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The amniotic sac is a tough but thin transparent pair of membranes which hold a developing embryo (and later fetus) until shortly before birth. The inner membrane, the amnion, contains the amniotic fluid and the fetus. The outer membrane, the chorion, contains the amnion and is part of the placenta. It is also called the amniotic bubble because of its resemblance to a bubble. When in the light, the amniotic sac is shiny and very smooth, but too tough to pierce through.
An artificial rupture of membranes (ARM), also known as an amniotomy, may be performed by a midwife or obstetrician. This is usually performed using an amnihook and is intended to induce or accelerate labour.
Amniotic fluid[edit | edit source]
Amniotic fluid is the watery liquid surrounding and cushioning a growing fetus within the Amnion. It allows the fetus to move freely without the walls of the uterus being too tight against its body. Buoyancy is also provided.
The amnion grows and begins to fill, mainly with water, around two weeks after fertilisation. After a further 10 weeks the liquid contains proteins, carbohydrates, lipids and phospholipids, urea and electrolytes, all which aid in the growth of the fetus. In the late stages of gestation much of the amniotic fluid consists of fetal urine.
Recent research by researchers led by Anthony Atala of Wake Forest University and a team from Harvard University has found that amniotic fluid is also a plentiful source of non-embryonic stem cells. These cells have demonstrated the ability to differentiate into a number of different cell-types, including brain, liver and bone.
The forewaters are released when the amnion ruptures, commonly known as when a woman's "waters break" or "spontaneous rupture of membranes" (SROM). The majority of the hindwaters remain inside the womb until the baby is born.
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Too little amniotic fluid (oligohydramnios) or too much (polyhydramnios or hydramnios) can be a cause or an indicator of problems for the mother and baby. In both cases the majority of pregnancies proceed normally and the baby is born healthy but this isn't always the case. Babies with too little amniotic fluid can develop contractures of the limbs, clubbing of the feet and hands, and also develop a life threatening condition called hypoplastic lungs. If a baby is born with hypoplastic lungs, which are small underdeveloped lungs, this condition is potentially fatal and the baby can die shortly after birth.
On every prenatal visit, the obstetrician/gynaecologist should measure the patient's fundal height with a tape measure. It is important that the fundal height be measured and properly recorded to insure proper fetal growth and the increasing development of amniotic fluid. The obstetrician/gynaecologist should also routinely ultrasound the patient—this procedure will also give an indication of proper fetal growth and amniotic fluid development. Oligohydramnios can be caused by infection, kidney dysfunction or malformation (since much of the late amniotic fluid volume is urine), procedures such as chorionic villus sampling (CVS), and preterm premature rupture of membranes (PPROM).
Polyhydramnios is a predisposing risk factor for cord prolapse and is sometimes a side effect of a macrosomic pregnancy. Hydramnios is associated with esophageal atresia. Amniotic fluid is primarily produced by the mother until 16 weeks of gestation.
Preterm premature rupture of membranes (PPROM) is a condition where the amniotic sac leaks fluid before 38 weeks of gestation. This can be caused by a bacterial infection or by a defect in the structure of the amniotic sac, uterus, or cervix. In some cases, the leak can spontaneously heal, but in most cases of PPROM, labor begins within 48 hours of membrane rupture. When this occurs, it is necessary that the mother receive treatment to avoid possible infection in the newborn.
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ABS occurs when the inner fetal membrane (amnion) ruptures without injury to the outer membrane (chorion). Fibrous bands from the ruptured amnion float in the amniotic fluid and can entangle the fetus, reducing blood supply and causing congenital limb abnormalities dysmelia. In some cases a complete "natural" amputation of a digit(s) or limb may occur before birth or the digit(s) or limbs may be necrotic (dead) and require surgical amputation following birth.
Multiple pregnancies[edit | edit source]
Twins and multiple pregnancies sometimes share the amnion and the chorion. Monoamniotic pregnancy is when each embryo or foetus from one single zygote (monozygotic, commonly known as identical twins) is located within the same amnion, which is itself in one chorion (monochorionic). Diamniotic pregnancy is when there is more than one amnion, either inside a single chorion or with each amnion having its own chorion (dichorionic). Dizygotic (fraternal, non-identical) twins each have their own amnion and chorion and may or may not share a placenta.
Sharing the same amnion (or the amnion and placenta) can cause complications in pregnancy. For example, the umbilical cords of monoamniotic twins can become entangled, reducing or interrupting the blood supply to the developing fetuses. Monochorionic twins, sharing one placenta, usually also share the placental blood supply. In rare cases, blood passes disproportionately from one twin to the other through connecting blood vessels within their shared placenta, which may lead to twin-to-twin transfusion syndrome. In other cases where the placenta is being shared disproportionately (a battledore placenta), the condition can lead to one twin getting less oxygen than the other, resulting in disproportionate growth rates. There is also a greater risk of developing amniotic band syndrome.
See also[edit | edit source]
References[edit | edit source]
- Mayes, M., Sweet, B. R. & Tiran, D. (1997). Mayes' Midwifery - A Textbook for Midwives 12th Edition, pp. 533–545. Baillière Tindall. ISBN 0-7020-1757-4
- Forewaters and hindwaters in Q&A section at babyworld.co.uk
|Mammalian development of embryo and development and fetus (some dates are approximate - see Carnegie stages) - edit|
Week 3: Hensen's node | Gastrula/Gastrulation | Trilaminar embryo Branchial arch (1st) | Branchial pouch | Meckel's cartilage | Somite/Somitomere | Germ layer (Ectoderm, Endoderm, Mesoderm, Chordamesoderm, Paraxial mesoderm, Intermediate mesoderm, Lateral plate mesoderm)
|Histogenesis and Organogenesis|
Circulatory system: Primitive atrium | Primitive ventricle | Bulbus cordis | Truncus arteriosus | Ostium primum | Foramen ovale | Ductus venosus | Ductus arteriosus | Aortic arches | Septum primum | Septum secundum | Cardinal veins
Urinary/Reproductive system: Urogenital folds | Urethral groove | Urogenital sinus | Kidney development (Pronephros | Mesonephros | Ureteric bud | Metanephric blastema) | Fetal genital development (Wolffian duct | Müllerian duct | Gubernaculum | Labioscrotal folds)
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