Monitor the condition of the fetus during labour.
Record the findings on the partogram.
Understand the significance of the findings.
Understand the causes and signs of fetal distress.
Interpret the significance of different fetal heart rate patterns and meconium-stained liquor.
Manage any abnormalities which are detected.
Multiple pregnancy is used to describe the development of more than one fetus in the uterus at the same time. It is a high risk pregnancy. Careful supervision and proper monitoring is needed for prevention of further complications.
Prolonged labor is the inability of a woman to proceed with childbirth upon going into labor. Prolonged labor typically lasts over 20 hours for first time mothers, and over 14 hours for women that have already had children.
Multiple pregnancy is used to describe the development of more than one fetus in the uterus at the same time. It is a high risk pregnancy. Careful supervision and proper monitoring is needed for prevention of further complications.
Prolonged labor is the inability of a woman to proceed with childbirth upon going into labor. Prolonged labor typically lasts over 20 hours for first time mothers, and over 14 hours for women that have already had children.
it contains a presentation on injuries that occur during baby birth
summary:
Maternal injuries following childbirth process are quite common.
VULVA
PERINEUM
RISK FACTORS FOR THIRD DEGREE PERINEL TEAR
REPAIR OF COMPLETE PERINEAL TEAR
VAGINA
CERVIX
PELVIC HEMATOMA
DIAGNOSIS OF RUPTURE UTERUS
it contains a presentation on injuries that occur during baby birth
summary:
Maternal injuries following childbirth process are quite common.
VULVA
PERINEUM
RISK FACTORS FOR THIRD DEGREE PERINEL TEAR
REPAIR OF COMPLETE PERINEAL TEAR
VAGINA
CERVIX
PELVIC HEMATOMA
DIAGNOSIS OF RUPTURE UTERUS
This presentation explains the basic concepts involved in CTG such as how to read it and how it works and the terms associated with it and a machine manufacture by Philips known as the Avalon FM30 : Fetal monitor
1.1 Define and use correctly all of the key terms
1.2 Describe the signs of true labour and distinguish between true and false labour
1.3 Explain to the mother how to recognise the onset of true labour
1.4 Describe the characteristic features and mechanisms of the four stages of labour
1.5 Describe the seven cardinal movements made by the baby as it descends the birth canal in a normal labour
Understand why an antepartum haemorrhage should always be regarded as serious.
Provide the initial management of a patient presenting with an antepartum haemorrhage.
Understand that it is sometimes necessary to deliver the fetus as soon as possible, in order to save the life of the mother or infant.
Diagnose the cause of the bleeding from the history and examination of the patient.
Correctly manage each of the causes of antepartum haemorrhage.
Diagnose the cause of a blood-stained vaginal discharge and administer appropriate treatment.
Abortion and other Causes of Early Pregnancy Bleeding.pdfChantal Settley
Describe common causes of bleeding in early pregnancy.
Describe the clinical classifications of abortion, the legal aspects of abortion in Ethiopia, and the safe methods used in health facilities.
Identify the warning signs and the emergency treatment required before referral for early pregnancy bleeding.
Describe the features of woman-friendly comprehensive post-abortion care, including the post-abortion family planning service
List the advantages of regionalised perinatal care.
Describe the functioning of a perinatal-care clinic.
Communicate better with patients and colleagues.
Safely transfer a patient to hospital.
Determine the maternal mortality rate.
Medical problems during pregnancy, labour and the puerperium.pdfChantal Settley
Diagnose and manage cystitis.
Reduce the incidence of acute pyelonephritis in pregnancy.
Diagnose and manage acute pyelonephritis in pregnancy.
Diagnose and manage anaemia during pregnancy.
Identify patients who may possibly have heart valve disease.
Manage a patient with heart valve disease during labour and the puerperium.
Manage a patient with diabetes mellitus.
Explain the wider meaning of family planning.
Give contraceptive counselling.
List the efficiency, contraindications and side effects of the various contraceptive methods.
List the important health benefits of contraception.
Advise a postpartum patient on the most appropriate method of contraception.
Define the puerperium.
List the physical changes which occur during the puerperium.
Manage the normal puerperium.
Assess a patient at the 6-week postnatal visit.
Diagnose and manage the various causes of puerperal pyrexia.
Recognise the puerperal psychiatric disorders.
Diagnose and manage secondary postpartum haemorrhage.
Teach the patient the concept of ‘the mother as a monitor’.
Uterine contractions continue, although less frequently than in the second stage.
The uterus contracts and becomes smaller and, as a result, the placenta separates.
The placenta is squeezed out of the upper uterine segment into the lower uterine segment and vagina. The placenta is then delivered.
The contraction of the uterine muscle compresses the uterine blood vessels and this prevents bleeding. Thereafter, clotting (coagulation) takes place in the uterine blood vessels due to the normal clotting mechanism.
Identify the onset of the second stage of labour.
Decide when the patient should start to bear down.
Communicate effectively with the patient during labour.
Use the maternal effort to the best advantage when the patient bears down.
Make careful observations during the second stage of labour.
Assess the fetal condition during the time the patient bears down.
Accurately evaluate progress in the second stage of labour.
Manage a patient with a prolonged second stage of labour.
Diagnose and manage impacted shoulders.
10.2 Preterm labour and preterm rupture of the membranes.pdfChantal Settley
Define preterm labour and preterm rupture of the membranes.
Understand why these conditions are very important.
Understand the role of infection in causing preterm labour and preterm rupture of the membranes.
List which patients are at increased risk of these conditions.
Understand what preventive measures should be taken.
Diagnose preterm labour and preterm rupture of the membranes.
Manage these conditions.
Define hypertension in pregnancy.
Give a simple classification of the hypertensive disorders of pregnancy.
Diagnose pre-eclampsia and chronic hypertension.
Explain why the hypertensive disorders of pregnancy must always be regarded as serious.
List which patients are at risk of developing pre-eclampsia.
List the complications of pre-eclampsia.
Differentiate pre-eclampsia from pre-eclampsia with severe features.
Give a practical guide to the management of pre-eclampsia.
Provide emergency management for eclampsia.
Manage gestational hypertension and chronic hypertension during pregnancy.
7.2 New Microsoft PowerPoint Presentation (2).pdfChantal Settley
Welcome the woman and ask her to sit near you and facing you.
Smile and make good eye contact with her.
Reassure her that you will always maintain her privacy and confidentiality
Without her permission, do not include a third person in the meeting.
Use simple non-medical language and terminologies throughout that she can understand, and check frequently that she has really understood.
Actively listen to her, using gestures and verbal communication to show her that you are paying attention to what she says.
Encourage her to ask questions, express her needs and concerns, and seek clarification of any information that she does not understand.
6.4 Assessment of fetal growth and condition during pregnancy.pdfChantal Settley
When you have completed this unit you should be able to:
• Assess normal fetal growth.
• List the causes of intra-uterine growth restriction.
• Understand the importance of measuring the symphysis-fundus height.
• Understand the clinical significance of fetal movements.
• Use a fetal-movement chart.
• Manage a patient with decreased fetal movements.
• Understand the value of antenatal fetal heart rate monitoring.
What possible complications to look for:
Antepartum haemorrhage
Pre-eclampsia
proteinuria and a rise in the blood pressure.
Cervical changes
Symphysis-fundus height measurement
below the 10th centile?
above the 90th centile?
To review and act on the results of the screening or special investigations done at the booking visit.
2. To perform the second assessment for risk factors.
If possible, all the results of the screening tests should be obtained at the first visit.
Assess normal fetal growth.
List the causes of intra-uterine growth restriction.
Understand the importance of measuring the symphysis-fundus height.
Understand the clinical significance of fetal movements.
Use a fetal-movement chart.
Manage a patient with decreased fetal movements.
Understand the value of antenatal fetal heart rate monitoring.
5.1 Placenta, membranes and amniotic fluid.pdfChantal Settley
Allows gas exchange so the fetus gets enough oxygen
Helps the fetus get sufficient nutrition (folate, vitamins, glucose, etc)
Helps regulate the fetus’ body temperature
Removes waste from the fetus for processing by the mother’s body (excretion)
Filters out some microbes that could cause infection
Transfers antibodies from the mother to the fetus, conferring some immune protection (immunity function).
Produces hormones that keep the mother’s body primed to support pregnancy (endocrine function)
Identify and describe the stages and factors that can affect human development from conception through birth
REVIEW THE STAGES OF FETAL DEVELOPMENT
EXPLORE FACTORS AFFECTING FETAL DEVELOPMENT
PROMOTE HEALTHY FETAL DEVELOPMENT
EXPLORE CONCEPTION
Gain a better understanding of how a fetus develops, and the mother physically changes during pregnancy.
Navigating the Health Insurance Market_ Understanding Trends and Options.pdfEnterprise Wired
From navigating policy options to staying informed about industry trends, this comprehensive guide explores everything you need to know about the health insurance market.
CRISPR-Cas9, a revolutionary gene-editing tool, holds immense potential to reshape medicine, agriculture, and our understanding of life. But like any powerful tool, it comes with ethical considerations.
Unveiling CRISPR: This naturally occurring bacterial defense system (crRNA & Cas9 protein) fights viruses. Scientists repurposed it for precise gene editing (correction, deletion, insertion) by targeting specific DNA sequences.
The Promise: CRISPR offers exciting possibilities:
Gene Therapy: Correcting genetic diseases like cystic fibrosis.
Agriculture: Engineering crops resistant to pests and harsh environments.
Research: Studying gene function to unlock new knowledge.
The Peril: Ethical concerns demand attention:
Off-target Effects: Unintended DNA edits can have unforeseen consequences.
Eugenics: Misusing CRISPR for designer babies raises social and ethical questions.
Equity: High costs could limit access to this potentially life-saving technology.
The Path Forward: Responsible development is crucial:
International Collaboration: Clear guidelines are needed for research and human trials.
Public Education: Open discussions ensure informed decisions about CRISPR.
Prioritize Safety and Ethics: Safety and ethical principles must be paramount.
CRISPR offers a powerful tool for a better future, but responsible development and addressing ethical concerns are essential. By prioritizing safety, fostering open dialogue, and ensuring equitable access, we can harness CRISPR's power for the benefit of all. (2998 characters)
Struggling with intense fears that disrupt your life? At Renew Life Hypnosis, we offer specialized hypnosis to overcome fear. Phobias are exaggerated fears, often stemming from past traumas or learned behaviors. Hypnotherapy addresses these deep-seated fears by accessing the subconscious mind, helping you change your reactions to phobic triggers. Our expert therapists guide you into a state of deep relaxation, allowing you to transform your responses and reduce anxiety. Experience increased confidence and freedom from phobias with our personalized approach. Ready to live a fear-free life? Visit us at Renew Life Hypnosis..
Defecation
Normal defecation begins with movement in the left colon, moving stool toward the anus. When stool reaches the rectum, the distention causes relaxation of the internal sphincter and an awareness of the need to defecate. At the time of defecation, the external sphincter relaxes, and abdominal muscles contract, increasing intrarectal pressure and forcing the stool out
The Valsalva maneuver exerts pressure to expel faeces through a voluntary contraction of the abdominal muscles while maintaining forced expiration against a closed airway. Patients with cardiovascular disease, glaucoma, increased intracranial pressure, or a new surgical wound are at greater risk for cardiac dysrhythmias and elevated blood pressure with the Valsalva maneuver and need to avoid straining to pass the stool.
Normal defecation is painless, resulting in passage of soft, formed stool
CONSTIPATION
Constipation is a symptom, not a disease. Improper diet, reduced fluid intake, lack of exercise, and certain medications can cause constipation. For example, patients receiving opiates for pain after surgery often require a stool softener or laxative to prevent constipation. The signs of constipation include infrequent bowel movements (less than every 3 days), difficulty passing stools, excessive straining, inability to defecate at will, and hard feaces
IMPACTION
Fecal impaction results from unrelieved constipation. It is a collection of hardened feces wedged in the rectum that a person cannot expel. In cases of severe impaction the mass extends up into the sigmoid colon.
DIARRHEA
Diarrhea is an increase in the number of stools and the passage of liquid, unformed feces. It is associated with disorders affecting digestion, absorption, and secretion in the GI tract. Intestinal contents pass through the small and large intestine too quickly to allow for the usual absorption of fluid and nutrients. Irritation within the colon results in increased mucus secretion. As a result, feces become watery, and the patient is unable to control the urge to defecate. Normally an anal bag is safe and effective in long-term treatment of patients with fecal incontinence at home, in hospice, or in the hospital. Fecal incontinence is expensive and a potentially dangerous condition in terms of contamination and risk of skin ulceration
HEMORRHOIDS
Hemorrhoids are dilated, engorged veins in the lining of the rectum. They are either external or internal.
FLATULENCE
As gas accumulates in the lumen of the intestines, the bowel wall stretches and distends (flatulence). It is a common cause of abdominal fullness, pain, and cramping. Normally intestinal gas escapes through the mouth (belching) or the anus (passing of flatus)
FECAL INCONTINENCE
Fecal incontinence is the inability to control passage of feces and gas from the anus. Incontinence harms a patient’s body image
PREPARATION AND GIVING OF LAXATIVESACCORDING TO POTTER AND PERRY,
An enema is the instillation of a solution into the rectum and sig
Telehealth Psychology Building Trust with Clients.pptxThe Harvest Clinic
Telehealth psychology is a digital approach that offers psychological services and mental health care to clients remotely, using technologies like video conferencing, phone calls, text messaging, and mobile apps for communication.
Leading the Way in Nephrology: Dr. David Greene's Work with Stem Cells for Ki...Dr. David Greene Arizona
As we watch Dr. Greene's continued efforts and research in Arizona, it's clear that stem cell therapy holds a promising key to unlocking new doors in the treatment of kidney disease. With each study and trial, we step closer to a world where kidney disease is no longer a life sentence but a treatable condition, thanks to pioneers like Dr. David Greene.
India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...Kumar Satyam
According to TechSci Research report, "India Clinical Trials Market- By Region, Competition, Forecast & Opportunities, 2030F," the India Clinical Trials Market was valued at USD 2.05 billion in 2024 and is projected to grow at a compound annual growth rate (CAGR) of 8.64% through 2030. The market is driven by a variety of factors, making India an attractive destination for pharmaceutical companies and researchers. India's vast and diverse patient population, cost-effective operational environment, and a large pool of skilled medical professionals contribute significantly to the market's growth. Additionally, increasing government support in streamlining regulations and the growing prevalence of lifestyle diseases further propel the clinical trials market.
Growing Prevalence of Lifestyle Diseases
The rising incidence of lifestyle diseases such as diabetes, cardiovascular diseases, and cancer is a major trend driving the clinical trials market in India. These conditions necessitate the development and testing of new treatment methods, creating a robust demand for clinical trials. The increasing burden of these diseases highlights the need for innovative therapies and underscores the importance of India as a key player in global clinical research.
2. Objectives
When you have completed this chapter you
should be able to:
• Monitor the condition of the fetus during labour.
• Record the findings on the partogram.
• Understand the significance of the findings.
• Understand the causes and signs of fetal distress.
• Interpret the significance of different fetal heart rate patterns and
meconium-stained liquor.
• Manage any abnormalities which are detected.
3. Monitoring the fetus
• Why should you monitor the fetus during labour?
• It is essential to monitor the fetus during labour in order to assess how it responds to
the stresses of labour. The stress of a normal labour usually has no effect on a
healthy fetus.
• What may stress the fetus during labour?
• Compression of the fetal head during contractions.
• A decrease in the supply of oxygen to the fetus.
• How does head compression stress the fetus?
• During uterine contractions compression of the fetal skull causes vagal stimulation
which slows the fetal heart rate.
• Head compression usually does not harm the fetus. However, with a long labour due
to cephalopelvic disproportion, the fetal head may be severely compressed. This may
result in fetal distress.
4. • What may reduce the supply of oxygen to the fetus?
• Uterine contractions
• Reduced blood flow through the placenta
• Abruptio placentae
• Cord prolapse or compression
5. • How do contractions reduce the supply of oxygen to the fetus?
• Uterine contractions may:
• Reduce the maternal blood flow to the placenta due to the increase in intra-uterine pressure.
• Compress the umbilical cord.
• When do uterine contractions reduce the supply of oxygen to the fetus?
• Usually uterine contractions do not reduce the supply of oxygen to the fetus, as
there is an adequate store of oxygen in the placental blood to meet the fetal needs
during the contraction. Normal contractions in labour do not affect the healthy fetus
with a normally functioning placenta, and, therefore, are not dangerous.
• However, contractions may reduce the oxygen supply to the fetus when:
• There is placental insufficiency.
• The contractions are prolonged or very frequent.
• There is compression of the umbilical cord.
6. • How does the fetus respond to a lack of oxygen?
• A reduction in the normal supply of oxygen to the fetus causes fetal hypoxia.
This is a lack of oxygen in the cells of the fetus. If the hypoxia is mild the fetus
will be able to compensate and, therefore, show no response. However,
severe fetal hypoxia will result in fetal distress. Severe, prolonged hypoxia will
eventually result in fetal death.
• How is fetal distress recognised during labour?
• Fetal distress caused by a lack of oxygen results in a decrease in the fetal
heart rate.
• How do you assess the condition of the fetus during labour?
• Two observations are used:
• The fetal heart rate pattern.
• The presence or absence of meconium in the liquor.
7. Fetal heart rate patterns
• What devices can be used to monitor the fetal heart rate?
• Any one of the following three pieces of equipment:
• A fetal stethoscope.
• A ‘doptone’ (Doppler ultrasound fetal heart rate monitor).
• A cardiotocograph (CTG machine).
• In most low-risk labours the fetal heart rate can be determined adequately
using a fetal stethoscope. However, a doptone is helpful if there is difficulty
hearing the fetal heart, especially if intra-uterine death is suspected. If
available, a doptone is the preferred method in primary-care clinics and
hospitals.
• Cardiotocograph is not needed in most labours but is an important and
accurate method of monitoring the fetal heart in high-risk pregnancies.
8. How should you monitor the fetal heart rate?
• Because uterine contractions may decrease the maternal blood flow
to the placenta, and thereby cause a reduced supply of oxygen to the
fetus, it is essential that the fetal heart rate should be monitored
during a contraction.
• In practice, this means that the fetal heart pattern must be checked
before, during and after the contraction. A comment on the fetal
heart rate, without knowing what happens during and after a
contraction, is almost valueless.
9. How often should you monitor the fetal heart
rate?
• For low-risk patients who have had normal observations on admission:
• 2-hourly during the latent phase of labour.
• Half-hourly during the active phase of labour.
• Patients with a high risk of fetal distress should have their observations done more
frequently.
• Intermediate-risk patients, high-risk patients, patients with abnormal
observations on admission, and patients with meconium-stained liquor
need more frequent recording of the fetal heart rate:
• Hourly during the latent phase of labour.
• Half-hourly during the active phase of labour.
• At least every 15 minutes if fetal distress is suspected.
10. What features of the fetal heart rate pattern
should you always assess during labour?
• There are two features that should always be assessed:
• The baseline fetal heart rate: This is the heart rate between contractions.
• The effect of uterine contractions on the fetal heart rate: If contractions are
present, the relation of the deceleration to the contraction must be
determined:
• Decelerations that occur only during a contraction (i.e. early decelerations).
• Decelerations that occur during and after a contraction (i.e. late decelerations).
• Decelerations that have no fixed relation to contractions (i.e. variable decelerations).
11. What fetal heart rate patterns can be recognised
with a fetal stethoscope?
• Normal.
• Early deceleration.
• Late deceleration.
• Baseline tachycardia.
• Baseline bradycardia.
• These fetal heart rate patterns (with the exception of variable
decelerations) can be easily recognised with a stethoscope or doptone.
• It is common to get a combination of patterns, e.g. a baseline bradycardia
with late decelerations. It is also common to get one pattern changing to
another pattern with time, e.g. early decelerations becoming late
decelerations.
12. • What is a normal fetal heart rate pattern?
• No decelerations during or after contractions.
• A baseline rate of 110–160 beats per minute.
• What are early decelerations?
• Early decelerations are characterised by a slowing of the fetal heart rate
starting at the beginning of the contraction, and returning to normal by the
end of the contraction. Early decelerations are usually due to compression of
the fetal head, which causes the heart rate to slow during the contraction.
13. • What is the significance of early
decelerations?
• Early decelerations do not indicate
the presence of fetal distress.
• However, these fetuses must be
carefully monitored as they are at
an increased risk of fetal distress.
• What are late decelerations?
• A late deceleration is a slowing of
the fetal heart rate during a
contraction, with the rate only
returning to the baseline 30
seconds or more after the
contraction has ended.
14. What are variable decelerations?
• Variable decelerations have no
fixed relationship to uterine
contractions.
• Therefore, the pattern of
decelerations changes from 1
contraction to another.
• Variable decelerations are usually
caused by compression of the
umbilical cord
• These fetuses must be carefully
monitored as they are at an
increased risk of fetal distress.
15. • What is a baseline tachycardia?
• A baseline fetal heart rate of more than 160 beats per minute.
• What are the causes of a baseline tachycardia?
• Maternal pyrexia.
• Maternal exhaustion.
• Salbutamol (Ventolin) administration.
• Chorioamnionitis (infection of the placenta and membranes).
• Fetal haemorrhage or anaemia.
• What is a baseline bradycardia?
• A baseline fetal heart rate of less than 100 beats per minute.
• A fetal heart rate of between 100 and 110 beats per minute with good
variability is normal but must be distinguished from the maternal heart rate.
16. • What is the cause of a baseline bradycardia of less than 100 beats per
minute?
• A baseline bradycardia of less than 100 beats per minute usually indicates
fetal distress which is caused by severe fetal hypoxia.
• If decelerations are also present, a baseline bradycardia indicates that the
fetus is at great risk of dying.
• How should you assess the condition of the fetus on the basis of the
fetal heart rate pattern?
• The fetal condition is normal if a normal fetal heart rate pattern is present.
• The fetal condition is uncertain if the fetal heart rate pattern indicates that
there is an increased risk of fetal distress.
• The fetal condition is abnormal if the fetal heart rate pattern indicates fetal
distress.
17. • What is a normal fetal heart rate pattern during labour?
• A normal baseline fetal heart rate without any decelerations.
• Which fetal heart rate patterns indicate an increased risk of fetal
distress during labour?
• Early decelerations.
• Variable decelerations.
• A baseline tachycardia.
• These fetal heart rate patterns do not indicate fetal distress but warn that the
patient must be closely observed as fetal distress may develop.
18. • What fetal heart rate patterns indicate fetal distress during labour?
• Late decelerations.
• A baseline bradycardia.
• How should the fetal heart rate pattern be observed during labour?
• The fetal heart rate must be observed before, during and after a contraction.
• The following questions must be answered and recorded on the partogram:
• What is the baseline fetal heart rate?
• Are there any decelerations?
• If decelerations are observed, what is their relation to the uterine contractions?
• If the fetal heart rate pattern is abnormal, how must the patient be managed?
19. • Which fetal heart rate pattern indicates that the fetal condition is
good?
• The baseline fetal heart rate is normal.
• There are no decelerations.
• What must be done if decelerations are observed?
• First the relation of the decelerations to the uterine contractions must be
observed to determine the type of deceleration. Then manage the patient as
follows:
• If the decelerations are early or variable, the fetal heart rate pattern warns that there
is an increased risk of fetal distress and, therefore, the fetal heart rate must be checked
every 15 minutes.
• If late decelerations are present, the management will be the same as that for fetal
bradycardia.
20.
21. • What must be done if a fetal bradycardia is observed?
• Fetal distress due to severe hypoxia is present. Therefore, you should
immediately do the following:
• Exclude other possible causes of bradycardia by turning the patient onto her side to
correct supine hypotension, and stopping the oxytocin infusion to prevent uterine
overstimulation.
• If the fetal bradycardia persists, intra-uterine resuscitation of the fetus must be
continued and the fetus delivered as quickly as possible.
23. How is intra-uterine resuscitation of the fetus
given?
• Turn the patient onto her side.
• Start an intravenous infusion of Ringer’s lactate and give 250 μg (0.5 ml) salbutamol (Ventolin)
slowly intravenously, after ensuring that there is no contraindication to its use. (Contraindications
to salbutamol are heart valve disease, a shocked patient or patient with tachycardia). The 0.5 ml
salbutamol is diluted with 9.5 ml sterile water and given slowly intravenously over 5 minutes.
• Deliver the infant by the quickest possible route. If the patient’s cervix is 9 cm or more dilated and
the head is on the pelvic floor, proceed with the delivery (a vacuum extraction may be
performed). Otherwise, perform a Caesarean section.
• If the patient cannot be delivered immediately (i.e. there is another patient in theatre) the dose
of salbutamol can be repeated if contractions start again, but not within 30 minutes of the first
dose or if the maternal pulse is 120 or more beats per minute.
• It is important that you know how to give fetal resuscitation, as it is a lifesaving procedure when
fetal distress is present, both during the antepartum period and in labour.
• Always prepare to resuscitate the infant after birth if fetal distress is diagnosed during labour.
25. The liquor
• Is the liquor commonly meconium stained?
• Yes, in 10–20% of patients, the liquor is yellow or green due to meconium staining. The incidence
of meconium-stained liquor is increased in the group of patients that go into labour after 41
completed weeks gestation.
• Is it important to distinguish between thick and thin, or yellow and green meconium?
• Although fetal and neonatal complications are more common with thick meconium, all cases of
meconium-stained liquor should be managed the same during the first stage of labour. The
presence of meconium is important and the management does not depend on the consistency of
the meconium.
• What is the importance of meconium in the liquor?
• Meconium-stained liquor usually indicates the presence of fetal hypoxia or an episode of fetal
hypoxia in the past. Therefore, fetal distress may be present. If not, the fetus is at high risk of
distress.
• There is a danger of meconium aspiration at delivery.
26. • How should you monitor the fetus during the first stage of labour if the
liquor is meconium stained?
• Listen carefully for late decelerations. If present, then fetal distress must be
diagnosed.
• If late decelerations are absent, then observe the fetus carefully during labour for
fetal distress, as about a third of fetuses with meconium-stained liquor will develop
fetal distress.
• If electronic monitoring is available, the fetal heart rate pattern must be monitored.
• How must the delivery be managed if there is meconium in the liquor?
• A normal delivery is conducted. There is no need to suction the mouth and nose
prior to the delivery of the shoulders and chest. Immediately dry the infant. No
further resuscitation is necessary if the infant is breathing well. This must be done
irrespective of whether a vaginal delivery or Caesarean section is done.
• Anticipate that the infant may need to be resuscitated at delivery if the infant is not
breathing well following drying. Infants not breathing at delivery have birth asphyxia
and need intubation. Suction the airways using an endotracheal tube before starting
ventilation.
27. • How and when are the liquor findings recorded?
• Three symbols are used to record the liquor findings on the
partogram:
• I = Intact membranes (i.e. no liquor draining).
• C = Clear liquor draining.
• M = Meconium-stained liquor draining.
• The findings are recorded in the appropriate space on the partogram
• The liquor findings should be recorded when:
• The membranes rupture.
• A vaginal examination is done.
• A change in the liquor findings is noticed, e.g. if the liquor becomes
meconium stained.
28. ADMISSION OF A WOMAN IN LABOUR
• History taking
• Physical examination
• Note the psychological state, heart rate, temperature, blood pressure,
respiratory rate and any oedema or
• Examine the abdomen
• Perform a vaginal examination:
29. GENERAL CARE OF WOMEN IN LABOUR
• Assessment of problems and risks
• Respect, privacy and companionship
• Diet and fluids
• Mobility and posture
• Enema, pubic hair shaving and insertion of urinary catheter
• Artificial rupture of membranes (amniotomy)
• Partogram
30. ROUTINE MONITORING IN THE FIRST STAGE OF
LABOUR
• Latent phase (cervix <4 cm dilated):
• Temperature, heart rate, respiratory rate and blood pressure 4 hourly.
• Uterine contractions and fetal heart rate 4 hourly.
• Vaginal examination 4 hourly.
• Any change in phase of labour, or abnormal observation, warrants
more frequent observation or action.
31. • Active phase (cervix ≥4 cm dilated, <1 cm long):
• Maternal condition
• Heart rate, BP, respiratory rate hourly.
• Temperature 4 hourly.
• Urine volume and test for protein and sugar when urine is passed
• Fetal condition
• Fetal heart rate half-hourly, before and immediately after contractions, ideally using a hand-
held
• Doppler device.
• Colour and odour of the liquor 2 hourly if the membranes have ruptured.
• Progress of labour
• Duration and frequency of uterine contractions half-hourly, per 10 minutes.
• Vaginal examination 2 hourly noting cervical dilation, sagittal moulding and caput.
• Treatment given
• All medications.
• All fluids, by whatever route.
• Summary of findings
• Identified problems.
• Management plan.
32. Analgesia in labour
• Pain relief should be offered to all women in labour:
• Support and companionship have been shown to reduce the need for
analgesic medication in labour. Promote companionship in labour.
• Pethidine 100 mg with promethazine 25 mg intramuscularly 4 hourly is
acceptable in both the latent and active phases, even up to full dilatation of
the cervix.
• Inhaled Entonox® (a mixture of 50% nitrous oxide and 50% oxygen) by mask is
useful in the late first stage (≥8 cm cervical dilatation).
• Epidural anaesthesia is generally not available in CHCs and district hospitals.
Some institutions may however have the necessary skills and equipment to
provide this form of pain management.
33.
34. First stage:
dilation and foetal descent, divided into 2 phases
• 1) Latent phase: from the start of labour to approximately 5 cm of dilation.
Its duration varies depending on the number of prior deliveries.
• 2) Active phase: from approximately 5 cm to complete dilation. During this
phase the cervix dilates faster than during the latent phase. The time to
dilate varies with the number of previous deliveries. As a rule, it does not
last longer than 10 hours in a multipara and 12 hours in a primipara.
• Second stage: delivery of the infant
• Begins at full dilation.
• Third stage: delivery of the placenta
35. Dilation curve in the primipara (in a multipara, the curve is
shifted to the left)
37. Amniotic sac
• – The amniotic sac bulges during contractions and usually breaks
spontaneously after 5 cm of dilation or at full dilation during delivery.
Immediately after rupture, check the fetal heart rate and if necessary
perform a vaginal examination in order to identify a potential prolapse of
the umbilical cord. Once the membranes are ruptured, always use sterile
gloves for vaginal examination.
• – Note the colour of the amniotic fluid: clear, blood-stained, or meconium-
stained.
• Meconium staining by itself, without abnormal fetal heart rate, is not
diagnostic of fetal distress, but does require closer monitoring—in
particular, a vaginal examination every 2 hours. Action must be taken if
dilation fails to progress after 2 hours.
38. Foetal progress
• – Assess foetal descent by palpating the abdomen (portion of the fetal
head felt above the symphysis pubis) before performing the vaginal
examination.
• – At each vaginal examination, in addition to dilation, check the
presentation, the position and the degree of fetal descent.
• – Look for signs that the fetal head is engaged:
• On vaginal examination, the presenting part prevents the examiner's fingers from
reaching the sacral concavity .
• The presence of caput (benign diffuse swelling of the fetal head) can lead to the
mistaken conclusion that the fetal head is engaged.
• The distance between the fetal shoulder and the upper edge of the
symphysis pubis is less than 2 finger widths
39. Diagnosing engagement
Presenting part not engaged: fingers in the
vagina can reach the sacral concavity
Presenting part engaged: fingers in the
vagina cannot reach the sacral concavity
(if caput absent)
40. Head not engaged: the shoulder is more
than 2 finger widths above the symphysis
Head engaged: the shoulder is less than 2
finger widths above the symphysis
41. SUMMARY: CTG
• Cardiotocography (CTG) is used during pregnancy to monitor fetal
heart rate and uterine contractions. It is most commonly used in the
third trimester and its purpose is to monitor fetal well-being and
allow early detection of fetal distress. An abnormal CTG may indicate
the need for further investigations and potential intervention. The
device used in cardiotocography is known as a cardiotocograph. It
involves the placement of two transducers onto the abdomen of a
pregnant woman. One transducer records the fetal heart rate using
ultrasound and the other transducer monitors the contractions of the
uterus by measuring the tension of the maternal abdominal wall
(providing an indirect indication of intrauterine pressure). The CTG is
then assessed by a midwife and the obstetric medical team.
42. How to read a CTG
• To interpret a CTG you need a structured method of assessing its various
characteristics. The most popular structure can be remembered using the
acronym DR C BRAVADO:
• DR: Define risk
• C: Contractions
• BRa: Baseline rate
• V: Variability
• A: Accelerations
• D: Decelerations
• O: Overall impression
43. Define risk
• When performing CTG interpretation, you first need to determine if
the pregnancy is high or low risk. This is important as it gives more
context to the CTG reading (e.g. if the pregnancy categorised as high-
risk, the threshold for intervention may be lower).
• Maternal factors
• Obstetric complications
• Other risks
45. Baseline rate of the fetal heart: The baseline rate is the
average heart rate of the fetus within a 10-minute window.
• Look at the CTG and assess what the average heart rate has been over
the last 10 minutes, ignoring any accelerations or decelerations.
• A normal fetal heart rate is between 110-160 bpm.
50. Decelerations: Decelerations are an abrupt decrease in the
baseline fetal heart rate of greater than 15 bpm for greater than 15
seconds.
51. Variable decelerations are observed as a rapid fall in baseline fetal heart rate
with a variable recovery phase. They are variable in their duration and may not have any relationship
to uterine contractions. They are most often seen during labour and in patients’ with reduced
amniotic fluid volume. All fetuses experience stress during the labour process, as a result of uterine
contractions reducing fetal perfusion. Whilst fetal stress is to be expected during labour, the challenge
is to pick up pathological fetal distress.
52. Late deceleration
Late decelerations begin at the peak of the uterine contraction and recover after the
contraction ends. This type of deceleration indicates there is insufficient blood flow
to the uterus and placenta. As a result, blood flow to the fetus is significantly
reduced causing fetal hypoxia and acidosis.
55. Overall impression
• Once you have assessed all aspects of the CTG you need to determine
your overall impression.
• The overall impression can be described as either reassuring,
suspicious or abnormal.
57. Case study 1
• A primigravida with inadequate uterine contractions during labour is
being augmented with an oxytocin infusion. She now has frequent
contractions, each lasting more than 40 seconds. With the patient in
the lateral position, listening to the fetal heart rate reveals late
decelerations.
58. Case study 2
• A patient who is 38 weeks pregnant presents with an antepartum
haemorrhage in labour. On examination, her temperature is 36.8 °C,
her pulse rate 116 beats per minute, her blood pressure 120/80 mm
Hg, and there is tenderness over the uterus. The baseline fetal heart
rate is 166 beats per minute. The fetal heart rate drops to 130 beats
per minute during contractions and then returns to the baseline 35
seconds after the contraction has ended.
59. Case study 3
• During the first stage of labour a patient’s liquor is noticed to have
become stained with thin green meconium. The fetal heart rate
pattern is normal and labour is progressing well.