Thursday, January 29, 2026

Isolated Abnormal Amniotic Fluid Volume in Pregnancy

This blogpost is the summary of the recent TOG article published in January 2026. It provides an overview of polyhydramnios / oligohydramnios; various cause; its impact on mother & fetus and management of pregnancy/delivery. This is an important resource for exam questions. 

I hope this blog post is helpful. Feel free to leave your feedback in the comments. 


To download the original article (free access) : Click here 

To Access ALL TOG articles: Click here


RK4 Courses

Introduction

  • Amniotic fluid volume (AFV) - vital measurement for fetal well-being
  • Amniotic fluid - produced by fetus & comprises fetal urine and lung fluid; protects fetus from trauma, allows fetal movements & prevents cord compression
  • Pathologies disrupting swallowing ± urine production or flow can directly affect AFV
  • AFV correlated with gestational age & size
  • Abnormal AFV could be due to placental, fetal or maternal pathology or a combination

Measuring AFV

  • Most accurate method to measure AFV - dye dilution test (limited diagnostic value as it requires amniocentesis)
  • Clinically AFV measured in 2 ways - Single Deepest Vertical Pocket (SDVP) or Amniotic Fluid Index (AFI)
  • SDVP preferred choice for AFV assessment
  • AFI measurement increases rates of oligohydramnios diagnosis

Polyhydramnios

  • Defined as - increase AFV, SVDP ≥8 cm or AFI ≥24 cm
  • No universal agreed classification
  • Complicate 1-2% of pregnancies
  • Most common cause of mild-to-moderate polyhydramnios - Idiopathic
  • Fetal abnormalities account for over 30% of severe polyhydramnios
  • Early severe polyhydramnios or in context of FGR or SGA confers poor prognosis

Ref: TOG

Ref: TOG
Ref: TOG

Ref: TOG

Isolated polyhydramnios
  • Most common cause of polyhydramnios - Idiopathic (isolated polyhydramnios)
  • Accounts for 60-70% of all cases & 1% of pregnancies overall
  • Most cases identified in 3rd tri - mild-to-moderate make up 80% overall & 90% of cases at term’
  • Evidence for correlation b/w macrosomia & polyhydramnios

Ref: TOG

Management of isolated polyhydramnios

  • 3 options - amnioreduction, conservative or expedite delivery
  • Consider individual risk factors
  • GTGs recommend regular fetal biometry scan monitoring for all cases of polyhydramnios
  • American Society for Maternal Fetal Medicine recommends amnioreduction only for severe maternal discomfort, dyspnoea or severe polyhydramnios
  • Amnioreduction may assist in aiding diagnosis in suspected fetal genetic abnormalities 
  • Indomethacin - no longer used

Delivery

  • Timing of delivery to be individualised - Need more studies
  • NICE recommends continuous CTG for all cases of polyhydramnios regardless of severity
  • IOL may be offered in moderate isolated polyhydramnios - exact timing decided on individual basis

Management after birth

  • No consensus on screening neonates after birth
  • Risk of neonatal abnormality with idiopathic polyhydramnios - 1% with mild 2% with moderate 10% with severe 
  • UK population risk 2019 -Genetic syndromes 6.3 per 10,000 births Chromosomal abnormalities 23.1 per 10,000
  • Early-onset polyhydramnios & severe polyhydramnios - linked to high rates of undiagnosed genetic abnormalities
  • Rate of genetic abnormalities with isolated polyhydramnios - 4.5% most common genetic abnormality - Bartter syndrome 21% (an autosomal recessive disorder that can be fatal in newborn due to polyuria, hypokalaemia, hyperchloremic metabolic alkalosis and hyperaldosteronism

Oligohydramnios and Anhydramnios

  • Oligohyrdamnios - AFV below normal limits AFI ≤5 cm SDVP <2cm
  • Anhydramnios - complete absence of amniotic fluid
  • Oligohyramnios associated with poor fetal outcomes Higher degree of adverse outcomes if diagnosed in 2nd trimester
  • Most common cause of oligohydramnios - Idiopathic

Ref: TOG

Ref: TOG

Early-onset oligohydramnios

  • Nearly always caused by fetal abnormalities or maternal effects
  • Associated with significant fetal morbidity
  • Most common causes - PPROM, bilateral renal agenesis or severe renal abnormalities (referred to as renal oligohydramnios)
  • Potter’s sequence - used to describe severe early-onset oligohydramnios/ anhydramnios
    • the sequence comprises of clubbed feet, pulmonary hypoplasia, cranial and skin abnormalities
    • It is incompatible with life
    • TOP offered
  • Methods to reduce fetal morbidity - amnioinfusion, fetal surgical procedures - have varying levels of success Area of ongoing research

Isolated oligohydramnios

  • Complicates 0.5 - 5% of pregnancies
  • Diagnosis of exclusion
  • Take a systematic approach to rule out common causes such as membrane rupture, placental disorders, FGR and fetal infection

Management of pregnancy

  • ACOG & NICE recommend increased surveillance and monitoring for signs of deteriorating fetus
  • Amnioinfusion in labour may be beneficial - but has methodological limitations not a common practice in UK

Timing of delivery

  • Continuous CTG advised due to risk of fetal hypoxia
  • IOL associated with increased risk of CS 
  • Timing of delivery to be individualised
  • Need more research in this area

Management after birth

  • Higher rate of respiratory distress & low APGAR scores in isolated oligohydramnios
  • Delivery should occur in a facility with access to neonatal services
  • Increased surveillance advised in subsequent pregnancies (as risk of placental disorders)
Ref: TOG
You may also be interested in

No comments:

Post a Comment