The Last Hour of Labour
Department of Women’s Health
PROMPT Course 2017/18
Considerat ions and Complicat ions
Contents
• Why the last hour?
• What normally happens?
• Progress
• CTG changes
• Cord bloods
Why the last hour?
Why the last hour?
• Peak level of activity
• Demands on staff for preparation, support, monitoring and
procedures
• Emotional peak
• Physical energy may be low
• Potential for more rapid deterioration in clinical picture
• Potential for sudden onset of complications
• Whilst providing a positive birth experience
Preparation for BirthWhat Are The Elements Involved?
Preparation - Environment
• Lighting, noise
• Space
• Hazards
• Temperature/warmth
• Position
• Calm & supportive
Preparation - Equipment
• Normal Equipment – open pack: forceps, scissors, clamps,
packs
• Cot - warmer on, blankets towels
• Resuscitaire – (inside or outside) on, warm, tested (Gas flow
PIP, PEEP, suction, intubation, drugs)
• Emergency equipment – stocked (vacuum, forceps, cord
bloods, PPH box)
• Drugs prescribed & ready – oxytocic (syntometrine vs
syntocinon)
• Cord blood syringes if indicated
Assessment
• Maternal observations
1st stage – temp 4hrly, BP 2hrly, pulse 1/2hrly
2nd stage – temp 4hrly, BP 1hrly, pulse 1/2hrly
• Fetal heart rate assessment (CTG vs IA). If IA:
1st stage - 15-30mins, from end of contraction 30-60secs
2nd stage - every 5 mins or each contn)
• Abdo palpation – engaged, position
• VE to confirm full dilatation, station, position, caput, moulding,
l iquor
Preparation – Team
• When pushing Inform ANUM or Obs registrar
• Obstetric Registrar Present if:
Abnormal presentation, multiples
Risk of shoulder dystocia
Risk of PPH
• Paeds registrar (The above plus)
Meconium, abnormal CTG, known anomaly
Prematurity, sepsis
• 2nd midwife assist when birth imminent
Preparation - Communication
• Documentation – baby bradma, notes & ID
document full dilation and pushing times
observations
confirm blood group, recent results
document who was informed
• Counsel woman, reassure, discuss likely events
• Engage partner & family - support
Progress
VE is the cornerstone of assessing progress in labour but:
• Needs to be taken in the context of the whole woman’s wellbeing
• Can be invasive, painful, distressing, may raise issues of sexual
int imacy or assault.
• Lack of information or an unsympathetic att i tude can cause trauma
or complaint
• Needs to be justif ied to the woman and her family, the f indings
carefully explained and the implications discussed.
• “Examinations carried out with sensit ivity, in privacy by one midwife
with whom the woman has a good relat ionship wil l be experienced
as very different from brusque examinations from different
professionals whom the woman hardly knows.”
RCM, UK, Assessing Progress in Labour 2012
Progress in the 2nd Stage
• Passive & Active Definitions
• Normal second stage has a broad range
• 95 th% is 4hrs in primp
• Chance of vaginal birth 85% at 1hr but 9% by 5hrs
• Higher risk of atony (PPH), perineal trauma, infection, (local
experience - higher risk of technically complicated births)
• Neonatal risks debated – possible increase in morbidity,
sepsis, low Apgars
• Variation in local & international protocols
3 Centres Labour & Birth Guideline, 2012
PH CPG for delay in 2nd Stage• Combined passive and active second stage over 3 hours in a nul l iparous
woman.
• Combined passive and active second stage over 2 hours in a muli t iparous
woman.
• Encourage pushing with natural expulsive urge, posit ion changes.
• VE recommended:
To initially confirm full dilation
To confirm descent after passive descent of 1hr (exclude obstruction and to consider
augmentation if no descent).
• After 1hr active pushing inform ANUM & Obs Reg, commence CTG
Peninsula Health CPG, 2017
• Better to identi fy & manage abnormal contractions early in the 2 nd stage
rather than after 2hrs of pushing.
CTG ChangesW hat is normal?
Who Should Be Monitored
• RANZCOG Guidelines
Antenatal risk factors – see CPG
Intrapartum (eg induction)
Risk that may develop during labour:
Abnormal ausculation (changing FH even if within normal range)
Augmentation
Epidural
Bleeding, meconium, absent liquor post amniotomy
Pyrexia = 380c or more
Prolonged 1st or 2nd stage
Tachysystole (5:10)
Hypertonus (Contn >2mins or resting phase <60secs)
Optimising the CTG
• Active pushing impairs uterine blood f low and cerebral oxygenation
(within 10mins cf 30mins if passive)
• Prolonged breath holding may worsen this
• A compromised fetus may decompensate with pushing
• Hypertonus or tachysystole can turn to hyperstimulation
• Waiting unti l the urge to push starts (passive 2 nd stage) does not
increase the total t ime of the 2 nd stage.
• Passive descent:
shortens the active phase.
Reduces CTG abnormalities
Reduces the impact on acid-base status
J Perinatal Ed 2006
Reviewing CTG – False reassurance
• Pushing increases maternal heart rate
• May be similar to fetal HR
• Changes in position may detect maternal pulse
• In second stage:
Monitor maternal HR (30mins)- caution if similar
Consider pulse oximeter
Consider scalp electrode if any abnormalities
Beware an ‘improving’ CTG with accelerations
• What CTG changes are more common in the second stage?
Common CTG changes in the second stage
• Absent accelerations
• Rise in baseline
• Reduced variabil i ty
• Variable decelerations
• Higher r isk of complicated variable decelerations
• Higher risk of late decelerations
• Which of these are ‘normal’
Normal CTG changes in the second stage
• Absent accelerations
• Rise in baseline
• Reduced variabil i ty
• Variable decelerations very common 85-90%
represent a physiological response
• Higher r isk of complicated variable decelerations
• Higher risk of late decelerations 8-10%
• There are no changes that are unique to the 2 nd stage
• Falsely attr ibuting abnormalit ies to 2 nd stage carries risk
M c D o n n e l l , B J M M R 2 0 1 5
Interpretation
• Context is everything
• Uncomplicated variable decelerations unlikely to be
associated with compromise
• Severe baseline changes, complicated variable or late
decelerations require action
• Action may be:
Proceed to normal birth if imminent
Intrauterine resuscitation (stop pushing, reduce contractions,
position, fluids)
Assisted birth (episiotomy, instrumental, caesarean)
Fetal Scalp Sampling in 2nd stage
• CTG abnormalities have a high false +ve rate
• In most cases an abnormal CTG in 2 nd stage would indicate
assisted birth
BUT
If vaginal birth is not easily achievable, consider a scalp sample
• Rarely indicated, consultant discussion
• Allow time for further descent
• Generally only if an ‘intermediate’ level of abnormality
• But no evidence of improved neonatal outcome (Eas t , Cochrane 2010)
CTG Discussion
• Women not having an active say in their decisions results in:
x6 risk of dissatisfaction in primips
x15 risk of dissatisfaction in multips
More likely to have unvoiced concerns about baby’s wellbeing
So:
• Careful explanation of indications, findings and plan for all
CTGs
• Reassurance not all CTG changes are serious
• Careful discussion if plans change
Cord BloodsW hy and interpretat ion
Benefits of Cord Blood Gas Analysis
• Record of the fetal acid – base status at birth
• Feedback to clinical staff – re appropriate decision making
• Information to paeds re risk of neonatal complications
• Education – case discussions
• Improves outcomes (reduces neonates born with Art pH<7.0)
• Medico-legal
White, ANZJOG 2010
Why a full blood gas
• pH results indicate fetal acidosis
• Best predictor of poor outcomes (along with lactate)
• Information from pCO2 and Base excess can indicate acute or
chronic picture and respiratory vs metabolic acidosis
• Birth Asphyxia:
Intrapartum hypoxia sufficient to cause neurological damage
Defined by: Art pH <7.00
Apgars at 5mins <4
Moderate or severe encephalopathy
Multi-organ dysfuction
Fetal Acid Production
• pH indicated concentration of hydrogen ions
• Stable pH is vital to maintaining body systems
• Dissolved carbon dioxide:
CO2 +H2O = HCO3- + H+ (hydrogen ion = acid)
Other Acids:
Lactic acid (product of anaerobic metabolism)
Keto-acids (breakdown of carbs and fatty acids)
Uric acid (breakdon of amino acids)
FETAL ACID
PRODUCTION
Glucose
Citric Acid
Cycle
Lactate - + H+Pyruvate
Glycolytic
Pathway
CO2 + H
20
(2 ATP)
(36 ATP)
CO2 + H20 H2CO3 H+ + HCO3-Respiratory
Aerobic
Anaerobic
Types of Acidosis
• Respiratory acidosis
CO2 + H20 H+ + HCO3-
• Metabolic acidosis
Glucose Lactate + H+
• Combined respiratory and metabolic acidosis
Causes of Metabolic Acidosis• Fetal:
Chronic metabolic derangement
Chronic utero-placental hypo-perfusion
anaerobic metabolism
• Maternal:
Sepsis
Reduction in acid excretion:
renal failure
alcoholic, diabetic or starvation keto-acidosis
Increased bicarbonate loss:
renal tubular acidosis
hyperparathyroidism
Diarrhoeal states
Causes of Metabolic Acidosis• Fetal:
Chronic metabolic derangement
Chronic utero-placental hypo-perfusion
anaerobic metabolism
• Maternal:
Sepsis
Reduction in acid excretion:
renal failure
alcoholic, diabetic or starvation keto-acidosis
Increased bicarbonate loss:
renal tubular acidosis
hyperparathyroidism
Diarrhoeal states
Normal Values
Artery Vein
pH 7.10 – 7.38 7.20 – 7.44
pCO2 39.1 – 73.5 14.1 – 43.3
pO2 4.1 - 31.7 30.4 – 57.2
HCO3- 19.7 – 28.5 18.4 – 26.8
Base Excess -9 – 1.8 -7.7 – 1.9
Practical Interpretation of pH<7.1
• Respiratory Acidosis
↑ pCO2 (>70 mmHg)
Base excess normal (-10 to 1)
• Metabolic
pCO2 normal (40-75 mmHg)
Low base excess (< -10)
Lactate (>6.1)
• Mixed
↑ pCO2
Low base excess
Indications
• Operative delivery (emergency CS or instrumental)
• Abnormal CTG
• Complex birth (breech, shoulder dystocia, twins)
• Low Apgars <7
• Any neonatal resuscitation
• Inform Paeds registrar if:
pH <7.1
Lactate >6.1
Summary
The Last Hour of Labour
• A key time period in labour with a combination of significantly
increased workload, greater risk and high expectations
• Vital to maintain situational awareness
• Assess risk factors & review them
• Monitor: The environment
The woman and her family
Observations and assessment (physical or CTG)
• Anticipate & prepare
• Consider a whole team approach