Ante-partum maternal factors | Ante-partum foetal factors | Intra-partum factors |
Infection | IUGR | Evidence of foetal compromise e.g. non-reassuring CTG |
GDM | <36 weeks or >40 weeks gestation | Meconium |
PIH | PET | Eclampsia | Multiple pregnancy | Breech delivery or other malpresentation |
High BMI | Oligohydramnios | Instrumental delivery e.g. forceps, ventouse |
Short stature | Polyhydramnios | LSCS <39 weeks |
Pre-term labour without steroids | Serious congenital abnormality | Emergency LSCS |
No antenatal care | Anaemia | General anaesthesia |
Macrosomia | MOH inc. placental abruption | |
Cord prolapse |
Neonatal Resuscitation
Neonatal Resuscitation
This topic is absent from the intermediate curriculum, which is replete of a smorgasbord of other neonatal topics.
The below-linked BJA Education article suggests that 'any anaesthetist providing obstetric care should maintain familiarity with current practices in neonatal resuscitation'.
Resources
- Most infants adapt well to extra-uterine life, though some require help with stabilisation or resuscitation
- 85% will breathe spontaneously without intervention
- 10% respond after drying/stimulation/airway opening
- 5% receive PPV
- 0.4 - 2% require intubation
- <0.3% require chest compression
- 0.05% receive adrenaline
Cord clamping
- Where immediate stabilisation or resuscitation is not required, aim to delay cord clamping for at least 60s (longer periods may be more beneficial)
- Where immediate stabilisation or resuscitation is required:
- Delay cord clamping if it is possible to safely undertake interventions with cord intact
- If delayed cord clamping not possible, consider milking the cord in those >28 weeks gestation
- Delayed cord clamping:
- Results in higher neonatal blood volumes after birth
- Improves iron stores in infancy and therefore fewer blood transfusions
- Improves haemodynamic stability during the transition from foetal to neonatal life
- Associated with lower incidence of intraventricular haemorrhage
- Associated with lower infant mortality rates
Temperature management
- Monitor temperature regularly e.g. with skin temperature probe
- Target temperature between 36.5°C and 37.5°C
- Methods for maintaining temperature:
- Dry neonate at birth
- Maintain a warm delivery room (between 23°C and 25°C, and >25°C for infants less than 28 weeks' gestation)
- Use a radiant warmer
- Plastic wrap and chemical mattress in pre-term infants to prevent hypothermia
- In appropriate circumstances, consider therapeutic hypothermia after resuscitation
Airway & ventilatory management
- If not breathing, stimulate ± suction nose/mouth if evidence of secretions obstructing the airway
- Consider tracheal suction if born through meconium-stained amniotic fluid and obstruction is suspected
- Start PPV using a mask if inadequate respiratory effort/apnoeic or HR <100bpm
- FiO2 0.21 and PIP 30cmH2O in term infants
- FiO2 0.21 - 0.35 and PIP 20-25cmH2O in pre-term infants <35 weeks
- Use PEEP 5-6cmH2O as it helps in the generation of FRC which will allow the lungs to stay inflated
- Target preductal SpO2 values (saturations on monitor on right hand) of 85% at 5mins and 90% at 10mins
- If HR <60bpm or chest compressions are required then:
- Use alternative airway e.g. intubate, supraglottic device
- Increase FiO2 to 1.0
Perform rapid assessment
- E.g. the Apgar score at 1min (i.e. the above steps should all take place within 60s if necessary)
- Developed by an obstetric anaesthetist to determine the effect of anaesthesia on neonates
- It should be performed at 1mins and 5mins ± 10mins if earlier scores low
- It consists of:
- Appearance i.e. skin colour
- Pulse i.e. heart rate (>100bpm satisfactory)
- Grimace e.g. reflex irritability
- Activity e.g. muscle tone
- Respiration
- Each is scored 0 - 2, with a maximum score of 10
Scoring and significance
- A 1min score of ≤3 does not predict any individual infants outcome
- A 5min score of ≤3 correlates with neonatal mortality, but does not predict individual future neurologic dysfunction
- Most infants with low Apgar scores will not develop cerebral palsy
- However, low 5min score increases the relative risk of cerebral palsy by 20 - 100x compared to an infant with an Apgar score of ≥7
- A 10min score of ≤3 is associated with increased risk of poor neurological outcome
- Continued respiratory support is required if, after initial assessment & intervention;
- There is inadequate or irregular breathing
- HR <100bpm
Lung inflation
- If evidence of inadequate respiration, aim to start PPV ideally within 60 seconds
- Give 5 inflation breaths, maintaining inflation pressure for 2 - 3s
- FiO2 0.21 and PIP 30cmH2O in term infants
- FiO2 0.21 - 0.35 and PIP 20-25cmH2O in pre-term infants <35 weeks
- PEEP of 5 - 6cmH2O
- Saturations monitoring is required and oxygen should be titrated to avoid hypoxia or hyperoxia
- Accept pre-ductal saturations of 85% at 5mins, 90% at 10mins and wean oxygen if >95%
CPR
- If HR <60bpm or absent after 30 seconds of ventilation, start CPR
- Increase FiO2 to 1.0
- Delivery of CPR:
- 3:1 compressions to ventilations
- 15 cycles every 30 seconds
- Two-thumb (encircling) technique
- Reassess HR and chest movement every 30s
- Consider vascular access and drugs if HR <60bpm after 30s
Vascular access
- Peripheral venous access is likely to be difficult, and suboptimal for vasopressor administration
- Options therefore include:
- Umbilical vein cannula
- IO access
- Peripheral or central access for post-resuscitation care
Drugs
- Adrenaline
- Indicated if HR <60bpm despite 60s of chest compressions
- 20μg/kg IV or IO
- 50-100μg/kg via trachea if intubated and no other access
- Subsequent doses every 3 - 5mins if HR <60bpm
- Volume resuscitation
- 10ml/kg of O-negative blood or isotonic crystalloid in suspected shock
- 2 - 4ml/kg of 4.2% NaHCO3 in prolonged, unresponsive resuscitation to reverse intracardiac acidosis
- Glucose
- 2.5ml/kg of 10% dextrose IV or IO
- For prolonged resuscitation to reduce likelihood of hypoglycaemia
Aetiologies
- If prolonged resusctiation consider alternative aetiologies such as:
- Pneumothorax
- Unrecognised congenital abnormalities e.g. congenital diaphragmatic hernia
- Hypovolaemia/haemorrhage