Pregnant women have routine monitoring of the baby's heart rate when in labour. Women with complicated pregnancies require continuous monitoring using an electronic recorder called a CTG. The CTG produces a paper based recording which is interpreted by the midwife as showing normal, suspicious or abnormal features of the baby's heart rate. Babies quite commonly demonstrate abnormal features from time to time during the course of labour. In some cases the abnormal features are of sufficient concern to warrant delivery by emergency caesarean section. In most of these cases the baby is born in good condition and the question arises whether the caesarean section was unnecessary. In order to reduce the chance of an unnecessary caesarean section additional "second-line" tests can be offered. One such test is where a small drop of blood is taken from the baby's scalp. This test involves an internal examination with an instrument to visualise the baby's head and a small scratch to the baby's scalp. The blood is tested for acid which is an indicator of whether or not the baby is receiving enough oxygen. The test is called a fetal blood sample or FBS. An alternative test is where the doctor or midwife performs a vaginal examination with two fingers and gently rubs the baby's scalp in an attempt to cause an increase in the baby's heart rate. This is a healthy response suggesting that the baby is receiving enough oxygen. The test is called digital fetal scalp stimulation or dFSS. These two "second-line" tests have never been compared in a properly conducted head-to-head comparison. This study aims to compare dFSS and FBS in a large clinical trial completed within four of Ireland's largest maternity hospitals. This trial will generate important evidence of direct relevance to clinical care and patient outcomes.
Continuous electronic fetal heart rate recording with cardiotocography (CTG) is a standard approach to monitoring fetal wellbeing in labour and is recommended for high-risk pregnancies. The aim is to identify fetal compromise early and intervene in order to reduce serious adverse events such as cerebral palsy and perinatal death. CTG abnormalities are relatively common and can lead to the decision to deliver by emergency caesarean section. In most cases the fetus is subsequently found to have been compensating for the stress of labour and is not actually compromised. Fetal blood sampling (FBS) is a second-line invasive test that provides information on the acid-base status of the fetus, reflecting hypoxia. It is used to provide either reassurance that labour can continue, or more objective evidence that delivery needs to be expedited. Clinical guidelines in the United Kingdom and Ireland have treated FBS as a gold standard test. Recent studies have questioned the validity and reliability of FBS, and also the logistic challenges of achieving a result in a timely manner. Fetal scalp stimulation (dFSS) by digital rubbing is an alternative less invasive test of fetal wellbeing in labour and is recommended in preference to FBS in US guidelines. This research aims to compare digital FSS and FBS in women with term singleton pregnancies and an abnormal intrapartum CTG, where additional information on fetal wellbeing is required. A multi-centre randomised controlled trial will be conducted. The clinical outcomes of interest will include caesarean section, assisted vaginal birth, low Apgar scores, cord blood acidosis, and admission to the neonatal unit. This trial will generate important evidence of direct relevance to clinical care and patient outcomes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
DOUBLE
Enrollment
40
Vaginal examination, insert amnioscope through cervix, visualise fetal scalp, clean fetal scalp, apply ethyl chloride spray, wipe scalp with petroleum gel, small scalp scratch with sharp instrument, collect sample in heparinised capillary tube, analyse sample.
Vaginal examination, insert one or two fingers through cervix onto fetal scalp, rub fetal scalp digitally for approximately 30-60 seconds, withdraw fingers and observe CTG for 5-10 minutes.
Coombe Women & Infants University Hospital
Dublin, Ireland
Caesarean section (CS)
All caesarean sections will be in labour in the context of an abnormal CTG
Time frame: at birth
Caesarean section , primary indication fetal concerns
abnormal CTG, or meconium, or low pH on FBS
Time frame: at birth
Caesarean section, primary indication poor progress
Poor progress in first or second stage of labour
Time frame: at birth
Caesarean section, failed attempt at assisted vaginal birth
Failed vacuum or forceps in second stage of labour
Time frame: at birth
Assisted vaginal birth (AVB) (all cases)
Vacuum or forceps or sequential (vacuum and forceps)
Time frame: at birth
Assisted vaginal birth, primary indication fetal concerns
abnormal CTG, or meconium, or low pH on FBS
Time frame: at birth
Assisted vaginal birth, primary indication poor progress
Poor progress in second stage of labour
Time frame: at birth
Spontaneous Vaginal Birth (SVB)
unassisted birth
Time frame: at birth
Decision Delivery Interval (DDI) for emergency CS >30 minutes
Decision delivery interval prolonged
Time frame: during labour up until time of birth
Decision Delivery Interval (DDI) for AVB >15 minutes
Decision delivery interval prolonged
Time frame: during labour up until time of birth
Perinatal death
intrapartum or early neonatal death
Time frame: up to 7 days of age
Late perinatal death
after 7 days up to 28 days of age
Time frame: 8-28 days of life
Apgar score at 5 minutes <7
low Apgar score at 5 minutes
Time frame: age 5 minutes
pH umbilical artery <7.00 or Base Excess artery <-12.0
arterial cord blood acidosis
Time frame: immediately after birth
Admission to neonatal unit (NNU)
admission all causes
Time frame: from birth up until 28 days
Neonatal encephalopathy (as defined by authors)
protocol definition
Time frame: from birth up until 28 days
Therapeutic hypothermia
treatment for encephalopathy
Time frame: indicated within 6 hours of birth
Abnormal neurological examination prior to discharge
clinical assessment recording abnormal findings - tone, reflexes, gag
Time frame: at time of hospital discharge, assessed up to 28 days after birth
FBS related injury/complication to baby (as reported on neonatal examination)
traumatic injury or abnormal bleeding
Time frame: at birth or with first 7 days of life
Major obstetric haemorrhage >1000mL
postpartum haemorrhage
Time frame: up to 24 hours after birth
Obstetric Anal Sphincter Injury (OASI - all degrees)
injury either spontaneous or with episiotomy
Time frame: at birth
Referral to perinatal mental health services
psychological symptoms warranting referral
Time frame: from birth up to six weeks after birth
Maternal acceptability of procedure (defined by questionnaire)
acceptability
Time frame: from birth up to 7 days after birth
Number of second-line tests (dFSS or FBS)
each event (rather than samples taken)
Time frame: during labour up until birth
Number of inconclusive/uninterpretable dFSS procedures
no clear acceleration or variability borderline
Time frame: during labour up until birth
Number of failed FBS procedures
no sample or reliable result achieved
Time frame: during labour up until birth
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