Ultrasound is useful in the first trimester for evaluating bleeding, pain, gestational sac location and development. A gestational sac is normally visible by 4 weeks ultrasound. The yolk sac appears by 5 weeks and the embryo with cardiac activity by 6 weeks. Abnormal findings include lack of growth, irregular sac shape, large yolk sac size. Doppler can assess blood flow. Ectopic pregnancies can be detected by visualizing an embryo outside the uterus combined with serum hCG levels. Multiple pregnancies are determined by membrane thickness and number of yolk sacs.
In this presentation we will discuss
First trimester US especially TVS is an integral part for confirmation of intrauterine pregnancy and to rule out ectopic pregnancy.
First trimester US helps us in suggesting conceptus viability.
First trimester US especially TVS is very efficient in approaching and evaluating the cause of vaginal bleeding.
In this presentation we will discuss
First trimester US especially TVS is an integral part for confirmation of intrauterine pregnancy and to rule out ectopic pregnancy.
First trimester US helps us in suggesting conceptus viability.
First trimester US especially TVS is very efficient in approaching and evaluating the cause of vaginal bleeding.
MRI ANATOMY OF WRIST AND ELBOW ; special emphasis on TFCC, planning of wrist and elbow mri, intrinsic and extrinsic ligaments, compartments of wrist, neurovascular anatomy of elbow and wrist,
Basics of Interventional Radiology and Vascular Interventions RVRoshan Valentine
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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
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
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.
Title: Sense of Taste
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 structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
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.
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.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
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.
Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
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.
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.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
2. INTRODUCTION
FIRST TRIMESTER
Most critical and tenuous period of human dvpt
Single cell into recognizable human being
Till 12 weeks
3. INTRODUCTION
WHY
Location and number of gsac
GA
Early pregnancy for normal appearance/impending failure
Evaluate pain/bleeding in maternity
Evaluate uterine contents before pregnancy termination
Screening for fetal anomalies
4. NORMAL SONOGRAPHIC ANATOMY
IDENTIFYING THE GESTATIONAL SAC
First definitive sonographic sign
Earliest appearance :small round fluid collection(chorionic cavity)
surrounded completely by a hyperechogenic rim of tissue(chorionic villi
+ decidual tissue).
Threshold(TVS) : 2-3mm size ; 4+1 weeks – 4+3 weeks
Hyperechoic rim : 2mm thick , hyperechoic than myometrium
GS measured as Mean Sac Diameter(MSD)
5.
6. IDENTIFYING THE GSAC
Normal position : mid – upper uterus
Double decidual sac sign : growing sac deforms the central cavity giving
a double bubble appearance
MSD : ≥ 10mm, 5-6 weeks (TAS)
8. BLOOD FLOW IN EARLY PREGNANCY
UTERINE ARTERY:
At uterocervical junction
High resistance flow with prominent diastolic notch(absent in some)
• diastolic notch – disappears by 2nd trimester
• Presence in 3rd trimester : umbilical cord and placental abnormalities
SPIRAL ARTERY
B/W myometrium and choriodecidual tissue
Low resistance flows
Changes to high velocity low resistance flow as pregnancy progress
9.
10. IDENTIFYING THE YOLK SAC
First anatomic structure within GS
TVS : 5th week ; 5mm MSD
Almost always : 5+5 weeks ; MSD 8mm
TAS : by 7 weeks ; MSD 20mm
Confirms IUP
Highest possible transducer frequency
Spherical in shape with sonolucent center and echogenic periphery
Max diameter : 5-6mm ;CRL 30-45mm
End of first trimester : no longer detected
11.
12. INDENTIFYING EMBRYO AND CARDIAC ACTIVITY
EMBRYONIC DISK :
Subtle focal thickening along the
periphery of yolk sac.
THRESHOLD : 5-6 wks; MSD 5-12mm
CARDIAC ACTIVITY
TVS : 34 gestational days; embryonic
length : 1.6mm(Earliest)
THRESHOLD : Length 4-5mm ; GA 6.0-
6.5 wks ; MSD 13-18mm
TAS: GA 8wks ; MSD 25mm.
13. 6 weeks : Flat disk changes to C-shaped embryo
7-8 weeks: paddle shaped upper and lower limbs
9th week : trunk elongates , extremities protrude ventrally and midgut
herniates into UC
10th week : CRL 30-35mm – human appearing embryo , opposed limbs.
14. FETAL MEMBRANES AND PLACENTA
Amnion normally
identified at 6-7 weeks ;
CRL 7mm
Double bleb sign :
anatomic relationship of
amniotic sac + yolk sac
CRL and amniotic sac inc
by 1mm/day
So CRL of 12mm =
amniotic cavity with mean
dia of 12mm
15. FETAL MEMBRANES AND PLACENTA
Amniotic membrane may or may
not be visible .
Inability to visualize ≠ pregnancy
failure
Presence of amnion = presence of
intra-uterine gestational sac
Chorion may/may note be visible
Low-level echoes may be seen
16. DETERMINING GESTATIONAL AGE
GSAC
Most accurate time : first trimester
First structure to be measured : GS(when no embryo or yolk sac is
visible) MSD is used
5-11 weeks : 30 + MSD(mm) = GA in days
YOLK SAC
YS – CA- embryo on TVS : 5.5weeks
YS+ CA – CRL (too small to measure) : 6wks
18. DETERMINING GESTATIONAL AGE
CRL
6-12 weeks : most accurate
± 4.7 days with 95% confidence
GA(days) : 42 + CRL(mm)
During end of first trimester , CRL
not accurate
rapid fetal development
flexion/extension positional
changes
Hence BPD and FL
19. FIRST TRIMESTER COMPLICATIONS
15% of clinically recognized pregnancies are spontaneously
Miscarried
Vaginal spotting or frank bleeding – MC presentation
Bleeding – implantation of the conceptus into the decidualized
endometrium.
Threatened abortion : vaginal bleeding with long cervix + closed cervix+ live
embryo
50% abort & 50% normal outcome
Missed abortion : does not adequately describe pathophysiologic
changes and should be abandoned.
Instead embryonic demise and blighted ovum
20.
21. Threatened abortion
Absent GS
Normal uterus and
normal ET
1)No pregnancy
2)early IUP
3)Ectopic
Thickened ET
/irregularly
echogenic
RPOC/IUBLEED(heavy
bleeding)
DOPPLER FOR RETAINED TISSUE
DECIDUAL RXN
ECTOPIC
(heavy bleeding rare)
EARLY IUP
(HCG >disc level)
GS w/o embryo GS w/ embryo
24. SAC WITHOUT EMBRYO
Normal early IUP
Abnormal IUP
Pseudogestational sac – ectopic pregnancy
IUS - within decidua & PseudoGS – within uterine cavity
Hard to differentiate – f/u required to see yolk sac /embryo.
25. ABNORMAL SAC CRITERIA
NORMAL
THRESHOLD(TVS): MSD 2-3mm ; GA :
4wks
TAS: 5mm ; 5wks
ABNORMAL: TAS (TVS)
No double decidual sac – MSD >10mm
No Yolk Sac - MSD > 20mm (8mm)
No embryo wd CA – MSD > 25mm
(16mm)
26. ABNORMAL SAC CRITERIA
GROWTH RATE
Blighted ovum and anembryonic pregnancy : dvpt arrest before formn
of embryo /before it is detectable using current available equipment.
Normal : 1.13 mm/day
Abnormal: <0.6 mm/d
28. ROLE OF DOPPLER
Differentiate a pseudogestational sac from an intrauterine GS
Flow around pseudo GS – absent or < 8cm/s PSV
Flow around IU GS: high velocity with low resistance
Not reliable as arterial flow with low resistance can also be seen with
pseudo-GS
Doppler delivers more energy , hence restricted to prevent harmful
exposure to early embryo.
31. DETECTING A SAC WITH EMBRYO
ABSENT CARDIAC ACTIVITY
Usually poor prognosis
THRESHOLD : 9mm(TAS) ; 5mm(TVS)
If length of embryo <discriminatory level , Expectant management /
BhCG for normal IUP
Care to be taken:
Highest transducer frequency
M mode if available
Real time clip/videotape documenting absent CA
2nd independent observer to confirm the finding.
32. DETECTING A SAC WITH EMBRYO
CARDIAC ACTIVITY PRESENT
Favourable prognosis
CA + asymptomatic women >8weeks GA – risk of loss only 2-3%.
33. RISK FACTORS FOR EARLY PREGNANCY FAILURE
GA – Inverse relation
<6weeks : 7-24% chance
>8weeks : 2%
First trimester vaginal bleeding : 2-3X spont abortion
HR
Bradycardia
• 6.2 weeks : < 100bpm
• 6.3-7.0 wks : < 120bpm
25% rate of demise
a/w trisomy 18 and triploidy
34. RISK FACTORS FOR EARLY PREGNANCY FAILURE
FIRST TRIMESTER OLIGOHYDRAMNIOS
MSD – CRL < 5mm
80-94% spont abortion despite normal CA
35. YOLK SAC EVALUATION
Both the size and appearance of
the yolk sac should be
considered in early pregnancy.
SIZE
Normal YS
Max Diameter : 5-6mm at
10wks GA
large yolk sac - increased risk for
spontaneous abortion.
37. AMNION EVALUATION
Not visualized normally till CRL 7mm
Abnormal amnion dvpt
Easy to see
Thickness and echogenicity ~ yolk sac
Amniotic cavity > CRL (normally both almost same size)
Double bleb sign - impending or frank pregnancy failure
Amnion without embryo ( usually embryo before the amnion)
• Empty amnion : MSD >16mm
• If MSD <16mm : correlate with b-hCG
38. AMNION EVALUATION
Differentiating YS and amnion is usually difficult
But any cystic structure > 6mm without live embryo – s/o pregnancy
failure
39. MATERNAL FACTORS
Age > 34 years : 1.5 X
Fibroids : 2 X
Septate uterus – inadequate implantation
Daughters of women who took diethylstilbestrol [DES
40. HCG LEVEL IN FIRST TRIMESTER
GS growth and hCG relate to trophoblast function.
HCG assay useful in equivocal cases and women at risk for recurrent
miscarriages – assess if pregnancy is progressing normally
In abnormal IUP , hCG is disproportionately low
Small intrauterine fluid collection with no DDS(TAS) or intra-decidual
sign (TVS) – to see if intrauterine findings are due to pseudoGS or early
IUP
Ectopic pregnancy : absent IU-GS with hCG > discriminatory
levels(1000-2000mIU/ml)
41. ROLE OF DOPPLER IN PREDICTING PREGNANCY
OUTCOME
Not routinely advocated – high energy
Increased indices(RI ,PI)in uterine vessels : increased risk of spont
abortion
By 6-12 weeks GA , indices within UA and spiral artery declines
By 11 wks GA , increased UA RI – risk of IUGR and PIH
42. ECTOPIC PREGNANCY
One of the leading cause of deaths
1.4% of all pregnancies and approximately 15% of maternal deaths.
CLINICAL FEATURES
Classical triad : pain + abnormal vaginal bleeding + palpable adnexal
mass( only 45% cases)
Others : amenorrhea , adnexal tenderness , cervical motion
tenderness.
INCREASED RISK : previous tubal pregnancy , CS , PID , tubal recanalization
, IUCD and increased age
43. ECTOPIC PREGNANCY
SONOGRAPHIC DIAGNOSIS
Pelvis USG and TVS – IOC
Adnexal tenderness on TVS
Initial examn: TAS through full bladder
Look for extrauterine GS or hematoma
FF in morrisons – sense of degree of blood loss(sense of urgency)
TVS: assess uterus , ovaries and adnexa
44. ECTOPIC PREGNANCY
SPECIFIC FINDINGS
Demonstration of IUP by TVS
intradecidual sign and the double-decidual sign can be used to identify
an IUP
DDS s`d be diff from decidual cast /pseudo GS(single decidual layer)
Demo of LIVE EMBRYO IN ADNEXA
45.
46.
47. ECTOPIC PREGNANCY
NON-SPECFIC FINDINGS
SERUM hCG correlation when sonography is non-specific
Negative b hCG rules out live pregnancy
B hCG positive by 23 days of GA
THRESHOLD : TAS : >1800 ; TVS : 500-1000mIU/ml
But If the β-hCG level is below the threshold level, the sonogram may
still identify an ectopic pregnancy.
Normally B hCG doubles in 2 days ; hence serial quantitiative assay will
be helpful as dead or dying gestation have a falling β-hCG level.
48. ECTOPIC PREGNANCY
Pts with ectopic has slower rise in B hCG .
An adnexal mass : ectopic pregnancy , hemorrhagic corpus luteum cyst,
endometriosis, and abscess. Hence not diagnostic.
But pelvis mass+ no e/o IUP + positive B hCG = ectopic mostly
TUBAL RING : concentric ring created by the trophoblast of the ectopic
pregnancy surrounding the chorionic sac.
Diff from corpus luteal cyst : cyst is in eccentric position , hypoechoic
compared to ovarian parenchyma (tubal ring > ovarian parenchyma)
49. ECTOPIC PREGNANCY
Useful in detecting free pelvic fluid.
HP or blood in cul-desac + no IUP : s/o ectopic
Small amout of NON-ECHOGENIC is seen in normal pts.
presence or the amount of intraperitoneal fluid was not a reliable
indicator of rupture.
Intraperitoneal fluid is possible if the blood escapes through the
fimbriated end of the intact fallopian tube.
55. MULTIPLE PREGNANCY
SONOGRAPHIC DETERMINATION
Chorionicity can be determined with high reliability in the first trimester with
accuracy of 98% to 100%
6-9 WEEKS : MEMBRANE THICKNESS for chorionicity and number of yolk sac
for amnionicity
Membrane thicker > 2mm : dichrionic gestn
If its thin and imperceptible – monochorionic gestation.
One yolk sac with 2 embryos : monoamniotic gestation
2 YS + 2 embryos +/- intervening memebrane : diamniotic gestation
56.
57. DETECTING FETAL ANOMALIES
IN > 50% CASES , cause is unknown
MC identifiable cause : chromosomal aberration
< 5 weeks exposure : all or none ( either die / normal)
5-10 weeks (organogenesis) : affects organ dvpt
58. DEVELOPMENT PITFALLS
In a developing embryo , normal
structures may be interpreted
as abnormal
DEVELOPING RHOMBENCEPHALON
In posterior cranium between 7-9
weeks
Seen as a cystic area
Eventually develop as 4th ventricle ,
brain stem and cerebellum.
Can be confused with
hydrocephalus/dandy walker
malformation
59. DEVELOPMENT PITFALLS
PROMINENCE OF FETAL
UMBILICAL CORD INSERTION
SITE
@ 8TH WK GA: physiological
herniation of bowel into
base of umbilical cord
creates a focal mass
Size ≤ 7m , prominent at 9-
10 weeks , resolve by end of
11th week , not seen once
CRL >45mm.
60. DIAGNOSING ANOMALIES
By 10 weeks’ GA, the fetal cranium, brain, neck, trunk, and
extremities can be visualized, and gross anomalies can be
detected in the first trimester.
ANENCEPHALY
Absence of dvpt of cranium with dystrophic brain tissue
Fetal head has an irregular contour /no calcified cranium with brain
tissue extending beyond the usual location.
63. DIAGNOSING ANOMALIES
HOLOPROSENCEPHALY
failure of cleavage of the
prosencephalon into the
cerebral hemispheres
large central cystic space
and the falx and choroid
plexus are absent
a/w trisomy 13
64. DIAGNOSING ANOMALIES
CYSTIC HYGROMA/LYMPHANGIECTASIA
large cystic spaces behind the fetal head, neck, and trunk
Trisomy 13,18 , 21 and turners syndrome
Can extend down the trunk appearing as halo or cofined to posterior
fetal neck
66. DIAGNOSING ANOMALIES
OMPHALOCELE AND GASTROSCHISIS
Diff rom physiological bowel herniation
Mass beyond 12 wks GA
Size > 7mm
Ompahlocele mass has a smooth and rounded contour due to
peritoneal covering.
Gastroschisis: irregular contour as protruding loops not contained by
membrane
69. DIAGNOSING ANOMALIES
AMNIOTIC BAND SYNDROME
entrapment of various fetal parts from a disrupted amnion.
Ventral wall defect + encephalocele + limb amputation
70. SCREENING FOR ANEUPLOIDY
FETAL NUCHAL TRANSLUCENY
Single most powerful marker for diff downs syndrome from euploidy.
Normal subcutaneous fluid-filled space etween the back of the fetal
neck and the overlying skin
Normally very small , increased in downs syndrome.
72. SCREENING FOR ANEUPLOIDY
The fetus should be imaged in the midsagittal plane, ideally with the fetal spine down.
Adequate magnified so that only the fetal head, neck, and upper thorax fill the viewable
area.
The fetal neck should be neutral, with care being taken toavoid measurements in the
hyperflexed or hyperextendedpositions.
The skin at the fetal back should be clearly differentiated from the underlying amniotic
membrane, either by visualizing separate echogenic lines or by noting that the skin line
moves with the fetus.
Measurement calipers should be placed on the inner borders of the echolucent space and
should be perpendicular to the long axis of the fetus (see Fig. 3–1).
Ultrasound and transducer settings should be optimized to ensure clarity of the image and
of the borders of the nuchal space in particular. This may require transvaginal sonography
in certain situations.
73. NUCHAL TRANSLUCENCY
a value of less than ~2.2-2.8 mm in thickness is not associated with
increased risk
Nuchal translucency cannot be adequately assessed if there is:
unfavourable fetal lie
unfavourable gestational age: CRL <45 or >84 mm
Mean nuchal translucency measurements increase by 15% to 20% each week
from 10 to 14 weeks’ gestation.
Hence no single value but preferably 95th percentile for a particular
gestational age.
75. SCREENING FOR ANEUPLOIDY
NASAL BONE SONOGRAPHY
a/w downs syn.
The fetal nasal bones could not be
visualized in 73% of Down syndrome
fetuses
TECHNIQUE
Mid-sagittal plane
The fetal spine should be posterior,
with slight neck flexion.
Two echogenic lines at the fetal nose
profile should be visualized
(nasal skin and bone)
76. SCREENING FOR ANEUPLOIDY
DUCTUS VENOUS SONOGRAPHY
adjunctive test for fetal aneuploidy screening.
Normal : forward triphasic pulsatile DV flow
Abnormal : reversed flow at the time of atrial contraction
a/w : aneuploidy and fetal cardiac malformn
This could be used to either improve the detection rate or
alternatively to reduce the false-positive rate.
PITFALL : contamination of the waveform from neighboring
Vessels.
78. SCREENING FOR ANEUPLOIDY
TRICUSPID REGURGITATION EVALUATION
fetus should be oriented so that the chest wall is anterior
the fetal heart should be insonated parallel to the ventricular septum
3mm gate at tricuspid valve
regurgitant jet of at least 60 cm/sec is noted extending to over half of
systole : significant
79. FETAL MEGACYSTIS
Unusually large bladder in a fetus.
Bladder diameter : > 7mm in 1st trimester
if the longitudinal bladder diameter of 7-15 mm there is a risk of a
chromosomal defects is estimated at ~25% 4
if the bladder diameter is >15 mm the risk of chromosomal defects is
estimated at ~10% (usually obstructive uropathy )
May be a/w oligohydramnios/renal anomalies
82. FIRST TRIMESTER MASSES
OVARIAN MASSES
MC : corpus luteum cyst
Corpus luteum
Secretes prog to support pregnancy
<5cm in diameter
Thick walled cyst with circumferential vascular flow
83. OVARIAN MASSES
CL CYST
Occasionally size > 10cm
Internal septation and echogenic debris – 2o H’age
extremely thick cyst wall and septations
Decrease in size on follow up at 16-18 wks(diff from pathological cysts)
Though not all regress
Adnexal cystic masses < 5 cm in diameter in the first trimester are usually
follicular or corpus luteum cysts and almost always resolve spontaneously.
84.
85. UTERINE MASSES
FIBROIDS
common pelvic mass often identified during pregnancy
Localized pain and tenderness.
Most do not change in size , though some enlarge rapidly – resulting in
infarction and necrosis
USG: solid, often hypoechoic uterine masses with areas of calcification
and may have cystic , avascular area related to necrosis.
Increased spontaneous loss rate in early singleton pregnancies
Editor's Notes
The gestational
sac (circle) does not displace or deform the central cavity complex (straight
black line). The white area represents thickened decidual tissue.
The sac is completely
imbedded within the thickened decidua and does not displace or deform
the central echo cavity complex (arrows).
The gestational sac (circle) protrudes into and displaces the central cavity echo complex
5.3-week intrauterine gestational sac. A. A transvaginal
scan using a 5MHz transducer failed to detect a yolk sac. B. With a
7.5 MHz transducer, a yolk sac is easily seen.
Embryonic demise : no cardiac activity, blighted ovum : gsac without embryo
Follow up warranted as exception s can occur
echogenic yolk sac,
>2k IU GS sd be visible by TVS
1)DCDA:2 sac 2 mbryo , thick membrane
2)MCDA: thin membrane around each embryo
3)MCDA: 2 YS + 2 embryo though no perceptible membrane enoted.
4)DC tri amniotic: one embryo its own amnion and chorion ,
5)Sextuples : 5 of 6 sacs seeneach separated by thck membrane
Three-dimensional image of a 10-week fetus with prominent physiologic bowel at the base of the umbilical cord (arrows).
Twelve-week fetus with absent
cranium and dystrophic brain tissue protruding above the face (arrows).
The head size is smaller than normal.
Omphaloceles. A. Eleven-week fetus with small rounded
mass at the base of the umbilical cord (between calipers) that persisted
on follow-up scan after 12 weeks’ gestational age. B. Color Doppler
sonogram of 12-week fetus with large omphalocele (arrows) demonstrating
umbilical vessels traveling through the omphalocele sac. C. Threedimensional
sonogram of same fetus as B demonstrating the rounded
omphalocele sac (arrow) anterior to the fetal abdomen.