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INTRAPARTUM FETAL MONITORING
CARDIOTOCOGRAPHS
INDICATIONS
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Indications for Electronic
Fetal Monitoring
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In pregnancies with recognised risk
factors continuous EFM should be offered and
recommended.
RCOG
ANTENATAL:
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Small
Fetus |
Small fetal size is
associated with a significant increased risk of cerebral palsy.8601 |
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Preterm Fetus
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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 |
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Hypertension |
Pre-eclampsia is a risk factor for neonatal
encephalopathy 9801
but also
increases the risk to the baby as a result of impaired fetal growth. |
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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 |
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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 |
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Diabetes; Antepartum haemorrhage; Cardiac disease (cyanotic);
Severe anaemia; Hyperthyroidism; Vascular disease; Renal disease;
Prematurity; Oligohydramnios; Abnormal umbilical artery Doppler
velocimetry; Isoimmunisation
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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.
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INTRAPARTUM:
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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. |
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Intrauterine
Infection |
Maternal pyrexia alone has been shown to be
associated with an increased risk of neonatal encephalopathy9501
9802 and cerebral palsy. 9701,
0501 |
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Meconium
Staining of the Liquor |
Meconium-stained liquor was found to be associated
with an increased risk of cerebral palsy0702
and death.0002
Meconium-stained liquor is a significant risk factor for neonatal
encephalopathy.9501
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Post-term
Pregnancy |
There was an increase in the rate of neonatal
encephalopathy with rising gestation after 39 week s.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
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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
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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
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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?.
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Augmented labour;
Hypertonic uterus;
Suspicious fetal heart
rate on auscultation.
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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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