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FETAL SURVEILLANCE

BY

Dr. A. E. EDUGBE (MBBS, FMCOG, FWACS)

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OUTLINE

  • Introduction
  • Aetiology of fetal deaths
  • Aims of fetal surveillance
  • Indications for fetal surveillance
  • Antepartum fetal surveillance
  • Intra-partum fetal surveillance
  • Conclusion

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INTRODUCTION

Fetal surveillance are the various methods or techniques employed to assess the risk of adverse perinatal outcome of a fetus at risk for antepartum and/or intra-partum fetal loss

Placenta is the only fetal supply line for nutrition and gas exchange, hence, the fetus is vulnerable to any strain in the utero-placental unit

Any utero-placental disorder becomes more critical as the fetus gets bigger

Currently, there are no treatment modalities for reversion of utero-placental insufficiency

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INTRODUCTION CONT;

  • Fetal monitoring (FS) is crucial for detection of fetuses at risk of jeopardy – early or late stages of hypoxia

Timely delivery is effected when findings suggest fetal compromise

  • The aim of FS is to deliver the most mature fetus in the best possible condition with minimal risk to the mother
  • Reduce the risk of fetal death in utero
  • Delay the need for inappropriate interventions
  • Prolong the gestation in pregnancies at risk for preterm delivery

  • Most authorities begin at 32 weeks, and the interval of testing is generally weekly to twice weekly
  • FS may done antepartum or intra-partum

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DEFINITION OF TERMS

  • Hypoxia: Decreased PO2 in tissues
  • Acidosis: Decreased PH in tissues
  • Asphyxia: Hypoxia with metabolic acidosis
  • Utero-placental insufficiency;
    • Inadequate delivery of nutrients or oxygen to appropriate fetal tissues
    • Inadequate exchange within the placenta could be due to decreased blood flow, decreased surface area or increased membrane thickness
  • Theoretical scheme of fetal deterioration: nutritional compromise → growth restriction → fetal hypoxia → acidosis → asphyxia → death

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Aetiology of fetal loss

Fetal deaths

Antepartum 70-90%

Intrapartum 10-30%

  • Chronic asphyxia
  • Anomalies
  • Pregnancy complications
  • Unexplained IUDs
  • Chronic asphyxia
  • Anomalies
  • Pregnancy complications
  • Unexplained IUDs

Asphyxia 30%

Maternal compl 30%

Malformations 15%

Infection 5%

Unexplained 20%

Asphyxia 30%

Maternal compl 30%

Malformations 15%

Infection 5%

Unexplained 20%

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AIMS OF FETAL SURVEILLANCE

1. To ensure satisfactory growth and well being of the fetus throughout pregnancy

2. To screen out high risk factors that affect the growth of the fetus

3. To determine when the risk of IUFD outweighs the risk of premature delivery

4. To determine optimum timing of delivery

5. To avoid unnecessary obstetric interventions

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INDICATIONS FOR FETAL SURVEILLANCE

  • Prolonged pregnancy
  • Diabetes mellitus
  • Hypertensive disorders in pregnancy
  • Previous Stillbirth
  • Suspected intra-uterine growth restriction
  • Rhesus isoimmunization
  • Decrease fetal movements
  • Amniotic fluid disorders – oligo/polyhydramnios
  • PPROM, Antepartum haemorrhage
  • Multiple pregnancy
  • Maternal medical disorders e.g renal, heart etc

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ANTEPARTUM FETAL SURVEILLANCE

  • Most fetal deaths occur in the antepartum period

  • Antepartum fetal deaths – causes;

- Asphyxia (IUGR, post dates) – 30%

- Maternal complications(PE, abruption, DM) – 30%

- Congenital malformations/chromosomal abnormalities – 15%

- Infection – 5%

  • About 20 percent of stillbirths have no obvious cause

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METHODS OF ANTENATAL FETAL SURVEILLANCE

This can be subclassified under:

  • Clinical

  • Biophysical

  • Biochemical – Prenatal diagnosis lecture e.g AFP

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CLINICAL METHODS OF ANTENATAL FS

  • Use mainly for fetal growth assessment
  • Useful as screening test for further investigation

1. Maternal weight gain

  • In second half of pregnancy, average weight gain is 0.5 Kg/week
  • Excess weight gain may be due to excess fluid retention – May be first sign of pre-eclampsia
  • Weight gain that is less than normal, stationary or even falling may points to IUGR

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2. SFH

  • Correspond to GA in second half of pregnancy up to 36 weeks with error margin of 1-2 cm
  • Aim is to compare SFH with GA calculated from LMP (certain date) or early USS
  • SFH > GA – causes include Wrong date (LMP), multiple pregnancy, polyhydramnios, pelvic tumours etc
  • SFH < GA – causes include wrong LMP, IUGR, oligohydramnios etc

3. Auscultation of fetal heart

  • Assessment of rate & rhythm using;

- Pinard stethoscope or doppler (Sonicaid)

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BIOPHYSICAL METHODS OF ANTENATAL FS

  • Principle - Biophysical profile is a screening test for utero-placental insufficiency
  • Fetal biophysical activities are initiated, modulated and regulated through fetal nervous system
  • The fetal CNS is very sensitive to diminished oxygenation
  • Hypoxia → metabolic acidosis → CNS depression → changes in fetal biophysical activity

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1. Fetal movement count

Decreased placental perfusion and fetal hypoxia are associated with decreased fetal movements

  • Cardiff count to 10 –
  • The patient counts fetal movements starting from a specific time e.g 9 am
  • The counting comes to an end as soon as 10 movements are perceived
  • She is instructed to report if;

(i) less than 10 movements occur during 12 hours on 2 successive days

(ii) no movement is perceived even after 12 hours in a single day

Biophysical methods of antenatal FS

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  • Daily fetal movement count (DFMC):
  • Three counts each of one hour duration (morning, noon and evening) are recommended
  • Total counts multiplied by four gives daily (12 hour) fetal movement count (DFMC)
  • If there is diminution of the number of kicksto less than 10 in 12 hours (or less than 3 in each hour), it indicates fetal compromise
  • Loss of fetal movements is commonly followed by disappearance of FHR within next 24 hours
  • Ominous fetal kick count is an indication for NST

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NOTE;

  • Maternal hypoglycemia is associated with increased fetal movements
  • Maternal perception of fetal movements may be reduced with;

- Fetal sleep (quiet)

- Fetal anomalies (CNS)

- anterior placenta

- Polyhydramnios

- Obesity

- Drugs (narcotics)

- Chronic smoking

- Hypoxia

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FETAL KICK CHART IN BHUTH

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BIOPHYSICAL METHODS OF ANTENATAL FS

2. Ultrasound;

  • late USS helps in detecting:

i) Fetal growth abnormalities – IUGR, fetal macrosomia

ii) Abnormalities in amniotic fluid volume

iii) Problems with placenta – calicifications etc

iv) Abnormalities of fetal position

v) Fetal wellbeing

  • IUGR can be diagnosed accurately with serial measurement of BPD, AC, HC, FL and amniotic fluid volume
  • AC is the single measurement which best reflects fetal nutrition

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  • Mean increase of BPD after 34 weeks is 1.7 mm/week
  • When HC/AC ratio is elevated (> 1.0) after 34 weeks, IUGR should be suspected

Amniotic fluid volume assessment;

  • A vertical pocket of amniotic fluid 2-8 cm is considered normal, <2 cm, > 8cm – oligo/polyhydramnios resp
  • AFI ranges;

- <5 cm, 5-7 cm, 7-10 cm denote severe, moderate and mild oligohydramnios respectively

- 10-25 cm – Normal

- >25 cm – Polyhydramnios

  • Oligohydramnios – Assoc fetal morbidity/mortality

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3. Fetal cardiotocography (NST);

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  • NST involves continuous electronic monitoring of the fetal heart rate along with recording of fetal movements
  • There is association of FHR acceleration with fetal movements
  • When present, indicates a healthy fetus
  • Tracing is done over 20-30 minutes usually in third trimester
  • Reactive (Reassuring) CTG consist of;

- Base line HR of 110–160 beats/minute

- Base line variability 5–25 bpm

- No deceleration

- Two or more accelerations of > 15 bpm above baseline, lasting at least 15 seconds or more

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  • Non reactive (Non reassuring ) CTG – absence of fetal reactivity

Normal CTG tracing

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FETAL SURVEILLANCE

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BIOPHYSICAL METHODS OF ANTENATAL FS

4. Fetal biophysical profile

  • It combines NST with four USS features of fetal behaviour and physiological characteristics
  • USS PROCEDURE: It is performed over 30 minutes and assesses fetal behaviour by observing
    • Fetal breathing movements
    • Body movement
    • Fetal muscle tone
    • Amniotic fluid volume

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NDUKA EMMANUELLA

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BIOPHYSICAL PROFILE SCORING

(OBSERVATION FOR 30MINS, NORMAL SCORE=2, ABNORMAL SCORE=0)

PARAMETERS

SCORE 2

SCORE 0

Cardiotocogrphy (NST)

Reactive Pattern

Non reactive Pattern

Fetal Breathing Movements

At least one episode lasting for more than 30seconds

None or one episode lasting less than 30seconds

Fetal gross body movements

> 3 discrete body limb movements

< 3 body movements

Fetal Muscle Tone

> 1 episode of active extension (lumbar trunk) with return to flexion or opening and closing of the hand

No movement

Amniotic Fluid Volume

At least > 1 cord & limb free fluid pocket >2cm by 2cm in 2 perpendicular planes

<2cm by 2cm fluid pocket

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BPP INTERPRETATION

  • 8-10 (8/8 if NST is not done)

- Interpretation: No fetal asphyxia

- Management: Repeat testing at weekly interval or more

- Interventions should be from obstetric or maternal factors

  • 4-6

- Interpretation: Equivocal test; suspect chronic asphyxia

- Management: if >34 weeks, deliver

If <34 weeks repeat test in 24 hours, if result is same, mature lungs and deliver within 48 hours

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  • 0-2

- Interpretation: Strongly suspect chronic fetal asphyxia

- Management: Evaluate patient for immediate CS delivery.

If 34 weeks, mature lungs and deliver

  • N.B Oligohydramnios alone is an indication for delivery

* Modified Biophysical Profile consists of NST and amniotic fluid index in USS

Interpretation - Considered abnormal (non reassuring) when the NST is non-reactive and/or the AFI is < 5

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BIOPHYSICAL METHODS OF ANTENATAL FS

5. Contraction stress test;

  • Evaluates response of the FHR to induced contractions
  • CST is NST done in the presence of at least 3 contractions in a 10 minute period
  • Designed to unmask poor placental function
  • Principle - contractions transiently decrease fetal oxygenation → decreased FHR in a marginally compromised fetus with limited placental function
  • Can be done with naturally occurring contractions or with induced nipple stimulation or IV oxytocin

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BIOPHYSICAL METHODS OF ANTENATAL FS

  • Advantage of CST - most closely approximates intra-partum surveillance of fetal risk even during the antepartum period
  • CST is rarely done

Interpretation;

* Negative result - No late or significant variable decelerations

* Positive result - Late decelerations (occurs after 50% contractions)

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BIOPHYSICAL METHODS OF ANTENATAL FS

6. Doppler velocimetry

  • Doppler USS uses sound waves to study blood circulation in the Uterus, placenta and fetus
  • Normal blood in tissues occur without resistance in diastole

Uterine artery Doppler

  • Resistance within the placenta can be measured from the maternal side, usually as a screening test at 23 weeks
  • High resistance in the uterine artery indicates; - Increased risk of development of early onset pre-eclampsia

- Risk of a fetus with IUGR

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BIOPHYSICAL METHODS OF ANTENATAL FS

Umbilical artery Doppler

  • Increasing resistance in the umbilical artery is an indicator of placental failure
  • Using this in high risk pregnancies reduces the risk of fetal death

Middle Cerebral artery (MCA) Doppler

  • The artery shows increasing diastolic flow as hypoxia increases due to redistribution of blood to the brain
  • Peak systolic velocity in MCA Doppler increases with fetal anemia as seen in Rhesus iso-immunization

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NORMAL DOPPLER WAVEFORM

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ABNORMAL DOPPLER WAVEFORMS

  • Reduced end diastolic flow

  • Reversed end diastolic flow

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INTRA-PARTUM FETAL SURVEILLANCE

  • Simply means watching fetal behavior during labour
  • AIM - To detect hypoxia during labour and to initiate management depending n the severity of the hypoxia
  • In labour, 3 major factors occurs - uterine contractions, cord accident & prolonged head compression

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UTERINE CONTRACTIONS

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METHODS OF INTRA-PARTUM FETAL MONITORING

  • 1. Intermittent auscultation – using pinard or hand held doppler (sonicaid)
  • Aim – To detect fetal bradycardia and tachycardia

  • 2. Liquor assessment – Clear liquor (Normal), meconium stain [fresh (green) or stale (brown)], blood stain

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3. CTG – continuous fetal heart monitoring

4. Fetal pulse oximetry

5. Fetal scalp sampling 🢡 PH determination

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PH INTERPRETATIONS

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CONCLUSION

  • Perinatal morbidity and mortality can be reduced with utilisation of robust antenatal and intra-partum monitoring approach

  • Training and Practice is the way forward

  • There is no one best test and none of the testing modalities has been shown to reduce perinatal morbidity nor increase long term fetal neurologic outcome

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  • THANK YOU