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assisted vaginal birth


Assisted Vaginal Birth


Purpose


To expedite vaginal birth of the infant when the risks of the procedure are less than the risks of waiting for spontaneous vaginal birth, and the conditions necessary for the procedure (below) are present.

Definition


The vaginal birth of an infant in a cephalic presentation with the assistance of forceps or vacuum extraction.

Classification of Types of Assisted Vaginal Birth



Classification of Types of Assisted Vaginal Birth
Outlet
  • Fetal scalp is visible without parting the labia
  • Fetal head is at, or on the perineum
  • Fetal skull has reached the pelvic floor
  • Sagittal suture is in the antero-posterior diameter, or right or left occipito-anterior or posterior position (rotation does not exceed 45o)
Low
  • Leading point of the skull (not caput) is at or below station +2cms and not on the pelvic floor.

(a) Sagittal suture is rotated 45o or less from the midline
(b) Sagittal suture is rotated more than 45
o from the midline
Mid
  • Fetal head should have no more than 2 cms (1/5) palpable per abdomen.
  • On vaginal examination the leading point of the fetal skull is above station +2cm but not above the ischial spines. Consider the need for a trial of vaginal birth in the operating theatre with obstetric consultant back-up.

(a) Sagittal suture is rotated 45o or less from the midline
(b) Sagittal suture is rotated more than 45
o from the midline
High
  • Not included in the classification


Indications for Assisted Vaginal Birth


(No indication is absolute. Actions should relate to the individual case).

Fetal
  • non-reassuring fetal status on CTG / scalp lactate measurement
  • abruptio placenta in second stage
  • cord prolapse in second stage (multigravida)
  • 'any condition that makes it unsafe for the fetus to remain in the uterus during second stage' (ALSO)

Maternal
  • Medical indications to avoid strong pushing (Valsalva technique) e.g. severe cardiac disease, hypertensive disorders, cerebral vascular disease/ uncorrected cerebral vascular malformations, myasthenia gravis, spinal cord injury.
  • Inadequate progress: (Approximate intervals for a prolonged second stage):
  • Nulliparous women: lack of continuing progress for 3 hours with epidural, or 2 hours without epidural. (passive + active second stage labour).
  • Multiparous women: lack of continuing progress for 2 hours with epidural, or one hour without epidural. (passive + active second stage labour)
  • Maternal fatigue/ exhaustion

Contraindications


Relative Contraindications


  • Fetal bleeding disorders (alloimmune thrombocytopenia, haemophilia, von Willebrand's disease - in these circumstances vacuum extraction should not be performed - non-rotational low or outlet forceps may be permissible after consultant discussion).
  • Risk of vertical transmission of Hepatitis C and HIV: Avoidance of acquired infection as a result of an increased chance of facial or scalp abrasions.

Contraindications


  • Fetal predisposition to fractures (e.g. osteogenesis imperfecta)
  • Face presentation - forceps only to be used
  • Prematurity of <34 weeks gestation - forceps only to be used

Note: The only indications for delivery by forceps or vacuum extraction prior to full dilation of the cervix are a prolapsed cord at 9cms in a multiparous woman or a second twin.


Assessment prior to Assisted Vaginal Birth


Assessment prior to Assisted Vaginal Birth
Abdominal Examination
  • Vertex presentation

  • <2 cm (1/5) head palpable above the pelvic brim (the presence of more than this above the pelvic brim should alert the operator to the fact that the head in the pelvis is not deep enough to allow vaginal delivery)

  • Uterus contracting adequately (consider use of oxytocin to augment labour in the second stage of labour for primiparous women with epidural anaesthesia in situ or inadequate contractions).
Vaginal Examination
  • Cervix fully dilated
  • Membranes ruptured
  • Station of presenting part - the vertex must be at or below the ischial spines (beware of caput and moulding in assessing the station)
  • Knowledge of the exact position of the fetal head aids appropriate and safe placement of instrument
  • Pelvis deemed to be adequate
Maternal
  • Provide explanation of procedure
  • Obtain informed (verbal) consent
  • Empty maternal bladder
  • Indwelling catheter should be removed or have balloon deflated.
  • Ensure anaesthesia/ analgesia is adequate for the procedure. For mid-cavity rotational deliveries (irrespective of instrument) this will usually be a regional block.
  • A pudendal block may be appropriate where there is no regional block in place, especially where there is a need for urgent delivery. Perineal infiltration alone is rarely adequate except for some outlet vacuum extractions.
  • Aseptic techniques
Clinical Requirements
  • Reasonable anticipation of successful outcome.
  • Operator must have the knowledge, experience and skill to use the instrument correctly.
  • Operator must have the ability to anticipate and manage potential complications
  • Adequate facilities and backup personnel available, including those skilled in neonatal resuscitation.
  • Back-up plan in case of failure to deliver


Precautions prior to undertaking assisted delivery


  • In primigravidas, the use of oxytocin (to augment labour) should be considered for managing delay in the second stage of labour before the fetal head reaches the pelvic floor, rather than initiating early instrumental intervention. The use of oxytocin at this stage in women who have previously had a baby has the potential to cause uterine rupture.

  • Assisted vaginal births with an anticipated higher rate of failure should be considered a trial and conducted in the operating theatre.

  • Higher rates of failure are associated with:

  • maternal body mass index greater than 30
  • estimated fetal weight greater than 4000 g or clinically big baby
  • occipitoposterior position

  • Mid-cavity delivery or when 1/5 head palpable per abdomen (consider the need for a trial of vaginal birth in the operating theatre with obstetric consultant back-up).

  • A consultant obstetrician should be present for all attempts at mid-cavity or rotational forceps, and all "trials of forceps".
  • The need for instrumental birth is associated with the potential for shoulder dystocia. Refer to the Women's CPG: Shoulder Dystocia.
  • The need for mediolateral episiotomy should be considered.
  • Paediatrician to be present for the delivery where neonatal morbidity can be reasonably anticipated, including but not limited to all cases of suspected fetal compromise, mid-cavity and rotational deliveries.
  • Attempted vaginal delivery should be abandoned where:

  • There is no evidence of progressive descent with traction with each pull.
  • For vacuum extraction, there is disengagement of the cup three times
  • When the birth is not imminent following traction over three consecutive contractions of a correctly applied instrument by an experienced operator.
NOTE:
1. Reassessment of the decision to deliver should be made after 3 consecutive 'pulls' by vaginal instrumental delivery.
2. The vacuum cup should be on for no longer than 20 minutes.



  • In the event of a failed vacuum extraction, a forceps delivery should only be attempted by a skilled operator. Delivery by Caesarean section should be considered.
  • Paired umbilical cord, blood gas samples should be processed following all attempts at an assisted vaginal birth and the results recorded in the birth documentation.


Potential and Relative Complications of Assisted Vaginal Birth


Comparison between Vacuum Extraction and Forceps

Choice of instrument is dependant on the skills and preference of the operator and the clinical situation.

Forceps
Vacuum extraction
Maternal Complications
Associated with a greater incidence in 3rd and 4th degree lacerations when episiotomy is performed.

Increase in the severity of genital tract trauma thereby increasing the likelihood of postpartum haemorrhage.

Associated with reductions in severe genital tract trauma.

Associated with an increase in anterior vaginal trauma.

More likely to fail at achieving vaginal delivery.

Mother more likely to be worried about baby.

Neonatal Complications
Has a greater association with external ocular injuries and facial nerve palsies.
Associated with an increase in mild scalp lacerations, cephalhaematoma and retinal haemorrhage.
The use of two operative interventions for delivery is more likely to result in a serious injury to the neonate than a single intervention.

Midwifery Responsibilities


  • Reassurance of woman, support person(s)
  • Continual monitoring and documentation of fetal status
  • Timing of contractions manually. Informing operator of onset prior to traction being applied and cessation of same to enable any manipulation of equipment.
  • Observation/ documentation of time of application of instrument and how many contractions required for birth of baby
  • Ensure Paediatrician is informed of event/ Check neonatal resuscitation equipment
  • Midwifery care & documentation according to the Women's procedure: Observations of Labouring Women (intranet only) and Midwifery Standards: Birth Suites pamphlet.


Documentation of Procedure


This MUST be documented by the accoucheur within the Progress Notes and the Instrumental Delivery summary and should include the following:

Progress Notes Labour Chart (MR/90077)
  • Indication for intervention
  • A record of discussion with the woman of the risks, benefits of the procedure and her options
  • Description of fetal CTG and contractions
  • Abdominal palpation: position of fetus & station of fetal head
  • Consultation with senior medical officer

Instrumental Delivery Summary (MR/90077A)
  • The findings of vaginal examinations including:

  • Station and position of the fetal head
  • Amount of caput and moulding present
  • Assessment of maternal pelvic capacity
  • Type of analgesia used
  • The number of attempts and ease of application of instrument
  • The duration of traction and force required
  • A description of maternal and neonatal injuries and their management
  • Record of the paired umbilical cord gases (venous and arterial)

Post Birth Management


  • Repair of perineal trauma: refer to the Women's CPGs:


  • Bladder management: Urinary output should be monitored for at least 24 hours post birth to detect postpartum urinary retention. A post-void residual urine should be measured if retention is suspected.
    For a woman who has experienced an assisted birth/ prolonged labour/ epidural anaesthesia, consider an indwelling urinary catheter for twelve hours following the birth to prevent asymptomatic bladder overfilling. Refer to the Women's CPG:
    Peripartum Bladder Management. Women should be offered physiotherapy-directed strategies to prevent urinary incontinence.

  • Analgesia: If there are no contraindications provide diclofenac and paracetamol at regularly prescribed intervals. Icepacks can be applied to the perineum at regular intervals for up to 48 hours.

  • Thromboprophylaxis: Assess woman in relation to individual risk factors.

  • Observe neonate for signs of jaundice, infection and any concerns about tissue or nerve related injury.

  • The accoucheur and primary midwife should review the woman prior to hospital discharge and discuss the indication for operative delivery, management of any complications and the prognosis for future deliveries.

References


References: Assisted Vaginal Birth link to a separate page.

Published: 10 Aug 2007

Royal Women's Hospital Clinical Practice Guidelines (CPGs) are intended to provide guidance to health care professionals, based on a thorough evaluation of research evidence, on the practical assessment and management of specific clinical issues or situations. The guidelines allow some flexibility on the part of the health care professional based on the needs of the specific patient for whom they are caring.

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