FOGSI Focus Imaging in Obstetrics and Gynecology Meenu Agarwal, Rohan Palshetkar, Nandita Palshetkar, Chinmay Umarji
INDEX
Page numbers followed by b refer to box, f refer to figure, and t refer to table
A
Abdomen 107
axial view of 157f159f
Abdominal circumference 70, 104, 105, 133, 134f
Abdominal distension 70
Abnormal ductus venosus waveforms 85f
Abortion 46
complete 75
incomplete 75
missed 75, 76f
threatened 74
Abruptio placentae 80, 80f
Absent end-diastolic flow 135, 137f
Acardiac twin 98
Acardius acephalus 99
Acardius amorphous 99
Acardius myelacephalus 99
Adenomyoma 29t, 32
Adenomyosis 29, 29f, 59, 61f
color flow pattern of 29f
ultrasound features of 61t
Adherent placenta 167
Adhesions 51
Adnexa 17, 52, 82
assessment of 68
solid masses of 72
ultrasound of 70
Adnexal mass 87f
classification of 28
near ovary 67f
Adnexal ovarian torsion 30
Adnexal pregnancy 68f
Adnexal torsion 70, 72
Allister-Hall syndrome 184
Alpha-fetoprotein 180, 181
American College of Obstetricians and Gynecologists 132, 136, 147
American College of Radiology 132
American Institute of Ultrasound in Medicine 132
Amniocentesis 146, 146f, 177, 184
indications for 145
Amniotic cavities 95f
Amniotic fluid 23, 124, 124f, 157f
assessment 124
dynamics 125f
index 126, 132, 173
percentile values 127t
technique for 126f
old blood-stained 146f
volume 124, 125f, 131, 136
assessment 129
measurement of 125
normal 125
Amniotic membrane 84f
Anal atresia 158, 161
Andometrioma, complex 51
Anembryonic pregnancy 75
Anencephaly 107
Aneuploidy
risks 189
screening for 94
Angiogenesis around follicle 35f
Angiotensin-converting enzyme inhibitors 127
Anorectal malformations 161
surgical repair of 162
Antenatal care 131
Antepartum fetal surveillance 135
Anteroposterior abdominal diameter 104, 105
Anti-Müllerian hormone 42
Antral follicle 36
count 42, 42f, 43, 62
Aortic isthmus Doppler 138
Arcuate uterus 59
Asherman's syndrome 60
Assisted reproductive technology 67, 187
Asynchronous color flow imaging 26
Atrial septal defect 95
Atrioventricular septal defect 108f
Atypical endometriotic cyst 50f
Axial diffusion-weighted imaging 51
B
Backache 70
Benign adnexal masses, causes of 70
Beta-human chorionic gonadotropin 74, 82, 177
Biophysical profile 135
score 135
Biopsy 52
Biparietal diameter 104, 105, 133, 134f
Bladder
outlet obstruction 185
wall-serosa interface 116f
Bleeding
causes of 74
in late pregnancy 78
in obstetrics, ultrasonography for 74
per vaginum 153
subacute 51
Blighted ovum 75f, 86, 86f
Blood velocity 25
Body mass index 42, 43
Bowel
atresia 158, 165
lumen 17f
muscularis 17f
Brain 22, 23, 107
Bronchopulmonary sequestration 140
C
Cancer antigen 125 50
Cardiac anomalies 141, 158
Cardiac defects 158
Cardiotocography 135
computerized 96
Cardiovascular system 129
Caudal regression syndrome 161
Cell-free deoxyribonucleic acid 94
Central cord insertion, normal 120f
Central nervous system 95, 129, 139
Cephalopagus conjoined twins 98f
Cerebral ventriculomegaly, bilateral 107f
Cerebroplacental ratio 135, 137
Cervical
canal 16f, 77f
glands 16f
insufficiency 80, 80f
length assessment 104, 109
pregnancy 77f
Cervix 16, 55, 66
assessment of 110f
carcinoma of 35
Chocolate cysts 32
Choledochal cyst 164
Chorioamnionitis 153
Chorioangioma
gross specimen of 119f
placental 119f
vascularity of 119f
Chorionic plate 167
Chorionic villus sampling 94, 145, 147, 147f, 177, 184
Chorionicity, ultrasound signs of 92t
Chronic endometriotic deposits 51
Chylothorax 153
Circle of Willis, HD-live flow of 21f
Circummarginate placenta 113f
Circumvallate placenta 113f
Clear cell carcinoma 28
Cleft lip 107, 108f, 184
Cleft palate 129, 184
Cobweb pattern 63f, 71
Cogwheel appearance 72
Coiling abnormalities 120
Color Doppler 3, 25
in infertility, role of 35
settings 6
Color flow, role of 25
Complex extra-adnexal cyst 78
Computed tomography scan 49, 51
Congenital anomalies, absence of 135t
Congenital cystic adenomatoid malformation 152
Congenital diaphragmatic hernia 141, 141f, 144, 152
repair of 152
treatment of 153
Congenital pulmonary airway malformation 140, 141
thoracoamniotic shunt for 152
Congenital pulmonary airway obstruction 154
Conjoined twins 97
classification of 97t
Continuous wave Doppler 26
Cord cyst 121, 121f
Cordocentesis 184
Corpus callosum agenesis 139f
Corpus luteal flow, normal 47f
Corpus luteum 34f, 63, 63f
color Doppler of 38f
Crescent sign 55, 56f
Crown-rump length 74, 82, 84f, 92, 133, 191f
Cul-de-sac 67f
Cyst adenoma 64
Cystic fibrosis 165
Cystic hygroma 129
Cytomegalovirus 146
infection, diagnosis of 112f
D
Decidual cyst 78
Deep infiltrating endometriosis 52, 65
Deep peritoneal implants 52
Deepest vertical pocket 101
Degenerating leiomyoma 176
Delivery, timing of 96, 102
Deoxyribonucleic acid 147
Dermoid cyst 64, 70, 71, 71f
Diaphragmatic hernia 107
Dichorionic diamniotic
pregnancy 95f
twins 125
Dichorionic pregnancy 9496
Dichorionic twins 126
Didelphys uterus 59
Dizygotic twins 90
Doppler 3, 56
angle 9
bold spectrum of 9f
calculations in 26
frequency 3
in gynecology, use of 27
safety of 11
types of 26
velocity waveform 25
Double bubble sign 140
Down syndrome 144, 158, 177, 178, 184
Ductus venosus 100, 105, 138f
agenesis 162
extrahepatic type of 162f
types of 162
Doppler 137
Duodenal atresia 158, 158t, 159f
differential diagnosis of 158b
Dysgerminoma 28
E
Early pregnancy 92, 190
failure 85
scan 85
Echogenic bowel 164, 165f
grading of 165t
Ectopic endometrial glands 51
Ectopic pregnancy 33, 34f, 67, 67f, 68f, 69, 87, 175
types of 68
ultrasound of 67
Edwards’ syndrome 177, 180
Electrical interferences 11
Electronic fetal monitoring 173f
Embryo 83
transfer 39
Endometrial blood flow 39
Endometrial carcinoma 34, 35f, 63f
ultrasound in 62
Endometrial cavity 37f
fluid in 60, 62f
Endometrial flow 6f, 18f
Endometrial motion 39
Endometrial polyp 29, 60, 62f
Endometrial thickness 39, 63f
Endometrial vascularity 45, 46t
Endometrioma 28, 32, 32f, 51, 63, 63f, 70, 71
Endometrio-myometrial junctional zone 116f
Endometriosis 31, 32, 49, 53, 65
imaging 49
techniques for 52
sites of 52, 52t
Endometriotic cyst 50f, 64
Endometriotic nodules 32f
Endometritis 34
Endometrium 15, 37f, 42, 47, 47f, 55, 66
changes in 37
Doppler features of 45
hypoechoic inner layer of 37f
like glands 32
measurement of 59
Endomyometrial junction 56, 57f
Enteric duplication cyst 163
Enterolithiasis 161
Epithelial carcinoma 28
Esophageal atresia 156, 157f, 157t
Estimated fetal weight 132, 135
Estriol 181
European Board and College of Obstetrics and Gynecology 194
European Society of Urogenital Radiology 51
Exomphalos 107
Extrachorial placentation 113
Extrauterine fetal cardiac activity 78
Extrauterine pregnancies 76, 78f
Extremities 22, 23
F
Face 23, 107
Fallot's tetralogy 141f
Federation of Obstetric and Gynaecological Societies of India 194
Female pelvis, ultrasound examination of 13
Femur length 104, 105
Fetal abdomen 156
Fetal activity 167
Fetal anomalies 107t
scan, targeted imaging for 104, 106
Fetal arrhythmias 150
Fetal biometry 104
Fetal blood
flow, disruption of 117
sampling 148
Fetal bradycardia 74
Fetal cardiac activity 132
Fetal central nervous system abnormalities 139
Fetal cord blood sampling 148f
Fetal disorders, prenatal diagnosis of 144
Fetal Doppler 136
Fetal face 22
HD-live mode for 21f
multiplanar view of 20f
surface rendering of 20f
Fetal gastrointestinal anomalies 140
Fetal genitourinary anomalies 140
Fetal growth 131
restriction 95, 96, 105, 127, 133, 135, 135t, 167, 184, 189
early-onset growth charts 134f
late-onset growth charts 134f
surveillance 133
Fetal head
attitude 170
descent 170
tomographic ultrasound imaging of 20f
Fetal heart
color spatiotemporal image correlation of 20f
inversion mode for 21f
rate 136
sound 173
Fetal infection 146
Fetal intervention 144
Fetal medical therapy 149
Fetal medicine 144, 184
Fetal middle cerebral artery 135
Fetal musculoskeletal abnormalities 142
Fetal occiput, position of 170, 171t
Fetal spinal column, omniview of 21f
Fetal structural abnormalities 129b
Fetal surgery 149, 152
prerequisites for 152
principles of 152
Fetal therapy 144, 149
Fetal tracheal occlusion 152
Fetal tumors 129
Fetal weight estimation 133
Fetal well-being, assessment of 168
Fetoscopic fetal surgery 153
Fetoscopic surgery 149
limitations of 153
Fetoscopic tracheal occlusion 153
Fetus papyraceus 96
Fibroids 29t, 59, 61f
ultrasound features of 61t
Fibroma 28
Fibrotic endometriotic deposits 51
First trimester
placenta, normal 112f
ultrasound in 82
Fission theory 97
Flow index 58f
Fluorescent in situ hybridization 177
Follicle 63
B-mode image of 4f
pulse Doppler image of 44f
stimulating hormone 42
Follicular ring sign 66
Fraternal twins 90
Free beta-human chorionic gonadotropin 94
Functional cysts 28
Fusion
defects 59
theory 97
G
Gastrointestinal system 129
Gastrointestinal tract 156
anomalies 156
malformations 156t
Gastroschisis 107
Genetic counseling 144
Genitourinary system 129
Germ cell tumor 28
Gestation sac 75f77f
Gestational age 134f, 135
appropriate for 105f
fetus growth charts, appropriate for 134f
function of 125f
growth charts, large for 135f
large for 133
Gestational sac 46, 82, 83, 83f, 84f, 86f, 88f
Gestational trophoblastic
disease 32, 65, 76
neoplasia 33
tumors 33
Goitre 129
Gonadotropin-releasing hormone 29
Granulosa cell tumor 28
Graves’ disease 150
Ground-glass appearance 63, 63f
Growth scan 191
Gynecology, ultrasound in 55
H
Head and neck 129
Head circumference 104, 105, 133
Head-perineum distance 171
measurement of 172f
Head-symphysis distance 171
measurement of 172f
Heart 22, 23, 107
block, complete 150
Hematoma 115f, 117
collection of 80f
Hematometra 61
Hemoglobin 100
Hemorrhage, subchorionic 74
Hemorrhagic cyst 32, 34f, 64, 70, 71
Hepatic calcification 161
Hepatic cyst 164
Heterogeneous myometrium 29f
Heterotopic pregnancy 78f
High pulse repetition frequency 10f
High-definition flow Doppler 18f
High-resistance
umbilical artery Doppler 137f
uterine artery flow waveform 46f
High-resolution ultrasonography 184
Human chorionic gonadotropin 32, 44, 67, 181
Hydrosalpinx 70, 72
Hydrothorax, primary 152
Hyperplasia
congenital adrenal 149
endometrial 60
Hyperthyroidism 150
Hypoplastic uterus 59
Hypothyroid fetus 150
Hysterectomy 116f
I
Iliac flow 28
In vitro fertilization 37, 43, 187
Inferior vena cava 162f
Infertility 63, 67
monitories 25
ultrasound in 42
Injury, mechanism of 96
Insonation, angle of 25, 56
International Endometrial Tumor Analysis Group 59
International Ovarian Tumor Analysis 28, 64, 72
Classification 28
Collaboration 64
Guidelines 72t
Terminologies 28
International Society of Ultrasound in Obstetrics and Gynecology 104, 133, 148, 194
Intertwin membrane, documentation of 191f
Intra-amniotic hemorrhage 165
Intracranial lesions 175
Intrapartum ultrasonography 142
Intrauterine adhesion 60
ultrasonography features of 60
Intrauterine contraceptive device 67
Intrauterine device 91
Intrauterine growth restriction 25, 105, 133, 157, 165
Intrauterine insemination 16, 39, 42
Intrauterine pregnancy 78, 78f
Intrauterine transfusion 150
Intravenous immunoglobulin, maternal administration of 149
Invasive diagnostic tests 49
Invasive mole 77f
Irregular gestational sac 74
Irregular periods 70
J
Jejunal atresia 159f
Jejunoileal atresia 159f
L
Labor, assessment of progress of 170
Lace-like pattern 71
Lambda sign 92
Laparoscopy 52
Large subchorionic hematoma 86f
Length abnormalities 120
Light-emitting diode 12
Limbs 107
abnormalities 158
Low spiral artery resistance index 35f
Lower segment uterine contraction 115f
Low-resistance tortuous vessels 32f
Lung
malformations, congenital 140
maturity, steroids for 149
Luteal phase scan 37
Luteinized unruptured follicle 36
Luteinizing hormone 44
M
Magnesium sulfate, maternal administration of 149
Magnetic resonance imaging 49, 51, 175
machines 187
Malignant adnexal masses 72
Malignant teratoma 28
Malignant uterine tumors 34
Marginal hematoma 167
Mass
ground-glass appearance of 32f
lesions 15
Maternal blood flow, disruption of 116
Maternal human immunodeficiency virus 150
Maternal serum alpha-fetoprotein 177
Maternal transmissible infectious disease 146
Mature cystic teratoma 71
Mature follicle
B-mode features of 43
B-mode ultrasound image of 44f
Mature teratoma 28
Mean sac diameter 74, 83
Meconium ileus 160, 160f
Meconium peritonitis 161
Meconium pseudocyst 164, 164f
Medical software, sample form of 189f
Meigs syndrome 28
Membranes
funneling of 110f
premature rupture of 127, 153, 167
Meningocele 139f
Meningomyelocele 144, 152
fetal surgery for 152
surgery for 152
Menstrual cycle 27, 28t
study of 35
Mesenteric cyst 164
Middle cerebral artery 138f, 189
Doppler 136
peak systolic velocity 100, 150
Midtrimester scan 106f
Miscarriage 88f
incomplete 85
missed 86, 86f
threatened 74
Modified biophysical profile 136
Molar pregnancy 86
Molar tissue, penetration of 77f
Monochorionic diamniotic twins 99f, 101f, 126, 185
Monochorionic fetuses, reduction in 152
Monochorionic monoamniotic twins 90, 102
Monochorionic pregnancy 9497
Monochorionic twin 90f, 95f, 100f, 126
pregnancy 94, 96, 97
classification of 96
Monozygotic twins 90, 90f
genesis of 91
Morbidly adherent placenta 79, 167, 175
Morphological uterus sonographic assessment 59
Mucinous cystadenocarcinoma 28
Mucinous cystadenoma 28
Mucopolysaccharidosis 184
Müllerian duct abnormalities 15
Multicystic dysplastic kidneys 108f
Multifetal gestation 91, 94, 95
invasive prenatal diagnosis in 94
mechanism of 90
Multifetal pregnancy
monitoring of 93
reduction 151
Multilocular cyst 64
Multiple gestation, diagnosis of 92
Multiple pregnancy 87, 90, 102, 149, 190
Multiplex ligation-dependent probe amplification 147
Myometrial blood flow 38f, 39
Myometrial contraction 39
Myometrial cysts 29f
Myometrial echogenicity 39
Myometrial lesions 61f
Myometrium 15, 16f, 55, 66, 116f
homogeneous 38f
homogenicity of 15
N
National Cancer Institute 35
Neck 107
Negative predictive values 92
Neonatal intensive care unit 127, 141
Next generation sequencing 147
Nodule, subcutaneous 53f
Nonassisted reproductive technology 39
Noninvasive diagnostic tests 49
Noninvasive prenatal testing 181
Noninvasive transplacental route 149
Nonsteroidal anti-inflammatory drugs 127
Nonstress test 135, 173
Nuchal translucency 82, 85f, 181, 184
nomogram of 191f
sampling of 191f
scan 190
thickness 94
O
Obgyn medical software 189f
Obstetrics
and gynecology, training in ultrasound in 193
four-dimensional ultrasound in 19
three-dimensional ultrasound in 19
Obstructive uropathy 152, 153
Occipitofrontal diameter 104, 105
OEIS syndrome 161
Oligohydramnios 101f, 112f, 127, 165
Open fetal surgery 149, 152
Open spina bifida 107
Ovarian cyst aspiration 152
Ovarian fibroma 72
Ovarian fossae, peritoneum of 52
Ovarian hyperstimulation syndrome 25, 42
Ovarian masses 28, 63
Ovarian polycystic sonomorphology 64f
Ovarian stimulation 25
Ovarian stromal
flow 18f, 43f
resistance index 42
Ovarian torsion 30f
Ovarian vessels 28
resistance index for 28t
Ovarian volume 36, 42, 43f
Ovary 51, 62, 66
changes in 35
corpus luteum in 65f
power Doppler in 58f
three-dimensional ultrasound image of 42f
P
Pain, acute abdominal 175
Painful umbilical swelling 54f
Parasitic twin 97
Paratubal cyst 70, 72
Partial hydatidiform mole 76
Partial vesicular mole 76f
Patau syndrome 177, 180
Peak systolic velocity 42, 43, 47, 136, 189
Pedicle artery sign 30, 30f
Pelvic
congestion syndrome 34
inflammatory disease 32, 72
mass 70
organs, sonography of 13
pain 70
wall scars 52
Percutaneous ultrasound-guided fetal shunts 153
Perifollicular flow 18f
Peritoneal cavity 78
Peritoneal endometriosis 32
Peritoneal inclusion cysts 70, 72
Persistent right umbilical vein 163
Placenta 109f
accreta 79, 116f
spectrum 114, 116f
anatomy of 112f
normal 111
percreta 79f
previa 78, 108f, 113, 114f
complete 79f
transvaginal ultrasound of 168f, 169f
separation of 80f
succenturiate lobe of 79f
thickening of 80
Placental abnormalities 111
Placental abruption 80, 113, 167, 176
Placental calcification 118
Placental cord insertion site 133
Placental growth factor 181
Placental hematoma, types of 117f
Placental lacuna 168f
Placental localization 104, 108
Placental location 133
Placental tumors 118
Plasma protein-A, pregnancy-associated 94, 181
Pleuroamniotic shunt 152
Polycystic ovary 28, 71
disease 70
syndrome 60, 63, 64f
Polyhydramnios 101f, 113f, 128, 129b
causes of 128b
Poor decidual reaction 75
Positive predictive value 30, 92
Positive urine pregnancy test 87f
Positron emission tomography scan 52
Postovulation corpus luteum 63
Potassium chloride 151f
Pouch of Douglas 32, 52
Power Doppler 5
settings 6
Pre-conception and Pre-natal Diagnostic Techniques 186
(Prohibition of Sex Selection) Act 189
Act 186, 187
Registered Center in India 145
Pre-eclampsia 189
Pregnancy 65, 111
first trimester of 22
loss, recurrent 60
medical termination of 186
poor prognostication of 88f
prognostication of 87
Preterm delivery 113, 189
Preterm labor, high chances of 153
Pretrigger endometrium, B-mode features of 45
Previous cesarean scar 87f
endometriosis 53f
Prostaglandin synthetase inhibitors 129
Pseudocysts 72
Pseudogestational sac 78
Pseudomyxoma peritonei 28
Pulsatility index 28, 39, 47, 135
Pulse
Doppler 47
repetition frequency 7, 9, 44
Pulsed wave Doppler 8, 26, 26f
Pyometra 61
Q
Quantitative fluorescent 147
polymerase chain reaction studies 177
Quintero classification 101t
R
Reactive nonstress test 174f
Renal anomalies 158
Reporting pelvic ultrasound 66, 66b
Reproduction, uterine scoring system for 39
Resistance index 28, 43
Resorption defects 59
Respiratory system 129
Reticular pattern 71
Retrochorionic hematoma 86f
Retroplacental collection 167
Retroplacental hematoma, two-dimensional ultrasound image of 117f
Retroplacental hypervascularity 168f
Retroplacental myometrium, thickening of 80
Ring of fire sign 78
Rubella 146
S
Sacrococcygeal teratoma 144
ligation of 152
surgery for 153
Saline infusion sonography 30, 30f
Scanning angle 1
Scanning depth 2
Scar
dehiscence 81
ectopic pregnancy 34
diagnostic criteria for 34
pregnancy 87f
tissues 15
Second trimester
biometry 105f
placenta, normal 112f
scan, scope of 104
ultrasound in 104
uterine artery Doppler studies in 108
Selective fetal
growth restriction 95, 96
reduction 151
Septate uterus 59
Serious cardiac abnormalities 107
Serious cystadenocarcinoma 28
Serosa 55
Serous cystadenoma 28
Sex cord tumor 28
Simple adnexal cyst 78
Simple cyst 70, 71f
Single gene disorder 184
Single umbilical artery 118, 120f
Sirenomelia 161
Skeletal system 129
Skills training 23
Skull 107
Sliding sign 51, 55
Small arteriovenous anastomoses 100f
Small bowel atresia 140f, 159
Small for gestational age 113, 133
age fetus growth charts 134f
Small gestational sac 74
Small stomach 157
Sonography-based automated volume count 19, 20, 64f
Sonography-based volume computer-aided display 19, 21
Spatiotemporal image correlation 19, 20
fetal heart 21f
Spectral Doppler 5
Spider web appearance 72
Spinal column, skeletal mode for 22f
Spine 107
Splenic cyst 164
Splitting sign 56
Standard fetal biometric measurements 105t
Stomach
absence of 157, 157f
nonvisualization of 157
String appearance, beads of 72
Stroma outside uterus 32
Subchorionic hematoma 75f, 167
two-dimensional ultrasound image of 117f
Subdiaphragmatic vestibulum 162f
Submucous myoma 62f
Succenturiate lobe 112f
Synchronous color flow imaging 26
T
Tachycardia, supraventricular 150
Telemedicine 19
Tetralogy of Fallot 95, 184
Thecoma 72
Third trimester ultrasound 131, 132
Thorax 107
axial view of 156
sagittal view of 156
Thrombosis 175
Thyroid
disorders 150
stimulating hormone 150
Tomographic ultrasound imaging 19, 20
Torsion 66
Toxoplasma 146
Tracheoesophageal fistula 158
Transabdominal diameter 104
Transabdominal route 13
Transabdominal scan 13f, 14f, 55, 56
Transabdominal sonography 82, 114
Transabdominal ultrasonography 113
scan 51
Transabdominal ultrasound 114f
imaging 171f
Transplacental route 149
Transrectal route 13
Transrectal ultrasonography 49
Transvaginal color Doppler 32
Transvaginal probe 14f
Transvaginal route 13
Transvaginal scan 42, 55, 56, 115f
Transvaginal sonography 45, 68, 70, 75, 82, 110, 114
Transvaginal ultrasonography 49, 50, 50f, 51, 53f
Transverse abdominal diameter 105
Triamniotic trichorionic triplet pregnancy 87f
Triploidy 177, 180
Trisomy 13 177, 180
Trisomy 18 177, 180
Trisomy 21 177, 178
screening for 181t
Trophoblastic diseases 76
T-sign 92
Tubal ectopic gestation 78f
Tubal ring sign 78
Tubo-ovarian abscess 70, 72
Turner syndrome 177, 180
Twin anemia polycythemia sequence 92, 99, 99f, 100
management of 92
Twin pregnancy
incidence of 92t
management of 94, 96
Twin reversed arterial perfusion sequence 98, 152
management of 92
Twin-to-twin transfusion syndrome 92, 100, 101, 101f, 144, 152
management of 92
Typical Doppler waveform 25f
Typical ovarian endometriomas 52
U
Ultrasonography 38, 50, 55, 70, 175
limitations of 51
Ultrasound 1, 42, 48, 90, 104
appearance 157
frequency 25
guided interventions 149, 150
machine, basic principles of 1
modalities of 56
practice, empowerment of 22
scan 50
screening 94
Umbilical artery 100, 135
Doppler 136
normal 137f
Umbilical coiling index 120
Umbilical cord 119f
abnormalities of 118
knot 122f
Umbilical endometriosis
primary 52
secondary 52
Umbilical vein 100, 162f
Unicornuate uterus 59
Unilocular cyst 64
Upper gastrointestinal obstruction 128
Ureteropelvic junction 95
Urinary bladder endometriosis 52
Urinary tract dilatation 140f
Uterine anomalies, congenital 58, 60f
Uterine artery 18f, 109f, 135
Doppler
flow 39
studies 104, 108
flows, normal 109f
high-resistance flows in 109f
pulsatility index 46
Uterine biophysical profile 38
Uterine cavity 87f
Uterine fundus 87f
Uterine masses 28
Uterine perfusion 36
Uterine rupture 81
Uterine scoring system for reproduction scores 39, 40t
Uterine wall 75f
Uterocervical gland 16f
Uterosacral ligament 53f
Uterus 52, 66, 78, 82
B-mode image of 3f, 4f, 16f
endometrium of 61f
high-definition flow of 58f
power Doppler in 58f
transverse
diameter measurement of 17f
section of 17f
ultrasound 57f
ultrasound color Doppler flow in 58f
V
Vaginal bleeding during pregnancy 74
Vasa previa 79, 79f, 111, 120
Vascular tissue, penetration of 79f
Vascularization-flow index 58
Velamentous cord insertion 120f
Ventriculoamniotic shunts 154
Vertebral anomalies 158
Vertebral defects 158
Vesicoamniotic shunt 152
Vesicouterine fold 52
Vesicular mole
complete 76f
snowstorm appearance of 87f
W
Waist sign 72
Wall motion filter 6, 7, 9
Weight loss 70
Whirlpool sign 31f
World Health Organization 131
Writing ultrasound report 189
Y
Yolk sac 75f, 77f, 83, 84f, 88f
Z
Z-score 133
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Chapter Notes

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Basic Principles of Ultrasound Machine1

Sonal Panchal,
Chaitanya Nagori
 
INTRODUCTION
Ultrasound (US) is the most essential modality for a gynecologist. A well done US may give maximum information about the anatomy and pathology of the female pelvic organs as well as the growing fetus. It is, therefore, essential that the operator is well-acquainted with the machine and can use its different functions for the best advantage of the patient. It is true that majority of us are reluctant to operate the different knobs available for obtaining the most expected image quality probably because we fear ruining the already made settings on the machine. This is well understood by the manufacturers and therefore several presets are available on the machines, with the names of the presets suggesting, what are these best for. These presets are made keeping in mind majority of the patients, but naturally would not suit to all and several adjustments are required to produce good quality images. Good quality images are essential for correct diagnosis.
This chapter will be divided under following heads:
  • Optimizing B-mode image
  • Optimizing Doppler image
  • Artifacts
  • Safety of US
  • Tips to make a good setup
 
OPTIMIZING B-MODE IMAGE
The image can be optimized by manipulating and adjusting the knobs on the control panel of the scanner (Fig. 1). It is essential to know about the knobs, what they do, and when to use them.
The settings that need to be often done during each scan to get an optimum information out of the scans are scanning angle, scanning depth, probe frequency, focal zone, zoom, gains, contrast, and probe power.
zoom view
Fig. 1: Switch board of the scanner.
  • Scanning angle: Each probe has a maximum scanning angle. This is the maximum angle up to which the US beam can fan out. It indicates as to how far sideward can an US beam see. Maximum scanning angle for transvaginal probes usually vary from 80° to 180°. Large scanning angle is very convenient for obtaining the bird's eye view of the pelvis to see the entire uterus or first trimester fetus on a single image (Fig. 2), but it decreases the speed of scanning which is indicated by frame rate.
    What is frame rate?
    The real time B-mode images that we are seeing on the scanner screen are several static images seen quickly one after the other. Faster the change in frames, more real time it looks. Frame rate is the number of static images displayed in a unit time by the scanner. This means that if the frame rate is low, the image less real time.2
zoom view
Fig. 2: B-mode image with a complete open angle.
zoom view
Fig. 3: Diagrammatic explanation of the sound beam direction in the central zone and in the side lobes.
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Figs. 4A and B: (A) B-mode image with more depth; and (B) B-mode image with appropriate depth.
Therefore, once the area of interest has been located, the scanning angle should be narrowed down to just a little larger than the area of interest. Narrowing the scanning angle increases frame rate. Moreover, when one decreases the scanning angle, area of interest is brought in the center. The sound beam from the transducer head then hits it at closer to right angle and gives sharper margin definition. When sound beam is emitted from the convex probe surface, the sound beam is vertical in the central part but is oblique on the sides (Fig. 3). This means that the structures that are not in the center of the image field are hit by the sound waves tangentially and lead to unsharp margins due to refraction.
  • Scanning depth: Each probe has a limit of maximum depth up to which the US beam can penetrate. This, of course, depends on frequency of the probe. Maximum achievable depth by any probe may be used for the initial survey, but then depending on the depth at which the area of interest, the scanning depth, is to be decreased. This also increases the frame rate, and improves resolution (Figs. 4A and B). The correct depth setting is when the organ/lesion of interest fills up two-thirds of the image.
  • Setting the focal zone: The US beam behaves like a light wave passing through the convex lens and therefore converges at a point called focal point, but since the probe (transducer) produces a series of similar sound beams the converging points of all make a plane called focal zone. Focal zone is the level at which the image is the sharpest because of the narrowest beam width. Therefore, focal zone is always set at the level of area of interest. The arrow head on right side of the image indicates the focal zone (Fig. 5). There is also an option of having more than one focal zone, when there are multiple levels at which the image needs to be sharp. But increasing the number of focal zones decreases the frame rate, and therefore usually single focal zone is selected.3
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    Fig. 5: B-mode image of the uterus showing yellow arrowhead on the left side indicating the focal zone.
  • Zoom: After the overview, decreasing the scanning angle and depth and setting the focal zone, further improvement in the image quality can be achieved by zooming the image. One may zoom the whole image (panzoom) (Figs. 6A to C) or may use a zoom box to decide and define which part of the image needs to be zoomed [high-definition (HD) zoom] (Figs. 6A to C). Panzoom only enlarges the image and therefore increases the distance between the image pixels and deteriorates the image quality unless it is used after freezing the image, whereas HD zoom concentrates pixels into a smaller box and thus improves image resolution. Larger image can depict more anatomical details. Image should be zoomed large enough to fill up at least two-thirds of the screen.
  • Gains: The US wave when travels into the body hit several tissue planes on its onward as well as return path. With each plane that it hits, the sound beam attenuates due to absorption of the energy and refraction of the sound wave. This leads to darker (hypoechoic) image of the structures that are far from the probe. Image can be made brighter by increasing the gains (Figs. 7A and B). This is potentiating of the returning beam to make the image brighter, but changing gains inadvertently may lead to erroneous diagnosis. Therefore, in all doubtful, difficult situations, the gains once set on the preset should then not be changed. If done, one must revert back to preset as soon as the scanning field is changed. Gains can be adjusted in two ways. Total gains can be increased/decreased, or gains can be adjusted layerwise, depending on the distance of the tissue plane from the probe. The latter one is known as time gain compensation (TGC) (Fig. 8). US wave returning from deeper structures takes longer time to return and is attenuated. This control compensates for the gains lost by time.
  • Probe power: Brightness of the image can also be adjusted by increasing the power of the incident beam. Gain adjustment potentiates the returning beam, and power affects the incident beam. Probe power can be increased maximum to 100%, but usually set at between 80% and 90%. This is to control total mechanical and thermal energy transmitted to the tissues. Power may be increased only when, in spite of all adjustments, an optimum image brightness is not achieved.
  • Contrast: Increased contrast means more black and white image with less shades of gray, and less contrast means more shades of gray in an image (Figs. 9A and B). Unoptimized contrast settings may, therefore, mask the details of soft tissues. Contrast setting may also be presented as dynamic contrast on the US machine.
 
OPTIMIZING DOPPLER IMAGE
 
What is Doppler?
Doppler effect is the change frequency of a sound wave when it hits a moving object. The difference in the emitted and the received frequency is known as Doppler shift. The shift depends on the angle at which the sound beam hits the moving object, velocity of the moving object, and the frequency of the incident beam. Looking into the equation used for calculation of the velocity from the frequency change on Doppler:
The Doppler effect can be displayed as color Doppler, power Doppler, and spectral Doppler.
 
Color Doppler
It displays the blood flow in two colors, and these are conventionally red and blue. The color indicates the direction of the flow. Flow toward the probe is red and away from the probe is blue (Fig. 10), but these can be interchanged by using the invert switch. When the flow is perpendicular to the sound beam, no color will be displayed in spite of presence of the flow. The arterial flow is pulsatile and the venous flow is nonpulsatile. The higher flow velocities display bright colors and the lower flow velocities display dull colors (Fig. 11).4
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Figs. 6A to C: (A) B-mode image of uterus; (B) B-mode image of uterus with panzoom; and (C) B-mode image of uterus with high-definition (HD) zoom.
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Figs. 7A and B: B-mode image of follicles with (A) Normal gains; (B) High gains.
5
Since color Doppler does not give exact velocity values, so it is a directional semiquantitative Doppler.
 
Power Doppler
Power Doppler is nonangle-dependent technology. It is known that movement of any object produces energy and this is used to depict the blood flow signals in power Doppler. This means that wherever there is a movement of blood or of body tissues, color signals will be generated. It displays color signals even in vessels that are perpendicular to the sound beam, but the disadvantage is that it is a single color display and does not show the flow direction (Fig. 12). It indigenously potentiates the signals and therefore is a useful technology for documentation of low velocity blood flows. The main application of the power Doppler, therefore, is to pick up flow in low velocity blood vessels and the blood flows in the vessels are perpendicular to the sound beam. High velocity movements show a bright color and the low velocity movements display dull color (Fig. 12).
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Fig. 8: Image of time gain compensation knobs.
High-definition flow is a new addition to the basic power Doppler technology. It is a directional power Doppler. Apart from high flow sensitivity, HD flow also has a color coding for the flow toward or away from the probe as in color Doppler (Fig. 13).
 
Spectral Doppler
Spectral Doppler is the spectral display of the blood flow/movement of a moving object. Trace above the baseline in the spectrum is the flow toward the probe and the trace below the baseline is the flow away from the probe (Fig. 14) on the spectrum. On the spectral Doppler, the arterial flow appears spiky and the venous flow appears flat. There is a scale on the side of the spectrum that calculates exact velocities of the flows can be calculated (Fig. 14).
The spectrum can be displayed for pulsed wave Doppler and the continuous wave Doppler. In pulsed wave Doppler, the sound waves are emitted in pulses and the frequency of this is called pulse repetition frequency (PRF).
To obtain the correct information about flow velocities with Doppler, certain settings and adjustments on the scanner are required.
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Figs. 9A and B: B-mode ultrasound image with (A) Low contrast; (B) High contrast.
6
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Fig. 10: Color Doppler image showing flow toward the probe in red and flow away from the probe in blue.
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Fig. 11: Color Doppler showing bright color for high velocity flow and dull color for low velocity flow.
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Fig. 12: Power Doppler image showing single color flow and bright color for high velocity flow and dull color for low velocity flow.
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Fig. 13: High-definition (HD) flow image showing endometrial flow.
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Fig. 14: Trace above the baseline in the spectrum is the flow toward the probe and the trace below the baseline is the flow away from the probe and scale on the side of the spectrum calculates the velocities.
Though most of these are set on the dedicated presets, it is important to understand how we can manipulate certain switches/knobs to achieve best flow information.
These are the Doppler box size, color gains, PRF, wall motion filter (WMF) and balance on color and power Doppler and sample volume, gains, PRF, WMF, and angle correction for the pulsed wave Doppler.
  • Color/power Doppler settings:
    • Box size: When one switches on the color Doppler, a box appears on the screen, on the B-mode image. This box defines in which area of the B-mode image, the blood flow information will be looked for. It is important to consider here that when the Doppler is switched on, the machine has to process the B-mode information as well as the flow information and therefore the frame rate significantly decreases.7
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      Fig. 15: Color box seen drawn by green line on the image.
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      Fig. 16: High gains showing color spill outside the vessels.
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      Figs. 17A and B: (A) High pulse repetition frequency (PRF) for low velocity flow shows nonfilling of the vessels (arrow); and (B) Low PRF for high velocity flow shows mixing of colors (arrow).
      The color box size is planned just large enough to cover the area of interest. The color box can be moved all across the B-mode image and the size can be altered based on the requirement (Fig. 15).
    • Gains: When the Doppler is switched on, it should show the blood vessels filled up with color but no color spilling out of the vessels. This is done by gain adjustment. When the gains are too high, the color will be seen spilling out of the vessels (Fig. 16). Whereas when the gains are low, the color will not completely fill up the vessel. This is because when the gains are low, the low velocity signals will not be picked up by Doppler. The correct gain, therefore, is when the entire lumen of the vessel is filled with color and there is no spill outside. Color gains can be adjusted by rotating the color knob.
    • Pulse repetition frequency: It is important to select an optimum PRF for the velocity of the blood vessels flow studied. High PRF if used for low velocity flow, it will not be possible to pick up the color where there are flows (Fig. 17A). Instead if low PRF is used for high velocity flows, there will be aliasing mixing of red and blue colors—appears like turbulence (Fig. 17B). The PRF setting would be optimum when the color homogeneously fills the entire vessel with single color—red or blue.
    • Wall motion filter: It is known that Doppler produces color signals wherever there is a movement and the brightness of the color depends on the velocity of the moving object.8
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      Figs. 18A and B: White patches on color Doppler due to low balance, normal color pick up with normal balance.
      This means that the color signals are produced by the red blood corpuscles in the blood, but are also produced by the wall movement of the artery and also by the pulsations transmitted to the surrounding tissues. The color signals of the blood flow are the brightest, those of wall motion are dull, and those due to transmitted pulsations from the surrounding tissues are the dullest, but these dull color signals corrupt the flow information and can be eliminated only if a low velocity filter is used. This filter is named as WMF. For larger vessels with high velocity flows, the arterial flow movement is more and higher WMF is required, whereas for small vessels with low velocity signals, the arterial wall movements are less and so low wall filters are required. Using higher wall filter for a low velocity blood, flow vessel will eliminate the slow flow information.
    • Balance: As the name suggests, this is a balancing tool between the two modalities—the B-mode and the color Doppler. When color/power Doppler is switched on, a gray bar and a color bar appear on the left side of the screen. On the gray bar, is a green line. This line indicates the balance adjustment. When the brightness of the grayscale on the image matches the brightness below the green line on the gray bar, the color predominates and the color filling is normal, but when the brightness on the grayscale image matches the brightness above the green line on the gray bar, the B-mode predominates and therefore in these areas if the color is present to show the flows, the color will be patched up with white (Figs. 18A and B). When this happens, the correct thing to do is to change the balance to higher, or decrease the B-mode gains (Figs. 18A and B).
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      Fig. 19: Power Doppler image with pulse wave Doppler showing a dashed line with a “= line” showing the sample volume.
  • Pulsed wave Doppler:
    • Sample volume: Sample volume is the selected length of the vessel to assess the flow. When pulsed wave Doppler is switched on, a dotted line appears on the screen. This line is parallel to the sound beam that can be swapped across the entire image. Two parallel short horizontal lines (=sign) appear on this line and is called sample volume/gate size (Fig. 19), this “=sign” can be moved up and down on the dotted line anywhere. This sign is to be placed on the vessel in which the flow is to be measured. The distance between the two lines decide, what length of the vessel will be evaluated for the flow assessment. If the vessel is not absolutely parallel to the sound beam (overlapping on the dotted line), the distance between the two line (sample volume) should be equal to the diameter of the vessel.9
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      Figs. 20A to C: (A) Pulse wave Doppler images showing bold spectrum of Doppler; (B) High gains showing noise on the spectrum; and (C) Scattered spectrum due to low gains on spectral Doppler.
      A sample volume smaller than the diameter will lead to error in the velocity assessment.
    • Gains: Gain settings on the pulsed wave Doppler should be such that it produces a clear well-defined bold spectrum of blood flows (Figs. 20A to C). If the gains are too high, the flow information will be corrupted by lot of noise (Figs. 20A to C). If the gains are too low, the entire spectrum will appear scarce and scattered (Figs. 20A to C).
    • Pulse repetition frequency: PRF is adjusted according to flow velocity to be assessed, high PRF for high velocity flow and low PRF for low velocity flow. If high PRF if used for low velocity flow, it will not be possible to differentiate between the systolic and diastolic flows as the systolic flow recordings will be subdued (Figs. 21A and B). If low PRF is selected for high-velocity blood flows, there will be overlapping of systolic and diastolic signals and is known as aliasing (Figs. 21A and B).
    • Wall motion filter: Like in color and power Doppler, the function of wall motion filter in pulsed Doppler also is to eliminate signals from low velocity movements, not to corrupt the image with wall motions. Again like color and power Doppler, the settings are low for low velocity vessels and high for high velocity vessels, but the wall filter setting in a pulsed Doppler spectrum is known to be correct only if the spectrum touches the baseline. When there is a black line or a gap between the baseline and the spectrum (Fig. 22), this trace is not to be accepted as this clearly indicates high wall filter for the case and may erroneously diagnose absence of diastolic flows. In that case if we say it eliminates low velocity information, means it interferes with the diastolic flow information and may lead to false diagnosis of absent end-diastolic flow and naturally then wrong interpretations.
    • Doppler angle: As is discussed earlier considering the equation for calculation of the blood flow velocity from frequency of incident sound beam, frequency of received sound beam, and cos of the angle of incidence, if the angle of incidence is 90°, then the cos θ being 0, the velocity value will be 0 and also that with increasing angle from more than 60°, the percentage of error in calculation is highly significant and so the Doppler angle is always set between 0° and 60°, preferably <30°.10
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      Figs. 21A and B: (A) Spectral Doppler image with high pulse repetition frequency (PRF) for low velocity flow, hardly any differentiation seen between systolic and diastolic velocities; and (B) Spectral Doppler image with low PRF for high velocity flow, showing overshooting of systolic flow on the other side of the spectrum (aliasing).
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      Fig. 22: High wall motion filter showing black line between the spectrum and the baseline.
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      Fig. 23: Short yellow line deviating out of the dashed line when angle adjustment is done.
      The Doppler angle can be set at 0° when the vessel is parallel to the dotted line. This is often times possible because the dotted line can be swapped across the entire B-mode image and the probe manipulation may also help in the alignment of the two. But if it is still not possible, after achieving the smallest angle between the vessel and the dotted line, angle correction is used. This deviates out a short line from the dotted line, and is tried to align this short line to the vessel (Fig. 23). In trying to do this, the angle between the dotted line and the short line is the Doppler angle. It is displayed on the screen or the touch pad of the scanner.
    • Setting the speed of the trace: An ideal spectral trace is when there are four to five cardiac cycles (Fig. 24) recorded on any one spectrum image. This can be done by setting the speed of the trace. For most scans, this is possible when the speed is set as 4 or 5. Higher speed gives trace of too few cardiac cycles and lesser speed gives too many cardiac cycles traced.
 
UNDERSTANDING THE ARTIFACTS
In spite of all these settings used to optimize the Doppler images, certain artifacts still cannot be completely eliminated. These are aliasing, mirror image artifact, and artifacts due to electrical interferences.11
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Fig. 24: Spectral Doppler showing five complete cardiac cycles on the baseline, suggesting normal speed adjustment.
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Fig. 25: Mirror image artifact seen on the spectral Doppler.
  • Aliasing: This is overlapping effect of systolic and diastolic velocities, across the baseline on both the sides of the spectrum (see Figs. 21A and B). This effect is similar to what we have often observed especially in movies. The car wheels suddenly appear to start rotating in the opposite direction when the car speeds up. Adjusting the PRF can eliminate this artifact.
  • Mirror image artifact: Mirror image artifact is when a similar spectrum is seen on both the sides of the baseline. This is especially possible when the sample volume is large and is tracing the flow in two vessels or two loops of the same vessel positioned, side by side (Fig. 25), or a large sample volume is placed on the curve of the loop, when in the proximal half of the loop the blood flow is observed away from the probe by the transducer and in the distal half of the sample volume the flow is perceived toward the probe. Decreasing the sample volume and planning to place it on one vessel only sorts out this problem.
  • Electrical interferences: These may appear as random signals on color, power, or spectral Doppler, especially when the scanner is sharing the same electrical line as some high voltage gadget and the only way to get rid of this is to plan the electrical supply to the scanner wisely.
 
SAFETY OF DOPPLER
The two major effects of sound wave when it passes through the human body are:
  1. Thermal effect: Production of heat that may damage the cells.
  2. Mechanical effect: Due to pressure changes on the molecule.
Thermal effect: As the sound waves pass through the body tissues, there is absorption of energy and transformation of US energy into heat. The energy absorption is minimal in fluid and maximum in bones. It is also dependent on the frequency of the US waves. The absorption is higher with high frequency waves and lower with low-frequency sound waves. A temperature rise of up to 1°C is considered absolutely safe, whereas if it is >2.5°C, it can lead to significant tissue damage. This thermal effect is measured and displayed as thermal index on the screen. It is generally found that the temperature rise of 2°C is thermal index 2. The thermal index should be limited at maximum 1.
Mechanical effect: When the sound wave passes through the body tissues, it leads to oscillations of the body molecules, resulting in cavitating (low pressure) phase and a compressing (high pressure) phase. The mechanical damage caused by the sound waves is quantified as mechanical index (MI). MI is defined as “maximum estimated in situ rarefaction pressure or maximum negative pressure (in MPa) divided by the square root of the frequency (in MHz)”. MI of up to 0.3 can be considered safe and more than 0.7 can lead to cavitation.1
 
APART FROM THIS A FEW PRACTICAL TIPS ON PLANNING YOUR SETUP
 
Ordering the Scanner
Apart from optimizing the image, it is essential to make the correct choice of the machine according to your requirements and also correctly ordering the probes and the softwares.
There is a huge choice available now in the market as there are several different brands available with a range of lower end only B-mode or portable machines to high-end 3D-4D machines loaded with lot of automations and softwares. Though the image quality, even on the B-mode, significantly improves as one moves on from lower end to the higher end scanners, 3D and 4D scanners are not essential for all. It depends on one's type of practice and the amount of work that the scanner should be selected. But as far as obstetrics and gynecology practice is con-cerned, in our opinion, a good quality scanner with a good quality Doppler is essential. Check for the service facilities of a particular brand around your place.12
Probes must also be selected according to one's practice. It should be kept in mind always that low frequency probes are better for penetration but have a poor resolution, whereas high frequency probes have poor penetration but high resolution. Always check the B-mode and the Doppler image quality with the same probes that is to be bought during presale demonstrations. Instead of depending on the demonstration images in presentations by the company, depend on the live scans that are being done, preferably by a colleague.
When ordering the machine, confirm which softwares are optional and decide which of those are required for one's practice and specifically order for those and confirm when the written order comes to you for signature.
It is also important that in your setup, the electrical power point supplying the scanner should not be in the same line as any other equipment that consumes high power voltage. Moreover, do not fit any light-emitting diode (LED) lights in the scanning room.
 
CONCLUSION
Doppler is a very useful modality for assessment of circulation in the human body. Correct settings on the scanner only can give optimum results and therefore it is very important to understand the basic principles and settings of the US scanner before starting to use Doppler for interpretation of vascular flows and information of oxygenation in human fetus. US and Doppler are generally safe modalities. Their safety can be related to frequency used and the length of exposure. Therefore, Doppler should not be used for long time on a single focus and therefore as low as reasonably achievable (ALARA)2 principle is now applied for all US scan.
REFERENCES
  1. The British Medical Ultrasound Society (BMUS) (2019). Safety of ultrasound. [online] Available from www.bmus.org/public-info/pi-safety01.asp. [Last accessed November, 2019].
  1. Auxier JA, Dickson HW. Guest editorial: concern over recent use of the ALARA philosophy. Health Phys. 1983;44(6):595–600.