SLCOG Clinical Practice Guideline

Management of Normal Labour

Guideline 18September 2022Labour and delivery31 tables6 figures
Open source PDF

1. Introduction

The aim of this guideline is to provide recommendations to healthcare providers in the management of a healthy woman with a single foetus in labour at term (37 weeks onwards). It does not cover the care of women with complicated pregnancies.

The objective of this guideline is to ensure optimal management of women in labour, detect any abnormality, take appropriate action, prevent complications and consequently make childbirth safer; and also to make sure that these women are treated with respect and compassion, kept well informed and well supported throughout the process of labour.

2. Diagnosis of labour

Labour is diagnosed by the presence of regular, painful, intermittent contractions, which are of increasing frequency, duration and intensity, leading to progressive cervical effacement, dilatation and expulsion of the conceptus.

Note: For the purpose of this guideline, labour is also diagnosed in the presence of painful contractions occurring at a frequency of 2 or more in 10 minutes.

Labour has four stages;

Definitions

The first stage of labour subdivided to two stages;

i. Latent phase of the first stage of labour – From the commencement of labour to a cervical dilatation of 6 cm. (This is a period of time, not necessarily continuous, where there are painful contractions and some cervical changes including cervical effacement and dilatation up to 6cm takes place).

ii. Active phase of the first stage of labour – Commences at a cervical dilatation of 6 cm and ends with full dilatation (There are regular painful contractions and progressive cervical dilatation from 6cm up to full dilatation)1.

If the diagnosis of labour is uncertain, observation should continue and reassessment should be done four hours apart.

Any woman who is diagnosed as not being in labour, but continues to complain of pain, would require careful assessment by an experienced medical professional. Possible diagnoses of placental abruption and nonobstetriccauses should be considered.

In all cases of suspected labour, foetal condition should be assessed.

Second stage of labour is from the full dilatation of the cervix till complete delivery of the foetus.

Third stage of labour is from the delivery of the foetus till the end of complete expulsion of placenta.

Fourth stage of labour is the immediate 2 hours following the delivery of the placenta.

3. Management of labour

3.1. General considerations

3.1.1. Communication between woman and healthcare professionals/workers

3.2. Cervical dilatation

Historical labour curve published in the 1950s by Friedman which divided latent and active phase of first stage at 4cm dilatation was replaced in 2010 by the publication of The Modern Labour Curve from the study of Zhang and colleagues1 which included 60000 patients from 19 hospitals in the United States with pregnancies at term who went on to have vaginal deliveries and normal perinatal outcomes. In that study both nulliparous and multiparous women progressed in a similar fashion up to 6cm of cervical dilatation.

After 6cm, the progress was more rapid (especially in multiparous women) hence indicating active phase of labour. They found that the active phase in nulliparous women took 1.4 to 2.2 hours for each centimeter and 0.8 to 1.8 hours in multiparous women.

In another study Wood and colleagues2 assessed 2000 patients regarding the risk of caesarean delivery in relation to cervical dilation on admission to labour ward when in spontaneous labour. Admission in the latent phase of labour of less than 6 cm was associated with increased risk of caesarean delivery, in comparison to women admitted with more than 6 cm of dilatation.

As stated in this study it is good to consider delaying admission to the labour ward of patients with intact membranes to reduce the risk of caesarean delivery especially when the dilatation is less than 6 cm.

3.2.1. Comparison of induced with spontaneous labour

Table 1
4 cm → 10 cmMedianRate: 95th percentile
NulliparousSpontaneous3.811.8 hr
Induced5.517 hr
MultiparousSpontaneous2.48.8 hr
Induced4.416.2 hr

3.3. Descent of the presenting part Concomitant descent of the presenting part needs to happen during labour7

In general, multipara had higher positioning of the presenting part than nullipara at the first stage. However, findings of the study showed that 95% of all patients were either at zero or + at cervical dilation of 10 cm. Though slow descent is not completely abnormal at 10 cm of dilatation, foetal presenting part at stations higher than zero should arouse caution in management.

3.4. Special populations to consider regarding labour

1. Obesity

Obesity is an independent risk factor for caesarean delivery and complications of caesarean delivery as shown in a study by Norman and colleagues4 which subjected more than 5000 women at term who reached full cervical dilatation. The study considered 4 cm as the transition dilatation from the latent to active. However, the graphs given in the study showed this transition took place at 6 cm dilatation. The latent phase for obese women with a BMI greater than 30 was significantly longer. The higher the BMI, the more evident was the lag in latent phase. However, the active phase showed no difference.

2. Preterm labour

Preterm labour is a common condition (<37 weeks). Spain and colleagues5 studied a sample of 5000 women in preterm and term labour. The active phase of labour was observed to be faster in preterm labour and the transition still took place at 6 cm of dilatation.

3. VBACs (Vaginal birth after caesarean delivery)

Graseck and collegues10 compared term spontaneous labour without scar with VBACS. This study included 2000 patients. They found that the labour curves were no different in two groups.

3.5. General preparation for labour

(These two steps should not be considered mandatory)

3.5.1. Documentation

3.5.2. Mobilisation and positioning

3.5.3. Eating and drinking during labour

3.5.4. Hygiene during labour

3.6. Management of the first stage of labour

3.6.1. Management of latent phase

It is important to recognize the duration of the latent phase of labour, since its prolongation could lead to maternal exhaustion, dehydration and acidosis, leading to eventual foetal compromise and dysfunctional labour.

Women in the latent phase of labour would be best managed in the antenatal ward.

Women in the latent phase of labour must be assessed on a regular basis, as follows:

It is important to inform the mother that it is common to have slow progress in the latent phase and reassure her.

The latent phase is considered prolonged when it lasts more than 12 hours in a primigravida and 8 hours in a multigravida. In these situations, an experienced medical officer must reassess the mother with a view of possible augmentation of labour.

3.6.2. Management of active phase

3.6.2.1. General management

All pregnant women diagnosed as being in the active phase of the first stage of labour need to be admitted to the labour ward.

The initial assessment of a woman at the labour room should include:

A vaginal examination should be offered whennecessary.

Health care professionals who conduct vaginal examination should:

It is extremely important that delay in progress is assessed by an experienced medical officer. This assessment must consider:

In women with delay in the active phase of the first stage, every effort must be made to find a cause for the delay. This may either be due to inadequate contractions or obstruction due to CPD (Cephalopelvic Disproportion), malpresentation or malposition (such as occipito-posterior position), or a combination of these.

3.6.2.2. In cases of inadequate contractions;

This should have been identified and corrected before the diagnosis of arrest is made

3.6.2.3. Multiparous women with delayed progress:

Attention must be paid to providing effective pain relief and correcting dehydration in these situations.

After paying attention to the above, caesarean delivery must be considered when the progress is diagnosed as arrested.

3.6.3. Diagnosis of arrest of active part of first stage of labour

Historical Friedman curve-based diagnosis of first stage arrest is done when there is no cervical change for more than 2 hours with adequate contractions and at least 4 cm of dilatation.

With the acknowledgement of current understanding of labour curve, the patient needs to be at least

6 cm dilated

Progressive but slow labour progression should not be considered as an indication for a caesarean delivery.

Previously defined prolonged latent phase of labour of more than 20 hours in nullipara and more than 14 hours in multipara are no longer considered as a factor for caesarean delivery8,9.

3.6.4. Diagnosis of induction failure

This requires that the patient

However, recent literature has shown no difference in the outcome of induction vs expectant management in gestations greater than 39 weeks. Ripening the cervix as a part of the induction protocol has shown to reduce the failure of induction and progress8,9.

3.7. Second stage of labour

This stage begins at complete cervical dilatation of the cervix and ends with the delivery of the neonate. ACOG practice bulletin #49 defines prolonged second stage as two hours for nullipara and one hour for multipara without epidural analgesia. With epidural anaesthesia one hour is added to both categories.

PEOPLE trial and a similar trial in Sweden11 showed that increased duration of the second stage of labour as well as the duration of pushing time, increased the risk of asphyxiation of foetus as well as increased probability of postpartum haemorrhage.

However, a specific absolute total length of second stage over which all women should be considered for instrumental/operative delivery has not been established.

A consensus document developed jointly by ACOG and Society for Maternal-Foetal Medicine recommends22 at least two hours of pushing for multiparous women and 3 hours for nulliparous women before diagnosis of arrest of labour. These timeframes are applicable only if foetal and maternal evaluation continues to be reassuring. Additional time for these time parameters are allowed with epidural analgesia or foetal malposition.

SLCOG recommends ACOG recommendation that advocates a very senior review for the decision to wait any longer.

Second stage of labour consists of passive and active stages.

3.7.1. Passive second stage of labour (descent phase)

3.7.2. Active second stage of labour (expulsive phase)

Use of a hand-held Doppler device is recommended (in preference to a Pinnard stethoscope) for foetal heart rate monitoring in the second stage.

Women must be encouraged to continue consuming clear fluids during the second stage.

Support by the labour companion must be continued.

Total time duration allowed for the second stage of labour are as follows:

3.7.2.1 Primigravida

3.7.2.2. Multigravida

One further hour is permitted for women in each category for women with epidural analgesia.

3.7.3. Observations for women and babies in the second stage of labour

All observations should be documented on the Labour Care Guide.

In addition:

3.7.4. Woman’s position and pushing in the second stage of labour

Although most deliveries in Sri Lanka are conducted in the dorsal/McRoberts position, women may be encouraged to adopt squatting, semi upright or lateral positions to aid the expulsion phase.

Women should be informed that in the second stage, they should be guided by their own urge to push.

If pushing is ineffective, strategies to assist birth such as support, encouragement and change of position is used.

3.7.5. Episiotomy

Where an episiotomy is performed, mediolateral episiotomy, performed at about 40-30 degrees from the midline directed to the right side, (angle is measured taking arbitrary longitudinal line drawn in the perineum going across on all midline orifices connecting in one line as the zero-degree line). (NICE guideline states it as 40-60 degrees but there is no comment on the zerodegree line making it difficult to interpret). Beginning at the vaginal fourchette is preferred to the median episiotomy. It should be performed at the time of crowning of the foetal head.

Episiotomy should be performed after infiltration of 1% lignocaine (up to 20 ml may be used).

In primigravida in whom contractions have become weak and there is no evidence of foetal compromise or obstruction, oxytocin may be administered as an infusion. In this case, the expulsive phase may be continued under close observation for a further 30 minutes. Delivery must be considered at the end of this period.

The mother may continue to consume clear fluids in the active phase.

She must be encouraged to assume any position that she is comfortable in and avoid the dorsal position if necessary.

In women with spontaneous labour progressing normally; routine early amniotomy and use of oxytocin is not recommended.

3.7.7. Intrapartum interventions to reduce perineal trauma

Either the ‘hands on’ (guarding the perineum and flexing the baby’s head) or the ‘hands poised’ (with hands off the perineum and baby’s head but in readiness) techniques can be used to facilitate spontaneous birth.

A routine episiotomy should not be carried out during spontaneous vaginal birth.

Episiotomy should only be performed selectively in women in whom there is a clinical need, instrumental birth, foetal maneuvering, suspected foetal compromise or a high chance of perineal tears.

3.7.8. Delivery

The foetal head should not be allowed to extend till occiput is felt below the symphysis pubis. The perineum should be supported during delivery of the head. Then the head is delivered with appropriate cleaning of the foetal oropharynx. Woman should be discouraged from bearing down during this period. Following restitution and external rotation, shoulders must be delivered with appropriately directed traction on the foetal head. The baby must be delivered onto the mother’s abdomen. Breastfeeding should be initiated within 30 minutes of birth.

3.8. Third stage of labour

The third stage of labour is the period from complete delivery of the baby to the complete delivery of the placenta and membranes.

3.8.1. Active management of the third stage of labour

Active management of the third stage of labour is recommended for all mothers. This includes;

Oxytocin given intravenously act with one circulation cycle, but action of ergometrine takes 45 seconds when it is given intravenously. Oxytocin given IM work in 5 minutes and ergometrine takes 7.5 minutes for its action when given IM.

3.8.1.1. Delayed cord clamping (2 minutes after the birth) and cutting of the cord

Delayed clamping of the cord allows for placental transfusion, which reduces neonatal and infant iron deficiency and anaemia. This policy should be followed unless the baby is born in a poor condition or if the mother is bleeding or risk of Rhesus / any iso immunization is a concern.

3.8.1.2. Controlled cord traction

Clamp and cut the cord close to the perineum. A hand should be placed above the symphysis pubis to stabilize the uterus by applying counter traction during controlled cord traction. Application of cord traction when the uterus is relaxed could lead to acute inversion of the uterus.

After delivering of the placenta it must be placed on a flat surface and its surface should be examined for completeness. On the foetal surface the blood vessels must be traced to exclude a succenturiate lobe. Completeness of the foetal membranes must be ensured.

40-30 degrees from midlne directed to right side (angle is measured taking arbitrary longitudinal line in the perineum going across all midline orifices in one line as the point of zero degrees.) NICE guidelines recommend it as 45-60 degrees however the reference point is not clear.

3.8.1.3. Observations in the immediate postpartum period include

3.8.1.3.1. Experienced medical personnel should be informed in any one the following instances

The level of the fundus must be marked on the skin using a marker for observations to be more objective when necessary.

3.8.2. Delayed third stage

Delayed third stage is diagnosed if the placenta is not delivered within 30 minutes of active management.

In managing delayed third stage of labour, options are:

A period of 30 minutes is allowed and again controlled cord traction is attempted provided that no ongoing bleeding is observed.

3.8.2.1. Induction of labour

Labour induction has increased by 140% since 1990. Several studies on induction of labour associated this observation with increased risk of caesarean delivery. In these studies, the comparison was induced pregnancies with spontaneous labour at the same gestation. This comparison is not fair because the alternative to induction is continuation of the pregnancy but not spontaneous labour. Furthermore, induction is a different physiological process when compared to a woman who is in spontaneous labour.

Definitions of normal spontaneous labour cannot be directly applied to induced labour. A study by Harper and colleagues3 showed that in comparison to normal labour progression, women who were induced had slower progress both for multi and nulliparous in comparison to their counterparts in spontaneous labour. Once reaching 6 cm both induced and spontaneous labour progressed at same rates.

It could be that the studies which showed higher caesarean delivery for induced labour concluded in this manner because they were expecting the induced labour to follow the same curve as spontaneous labour.

3.8.2.2. Labour induction techniques

Taking modified Bishops score into consideration, a score of less than 6 (simple Bishop’s score of 5 or less) is considered to be an indicator predicting poor outcome of induction methods in achieving vaginal delivery.

In this group there are two broad categories. These are

Though not widely used, assessment of the cervix by transvaginal imaging and measurement of Foetal Fibronectin are possible predictors of success of labour induction.

3.8.2.3. Methods of cervical ripening

• Mechanical methods

1. Membrane stripping

Though it is widely practiced, it is not being properly assessed. This is primarily used as a preventive measure for formal induction rather than an induction technique,

2. Balloon catheter

There are various catheters specifically made for the purpose of ripening the cervix but most units use Foley catheters either 16 or 18 gauge for cervical ripening. Taking the low cost of Foley catheters, the results show very encouraging outcome compared to purposemade balloon catheters.

Foley catheter is placed in the extra-amniotic space between the membranes and the internal cervical os. Catheter is then dilated with fluid of 60 to 80 ml of sterile water or saline. The open catheter end is usually closed with a sterile syringe piston of 3 ml size. There is no agreed upon volume of optimal dilatation or the duration to keep in the catheter12.

The experience of SLCOG is that allowing the catheter for spontaneous expulsion of up to 48 hours is safe in the presence of appropriate monitoring regarding infection or membrane rupture. Recent metanalysis shows no additional risk of infectious morbidity associated with this technique13. Recent publication of RCOG advocates even the outpatient use of balloon Foley catheter for induction although SLCOG is advocating only in-ward use of Foley catheter for cervical ripening unless the obstetrician is very confident about the monitoring reliability of the patient.

• Pharmacological methods

Use of prostaglandins could be considered for cervical ripening if there are no pre-existing uterine activity. (i.e. two or more contractions per ten minutes) Prostaglandin E1, i.e. misoprostol and prostaglandin E2 (Glandin E2 vaginal tablet or gel) could be used for cervical ripening.

Although there is no FDA approval, both ACOG and The Society of Obstetricians and Gynaecologists of Canada consider E1, i.e. misoprostol to be both

effective and safe as a cervical ripening agent14,15.

Very recently RCOG recommended the use of misoprostol in doses of 25μg with re-dosing allowed in 6 hours. Redosing at 4 to 6 hours for maximum of 6 consecutive doses has been advocated by WHO16,17 allowed in 6 hours. Although 50μg single dose was more effective than 25μg (single dose) in achieving delivery within 24 hours and a lower oxytocin use, 25μg dose. 25μg dose was safer with lower rate of hyperstimulation, Caesarean delivery for foetal concern and meconium18.

Though E1 could be given sublingually, orally and vaginally, one route has not been shown to have better results in comparison with the other.

Oral misoprostol could have a higher advantage because of consistency in the dosing.

3.8.2.3.1. Prostaglandin E2

The studies have not shown advantage of gel over the tablet. However, most clinicians prefer application of E2 cervical gel. The pessary has an advantage of being able to be removed if hyperstimulation occurs following application.

Contraindications for the use of prostaglandins

In this, only removable pessaries should be tried if needed on expert guidance.

Caution is needed if oxytocin to be used within 4-6 hours of use of prostaglandin.

3.8.2.3.2. Oxytocin

One of the most widely used drugs for induction. But the oxytocin’s usefulness as a ripening agent has to be weighed against prolonged time needed for achieving the objective. For this purpose, oxytocin has been shown to be inferior to vaginal prostaglandins19.

Lastly, combination of mechanical and pharmacological agents can be used to achieve the objective of induction of labour. Two randomized studies showed combination of balloon catheter with either misoprostol given vaginally or orally reduced the time to delivery in comparison to treatment with vaginal misoprostol alone20,21. In another study 55 women who received balloon catheter and misoprostol was twice as likely to deliver the baby faster than the woman who received balloon or misoprostol alone.

However, the combination of balloon catheter and oxytocin infusion has shown conflicting results on the efficacy of combination versus using one method alone. Therefore, cannot be recommended by SLCOG other than for research purposes or in rare clinical scenarios.

3.8.2.4. Induction techniques with favourable cervix

3.9. Fourth stage of labour

This is the time period from the end of third stage until two hours. This is the time for careful monitoring of the maternal parameters for mainly postpartum haemorrhage.

3.9.1. General advice on labour care

The practice of maintaining a labour room ‘Notice Board’ – a ‘White Board’ in which the status of all women in labour is summarised and updated regularly is encouraged. This would convey at a glance to all care providers women who require additional attention. The age, parity status, risk factors, salient findings at each assessment and any abnormalities noted must be included in this.

4. Pain relief in labour

Labour analgesia Objectives

Adequate pain relief Improves the maternal and foetal well-being by minimizing the adverse effects like

Prenatal education about available analgesic methods can be done in clinics.

It is important to keep the mother informed of the progress of labour and the condition of the foetus throughout the process to get a better support to control pain.

4.1. Methods of pain relief in labour

The selection of the method of pain relief should be based on the patient preference and availability of resources in your institute and contra indications for each method

• Non-pharmacological methods

The advantages of non-pharmacological techniques include their relative ease of administration and minimal side-effects; however, there is little evidence to support the efficacy of many of these techniques, and some may be costly and time consuming.

A selection of non-pharmacological techniques are listed below:

(TENS);

Breathing exercises, massage and being in water may help to ease pain during the early stage of labour. There is not much evidence that aromatherapy, yoga or acupressure work to relieve pain, but you can use them if the patient wants to.

• Pharmacological methods

Entonox: 50% nitrous oxide in 50% oxygen, provides analgesia within 20-30 seconds of inhalation, with a maximum effect after about 45 seconds.

Advantages are:

Disadvantages are:

(observed in 0.4% of cases after prolonged use)

 Does not provide complete analgesia.

4.2. Systemic analgesics

4.2.1. Pethidine: Pethidine is safe and effective in the latent and early active phase. The dose is 1-1.5 mg/kg IM, repeated after 4-6 hours. Administration of a third dose should be done only with the concurrence of senior personnel. It is generally avoided where delivery is anticipated within 4 hours.

Maternal side effects include nausea, vomiting, sedation, dose dependent respiratory depression and a reduction in gastric motility with a subsequent increase in gastric acidity. Therefore, it should be administered coupled with metoclopramide 5 mg IV or 10 mg IM. Neonatal respiratory depression is a recognized consequence as it crosses the placenta. The highest fetal plasma concentration occurs 2-3 hours after maternal IM administration. Naloxone, a pure opioid antagonist should be available for treatment in all facilities administering opioids for analgesia. Naloxone is given to the baby in a dose of 100μg /kg IV. It has a short duration of action and additional doses may be required. If no improvement is seen with the first dose of naloxone, the cause of neonatal respiratory depression is more likely to be a factor other than opioids.

Despite these disadvantages, meperidine remains popular in many obstetric units, is easy to administer and may be a useful analgesic modality where other methods are not available or are contraindicated.

4.2.2. Morphine: Morphine shares many of the sideeffects of meperidine and rapidly crosses the placenta; however, its metabolites do not have convulsant effects. The dose used for maternal analgesia is 0.1-0.15 mg/kg.

4.2.3. Fentanyl: This has a rapid onset of action. It has a longer terminal half-life than both meperidine and morphine, and repeated dosing may result in drug accumulation in both the foetus and the mother. Advantages include absence of active metabolites and rapid onset of action, making it useful for patientcontrolled analgesia.

4.3. Patient-controlled analgesia (PCA)

If regional analgesia is unavailable or contraindicated, then PCA is a useful method of pain control as long as the equipment and staffing are available. It is important that women are instructed on how to use the device effectively.

This itself is associated with greater satisfaction; however,

Many opioids have been used in PCA devices; drugs currently used include fentanyl and, more recently, remifentanil.

A suggested regimen for fentanyl PCA is a 20 µg bolus with 5 minute lockout; however, the ideal loading dose, bolus dose, lockout time and maximum hourly dose remain unclear. Both parturient and neonate should be carefully monitored during labour, and post-partum and PCA settings altered accordingly.

4.3.1. Remifentanil, an ultra-short-acting opioid, does not accumulate, even after prolonged infusions. There are increasing reports of its use in PCA, although, like fentanyl, the ideal regimen remains unclear. A bolus dose of 0.25-0.5 µg/kg with a 2 minute lockout has been used successfully. However, close monitoring is essential and supplementary oxygen may be required.

If an intravenous or intramuscular opioid is used, also administer an antiemetic.

4.4. Regional techniques

Regional techniques represent the “gold standard” for labour analgesia.

Currently, four different neuraxial techniques for labour analgesia:

CSE (Combined Spinal epidural)

DPE (Dural Puncture epidural) techniques aredefined.

4.4.1. Epidural analgesia: is the most effective / gold standard form of pain relief in labour.

4.4.1.1. Indications/contraindications

The main indications for epidural analgesia during labour are:

1) Patient choice. 2) Twins.

4.4.1.2. Other relative indications

4.4.1.3. Absolute contraindications

4.4.1.4. Relative contraindications (discuss with Consultant Anaesthetist):

4) Certain neurological conditions.

4.4.1.5. Epidural – During 2nd stage pain frequently requires more local anaesthetic for successful relief, and depends on caudal spread of local anaesthetic from the lumbar epidural catheter. However, the dermatomal effects of epidural analgesia may be affected by the level of catheter placement, and caudal spread does not always occur, or takes a prolonged period of time, accounting for sometimes ineffective second stage analgesia.

4.4.2. Spinal – When a woman appears close to delivery, a single injection of local anaesthetic (e.g., bupivacaine or ropivacaine 2-4 mg) with opioid (fentanyl 10-15 μg or sufentanil 1-4 μg) using a 25 or 27 gauge (G) pencil-point spinal needle can provide analgesia for 1-2 h. Its place is limited because of the fixed duration of a single-shot technique, and by the high risk of headache when a large-bore needle is used to place a catheter in the subarachnoid space.

4.4.3. CSE – Combined Spinal Epidural has been shown to provide more rapid, more reliable and more effective analgesia than epidural analgesia, as it provides a more reliable sacral block, leading some practitioners to a strong preference for spinal or CSE procedures in women receiving analgesia late in labour.

CSE techniques performed with high dose spinal opioid (20-25 μg fentanyl) and no local anaesthetic had a higher risk of FHR decelerations (24% compared with 12%) and of uterine hyperactivity (tachysystole) (12% compared with 2%) when compared to CSEs done with local anaesthetic and a lower dose of opioid (fentanyl 10-15 μg).

Foetal bradycardia resulting from a CSE procedure should be managed with maternal blood pressure management and occasionally tocolytic drugs (e.g. terbutaline, nitroglycerine) if tachysystole is suspected, and should rarely lead to emergency delivery. An existing poor FHR tracing is a reasonable factor to consider when deciding between CSE and epidural techniques.

4.4.4. Dural puncture epidural is a recently described technique that can be used when some potential effects of a spinal dose might be inappropriate or undesirable, such as in the case of significant maternal cardiovascular disease or a pre-existing poor fetal tracing. The same technique is used as with a CSE procedure, but no spinal medication is injected after observation of CSF. The backflow of CSF confirms midline epidural placement, one of the technical advantages of the CSE procedure, whereas the lack of spinal dose avoids adverse effects (pruritus, FHR effects, hypotension). Analgesia provided by the DPE technique is more reliable with fewer failed and unilateral blocks compared with an epidural technique. Analgesia, including sacral coverage, may also occur more rapidly because medications are injected into the epidural space translocating into the subarachnoid space via the dural hole.

However, this potential advantage of DPE may depend on the size of the dural hole, and there may be little or no benefit when using needles smaller than 26 G.

Table 1. Advantages and disadvantages of epidural, combined spinal-epidural, and dural puncture epidural analgesia. Indicates some degree of uncertainty. FHR, fetal heart rate

Table 2
EpiduralCombined spinal epidural (CSE)Dural puncture epidural (DPE)
AdvantagesAdvantagesAdvantages
Default technique/long history‘Anatomical’ confirmation of‘Anatomical’ confirmation of
epidural placementepidural placement
Less equipment/less expensiveFaster analgesiaStable haemodynamics
Stable haemodynamicsImproved analgesiaFaster analgesia
‘Proven’ catheter effectBetter second stage analgesiaImproved analgesia
 Accidental dural puncturesBetter second stage analgesia
Increased maternal satisfaction Accidental dural punctures
Useful in training environment  Need for catheter replacementUseful in training environment
DisadvantagesDisadvantagesDisadvantages
No objective determination of Paraesthesia (spinal needle)Larger spinal needle (25G)
epidural spaceneeded
 Pruritus Paraesthesia (spinal needle)
Unreliable second-stage analgesiaFHR effects (hypotension, uterine tone)Dural puncture for no purpose

Table 2. Common dosing regimens for neuraxial analgesia in labour. In Europe, levobupivacaine (not available in the USA) may be substituted for bupivacaine at comparable doses.

DPE, dural puncture epidural; PCEA, Patient-Controlled Epidural Analgesia;

PIEB, Programmed Intermittent Bpidural bolus

Table 3
Labour spinal dosing Local anaesthetic Opioid Bupivacaine 2.5 μg Fentanyl 10-15 μg Ropivacaine 2.5-3.5 μg Sufentanil 1.5-5 μg Epidural (DPE) loading dose Local anaesthestic Opioid 10-15 ml bupivacaine 0.125% Fentanyl 50-100 μg (50 μg probably enough) 10-15 ml ropivacaine 0.2% Sufentanil 10 μg Epidural infusion (10-15 ml h-1) Bupivacaine 0.0625-0.125% with fentanyl 2 μg ml-1 or sufentanil 0.2-0.5 μg ml-1 Ropivacaine 0.10-0.20% with fentanyl 2 μg ml-1 or sufentanil 0.2-0.5μg ml-1 PCEA recipes (Patient-Controlled Epidural Analgesia) 4-6 ml of infusion drug, lockout 5-10 min, maximum 30-35 ml h-1 total infusion plus boluses PIEB (Programmed Intermittent Epidural Bolus) strategy (essentially replace 10-12 ml h-1 infusion with timed bolus, similar hourly dose, usually with additional PCEA doses) 6-8 ml q 30 min 9-10 ml q 45 min 12 ml q 60 min

Adrenaline in concentrations as low as 1:1,000,000 (1-2.2 μg ml-1) may improve analgesia, either by local vasoconstriction maintaining higher concentration of analgesics, or via α2 adrenoceptor-mediated analgesia. Clonidine prolongs the effect of bupivacaine in the epidural space by 25-40% and provides additional analgesia via α2 adrenoceptor agonism.

It can be particularly useful and effective in women with opioid tolerance, where the direct effect of neuraxial opioids or synergism with local anaesthetics may be blunted.

Clonidine can be substituted for fentanyl in similar doses, with similar effects. Preservative-free clonidine 25-100 μg added to an epidural bolus or at a concentration of 2-3 μg ml-1 in standard epidural infusions can supplement analgesia, decrease sacral nerve sparing, improve patients’ satisfaction and reduce the dose of bupivacaine required over the duration of labour.

The most common adverse effect is mild sedation, which can be beneficial in some anxious patients.

4.4.5. Caudal analgesia: Since the development of epidural catheters, caudal epidural injections have become a less popular technique for labour analgesia. Not only do they provide less effective and less flexible analgesia than lumbar epidurals, there is also a higher risk of inadvertent IV injection.

Relief of pain in labour should be a major consideration. The pertinent references for pain management in labour is found under Reference numbers 28, 29, 31, 32 and 33. (Please see ‘References for Management of Pain during Labour’).

5. Care for the new-born baby

Effective care at birth is needed for anticipation of problems with the transition from in-utero dependent life to extra-uterine independent existence and to provide support to ensure stabilization.

The aims of neonatal care following birth include the following:

Guideline)25

5.1. Following basic steps should be followed at the time of birth;

The Apgar score at 1 and 5 minutes should be recorded for all births.

Initiation of breastfeeding should be aimed for within 1 hour after birth.

Head circumference, birth weight, length and other measurements should be carried out once the first feed is complete. A healthcare professional should examine the baby to detect any physical abnormality and to identify any problems that require referral.

6. Perineal care

Perineal or genital trauma caused by either episiotomy or tearing need to be repaired.

Before assessing for genital trauma:

The initial assessment should be performed gently and with sensitivity and may be done in the immediate period following birth preferably as soon as the placenta is delivered.

6.1. Classification of perineal trauma

Perineal repair should only be undertaken with tested effective analgesia in place using infiltration with up to 20 ml of 1% lignocaine, pudendal block or by topping up the epidural, as soon as possible by a medical officer.

The preferred suture material is Rapidly absorbed Polyglycolic Acid. However appropriate normal polyglycolic acid sutures are to be used for repair of anal sphincter.

The following basic principles should be observed when performing perineal repairs:

7. Staffing of the labour room

Achievement of above staffing level is a responsibility of the relevant hospital administration.

8. Equipment necessary for the labour room

Basic Equipment

The list itemized and revised by Family Health Bureau in 2020 is listed below

Equipment, Furniture and Linen List of basic items needed in labour room for providing EMOC services (300-400 deliveries)

MATERNAL

Basic furniture and general items

Table 4
Delivery bed with stirrups08
Spot lamps (movable)08
Revolving stools08
Instrument cabinets (Preferably less than 4 feet)02
Wall clock01
Emergency drugs trolleys01
Patient trolleys02
Instrument trolleys08
Oxygen cylinder stands and regulators04

(Continued)

Table 5
Wall oxygen (Oxygen cylinders for transfer)02
Refrigerator01
Rechargeable lamp in emergency (If no generator)02
Waste baskets with colour coordination system08
Mobile sucker stands for mobile sucker01
Chairs04
Wheel chair commode Stands for entonox cylinders01

Surgical equipment

Table 6
Sphygmomanometers (medium/large)03
Pinard foeal stethoscope/Dopplar08
Adult stethoscope03
Adult laryngoscope02
Ambu bag (adult)02
Hand held Doppler (Foetal heart detector) 04
CTG machine05
Pulse Oxymeter (with paediatric probe)01
Hand held disposable vacuum extractors/Hand held vacuum pump01
Different size cups02
Suction apparatus (adult)01
Nebulizer01
Defibrillator01
Multipara monitor01

(Continued)

Table 7
Patient warmer01
Blood warmer01
Mini autoclave (If CSSD not available)01
Cut down set01
Female urinary catheter metal05
Surgical drums06
Delivery sets30
Episiotomy sets30
Sets for artificial rupture of members20
Cervical repair kit06
Perineal repair kit02
Specula sims04
Specula Cusco’s (large, medium & small)02 each
Artery forceps06
Cheatle forceps04
Dressing scissors02
Obstetric forceps (Mid cavity)02
Wrigley’s forceps01
Rotational forceps (high forceps)01
Douche can (for use in acute inversion)01
Three way tap02
Double balloon cervical catheter03
Infusion pumps06
Kelly’s Forceps04
ET tubes 6, 7, 7.5, 8 Patient control analgesia (PCA) pump02
Multi parameter monitor1per bed
Syringe pumps1per bed
Table 8
Artery forceps02 (Kosher 140 mm straight)
Episiotomy scissors01 (200 mm curved blut)
Umbilical scissors01
Kidney trays02 or one kidney tray and large rectangle tray to be used for wrapping
General surgical towels02 – need packing separately
SwabsAdequate amount
Sterile pads05

Delivery packs (each pack to contain)

Episiotomy packs

Table 9
Blunt operating scissors01 (Mayo 230 mm curved blunt)
Needle holder01 (Mayo Hagar 180 mm Straight)
Toothed dissecting forceps01 (250mm straight)
Kidney tray01
Round body needles/ Cutting needles01 each
SwabsAdequate amount
GS towels02

Perineal / cervical repair kit

Sets for artificial rupture of membranes (ARM)

Table 10
Long artery forceps01
Kidney tray large01
Cotton woolAdequate amount
SwabsAdequate amount

Other surgical consumables

Table 11
Adult endotracheal tubes (Size 6, 7 & 8)each 01 / adequate amounts
IV Cannulae (Different sizes)Adequate amount / size 14, 16, 17,18
Urinary catheters (Foley catheter)Adequate amount / 14,16,18
Syringes (Different size)Adequate amount
Suture materialsAdequate amount
Vicryl Rapid 0, 2/0, 3/0Adequate amount
Vicryl 0, 1, 2/0, 3/0Adequate amount
Distilled waterAdequate amount

Linen and others

Table 12
Gowns25
Washable aprons12
Sterile mackintosh (1.5 meters)24
Boots10 sets
Sterile vaginal packsAdequate amount
Sterile sanitary padsAdequate amount
Washable curtainsAdequate amount
Sterile sanitary padsAdequate amount
Epidural catheter sets (Completed) 18 G25

Cleaning items

Table 13
Anti-SepticsCleaning-surface-isopropyl alcoholAdequate amount
Chlorhexidine for isolation roomAdequate amount
DisinfectantFloor-sodium hypochlorite/peracetic acidAdequate amount
TCLAdequate amount
DetergentAny General-purpose detergentAdequate amount
Reusable equipment - per acetic acidAdequate amount

NEONATAL Equipment

Table 14
Seca weighing scale01 (Preferably digital)
Neonatal suckers04
Infant Magill’s laryngoscope (straight blade)02
Neonatal Resuscitaire01
Neonatal cots08
Oxygen source01
Neonatal stethoscope01
Glucometer01
BP apparatus with neonatal cups01
Guedel airway different neonatal sizes04
Neonatal laryngoscope02
Low tech Incubator (not necessary if transport Incubator is available)01
Rectal thermometer05

Surgical consumables

Table 15
Cord clamps Neonatal Ambu bags03 (preferable. Twins need – 2, one for disinfected)
Nasogastric tubes Endo tracheal tube (size 2.5, 3.0, 3.5, 4.0)02 each
Flexible stiletto (for stiffening Endo tracheal tube)02
IV Cannulae Pen torch batteries05 (buffer stock)

Linen and others

Table 16
Umbilical sets (wrapped in GS towels – to be issued from CSSD) Mackintosh24
Masks03
Umbilical catheters02
Scalpel blades02
Catch forceps02
Pen torch batteries04
EDTA bottles for FBC Plain bottles Microbiological swabs Notice board On call doctor’s information Kidney tray01
Sterile gauze packet01
Cord scissors01

Advantages in umbilical sets

Cord blood for investigation (RH negative mother)

EDTA bottle to FBC

Microbiological swabs

 To take deep ear swabs for culture

EMERGENCY TRAY – Adults

Table 17
ESSENTIAL ITEMS
IV Cannulae (size 14,16,18,20)Each 01
Disposable syringes 2cc, 5cc, 10ccEach 01
Oral air way - Size 3 airway01
Foley catheters (size 12-14)Each 01
Adult Laryngoscope - medium long blades01
Endo-tracheal tube - 6.5,7, 7.5 mm diameter01+introducer
Laryngeal mask airway - Size 0303
Adult Ambu bag/ face mask and (scissors, plaster, cotton, gauze swabs)01
Suction catheter (16,18,14) gage05 from each size
Burette set01
Suction handles01

9. Medications

Basic medication list

Drugs needed in labour room

ANTIBIOTICS

Table 18
Amoxicillin250mg, 500mg tab
AmpicillinIV 250mg, 500mg
Benzyl Penicillin600mg (1 million units vial)
Cefalexin125mg, 250mg tab
Cefotaxime1g vial
Ceftriaxone1g vial
Cefuroxime750mg vial, 500mg tab
Cloxacillin250mg, 500mg tab
Co-Amoxiclav375mg, 625mg
Erythromycin250mg tab
Gentamycin20mg in 2ml, 80mg/ml in 2ml ampule
Metronidazole500mg/ 100ml ampule

ANALGESIC MEDICATIONS

Table 19
Morphine10mg, 15mg, 15mg/ml
Entonox Bupivacaine HCl (plain)10 ml
Morphine30mg tab
Pethidine75mg/ 50mg ampule
Fentanyl100 µg vials
Lignocaine2% in 20ml vial
Paracetamol500mg tab/suppositories
Diclofenac sodium25mg, 25mg, 100mg suppositories
Co-codamol (Panadeine) tabs500 mg
Tramadol Hydrochloride50mg tab
Tramadol Hydrochloride50 mg /2ml ampule

ANTIEMITIC

Table 20
Phenergan (Promethazine) injection25 mg
Metoclopramide HCl10 mg
Ondansetron injections/ tabs4 mg tablets/ 4 mg IV vials

UTEROTONICS

Table 21
Oxytocin/ Syntocinon injection2 units/2 ml, 5 units/ml ampule
Ergometrine injection0.5mg in 1 ml
Oxytocin + Ergometrine Misoprostol200 µg tabs
Tranexamic acid1 g injection

Treatment of toxicity

Table 22
Sodium bicarbonate (NaHCO3) Naloxone Calcium gluconate10 ml
Intralipid 20%ampules

ANTIHYPERTENSIVE MEDICATIONS

Table 23
Hydralazine IV/Oral50mg tab, 20mg in 1ml ampule
Labetalol IV/Oral100mg, 100mg in 20ml ampule
Methyldopa250mg tab
Nifedipine (SR)20mg
Prazosin1mg tab

EMERGENCY DRUGS

IV FLUIDS

5% Dextrose

10% Dextrose

50% Dextrose

Normal saline

Ringer’s lactate

4% Albumin

OTHER DRUGS

Table 24
Vitamin K1mg in 0.5 ml ampule
Heparin25000 IU/5 ml ampule
Famotidine150 mg
Rhogam / anti Rho (D) Immune Globulin Vitamin A mega dose100,000 IU
Ranitidine25 mg/ml in 2 ml ampule
Metoclopramide10 mg tab, 10 mg in 2 ml ampule
Cabergoline500 mg
LMW Heparin (Enoxaparin)40/60 mg

ANTICONVULSANTS

Table 25
Magnesium sulphate injection10 ml ampule
Diazepam injection10 mg/2ml
Phenobarbital15mg, 30mg, 60mg tab
Phenobarbital injection200mg/ 1ml ampule
Levetiracetam midazolam5 mg

TOCOLYTICS

Table 26
Nifedipine capsule20 mg tab

STEROIDS

Table 27
Dexamethasone0.5 mg tabs
Dexamethasone8 mg in 2 ml vial, 4 mg in 1ml vial
Prednisolone5 mg tab
Hydrocortisone100 IV

ANTIRETROVIRALS

Table 28
Contraceptives
Table 29
IUD Implants Condoms

Waste

Sterilization

For Instrumental deliveries

Miscellaneous

Basic Supplies

IV tubing

Following items are available as boxes and labelled as

PPH Box – all needed to manage PPH in a box

A separate Neonatal Resuscitation Box with

10. Guidance on environmental infections in healthcare facilities

10.1. Infection control in the labour room

This is very important in the final outcome of labour management. Infections resulting or originating in the labour room should be prevented from adhering to strict protocols and guidelines developed by institutions caring for labour. Input of microbiologist infection control units and administration and the clinicians caring for labor should have policies decided on keeping environment clean and sterile avoiding introduction and cross infection of patients in labour. Following references are suggested for assistance.

Guidance on this subject is provided in Hospital Infection Prevention and Control Manual26 © SLCM 2021, developed by Sri Lanka College of Microbiologists and updated in 2021, Labour Room Chapter 7.4, 155-158.

(Please see Annexure #5)

Guidance on Environmental Infections in Healthcare Facilities27 can be referred to at https://www.cdc.gov/infectioncontrol/guidelines/environmental/index.html as well as

For management of labour in COVID-19 patients, please refer to SLCOG Guidelines of 202128.

11. Layout plan for a labour suite

Attached herewith is an annexure developed and accepted by the Famiy Health Bureau of Sri Lanka as a suggested layout plan for a labour suite. Please refer to annexure #4.

12. Respectful maternity care during labour and childbirth

WHO recommendations on respectful maternity care during labour and childbirth updated in 2021 can be found at the source https://srhr.org/rhl/article/who-recommendation-on-respectful-maternity-care-duringlabour-andchildbirth

12.1. Communication

A separate line of intercom system should be available 24 hours. When there is no intercom system, a separate landline for the labour room is a must.

Annexure 1.

Contemporary labour curves by parity

Figure from Management of Normal Labour
Figure from the source guideline

Above is a graphical depiction of average labour curves by parity in singleton term pregnancies with spontaneous onset of labour, vaginal delivery, and normal neonatal outcomes. The main point here is that for parous women, the inflection point for acceleration of cervical dilation is at approximately 6 cm and that there is no clear inflection point for nulliparous women.

Data from: Zhang J, Landy HJ, Branch DW, et al. Contemporary patterns of spontaneous labor with normal neonatal outcomes. Obstet Gynecol 2010; 116:128

Annexure 2.

Figure from Management of Normal Labour
Figure from the source guideline

Annexure 3.

Figure from Management of Normal Labour
Figure from the source guideline

Annexure 4.

Labour room layout

Option 1

Figure from Management of Normal Labour
Figure from the source guideline

Option 2

Figure from Management of Normal Labour
Figure from the source guideline

Annexure 5.

Figure from Management of Normal Labour
Figure from the source guideline

7.4 LABOUR ROOM

Introduction

Infection prevention and control (IPC) measures in the labour room are necessary to reduce the risk of transmission of infections to the mother, newborn and health care workers (HCWs). Potential sources of infections include blood and other body fluids (e.g. amniotic fluid), secretions, excretions, any contaminated equipment, linen and other items used in the labour room or contaminated environment. The risk of these infections can be substantially reduced by simple IPC measures.

7.4.1 Design and layout

Location

Space

Functional areas

Hospital Infection Prevention & Control Manual © SLCM 2021 155 CHAPTER 7 7.4 LABOUR ROOM

Handwashing area

7.4.2 Staffing and discipline

Other measures to prevent infections

7.4.3 Cleaning, disinfection and sterilization of instruments and equipment

Table 1. Method of cleaning/disinfection/sterilization of instruments and equipment

Table 30
ItemMethod of cleaning/disinfection/sterilization
Baby cot, warmer and weighing scaleWipe with 70% alcohol daily and after each use
Re-usable metal speculumsClean with GPD and sterilize by autoclaving before reuse Disposable plastic specula are single use only
Mackintosh (contaminatedImmerse in 1% hypochlorite for 30-minute, wash with GPD
with blood and body fluids)and hang to dry
Mattresses - withWipe thoroughly with GPD in between patients and dry
impermeable, intactWipe with 1% hypochlorite if contaminated with blood or
coveringbody fluids
Delivery setUse a sterilized delivery set for each patient. After use, wash instruments with GPD and send for autoclaving
Newborn resuscitationShould be disinfected using a high-level disinfectant
equipment(HLD) or sterilized
Newborn resuscitation equipmentShould be disinfected using a HLD or sterilized

Cleaning, disinfection and sterilization of other patient care equipment/items Refer Chapter 4.5

7.4.4 Environmental cleaning

Table 2. Method of cleaning/disinfection of environmental surfaces

Table 31
ItemMethod of cleaning/disinfection
FloorsMop three times per day with 0.1% hypochlorite, with dedicated mops for each area. Dry the mops in sunlight and store them dry. Wash mops in 0.1% hypochlorite after each use
WallsWet mop with GPD weekly

Cleaning and disinfection of other environmental surfaces and management of spill

Refer Chapter 4.6

7.4.5 Linen

7.4.6 Handling and disposal of sharps Refer Chapters 4.4 and 4.8

7.4.7 Waste management

7.4.8 Occupational health Refer Chapter 9

References

References

Evaluation of a transcervical Foley catheter as a source of infection. Obstet Gynecol 2015; 126(3): 539-51.

ACOG Committee on Practice BulletinsObstetrics, ACOG Practice Bulletin No. 107: Induction of labor, Obstet Gynecol 2009; 114 (2 Pt 1): 386-97.

for developing countries Sri Lanka Journal of Child Health, 2021; 50(2): 329-33.

2020 National Guidelines for Newborn Care Revision 2020; Family Health Bureau, The Sri Lanka College of Paediatricians 2014; ISBN 978955-1503-65-9.

19-in-pregnancy.pdf

References on Management of Pain during Labour

KK Lam, MB, et al. Labour analgesia: update andliterature review, Hong Kong Med J 2020 Oct; 26 (5): 413-20.

WHO recommendation on epidural analgesia forpain relief during labour, 2018; https://srhr.org/rhl/ article/who-recommendation-on-epidural-

analgesia-for-pain-relief-during-labour