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Fig. 5.29 Feet. Axial view shows normal paired feet (F).
to the next, adjusting probe position as needed to obtain the desired images.82 Scanning beyond the femur will outline the hypoechoic cartilages of the distal femur and proximal tibia. Subsequently the tibia and fibula and orientation of
Normal fetal anatomy at 18–22 weeks
Fig. 5.30 View of a normal hand including the thumb. Note three bones (proximal phalanx, middle phalanx and distal phalanx) of each finger.
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Ultrasound in obstetrics and gynaecology
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Fig. 5.31 Hand, 3D view. Three-dimensional ultrasound with surface rendering better shows the complex shape of the hand.
the leg to the foot can be shown. Measurement of foot length and documenta­tion of digits are possible with appropriate fetal positioning and careful scanning. Similar scanning through the upper extremities can detail the humerus, radius and ulna, and hand.
The clavicle and scapula define the shoulder girdle. The scapula imaged in long axis coronally has a characteristic shape resembling a ‘Y’ with the supraspinatus, subscapularis and infraspinatus muscles in their respective fossae. The scapula has a triangular shape when imaged posteriorly. The clavicles can be seen if not
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obscured by flexion of the fetal head. They grow at a linear rate of approxi­mately 1 mm per week, reaching a length of 20 mm at 20 weeks and 40 mm at 40 weeks.
The humeral head epiphyseal cartilage lies between the ossified distal clavicle, scapula and proximal humeral diaphysis. At the elbow, the non-ossified coronoid fossa delineates the medial and lateral humeral epicondyles. The more proximal extent of the ulna at the elbow distinguishes it from the radius. Demonstration of the ulna and radius ending at the same level at the wrist effectively excludes many radial ray defects. The non-ossified carpals produce a conglomerate zone of grey echoes antenatally, but the ossified metacarpal and phalanges are readily visualized if the fetus extends the hand. The foot length is similar to the ossified femoral shaft throughout much of pregnancy.
83

CONCLUSION

A second-trimester scan has now become widely accepted throughout much of the developed world. We believe it should be considered an essential part of obstetric care, but only when performed by experienced sonographers or sonolo­gists. Armed with a systematic approach, a good understanding of normal fetal anatomy and familiarity with normal sonographic appearances and common vari­ants, the sonographer/sonologist can offer accurate reassurance in the vast major­ity of normal pregnancies, and at the same time detect the majority of major defects in anomalous fetuses. Finally, it will be of interest to see to what extent new techniques like echo-planar magnetic resonance will complement or even replace certain areas of fetal anatomic assessment.
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Normal fetal anatomy at 18–22 weeks

References

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32. Pretorius DH, Kallman CE, Grafe MR, Budorick NE, Stamm ER. Linear echoes in the fetal cisterna magna. J Ultrasound Med 1992;11:125–128
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34. Jeanty P, Cantraine F, Cousaert E et al. The binocular distance: a new way to estimate fetal age. J Ultrasound Med 1984;3: 241–243
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37. Petrikovsky BM, Vintzileos AM, Rodis JF. Sonographic appearance of occipital fetal hair. J Clin Ultrasound 1989;17:425–427
38. Benacerraf B, Frigoletto F, Laboda L. Sonographic diagnosis of Down syndrome in the second trimester. Am J Obstet Gynecol 1985;153:49–52
39. Gray DL, Crane JP. Optimal nuchal skin­fold thresholds based on gestational age for prenatal detection of Down syndrome. Am J Obstet Gynecol 1994;171:1282–1286
40. Bahado-Singh RO, Oz UA, Kovanci E et al. Gestational age standardized nuchal thickness values for estimating mid­trimester Down's syndrome risk. J Matern Fetal Med 1999;8(2):37–43
41. Ho SS, Metreweli C. Normal fetal thyroid volume. Ultrasound Obstet Gynecol 1998;11:118–122
42. Filly RA, Simpson GF, Linkowski G. Fetal spine morphology and maturation during the second trimester. J Ultrasound Med 1987;6:631–636
43. Gray DL, Crane JP, Rudloff MA. Prenatal diagnosis of neural tube defects: origin of midtrimester vertebral ossification centers as determined by sonographic water-bath studies. J Ultrasound Med 1988;7: 421–427
44. Yoo SJ, Lee YH, Cho KS, Kim DY. Sequential segmental approach to fetal congenital heart disease. Cardiol Young 1999;9(4):430–444
45. McGahan JP. Sonography of the fetal heart: findings on the four-chamber view. Am J Roentgenol 1991;156:547–553
46. Copel JA, Gianluigi P, Green J et al. Fetal echocardiographic screening for congenital heart disease: the importance of the four­chamber view. Am J Obstet Gynecol 1987;157:648–655
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48. Brown DL, DiSalvo DN, Frates MC et al. Sonography of the fetal heart: normal variants and pitfalls. Am J Radiol 1993;160:1251–1255
49. Frates MC. Sonography of the normal fetal heart: a practical approach. Am J Roentgenol 1999;173:1363–1370
50. Comstock CH. Normal fetal heart axis and position. Obstet Gynecol 1987;70:255–259
51. Paladini D, Chita SK, Allan LD. Prenatal measurement of cardiothoracic ratio in evaluation of heart disease. Arch Dis Child 1990;65(1 Spec No):20–23
52. Brown DL, Cartier MS, Emerson DS et al. The peripheral hypoechoic rim of the fetal heart. J Ultrasound Med 1989;8: 603–608
53. Schechter AG, Fakhry J, Shapiro LR, Gewitz MH. In utero thickening of the chordae tendinae. A cause of intracardiac echogenic foci. J Ultrasound Med 1987;6(12):691–695
54. Bromley B, Lieberman E, Laboda L, Benacerraf BR. Echogenic intracardiac focus: a sonographic sign for fetal Down syndrome. Obstet Gynecol 1995;86(6):998–1001
55. Manning JE, Ragavendra N, Sayre J et al. Significance of fetal intracardiac echogenic foci in relation to trisomy 21: a prospective sonographic study of high­risk pregnant women. Am J Roentgenol 1998;170(4):1083–1084
56. DeVore GR. The aortic and pulmonary outflow tract screening examination in the human fetus. J Ultrasound Med 1992;11:345–348
57. DeVore GR. Color Doppler examination of the outflow tracts of the fetal heart: a technique for identification of cardiovascular malformations. Ultrasound Obstet Gynecol 1994;4:463–471
58. Yoshimura S, Masuzaki H, Gotoh H, Fukuda H, Ishimaru T. Ultrasonographic prediction of lethal pulmonary hypoplasia: comparison of eight different ultrasonographic parameters. Am J Obstet Gynecol 1996;175(2):477–483
59. D'Arcy TJ, Hughes SW, Chiu WS et al. Estimation of fetal lung volume using enhanced 3-dimensional ultrasound: a new method and first result. Br J Obstet Gynaecol 1996;103:1015–1020
60. Laudy JA, Janssen MM, Struyk PC, Stijnen T, Wladimiroff JW. Three-dimensional ultrasonography of normal fetal lung volume: a preliminary study. Ultrasound Obstet Gynecol 1998;11(1):13–16
61. Vintzileos AM, Neckles S, Campbell WA et al. Fetal liver ultrasound measurements during normal pregnancy. Obstet Gynecol 1985;66:477–480
62. Schmidt W, Yarkoni S, Jeanty P et al. Sonographic measurements of the fetal spleen: clinical implications. J Ultrasound Med 1985;4:667–672
63. Rosenberg ER, Bowie JD, Andreotti RF et al. Sonographic evaluation of the fetal adrenal glands. Am J Roentgenol 1982;139:1145–1147
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64. Hata K, Aoki S, Hata T et al. Ultrasonographic identification of the human fetal gall bladder in utero. Gynecol Obstet Invest 1987;23:79–83
65. Millener PB, Anderson NG, Chisholm RJ. Prognostic significance of non-visualization of the fetal stomach by sonography. Am J Roentgenol 1993;160:827–830
66. Pretorius DH, Gosink BB, Clautice-Engle T et al. Sonographic evaluation of the fetal stomach: significance of nonvisualization. Am J Roentgenol 1988;151:987–989
67. Pekindil G, Varol F, Yuce MA, Yardim T. The fetal stomach circumference/abdominal circumference ratio: a possible parameter in assessing fetal stomach size. Yonsei Med J 1998;39(3):222–228
68. Levine D, Goldstein RB, Cadrin C. Distention of the fetal duodenum: abnormal finding? J Ultrasound Med 1998;17(4):213–215
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70. Nyberg DA, Mack LA, Pattern RM et al. Fetal bowel: normal sonographic findings. J Ultrasound Med 1987;6:3–6
71. Parulekar SG. Sonography of normal fetal bowel. J Ultrasound Med 1991;10: 211–220
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73. Nyberg DA, Dubinsky, Mahony BS, Luthy DA, Hickok DE, Sorenson T. Echogenic fetal bowel: clinical importance. Radiology 1993;188:527–531
74. Hashimoto BE, Filly RA, Callen PW. Fetal pseudoascites: further observations. J Ultrasound Med 1986;5:151–152
75. Cohen HL, Cooper J, Eisenberg P et al. Normal length of fetal kidneys: sonographic study in 397 obstetric patients. Am J Roentgenol 1991;157:545–548
76. Grannum P, Bracken M, Silverman R et al. Assessment of fetal kidney size in normal gestation by comparison of ratio of kidney circumference to abdominal circumference. Am J Obstet Gynecol 1980;136:249–254
77. Anderson N, Clautice-Engle T, Allan R et al. Detection of obstructive uropathy in the
fetus: predictive value of sonographic measurements of renal pelvic diameter at various gestational ages. Am J Roentgenol 1995;164:719–723
78. Kent A, Cox D, Downey P, James SL. A study of mild fetal pyelectasia – outcome and proposed strategy of management. Prenat Diagn 2000;20(3):206–209
79. Shapiro E. The sonographic appearance of normal and abnormal fetal genitalia. J Urol 1999;162:530–533
80. Goldstein RB, Filly RA, Simpson G. Pitfalls in femur length measurements. J Ultrasound Med 1987;6:203–207
81. Lessoway VA, Schulzer M, Wittmann BK. Sonographic measurement of the fetal femur: factors affecting accuracy. J Clin Ultrasound 1990;18:471–476
82. Mahony BS, Filly RA. High resolution sonographic assessment of the fetal extremities. J Ultrasound Med 1984;3: 489–498
83. Mercer BM, Sklar S, Shariatmadar A. Fetal foot length as a predictor of gestational age. Am J Obstet Gynecol 1987;156:350–355
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85. Garel C. Fetal cerebral biometry: normal parenchymal findings and ventricular size. Eur Radiol 2005;15:809–813
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88. Allan L. Technique of fetal echocardiography. Paediatric Cardiol 2004;25:223–233
89. De Vore GR. Three-dimensional and four­dimensional fetal echocardiography: a new frontier. Curr Opin Pediatr 2005;17: 592–604
90. Duncan KR, Issa B, Moore R, Baker PN, Johnson IR, Gowland PA. A comparison of fetal organ measurements by echo-planar magnetic resonance imaging and ultrasound. Br J Obstet Gynaecol 2005;112:43–49
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Amniotic fluid and placental localization

Juriy W Wladimiroff Sturla H Eik-Nes
ABSTRACT
Various pathways determine amniotic fluid production and absorption, which include fetal swallowing, lung fluid and urine production and flow across the chorionic plate. Measurements of the amount of amniotic fluid include the 1 or 2 cm pocket rule and the amniotic fluid index.
Oligohydramnios is associated with fetal renal pathology and fetal growth restriction, whereas polyhydramnios is often associated with a wide range of fetal congenital anomalies, maternal diabetes mellitus, multiple pregnancy and non­immune hydrops.
Ultrasound is the method of choice to locate the placenta. The most common indications for locating the placenta are in connection with first-trimester invasive procedures, bleeding in the second and third trimesters, as part of the routine second-trimester exam and prior to external version of the fetus in late pregnancy. The placenta is located in the fundal area, on the left or right lateral side, the posterior or the anterior side or a combination thereof. Clinically it is most useful to distinguish the relation between the inner os of the cervical canal and the edge of the placenta.
KEYWORDS
Amniotic fluid absorption, amniotic fluid production, amniotic fluid volume, management of abnormal placental location, oligohydramnios, placenta praevia, placental embryology, placental functional anatomy, placental location, polyhydramnios.

AMNIOTIC FLUID

The amount of amniotic fluid surrounding the fetus provides us with informa­tion about the fetal condition. To appreciate abnormal changes in amniotic fluid
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volume, it is necessary not only to reliably measure amniotic fluid volume but also to understand the various pathways which determine amniotic fluid produc­tion and absorption.

AMNIOTIC FLUID PHYSIOLOGY

It is during the period of embryonic development that the amnion is formed and surrounds the embryo. In the beginning the amnion itself is surrounded by coelo­mic fluid which will disappear from 9–10 weeks of gestation and a rapid expan­sion of amniotic fluid volume will occur thereafter. Amniotic fluid is 98–99% water and its chemical composition varies with gestational age.10 There are five pathways playing a major role in the exchange of water and solutes between fetus and amniotic fluid.14 Excretion from the fetus into the amniotic cavity consists of fetal urine flow and lung flow. The onset of fetal micturition is associated with a reduction of amniotic osmolarity which will continue with advancing gestational age.10 Reabsorption of amniotic fluid takes place through fetal swallowing and absorption into the fetal circulation across the fetal surface of the placenta1 and
Ultrasound in obstetrics and gynaecology
exchange across the fetal skin before completion of the keratinization process at approximately 22 weeks of gestation. Finally, there appears to be excretion from the fetal salivary glands into the amniotic fluid. A short resumé of a few of the most important pathways will now follow.
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Fetal urinary production
Fetal urine flow constitutes an important source of amniotic fluid, hence the devel­opment of severe oligohydramnios in bilateral renal agenesis or urethral obstruc­tion. Diagnostic ultrasound has provided data on hourly fetal urinary production rates, with values from 2–3 mL/h at 20 weeks to 30–35 mL/h at term.17 This would result in a urinary production rate of 700–800 mL/24 h, which is approximately 25% of fetal body weight/day. Over the years different urine production rates have been reported as a result of different measuring techniques. It seems that the above figures are probably more or less correct. Fetal urine contributes not only to amniotic fluid volume but also to its composition, since osmolarity is about one­half and chloride and sodium concentration are about one-third of plasma values.
Lung fluid
The production of lung fluid is 250–300 mL/24 h at term, which is approximately 10% of fetal body weight.9 A very small percentage of this fluid remains in the lungs for expansion with growth. Nearly 99% of the fluid leaves the lungs through the trachea. Beyond the trachea about 50% is swallowed and the remaining 50% will appear in the amniotic fluid.
Flow across the chorionic plate
It is likely that the exchange from the amniotic cavity to the fetal blood compart­ment of water and solutes is quite considerable, with figures of 200–250 mL/day of water in normal fetal development near term.
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AMNIOTIC FLUID VOLUME

Both amniotic fluid volume and its composition reflect the status of mother and fetus.
Methods of assessment
Several methods of amniotic fluid assessment have been employed to detect adverse fetal conditions. Determination of total intrauterine volume reflecting the sum of the volume of all intrauterine contents (fetus, placenta, amniotic fluid) is achieved from longitudinal, transverse and anteroposterior uterine dimensions. This method was particularly applied for the early detection of fetal growth restriction, but has a low accuracy. A quantitative approach of assessing amniotic fluid volume is the 1 cm or, even better, the 2 cm pocket rule. Using ultrasound, the largest cord-free pocket of amniotic fluid is detected and the vertical and transverse diameter of this pocket is measured with the transducer always at right angles to the mater­nal abdominal wall. Amniotic fluid volume was considered normal if the pocket measured 1 cm or more in its largest vertical diameter and reduced if the diam­eter was less than 1 cm.8 However, this approach leads to a pick-up rate of fetal growth restriction of only 4%. Later it was demonstrated that amniotic fluid pock­ets greater than 1 cm but less than 2 cm should also undergo further investigation for fetal underdevelopment.2 Here, the single deepest pocket was identified.
A semi-quantitative method of assessing amniotic fluid volume is the amni­otic fluid index technique.13 Using the umbilicus as a reference point, the uterus is divided into an upper and a lower half. The linea nigra is subsequently used to divide the uterus into a right and a left half, resulting in four uterine quadrants. The ultrasound transducer is placed in each quadrant with the transducer head always at right angles to the floor. A more oblique positioning of the transducer head will result in an inaccurate amniotic fluid volume measurement. Moreover, the inves­tigation should extend to the lateral margins of the uterus since often substantial amniotic fluid may be situated in the flanks of the pregnant woman when in the supine position. In each quadrant the largest pocket of fluid is sought according to the above technique. The vertical diameter of each of the pockets is then mea­sured (Fig. 6.1). The numbers obtained from each quadrant are added up. The resulting figure in centimetres represents the amniotic fluid index for that particu­lar pregnant woman. A normal amniotic fluid index ranges between 5 and 25 cm.
The amniotic fluid index and single deepest pocket measurement appear to perform best for the identification of normal amniotic fluid volumes, whereas the identification of oligo- and polyhydramnios is of limited value.7 In another study, the amniotic fluid index was not significantly correlated with perinatal out­come.11 The amniotic fluid index seems to offer no advantage in detecting adverse outcomes compared with the single deepest pocket when performed with the biophysical profile.
Three-dimensional ultrasound has been used in measuring amniotic fluid or gestational sac volume at 11–14 weeks of gestation,4 whereas later in pregnancy magnetic resonance imaging was found to be comparable with ultrasound evalu­ation for the prediction of oligohydramnios.
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Amniotic fluid and placental localization
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4.7 cm 5.8 cm
4.9 cm 6.2 cm
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Fig. 6.1 Measurement of the vertical diameter in each of the four quadrants of the uterus. The numbers are added up to calculate the amniotic fluid index.
Normal amniotic fluid volume values
Amniotic fluid volume increases from approximately 70 mL at 11 weeks of ges­tation to 800 mL at 28 weeks followed by a slower increase to about 1000 mL at 34 weeks. A decline in volume takes place during the last 6 weeks of gestation to about 800 mL at 40 weeks. Gestational sac volume appears to be a poor predictor of major chromosomal defects.
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Abnormal amniotic fluid volumes
Abnormalities in amniotic fluid volume are associated with increased perinatal mortality and morbidity.
Oligohydramnios
Oligohydramnios is defined as a deepest fluid pocket of less than 2 cm or an amniotic fluid index of 5 cm or less. It develops in 0.5–4.0% of all pregnancies and can be associated with fetal growth restriction as a result of reduced renal perfusion and urinary output. Severe oligohydramnios (deepest fluid pocket smaller than 1 cm) or even anhydramnios may develop in the presence of bilat­eral renal agenesis or urethral obstruction/stenosis. Pregnancies beyond 40 weeks may be complicated by reduced amounts of amniotic fluid with volumes down