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INTRAPARTUM FETAL MONITORING

CARDIOTOCOGRAPHS

INDICATIONS

Indications for Electronic Fetal Monitoring

 

 

In pregnancies with recognised risk factors continuous EFM should be offered and recommended. RCOG

 

 

ANTENATAL:

Small Fetus

Small fetal size is associated with a significant increased risk of cerebral palsy.8601

Preterm Fetus

 

Prematurity of less than 32 weeks is associated with a significant increased risk of cerebral palsy and death.8601, 9401Intrauterine growth restriction, in combination with prematurity, results in significantly increased rates of neonatal encephalopathy.

9801

Hypertension

Pre-eclampsia is a risk factor for neonatal encephalopathy9801 but also increases the risk to the baby as a result of impaired fetal growth.

Multiple Pregnancy

The risks associated with multiple pregnancy are complex. Fetal risks are complicated by increased rates of prematurity, intrauterine growth restriction and placental abruption. However, rates of cerebral palsy and neonatal death are independently significantly increased with multiple order pregnancies and also increase with plurality. There is an increased risk of cerebral palsy.0601

Breech Presentation

Breech presentation is associated with an increase in both cerebral palsy and death.8601 This is independent of mode of delivery and gestation. However, an RCT comparing planned caesarean section versus planned vaginal birth found a significant reduction in perinatal mortality and neonatal morbidity in association with planned caesarean section.0001

Diabetes; Antepartum haemorrhage; Cardiac disease (cyanotic);      Severe anaemia; Hyperthyroidism; Vascular disease; Renal disease; Prematurity; Oligohydramnios; Abnormal umbilical artery Doppler velocimetry; Isoimmunisation

 

EFM has not been extensively and prospectively evaluated with respect to individual risk factors. Furthermore, the systematic reviews and the constituent trials do not contain sufficient participants to allow a subgroup analysis with respect to individual indications even if those data were provided.

 
 
 

 INTRAPARTUM:
Vaginal Bleeding

Placental abruption is associated with an increased risk of death and cerebral palsy.0701 Clearly when placental abruption occurs there is an indication for caesarean section.

Intrauterine Infection

Maternal pyrexia alone has been shown to be associated with an increased risk of neonatal encephalopathy9501 9802 and cerebral palsy.9701, 0501

Meconium Staining of the Liquor

Meconium-stained liquor was found to be associated with an increased risk of cerebral palsy0702 anddeath.0002 Meconium-stained liquor is a significant risk factor for neonatal encephalopathy.9501

Post-term Pregnancy 

There was an increase in the rate of neonatal encephalopathy with rising gestation after 39 weeks.9801 Furthermore, there was a rise in perinatal death rate from 41 weeks.9803 Recent data have suggested that the risks of stillbirth increases from 1 per 3000 continuing pregnancies at 37 weeks, to 3 per 3000 continuing pregnancies at 42 weeks, to 6 per 3000 continuing pregnancies at 43 weeks. A similar increase in neonatal mortality is also reported.9803

 
Prolonged Membrane rupture

Prolonged rupture of the membranes has been reported to be associated with an increased risk of death and cerebral palsy particularly with increasing prematurity.9803

 
Induction and Augmentation of Labour

If induction or augmentation of labour is undertaken with oxytocin there is a significant risk of hypercontractility and EFM should be used. RCOG

 

Previous Caesarean Section

The rate of spontaneous scar dehiscence with a previous caesarean section is 0.3?0.7%. This may present with a variety of warning signs, including poor progress in labour, scar tenderness, vaginal bleeding or FHR abnormality. The RCOGtherefore recommends ?attentive intrapartum fetal an maternal surveillance in a setting where the baby can be delivered within 30 minutes?.

 

Augmented labour;

Hypertonic uterus;

Suspicious fetal heart rate on auscultation.

 

EFM has not been extensively and prospectively evaluated with respect to individual risk factors. Furthermore, the systematic reviews and the constituent trials do not contain sufficient participants to allow a subgroup analysis with respect to individual indications even if those data were provided.

 

Both the maternal notes and CTG are continuous records of intrapartum events. It is imperative that any events occurring during labour that may affect FHR are contemporaneously noted in both these records. These include change in maternal position, vaginal examination and administration of drugs. The notes should be timed, dated and signed. If intermittent auscultation is being used then details of the features of FHR should be recorded contemporaneously in the maternal notes, together with any other intrapartum events that might affect the FHR.

There should be established paths of communication to allow concerns regarding intrapartum FHR traces to be dealt with effectively there should be established guidelines for communicating the urgency of situations and decisions about fetal wellbeing on an interprofessional level, to avoid unwarranted delays.

There is debate about the value of intrapartum electronic fetal monitoring. At one extreme,

Natale and Dodman

0301  believe, that as practitioners of and investigators in fetal health surveillance, that there is not good supporting evidence for recommending continuous intrapartum EFM for pregnancies in which there is an increased risk of perinatal death, cerebral palsy, or neonatal encephalopathy, or when oxytocin is being used for induction of labour, and that if we recommend that the fetal heart be electronically monitored while the nurse is elsewhere, we are on a slippery slope. Difficulty would arise, however, when there is an unfavourable outcome and frequently accepted indications for electronic fetal monitoring have been ignored.

 

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