The use of cardiotocogragh in obstetric practice is a sure way for early identification of fetal compromise. Thus there is need for regular and structured training of labour ward staff to ensure proper use of this technology, thereby decreasing perinatal mobidity and mortality.
CTG - Cardiotocography or Non stress test
A nonstress test is a screening test used in pregnancy to assess fetal status by means of the fetal heart rate and its responsiveness.
A cardiotocograph is used to monitor the fetal heart rate and presence or absence of uterine contractions. The test is typically termed "reactive" or "nonreactive".
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
CTG - Cardiotocography or Non stress test
A nonstress test is a screening test used in pregnancy to assess fetal status by means of the fetal heart rate and its responsiveness.
A cardiotocograph is used to monitor the fetal heart rate and presence or absence of uterine contractions. The test is typically termed "reactive" or "nonreactive".
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
CTG Interpretation, evidence based approach
Cardiotocography (CTG) or electronic fetal monitoring (EFM) is the most widely used technique for assessing fetal wellbeing in labour in the developed world. The primary purpose of fetal surveillance by CTG is to prevent adverse fetal outcomes. Continuous electronic foetal monitoring is recommended to assure fetal wellbeing in labour in high risk pregnant women. Understanding pathophysiology of fetal heart rate variation will help appropriate interpretation of the CTG.
Features & classification of CTG according to RCOG will be demonstrated in this presentation with sufficient trace demonstration.
Ultrasound can be used to assess fetal wellbeing by measuring various parameters of the fetus such as the fetal heart rate, amniotic fluid volume, and fetal movements.
Fetal Heart Rate (FHR) : A normal FHR is usually between 120-160 beats per minute (bpm) and it can be assessed using ultrasound. Abnormal FHR patterns such as tachycardia or bradycardia may indicate fetal distress and require further evaluation.
Amniotic Fluid Volume (AFV) : A normal AFV is essential for fetal wellbeing as it cushions the fetus and allows for proper fetal movement and growth. An abnormal AFV such as oligohydramnios (low fluid) or polyhydramnios (excess fluid) can indicate a problem with the fetus or the placenta.
Fetal Movements : Fetal movements can be observed using ultrasound, and a lack of fetal movement can indicate fetal distress.
Biometric parameters such as the measurement of the head, abdominal circumference, femur length, and others can be used to assess fetal growth and development.
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
CTG Interpretation, evidence based approach
Cardiotocography (CTG) or electronic fetal monitoring (EFM) is the most widely used technique for assessing fetal wellbeing in labour in the developed world. The primary purpose of fetal surveillance by CTG is to prevent adverse fetal outcomes. Continuous electronic foetal monitoring is recommended to assure fetal wellbeing in labour in high risk pregnant women. Understanding pathophysiology of fetal heart rate variation will help appropriate interpretation of the CTG.
Features & classification of CTG according to RCOG will be demonstrated in this presentation with sufficient trace demonstration.
Ultrasound can be used to assess fetal wellbeing by measuring various parameters of the fetus such as the fetal heart rate, amniotic fluid volume, and fetal movements.
Fetal Heart Rate (FHR) : A normal FHR is usually between 120-160 beats per minute (bpm) and it can be assessed using ultrasound. Abnormal FHR patterns such as tachycardia or bradycardia may indicate fetal distress and require further evaluation.
Amniotic Fluid Volume (AFV) : A normal AFV is essential for fetal wellbeing as it cushions the fetus and allows for proper fetal movement and growth. An abnormal AFV such as oligohydramnios (low fluid) or polyhydramnios (excess fluid) can indicate a problem with the fetus or the placenta.
Fetal Movements : Fetal movements can be observed using ultrasound, and a lack of fetal movement can indicate fetal distress.
Biometric parameters such as the measurement of the head, abdominal circumference, femur length, and others can be used to assess fetal growth and development.
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
263778731218 Abortion Clinic /Pills In Harare ,sisternakatoto
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Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Are There Any Natural Remedies To Treat Syphilis.pdf
ELECTRONIC FETAL MONITORING CARDIOTOCOGRAPH IN THE MANAGEMENT OF LABOUR
1. ELECTRONIC FETAL MONITORING _CARDIOTOCOGRAPH
IN THE MANAGEMENT OF LABOUR
PRESENTED BY
DR COURAGE J. ILUMA
NDUTH OKOLOBIRI
2. OUTLINE
• INTRODUCTION
• INDICATIONS
• COMPONENT OF THE CTG MACHINE
• MATERNAL POSITION FOR CTG ACQUISITION
• ANALYSIS OF TRACINGS
• DESCRIPTION OF CTG TRACINGS
• MANAGEMENT BASED ON CTG TRACING
• ADVANTAGES
• DISADVANTAGES
• CONCLUSION
3. INTRODUCTION
• Cardiotocograph is a technical continuous non invasive
monitor of foetal heart rate and uterine contraction during
pregnancy.
• Foetal cardiac behaviour is regulated through the autonomic
nervous system and by vasomotors, chemoreptors and
baroreceptors.
4. INTRODUCTION
• Pathological events, such as foetal hypoxia
modify these signals and hence cardiac
response, including foetal heart rate patterns,
can be detected and recorded in the CTG.
• It is used both in antepartum and
intrapartum to monitor and assess fetal well
being.
5. INTRODUCTION
• Cardiotocograph remains one of the cornerstones of
making diagnosis in foetal distress. The monitoring of foetal
heart rate in labour aims to identify hypoxia before it is
sufficient to lead to long term poor neurological
outcome(cerebral palsy) and mortality.
6. INTRODUCTION CONT.
• Continuous electronic fetal monitoring was
introduced into obstetrics practice during the late
1960s.
• Invented by Orvan Hess, Edward Hon and
developed by Hammacher.
• When first introduced EFM was used primarily in
complicated pregnancies but gradually it is being
used in most pregnancies.
• By 1978 it was estimated that nearly two-third of
American women were being monitored
electronically in labour.
7. • In 2002 approximately 3-4 million American women,
comprising 85% of all live births underwent electronic fetal
monitoring( EFM).
• In Nigeria, it is not used generally except in most tetiary
hospitals.
8. COMPONENTS OF CTG
MACHINE
• MONITOR
• TWO TRANSDUCERS:
1. ULTRASOUND TRANSDUCER THAT MEASURES FHR.
2. PRESSURE SENSITIVE TRANSDUCER(TOCODYNAMOMETER)
10. INDICATIONS FOR CTG
MONITORING IN LABOUR
• Previous C/S
• Hypertensive disorders in pregnancy
• Antepartum haemorrhage
• IUGR
• twin pregnancy
• Breech presentation
• Preterm labour
• Meconium stained liquor
• DM in pregnancy
• Sickle cell disease in pregnancy
• Thyroid disease in pregnancy
11. INDICATIONS CONTD
• Abnormal FHR detected by intermittent
auscultation
• Maternal pyrexia
• Fresh bleeding developing in labour
• Oxytocin use for induction and augmentation of
labour
• Pregnancy following IVF.
• Elderly primigravida.
• Patient request etc
12. MATERNAL POSITION FOR
CTG ACQUISITION
• Preferred maternal position for CTG
acquisition :
•Lateral recumbent position
•Half sitting position
•Upright position
The CTG machine is connected to the pregnant
woman’s abdomen using two transducers.
1. The ultrasound transducer for FHR
measurement
2. The TOCODYNAMOMETER for uterine
contractions.
15. STORAGE OF TRACINGS
• All CTG tracings need to be identified with patient’s name,
place of recording, paper print out, date and time when
acquisition started and ended and indication.
• This CTG tracings should be stored securely with the
woman’s medical records for at least 25years.
16. ANALYSIS OF TRACINGS
B Ra V A D O
• 1. Baseline heart rate
• 2. Variability
• 3. Acceleration
• 4.Deceleration
• 5 Overall impression
- Reassuring
- Non reassuring
- omnious
17. BASELINE FHR
• This is the mean level of most horizontal and
less oscillatory FHR Segment. It is estimated
in a time period of 10mins.
• Normal baseline FHR_ 110-160bpm
• Greater than 160pm_ fetal tachycardia
• Less than 110bpm_ fetal bradycardia
18.
19. FETAL TACHYCARDIA
• FHR greater than 160bpm.
• 161-180bpm _mild
• 181-200bpm _ severe
• Greater than 200bpm _ severe, omnious
20. CAUSES OF TACHYCARDIA
• Maternal fever
• Fetal infection
• Maternal dehydration and anxiety
• Maternal thyrotoxicosis
• Fetal anaemia
• Fetal tachyarrhythmias
• Drugs like sympathomimetics and
parasympatholytics
23. CAUSES OF BRADYCARDIA
• Post date pregnancy
• Maternal hypothermia
• Congenital heart block
• Uterine hypertonicity
• Maternal medications like sedative opiates
and beta blockers
• Prolong cord compression
• Vigorous vaginal examination
24.
25. BASELINE VARIABILITY
• It is the fluctuation of FHR resulting from influence of
autonomic nervous system.
• It is evaluated as the average bandwidth in 1minute
segment.
• NORMAL VARIABILITY: 5- 25bpm
• REDUCED VARIABILITY: less than 5bpm for more than
30minutes in baseline segment or for 3 minutes during
deceleration.
26. BASELINE VARIABILITY
REDUCED BASELINE VARIABILITY
• Central nervous system hypoxia
• Fetal acidosis
• Resulting decreased sympathetic and parasympathetic
activity.
• Previous cerebral injury,
• Infection
• Administration of CNS depressant or parasympathetic
blockers.
• Fetal sleep
• Prematurity
27. BASELINE VARIABILITY
INCREASED BASELINE VARIABILITY
• > 25bpm lasting more than 30mins.
• The pathophysiology of this pattern is incompletely
understood.
• May be linked with recurrent decelerations.
• When hypoxia/acidosis evolves very rapidly.
• Presumed to be caused by fetal autonomic
instability/ hyperactive autonomic system.
28.
29.
30. ACCELERATION
• It is an increase in FHR over baseline of at least
15bpm for at least 15 seconds but less than
10minutes.
• Most acceleration coincides with foetal movement
and are a sign of neurologically responsive foetus
that does not have hypoxia/acidosis.
• Reassuring.
31.
32. DECELERATION
• It is decrease in FHR below the baseline of at
least 15bpm for at least 15seconds.
• Deceleration could be:
• EARLY
• LATE
• VARIABLE
• PROLONGED
33. EARLY DECELERATION
• Early deceleration are uniform .
• Repetitive in association with uterine
contractions .
• The nadir of deceleration coincides with
the peak of uterine contraction.
• Due to foetal head compression at the
later stage of labour .
• Does not indicate foetal hypoxia/ acidosis.
34.
35. LATE DECELERATION
• Also uniform and repetitive in relation to uterine
contractions .
• Delayed in timing with nadir late in relation to
peak uterine contractions (ocurring 20secs after the
peak of contraction) .
• Recovers after the end of contraction.
• Late deceleration is almost always indicative of
uteroplacental insufficiency and decreased
intervillous exchange between the mother and
fetus resulting in fetal hypoxia.
38. VARIABLE DECELERATION
• Deceleration that exhibit a rapid drop (onset
to nadir in less than 30seconds)
• Good variability within deceleration.
• Rapid recovery to baseline.
• Varying size, shape and relationship to
uterine contractions.
• It constitute the majority of deceleration in
labour.
• It is seen in cord compression.
39.
40. PROLONGED DECELERATION
• Deceleration lasting more than 3 minutes.
• These are likely to include chemoreceptor mediated
component and thus indicate hypoxaemia.
• Prolonged deceleration causes include:
-Uterine hyperactivity.
-Cord entanglement,
-Maternal supine position.
-Others include: epidural, spinal and para cervical
analgesia.
41.
42. CONTRACTIONS
They are ball shaped gradual increase in the uterine signals
followed by a roughly symmetrical decrease.
TACHYSYSTOLE: excessive frequency of contractions in the
excess of 5 contractions in 10minutes.
43. PRINCIPLES FOR
INTRAPARTUM CTG TRACE
INTERPRETATION
When reviewing the CTG trace, assess
and document contractions and all 4
features of FHR. If there is a stable
baseline FHR between 110- 160bpm
and normal variability, continue usual
care as the risk of foetal acidosis is
limited.
44. DESCRIPTION OF CTG
TRACE
DESCRIPTION BASELINE
FHR(BPM)
BASELINE
VARIABILITY(BP
M)
DECELERATION
REASSURING 110 - 160 5 - 25 None or early
Variable
deceleration with
no concerning
characteristics for
less than 90
minutes.
45. DESCRIPTION OF CTG TRACE
DESCRIPTIO
N
BASELINE
FHR(BPM)
BASELINE
VARIABILIT
Y (BPM)
DECELERATION
NON
REASSURING
100 – 109
OR 161 -
180
<5 for 30 –
50 minutes
OR > 25 for
15 – 25
minutes
Variable deceleration with no
concerning characteristics for 90
minutes or more OR
Variable deceleration with any
concerning characteristics in up to
50% of contraction for 30 minutes or
more OR
Variable deceleration with any
concerning characteristics in over 50%
of contractions for < 30mins OR
Late deceleration in over 50% of
contractions for < 30mins with no
maternal or fetal clinical risk factor
such as vaginal bleeding or significant
meconium.
46. DESCRIPTION OF CTG TRACE
DESCRIPTION BASELINE
FHR(BPM)
BASELINE
VARIABILI
TY(BPM)
DECELERATION
ABNORMAL < 100 OR
>180
< 5 for
more than
50mins or
>25 for
more than
25mins
Variable deceleration with any
concerning characteristics in over
50% of contractions for 30minutes
(or less if any maternal or foetal
clinical risk factors)OR
late deceleration for 30mins(or
less if any maternal or foetal
clinical risk factors)OR
Acute bradycardia OR
Prolonged deceleration lasting
3mins or more.
47. Concerning characteristics for variable
deceleration are:
• Variable deceleration lasting> 60secs
• Reduced baseline variability within
deceleration
• Failure to return to baseline
• Biphasic shape
• No shouldering
48. MANAGEMENT BASED ON
INTERPRETATION OF CTG TRACING
CATEGORY DEFINITION MANAGEMENT
NORMAL All features are
reassuring
• Continue CTG and usual care
• Talk to the woman and her birth
companion about what is happening
SUSPICIOUS 1 non reassuring
feature and 2
reassuring features
• Correct any underlying causes or
uterine hyper stimulation
• Perform a full set maternal observation
• Start one or more conservative
measures
• Inform an obstetrician or a senior
midwife
• Document a plan for reviewing the
whole clinical picture and the CTG
findings
• Talk to the woman and her birth
companion about what is happening
and take her preferences into account
49. MANAGEMENT BASED ON
INTERPRETATION OF CARDIOTOCOGRAPH
TRACES
CATEGORY DEFINITION MANAGEMENT
PATHOLOGIC
AL
1 abnormal OR
2 non reassuring
features
• Obtain a review by an obstetrician or
senior midwife
• Exclude acute events( e,g cord prolapse,
suspected placental abruption or
suspected uterine rupture)
• Correct any underlying causes such as
hypotension or uterine hyperstimulation
• Start 1 or more conservative measures
• Talk to the woman and her birth
companion about what is happening and
take her preference into account.
• If the CTG trace is still pathological after
implementing conservatives measures:
• Obtain a further review by obstetrician or
senior midwife
• Offer digital fetal scalp stimulation and
document the outcome.
50. • If the CTG trace is still
pathological after fetal
scalp stimulation:
• Consider fetal blood
sampling
• Consider expediting
the birth
• Take the woman`s
preferences into
account.
51. NEEDS FOR
URGENT
INTERVENTI
ON
Acute bradycardia, or a
single prolonged
deceleration for 3mins
or more
• Urgently seek obstetric help
• If there has been an acute event
(e.g cord prolapse, suspected
placental abruption or suspected
uterine rupture), expedite the birth
• Correct any underlying causes
such as hypotension or uterine
hyperstimulation
• Start 1 or more conservatives
• Make preparation for an urgent
birth
• Talk to the woman and her birth
companion about what is
happening and take her
preference into account
• Expedite the birth if the acute
bradycardia persists for nine
minutes
• If the FHR recovers at any time up
to 9 mins, assess any decision to
expedite the birth, in discussion
with the woman.
52. ADVANTAGES
OF CTG IN LABOUR
• Early identification of fetal compromise.
• Reduces the stress of continuous manual monitoring.
• Decreases the rate of birth injury due to hypoxia.
53. • Its use is associated with high caeserean section rate and
instrumental vaginal delivery .
• Cost of equipment.
• It requires training to use equipment and analyse results.
• One on one use of device.
DISADVANTAGES/
DRAWBACKS OF CTG IN
LABOUR
54. SINUSOIDAL PATTERN
• A regular, smooth, undulating signal, resembling a
sine wave.
• Amplitude of 5 – 15bpm and a frequency of 3 – 5
cycles per minute.
• Last > 30mins.
• Pathological basis is incompletely understood, but
it occurs in association with-
• severe anaemia, as is found in anti-D
alloimunization, fetal-maternal haemorrhage, twin-
twin transfusion syndrome and ruptured vasa
previa.
55. PSEUDOSINUSOIDAL
PATTERN
• A pattern resembling the sinusoidal pattern.
• more jagged “saw- tooth” appearance.
• Its duration seldom exceeds 30minutes and it is
characterized by normal pattern before and after.
• It is described after analgesic administration to the
mother, and during periods of sucking and other
mouth movement.
56. CONCLUSION
• The use of cardiotocogragh in obstetric
practice is a sure way for early identification
of fetal compromise. Thus there is need for
regular and structured training of labour
ward staff to ensure proper use of this
technology, thereby decreasing perinatal
mobidity and mortality.