Chapter 14. Obstetrical Imaging. Will Obs

 Chapter 14. Obstetrical Imaging

BS. Nguyễn Hồng Anh

Obstetrical ultrasound is undamental to prenatal care. It is

used to conrm gestational age and viability; to detect and

characterize abnormalities o the etus, amnionic uid, and

placenta; and to assist with diagnostic and therapeutic procedures.

Ultrasound practice continues to evolve. Te number o

components included in the second-trimester standard and

detailed etal anatomical surveys has expanded. With improved

image resolution, etal abnormalities are increasingly identied

in the late rst trimester. Tis has prompted the requirement or

a limited anatomical survey during the standard rst-trimester

examination and has led to the development o a new detailed

rst-trimester examination. Detailed placental evaluation is a

new specialized examination to aid detection and characterization o placenta accreta spectrum.

Across the United States, pregnant women receive ultrasound examinations in various practice settings staed by

obstetrician–gynecologists, maternal–etal medicine specialists, and radiologists. Ideally, examinations are perormed by

registered diagnostic medical sonographers or physicians with

certication in their area(s) o practice and in units accredited

by the American Institute o Ultrasound in Medicine (AIUM)

or American College o Radiology. Components o accreditation include evidence o physician training, sonographer credentialing, continuing medical education, and protocols and

procedures to ensure proper and sae ultrasound practice. One

important component is independent review o submitted

images.

o standardize ultrasound education or residents in obstetrics and gynecology and ellows in maternal-etal medicine,

the American College o Obstetricians and Gynecologists,

the Society or Maternal-Fetal Medicine, and the AIUM have

developed consensus documents (Abuhamad, 2018; Benacerra, 2018). A ocus o training—and o ultrasound practice—is

standardization o an ultrasound curriculum and provision o

competency assessment tools or image acquisition.

TECHNOLOGY AND SAFETY

Te image on the ultrasound screen is produced by sound

waves that are reected back rom uid and tissue interaces o

the etus, amnionic uid, and placenta. Ultrasound transducers

contain groups o piezoelectric crystals that convert electrical

energy into sound waves and convert returning sound waves

back into electrical energy. Te sound waves are emitted in

synchronized pulses. As these pulses pass through tissue layers, dense tissue such as bone produces high-velocity reected

waves. With routine gray-scale imaging, which is also known as

brightness-mode (B-mode), these reected waves are displayed

as bright echoes on the screen. Conversely, uid generates ew

reected waves and appears dark. Digital images generated at

50 to more than 100 rames per second undergo postprocessing

that yields the appearance o real-time imaging.

Ultrasound reers to sound waves traveling at a requency

above 20,000 hertz (Hz [cycles per second]). ransducers use

wide-bandwidth technology to perorm within a range o requencies. Higher-requency transducers yield better image

resolution, whereas lower requencies penetrate tissue more

eectively. In early pregnancy, a 5- to 12-megahertz (MHz)

transvaginal transducer usually provides excellent resolution,

because the early etus lies close to the transducer. In the rst and

second trimesters, a 4- to 6-MHz transabdominal transducer is

similarly sufciently close to the etus to yield precise images.

By the third trimester, however, a lower-requency 2- to 5-MHz

transducer may be needed or tissue penetration— particularly

in obese patients—and this can lead to compromised image

resolution.

■ Embryo and Fetal Safety

Sonography should be perormed only or a valid medical

indication and use the lowest possible exposure setting to gain

necessary inormation. Tis is the ALARA principle—as low

as reasonably achievable. Examinations are perormed only by

those trained to recognize etal abnormalities and artiacts that

may mimic pathology and with techniques to avoid ultrasound

exposure beyond what is considered sae or the etus (American

College o Obstetricians and Gynecologists, 2020; American

Institute o Ultrasound in Medicine, 2018a). No causal relationship has been demonstrated between diagnostic ultrasound

and any recognized adverse eect in human pregnancy. Te

International Society o Ultrasound in Obstetrics and Gynecology (2016) urther concludes that there is no scientically

proven association between ultrasound exposure in the rst or

second trimesters and autism spectrum disorder or its severity.

All ultrasound machines are required to display two indices: the thermal index and the mechanical index. Te thermal

index measures the relative probability that the examination

may raise the temperature enough to induce injury. However,

etal damage resulting rom commercially available ultrasound

equipment in routine practice is extremely unlikely. Te potential or temperature elevation is higher with longer examination

time and is greater near bone than in sot tissue. Teoretical

risks are higher during organogenesis than later in gestation.

Te thermal index or sot tissue, Tis, should be used beore

10 weeks’ gestation, and that or bone, Tib, at or beyond

10 weeks (American Institute o Ultrasound in Medicine, 2018a).

Te thermal index is higher with pulsed Doppler applications than with routine B-mode scanning. In the rst trimester, i pulsed Doppler is clinically indicated, the thermal

index should be ≤0.7, and the exposure time should be as

brie as possible (American Institute o Ultrasound in Medicine, 2020b). Tis is an important consideration when pulsed

Doppler is applied to assist with identication or characterization o suspected abnormalities at 11 to 14 weeks’ gestation.

o document the embryonic or etal heart rate, motion-mode

(M-mode) scanning is used instead o pulsed Doppler imaging.

Te mechanical index is a measure o the likelihood

o adverse eects related to rareactional pressure, such as

cavitation, which is relevant only in tissues that contain air.

Microbubble ultrasound contrast agents are not used in pregnancy or this reason. In mammalian tissues that do not contain

gas bodies, no adverse eects have been reported over the range

o diagnostically relevant exposures. Fetuses cannot contain gas

bodies and thus are not considered at risk.

Te use o ultrasound or any nonmedical purpose, such as

“keepsake etal imaging,” is considered contrary to responsible

medical practice and is not condoned by the Food and Drug

Administration (FDA) (2019), the American Institute o Ultrasound in Medicine (2020b), or the American College o Obstetricians and Gynecologists (2020b). However, images or video

clips rom medically indicated ultrasound examinations may be

shared with patients.

■ Operator Safety

Te reported prevalence o work-related musculoskeletal discomort or injury among sonographers approximates 70 percent (Janga, 2012; Roll, 2012). Te most common injuries are

capsulitis and tendonitis o the shoulder, epicondylitis o the

elbow, carpal and cubital tunnel syndrome, and neck or back

strain (Murphey, 2018). Te main risk actors or injury during

transabdominal ultrasound examinations are awkward posture,

sustained static orces, and various pinch grips used to maneuver the transducer (Centers or Disease Control and Prevention, 2006). Excessive exion, extension, or abduction while

scanning places stress on joints and muscles. ask repetition

without adequate recovery time may compound risks. Maternal

habitus can be contributory because more orce is oten needed

when imaging obese patients.

Te ollowing guidelines may help avert injury:

1. Position the patient close to you on the examination table.

As a result, your elbow is close to your body, shoulder abduction is <30 degrees, and your thumb is acing up.

2. Adjust the table or chair height so that your orearm is parallel to the oor.

3. Use a chair with back support, i seated. Avoid leaning

toward the patient or monitor. Support your eet, and keep

ankles in neutral position.

4. Face the monitor squarely and position it so that it is viewed

at a neutral angle rom the horizon, such as 15 degrees

downward.

5. Avoid reaching, bending, or twisting while scanning.

6. ake requent breaks to help prevent muscle strain. Stretching and strengthening exercises can be helpul.

GESTATIONAL AGE ASSESSMENT

Gestational age is based on two things: the certainty o the

woman’s last menstrual period (LMP) date and measurements

o the embryo or etus at the initial ultrasound examination.

Gestational sac measurement is not suitable or gestational

age assignment. I the LMP is certain, the estimated due date

(EDD) is based on LMP unless the date–measurement discrepancy exceeds thresholds listed in Table 14-1 (American

College o Obstetricians and Gynecologists, 2019b,c). I the248 The Fetal Patient

Section 6

discrepancy exceeds these thresholds, or i the LMP is uncertain or unknown, ultrasound measurements establish the

EDD.

Ultrasound measurement o the crown-rump length (CRL)

is the most accurate method to establish or conrm gestational

age (Appendix, p. 1234). ransvaginal imaging yields higher

resolution images. Te CRL is measured in the midsagittal

plane with the embryo or etus in a neutral, nonexed position. Tis allows its length to be measured in a straight line

(Fig. 14-1). Te mean o three discrete measurements is used.

Beore 14 weeks’ gestation, the CRL is accurate to within 5 to

7 days (American College o Obstetricians and Gynecologists,

2019c).

Starting at 140/7 weeks’ gestation, the biparietal diameter,

head circumerence, abdominal circumerence, and emur

length should be measured. Equipment sotware ormulas calculate estimated gestational age and etal weight rom these

our biometric parameters. Te accuracy o the etal weight estimate is assumed to be within 15 percent o the actual weight

(American Institute o Ultrasound in Medicine, 2018a). Measurement criteria are discussed in Chapter 15 (p. 272).

Beore 22 weeks, gestational age assessment using these

our biometric parameters is accurate to within 7 to 10 days

(American College o Obstetricians and Gynecologists, 2019c).

Various nomograms are available or other structural measurements, including the transverse cerebellar diameter, orbital distances, thoracic circumerence, and length o the ear, kidney,

long bones, and eet. Tese may be used to address specic

questions regarding organ system abnormalities or syndromes

(Appendix, pp. 1238–1241).

I the initial ultrasound examination is perormed at or

beyond 22 weeks’ gestation, the pregnancy is suboptimally dated

(American College o Obstetricians and Gynecologists, 2019b).

In such cases, subsequent ultrasound evaluation in 3 to 4 weeks

may be considered. Tis is especially true i the ultrasound measurements are smaller than expected or gestational age based

on LMP and thus poor etal growth is a possibility.

Fertilization is presumed to occur 2 weeks ater a condent

LMP. Tereore, or pregnancies achieved with in vitro ertilization and resh transer, 266 days are added to the egg-retrieval/

ertilization date to calculate the EDD. Similarly, i using a

day-3 rozen embryo, adding 263 days accounts or the days o

embryo culture. For pregnancies conceived with intrauterine

insemination, LMP is used.

FIRST-TRIMESTER ULTRASOUND

Te three types o rst-trimester examinations include standard

ultrasound; nuchal translucency evaluation—between 11 and

14 weeks’ gestation; and detailed rst-trimester anatomy evaluation between 12 and 14 weeks’ gestation.

Indications or the standard rst-trimester examination

are listed in Table 14-2 (American College o Obstetricians

and Gynecologists, 2020; American Institute o Ultrasound

in Medicine, 2018a). Early pregnancy can be evaluated with

transabdominal or transvaginal sonography, or both. Te components listed in Table 14-3 should be assessed (American



TABLE 14-1. Assessment of Gestational Age

Gestational Agea Parameter(s)

Threshold Value

to Redateb

<9 wks CRL >5 d

9 to <14 wks CRL >7 d

14 to <16 wks BPD, HC, AC, FL >7 d

16 to <22 wks BPD, HC, AC, FL >10 d

22 to <28 wks BPD, HC, AC, FL >14 d

≥28 wks BPD, HC, AC, FL >21 d

aBased on last menstrual period (LMP).

bUltrasound gestational age should be used if it differs

from the LMP-derived gestational age by more than the

threshold value.

AC = abdominal circumference; BPD = biparietal diameter; CRL = crown-rump length; FL = femur length;

HC = head circumference.

A B



FIGURE 14-1 A. The measured crown-rump length is approximately 7 mm in this 6-week embryo. B. M-mode demonstrates embryonic

cardiac activity and a heart rate of 124 beats per minute.Obstetrical Imaging 249

CHAPTER 14

College o Obstetricians and Gynecologists, 2020; American

Institute o Ultrasound in Medicine, 2018a). Te rst trimester

is the ideal time to evaluate the uterus, adnexa, and cul-desac. Ultrasound interrogation at this time can reliably diagnose

anembryonic gestation, embryonic demise, ectopic pregnancy,

and gestational trophoblastic disease. In a multietal gestation,

determination o chorionicity is most accurate in the rst trimester (Chap. 48, p. 841). Gestational sac implantation in a

prior cesarean scar is increasingly detected in the rst trimester

as well.

An intrauterine gestational sac may be consistently visualized with transvaginal sonography by 5 weeks’ gestation, and an

embryo with cardiac activity by 6 weeks. Te embryo should be

visible transvaginally once the mean sac diameter has reached

25 mm—otherwise the gestation is anembryonic. Whenever

an embryo or etus is identied, it should be measured, and

cardiac motion should be documented with either video clip

or M-mode scanning (see Fig. 14-1B). Cardiac motion may

be visible with transvaginal imaging when the length o the

embryo is 2 mm and should be visible at 7 mm in a live embryo

(American College o Obstetricians and Gynecologists, 2020).

I an embryo measures <7 mm and has no visible cardiac activity, subsequent examination is recommended in 1 week (American Institute o Ultrasound in Medicine, 2018a). At Parkland

Hospital, rst-trimester demise is diagnosed with transvaginal

ultrasound i the embryo has reached 10 mm and lacks cardiac

motion, taking measurement error into consideration. Criteria to diagnose rst-trimester demise are ound in able 11-2

(p. 202).

A recent addition to the standard rst-trimester examination

is an assessment o selected anatomical components when etal

size permits. Tese include the calvarium, umbilical cord insertion into the ventral wall, and presence o extremities (American Institute o Ultrasound in Medicine, 2018a).

■ Nuchal Translucency

Tis represents the maximum thickness o the subcutaneous

translucent area between the skin and sot tissue overlying the

etal spine at the back o the neck. Te nuchal translucency

(N) is measured in the sagittal plane between 11 and 14

weeks’ gestation using precise criteria (Table 14-4) (American

Institute o Ultrasound in Medicine, 2018a; International Society o Ultrasound in Obstetrics and Gynecology, 2016). When

the N measurement is increased, the risk or etal aneuploidy

and various structural anomalies—in particular heart deects—

is signicantly elevated. It is a component o rst-trimester



TABLE 14-3. Components of Standard Ultrasound Examination by Trimester

First Trimestera Second and Third Trimester

Gestational sac size, location, and number

Embryo and/or yolk sac identification

Crown-rump length

Gestational age assessment

Fetal number, including amnionicity and chorionicity

of multifetal gestations

Embryonic/fetal cardiac activity, documented with

M-mode or 2-dimensional video clip

Fetal anatomy assessment including calvarium,

nuchal region, ventral wall cord insertion, and

presence of limbs (depending on gestational age

and fetal size)

Fetal nuchal translucency assessment

Maternal uterus, adnexa, and cul-de-sac evaluation

Gestational age assessment

Fetal number, including amnionicity and chorionicity of multifetal

gestations

Fetal weight estimation

Fetal anatomical survey, including documentation of technical

limitations

Fetal cardiac activity, documented with M-mode or 2-dimensional

video clip

Fetal presentation

Amnionic fluid measurement (single deepest pocket, amniotic fluid

index, or qualitative assessment)

Placental location, appearance, and relationship to internal

cervical osa

Placental cord insertion site documentation when technically

possible

Evaluation of the maternal uterus, adnexa, and cervixa

aIf a transabdominal examination is not definitive, transvaginal (or transperineal) evaluation is recommended.



TABLE 14-2. Indications for First-Trimester Ultrasound

Examination

Confirm an intrauterine pregnancy

Estimate gestational age

Confirm cardiac activity

Diagnose/evaluate a multifetal gestation, including

chorionicity and amnionicity

Assess for certain fetal anomalies, such as anencephaly

Measure fetal nuchal translucency, when part of an

aneuploidy screening program

Evaluate for uterine abnormalities or pelvic masses

Evaluate for suspected ectopic pregnancy

Evaluate for suspected gestational trophoblastic

disease

Evaluate for the cause of vaginal bleeding

Evaluate for the cause of pelvic pain

Serve as adjunct to embryo transfer, chorionic villus

sampling, and intrauterine device localization and

removal250 The Fetal Patient

Section 6

TABLE 14-5. Indications for Standard Second- and

Third-trimester Ultrasound Examinations

Routine evaluation of gestational age and fetal anatomya

Fetal growth evaluation or size-date discrepancy

Fetal abnormality (follow-up evaluation)

Amniocentesis or other procedure

Cervical length assessment

Multifetal gestation

Vaginal bleeding

Placenta previa or low-lying placentab

Vasa previab

Placenta accreta spectrumb

Placental abruptionb

Uterine or adnexal abnormalityb

Gestational trophoblastic diseaseb

Amnionic fluid volume abnormalityb

Preterm rupture of membranes or preterm labor

Inability to document fetal heart tones

Assessment of fetal well-being

Assessment of fetal presentation

Adjunct to external cephalic version

aStandard ultrasound examination should be offered in all

pregnancies, ideally at 18–20 weeks’ gestation.

bIncludes evaluation of suspected cases.



TABLE 14-4. Guidelines for Nuchal Translucency (NT)

Measurement

Angle of insonation is perpendicular to NT line

Fetus is measured in midsagittal plane, with nasal tip,

palate, and diencephalon visible

Margins of NT edges are visible

Majority of image is filled by the fetal head, neck, and

upper thorax

Fetal neck lies in a neutral position, not flexed or

hyperextended

Amnion line must be separate from the NT line

+ calipers are placed perpendicular to the fetal long axis,

on the inner borders of the nuchal membranes, with

none of the horizontal crossbar protruding into the

space

Measurement should be obtained at the widest NT space

Largest of 3 NT measurements should be used

SECOND- AND THIRD-TRIMESTER

ULTRASOUND

Ultrasound should be routinely oered to all pregnant

women between 18 and 22 weeks’ gestation (American College o Obstetricians and Gynecologists, 2020). Recognizing

that the gestational age at which an abnormality is identied

may aect pregnancy management options, providers oten

opt to perorm the examination beore 20 weeks. Indications or second- and third-trimester sonograms are listed in



Table 14-5 (American College o Obstetricians and Gynecologists, 2020; American Institute o Ultrasound in Medicine, 2018a). Based on data rom large insurance providers,

pregnant women typically receive at least 4 to 5 sonograms

per pregnancy (O’Keee, 2013). Examinations are classied

as standard, specialized, or limited. Specialized examination

types include the detailed etal anatomy examination, detailed

evaluation or placenta accreta spectrum (p. 253), etal echocardiography, Doppler velocimetry (p. 262), and the biophysical prole (Chap. 20, p. 389).

■ Standard Second and ThirdTrimester

Ultrasound Examinations

Te standard examination includes evaluation o etal number

and presentation, cardiac activity, etal biometry, amnionic

uid volume, placental location, cervical length, and a survey

o etal anatomy (see able 14-3). Anatomical components are

listed in able 15-1 (p. 273). With twins or other multiples,

documentation should also include the number o chorions

aneuploidy screening, which is discussed in Chapter 17

(p. 337). Te aneuploidy risk calculation depends on the

crown-rump length. However, an N measurement ≥3 mm

is associated with increased risk or etal structural or genetic

abnormalities and is an indication or a detailed etal anatomical survey.

■ Detailed FirstTrimester Ultrasound

Examination

Assessment or etal abnormalities in an at-risk pregnancy may

include a detailed survey o etal anatomy at 12 to 14 weeks’

gestation. Such examinations are a recent addition and limited

to specialized centers with advanced imaging skills, although

use may be expected to expand. Despite improvements in imaging technology, it is not realistic to expect that all major abnormalities detectable in the second trimester may be visualized in the

rst trimester. Abnormalities may change in appearance as the

etus develops, and new ndings may become evident. I an

abnormality is identied in the rst trimester, detailed secondtrimester sonography will be important to urther characterize

the ndings or identiy associated abnormalities. In an at-risk

pregnancy, a normal rst-trimester examination does not obviate the recommendation or a detailed second-trimester etal

anatomical survey.

In a systematic review o more than 118,000 pregnancies

undergoing etal N assessment, 46 percent o major abnormalities were detected in low-risk or unselected pregnancies

(Karim, 2017). In high-risk pregnancies, anomaly detection

exceeded 60 percent. Detection rates are high or etal anencephaly, alobar holoprosencephaly, and ventral wall deects.

However, in one series o 40,000 pregnancies with etal anatomical evaluation at the time o N assessment, only a third

o major cardiac anomalies were identied. No cases o microcephaly, agenesis o the corpus callosum, cerebellar abnormalities, congenital pulmonary airway malormations, or bowel

obstruction were detected (Syngelaki, 2011). Some o these

abnormalities had not yet developed by the end o the rst

trimester, and this is an important caveat or counseling.Obstetrical Imaging 251

CHAPTER 14

and amnions, comparison o etal sizes, estimation o amnionic

uid volume within each sac, and etal phenotypic gender.

Te American Institute o Ultrasound in Medicine (2018a)

revised its prior 2013 standard ultrasound practice parameter to

include the ollowing updates:

1. Components added to the standard etal anatomical survey

are presence o the hands and eet, and when easible, the

three-vessel view and three-vessel trachea views o the heart

(Fig. 15-37, p. 290).

2. I the relationship between placenta and cervix cannot be

assessed transabdominally, transvaginal evaluation should be

perormed. ransperineal evaluation remains an option but

in our experience is rarely used.

3. I the cervix appears abnormal or is not adequately visualized

transabdominally, transvaginal (or transperineal) examination

is recommended. I cervical length assessment is requested,

measurement should be based on a transvaginal image.

4. In the setting o velamentous cord insertion, color and

pulsed Doppler ultrasound should be used to evaluate or

vasa previa (Figs. 6-6 and 6-7, p. 115).

■ Detailed Second and ThirdTrimester

Ultrasound Examinations

Te detailed etal anatomy examination is also known as a targeted or 76811 examination. It is perormed when the risk or a

etal structural or genetic abnormality is elevated because o history, screening test result, or abnormal nding during standard

examination (Table 14-6) (American Institute o Ultrasound

in Medicine, 2019). Te detailed ultrasound examination is

intended to be indication-driven and is not repeated without an

extenuating circumstance, such as a new risk actor (American

Institute o Ultrasound in Medicine, 2019). Physicians who

perorm or interpret these ultrasound examinations should

have gained expertise in etal imaging through both training

and ongoing experience (American College o Obstetricians

and Gynecologists, 2020).

Components o the detailed examination are intended to

be determined on a case-by-case basis. able 15-1 (p. 273)

lists nearly 70 anatomical components that may be included.

When practices apply or adjunct accreditation in perormance

o the detailed etal anatomic survey, the American Institute o

Ultrasound in Medicine species 50 components that must be

included when submitting normal cases or review. At Parkland

Hospital, we attempt to image these components in all detailed

anatomic surveys. When perorming a given detailed examination, one challenge is determining which components are

needed or a given indication, as these have not been codied.

Te most prevalent risk actors and thus indications or detailed

ultrasound examinations are maternal obesity and maternal

age ≥35 years. In a systematic review o more than 16,000

pregnancies aected by anomalies, obesity conerred modestly



TABLE 14-6. American Institute for Ultrasound in Medicine Indications for Detailed

Second- and Third-trimester Ultrasound Examinations

Prior fetus or infant with a structural or genetic abnormality

Current pregnancy with known or suspected fetal abnormality or growth restriction

Increased risk for fetal structural abnormality in current pregnancy

Teratogen exposure (Chap. 8)

Diabetes diagnosed before 24 weeks’ gestation

Nuchal translucency ≥3.0 mm

Abnormal serum analyte levels (e.g., elevated alpha fetoprotein)

Assisted reproductive technology used to achieve conception

Prepregnancy body mass index ≥30 kg/m2

Multifetal gestation

Increased risk for fetal genetic abnormality in current pregnancy

Woman or her partner carries a genetic abnormality

Maternal age ≥35 years at delivery

Nuchal translucency ≥3.0 mm

Abnormal aneuploidy screening test result (Chap. 17, p. 333)

Minor aneuploidy marker found during standard ultrasound examination

Other condition affecting the fetus

Congenital infection (Chaps. 67, 68)

Substance abuse

Alloimmunization (Chap. 18, p. 352)

Amnionic fluid volume abnormality

Suspected placenta accreta spectrum or associated risk factors

Adapted with permission from American Institute of Ultrasound in Medicine (AIUM):

Practice parameter for the performance of detailed second- and third-trimester diagnostic

obstetric ultrasound examinations. J Ultrasound Med 38(12):3093, 2019.252 The Fetal Patient

Section 6

increased odds o a neural-tube deect (1.9), ventriculomegaly

(1.7), cardiovascular anomaly (1.3), clet lip/palate (1.2), anorectal atresia (1.5), and limb reduction deect (1.7) (Stothard,

2009). Subsequently, Biggio and colleagues (2010) reported

that obesity was associated with a higher anomaly prevalence

only in the setting o diabetes. Maternal age ≥35 years is considered another indication or detailed sonographic examination. However, the etal anomaly risk may be related to the

associated increase in aneuploidy. Goetzinger and colleagues

(2017) ound that the anomaly rate among euploid etuses

born to older mothers was not increased.

■ Fetal Echocardiography

Tis specialized examination o etal cardiac structure and unction is designed to identiy and characterize abnormalities.

Echocardiography indications include suspected etal cardiac

structural or unctional abnormality; heart rate abnormality or

arrhythmia; extracardiac anomaly or hydrops; chromosomal

abnormality; nuchal translucency ≥3.5 mm; in vitro ertilization; monochorionic twin gestation; rst-degree relative to the

etus with a congenital cardiac deect; rst- or second-degree

relative to the etus with a Mendelian syndrome and childhood

cardiac maniestation; prior etus with heart block in the setting

o maternal anti-Ro or La antibodies; retinoid exposure; and

metabolic risk actor such as pregestational diabetes or phenylketonuria (American Institute o Ultrasound in Medicine, 2020a).

Selected cardiac anomalies are reviewed in Chap. 15 (p. 291).

■ Limited Ultrasound Examination

A limited second- or third-trimester examination is perormed

to address a specic clinical question. Evaluation o etal number, presentation, and cardiac activity; amnionic uid volume;

and placental location with respect to the internal os are common indications (American Institute o Ultrasound in Medicine, 2018b). Te examination may include etal biometry but

not a complete anatomical survey. In the absence o an emergency, a limited examination is perormed only i a standard

ultrasound survey has already been completed. Otherwise, provided that the gestational age is at least 18 weeks, a standard

ultrasound examination is recommended.

■ Fetal Anomaly Detection

With current advances in imaging technology, approximately

60 percent o major etal abnormalities may be detected during standard ultrasound examinations (Byrne, 2020; Rydberg,

2017). For detailed ultrasound surveys perormed in pregnancies at increased risk or anomalies, detection rates may exceed

90 percent (Dashe, 2009; Levi, 1998). Te sensitivity o the

examination varies according to actors such as gestational age,

maternal habitus, etal position, equipment eatures, examination type, operator skill, and the specic abnormality. For

example, maternal obesity lowers the anomaly detection rate by

20 percent (Dashe, 2009).

Detection rates vary considerably according to the abnormality. In the EUROCA network o 28 population-based

registries, 40 percent o major etal abnormalities are detected

prenatally (EUROCA, 2019). Detection rates o selected

abnormalities are as ollows: anencephaly, 98 percent; spina

bida, 89 percent; hydrocephaly, 82 percent; clet lip/palate,

70 percent; hypoplastic let heart, 88 percent; transposition o

the great vessels, 69 percent; diaphragmatic hernia, 73 percent;

gastroschisis, 92 percent; omphalocele, 90 percent; bilateral

renal agenesis, 94 percent; posterior urethral valves, 80 percent;

limb reduction deects, 60 percent; and cluboot, 60 percent.

In contrast, anomalies with poor sonographic detection rates

in the second trimester include microcephaly, choanal atresia,

clet palate, Hirschsprung disease, anal atresia, and congenital

skin disorders. Although clinicians tend to ocus on abnormalities amenable to sonographic detection, those that are undetectable can be no less devastating to amilies. Every sonographic

examination should include a rank discussion o examination

limitations.

■ ThreeDimensional Ultrasound Examination

Over the past three decades, three-dimensional (3-D) ultrasound has gone rom a novelty to a eature o all modern

equipment. Ater a region o interest is identied, a volume is

acquired using a 3-D transducer. Tis volume can be rendered

to display axial, sagittal, coronal, or oblique images. Sequential slices may be generated, similar to computed tomographic

(C) images. Unlike two-dimensional (2-D) scanning, which

appears to be happening in real time on the screen, 3-D imaging is static and obtained by processing a volume o stored

images. With our-dimensional ultrasound, rapid reconstruction

o the rendered images conveys the impression that the scanning is in real time.

For selected anomalies, such as those o the ace and skeleton, or tumors, and or some cases o neural-tube deects, 3-D

sonography can add useul inormation (American College o

Obstetricians and Gynecologists, 2020; Goncalves, 2005). Tat

said, comparisons o 3-D and conventional 2-D sonography or

the diagnosis o most congenital anomalies have not demonstrated better overall detection rates (Goncalves, 2006; Reddy,

2008). Te American College o Obstetricians and Gynecologists (2020b) has concluded that proo o a clinical advantage

o 3-D ultrasound or prenatal diagnosis is generally lacking.

PLACENTA AND CERVIX

Te standard examination includes evaluation o the anatomical relationship between the placenta and the internal cervical

os, the umbilical cord insertion into the placenta, and cervical length assessment. (American Institute o Ultrasound in

Medicine, 2018a). Evaluation or placenta accreta spectrum is

a detailed examination type (see able 14-6).

■ Placenta Previa and Lowlying Placenta

Te location o the placenta with respect to the cervix may

be accurately assessed by approximately 16 weeks’ gestation. I transabdominal visualization is limited, transvaginal

ultrasound is recommended. Placenta previa is diagnosed i

the placenta overlies the internal cervical os to any degree orObstetrical Imaging 253

CHAPTER 14

reaches its margin (Fig. 14-2A). I the inerior placental edge

is within 2 cm o the internal os but does not reach the cervix,

the diagnosis is low-lying placenta (see Fig. 14-2B). Whenever

placenta previa or low-lying placenta are diagnosed, a ollowup ultrasound examination is recommended at approximately

32 weeks’ gestation, with transvaginal evaluation i needed to

veriy the relationship between the placenta and cervix. I ndings persist, a 36-week ultrasound examination also is recommended. Management o these placenta types are discussed in

Chapter 43 (p. 757).

Te umbilical cord insertion into the placenta should be

interrogated. Marginal cord insertion, also known as battledore

placenta, is diagnosed i the umbilical cord inserts into the edge

o the placenta or within 2 cm o the placental margin. I the

umbilical cord does not insert into the placenta—but rather

into the membranes—the diagnosis is velamentous cord insertion

(Fig. 6-6, p. 115). With the latter, the umbilical arteries and

vein traverse the membranes along the uterine wall unprotected

by Wharton jelly beore entering the placental margin. I umbilical vessels course within the portion o membrane overlying the

cervix or within 2 cm o the cervix, the diagnosis is vasa previa

(Fig. 6-7, p. 116). Vasa previa may also occur i there are two

or more placental lobes—as with a succenturiate lobe—and the

interconnecting vessels traverse the intervening membranes over

or in proximity to the internal cervical os. ransvaginal ultrasound with color Doppler highlights the vessels, and pulsedwave Doppler o the spanning arterial vessel demonstrates a etal

heart rate, which conrms the diagnosis. A subsequent detailed

ultrasound examination is recommended at 32 weeks’ gestation (Society or Maternal-Fetal Medicine, 2015b). Chapter 6

(p. 114) contains content on management o these entities.

■ Placenta Accreta Spectrum

Placenta accreta, increta, and percreta comprise the placenta

accreta spectrum (PAS). Tey are characterized by abnormal placental invasion onto, into, or through the myometrium, respectively (Chap. 43, p. 759). Evaluation includes transabdominal

and transvaginal imaging, with and without color or power

Doppler and with the patient’s bladder partially lled. In one

metaanalysis that included more than 3200 pregnancies, the

sensitivity o ultrasound to identiy placenta accreta, increta,

and percreta was 91, 93, and 89 percent, respectively. Corresponding specicities were 97, 98, and 99 percent, respectively

(Pagani, 2018). Five ultrasound criteria assist with detection

and characterization o PAS (Fig. 14-3):

1. Placental lacunae, which are vascular spaces that may contain

prominent color Doppler ow

2. Attenuation or thinning o the retroplacental myometrium,

such that the smallest myometrial thickness measurement is

<1 mm. Tis is also reerred to as loss o the retroplacental

clear space

3. Disruption o the bladder-uterine serosal interace, which

appears as an irregular, echogenic boundary between the

bladder and uterine serosa with gray-scale imaging

4. Bridging vessels, which are demonstrated with color Doppler

to course rom the placenta to the bladder-serosal interace

5. A placental “bulge” that pushes outward and distorts the

contour o the uterus or other organs. In some cases o placenta percreta, a ocal exophytic mass also is seen.

Te accuracy o these criteria varies in published series

and is aected by the number and predictive value o given

ndings and by associated risk actors such as placenta previa

and number o prior cesarean deliveries (Jauniaux, 2016; Rac,

2015). Serial evaluation may be helpul, particularly in the

third trimester. With concurrent placenta previa and history o

cesarean delivery, any o these ultrasound ndings prompts a

detailed ultrasound evaluation. Te role o magnetic resonance

(MR) imaging as an adjunct in pregnancies with suspected PAS

is reviewed later (p. 268).

■ Cesarean Scar Pregnancy

Placental implantation within a prior hysterotomy scar—

termed cesarean scar pregnancy (CSP)—is oten a precursor

A B



FIGURE 14-2 A. Placenta previa. In this transvaginal image, the inferior edge (arrow) of the posterior placenta (P) overlies the internal

cervical os (arrowhead). H = head. B. Low-lying placenta. The inferior placental edge (arrow) is within 2 cm of the internal cervical os (arrowhead) in this transvaginal image. The bladder (B) is seen anterior to the cervix.254 The Fetal Patient

Section 6

to second- or third-trimester PAS (Happe, 2020; Rac, 2016;

imor-risch, 2014). Sonographically, the gestational sac

lies low and anteriorly in the uterus. CSPs may appear to

rest on the prior scar or may ll the niche, which is a myometrial pocket deect in the thinned hysterotomy scar (Kaelin Agten, 2017). Placental sonolucencies, a precursor to

PAS lacunae, may be seen. Te retroplacental myometrium

may be attenuated to a degree that the distance rom the

anterior trophoblastic border to the uterine serosa measures

<3 mm (D’Antonio, 2018; Moschos, 2014; Happe, 2020).

Color Doppler may demonstrate prominent vascularity

in the region o the prior hysterotomy scar (Fig. 14-4). In

some cases, the gestational sac may bulge toward the bladder.

CSP evaluation and management are discussed in Chapter

12 (p. 229).

■ Cervical Length

Although the cervix may be imaged transabdominally

(Fig. 14-5A), visualization is oten limited by maternal habitus,

cervical position, or shadowing by the etal presenting part. In

addition, the maternal bladder or pressure rom the transducer

may articially elongate the cervix’s appearance. As a result,

values rom transabdominal or transvaginal measurement o the

cervix can dier signicantly.

I the cervix appears short or is inadequately visualized during transabdominal evaluation, transvaginal assessment should

be considered (American Institute o Ultrasound in Medicine,

2018a). Clinical decision-making should use only cervical

length measurements obtained transvaginally (Fig. 14-5B).

Measurement should be perormed at or beyond 16 weeks’

gestation. A short cervix is associated with an elevated risk or

preterm birth, particularly in those with prior preterm birth.

Risk rises proportionally with the degree o cervical shortening

(Chap. 45, p. 793).

o measure the cervix transvaginally, the imaging criteria shown in Table 14-7 are ollowed. Te endocervical canal

should be visible in its entirety, and images ideally are obtained

over several minutes to capture dynamic change. Funneling is a

protrusion o amnionic membranes into a portion o the endocervical canal that has dilated (Fig. 14-6). Funneling is not an

independent predictor o preterm birth but is associated with

cervical shortening. ransvaginal assessment is recommended

i a unnel is suspected transabdominally. Te cervical length is

measured distal to the unnel, because the unnel’s base becomes

the unctional internal os. I the cervix is dilated, as with cervical

insufciency, the membranes may prolapse through the endocervical canal and into the vagina to produce an hourglass appearance. Sludge represents an aggregate o particulate matter (debris)

within the amnionic sac and close to the internal os. In pregnancies at risk or preterm birth, sludge urther raises the risk.

AMNIONIC FLUID

■ Physiology

Amnionic uid serves several roles. Fetal breathing is essential or normal lung growth, and etal swallowing permits

A B C



FIGURE 14-3 These third-trimester sonograms demonstrate findings that characterize placenta accreta spectrum. A. Transabdominal color mapping depicts bridging vessels between the bladder

and the uterine serosa (arrowheads) and shows large intraplacental

lacunae (arrow). B. Transvaginal transverse image showing a large

bulge (suggesting placenta percreta) along the bladder-uterine

serosal interface (arrowheads) and multiple large, irregular lacunae (arrows). C. Disruption of the bladder-serosal interface. The

echogenic interface between bladder and serosa appears irregular

(arrowheads). The smallest myometrial thickness measures <1 mm,

and bridging vessels are highlighted by color Doppler. Large lacunae also are shown (arrows).Obstetrical Imaging 255

CHAPTER 14

A B

C D



FIGURE 14-4 Cesarean scar pregnancy, transvaginal images. A. The trophoblast appears to fill the scar “niche” (arrows). B. Outward

bulging of the gestational sac toward the bladder (arrowheads). C. Placental sonolucencies (arrows). D. Attenuation of the retroplacental

myometrium. The distance from the anterior trophoblastic border to the uterine serosa is <1 mm (arrows). Color Doppler demonstrates

vascularity in the region of the prior hysterotomy scar.

A B



FIGURE 14-5 A. Transabdominal image of the cervix depicting the internal os and external os. B. Transvaginal imaging provides a more

accurate evaluation of the cervix and should be used for medical decision-making. In this image, arrowheads mark the endocervical canal.

(Reproduced with permission from Dr. Emily Adhikari.)256 The Fetal Patient

Section 6

Early in pregnancy, amnionic uid is similar in composition

to extracellular uid. Amnionic uid arises as a transudate o

plasma either rom the etus through its nonkeratinized skin

or rom the mother across the uterine decidua and placenta

surace (Beall, 2007). Specically, early transer o water and

other small molecules occurs via three mechanisms: across the

amnion—transmembranous fow; across etal vessels on the placental surace—intramembranous fow; and across etal skin—

transcutaneous fow. Fetal urine production does not become a

major component o amnionic uid until the second trimester, which explains why etuses with lethal renal abnormalities

may not maniest severe amnionic volume declines until ater

18 weeks’ gestation. Water transport across the etal skin continues until keratinization occurs at 22 to 25 weeks. In the second hal o pregnancy, etal urination is the primary source

o amnionic uid. In late gestation, the etal respiratory tract

also produces approximately 350 mL o lung uid per day.

Fetal swallowing is the primary mechanism or amnionic uid

resorption and averages 500 to 1000 mL per day (Mann, 1996).

By term, the entire amnionic uid volume is recirculated on a

daily basis (Table 14-8). However, impaired swallowing, secondary to either a central nervous system (CNS) abnormality

or GI tract obstruction, can result in impressive amnionic uid

volume expansion.

Te osmolality o amnionic uid is similar to that o etal

urine and hypotonic to that o maternal and etal plasma. Specically, the osmolality o maternal and etal plasma approximates 280 mOsm/mL, whereas that o amnionic uid is about



FIGURE 14-6 Transvaginal image depicting a foreshortened

cervix with funneling. Funneling is a protrusion of amnionic membranes into a portion of the endocervical canal that has dilated.

The distal protruding edge of the funnel becomes the functional

internal os (left arrow). Thus, the measured cervical length, which lies

between the arrows, should not include the funnel. (Reproduced

with permission from Dr. Emily Adhikari.)



TABLE 14-7. Criteria for Transvaginal Evaluation of the Cervix

Imaging the Cervix

Maternal bladder should be empty.

Transducer is inserted under real-time observation, identifying midsagittal plane, internal os, and then external os, while

keeping the internal os in view.

Internal os, external os, and entire endocervical canal should be visible. The internal os may appear as a small triangular

indentation at the junction of the amnionic cavity and endocervical canal.

Image is enlarged so that the cervix fills approximately 75% of the screen.

Anterior and posterior width of the cervix should be approximately equal.

Transducer is pulled back slightly until the image begins to blur, ensuring that pressure is not placed on the cervix, then

inserted only enough to restore a clear image.

Images should be obtained with and without fundal or suprapubic pressure, to assess for dynamic change or shortening

on real-time imaging.

Measuring the Cervix

Calipers are placed at the point where anterior and posterior walls of cervix meet.

Endocervical canal appears as a faint, linear echodensity.

If canal has a curved contour, a straight line between the internal and external os will deviate from the path of the

endocervical canal.

If midpoint of the line between the internal and external canal deviates by ≥3 mm from the endocervical canal, measure

the cervical length in two linear segments.

Funneling, sludge (debris), or dynamic change is noted.

At least three separate images are measured during a period of at least 3 minutes to allow for dynamic change.

Visualization of cervical shortening on real-time imaging, with or without fundal or suprapubic pressure, raises preterm

birth risks.

Shortest cervical length image that meets all criteria should be used.

Adapted from American Institute of Ultrasound in Medicine, 2018a; Iams, 2013.

gastrointestinal (GI) tract development. Te uid also creates a

physical space or etal movement, which is necessary or neuromusculoskeletal maturation. Amnionic uid urther guards

against umbilical cord compression and protects the etus rom

trauma. It also has bacteriostatic properties.Obstetrical Imaging 257

CHAPTER 14

260 mOsm/L. Te hypotonicity o amnionic uid accounts or

up to 400 mL per day o intramembranous uid transer across

and into etal vessels on the placental surace (Mann, 1996).

Maternal dehydration can lead to higher maternal osmolality,

which avors uid transer rom the etus to mother and then

rom the amnionic uid compartment into the etus (Moore,

2010).

Amnionic uid volume expands rom approximately 30 mL

at 10 weeks’ gestation to 200 mL by 16 weeks and reaches

800 mL by the mid-third trimester (Brace, 1989; Magann,

1997). Using dye dilution, Magann and associates (1997)

reported that the average amnionic uid volume was approximately 400 mL between 22 and 30 weeks’ gestation, then rose

to 800 mL until 40 weeks, and subsequently declined by 8

percent per week. Tere was a wide normal range, particularly

in the third trimester. Abnormally decreased uid volume is

termed oligohydramnios, whereas abnormally increased uid

volume is termed hydramnios or polyhydramnios.

■ Semiquantitative Assessment

Evaluation o amnionic uid volume is a component o every

second- or third-trimester ultrasound examination. Volume is

measured semi-quantitatively using the single deepest pocket o

uid or the amnionic uid index (AFI). Both measurements are

reproducible and, in the setting o a uid abnormality, can be

ollowed serially over time to assess trends and aid communication among providers. For this reason, subjective assessment

alone is not recommended.

Te single deepest pocket o uid is measured in a sagittal plane with the ultrasound transducer held perpendicular to

the oor and parallel to the long axis o the woman. A pocket

should be at least 1 cm wide to be considered adequate, and the

measurement should not include etal parts or loops o umbilical cord. Color Doppler is generally used to veriy that umbilical cord is not within the measurement. Te measurement is

considered normal i it is >2 cm and <8 cm. Values below and

above this range indicating oligohydramnios and hydramnios,

respectively. Tese thresholds correspond to the 3rd and 97th

percentiles (Chamberlain, 1984). When evaluating twins and

other multietal gestations, a single deepest pocket is assessed in

each gestational sac, using the same normal range (Hernandez,

2012; Society or Maternal-Fetal Medicine, 2013). Te etal

biophysical prole similarly uses a single deepest vertical pocket

threshold o >2 cm to indicate normal amnionic uid volume

(Chap. 20, p. 389).

o measure the AFI, the uterus is divided into our equal

quadrants—the right and let upper and lower quadrants,

respectively. Te AFI is the sum o the single deepest pocket

rom each quadrant. In a study o 1400 measurements obtained

rom the INERGROWH-21st trial, the mean intra- and

interobserver variability o AFI measurements were each below

1 cm (Sande, 2015). wo standard deviations rom the mean,

however, reached 5 and 7 cm, respectively. As useul rule o

thumb, the AFI is generally three times higher than the single

deepest pocket o uid.

Te AFI is considered normal i >5 cm and <24 or 25 cm.

Using an AFI nomogram based on cross-sectional evaluation o

nearly 800 uncomplicated pregnancies, the mean AFI ranged

between 12 and 15 cm rom 16 weeks until 40 weeks’ gestation

(Moore, 1990). Other investigators have published nomograms

with similar mean values (Fig. 14-7) (Hinh, 2005; Machado,

2007).

■ Hydramnios

Abnormally increased amnionic uid volume complicates 1 to

2 percent o singleton pregnancies (Dashe, 2002; Khan, 2017;

Pri-Paz, 2012). Hydramnios may be categorized as mild i the

AFI is 25 to 29.9 cm; moderate, i 30 to 34.9 cm; and severe,

i ≥35 cm (Luo, 2017; Odibo, 2016). Using a single deepest

pocket o amnionic uid, as is done in multietal gestations,

mild hydramnios is dened as 8 to 9.9 cm, moderate as 10 to

11.9 cm, and severe hydramnios as ≥12 cm (Fig. 14-8). Mild

hydramnios accounts or approximately two thirds o cases and

is requently idiopathic and benign. By comparison, severe

hydramnios is ar more likely to have an underlying etiology

and to have consequences or the pregnancy.

Underlying causes o hydramnios include etal structural

abnormalities or genetic syndromes in approximately 15 percent and diabetes in 15 to 20 percent (Table 14-9). Selected

anomalies and the likely mechanism by which they cause

hydramnios are shown in Table 14-10. Congenital inection,

red blood cell alloimmunization, and placental chorioangioma

are less requent etiologies. Hydramnios may also complicate

syphilis and cytomegalovirus, toxoplasmosis, and parvovirus

inections (Chaps. 67 and 68, pp. 1183 and 1206). Hydramnios is oten seen with hydrops etalis (Chap. 18, p. 360). Te



TABLE 14-8. Amnionic Fluid Volume Regulation in Late Pregnancy

Pathway

Effect on

Volume

Approximate Daily

Volume (mL)

Fetal urination Production 1000

Fetal lung fluid secretion Production 350

Fetal swallowing Resorption 750

Intramembranous flow across fetal vessels on the

placental surface

Resorption 400

Transmembranous flow across amnionic membrane Resorption Minimal

Data from Magann, 2011; Modena, 2004; Moore, 2010.258 The Fetal Patient

Section 6

and 10 percent i hydramnios

was severe. Te overall reported

risk that an underlying anomaly

will be discovered ater delivery

ranges rom 9 percent in the

neonatal period to 28 percent

among inants ollowed to 1

year o age (Abele, 2012; Dorleijn, 2009).

Te amnionic uid glucose concentration is higher in

diabetic women than in those

without diabetes, and the AFI

may correlate positively with the

amnionic uid glucose concentration (Dashe, 2000; Spellacy,

1973; Weiss, 1985). Such ndings support the hypothesis that

maternal hyperglycemia causes

etal hyperglycemia, which leads

to etal osmotic diuresis into the

amnionic uid compartment.

Repeat screening or gestational

diabetes in pregnancies with

hydramnios does not appear to

be benecial i the second-trimester glucose tolerance test result

was normal (Frank Wol, 2017).

Hydramnios is more requently noted in multietal gestations than in singleton ones. In a review o nearly 2000

twin gestations, Hernandez and coworkers (2012) identied

hydramnios in 18 percent o both monochorionic and dichorionic pregnancies. In monochorionic gestations, hydramnios

in one sac and oligohydramnios in the other are diagnostic criteria or twin-twin transusion syndrome (S) (Chap. 48,

p. 848). Isolated hydramnios solely in one sac also may precede

this syndrome’s development (Chon, 2014). In the absence o a

etal abnormality or S, complication risks are not generally

higher (Hernandez, 2012).

Idiopathic hydramnios is a diagnosis o exclusion. It accounts

or up to 70 percent o all hydramnios cases, is mild in approximately 80 percent o idiopathic cases, and subsequently resolves

in more than one third (Odibo, 2016; Wiegand, 2016).

Management

Severe hydramnios occasionally results in early preterm labor or

maternal respiratory compromise. In such cases, large-volume

amniocentesis—termed amnioreduction—may be needed. Te

technique is similar to that or genetic amniocentesis but is generally done with an 18- or 20-gauge needle. Fluid is collected

in either a vacuum container bottle or a larger syringe (Chap.

17, p. 344). Approximately 1000 to 2000 mL o uid is slowly

withdrawn over 20 to 30 minutes, depending on the severity o

hydramnios and gestational age. Te goal is to restore amnionic

uid volume to the upper normal range. Subsequent amnioreduction procedures may be required as oten as weekly or semiweekly.

In a review o 138 singleton pregnancies requiring amnioreduction or hydramnios, a etal GI malormation was identied

in 20 percent, a chromosomal abnormality or genetic condition



FIGURE 14-8 Severe hydramnios. This pocket of amnionic fluid

measured >15 cm, and the amnionic fluid index measured nearly

50 cm.

underlying pathophysiology in such cases is requently related

to a high-cardiac-output state, and severe etal anemia a classic

example. A detailed ultrasound examination is indicated whenever hydramnios is identied. I a etal abnormality is identied

at that time, the aneuploidy risk is signicantly elevated.

Te degree o hydramnios positively correlates with the likelihood o an anomalous etus. At Parkland Hospital, the prevalence o an anomalous neonate approximated 8 percent with

mild hydramnios, 12 percent with moderate hydramnios, and

more than 30 percent with severe hydramnios (Dashe, 2002).

Even i no abnormality was detected during targeted sonographic evaluation, the likelihood o a major anomaly identied

at birth was 1 to 2 percent i hydramnios was mild or moderate

97.5th percentile

50th percentile

2.5th percentile

8 6 4 2 0

10

12

14

16

18

22

26

30

Mild hydramnios

Oligohydramnios

20

24

28

16 18 20 22 24 26 28 30 32 34 36 38 40 42

Weeks’ gestation

Amnionic fluid index (cm)

Moore, 1990 Machado, 2007 Hinh, 2005



FIGURE 14-7 Amnionic fluid index (AFI) according to gestational age–specific and threshold values. The blue curves represent the 2.5th, 50th, and 97.5th AFI percentile values, based on the nomogram by Moore (1990). Red and tan curves represent 50th percentile values for AFI from Machado

(2007) and from Hinh and Ladinsky (2005), respectively. The light blue and yellow shaded bars indicate threshold values used to define hydramnios and oligohydramnios, respectively.Obstetrical Imaging 259



CHAPTER 14

TABLE 14-10. Selected Anomalies and Mechanism for Hydramnios

Mechanism Anomaly Examples

Impaired swallowing (CNS) Anencephaly

Hydranencephaly

Holoprosencephaly

Impaired swallowing (craniofacial) Cleft lip/palate

Micrognathia

Tracheal compression or obstruction Neck venolymphatic abnormality

CHAOSa

Thoracic etiology (mediastinal shift) Diaphragmatic herniaa

Cystic adenomatoid malformationa

Pulmonary sequestrationa

High-output cardiac state Ebstein anomalya

Tetralogy of Fallot with absent pulmonary valvea

Thyrotoxicosisa

Functional cardiac etiology Cardiomyopathy, myocarditisa

Cardiac arrhythmia Tachyarrhythmiaa: atrial flutter, atrial fibrillation, supraventricular tachycardia

Bradyarrhythmiaa: heart block

GI obstruction Esophageal atresia

Duodenal atresia

Renal-urinary Ureteropelvic junction obstruction (“paradoxical hydramnios”)

Bartter syndrome

Neurological or muscular etiology Arthrogryposis, akinesia sequence

Myotonic dystrophy

Neoplastic etiology Sacrococcygeal teratomaa

Mesoblastic nephromaa

Placental chorioangiomaa

aPoses risk for hydrops.

CNS = central nervous system; CHAOS = congenital high-airway obstruction sequence; GI = gastrointestinal.



TABLE 14-9. Hydramnios: Prevalence and Associated Etiologies—Values in Percent

Golan (1993)

n = 149

Many (1995)

n = 275

Biggio (1999)

n = 370

Dashe (2002)

n = 672

PriPaz (2012)

n = 655

Prevalence 1 1 1 1 2

Amnionic fluid index

Mild 25–29.9 cm

Moderate 30–34.9 cm

Severe >35 cm

— 72

20

8

— 66

22

12

64

21

15

Etiology

Idiopathic

Fetal anomalya

Diabetes

65

19

15

69

15a

18

72

8

20

82

11a

7

52

38a

18

aA significant correlation was identified between severity of hydramnios and likelihood of an anomalous infant.

in almost 30 percent, and a neurological abnormality in 8 percent (Dickinson, 2014). In only 20 percent o cases was the

hydramnios idiopathic. Te initial amnioreduction procedure

was perormed at 31 weeks’ gestation, and the median gestational age at delivery was 36 weeks.

Outcomes

Hydramnios can be associated with preterm birth, placental

abruption, uterine dysunction during labor, and postpartum

hemorrhage. When an underlying cause is identied, the severity o hydramnios positively correlates with risk or preterm

delivery, small-or-gestational age newborn, and perinatal

mortality (Pri-Paz, 2012). However, idiopathic hydramnios is

generally not associated with preterm birth (Magann, 2010;

Many, 1995; Panting-Kemp, 1999). Placental abruption may

result rom rapid decompression o an overdistended uterus

ollowing rupture o membranes or therapeutic amnioreduction, occasionally days or weeks later. Uterine dysunction rom260 The Fetal Patient

Section 6

overdistention may lead to postpartum atony and associated

postpartum hemorrhage.

With idiopathic hydramnios, birthweight exceeds 4000 g in

nearly 25 percent o cases, and the likelihood is greater i the

hydramnios is moderate or severe (Luo, 2017; Odibo, 2016;

Wiegand, 2016). A rationale or this association is that larger

etuses have higher urine output, by virtue o their increased

volume o distribution, and etal urine is the largest contributor to amnionic uid volume. Cesarean delivery rates are also

higher in pregnancies with idiopathic hydramnios, and reported

rates range rom 35 to 55 percent (Dorleijn, 2009; Khan, 2017;

Odibo, 2016).

An unresolved question is whether hydramnios alone raises

the risk or perinatal mortality (Khan, 2017; Pilliod, 2015;

Wiegand, 2016). Using birth certicate data rom Caliornia,

Pilliod and colleagues (2015) reported that at 37 weeks’ gestation, the stillbirth risk was sevenold higher in pregnancies

with hydramnios. Risks appear to be compounded when etalgrowth restriction is comorbid with hydramnios (Erez, 2005).

■ Oligohydramnios

Abnormally decreased amnionic uid volume complicates 1 to

2 percent o pregnancies (Casey, 2000; Petrozella, 2011). Oligohydramnios is diagnosed i the AFI measures <5 cm or the

single deepest pocket is <2 cm (American College o Obstetricians and Gynecologists, 2020). An AFI threshold o 5 cm is

below the 2.5th percentile throughout the second and third

trimesters (see Fig. 14-7). Importantly, use o AFI rather than

single deepest pocket will identiy more pregnancies as having

oligohydramnios but without evidence o improved pregnancy

outcomes (Kehl, 2016; Nabhan, 2010). When evaluating multietal pregnancies or S, a single deepest pocket <2 cm is

used to dene oligohydramnios (American College o Obstetricians and Gynecologists, 2021c). When no measurable pocket

o amnionic uid is identied, the term anhydramnios is used.

By 18 weeks’ gestation, the etal kidneys are the main contributor to amnionic uid volume. Selected renal abnormalities that lead to absent etal urine production include bilateral

renal agenesis, bilateral multicystic dysplastic kidney, unilateral

renal agenesis with contralateral multicystic dysplastic kidney,

and the inantile orm o autosomal recessive polycystic kidney

disease. Lower urinary abnormalities may also cause oligohydramnios because o etal bladder outlet obstruction (Figs.

15-58 through 15-61, p. 300). Complex etal genitourinary

abnormalities such as persistent cloaca and sirenomelia similarly

may result in a lack o amnionic uid. With oligohydramnios beore the mid-second trimester, particularly beore 20 to

22 weeks, pulmonary hypoplasia is a signicant concern. Te

prognosis is extremely poor unless etal therapy is an option

(Chap. 19, p. 377).

Oligohydramnios is also associated with exposure to drugs

that block the renin-angiotensin system. Tese include angiotensin-converting enzyme (ACE) inhibitors, angiotensinreceptor blockers, and nonsteroidal antiinammatory drugs

(NSAIDs). When taken in the second or third trimester, ACE

inhibitors and angiotensin-receptor blockers may result in etal

hypotension, renal hypoperusion, and renal ischemia, leading

to subsequent anuric renal ailure (Bullo, 2012; Guron, 2000).

Fetal skull bone hypoplasia and limb contractures also have

been described (Schaeer, 2003). Additionally, NSAIDs can

be associated with etal ductus arteriosus constriction and

impaired etal urine production (Chap. 8, p. 151).

Oligohydramnios in the late second trimester or in the third

trimester is oten associated with uteroplacental insufciency.

A placental abnormality or a maternal complication such as

preeclampsia or vascular disease are examples. Initially, ruptured membranes should be excluded. Ten, particularly in

the second trimester, a detailed ultrasound examination should

be perormed to search or etal and placental abnormalities.

I a placental hematoma or chronic abruption is sufciently

severe to result in oligohydramnios—the chronic abruptionoligohydramnios sequence (CAOS)—then it commonly also

causes growth restriction (Chap. 43, p. 750).

Management

Oligohydramnios detected beore 36 weeks’ gestation in the

presence o normal etal anatomy and growth is generally managed expectantly and coupled with etal surveillance (Chap. 20,

p. 392). For late-preterm and early-term pregnancies, risks o

etal compromise outweigh potential complications o preterm

delivery. Te American College o Obstetricians and Gynecologists (2021b) recommends delivery between 360/7 and 376/7

weeks. In a review o 16 trials o pregnancies with apparent

isolated oligohydramnios, oral or intravenous hydration was

associated with a signicantly improved AFI. However, it was

unclear whether this translated into better pregnancy outcomes

(Gizzo, 2015).

Outcomes

In a review o pregnancies with oligohydramnios at Parkland

Hospital, Petrozella and associates (2011) ound that an AFI

<5 cm identied between 24 and 34 weeks’ gestation was

associated with increased risks or perinatal morbidity and

mortality (Table 14-11). Similarly, a metaanalysis comprising

more than 10,000 pregnancies ound that oligohydramnios

conerred a twoold risk or cesarean delivery due to nonreassuring etal status and a veold risk or an Apgar score <7

at 5 minutes compared with pregnancies with a normal AFI

(Chauhan, 1999).

As discussed, i oligohydramnios is dened as an AFI <5 cm

rather than a single deepest pocket <2 cm, more pregnancies

will be classied as such. Kehl and coworkers (2016) perormed

a prospective trial with more than 1000 term pregnancies in

which women with an AFI <5 cm or a single deepest pocket

<2 cm were randomly assigned to labor induction or expectant

care. Signicantly more pregnancies were diagnosed with oligohydramnios using the AFI criterion—10 percent compared

with just 2 percent—when single deepest pocket was used. Tis

led to a higher rate o labor induction in the AFI group but not

to a dierence in neonatal outcomes.

Borderline Oligohydramnios

Tis diagnosis is somewhat controversial. Also called borderline

AFI. It usually reers to an AFI between 5 and 8 cm (Magann,

2011; Petrozella, 2011). During the mid-third trimester, anObstetrical Imaging 261

CHAPTER 14

AFI value o 8 cm is below the 5th percentile on the Moore

nomogram (see Fig. 14-7). Petrozella (2011) ound that pregnancies between 24 and 34 weeks’ gestation with an AFI

between 5 and 8 cm were not more likely than those with an

AFI >8 cm to have maternal hypertensive complications or an

increased risk or stillbirth and neonatal death. Wood and colleagues (2014) reported a higher rate o etal-growth restriction

in pregnancies with borderline AFI but not an increase in rates

o preterm delivery or need or neonatal intensive care. In a

study o late-preterm pregnancies that were otherwise uncomplicated, borderline AFI conerred no increased risk or preterm

delivery, nonreassuring etal heart rate tracing, low Apgar score,

or neonatal respiratory compromise (Sahin, 2018). Evidence

is insufcient to support etal surveillance or delivery in this

setting (Magann, 2011).

DOPPLER

When sound waves strike a moving target, the requency o

the waves reected back is shited in proportion to the velocity

and direction o that moving target—a phenomenon known

as the Doppler shit. Because magnitude and direction o the

requency shit depend on the motion o a moving target, Doppler can help evaluate ow within blood vessels.

An important component o the Doppler equation is the

angle o insonation, abbreviated as theta (θ) (Fig. 14-9). Tis

is the angle between the sound waves rom the transducer and

ow within the vessel. Measurement error becomes large when

θ is not close to zero, in other words, when blood ow is not

coming directly toward or away rom the transducer. For this

reason, ratios are oten used to compare dierent waveorm

components and allow cosine θ to cancel out o the equation.

Figure 14-10 is a schematic o the Doppler waveorm and

describes the three ratios commonly used. Te simplest is the

systolic-diastolic ratio (S/D ratio), which compares the maximal (or peak) systolic ow with end-diastolic ow to evaluate

downstream impedance to ow. Currently, two types o Doppler modalities are available or clinical use.

Continuous-wave Doppler equipment contains two types

o crystals, one to transmit high-requency sound waves and

another to continuously capture signals. In M-mode imaging,

continuous-wave Doppler is used to evaluate motion through

time, however, it cannot image individual vessels.

Pulsed-wave Doppler uses only one crystal, which transmits

the signal and then waits until the returning signal is received

beore transmitting another one. It allows precise visualization

and color-ow mapping o the vessel o interest. By convention,



TABLE 14-11. Pregnancy Outcomes in Women Diagnosed with Oligohydramnios

between 24 and 34 Weeks’ Gestation at Parkland Hospital

Factor

AFI ≤5 cm

(n = 166)

AFI 8 to 24 cm

(n = 28,185) p Value

Major malformation 42 (25) 634 (2) <.001

Stillbirth 8 (5) 133 (<1) <.001

Gestational age at deliverya 35.1 ± 3.3 39.2 ± 2.0 <.001

Preterm birth, spontaneousa 49 (42) 1698 (6) <.001

Preterm birth, indicateda 23 (20) 405 (2) <.001

Cesarean delivery for nonreassuring fetal

statusa

10 (9) 1083 (4) <.001

Birthweight <10th percentilea 61 (53) 3388 (12) <.001

<3rd percentilea 43 (37) 1130 (4) <.001

Neonatal deatha 1 (1) 24 (<1) <.001b

Data expressed as No. (%) and mean ± standard deviation.

aAnomalous infants excluded.

bThis difference was no longer significant after adjustment for gestational age at delivery.

Data from Petrozella LN, Dashe JS, McIntire DD, et al: Clinical significance of borderline

amniotic fluid index and oligohydramnios in preterm pregnancy. Obstet Gynecol

117(2 pt 1):338, 2011.



FIGURE 14-9 Doppler equation. Ultrasound emanating from the

transducer with initial frequency fo strikes blood moving at velocity v.

Reflected frequency fd is dependent on angle θ between beam of

sound and vessel.262 The Fetal Patient

Section 6

blood owing toward the transducer is displayed in red and

that owing away rom the transducer appears in blue.

■ Umbilical Artery

Te umbilical artery diers rom other vessels in that it normally has orward ow throughout the entire cardiac cycle.

With advancing gestation, the amount o ow during diastole

increases because o decreasing placental impedance. Te S/D

ratio approximates ≤4.0 ater 20 weeks’ gestation, <3.0 ater

30 weeks’, and close to 2.0 at term. More end-diastolic ow is

observed at the placental cord insertion than at the etal ventral wall, a reection o downstream impedance to ow. Tus,

abnormalities such as absent or reversed end-diastolic ow will

appear rst at the cord insertion site into the etus. Te International Society o Ultrasound in Obstetrics and Gynecology

recommends that umbilical artery Doppler measurements be

made in a ree loop o cord (Bhide, 2013). However, assessment close to the ventral wall insertion may optimize measurement reproducibility in cases in which ow is diminished

(Berkley, 2012).

Te waveorm is considered abnormal i the S/D ratio is

>95th percentile or gestational age. Treshold values are listed

in the Appendix (p. 1242). In extreme cases o growth restriction, end-diastolic ow can become absent or even reversed

(Fig. 47, p. 830). Such reversal o end-diastolic ow has been

associated with greater than 70-percent obliteration o the

small muscular arteries in placental tertiary stem villi (Kingdom,

1997; Morrow, 1989).

Umbilical artery Doppler has been rigorously investigated to test o etal well-being. As described in Chapter 47

(p. 830), this tool aids management o etal-growth restriction and is associated with improved outcome in these cases

(American College o Obstetricians and Gynecologists, 2019a).

It is not recommended or other indications. Similarly, its use

as a screening tool or growth-restriction is not advised (Berkley, 2012). Abnormal umbilical artery Doppler ndings should

prompt a detailed etal evaluation, i not already done, because

abnormal measurements are oten associated with major etal

anomalies and aneuploidy (Wenstrom, 1991).

■ Ductus Arteriosus

Doppler evaluation o the ductus arteriosus is used primarily to

monitor etuses exposed to indomethacin and other NSAIDs.

Indomethacin may cause ductal constriction or closure, particularly when used in the third trimester (Huhta, 1987). Te

resulting increased pulmonary ow can cause reactive hypertrophy o the pulmonary arterioles and eventual development

o etal pulmonary hypertension. In a review o 12 randomized

trials involving more than 200 exposed pregnancies, Koren

and coworkers (2006) reported that NSAIDs raised the odds

o ductal constriction 15-old. Te risk is typically limited to

drug use greater than 72 hours’ duration. Monitoring or ductal constriction should be considered in such cases, so that the

NSAID can be discontinued i ductal constriction is identied.

Fortunately, eects are oten reversible ater NSAID discontinuation.

■ Uterine Artery

Uterine blood ow is estimated to rise rom 50 mL/min

early in gestation to 500 to 750 mL/min by term. Te uterine artery Doppler waveorm is characterized by high diastolic

ow velocities and turbulent ow. Greater resistance to ow

and development o a diastolic notch are associated with later

development o gestational hypertension, preeclampsia, and

etal-growth restriction. Zeeman and associates (2003) also

ound that women with chronic hypertension who had elevated

uterine artery impedance at 16 to 20 weeks’ gestation were at

greater risk to develop superimposed preeclampsia. However,

the technique, best testing interval, and dening criteria or this

indication have not been standardized. As the predictive value

o uterine artery Doppler testing is considered to be low, its use

or screening or hypertensive complications o pregnancy or

or etal-growth restriction is not recommended in either highrisk or low-risk pregnancies (American College o Obstetricians

and Gynecologists, 2019a, 2020b).

■ Middle Cerebral Artery

Doppler velocimetry o the middle cerebral artery (MCA) has

become the primary method o detecting etal anemia and is

central to surveillance o alloimmunized pregnancies. Anatomically, the path o the MCA is such that ow oten approaches

the transducer “head-on,” which allows accurate determination

o ow velocity (Fig. 14-11). Te MCA is imaged in an axial

view o the head at the base o the skull and ideally within

2 mm o the internal carotid artery origin. Velocity measurement is optimal when the insonating angle θ is close to zero,

and no more than 30 degrees o angle correction should be

used. In general, other etal vessels are not suitable or velocity assessment, because a larger insonating angle is needed and

coners signicant measurement error.



FIGURE 14-10 Doppler systolic–diastolic waveform indices of

blood flow velocity. S represents the peak systolic flow or velocity,

and D indicates the end-diastolic flow or velocity. The mean, which

is the time-average mean velocity, is calculated from computerdigitized waveforms.Obstetrical Imaging 263

CHAPTER 14

With etal anemia, the peak systolic velocity is enhanced due

to greater cardiac output and decreased blood viscosity (Segata,

2004). Tis permits the reliable, noninvasive detection o etal

anemia in cases o blood-group alloimmunization. Mari and

colleagues (2000) demonstrated that an MCA peak systolic

velocity threshold o 1.50 multiple o the median (MoM) could

reliably identiy etuses with moderate or severe anemia. As discussed in Chapter 18 (p. 355), MCA peak systolic velocity has

replaced invasive testing with amniocentesis as the preerred

test or etal anemia detection (Society or Maternal-Fetal Medicine, 2015a).

MCA Doppler has also been studied as an adjunct in evaluation o etal-growth restriction (Chap. 47, p. 830). Fetal

hypoxemia is associated with increased blood ow to the brain,

heart, and adrenal glands, which leads to greater end-diastolic

ow in the MCA. Tis phenomenon, called “brain-sparing,” is

actually a misnomer, as it does not protect the etus but rather

is associated with perinatal morbidity and mortality (BahadoSingh, 1999; Cruz-Martinez, 2011). o evaluate redistribution o blood ow, investigators have studied a ratio o the

MCA pulsatility index (PI) to the umbilical artery PI–termed

the cerebroplacental ratio. Like the S/D ratio, the PI estimates

downstream impedance to ow (Fig. 14-10). In the PORO

(Prospective Observational rial to Optimize Paediatric Health

in IUGR) study o ultrasound-dated pregnancies with estimated etal weights <10th percentile, etuses with a cerebroplacental PI ratio <1 had an 11-old greater risk or adverse

perinatal outcomes (Flood, 2014). Such ndings can urther

our understanding o etal pathophysiology. However, the utility o MCA Doppler to aid the timing o delivery is uncertain,

and it has not been adopted as standard practice in the management o growth restriction (American College o Obstetricians

and Gynecologists, 2021a; Martins, 2020).

■ Ductus Venosus

Te etal ductus venosus shunts oxygenated blood rom the

intrahepatic portion o the umbilical vein directly to the

inerior vena cava, thus bypassing the liver (Fig. 7-9, p. 127).

Te ductus venosus is imaged as it branches rom the umbilical

vein at approximately the level o the diaphragm. Te wave-

orm is biphasic and normally has orward ow throughout

the entire cardiac cycle (Fig. 14-12). Te rst peak reects

ventricular systole, and the second is ventricular diastolic lling. Tese are ollowed by a nadir during atrial contraction—

termed the a-wave.

It is believed that Doppler ndings in preterm etuses with

growth restriction show a progression in which umbilical artery

Doppler abnormalities are ollowed by ones in the MCA and

then in the ductus venosus. With severe etal-growth restriction, cardiac dysunction may lead to ow in the a-wave that is

decreased, absent, and eventually reversed and to pulsatile ow

in the umbilical vein (see Fig. 14-12). However, ductus venosus Doppler assessment has not improved perinatal outcomes,

and neither the American College o Obstetricians and Gynecologists (2021a) nor the Society or Maternal-Fetal Medicine

(Martins, 2020) recommend its use in the routine management

o etal growth-restriction.

MAGNETIC RESONANCE IMAGING

MR imaging is based on the excitation o hydrogen ions in

the body by pulsing radiorequencies with high eld-strength

magnets (1.5 to 3 esla). High-resolution etal imaging is now

possible, in part due to aster acquisition times o less than one

second per slice. Te relaxing hydrogen ions can be manipulated through various pulse sequences to produce dierent representations on images. Te classic example is simple uid, such

as amnionic uid or urine in the bladder, which appears bright

on 2-weighted and dark on 1-weighted image acquisitions.

Image resolution with MR is oten superior to that with

sonography because MR is less hindered by bony interaces,

maternal obesity, oligohydramnios, or an engaged etal head.

Tus, it can complement sonography in evaluating suspected

etal abnormalities. Examples include complex abnormalities o

the etal thorax and o the central nervous, GI, genitourinary,

A B



FIGURE 14-11 Middle cerebral artery (MCA) Doppler. A. Color Doppler of the circle of Willis demonstrates the correct location to sample

the MCA. B. The waveform shows a peak systolic velocity exceeding 70 cm/sec in a 32-week fetus with severe fetal anemia secondary to Rh

alloimmunization.264 The Fetal Patient

Section 6

and musculoskeletal systems. MR imaging is also used to

evaluate maternal pelvic masses and placental invasion. Tis

modality, however, is not portable, is time-consuming, and

is generally limited to reerral centers with expertise in etal

imaging.

o guide clinical use, the American College o Radiology

and Society or Pediatric Radiology (2020b) have developed

a practice guideline or etal MR imaging. Tis document

acknowledges the primacy o sonography as the preerred

screening modality. Moreover, it recommends that etal MR

imaging be used or problem solving to contribute to prenatal diagnosis, counseling, treatment, and delivery planning. At

Parkland Hospital, MR imaging is perormed in 15 percent

o pregnancies with major etal abnormalities (Herrera, 2020).

Specic indications are listed in Table 14-12 and are discussed

subsequently (American College o Radiology, 2020b).

■ Safety

MR imaging is not associated with known adverse etal eects

i perormed without administration o contrast media (Ray,

2016). It uses no ionizing radiation, and human and tissue studies support its saety (Clements, 2000; Reeves, 2010; Vadeyar,

2000; Wiskirchen, 1999). Te strength o the magnetic eld

is measured in tesla (T). Both 1.5 and 3 etal MR imaging can be done saely and successully, assuming expertise o

the imagers with the physical principles o MR (Prayer, 2017).

All clinical examinations must adhere to the specic absorption

rate, which is regulated by the FDA, and the ALARA principle

should be ollowed. Specically, the amount o heat generated

in the MR is reected in the specic absorption rate and must

be monitored.

Te Society or Pediatric Radiology recommends 3 MR

imaging because o its improved signal-to-noise ratio, which

results in better resolution (Barth, 2017). We preer 1.5 or

diagnostic imaging given its better eld homogeneity. We

reserve 3 or unctional imaging, which requires higher eld

strength.

Gadolinium-based MR contrast agents are gadolinium

(Gd3+) chelates. Tese contrast agents enter the etal circulation and are excreted via etal urination into amnionic uid.

Here, they may remain or an indeterminate period beore

being ingested and reabsorbed. Te longer time the gadolinium-chelate molecule remains in a protected space such as the

amnionic sac, the greater the potential or dissociation o the

toxic Gd3+ ion. In a population-based review rom Ontario,

children exposed to gadolinium-enhanced MR imaging in

utero were at slightly increased risk or a broad set o rheumatological, inammatory, or inltrative skin conditions (Ray,

2016). In adults with renal disease, this contrast agent is associated with development o nephrogenic systemic brosis, a

potentially severe complication. MR imaging with gadolinium

is not recommended in pregnancy without a lie-threatening

indication.

■ Technique

Beore MR imaging, all women complete a written saety questionnaire that includes inormation about metallic implants,

pacemakers, or other metal- or iron-containing devices. Highlevel magnetization may cause dangerous movement in these

devices, causing adjacent tissue damage and malunction.

(American College o Radiology, 2020a). Iron supplementation may cause image artiact in the colon but does not usually aect the resolution o etal images. In more than 4500

MR procedures perormed at Parkland Hospital in pregnancy

during the past 18 years, <1 percent o our patients suered

maternal anxiety secondary to claustrophobia. o reduce anxiety in this small group, a single oral dose o diazepam, 5 to 10

mg, or lorazepam, 1 to 2 mg, may be given.

A B



FIGURE 14-12 Venous Doppler abnormalities. A. Reversal of

a-wave flow in the ductus venosus. Arrows depict a-waves below

the baseline. This finding may be identified with cardiac dysfunction in the setting of severe fetal-growth restriction. B. Pulsatile

flow in the umbilical vein. The undulating umbilical venous waveform below the baseline indicates tricuspid regurgitation. Above

the baseline is the umbilical artery waveform, in which there is no

visible end-diastolic flow. Because the venous waveform is below

the baseline in this image, it is not possible to determine whether

the umbilical artery end-diastolic flow is reversed.Obstetrical Imaging 265

CHAPTER 14



TABLE 14-12. Fetal Conditions for Which Magnetic Resonance Imaging May Be Indicateda

Brain and spine

Agenesis of the corpus callosum

Cavum septum pellucidum abnormalities

Cephalocele

Cerebral cortical malformation or migrational abnormalities

Family history conferring a risk for brain anomaly

Hemorrhage

Holoprosencephaly

Hydranencephaly

Infarctions

Monochorionic twin pregnancy complications

Neural-tube defects

Posterior fossa abnormalities

Sacral agenesis (caudal regression)

Sacrococcygeal teratoma

Sirenomelia

Solid or cystic masses

Vascular malformations

Ventriculomegaly

Vertebral anomalies

Skull, face, and neck

Facial clefts

Goiter

Hemangiomas

Teratomas

Venolymphatic malformations

Other abnormalities with potential airway obstruction

Thorax

Bronchogenic cyst or congenital lobar overinflation

Congenital cystic adenomatoid malformation

Diaphragmatic hernia

Effusions

Extralobar pulmonary sequestration

Esophageal atresia

Mediastinal masses

Evaluation of pulmonary hypoplasia secondary to diaphragmatic hernia, oligohydramnios, chest mass, or skeletal dysplasia

Abdomen, pelvis, and retroperitoneum

Abdominopelvic cystic mass

Bowel anomalies (anorectal malformations, complex obstructions)

Complex genitourinary anomalies (bladder outlet obstruction syndromes, bladder exstrophy, cloacal exstrophy)

Renal anomalies with oligohydramnios

Tumors (sacrococcygeal teratoma, neuroblastoma, hemangioma, suprarenal or renal masses)

Complications of monochorionic twins

Assess morbidity after death of a monochorionic co-twin

Determine vascular anatomy prior to laser treatment

Evaluate conjoined twins

Fetal surgery assessment

Anomalies for which fetal surgery is planned

Fetal brain anatomy before and after surgical intervention

aIn some cases, magnetic resonance imaging is indicated only if the anomaly is suspected but cannot be adequately

characterized sonographically, which is assessed on a case-by-case basis.

Summarized from American College of Radiology, Society for Pediatric Radiology: ACR-SPR practice parameter for the safe

and optimal performance of fetal magnetic resonance imaging (MRI). Resolution No. 45, 2020.266 The Fetal Patient

Section 6

o begin an MR examination, women are placed in a supine

or let lateral decubitus position. A torso coil is used in most

circumstances to send and receive the radiorequency pulses,

but a body coil can be used alone to accommodate large maternal habitus. A series o three-plane localizers, or scout views,

are obtained relative to the maternal coronal, sagittal, and

axial planes. Te gravid uterus is imaged in the maternal axial

plane (7-mm slices, 0 gap) with a 2-weighted ast acquisition.

ypically, these may be a single-shot ast spin echo sequence

(SSFSE), hal-Fourier acquisition single-shot turbo spin echo

(HASE), or rapid acquisition with relaxation enhancement

(RARE), depending on the machine. Next, a ast 1-weighted

acquisition such as spoiled gradient echo (SPGR) is perormed

(7-mm thickness, 0 gap). Tese large-eld-o-view acquisitions

through the maternal abdomen and pelvis are particularly good

or identiying etal and maternal anatomy.

Orthogonal images o targeted etal or maternal structures

are then obtained. In these cases, 3- to 5-mm slice thickness,

0 gap 2-weighted acquisitions are perormed in the coronal, sagittal, and axial planes. Depending on the anatomy and

underlying suspected abnormality, 1-weighted images can be

perormed to evaluate or subacute hemorrhage, at, or location

o normal structures that appear bright on these sequences, such

as liver and meconium in the colon (Brugger, 2006; Zaretsky,

2003b).

Short T1 inversion recovery (STIR) and requency-selective

at-saturated 2-weighted images may help dierentiation in

cases in which the water content o the abnormality is similar

to that o the normal structure. An example is a thoracic mass

compared with normal lung. Diusion-weighted imaging may

be employed to evaluate or restricted diusion, which can be

seen in ischemia, cellular tumors, or clotted blood (Brugger,

2006; Zaretsky, 2003b).

■ Fetal Anatomy Evaluation

A etal anatomical survey is generally completed during the

MR examination, regardless o the etal indication. Nearly

95 percent o anatomical components recommended by the

International Society o Ultrasound in Obstetrics and Gynecology were visible at 30 weeks’ gestation (Millischer, 2013). Te

aorta and pulmonary artery were the most difcult to evaluate.

Zaretsky and coworkers (2003a) similarly ound that with the

exclusion o cardiac structures, etal anatomical evaluation was

possible in 99 percent o cases.

■ Central Nervous System

For intracranial anomalies, ast 2-weighted images produce

excellent tissue contrast. Cerebrospinal uid–containing structures appear bright, which allows exquisite detail o the posterior ossa, midline structures, and cerebral cortex. 1-weighted

images are used to identiy hemorrhage. CNS biometry

obtained with MR imaging is comparable with that obtained

using sonography, and nomograms are available or the corpus

callosum and cerebellar vermis (Harreld, 2011; Katorza, 2016;

wickler, 2002; Xi, 2016).

MR imaging may provide valuable added inormation when

cerebral abnormalities are identied or suspected sonographically (Benacerra, 2007; Li, 2012). Additional inormation is

more likely to be gained when the examination is perormed

beyond 24 weeks’ gestation. In studies, MR imaging has identi-

ed additional CNS ndings or led to a changed diagnosis in

nearly 50 percent o cases and aected prognosis or management in 20 percent (Grifths, 2017, wickler, 2003).

MR imaging accurately portrays cerebral gyration and sulcation patterns (Fig. 14-13) (Levine, 1999). It may assist with

identiying agenesis or dysgenesis o the corpus callosum and

characterizing migrational abnormalities (Benacerra, 2007;

Li, 2012; wickler, 2003). In cases o septo-optic dysplasia,

MR imaging may conrm absence o the septum pellucidum

and display hypoplastic optic tracts (Fig. 14-14). When etal

intracranial hemorrhage (ICH) is suspected, MR imaging can

help to characterize the extent o bleeding and to estimate when

bleeding occurred. Risk actors or etal ICH include atypicalappearing ventriculomegaly, concern or neonatal alloimmune

thrombocytopenia, and severe S or demise o one monochorionic twin (Hu, 2006). With congenital etal inections,

MR imaging can delineate the variable

degrees o neural parenchymal abnormality and subsequent maldevelopment

(Soares de Oliveira-Szejneld, 2016).

■ Thorax

MR imaging can delineate the location

and size o space-occupying thoracic

lesions and quantiy the volume o lung

tissue. I needed, it can characterize blood

ow to a thoracic mass to dierentiate

cystic adenomatoid malormation rom

pulmonary sequestration (Chap. 15, p.

287). With congenital diaphragmatic

hernia, MR imaging can help veriy and

quantiy the abdominal organs within the

thorax (Debus, 2013; Lee, 2011; Mehollin-Ray, 2012). Tis includes the volume

A B



FIGURE 14-13 Axial images of the fetal brain demonstrate the normal gyration and sulcation progression during fetal development. A. 23 weeks’ gestation. B. 33 weeks’ gestation. These images were obtained using a Half Fourier Acquisition Single Shot Turbo Spin

Echo (HASTE) sequence because it is relatively motion insensitive.Obstetrical Imaging 267

CHAPTER 14

o herniated liver and o compressed lung

tissue (Fig. 14-15). MR imaging can also

measure lung volumes in pregnancies with

prolonged oligohydramnios secondary to

renal abnormalities or ruptured membranes (Messerschmidt, 2011; Zaretsky,

2005).

■ Abdomen

Meconium accumulation within the GI

tract gives a predictable pattern and has

high signal intensity on 1-weighted

sequences. Tus, MR imaging is a

complementary tool in diagnosing GI

abnormalities and complex cloacal mal-

ormations (Furey, 2016). With cystic

abdominal abnormalities, dierences in

signal characteristics may also help distinguish between meconium in the etal colon and urine in the bladder (Farhataziz,

2005). Peritoneal calcications related to meconium peritonitis

are more readily apparent sonographically, whereas pseudocysts

and resultant abnormalities o meconium

migration are better delineated with MR

imaging.

■ Adjunct to Fetal Therapy

Prior to etal surgery, MR imaging is

oten used. In cases o myelomeningocele, it precisely displays brain and spine

anatomy. For sacrococcygeal teratomas,

i etal surgery is considered, MR imaging may identiy tumor extension into the

etal pelvis (Avni, 2002; Neubert, 2004;

Perrone, 2018). When a etal neck mass is

identied with ultrasound, MR imaging

may help delineate a lesion’s extent and its

mass eect on the oral cavity and trachea.

Tis can help identiy cases that are at risk

or adverse outcome and that may benet

rom an ex utero intrapartum treatment

(EXI) procedure (Lazar, 2012; Ogamo,

2005; Ng, 2019). MR imaging can also

calculate a jaw index when an EXI procedure may be needed or severe micrognathia (Kooiman, 2018; Morris, 2009).

At some centers, beore laser ablation o

placental anastomoses or S, MR

imaging is perormed to identiy etal

ICH or periventricular leukomalacia (Hu,

2006; Kline-Fath, 2007). Fetal therapy is

discussed in Chapter 19 (p. 367).

■ Placenta

Despite improvements in ultrasound

detection o PAS, particularly when the

placenta is anterior, characterization o

the extent o invasion remains a challenge. MR ndings concerning or invasion are depicted in Figure 14-16. Tey include

dark intraplacental bands on 2-weighted images, a ocal bulge,

placental heterogeneity, involvement o the bladder-uterine

A B



FIGURE 14-14 Septo-optic dysplasia. A. Axial. B. Coronal. Images at 30 weeks’ gestation

confirm absence of the cavum septum pellucidum (arrowheads) in both. There is also

associated mild ventriculomegaly (arrow).

H

A B

C D



FIGURE 14-15 A. Coronal image of normal lungs on a balanced sequence at 29 weeks’

gestation. The liver (L) and stomach (S) lie below the diaphragm. B. Left-sided congenital

diaphragmatic hernia (CDH) (dotted ellipse) seen on balanced sequence at 33 weeks.

C. The T1-weighted sequence confirms the subdiaphragmatic position of the liver and

better delineates the small bowel (arrow) and meconium-containing colon (arrowhead)

that have herniated into the chest. D. Another image of a left-sided CDH at 22 weeks demonstrates no normal lung, the heart (H) displaced into the right chest, and an elevated liver

(dotted ellipse).268 The Fetal Patient

Section 6

serosal interace, and brin deposition (Clark, 2020; Leyendecker, 2012). When used to complement ultrasound, MR

imaging’s sensitivity to detect invasion is high. Clark and associates (2020) reported that MR imaging ndings positively

correlated with need or cesarean hysterectomy and with histological and surgical impressions o invasion. Clinical risk actors

and ultrasound ndings (p. 253) should be incorporated when

interpreting MR placental images (Chap. 43, p. 759).

wo emerging technologies also are being employed to

investigate placental insufciency and PAS. Arterial spin labelling is a technique or unctional assessment o perusion and

excites maternal red blood cells to serve as endogenous contrast

agents (Zun, 2018). Second, radiomics textural analysis characterizes placental morphology in vivo. MR textural eatures may

help select pregnancies requiring cesarean hysterectomy (Do,

2020).



FIGURE 14-16 A. Sagittal T2-weighted image of the placenta

demonstrates placenta accreta spectrum (PAS), in this case placenta percreta. There are intraplacental, dark, linear bands (arrows),

a large bulge along the bladder-serosal interface (arrowheads), and

a central area of marked inhomogeneity (asterisk). B. A coronal

image from the same study demonstrates the bulge with right

lateral extension (arrowheads) and multiple, dark, linear bands

(arrows). C. A sagittal, balanced, steady state free precession (SSFE)

image shows a bulge, retroplacental vessels, and irregularity of

the bladder-serosal interface (arrowheads). These contrast with the

large maternal varices (arrows). F = fetus

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