent in patients without previa in one study [65], 22 versus 1.2 percent in
another [8]). They are also more likely to undergo postpartum hysterectomy (5.3 versus 0.04 percent in one
study [8]), uterine/iliac artery ligation, or embolization of pelvic vessels. The risks of hemorrhage and postpartum
hysterectomy are particularly high for women with previa-accreta. (See "Clinical features and diagnosis of
placenta accreta spectrum (placenta accreta, increta, and percreta)", section on 'Consequences'.)
In women with severe hemorrhage, rapid, significant loss of intravascular volume can lead to hemodynamic
instability, decreased oxygen delivery, decreased tissue perfusion, cellular hypoxia, organ damage, and death. In
First cesarean birth, 3 percent●
Second cesarean birth, 11 percent●
Third cesarean births, 40 percent●
Fourth cesarean births, 61 percent●
Fifth or greater cesarean birth, 67 percent●
Malpresentation – The large volume of placenta in the lower portion of the uterine cavity predisposes the
fetus to assume a noncephalic lie [43,63-65].
●
Vasa previa and velamentous umbilical cord – Placenta previa is a risk factor for vasa previa and
velamentous umbilical cord insertion. (See "Velamentous umbilical cord insertion and vasa previa".)
●
Intrauterine growth restriction – An increased risk of intrauterine growth restriction has been reported by
multiple [8,32,66-71], but not all [34,35,66,72-74], investigators, and remains controversial. If a reduction in
fetal growth occurs, it is likely to be mild or due to confounding factors. For example, decreased placental
perfusion can lead to both fetal growth restriction and a suboptimal site of placental implantation. (See "Fetal
growth restriction: Evaluation and management".)
●
Congenital anomalies – Population-based cohort studies have reported a small increase in the overall rate
of congenital anomalies in pregnancies complicated by placenta previa, but no single anomaly or syndrome
was associated with the disorder [8,35,75,76].
●
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resource-rich countries, the maternal mortality rate associated with placenta previa is less than 1 percent [79],
but remains high in resource-poor countries where maternal anemia, lack of medical resources, and home births
are more common [65].
Severe maternal morbidity and maternal mortality can also be a consequence of amniotic fluid embolism
syndrome. Several studies have observed a strong association between placental pathology, such as placenta
previa, and amniotic fluid embolism syndrome [80-82]. (See "Amniotic fluid embolism syndrome".)
Neonatal — The principal causes of neonatal morbidity and mortality are related to preterm delivery [83]. In a
systematic review and meta-analysis of placental implantation abnormalities and risk of preterm delivery,
compared with no placenta previa, placenta previa was associated with a three- to fivefold increase in risk of
[84]:
In large studies, approximately 15 percent of patients with placenta previa delivered before 34 weeks of gestation
[69,85]. However, neonatal morbidity and mortality rates in pregnancies complicated by placenta previa have
fallen over the past few decades because of improvements in obstetrical management (eg, antenatal
corticosteroids), the liberal use of planned late preterm cesarean delivery, and improved neonatal care.
Neonatal anemia is also increased in pregnancies with placenta previa [86,87].
Morbidity of low-lying placenta — The morbidity of low-lying placenta (placental edge is <2 cm from, but not
over, the internal os) is less than that for placenta previa and decreases as the distance between the placental
edge and internal cervical os increases. A study that compared pregnancy outcomes of 53 women with placental
edge 1 to 10 mm versus 11 to 20 mm from the internal cervical os reported the following [88]:
RECURRENCE — Placenta previa recurs in 4 to 8 percent of subsequent pregnancies [16].
MANAGEMENT — (See "Placenta previa: Management".)
INFORMATION FOR PATIENTS — UpToDate offers two types of patient education materials, "The Basics" and
"Beyond the Basics." The Basics patient education pieces are written in plain language, at the 5 to 6 grade
reading level, and they answer the four or five key questions a patient might have about a given condition. These
articles are best for patients who want a general overview and who prefer short, easy-to-read materials. Beyond
the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written
at the 10 to 12 grade reading level and are best for patients who want in-depth information and are
comfortable with some medical jargon.
Preterm delivery <37 weeks (44 percent, relative risk [RR] 5.32, 95% CI 4.39-6.45)●
Neonatal intensive care unit admission (RR 4.09, 95% CI 2.80-5.97)●
Neonatal death (RR 5.44, 95% CI 3.03-9.78)●
Perinatal death (RR 3.01, 95% CI 1.41-6.43)●
Antepartum hemorrhage: 29 versus 3 percent●
Postpartum hemorrhage: 21 versus 10 percent●
Preterm birth: 29 versus 3 percent●
Cesarean delivery: 75 versus 31 percent●
th th
th th
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One to 6 percent of pregnant women display sonographic evidence of a placenta previa between 10 and 20
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●
The characteristic symptom of placenta previa is painless vaginal bleeding, which occurs in up 90 percent of
persistent cases. Ten to 20 percent of symptomatic women present with both uterine contractions and
bleeding, similar to the presentation of abruptio placenta. In approximately one-third of pregnancies with
persistent previa, the initial bleeding episode occurs prior to 30 weeks of gestation. (See 'Bleeding' above.)
●
Placenta previa should be suspected in any woman beyond 20 weeks of gestation who presents with
vaginal bleeding. For women who have not had a second or third trimester ultrasound examination,
antepartum bleeding should prompt sonographic determination of placental location before digital vaginal
examination is performed because palpation of the placenta can cause severe hemorrhage. (See 'Diagnosis'
above.)
●
The diagnosis of placenta previa is based on identification of placental tissue over the internal cervical os on
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●
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●
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●
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●
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●
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2000; 17:101.
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Previa: A Systematic Review and Meta-Analysis. PLoS One 2017; 12:e0170194.
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e: Principles and Practice. WB Saunders, Philadelphia 1999. p. 616.
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demographic factors. J Matern Fetal Neonatal Med 2015; 28:793.
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J Matern Fetal Neonatal Med 2009; 22:439.
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States. Am J Obstet Gynecol 2003; 188:1305.
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delivery: a systematic review and metaanalysis. Am J Obstet Gynecol 2015; 213:S78.
6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 13/17
85. Zlatnik MG, Cheng YW, Norton ME, et al. Placenta previa and the risk of preterm delivery. J Matern Fetal
Neonatal Med 2007; 20:719.
86. Schneiderman M, Balayla J. A comparative study of neonatal outcomes in placenta previa versus cesarean
for other indication at term. J Matern Fetal Neonatal Med 2013; 26:1121.
87. Jang DG, Jo YS, Lee SJ, Lee GS. Risk factors of neonatal anemia in placenta previa. Int J Med Sci 2011;
8:554.
88. Vergani P, Ornaghi S, Pozzi I, et al. Placenta previa: distance to internal os and mode of delivery. Am J
Obstet Gynecol 2009; 201:266.e1.
Topic 6772 Version 28.0
6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 14/17
GRAPHICS
Complete placenta previa
Transabdominal study shows the placenta completely covering the internal os (arrow). A
central placenta previa occurs when the internal os is approximately equidistant from the
anterior and posterior placental edges; 20 to 30 percent of complete previas are central.
Courtesy of Deborah Levine, MD.
Graphic 74665 Version 4.0
6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 15/17
Low lying placenta
Transvaginal study shows a posterior placenta with the tip of the placenta on the internal
os (arrow). The placenta is adjacent to the internal os, but does not cover it.
Courtesy of Deborah Levine, MD.
Graphic 55703 Version 4.0
6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 16/17
Overdistended bladder mimicking placenta previa
Transabdominal study shows an over-distended bladder giving the appearance of a previa
in a patient with NO placenta previa. An over-distended bladder can compress the
anterior lower uterine segment against the posterior lower uterine segment, thereby
mimicking placenta previa. The arrow points to the cervical os.
Courtesy of Deborah Levine, MD.
Graphic 76545 Version 3.0
6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate
https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 17/17
Contributor Disclosures
Charles J Lockwood, MD, MHCM Nothing to disclose Karen Russo-Stieglitz, MD Nothing to
disclose Deborah Levine, MD Nothing to disclose Vincenzo Berghella, MD Nothing to disclose Vanessa A
Barss, MD, FACOG Nothing to disclose
Contributor disclosures are reviewed for conflicts of interest by the editorial group. When found, these are
addressed by vetting through a multi-level review process, and through requirements for references to be
provided to support the content. Appropriately referenced content is required of all authors and must conform to
UpToDate standards of evidence.
Conflict of interest policy

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Placenta previa epidemiology, clinical features, diagnosis, morbidity and mortality up-todate

  • 1. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 1/17 Official reprint from UpToDate www.uptodate.com ©2018 UpToDate, Inc. and/or its affiliates. All Rights Reserved. Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality Authors: Charles J Lockwood, MD, MHCM, Karen Russo-Stieglitz, MD Section Editors: Deborah Levine, MD, Vincenzo Berghella, MD Deputy Editor: Vanessa A Barss, MD, FACOG All topics are updated as new evidence becomes available and our peer review process is complete. Literature review current through: May 2018. | This topic last updated: Aug 04, 2017. INTRODUCTION — Placenta previa refers to the presence of placental tissue that extends over the internal cervical os. Sequelae include the potential for severe bleeding and preterm birth, as well as the need for cesarean delivery. Placenta previa should be suspected in any pregnant woman beyond 20 weeks of gestation who presents with vaginal bleeding. For women who have not had a second-trimester ultrasound examination, bleeding after 20 weeks of gestation should prompt sonographic determination of placental location before digital vaginal examination is performed because palpation of the placenta can cause severe hemorrhage. This topic will discuss the epidemiology, clinical features, diagnosis, morbidity, and mortality of placenta previa. The natural history of placenta, risk of bleeding, and management are reviewed separately. (See "Placenta previa: Management".) EPIDEMIOLOGY Prevalence — In systematic reviews, the pooled prevalence of placenta previa is about 4 per 1000 births, but varies worldwide [1,2]. The prevalence is several-fold higher around 20 weeks of gestation (as high as 2 percent), but most previas identified early in pregnancy resolve before delivery. (See 'Natural history' below.) Risk factors — Major risk factors for placenta previa include [3-15]: Other risk factors, some of which are interdependent, include: ® Previous placenta previa – Placenta previa recurs in 4 to 8 percent of subsequent pregnancies [16].● Previous cesarean delivery – In two systematic reviews, previous cesarean delivery was found to increase the risk for placenta previa by 47 percent [17] and 60 percent [3]. The risk increases with an increasing number of cesarean deliveries [18-20]. Prelabor cesarean delivery may increase previa risk in a subsequent delivery more than previous intrapartum cesarean or vaginal delivery [13]. ● Multiple gestation – The prevalence of placenta previa was 40 percent higher among twin births than among singleton births (3.9 and 2.8 per 1000 births, respectively) in one study [5]. In another study, dichorionic twin pregnancies were more likely to have a placenta previa than monochorionic twin pregnancies (odds ratio [OR] 3.3) or singleton pregnancies (OR 1.5) [21]. ● Increasing parity● Increasing maternal age●
  • 2. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 2/17 PATHOGENESIS — The pathogenesis of placenta previa is unknown. One hypothesis is that the presence of areas of suboptimally vascularized decidua in the upper uterine cavity due to previous surgery or multiple pregnancies promotes implantation of trophoblast in, or unidirectional growth of, trophoblast toward the lower uterine cavity [1,3,22]. Another hypothesis is that a particularly large placental surface area, as in multiple gestation, increases the probability that the placenta will encroach upon/cover the cervical os. PATHOPHYSIOLOGY OF BLEEDING — Placental bleeding is the major adverse sequelae of placenta previa. It is thought to occur when uterine contractions or gradual changes in the cervix and lower uterine segment apply shearing forces to the inelastic placental attachment site, resulting in partial detachment. Vaginal examination or coitus can also disrupt this site and cause bleeding. Bleeding is primarily maternal blood from the intervillous space, but fetal bleeding can occur if fetal vessels in the terminal villi are disrupted. CLINICAL PRESENTATION AND COURSE Asymptomatic finding on midtrimester ultrasound examination — The most common presentation of placenta previa is as a finding on routine ultrasound examination at about 16 to 20 weeks of gestation for assessment of gestational age, fetal anatomic survey, or prenatal diagnosis. One to 6 percent of pregnant women are found to have sonographic evidence of a placenta previa on these examinations. (See 'Ultrasonography' below.) Natural history — Approximately 90 percent of placenta previas identified on ultrasound examination before 20 weeks of gestation resolve before delivery [23]. Two theories have been proposed to account for this phenomenon: In either case, the placental edge overlying the cervix atrophies. Predicting presence at delivery — Findings that suggest that a placenta previa will persist until delivery include lack of resolution by the third trimester and extension over the os by more than 25 mm. In a retrospective cohort study of 714 women with placenta previa, singleton gestation, and a liveborn infant ≥25 weeks of gestation, when the most recent ultrasound showed placenta previa at [24]: Infertility treatment● Previous abortion● Previous uterine surgical procedure● Maternal smoking● Maternal cocaine use● Male fetus● Non-white race● The lower uterine segment lengthens from 0.5 cm at 20 weeks of gestation to more than 5 cm at term [16]. This development of the lower uterine segment relocates the stationary lower edge of the placenta away from the internal os. ● Progressive unidirectional growth of trophoblastic tissue toward the fundus results in upward migration of the placenta away from the cervix. This phenomenon has been termed "trophotropism." ●
  • 3. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 3/17 The more the placenta extends over the internal os, the more likely it is to persist until delivery. Although available data are insufficient to make precise predictions, pooled data suggest that when the placenta extends at least 14 to 15 mm but <25 mm over the cervical os at 18 to 23 weeks of gestation, then the probability of placenta previa at delivery is about 20 percent; extension ≥25 mm is associated with a 40 to 100 percent probability of placenta previa at delivery [25-29]. Low-lying placentas and placentas formerly called partial previa are most likely to resolve (eg, only 6 to 7 percent of those diagnosed at 15 to 19 weeks and 39 to 63 percent of those diagnosed at 32 to 35 weeks were present at delivery). Anterior placenta previas are more likely to resolve than posterior placenta previa [30]. Recommendations for follow-up sonography to determine resolution are discussed separately. (See "Placenta previa: Management", section on 'Monitoring placental position'.) Bleeding — In the second half of pregnancy, the most common symptom of placenta previa is relatively painless vaginal bleeding, which occurs in up to 90 percent of persistent cases [31]. Ten to 20 percent of women present with uterine contractions, pain, and bleeding, similar to the presentation of abruptio placenta [32,33]. (See "Placental abruption: Pathophysiology, clinical features, diagnosis, and consequences".) In approximately one-third of pregnancies with persistent previa, the initial bleeding episode occurs prior to 30 weeks of gestation; this group is more likely to require blood transfusions and is at greater risk of preterm delivery and perinatal mortality than women whose bleeding begins later in gestation [32-35]. An additional one- third of patients becomes symptomatic between 30 and 36 weeks, while most of the remaining patients have their first bleed after 36 weeks [32,33]. About 10 percent of women reach term without bleeding. The number of antepartum bleeding episodes and need for blood transfusion have been identified as independent predictors for emergency cesarean delivery [36]. Antepartum bleeding from any cause is a risk factor for preterm labor and preterm premature rupture of membranes. (See "Pathogenesis of spontaneous preterm birth", section on 'Decidual hemorrhage' and "Preterm prelabor rupture of membranes", section on 'Risk factors'.) DIAGNOSIS — The diagnosis of placenta previa is based on sonography and requires the identification of echogenic homogeneous placental tissue over the internal cervical os. Placenta previa should be suspected in any woman beyond 20 weeks of gestation who presents with vaginal bleeding. For women who have not had a second- or third-trimester ultrasound examination, antepartum bleeding should prompt sonographic determination of placental location before digital vaginal examination is performed because palpation of the placenta can cause severe hemorrhage. 15 to 19 weeks – 20 percent were present at delivery if no prior cesarean delivery, and 41 percent if a prior cesarean delivery ● 20 to 23 weeks – 45 percent were present at delivery if no prior cesarean delivery, and 73 percent if a prior cesarean delivery ● 24 to 27 weeks – 56 percent were present at delivery if no prior cesarean delivery, and 84 percent if a prior cesarean delivery ● 28 to 31 weeks – 88 to 89 percent were present at delivery whether or not there was a prior cesarean delivery ● 32 to 35 weeks – 89 to 90 percent were present at delivery whether or not there was a prior cesarean delivery ●
  • 4. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 4/17 Diagnostic criteria — The diagnosis of placenta previa is based on identification of placental tissue extending over the internal cervical os on a second or third trimester imaging study (image 1), preferably transvaginal ultrasound [37]. The distance (millimeters) that the placenta extends over the internal cervical os should be described in the diagnostic report. Of note, when the placental edge is <2 cm from, but not over, the internal os, the placenta is labeled "low-lying" (image 2). The distance (millimeters) between the internal cervical os and the inferior edge of the placenta should be described in the diagnostic report [38]. (See 'Morbidity of low-lying placenta' below.) The historic terms "marginal" and "partial" for characterizing a placenta previa are no longer used, as they referred to information gathered on a digital vaginal examination, which should be avoided and is not needed given the superiority of ultrasound diagnosis. Ultrasonography Transabdominal — Transabdominal sonographic assessment of placental location is one of the standard components of the basic obstetrical ultrasound examination, and thus can be considered a screening test for placenta previa. Screening performance — If the placenta-cervix distance is ≤2 cm on transabdominal ultrasound, we perform transvaginal sonography to better define placental position and make the diagnosis. The overall false positive rate of transabdominal ultrasound for diagnosis of placenta previa is up to 25 percent, and varies by study design [39,40]. In a planned secondary analysis of a prospective cohort study of women with singleton gestations undergoing both transabdominal and transvaginal cervical length measurement during the second trimester anatomic survey, a transabdominal placenta-cervix distance threshold of 4.2 cm had sensitivity 93.3 percent, specificity 76.7 percent, negative predictive value 99.8 percent, and screen-positive rate 25.0 percent for detection of previa [41]. A threshold of 2.8 cm yielded a sensitivity 86.7 percent, specificity 90.5 percent, negative predictive value 99.6 percent, and screen-positive rate of 11.4 percent. Thus, a threshold of 2.8 cm maximizes specificity while a threshold of 4.2 cm maximizes sensitivity. Technique and pitfalls — Sagittal, parasagittal, and transverse sonographic views should be obtained with the patient's bladder partially full. Specific points that should be appreciated when performing transabdominal sonographic examination for placenta previa include: An over-distended bladder can compress the anterior lower uterine segment against the posterior lower uterine segment to give the appearance of a previa (image 3). The diagnosis of placenta previa should not be made without confirming placental position after the patient has emptied her bladder. Care should be taken to not make the diagnosis of placenta previa when the lower uterine segment is contracting, which commonly occurs after a woman empties her bladder, and obscures the relationship between the placental edge and the cervical os. ● A previa can be missed near term if the fetal head is low in the pelvis since acoustic shadowing from or compression of placental tissue by the fetal skull may obscure the placental location. In these cases, the cervix may be better visualized by placing the patient in Trendelenburg position and/or gently pushing the fetal head cephalad with an abdominal hand or the transducer. ● The sonographic diagnosis of a central placenta previa is readily made since the placenta is centered over the cervix and placental tissue is imaged anterior and posterior to the cervix. Complete noncentral previas, particularly when lateral, are more difficult to confirm. Transverse views at and above the internal cervical os should facilitate an accurate diagnosis. ●
  • 5. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 5/17 Transvaginal — Transvaginal ultrasound (TVS) can be performed safely in patients with placenta previa since the optimal position of the vaginal probe for visualization of the internal os is 2 to 3 cm away from the cervix, and the angle between the cervix and vaginal probe is sufficient to prevent the probe from inadvertently slipping into the cervical canal [42]. Performance — TVS generally provides a clearer image of the relationship between the edge of the placenta and the internal cervical os than transabdominal ultrasound. Randomized trials and prospective comparative studies have established the superior performance of TVS over transabdominal sonography for diagnosis of placenta previa [43-45]. In one study of 100 suspected cases, sensitivity, specificity, and positive and negative predictive values of TVS for diagnosis of placenta previa at cesarean were 87.5, 98.8, 93.3, 97.6 percent, respectively [46]. Use of color Doppler is employed in the cases of suspected morbidly adherent placentation (eg, accreta) or umbilical cord in the lower uterine segment, to rule out a vasa previa. (See "Clinical features and diagnosis of placenta accreta spectrum (placenta accreta, increta, and percreta)" and "Velamentous umbilical cord insertion and vasa previa".) Characteristics predictive of bleeding — Although the magnitude of bleeding risk may differ according to the following characteristics, all patients with placentas over or in close proximity to the cervical os are at risk of significant antepartum, intrapartum, and postpartum bleeding. Characteristics that appear to be predictive of antepartum bleeding include: Other ultrasound techniques — Translabial (transperineal) ultrasound imaging is an alternative technique that provides excellent images of the cervix and placenta [58]. The use of three-dimensional ultrasound may also improve accuracy [59]. Magnetic resonance imaging — Magnetic resonance imaging (MRI) is well-suited to the assessment of placental-cervical relationships because of the differing magnetic resonance characteristics of the two tissues. However, it is not used for diagnosis of placenta previa because of its high cost, limited availability, and the well- established safety and accuracy of transvaginal sonography [38]. MRI is most useful for diagnosis of complicated placenta previa, such as previa-accreta and previa-percreta [60]. (See "Clinical features and diagnosis of placenta accreta spectrum (placenta accreta, increta, and percreta)", section on 'Magnetic resonance imaging'.) ASSOCIATED FINDINGS A posterior placenta previa may be more difficult to visualize than an anterior placenta previa, even on transvaginal ultrasound. ● Bleeding can result in formation of a hematoma under and/or proximate to the placenta, which can obscure the relationship between the placental edge and the cervical os. ● Extension over the internal os rather than lying proximate to it [47-50].● Thick (>1 cm) placental edge and/or angle between the basal and chorionic plates greater than 45 degrees [51,52]. ● Echo-free space in the placental edge over the internal os [53].● Cervical length ≤3 cm [52,54,55].● Decrease in cervical length in the third trimester [56,57].●
  • 6. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 6/17 Placenta previa-accreta — When placenta previa is diagnosed, the possibility of placenta previa-accreta (or more) should be considered. In a prospective study including 723 women with placenta previa undergoing cesarean delivery, the frequency of placenta accreta increased with an increasing number of cesarean deliveries as follows [61]: In another large series, composite maternal morbidity in women with placenta previa and zero, one, two, or three prior cesarean deliveries was 15, 23, 59, and 83 percent, respectively, and almost all of the excess composite maternal morbidity in women with a prior cesarean was related to complications associated with placenta accreta, such as peripartum hysterectomy [62]. (See "Clinical features and diagnosis of placenta accreta spectrum (placenta accreta, increta, and percreta)", section on 'Prenatal diagnosis'.) Other associated findings MORBIDITY AND MORTALITY Maternal — Maternal morbidity from placenta previa is primarily related to antepartum and/or postpartum hemorrhage [77]. In systematic reviews, 52 percent of women with placenta previa had antepartum bleeding (95% CI 42.7 to 60.6 percent) [31] and 22 percent had postpartum hemorrhage (95% CI 15.8 to 28.7 percent) [78]. Because of antepartum and/or postpartum bleeding, women with placenta previa are more likely to receive blood transfusions (12 versus 0.8 percent in patients without previa in one study [65], 22 versus 1.2 percent in another [8]). They are also more likely to undergo postpartum hysterectomy (5.3 versus 0.04 percent in one study [8]), uterine/iliac artery ligation, or embolization of pelvic vessels. The risks of hemorrhage and postpartum hysterectomy are particularly high for women with previa-accreta. (See "Clinical features and diagnosis of placenta accreta spectrum (placenta accreta, increta, and percreta)", section on 'Consequences'.) In women with severe hemorrhage, rapid, significant loss of intravascular volume can lead to hemodynamic instability, decreased oxygen delivery, decreased tissue perfusion, cellular hypoxia, organ damage, and death. In First cesarean birth, 3 percent● Second cesarean birth, 11 percent● Third cesarean births, 40 percent● Fourth cesarean births, 61 percent● Fifth or greater cesarean birth, 67 percent● Malpresentation – The large volume of placenta in the lower portion of the uterine cavity predisposes the fetus to assume a noncephalic lie [43,63-65]. ● Vasa previa and velamentous umbilical cord – Placenta previa is a risk factor for vasa previa and velamentous umbilical cord insertion. (See "Velamentous umbilical cord insertion and vasa previa".) ● Intrauterine growth restriction – An increased risk of intrauterine growth restriction has been reported by multiple [8,32,66-71], but not all [34,35,66,72-74], investigators, and remains controversial. If a reduction in fetal growth occurs, it is likely to be mild or due to confounding factors. For example, decreased placental perfusion can lead to both fetal growth restriction and a suboptimal site of placental implantation. (See "Fetal growth restriction: Evaluation and management".) ● Congenital anomalies – Population-based cohort studies have reported a small increase in the overall rate of congenital anomalies in pregnancies complicated by placenta previa, but no single anomaly or syndrome was associated with the disorder [8,35,75,76]. ●
  • 7. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 7/17 resource-rich countries, the maternal mortality rate associated with placenta previa is less than 1 percent [79], but remains high in resource-poor countries where maternal anemia, lack of medical resources, and home births are more common [65]. Severe maternal morbidity and maternal mortality can also be a consequence of amniotic fluid embolism syndrome. Several studies have observed a strong association between placental pathology, such as placenta previa, and amniotic fluid embolism syndrome [80-82]. (See "Amniotic fluid embolism syndrome".) Neonatal — The principal causes of neonatal morbidity and mortality are related to preterm delivery [83]. In a systematic review and meta-analysis of placental implantation abnormalities and risk of preterm delivery, compared with no placenta previa, placenta previa was associated with a three- to fivefold increase in risk of [84]: In large studies, approximately 15 percent of patients with placenta previa delivered before 34 weeks of gestation [69,85]. However, neonatal morbidity and mortality rates in pregnancies complicated by placenta previa have fallen over the past few decades because of improvements in obstetrical management (eg, antenatal corticosteroids), the liberal use of planned late preterm cesarean delivery, and improved neonatal care. Neonatal anemia is also increased in pregnancies with placenta previa [86,87]. Morbidity of low-lying placenta — The morbidity of low-lying placenta (placental edge is <2 cm from, but not over, the internal os) is less than that for placenta previa and decreases as the distance between the placental edge and internal cervical os increases. A study that compared pregnancy outcomes of 53 women with placental edge 1 to 10 mm versus 11 to 20 mm from the internal cervical os reported the following [88]: RECURRENCE — Placenta previa recurs in 4 to 8 percent of subsequent pregnancies [16]. MANAGEMENT — (See "Placenta previa: Management".) INFORMATION FOR PATIENTS — UpToDate offers two types of patient education materials, "The Basics" and "Beyond the Basics." The Basics patient education pieces are written in plain language, at the 5 to 6 grade reading level, and they answer the four or five key questions a patient might have about a given condition. These articles are best for patients who want a general overview and who prefer short, easy-to-read materials. Beyond the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written at the 10 to 12 grade reading level and are best for patients who want in-depth information and are comfortable with some medical jargon. Preterm delivery <37 weeks (44 percent, relative risk [RR] 5.32, 95% CI 4.39-6.45)● Neonatal intensive care unit admission (RR 4.09, 95% CI 2.80-5.97)● Neonatal death (RR 5.44, 95% CI 3.03-9.78)● Perinatal death (RR 3.01, 95% CI 1.41-6.43)● Antepartum hemorrhage: 29 versus 3 percent● Postpartum hemorrhage: 21 versus 10 percent● Preterm birth: 29 versus 3 percent● Cesarean delivery: 75 versus 31 percent● th th th th
  • 8. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 8/17 Here are the patient education articles that are relevant to this topic. We encourage you to print or e-mail these topics to your patients. (You can also locate patient education articles on a variety of subjects by searching on "patient info" and the keyword(s) of interest.) SUMMARY AND RECOMMENDATIONS Use of UpToDate is subject to the Subscription and License Agreement. REFERENCES 1. Faiz AS, Ananth CV. Etiology and risk factors for placenta previa: an overview and meta-analysis of observational studies. J Matern Fetal Neonatal Med 2003; 13:175. 2. Cresswell JA, Ronsmans C, Calvert C, Filippi V. Prevalence of placenta praevia by world region: a systematic review and meta-analysis. Trop Med Int Health 2013; 18:712. Basics topics (see "Patient education: Placenta previa (The Basics)")● One to 6 percent of pregnant women display sonographic evidence of a placenta previa between 10 and 20 weeks of gestation when they undergo routine obstetrical ultrasound examination. The majority of these women are asymptomatic and 90 percent of these early cases resolve. (See 'Asymptomatic finding on midtrimester ultrasound examination' above.) ● The characteristic symptom of placenta previa is painless vaginal bleeding, which occurs in up 90 percent of persistent cases. Ten to 20 percent of symptomatic women present with both uterine contractions and bleeding, similar to the presentation of abruptio placenta. In approximately one-third of pregnancies with persistent previa, the initial bleeding episode occurs prior to 30 weeks of gestation. (See 'Bleeding' above.) ● Placenta previa should be suspected in any woman beyond 20 weeks of gestation who presents with vaginal bleeding. For women who have not had a second or third trimester ultrasound examination, antepartum bleeding should prompt sonographic determination of placental location before digital vaginal examination is performed because palpation of the placenta can cause severe hemorrhage. (See 'Diagnosis' above.) ● The diagnosis of placenta previa is based on identification of placental tissue over the internal cervical os on an imaging study (image 1). Transvaginal sonography should be performed to confirm a diagnosis made on transabdominal imaging. The distance (millimeters) that the placenta extends over the internal cervical os should be described in the diagnostic report. (See 'Diagnosis' above.) ● Previous placenta previa, previous cesarean deliveries, and multiple gestation are major risk factors for placenta previa. (See 'Epidemiology' above.) ● The likelihood of placenta previa at delivery is high when the previa persists into the third trimester and extends over the cervical os by ≥25 mm. (See 'Asymptomatic finding on midtrimester ultrasound examination' above.) ● Some conditions that may be associated with placenta previa include placenta accreta, malpresentation, preterm labor or premature rupture of the membranes, vasa previa and velamentous insertion of the umbilical cord. (See 'Placenta previa-accreta' above.) ● When placenta previa is diagnosed, the possibility of placenta previa-accreta/percreta should be considered and excluded, especially in women with a previous cesarean delivery. (See 'Placenta previa-accreta' above.) ●
  • 9. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previa… 9/17 3. Ananth CV, Smulian JC, Vintzileos AM. The association of placenta previa with history of cesarean delivery and abortion: a metaanalysis. Am J Obstet Gynecol 1997; 177:1071. 4. National Institutes of Health Consensus Development Conference Statement. NIH consensus development conference: Vaginal birth after cesarean: New insights. March 8–10, 2010. 5. Ananth CV, Demissie K, Smulian JC, Vintzileos AM. Placenta previa in singleton and twin births in the United States, 1989 through 1998: a comparison of risk factor profiles and associated conditions. Am J Obstet Gynecol 2003; 188:275. 6. Demissie K, Breckenridge MB, Joseph L, Rhoads GG. Placenta previa: preponderance of male sex at birth. Am J Epidemiol 1999; 149:824. 7. Yang Q, Wu Wen S, Caughey S, et al. Placenta previa: its relationship with race and the country of origin among Asian women. Acta Obstet Gynecol Scand 2008; 87:612. 8. Rosenberg T, Pariente G, Sergienko R, et al. Critical analysis of risk factors and outcome of placenta previa. Arch Gynecol Obstet 2011; 284:47. 9. Iyasu S, Saftlas AK, Rowley DL, et al. The epidemiology of placenta previa in the United States, 1979 through 1987. Am J Obstet Gynecol 1993; 168:1424. 10. Macones GA, Sehdev HM, Parry S, et al. The association between maternal cocaine use and placenta previa. Am J Obstet Gynecol 1997; 177:1097. 11. Rasmussen S, Albrechtsen S, Dalaker K. Obstetric history and the risk of placenta previa. Acta Obstet Gynecol Scand 2000; 79:502. 12. Gurol-Urganci I, Cromwell DA, Edozien LC, et al. Risk of placenta previa in second birth after first birth cesarean section: a population-based study and meta-analysis. BMC Pregnancy Childbirth 2011; 11:95. 13. Downes KL, Hinkle SN, Sjaarda LA, et al. Previous prelabor or intrapartum cesarean delivery and risk of placenta previa. Am J Obstet Gynecol 2015; 212:669.e1. 14. Karami M, Jenabi E, Fereidooni B. The association of placenta previa and assisted reproductive techniques: a meta-analysis. J Matern Fetal Neonatal Med 2018; 31:1940. 15. Shobeiri F, Jenabi E. Smoking and placenta previa: a meta-analysis. J Matern Fetal Neonatal Med 2017; 30:2985. 16. Lavery JP. Placenta previa. Clin Obstet Gynecol 1990; 33:414. 17. Klar M, Michels KB. Cesarean section and placental disorders in subsequent pregnancies--a meta- analysis. J Perinat Med 2014; 42:571. 18. Clark SL, Koonings PP, Phelan JP. Placenta previa/accreta and prior cesarean section. Obstet Gynecol 1985; 66:89. 19. Getahun D, Oyelese Y, Salihu HM, Ananth CV. Previous cesarean delivery and risks of placenta previa and placental abruption. Obstet Gynecol 2006; 107:771. 20. Gilliam M, Rosenberg D, Davis F. The likelihood of placenta previa with greater number of cesarean deliveries and higher parity. Obstet Gynecol 2002; 99:976. 21. Weis MA, Harper LM, Roehl KA, et al. Natural history of placenta previa in twins. Obstet Gynecol 2012; 120:753. 22. Rose GL, Chapman MG. Aetiological factors in placenta praevia--a case controlled study. Br J Obstet Gynaecol 1986; 93:586. 23. Oyelese Y, Smulian JC. Placenta previa, placenta accreta, and vasa previa. Obstet Gynecol 2006; 107:927.
  • 10. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 10/17 24. Dashe JS, McIntire DD, Ramus RM, et al. Persistence of placenta previa according to gestational age at ultrasound detection. Obstet Gynecol 2002; 99:692. 25. Mouer JR. Placenta previa: antepartum conservative management, inpatient versus outpatient. Am J Obstet Gynecol 1994; 170:1683. 26. Becker RH, Vonk R, Mende BC, et al. The relevance of placental location at 20-23 gestational weeks for prediction of placenta previa at delivery: evaluation of 8650 cases. Ultrasound Obstet Gynecol 2001; 17:496. 27. Taipale P, Hiilesmaa V, Ylöstalo P. Transvaginal ultrasonography at 18-23 weeks in predicting placenta previa at delivery. Ultrasound Obstet Gynecol 1998; 12:422. 28. Rosati P, Guariglia L. Clinical significance of placenta previa detected at early routine transvaginal scan. J Ultrasound Med 2000; 19:581. 29. Oppenheimer L, Holmes P, Simpson N, Dabrowski A. Diagnosis of low-lying placenta: can migration in the third trimester predict outcome? Ultrasound Obstet Gynecol 2001; 18:100. 30. Cho JY, Lee YH, Moon MH, Lee JH. Difference in migration of placenta according to the location and type of placenta previa. J Clin Ultrasound 2008; 36:79. 31. Fan D, Wu S, Liu L, et al. Prevalence of antepartum hemorrhage in women with placenta previa: a systematic review and meta-analysis. Sci Rep 2017; 7:40320. 32. Cotton DB, Read JA, Paul RH, Quilligan EJ. The conservative aggressive management of placenta previa. Am J Obstet Gynecol 1980; 137:687. 33. Silver R, Depp R, Sabbagha RE, et al. Placenta previa: aggressive expectant management. Am J Obstet Gynecol 1984; 150:15. 34. McShane PM, Heyl PS, Epstein MF. Maternal and perinatal morbidity resulting from placenta previa. Obstet Gynecol 1985; 65:176. 35. Crane JM, van den Hof MC, Dodds L, et al. Neonatal outcomes with placenta previa. Obstet Gynecol 1999; 93:541. 36. Ruiter L, Eschbach SJ, Burgers M, et al. Predictors for Emergency Cesarean Delivery in Women with Placenta Previa. Am J Perinatol 2016; 33:1407. 37. Reddy UM, Abuhamad AZ, Levine D, et al. Fetal imaging: executive summary of a joint Eunice Kennedy Shriver National Institute of Child Health and Human Development, Society for Maternal-Fetal Medicine, American Institute of Ultrasound in Medicine, American College of Obstetricians and Gynecologists, American College of Radiology, Society for Pediatric Radiology, and Society of Radiologists in Ultrasound Fetal Imaging workshop. Obstet Gynecol 2014; 123:1070. 38. Thurmond A, Mendelson E, Böhm-Vélez M, et al. Role of imaging in second and third trimester bleeding. American College of Radiology. ACR Appropriateness Criteria. Radiology 2000; 215 Suppl:895. 39. McClure N, Dornal JC. Early identification of placenta praevia. Br J Obstet Gynaecol 1990; 97:959. 40. Oppenheimer L, Society of Obstetricians and Gynaecologists of Canada. Diagnosis and management of placenta previa. J Obstet Gynaecol Can 2007; 29:261. 41. Quant HS, Friedman AM, Wang E, et al. Transabdominal ultrasonography as a screening test for second- trimester placenta previa. Obstet Gynecol 2014; 123:628. 42. Timor-Tritsch IE, Yunis RA. Confirming the safety of transvaginal sonography in patients suspected of placenta previa. Obstet Gynecol 1993; 81:742. 43. Sunna E, Ziadeh S. Transvaginal and transabdominal ultrasound for the diagnosis of placenta praevia. J Obstet Gynaecol 1999; 19:152.
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  • 13. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 13/17 85. Zlatnik MG, Cheng YW, Norton ME, et al. Placenta previa and the risk of preterm delivery. J Matern Fetal Neonatal Med 2007; 20:719. 86. Schneiderman M, Balayla J. A comparative study of neonatal outcomes in placenta previa versus cesarean for other indication at term. J Matern Fetal Neonatal Med 2013; 26:1121. 87. Jang DG, Jo YS, Lee SJ, Lee GS. Risk factors of neonatal anemia in placenta previa. Int J Med Sci 2011; 8:554. 88. Vergani P, Ornaghi S, Pozzi I, et al. Placenta previa: distance to internal os and mode of delivery. Am J Obstet Gynecol 2009; 201:266.e1. Topic 6772 Version 28.0
  • 14. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 14/17 GRAPHICS Complete placenta previa Transabdominal study shows the placenta completely covering the internal os (arrow). A central placenta previa occurs when the internal os is approximately equidistant from the anterior and posterior placental edges; 20 to 30 percent of complete previas are central. Courtesy of Deborah Levine, MD. Graphic 74665 Version 4.0
  • 15. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 15/17 Low lying placenta Transvaginal study shows a posterior placenta with the tip of the placenta on the internal os (arrow). The placenta is adjacent to the internal os, but does not cover it. Courtesy of Deborah Levine, MD. Graphic 55703 Version 4.0
  • 16. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 16/17 Overdistended bladder mimicking placenta previa Transabdominal study shows an over-distended bladder giving the appearance of a previa in a patient with NO placenta previa. An over-distended bladder can compress the anterior lower uterine segment against the posterior lower uterine segment, thereby mimicking placenta previa. The arrow points to the cervical os. Courtesy of Deborah Levine, MD. Graphic 76545 Version 3.0
  • 17. 6/17/2018 Placenta previa: Epidemiology, clinical features, diagnosis, morbidity and mortality - UpToDate https://www.uptodate.com/contents/placenta-previa-epidemiology-clinical-features-diagnosis-morbidity-and-mortality/print?search=placenta%20previ… 17/17 Contributor Disclosures Charles J Lockwood, MD, MHCM Nothing to disclose Karen Russo-Stieglitz, MD Nothing to disclose Deborah Levine, MD Nothing to disclose Vincenzo Berghella, MD Nothing to disclose Vanessa A Barss, MD, FACOG Nothing to disclose Contributor disclosures are reviewed for conflicts of interest by the editorial group. When found, these are addressed by vetting through a multi-level review process, and through requirements for references to be provided to support the content. Appropriately referenced content is required of all authors and must conform to UpToDate standards of evidence. Conflict of interest policy