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to about 350 mL at 42 weeks of gestation. Oligohydramnios may also develop in association with drug therapies such as indometacin treatment in prema­ture labour. Decreased renal perfusion may be the underlying mechanism for this. Another cause of oligohydramnios is premature rupture of the membranes (PROM), which occurs in approximately 10% of all pregnancies and is associ­ated with increased perinatal mortality and morbidity due to premature labour, chronic fetal distress or infection. When severe oligohydramnios develops before 20–25 weeks of gestation, there is a high association with fetal pulmonary hypo­plasia, fetal facial compression and abnormal position/contractures of hands/feet (oligohydramnion sequence).
Polyhydramnios
Polyhydramnios is defined as a deepest fluid pocket of more than 8 cm or an amniotic fluid index of at least 25 cm or more. Its incidence has been reported to range from 0.4% to 3.3%. Chronic polyhydramnios which develops gradually over weeks or months is more common than acute polyhydramnios.
The aetiology of polyhydramnios is diverse and includes fetal congenital anom­alies, notably neural tube defects and neuromuscular defects preventing adequate swallowing, on the one hand, and gastrointestinal obstruction resulting in fluid congestion on the other. Nearly one in five pregnancies with chronic polyhy­dramnios has been associated with fetal anomalies. Other abnormal maternal and fetal conditions associated with polyhydramnios are maternal diabetes mellitus, macrosomia, multiple pregnancy and non-immune fetal hydrops. Also, lesions of the umbilical cord and placenta have been associated with polyhydramnios. However, in approximately two-thirds of pregnancies with polyhydramnios, no specific cause can be established. Idiopathic polyhydramnios12 does not seem to be less associated with adverse perinatal outcomes than polyhydramnios in which one of the above fetal or maternal conditions has been identified. Polyhydramnios in itself may create obstetric problems such as premature labour, postpartum haemorrhage and PROM resulting in prolapsed cord.
Amniotic fluid and placental localization

CONCLUSIONS

Various pathways determine production and absorption of amniotic fluid, amongst which are fetal swallowing, fetal urinary production, fetal lung fluid excretion, fluid transfer through the chorionic plate and to a minor extent fluid excretion by the fetal salivary glands. Normal amniotic fluid volumes display a wide distribu­tion with a marked increase up to about 34 weeks and a gradual reduction there­after. Determination of amniotic fluid volume includes single deepest pocket and amniotic fluid index measurement. Abnormal amniotic fluid volumes include both oligohydramnios and polyhydramnios. Whereas oligohydramnios is mostly associated with fetal pathology, polyhydramnios may be due to abnormal fetal or maternal conditions or may be idiopathic. The predictive value of amniotic fluid index and single deepest amniotic fluid pocket for oligo- and polyhydramnios appears to be limited.
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Chorion frondosum
Decidua basalis
Decidua
parietalis
Decidua
capsularis
Chorion laeve
Measurement of the vertical diameter in each of the four quadrants of the uterus is undertaken. The numbers are added up to calculate the amniotic fluid index.

PLACENTA LOCALIZATION

The introduction of ultrasound technology represented a unique step forward in our ability to make a diagnosis regarding the human placenta. Rapidly, it became clear that the new technology had far more advantages than x-ray, thermography and scintigraphy in the ability to locate the placenta, and it left the old techniques obsolete. Even the particularly difficult problem of defining the exact delineation of the border in cases where placenta praevia was suspected is now of historical interest only as a consequence of high-resolution ultrasound and the transvaginal scanning approach.

EMBRYOLOGY

Ultrasound in obstetrics and gynaecology
The placenta is regarded as an organ of fetal origin as it develops solely from the outer cell layer of the blastocyst, the trophoblast. The contact with the uter­ine endometrium and the trophoblast induces a proliferation of the trophoblast. Some of the trophoblast cells lose their cell membrane and form a syncytium, the so-called syncytioblast. This process stimulates a decidual reaction in the endo­metrium that causes the stroma to become thicker and highly vascularized, then called decidua. A thin capsule of the decidua called decidua capsularis covers the part of the embryo which is protruding into the endometrial cavity. The decidua at the embryonic pole develops into the decidua basalis, which takes part in the formation of the future placenta. During early development, the vessels support­ing the decidua capsularis regress and the smooth chorion or chorion laeve devel­ops.6 The vessels supporting the decidua basalis are retained and the leafy chorion or chorion frondosum is developed and the growth process of the placenta, which takes most of the remaining time of the pregnancy, then commences (Fig. 6.2).
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Fig. 6.2 Status of the chorion and the decidua at approximately 8 weeks' gestational age.
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Functional anatomy
The human placenta is the interface between the circulations of the mother and fetus for the exchange of nutrients, respiratory gases and waste products.3 The physiological mechanism of the transfer of specific substances is complicated and remains a field for advanced research. This is in contrast to other organ systems where such a mechanism is mostly understood.
The human placenta has approximately 120 cotyledons that together com­prise the functional unit of the organ. Each of these cotyledons has a primary villus stem which arises from the chorionic plate and is supplied by the primary branches of the fetal vessels. Further down the vascular tree, these branches form the secondary and tertiary stem where the vascular exchange takes place. From the maternal side, the pulsative blood flow from the spiral arteries enters the intercotyledonary space and flushes the maternal side of the vascular space all the way up to the chorionic plate. Between the cotyledons, the blood filters into venous channels and returns to the decidual plate. There is complete separation between the fetal and the maternal blood and all exchange of nutrients and blood gases takes place through the vasculosyncytial membranes separating the two circulatory systems.
Development of the placenta as evaluated by ultrasound technology
During weeks 8–12 the development of the placenta may be followed and the chorion frondosum (placenta) may be easily differentiated from the chorion laeve (chorion) (Fig. 6.3). From week 12 onwards it becomes possible to differentiate between the placenta, the basal plate facing the maternal side of the placenta and the chorionic plate facing the fetus. The placenta grows as pregnancy progresses, allowing easy identification.
Amniotic fluid and placental localization

INDICATIONS FOR THE LOCATION OF THE PLACENTA

First-trimester invasive procedures such as abdominal or transvaginal
•
chorion villus biopsy Transabdominal amniocentesis in the second trimester and other invasive
•
procedures performed any time later in the pregnancy Bleeding in the second and third trimesters
•
Evaluation of the placenta and its location and relation to the uterine wall
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in cases of suspected placental abruption Routine fetal examination performed at 18–20 weeks
•
Prior to external version of the fetus in late pregnancy.
•
The most common indication for location of the placenta is during systematic evaluation of the uterus and the intrauterine contents during the second-trimes­ter fetal examination or ‘routine fetal examination’ as it is frequently called. The fetal examination is best initiated by the inverted U-movement of the transducer starting at the symphysis, slowly moving the transducer in a transverse plane on one side of the uterus to the top of the uterus and then down to the symphysis
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Fig. 6.3 Pregnancy at 10 weeks' gestational age. The placenta and the chorion are clearly imaged, as is the amniotic sac surrounding the fetus. The amnion has not yet fused with the chorion.
on the contralateral side. During this procedure the placenta may be located and other important features such as the viability of the fetus, the position and the
Ultrasound in obstetrics and gynaecology
number of fetuses may be established.
In early pregnancy, i.e. before the 18–20-week routine fetal examination, there is no reason to register the location of the placenta except for those indicated above.
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Various locations of the placenta
In the second trimester, the chorionic plate or the fetal surface of the placenta is usually seen as a white line. The placenta is usually relatively echogenic, with equally distributed, fine-grained echoes through the full extent of the organ. The basal plate is not always easy to distinguish but the uterine tissue, which is about
1.5 cm thick, appears slightly darker in its fine-grained echo setting compared to the placenta, making the delineation between the placenta and the uterine tis­sue possible (Fig. 6.4). Normally, the placenta is located in the fundal area on the left or right lateral side, the posterior or the anterior side (Fig. 6.5) or a combi­nation thereof. The most important clinically useful distinction of the location is
Fig. 6.4 Placenta located on the anterior wall. The uterine wall, the basal plate of the placenta facing the uterus and the chorionic plate facing the fetus are clearly seen.
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Fig. 6.5 Placenta located on the anterior wall including a velamentous insertion of the cord.
Amniotic fluid and placental localization
the relation between the lower portions of the placenta and the internal os of the uterus (Fig. 6.6). Attempts should be made to demonstrate the lower portion of the placenta and the internal os on the same image. Care must be taken to dis­tinguish between Braxton Hicks contractions and the placenta. The contraction appears darker and less echogenic (Fig. 6.7).
The final location of the placenta may require additional sagittal and parasag­ittal scans. It is not difficult to locate the placenta except when it is on the lower posterior wall. The overview might be difficult due to extremities or a larger pre­senting part of the fetus casting a shadow on the deeper portion of the image. Scanning from the right or left side of the uterus or scanning transvaginally can help overcome the problem.
Fig. 6.6 The placenta is located on the posterior wall, covering the internal os of the cervical canal. The placental edge is marked with +.
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Fig. 6.7 The placenta is located on the posterior wall. A local contraction of the uterus behind the placenta can clearly be distinguished, making the placenta seem to be protruding into the amniotic fluid.
Placenta praevia
The placenta may cover the internal uterine os (see Fig. 6.6). When this is the case, an exact delineation of the location of the placenta and a specific manage-
Ultrasound in obstetrics and gynaecology
ment protocol are required. If more than 2.5 cm of the placenta covers the inter­nal os, it is characterized as placenta praevia. A transvaginal scan may assist in providing a more detailed location of the lower portion of the placenta. In addi­tion to the detailed relation to the internal os, it is important to describe the main location of the placenta. Particular attention is required when the placenta covers the internal os and a major part of the placenta is located in the lower anterior portion of the uterus, which may interfere with a surgical approach to deliver the fetus.
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Suggested management protocol for suspected placenta praevia
Management when the placental edge related to the internal os at 18–20 weeks is:
=1 cm from internal os. No further scans. Placenta praevia is unlikely.
•
<1 cm from or <2.5 cm overlying the internal os. Repeat scan at 35 weeks
•
(or earlier in case of bleeding).
2.5 cm overlying the internal os. Most likely placenta praevia at term. Plan for
•
a caesarean section at 38 weeks following verification of placental location.

PLACENTAL MORPHOLOGY

Sometimes small sonolucent areas may be located within the regular fine-grained texture of the placenta, usually towards the basal plate (Fig. 6.8). They are usu- ally referred to as placental lakes and represent areas without any fetal villi which consist of slowly moving blood. They have no clinical significance.
Placental cysts may be located close to the chorionic plate. They are superfi-
cial vessels seen in cross-section or as longitudinal tubes. They have no clinical significance.
The placental texture changes during the course of a pregnancy. These mor-
phological changes have not been proven to have any clinical implications16 but
15
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Fig. 6.8 Anterior placenta with a placental lake.
it is useful to have knowledge of the described changes, which are part of the gradual ageing process of the placenta.
Grannum, who classified them into grades 0, I, II and III, has described these changes, called placental grading, in detail.5 Grade 0 represents the normal fine­grained homogenic placenta. Grade I presents with multiple echogenic areas, grade II has echogenic areas towards the base and comma-like indentions in the chorionic plate. Grade III has, in addition to grade II, cystic areas within the pla­centa and echogenic irregular areas beneath the chorionic plate.
Amniotic fluid and placental localization

CONCLUSION

The placenta is regarded as an organ of fetal origin as it develops from the tro­phoblast. It is the interface between the maternal and fetal circulation. The human placenta has approximately 120 cotyledons, each of which derives its vascular supply from the fetus. The development of the placenta may be fol­lowed from week 8 onwards. By week 12, distinction of the placenta, with the basal plate facing the uterus and the chorionic plate facing the fetus, is possible. The indications for localization of the placenta are in connection with intra­uterine invasive procedures, with bleeding in the second trimester, as part of the routine second-trimester scan and prior to external version in late pregnancy. The distinction of the relation of the inner cervical os and the placental edge is important. A management protocol for placenta praevia must be followed.

References

1. Brace RA. Current topic: progress toward
understanding the regulation of amniotic fluid: water and solute fluxes in and through the fetal extraplacental membranes. Placenta 1995;16:1–18
2. Chamberlain PF, Manning FA, Morrison I,
Harman CR, Lange IR. Ultrasound
evaluation of amniotic fluid volume. I. The relationship of marginal and decreased amniotic fluid volumes to perinatal outcome. Am J Obstet Gynecol 1984;150:245–249
3. Doughty IM, Sibley CP. Placental transfer. In: Hanson A, Spencer JAD, Rodeck C (eds)
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Fetus and neonate. Physiology and clinical applications. Cambridge University Press, New York, 1995: 3–29
4. Falcon O, Wegrzyn P, Faro C, Peralta CF, Nicolaides KH. Gestational sac volume measured by three-dimensional ultrasound at 11 to 13+6 weeks of gestation: relation to chromosomal defects. Ultrasound Obstet Gynecol 2005;25:546–550
5. Grannum PAT, Berkowitz RL, Hobbins JC. The ultrasonic changes in the maturing placenta and their relations to fetal pulmonic maturity. Am J Obstet Gynecol 1982;133:915–922
6. Larsen W. Fetal development and the fetus as a patient. In: Essentials of human embryology. Churchill Livingstone, New York, 1998: 317–330
7. Magann EF, Doherty DA, Field K et al. Biophysical profile with amniotic fluid volume assessments. Obstet Gynecol
Ultrasound in obstetrics and gynaecology
2004;104:5–10
8. Manning FA, Hill M, Platt LD. Qualitative amniotic fluid determination by ultrasound. Am J Obstet Gynecol 1981;139:254–260
9. Mescher EJ, Platzker ACG, Ballard PL, Kitterman JA, Clements JA, Tooley WH. Ontogeny of tracheal fluid, pulmonary surfactant and plasma corticoids in the fetal lamb. J Appl Physiol 1975;39:1017–1021
10. Modena AB, Freni S. Amniotic fluid dynamics. Acta Biomed Ateneo Parmense 2004;75:11–18
11. Ott WJ. Reevaluation of the relationship between amniotic fluid volume and perinatal outcome. Am J Obstet Gynecol 2005;192:1803–1809
12. Panting-Kemp A, Nguyen T, Chang E, Quillen E, Castro L. Idiopathic polyhydramnios and perinatal outcome. Am J Obstet Gynecol 1999;181:1079–1082
13. Phelan JP, Smith CV, Broussard P, Small M. Amniotic fluid volume assessment with the four-quadrant technique at 36–42 weeks gestation. J Reprod Med 1987;32:540–542
14. Seeds AE. Current concepts of amniotic fluid dynamics. Am J Obstet Gynecol 1980;138:575–586
15. Thompson MO, Vines SK, Aguilina J, Wathen NC, Harrington K. Are placental lakes of any clinical significance? Placenta 2002;23:685–690
16. Vosmar MB, Jongsma HW, van Dongen PW. The value of ultrasonic placental grading: no correlation with intrauterine growth retardation or with maternal smoking. J Perinat Med 1989;17:137–143
17. Wladimiroff JW, Campbell S. Fetal urinary production rates in normal and complicated pregnancy. Lancet 1974;ii:151–154
18. Zaretsky MV, McIntire DD, Reichel TF, Twickler DM. Correlation of measured amniotic fluid volume to sonographic and magnetic resonance predictions. Am J Obstet Gynecol 2004;191:2148–2153
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Assessment of the placenta and umbilical cord

Eric Jauniaux
ABSTRACT
With improvement of ultrasound equipment, obstetricians are now able to examine the placenta and the cord in detail before delivery and to investigate the placental circulations in vivo. Over the last two decades ultrasound has gained an important role in the prenatal diagnosis and management of:
first- and second-trimester intrauterine haematomas which are associated

with premature rupture of the membranes and preterm onset of labour placenta accreta which is characterized by myometrial invasion by villi
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tissue and occurs when the decidua basalis is partially or completely absent vascular chorioangiomas which are associated with an increased incidence of
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polyhydramnios and fetal growth retardation complete and partial hydatidiform mole which can both be associated with
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persisting gestational trophoblastic tumours vascular placental lesions such as large thrombosis and infarcts which are
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usually found during the third trimester and are associated with fetal growth restriction the absence of one umbilical artery which is found in association with many
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fetal anatomical defects and which when isolated leads to poor fetal growth in about 20% of the cases abnormal cord insertion and position which can be associated with severe
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obstetric complications.
These findings demonstrate that the differential diagnosis of placental and cord abnormalities is now possible in utero and that placental examination should be part of all routine ultrasound examinations.
KEYWORDS
Placenta, trophoblast, tumour, umbilical cord.
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INTRODUCTION

Before the development of ultrasound imaging, morphological examination of the placenta and the cord was only of epidemiological value and was therefore of little influence on pregnancy management. With the advent of modern ultrasound equip­ment, it is now possible to examine the placenta and the cord in detail from the beginning of the first trimester. A gestational sac of 2–3 mm can be detected as early as 4 weeks and 1 or 2 days menstrual age. In fact, the term ‘gestational sac’ refers to the chorionic cavity and the rim of placental villi and underlying decidual prolifera­tion, which is the first evidence of a pregnancy.
Determining placental position in utero was one of the first aims of ultra­sound examination in the 1960s. Visualization and localization of the placenta by ultrasound became rapidly superior to all other imaging techniques such as radiographic placentography or scintigraphy and is now an essential part of rou­tine prenatal examinations. The ultrasound features of most placental or cord vascular lesions may undergo major changes within a few days. When a placental or cord abnormality, which could be associated with perinatal complications, is
Ultrasound in obstetrics and gynaecology
suspected, serial sonographic examinations should be performed.
The information which can now be obtained by high-resolution ultrasound or Doppler techniques places additional demands on the clinician who requires more extensive knowledge of the anatomy and physiology of the vascular circu­latory changes that occur during pregnancy. differential diagnoses and pathophysiology of the principal abnormalities of the placenta and the umbilical cord will be presented.
1–30
In this chapter, the sonographic
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MAJOR STRUCTURAL ABNORMALITIES OF THE PLACENTA

In describing placental lesions, ultrasonographers have used many inaccurate and misleading expressions. This is probably due to the fact that little attempt has been made to compare ultrasound and pathological findings. One should always refer to the histopathological terminology to categorize these lesions and evaluate their clinical significance.

CONGENITAL ABNORMALITIES

Abnormalities of placentation
Placenta extrachorialis
This is a common abnormality, found in about 25% of all placentas, and charac­terized by a transition of membranous to villous chorion at a distance from the placental edge.9 Insertion of the membranes within the placental margin results in placental tissue not covered by the chorionic plate (extrachorialis) and in a smaller than normal amniotic cavity.9 Two forms can be distinguished: the circummargin­ate placentas and the circumvallate. Only the latter has clinical significance because the abnormal insertion of membrane contains amnion, chorion and decidual tissue. As the uterine wall stretches during the second half of gestation, the placenta can­not adapt and there is tearing of membranes from the edge of the chorionic plate