Polyhydramnios
Updates to Article Attributes
Polyhydramnios refers to a situation where the amniotic fluid volume is more than expected for gestational age.
It is generally defined as:
- amniotic fluid index (AFI) > 25 cm
- largest fluid pocket depth (maximal vertical pocket (MVP)) greater than 8 cm 6: although some centres particularly in Australia, NZ and the UK use a cut off of 10 cm
- overall amniotic fluid volume larger than 1500-2000 cc3
- two diameter pocket (TDP) > 50 cm 2
Epidemiology
It can occur in approximately 1-1.5% of pregnancies.
Clinical presentation
The patient may clinically present as alarge for dates uterus.
Pathology
Polyhydramnios occurs as a result of either increased production or decreased removal of amniotic fluid. The aetiology of polyhydramnios can be due to a vast variety of maternal and fetal disorders.
It is usually detected after 20 weeks (often 3rd trimester).
Causes
The potential causes of polyhydramnios are protean
- idiopathic: 60-65%: this is a diagnosis of exclusion despite accounting for a majority of cases, also termedidiopathic polyhydramnios
-
maternal: 25-30%
- diabetes: commonly gestational diabetes
- maternal congestive heart failure 8
-
fetal: 10-20%
- CNS lesions (e.g. neural tube defects): fetal CNS abnormalities tend to be the commonest out of all fetal causative associations 3
- proximal gastro-intestinal obstruction
- gastrointestinal atresia(s)
- abdominal wall defects
- fetal intestinal volvulus, e.g. from an intestinal malrotation
- fetal cervico-thoracic
abnormalitiesabnormalities- fetal cervical masses
- thoracic masses
- fetal cardiovascular anomalies
- sustained fetal tachycardia (e.g. supraventricular tachycardia (SVT), atrial flutter, ventricular tachycardia) 12
- twin pregnancy related complications
- twin-twin transfusion: occurs in recipient
- hydrops fetalis: immune and non immune
- fetal sketetal abnormalities
- reduced fetal movement
Associations
- fetal macrosomia: independant of maternal diabetes2,in idiopathic form
- mesoblastic nephroma
- Pena Shokeir syndrome
- maternal overhydration ref
Polyhydramios is associated with poor outcome if present in combination with intra uterine growth restriction (IUGR); usually seen in aneuploidies 18,13, and 21.
Classification
Some classify the severity of polyhydramnios as
- mild: single deepest pocket at 8-11 cm
- moderate: single deepest pocket at 12-15 cm
- severe: single deepest pocket >16 cm
Treatment and prognosis
The prognosis is variable dependent on associated conditions. Usually minimal or no interventional required for idiopathic mild uncomplicated cases. Options include:
- improved maternal diabetes control
- caesarian section if there is profound macrosomia
- therapeutic amniocentesis / amnioreduction
- Indomethacin 9-10
See also
-</ul><h4>Epidemiology</h4><p>It can occur in approximately 1-1.5% of pregnancies.</p><h4>Clinical presentation</h4><p>The patient may clinically present as a <a href="/articles/large-for-dates-uterus">large for dates uterus</a>. </p><h4>Pathology</h4><p>Polyhydramnios occurs as a result of either increased production or decreased removal of amniotic fluid. The aetiology of polyhydramnios can be due to a vast variety of maternal and fetal disorders. </p><p>It is usually detected after 20 weeks (often 3<sup>rd</sup> trimester).</p><h5>Causes</h5><p>The potential causes of polyhydramnios are protean</p><ul>- +</ul><h4>Epidemiology</h4><p>It can occur in approximately 1-1.5% of pregnancies.</p><h4>Clinical presentation</h4><p>The patient may clinically present as a <a href="/articles/large-for-dates-uterus">large for dates uterus</a>. </p><h4>Pathology</h4><p>Polyhydramnios occurs as a result of either increased production or decreased removal of amniotic fluid. The aetiology of polyhydramnios can be due to a vast variety of maternal and fetal disorders. </p><p>It is usually detected after 20 weeks (often 3<sup>rd</sup> trimester).</p><h5>Causes</h5><p>The potential causes of polyhydramnios are protean</p><ul>
-<strong>idiopathic: 60-65%</strong>: this is a diagnosis of exclusion despite accounting for a majority of cases, also termed <a href="/articles/idiopathic-polyhydramnios">idiopathic polyhydramnios</a>- +<strong>idiopathic: 60-65%</strong>: this is a diagnosis of exclusion despite accounting for a majority of cases, also termed <a href="/articles/idiopathic-polyhydramnios">idiopathic polyhydramnios</a>
-<li><a href="/articles/jejunoileal-atresia-1">jejuno-ileal atresia</a></li>- +<li><a href="/articles/jejunal-atresia">jejuno-ileal atresia</a></li>
-<li>fetal cervico-thoracic abnormalities <ul>- +<li>fetal cervico-thoracic abnormalities <ul>
-<li>thoracic masses</li>- +<li>thoracic masses<ul>
-<li>fetal cardiovascular anomalies</li>- +</ul>
- +</li>
- +<li>fetal cardiovascular anomalies<ul><li>sustained fetal tachycardia (e.g. supraventricular tachycardia (SVT), atrial flutter, ventricular tachycardia) <sup>12</sup>
- +</li></ul>
- +</li>
-<a href="/articles/fetal-macrosomia">fetal macrosomia</a>: independant of maternal diabetes <sup>2</sup>,<sup> </sup>in idiopathic form</li>- +<a href="/articles/fetal-macrosomia">fetal macrosomia</a>: independant of maternal diabetes <sup>2</sup>,<sup> </sup>in idiopathic form</li>
-</ul><p>Polyhydramios is associated with poor outcome if present in combination with <a href="/articles/intra-uterine-growth-restriction-2">intra uterine growth restriction (IUGR)</a>; usually seen in aneuploidies 18,13, and 21.</p><h5>Classification</h5><p>Some classify the severity of polyhydramnios as </p><ul>- +</ul><p>Polyhydramios is associated with poor outcome if present in combination with <a href="/articles/intrauterine-growth-restriction">intra uterine growth restriction (IUGR)</a>; usually seen in aneuploidies 18,13, and 21.</p><h5>Classification</h5><p>Some classify the severity of polyhydramnios as </p><ul>
References changed:
- 12. Simcha Yagel (Editor), Norman H Silverman (Editor), Ulrich Gembruch (Editor). Fetal Cardiology: Embryology, Genetics, Physiology, Echocardiographic Evaluation, Diagnosis and Management of Cardiac Diseases, Second Edition. (2008) ISBN: 0415432650 - <a href="http://books.google.com/books?vid=ISBN0415432650">Google Books</a>