eMedicine Specialties > Radiology > Obstetrics/Gynecology

Biophysical Profile, Ultrasound

Author: Peter A Gearhart, MD, Assistant Professor of Obstetrics and Gynecology, University of Pennsylvania School of Medicine
Coauthor(s): Harish M Sehdev, MD, Associate Professor of Clinical Obstetrics and Gynecology, Department of Obstetrics and Gynecology, University of Pennsylvania; Consulting Staff, Pennsylvania Hospital, University of Pennsylvania Health System; William GM Ritchie, MB, BCh, Former Clinical Professor of Radiology, University of Pennsylvania School of Medicine; Former Chief, Department of Radiology, Section of Ultrasound, Pennsylvania Hospital
Contributor Information and Disclosures

Updated: Oct 17, 2008

Introduction

The biophysical profile (BPP) is a noninvasive test that predicts the presence or absence of fetal asphyxia and, ultimately, the risk of fetal death in the antenatal period.1 When the BPP identifies a compromised fetus, measures can be taken to intervene before progressive metabolic acidosis leads to fetal death.2,3,4

The BPP combines data from 2 sources (ie, ultrasound imaging and fetal heart rate [FHR] monitoring). Dynamic realtime B-mode ultrasound is used to measure the amniotic fluid volume (AFV) and to observe several types of fetal movement. The FHR is obtained using a pulsed Doppler transducer integrated with a high-speed microprocessor, which provides a continuously updated reading.5

Originally described by Manning and colleagues,6,7 the BPP has become a standard tool for providing antepartum fetal surveillance. The BPP integrates 5 parameters to yield a biophysical profile score (BPS) and includes (1) the nonstress test (NST), (2) ultrasound measurement of the AFV, (3) observation of the presence or absence of fetal breathing movements, (4) gross body movements, and (5) tone. Table 1 (see below) describes specific criteria for the BPS.

The BPP allows 2 points for each parameter that is present, yielding a maximum score of 10; however, if all the ultrasound variable findings are normal, the FHR variable may be excluded because no change is made in the predicative accuracy of the BPP by including the FHR. If one or more ultrasound variable findings are abnormal, the NST should be performed.

A basic principle of antepartum testing is that a more accurate prediction of fetal wellness is achieved in direct proportion to the number of variables considered. The BPP is a clinical tool that integrates levels of dynamic biophysical activities into a usable standard.8 The BPP allows 2 points for each parameter that is present, yielding a maximum score of 10; however, if all ultrasound variables are normal, the FHR variable may be excluded because no change is made in the predictive accuracy of the BPP by including the FHR. If one or more ultrasound variables are abnormal, the NST should be performed.9


Table 1. Criteria for Coding Fetal Biophysical Variables as Normal or Abnormal

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Table
Biophysical
Variable
Normal
(Score = 2)
Abnormal
(Score = 0)
Fetal breathing movements1 or more episodes of >20 s within 30 min

Absent or no episode of >20 s within 30 min

Gross body movements2 or more discrete body/ limb movements within 30 min (episodes of active continuous movement considered as a single movement)

<2 episodes of body/limb movements within 30 min

Fetal tone1 or more episodes of active extension with return to flexion of fetal limb(s) or trunk (opening and closing of hand considered normal tone)

Slow extension with return to partial flexion, movement of limb in full extension, absent fetal movement, or partially open fetal hand

Reactive FHR

2 or more episodes of acceleration of >15 bmp* and of >15 s associated with fetal movement within 20 min

1 or more episodes of acceleration of fetal heart rate or acceleration of <15 bmp within 20 min

Qualitative AFV

1 or more pockets of fluid measuring >2 cm in vertical axis

Either no pockets or largest pocket <2 cm in vertical axis

Biophysical
Variable
Normal
(Score = 2)
Abnormal
(Score = 0)
Fetal breathing movements1 or more episodes of >20 s within 30 min

Absent or no episode of >20 s within 30 min

Gross body movements2 or more discrete body/ limb movements within 30 min (episodes of active continuous movement considered as a single movement)

<2 episodes of body/limb movements within 30 min

Fetal tone1 or more episodes of active extension with return to flexion of fetal limb(s) or trunk (opening and closing of hand considered normal tone)

Slow extension with return to partial flexion, movement of limb in full extension, absent fetal movement, or partially open fetal hand

Reactive FHR

2 or more episodes of acceleration of >15 bmp* and of >15 s associated with fetal movement within 20 min

1 or more episodes of acceleration of fetal heart rate or acceleration of <15 bmp within 20 min

Qualitative AFV

1 or more pockets of fluid measuring >2 cm in vertical axis

Either no pockets or largest pocket <2 cm in vertical axis


*Beats per minute

Reprinted with permission from Manning, 1999

Related eMedicine topics:
The Fetus as a Patient: Prenatal Diagnosis and Fetal Therapy - Pediatrics
Evaluation of Fetal Death - Obstetrics & Gynecology
Fetal Growth Restriction - Obstetrics & Gynecology

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Nonstress Test

The nonstress test (NST) is a noninvasive method used to evaluate fetal well-being. The NST is derived from observations that a fetus that is not acidotic and has an intact normally functioning autonomic nervous system will have periodic accelerations of the fetal heart rate (FHR). Acceleration is defined as a rise in the FHR-baseline rate that peaks at least 15 bmp above the baseline and lasts for at least 15 seconds from the beginning of the rise until the return to the FHR baseline.

Accelerations almost always occur with fetal movement. Partial umbilical cord compression with transient occlusion of the umbilical vein also can cause accelerations. This occurs with normal autonomic function, which acts to preserve cardiac output by increasing heart rate in response to decreased blood return to the fetal heart.

NSTs are described as either reactive or nonreactive. An NST is considered reactive if at least 2 accelerations are present in a 20-minute period. Occasionally, the NST may require 40 minutes or more of FHR recording to account for variations of the fetal sleep-wake cycle. An NST is considered nonreactive if sufficient accelerations are absent within a 40-minute period.

Decelerations of the FHR may be seen in as many as 50% of NSTs.10 If decelerations are nonrepetitive and less than 30 seconds in duration, obstetric intervention is not needed; however, repetitive decelerations or decelerations that last longer than 60 seconds are associated with an increased risk of fetal demise and cesarean delivery for the diagnosis of nonreassuring FHR pattern.11 Image 1 shows a reactive NST.

Pathophysiologic Basis of the Biophysical Profile

Hypoxemia and acidemia have been shown to interfere with measures of central nervous system (CNS) performance, such as fetal heart rate (FHR) patterns, fetal movement, and tone, in both animals and humans.12 Most likely, oligohydramnios results from decreased fetal urine production, which is seen with fetal hypoxemia as a result of blood flow redistributed away from the fetal kidneys and viscera in favor of the brain, heart, and adrenal glands.13

Each of the movements evaluated in the biophysical profile (BPP) results from efferent signals originating in different CNS centers, which mature at different gestational ages (see Table 2). When activities known to originate from each of these oxygen-dependent centers are observed, it can be assumed that brain function is normal and systemic hypoxia is not present. Conversely, if one or more of the BPP activities is not observed within the prescribed observation period of 30 minutes, hypoxemia must be assumed to be the cause of the absence of that activity.

Table 2. Maturation of Central Nervous System Regulatory Centers

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Table
ActivityGestational Age
of Maturation
(wk)
Gross body movements6
Breathing movements12-14
FHR accelerations resulting from fetal movement18-20
Sleep-wake cycles18-22
Integrated behavioral patterns28
ActivityGestational Age
of Maturation
(wk)
Gross body movements6
Breathing movements12-14
FHR accelerations resulting from fetal movement18-20
Sleep-wake cycles18-22
Integrated behavioral patterns28

However, the clinical reality is that hypoxemia is the least likely reason for the absence of a particular activity. In most fetuses, absence of a particular activity results from normal variations in fetal movements.14 Usually, this results from fetal sleep-wake cycles, which are approximately 20 minutes in length. The observation period of 30 minutes was chosen arbitrarily to exclude the effects of the fetal sleep-wake cycle on the majority of biophysical activities. Table 3 shows a variety of factors, other than hypoxemia, that have been shown to affect different BPP parameters.

Table 3. Factors Affecting the Biophysical Profile

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Table
ActivityFHR
Accelerations
ToneGross
Movement
Fetal
Breathing
AFV
Fetal sleepßßßß 
Early gestational age (<33 wk)ß  ß 
Late gestational age (>42 wk)ßß ßß
Maternal glucose ingestion Ý 
Maternal alcohol ingestion ß/— Ý/— 
Maternal magnesium administrationß  ß 
Artificial rupture of membranes   ßß
Premature rupture of membranes    ß
Labor   ß 
ActivityFHR
Accelerations
ToneGross
Movement
Fetal
Breathing
AFV
Fetal sleepßßßß 
Early gestational age (<33 wk)ß  ß 
Late gestational age (>42 wk)ßß ßß
Maternal glucose ingestion Ý 
Maternal alcohol ingestion ß/— Ý/— 
Maternal magnesium administrationß  ß 
Artificial rupture of membranes   ßß
Premature rupture of membranes    ß
Labor   ß 

Key: A blank box indicates that no data are available for that parameter.

Horizontal lines indicate that the parameter has been studied and that no change is demonstrated.

Arrows indicate that the parameter has been studied and that it increases or decreases as shown.

Biophysical Profile Procedure

The ultrasound portion of the biophysical profile (BPP) should begin by noting the starting time.2 The profile may be completed when all of the variables have been observed; however, a full 30 minutes must elapse before the profile is judged to be abnormal. The scan should start with a general survey, noting the position of the fetus and the presence of cardiac activity. Although not part of the BPP, surveying the placental position and grade and the fetal morphology is common practice during observation of fetal activity.

Amniotic fluid volume (AFV) is assessed as normal if one or more pockets of fluid are detected that measure at least 2 cm along the vertical axis. Oligohydramnios is present if the largest pocket measures less than 2 cm. The video in Image 6 shows 4 pockets of fluid being measured.

The pressure applied to the transducer by the sonographer is inversely proportional to the depth of the fluid pocket.15 Careful attention to transducer pressure is required to avoid a false diagnosis of oligohydramnios, which can result from excessive transducer pressure compressing the maternal abdomen.

Fetal movements are judged as normal or abnormal according to the criteria established in Table 1 (see Introduction). The video in Image 2 shows breathing movements, while the video in Image 3 shows movements that can be mistaken for fetal breathing. The videos in Image 4 and Image 5 demonstrate gross movements and tone. The video in Image 6 demonstrates the amniotic fluid index (AFI).

Amniotic Fluid Index

The amniotic fluid index (AFI) is a semiquantitative method for evaluating the amniotic fluid volume (AFV). The AFI is derived by adding the largest vertically measured fluid pocket from each uterine quadrant. This method appears to be at least as accurate as the largest–pocket-of-fluid method and can be reasonably substituted as an alternative method for evaluating AFV in the biophysical profile (BPP). Using this method, oligohydramnios is defined as an AFI of less than 5.

To obtain an AFI, the mother must be in the supine position and the linear ultrasound probe must be parallel to the maternal spine and perpendicular to the floor for all measurements. The abdomen is divided into 4 quadrants, with the umbilicus delineating the upper and lower halves and the linea nigra delineating the left and right halves.16 The largest pocket of fluid in each quadrant is measured along the vertical dimension, which is the dimension perpendicular to the ultrasound probe.17 The pockets must be free of umbilical cord or fetal extremities, although brief appearances of these are acceptable. The video in Image 6 demonstrates measurement of the AFI.

The Modified Biophysical Profile

A modified biophysical profile (BPP) consisting of a nonstress test (NST) and an amniotic fluid index (AFI) is used widely.18 If either the NST or the AFI is abnormal, a complete BPP or a contraction stress test (CST) is performed. The modified BPP, CST, and complete BPP have similarly low false-negative mortality rates, defined as the number of fetal deaths within 1 week of a normal test result.19 Nevertheless, no clear evidence exists that the 2 variables used in the modified BPP are better predictors than the other variables omitted from the BPP.20 Furthermore, this method requires 2 modalities for fetal evaluation, while normal ultrasound findings in a BPP eliminate the need for an NST.

Application of the Biophysical Profile

Antepartum testing using the biophysical profile (BPP) or any other method should not be performed earlier than the gestational age at which extrauterine survival or active intervention for fetal compromise is possible. Furthermore, no indications exist for testing in a fetus at term when likelihood of successful induction is high or when vaginal delivery is contraindicated for obstetric reasons. For patients with a low probability of successful induction, the BPP is a useful tool that can be used while waiting for cervical ripening. In these patients, the purpose of the BPP is to avoid the maternal morbidity resulting from failed induction followed by cesarean delivery.

The frequency of testing varies according to the clinical variables in each patient. In most high-risk pregnancies, testing plans start with weekly testing,3 although twice-weekly testing is the standard for pregnancies beyond 42 weeks and for patients with insulin-dependent diabetes.12 Frequency of testing increases in direct proportion to the severity of the maternal or fetal condition. In unstable pregnancies with progressive deterioration of the fetal condition, abnormal umbilical cord blood flow patterns occur first. Subsequently, fetal heart rate (FHR) variation is reduced, followed by loss of breathing movements, while general fetal movements and tone are the last parameters to demonstrate abnormal results. Frequent assessment of fetal BPP movements may help prolong the pregnancy in fetuses with a marginally reduced FHR variation.

An abnormal BPS should prompt further evaluation or intervention depending on the circumstances. If an abnormal score occurs in a term fetus, preparation should be made for delivery. An abnormal score in a fetus remote from term requires conservative management, since the risk of fetal death is similar to the neonatal mortality rate resulting from prematurity. In these patients, daily testing often is performed. Table 4 provides general guidelines for treatment following the BPS.

Table 4. Recommended Fetal Treatment According to the Biophysical Profile Score

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Table
ResultInterpretationRisk
of Asphyxia*
(%)
Risk of Fetal
Death (per
1000/wk)
Recommended Treatment
10/10Nonasphyxiated00.565Conservative
8/10 (normal AFV)Nonasphyxiated00.565Conservative
8/8 (NST not performed)Nonasphyxiated00.565Conservative
8/10 (decreased AFV)Chronic compensated
asphyxia
5-10 (estimate)20-30
    If mature (³ 37 wk), deliverIf immature, serial testing(twice weekly)
6/10 (normal AFV)Acute asphyxia
possible
050
    If mature (³ 37 wk), deliverIf immature, repeat test in 24 hand if £ 6/10, deliver
6/10 (decreased AFV)Chronic asphyxia with
possible acute asphyxia
>10>50
    Factor in gestational ageIf ³ 32 wk, deliverIf <32 wk, test daily
4/10 (normal AFV)Acute asphyxia likely36115
    Factor in gestational ageIf ³ 32 wk, deliverIf £ 32 wk, test daily
4/10 (decreased AFV)Chronic asphyxia with
acute asphyxia
likely
>36>115If ³ 26 wk, deliver
2/10 (normal AFV)Acute asphyxia almost
certain
73220If ³ 26 wk, deliver
0/10Gross severe asphyxia100100If ³ 26 wk, deliver
ResultInterpretationRisk
of Asphyxia*
(%)
Risk of Fetal
Death (per
1000/wk)
Recommended Treatment
10/10Nonasphyxiated00.565Conservative
8/10 (normal AFV)Nonasphyxiated00.565Conservative
8/8 (NST not performed)Nonasphyxiated00.565Conservative
8/10 (decreased AFV)Chronic compensated
asphyxia
5-10 (estimate)20-30
    If mature (³ 37 wk), deliverIf immature, serial testing(twice weekly)
6/10 (normal AFV)Acute asphyxia
possible
050
    If mature (³ 37 wk), deliverIf immature, repeat test in 24 hand if £ 6/10, deliver
6/10 (decreased AFV)Chronic asphyxia with
possible acute asphyxia
>10>50
    Factor in gestational ageIf ³ 32 wk, deliverIf <32 wk, test daily
4/10 (normal AFV)Acute asphyxia likely36115
    Factor in gestational ageIf ³ 32 wk, deliverIf £ 32 wk, test daily
4/10 (decreased AFV)Chronic asphyxia with
acute asphyxia
likely
>36>115If ³ 26 wk, deliver
2/10 (normal AFV)Acute asphyxia almost
certain
73220If ³ 26 wk, deliver
0/10Gross severe asphyxia100100If ³ 26 wk, deliver

*Umbilical venous blood pH less than 7.25

Reprinted with permission of Manning, 1999

Reliability of the Biophysical Profile

The biophysical profile (BPP) is a reliable method of predicting fetal survival. Data have been collected on this and other antepartum testing procedures for more than 20 years. Testing methods usually are evaluated by comparing the false-negative mortality rate for each method. The false-negative mortality rate is defined as the number of fetal deaths, corrected for lethal congenital anomalies and unpredictable causes of demise, that occur within 1 week of a normal test result.

The BPP has a false-negative mortality rate of 0.77 deaths per 1000 tests. Furthermore, the BPS highly correlates with the antepartum fetal umbilical venous cord pH level.21,22 Cordocentesis performed immediately following a BPP demonstrated that a poor BPS was always associated with a pH of less than 7.20, while a score of 10 of 10 always yielded a pH of greater than 7.20. The false-negative mortality rate for the nonstress test (NST) alone is 1.9 per 1000 tests, more than twice that of the BPP. The modified BPP has a mortality rate of 0.8. The low false-negative rates of these testing methods depend on an appropriate response to an abnormal result. Intervention and retesting are the usual responses.

Multimedia

Reactive nonstress test. The top graph plots the ...Media file 1: Reactive nonstress test. The top graph plots the fetal heart rate over time. Each small box represents 10 seconds along the horizontal axis and 10 beats per minute along the vertical axis. The baseline fetal heart rate is from 140-150 beats per minute. This tracing is reactive, since at least 2 accelerations of the fetal heart rate occur within less than 20 minutes.
Reactive nonstress test. The top graph plots the ...

Reactive nonstress test. The top graph plots the fetal heart rate over time. Each small box represents 10 seconds along the horizontal axis and 10 beats per minute along the vertical axis. The baseline fetal heart rate is from 140-150 beats per minute. This tracing is reactive, since at least 2 accelerations of the fetal heart rate occur within less than 20 minutes.

This feature requires the newest version of Flash. You can download it here.
Media file 2: Fetal breathing movements. Video shows a rhythmic deflection of the fetal chest wall and diaphragm that is clearly distinct from the rhythmic motion of the fetal heart. Note that the image begins in the transverse view, but the ultrasound transducer is then rotated to show a sagittal view and, finally, an oblique view. The episode of continuous fetal breathing lasts well in excess of the required 20-second period.
Fetal breathing movements. Video shows a rhythmic...

Fetal breathing movements. Video shows a rhythmic deflection of the fetal chest wall and diaphragm that is clearly distinct from the rhythmic motion of the fetal heart. Note that the image begins in the transverse view, but the ultrasound transducer is then rotated to show a sagittal view and, finally, an oblique view. The episode of continuous fetal breathing lasts well in excess of the required 20-second period.

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Media file 3: False fetal breathing movements. Although some transient fetal breathing movements are seen, the video does not include 20 seconds of continuous fetal breathing. Note that the maternal breathing and aortic pulse seen posteriorly and the fetal aortic pulse seen on the sagittal view, along with fetal cardiac activity, can cause deflections of the fetal chest wall, which can be mistaken for fetal breathing movements.
False fetal breathing movements. Although some tr...

False fetal breathing movements. Although some transient fetal breathing movements are seen, the video does not include 20 seconds of continuous fetal breathing. Note that the maternal breathing and aortic pulse seen posteriorly and the fetal aortic pulse seen on the sagittal view, along with fetal cardiac activity, can cause deflections of the fetal chest wall, which can be mistaken for fetal breathing movements.

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Media file 4: Gross fetal movements and tone. Video demonstrates generalized movements of the fetal lower extremities, including 1 episode of flexion and extension.
Gross fetal movements and tone. Video demonstrate...

Gross fetal movements and tone. Video demonstrates generalized movements of the fetal lower extremities, including 1 episode of flexion and extension.

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Media file 5: Gross fetal movements and tone. Video demonstrates generalized movements of the fetal upper extremities. The upper extremity rests in front of the fetal chest and chin. Although the ultrasound transducer is moving laterally across the maternal abdomen, 2 distinct episodes of flexion and extension are seen. Note the many cross-sectional views of the 3-vessel umbilical cord and the floating echogenic particles of vernix in the amniotic fluid.
Gross fetal movements and tone. Video demonstrate...

Gross fetal movements and tone. Video demonstrates generalized movements of the fetal upper extremities. The upper extremity rests in front of the fetal chest and chin. Although the ultrasound transducer is moving laterally across the maternal abdomen, 2 distinct episodes of flexion and extension are seen. Note the many cross-sectional views of the 3-vessel umbilical cord and the floating echogenic particles of vernix in the amniotic fluid.

This feature requires the newest version of Flash. You can download it here.
Media file 6: Amniotic fluid index. The largest pocket of fluid is measured in each quadrant of the maternal abdomen in the vertical dimension. Then, each value is added to yield the amniotic fluid index.
Amniotic fluid index. The largest pocket of fluid...

Amniotic fluid index. The largest pocket of fluid is measured in each quadrant of the maternal abdomen in the vertical dimension. Then, each value is added to yield the amniotic fluid index.

Keywords

biophysical profile, antenatal ultrasound fetal surveillance, prenatal ultrasound, BPP, fetal asphyxia, fetal heart rate monitoring, FHR monitoring, FHR, amniotic fluid volume, AFV, antepartum fetal surveillance, biophysical profile score, BPS, nonstress test, antepartum testing, antenatal testing, prenatal testing

 


More on Biophysical Profile, Ultrasound

References
Further Reading

References

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Further Reading

Growth disturbances: risk of intrauterine growth restriction.
American College of Radiology.  1996 (revised 2007).  10 pages.  NGC:006006
 
Ultrasound scanning during pregnancy.
Finnish Medical Society Duodecim.  2000 Apr 3 (revised 2004 Jun 28).  Various pagings. [NGC Update Pending] NGC:004106
 
Intrapartum fetal heart rate monitoring.
American College of Obstetricians and Gynecologists.  2005 Dec.  9 pages.  NGC:005707

Keywords

biophysical profile, antenatal ultrasound fetal surveillance, prenatal ultrasound, BPP, fetal asphyxia, fetal heart rate monitoring, FHR monitoring, FHR, amniotic fluid volume, AFV, antepartum fetal surveillance, biophysical profile score, BPS, nonstress test, antepartum testing, antenatal testing, prenatal testing

Contributor Information and Disclosures

Author

Peter A Gearhart, MD, Assistant Professor of Obstetrics and Gynecology, University of Pennsylvania School of Medicine
Peter A Gearhart, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists
Disclosure: Schering Plough Honoraria Speaking and teaching

Coauthor(s)

Harish M Sehdev, MD, Associate Professor of Clinical Obstetrics and Gynecology, Department of Obstetrics and Gynecology, University of Pennsylvania; Consulting Staff, Pennsylvania Hospital, University of Pennsylvania Health System
Harish M Sehdev, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Obstetricians and Gynecologists, American Institute of Ultrasound in Medicine, Phi Beta Kappa, and Society for Maternal-Fetal Medicine
Disclosure: Nothing to disclose.

William GM Ritchie, MB, BCh, Former Clinical Professor of Radiology, University of Pennsylvania School of Medicine; Former Chief, Department of Radiology, Section of Ultrasound, Pennsylvania Hospital
William GM Ritchie, MB, BCh is a member of the following medical societies: American College of Radiology, American Institute of Ultrasound in Medicine, Philadelphia County Medical Society, and Radiological Society of North America
Disclosure: Nothing to disclose.

Medical Editor

Christopher L Sistrom, MD, Associate Chair for Research, Assistant Professor, Department of Radiology, University of Florida School of Medicine
Christopher L Sistrom, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Radiology, American Institute of Ultrasound in Medicine, American Roentgen Ray Society, Association of University Radiologists, Phi Beta Kappa, and Radiological Society of North America
Disclosure: Nothing to disclose.

Pharmacy Editor

Bernard D Coombs, MB, ChB, PhD, Consulting Staff, Department of Specialist Rehabilitation Services, Hutt Valley District Health Board, New Zealand
Disclosure: Nothing to disclose.

Managing Editor

Karen L Reuter, MD, FACR, Professor, Department of Radiology, Lahey Clinic Medical Center
Karen L Reuter, MD, FACR is a member of the following medical societies: American Association for Women Radiologists, American College of Radiology, American Institute of Ultrasound in Medicine, American Roentgen Ray Society, and Radiological Society of North America
Disclosure: Nothing to disclose.

CME Editor

Robert M Krasny, MD, Consulting Staff, Department of Radiology, The Angeles Clinic and Research Institute
Robert M Krasny, MD is a member of the following medical societies: American Roentgen Ray Society and Radiological Society of North America
Disclosure: Nothing to disclose.

Chief Editor

Eugene C Lin, MD, Consulting Radiologist, Virginia Mason Medical Center; Clinical Assistant Professor of Radiology, University of Washington School of Medicine
Eugene C Lin, MD is a member of the following medical societies: American College of Nuclear Medicine, American College of Radiology, Radiological Society of North America, and Society of Nuclear Medicine
Disclosure: Nothing to disclose.

 
 
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