Engagement is delayed or difficult – called floating head or non-engaged head even in labor.
Common complications:
Transverse arrest.
Prolonged labor.
Cesarean section may be required.
SUMMARY TABLE: PELVIC TYPES & DELIVERY OUTCOMES
Pelvis Type
Shape
Delivery Likelihood
Common Issues
Gynecoid
Round
Spontaneous Vaginal
Few, if any complications
Android
Heart-shaped
Often Difficult
Arrest, OP, Instrumental
Anthropoid
Oval (AP > T)
Often Possible
OP, Long labor
Platypelloid
Flat
Rare Vaginal
Non-engagement, C-Section
Clinical Assessment in Midwifery
Clinical Pelvimetry – Estimating pelvic adequacy:
Diagonal conjugate measurement via vaginal exam.
Ischial spines prominence and sacral curvature felt digitally.
Engagement of fetal head before labor suggests favorable pelvis.
Cephalopelvic Disproportion (CPD):
Occurs when fetal head is too large or pelvis too small:
Seen more in android and platypelloid pelvis.
Leads to prolonged or obstructed labor.
Requires C-section or operative intervention.
Practical Midwifery Implications:
Antenatal period:
Identify at-risk pelvis via pelvimetry or imaging (X-ray, MRI pelvimetry).
Counsel patients on labor expectations.
Intrapartum:
Monitor fetal descent, station, and rotation.
Be alert for signs of labor dystocia (delay or arrest).
Decide timely on augmentation, instrumental, or surgical delivery.
FETAL SKULL
The fetal skull plays a crucial role in labor and delivery. Its structure allows for:
Moulding (overlapping of bones),
Passage through the birth canal,
And clinical assessment of fetal position.
1. BONES OF THE FETAL SKULL
The fetal skull is divided into 3 main parts:
A. Vault of the Skull (Calvaria) – Soft and compressible
2 Parietal bones
2 Frontal bones
1 Occipital bone
👉 These bones are separated by sutures and fontanelles – allowing moulding during labor.
B. Base of the Skull
Made up of the sphenoid, ethmoid, parts of temporal and occipital bones.
It is rigid and non-compressible.
C. Face
Made up of maxilla, mandible, nasal bones, etc.
Plays no significant role during birth.
2. SUTURES OF THE FETAL SKULL
Sutures are membranous joints where two bones meet. They allow movement and moulding during birth.
Suture
Location
Sagittal
Between the two parietal bones (midline)
Coronal
Between frontal and parietal bones
Lambdoid
Between parietal and occipital bones
Frontal (metopic)
Between the two frontal bones (may close early)
Clinical Use: During vaginal examination, sutures help assess:
Position (e.g., anterior vs posterior fontanelle),
Attitude (flexion/extension),
Moulding (overriding of bones).
3. FONTANELLES OF THE FETAL SKULL
Fontanelles are wide membrane-covered spaces at junctions of sutures.
A. Anterior Fontanelle (Bregma)
Diamond-shaped
At the junction of sagittal, coronal, and frontal sutures
Size: ~3×2 cm
Closes: by 18 months
Midwifery Use:
Felt during vaginal exam to identify position of fetal head.
If easily felt → suggests deflexion or malposition.
B. Posterior Fontanelle (Lambda)
Triangular-shaped
Junction of sagittal and lambdoid sutures
Smaller than anterior fontanelle
Closes by 6–8 weeks after birth
Midwifery Use:
Preferred landmark during labor → indicates well-flexed vertex position.
4. DIAMETERS OF THE FETAL SKULL
These are anteroposterior and transverse measurements of the fetal skull.
A. Anteroposterior Diameters (Front to Back)
Diameter
Extends From
Length
Significance
Suboccipitobregmatic
Below occiput → anterior fontanelle (bregma)
9.5 cm
Engaged in well-flexed vertex (ideal)
Suboccipitofrontal
Below occiput → center of frontal bone
10 cm
Incomplete flexion
Occipitofrontal
Occipital eminence → glabella
11.5 cm
Deflexed head, causes difficulty
Mentovertical
Chin → highest point of vertex
13.5 cm
Brow presentation, largest diameter
Submentovertical
Below chin → highest point of vertex
11.5 cm
Incomplete extension
Submentobregmatic
Below chin → bregma
9.5 cm
Fully extended head, face presentation
B. Transverse Diameters
Diameter
Extends Between
Length
Importance
Biparietal
Between two parietal eminences
9.5 cm
Engaging diameter of head
Bitemporal
Between temporal bones
8 cm
Narrowest transverse diameter
5. MOULDING OF THE FETAL SKULL
Definition: Overlapping of skull bones to reduce head size and allow passage through birth canal.
Caused by uterine pressure during labor.
Grades:
0 – bones not touching.
+1 – bones touching, not overlapping.
+2 – bones overlapping, reducible.
+3 – bones overlapping, not reducible → sign of obstructed labor.
6. PRESENTING PARTS RELATED TO SKULL
Presentation
Part Presenting
Skull Diameter Involved
Vertex
Area between anterior and posterior fontanelles
Suboccipitobregmatic (9.5 cm)
Face
Mentum (chin)
Submentobregmatic (9.5 cm)
Brow
Forehead
Mentovertical (13.5 cm)
Sinciput
Frontal part of skull
Occipitofrontal (11.5 cm)
Clinical & Midwifery Application
During vaginal examination, you feel:
Fontanelles → to determine position and flexion.
Sutures → to detect degree of rotation and moulding.
Obstructed labor may be suspected if:
Moulding is excessive (+3).
Large diameters (e.g., brow presentation) are present.
Summary Chart
Feature
Value/Structure
Importance
Fontanelles
Anterior & Posterior
Landmarks for position
Sutures
Sagittal, Coronal, etc.
Aid moulding & position
AP Diameters
9.5 – 13.5 cm
Affect labor progress
Biparietal Diameter
9.5 cm
Key for engagement
Moulding
0 to +3
Indicates labor progress
MOULDING OF THE FETAL SKULL
Definition:
Moulding is the overlapping of the bones of the fetal skull at the sutures during labor to facilitate passage through the birth canal.
It is a physiological process that helps the fetal head reduce its diameter to accommodate the shape and size of the maternal pelvis.
Why Does Moulding Occur?
The bones of the fetal skull (mainly the vault) are not fused – they are connected by sutures and fontanelles.
These allow mobility of the bones under pressure.
During uterine contractions and descent of the head, bones override each other to make the skull more adaptable to the pelvis.
Where Does Moulding Occur?
Moulding commonly occurs at:
Sagittal suture
Coronal sutures
Lambdoid sutures
Usually between:
Frontal and parietal bones
Parietal bones and occipital bone
Grades of Moulding (Clinical Assessment)
Grade
Description
Clinical Significance
0
Bones are not touching
Normal
+1
Bones are just touching
Normal
+2
Bones are overlapping, but reducible (can be pressed back)
Acceptable
+3
Bones are firmly overlapping, not reducible
Suggests obstructed labor – danger sign
Grade +3 Moulding with poor progress in labor may require cesarean section.
Positive Effects of Moulding:
Helps the head adjust and pass through the maternal pelvis.
Reduces the risk of prolonged second stage in favorable conditions.
Facilitates normal vaginal delivery in most vertex presentations.
Negative Effects / When Moulding Is Excessive:
Cephalopelvic Disproportion (CPD) – fetal head too big or pelvis too small.
Obstructed labor – failure of descent despite strong contractions.
May result in:
Caput succedaneum (soft tissue swelling)
Intracranial hemorrhage (rare, in excessive moulding)
Fetal distress
Moulding vs. Caput Succedaneum
Feature
Moulding
Caput Succedaneum
Definition
Bone overlapping
Edema (fluid) under scalp
Cause
Pressure on bones
Pressure on presenting part
Location
Over sutures
Over presenting part
Disappears
Within hours
Within days
Midwifery & Clinical Use
During vaginal examination, feel sutures and fontanelles to detect moulding.
Monitor labor progress in relation to moulding and descent.
Excessive moulding (+3) is a warning sign – may require operative intervention.
Summary
Moulding is normal and essential during labor.
It helps the fetal head adapt to the maternal pelvis.
Grade +3 moulding → think obstruction or CPD.
Proper monitoring can guide safe labor and delivery decisions.
FETOPELVIC RELATIONSHIP
(Also called: Fetal-Pelvic Relationship or Fetal Disposition in Uterus)
Definition:
Fetopelvic relationship refers to how the fetus is positioned within the maternal pelvis during late pregnancy and labor. It determines how the fetal presenting part aligns and engages in the birth canal, affecting the mode and ease of delivery.
COMPONENTS OF FETOPELVIC RELATIONSHIP
There are 5 key components:
Lie
➤ Relation between the long axis of the fetus and the long axis of the mother.
Type
Description
Longitudinal Lie
Fetal spine is parallel to maternal spine (most common)
Transverse Lie
Fetal spine is perpendicular to maternal spine (abnormal)
Oblique Lie
Fetal spine is diagonal to maternal spine (unstable/abnormal)
Presentation
➤ Part of the fetus that lies over the pelvic inlet.
Type
Presenting Part
Cephalic (Head)
Vertex, Brow, or Face
Breech (Pelvis)
Buttocks or feet
Shoulder
In transverse lie
Vertex presentation (head-first) is ideal for vaginal delivery.
Attitude (Posture)
➤ Relationship of fetal parts to each other.
Type
Description
Flexed (Normal)
Head and limbs flexed toward torso
Deflexed / Extended
Head partially or fully extended → Brow or Face presentation
Flexion is ideal → allows smallest diameter of head to pass.
Position
➤ Relationship of a denominator (fixed point) of the presenting part to the quadrants of maternal pelvis.
For example, in cephalic vertex presentation:
Denominator = Occiput (O)
Common Positions
Full Form
LOA
Left Occipito-Anterior (most common)
ROA
Right Occipito-Anterior
LOP
Left Occipito-Posterior
ROP
Right Occipito-Posterior
Anterior positions (OA) are favorable for delivery. Posterior positions (OP) may cause prolonged labor or back pain.
Engagement
➤ When the widest part of the presenting part (usually biparietal diameter of the fetal head – 9.5 cm) passes through the pelvic brim/inlet.
Type
Description
Engaged
Head is fixed in pelvis (station 0 or lower)
Floating
Head is still above the brim
Engagement typically occurs before labor in first-time mothers and during labor in multiparas.
Ovulation timing (Day 14) helps with conception or contraception
Menstrual irregularities
PCOS, amenorrhea, dysmenorrhea, etc.
Hormonal therapy
Use of estrogen/progesterone in contraceptives
Implantation failure
Luteal phase defects
Prenatal education
Cycle understanding helps explain early pregnancy signs
Key Points to Remember:
Normal cycle = 28 ± 7 days.
Ovulation occurs ~14 days before next period, not always on Day 14.
Hormonal balance is key to a healthy menstrual cycle.
Stress, illness, weight changes can disrupt the cycle.
MENSTRUAL HYGIENE
Definition:
Menstrual hygiene refers to personal hygiene practices during menstruation, including the proper use, changing, and disposal of menstrual products, as well as cleanliness of the body and genital area to prevent infections, discomfort, and ensure dignity.
Importance of Menstrual Hygiene
Benefit
Explanation
Prevents infections
Poor hygiene can cause urinary tract infections (UTIs), reproductive tract infections (RTIs), and skin irritations.
Boosts confidence and comfort
Good hygiene allows women to participate in school, work, and daily activities confidently.
Maintains reproductive health
Clean menstrual practices protect the uterus, ovaries, and vaginal health.
Promotes dignity and rights
Managing menstruation with comfort and privacy is a basic human right.
Key Components of Menstrual Hygiene
1. Use of Clean Menstrual Products
Sanitary pads (disposable or reusable)
Tampons
Menstrual cups
Cloth pads (only if clean and properly dried)
✅ Choose breathable and absorbent materials. ❌ Avoid using dirty rags or synthetic cloths.
2. Regular Changing of Menstrual Products
Every 4–6 hours depending on flow.
Avoid prolonged use of a single pad/tampon → prevents bacterial growth (e.g., Toxic Shock Syndrome in tampon use).
3. Proper Cleaning of Genital Area
Wash vulva (external genitalia) with clean water at least twice a day.
Use mild soap (avoid perfumed/harsh products).
Always wipe front to back to avoid infections.
4. Safe Disposal of Menstrual Waste
Wrap used pads in paper before disposal.
Use covered dustbins or incinerators.
Reusable cloths or cups should be washed with soap and dried in sunlight.
5. Nutrition and Hydration
Eat iron-rich and protein-rich foods.
Stay hydrated.
Helps in reducing fatigue, cramps, and overall discomfort.
Special Considerations in Schools & Communities
Availability of private toilets and water.
Provision of low-cost sanitary napkins.
Menstrual hygiene education from puberty onwards.
Remove stigma, taboos, and myths around menstruation.
Role of Nurse / Midwife / ANM
Role
Responsibilities
Health education
Teach adolescent girls and women about menstrual hygiene.
Counseling
Reduce stigma and promote healthy practices.
Distribution
Provide or guide on low-cost sanitary products (e.g., ASHA kits).
School programs
Conduct awareness sessions in schools and anganwadis.
Myths vs Facts (For Awareness)
Myth
Reality
“Girls should not bathe during periods.”
Bathing is essential for hygiene.
“Menstruation is impure.”
It is a natural biological process.
“You can’t exercise during periods.”
Light exercise reduces cramps and improves mood.
Government Programs in India Supporting Menstrual Hygiene
Menstrual Hygiene Scheme (MHS) – Launched by Ministry of Health & Family Welfare for rural girls.
WIFS (Weekly Iron and Folic Acid Supplementation) – Often integrated with menstrual health education.
Summary:
Menstrual hygiene is vital for health, dignity, education, and empowerment.
Nurses, midwives, and teachers play a key role in promoting safe practices and awareness.
Ensuring clean products, proper washing, frequent changing, and safe disposal are the pillars of menstrual hygiene.
FERTILIZATION
(Also called: Conception or Syngamy)
Definition:
Fertilization is the process by which a male sperm cell unites with a female ovum (egg) to form a zygote, which marks the beginning of a new life.
It restores the diploid number of chromosomes (46) and initiates embryonic development.
Site of Fertilization:
Takes place in the ampulla (outer third) of the fallopian tube (uterine tube), within 12–24 hours after ovulation.
Timing of Fertilization:
Ovum survives for about 24 hours after ovulation.
Sperm survives for 3–5 days in the female reproductive tract.
Fertilization is most likely when intercourse occurs 1–2 days before or on the day of ovulation.
Pre-Fertilization Events:
1. Ovulation
Mature ovum is released from the Graafian follicle in the ovary around Day 14 of the menstrual cycle.
2. Sperm Transport
Millions of sperm are deposited in the vagina during intercourse.
Sperm travel through:
Vagina → Cervix → Uterus → Fallopian Tube.
Only around 200–300 sperm reach the ampulla, and 1 sperm fertilizes the ovum.
Fertilization Process – Step-by-Step
1. Capacitation of Sperm
Functional maturation of sperm in female tract.
Sperm become capable of penetrating the ovum.
2. Acrosomal Reaction
Enzymes (like hyaluronidase) are released from the sperm’s acrosome (cap-like head) to break down the outer layer of the ovum.
3. Penetration of Ovum Layers
Sperm penetrates:
Corona radiata (outermost)
Zona pellucida (middle layer)
Oolemma (plasma membrane)
4. Fusion of Sperm and Egg Membranes
Sperm head enters ovum.
Tail remains outside.
5. Cortical Reaction (Block to Polyspermy)
Ovum releases substances to prevent entry of additional sperm.
Ensures only one sperm fertilizes the egg.
6. Completion of Meiosis II by Ovum
After sperm entry, the ovum completes second meiotic division.
Forms female pronucleus.
7. Formation of Male Pronucleus
Sperm nucleus swells and forms male pronucleus.
8. Syngamy (Fusion of Pronuclei)
Male and female pronuclei fuse.
Forms diploid zygote (46 chromosomes: 23 from each parent).
Outcome of Fertilization
Feature
Description
Zygote Formation
Diploid cell formed (1-cell embryo)
Sex Determination
X (female) or Y (male) chromosome from sperm decides sex
Initiation of Cleavage
Zygote undergoes mitotic divisions as it travels toward uterus
Restores Diploid Number
23 (egg) + 23 (sperm) = 46 chromosomes
After Fertilization – Early Development
Stage
Time After Fertilization
Zygote
Day 1
2-cell, 4-cell stage
Day 2
Morula (16 cells)
Day 3–4
Blastocyst
Day 5–6
Implantation
Day 6–10 in uterus
Clinical and Nursing Relevance
Topic
Importance
Infertility
Failure of fertilization is a cause of infertility.
Contraception
Most methods (e.g., IUCD, pills) aim to prevent fertilization.
Assisted Reproduction
IVF involves fertilization outside the body.
Genetic Counseling
Fertilization errors can lead to chromosomal anomalies (e.g., Down syndrome).
Emergency Contraception
Works by inhibiting ovulation or fertilization.
Summary:
Step
Description
1. Ovulation
Egg released from ovary
2. Sperm travels
Through female tract to fallopian tube
3. Fertilization
In ampulla – one sperm penetrates egg
4. Zygote forms
46 chromosomes, diploid
5. Early embryo
Cleavage, blastocyst, then implantation
CONCEPTION
(Also called: Fertilization + Early Development)
Definition:
Conception is the successful union of a sperm and an ovum (fertilization), followed by the formation of a zygote, and its implantation into the uterus — marking the beginning of pregnancy.
In short: Fertilization + Zygote formation + Implantation = Conception
STEPS OF CONCEPTION:
1. Ovulation
A mature ovum is released from the ovary (around Day 14 of the menstrual cycle).
The ovum is picked up by the fimbriae of the fallopian tube.
2. Fertilization
Occurs in the ampulla of the fallopian tube.
One sperm successfully penetrates the ovum → zygote (single-cell embryo) is formed.
3. Zygote Formation
Fusion of male and female pronuclei restores the diploid number (46 chromosomes).
Sex of the baby is determined at this point (XX = girl, XY = boy).
4. Cleavage (Early Cell Division)
The zygote undergoes mitotic divisions while moving down the fallopian tube.
Forms 2-cell, 4-cell, 8-cell, and morula (16-cell) stages.
5. Blastocyst Formation
By Day 5–6, the morula becomes a blastocyst — a hollow ball of cells.
The blastocyst has:
Inner cell mass → future embryo
Trophoblast → future placenta
6. Implantation
Occurs between Day 6–10 after fertilization.
The blastocyst attaches to the endometrium of uterus, usually in the upper posterior wall.
Trophoblast cells release hCG (human chorionic gonadotropin) → signals the body to maintain pregnancy.
HORMONAL SUPPORT FOR CONCEPTION
Hormone
Function
FSH
Stimulates follicle growth (prepares ovum)
LH
Triggers ovulation
Estrogen
Builds up endometrial lining
Progesterone
Maintains endometrium after ovulation
hCG
Secreted after implantation to maintain corpus luteum and progesterone production
TIMING OF CONCEPTION
Factor
Timing
Ovulation
Around Day 14 of cycle
Fertilization window
Within 12–24 hours of ovulation
Sperm survival
Up to 5 days in female tract
Implantation
6–10 days after fertilization
OUTCOME OF CONCEPTION
If successful:
Pregnancy begins.
Menstrual cycle is halted.
Embryo continues development.
If unsuccessful:
No implantation.
Corpus luteum degenerates.
Hormones fall → Menstruation occurs.
NURSING & MIDWIFERY IMPORTANCE
Relevance
Explanation
Pregnancy planning
Understanding fertile period helps couples conceive or avoid pregnancy.
Family planning
Contraceptives work by preventing any step in the conception process.
Infertility
Failure of fertilization or implantation can cause infertility.
Antenatal care
Knowledge of conception helps in accurate pregnancy dating and care.
KEY POINTS TO REMEMBER:
Conception = Fertilization + Implantation
Occurs in the fallopian tube and uterus.
Requires precise hormonal coordination.
Failure at any step → no pregnancy.
hCG is the first hormone detected in pregnancy tests.
IMPLANTATION
(Also called: Nidation)
Definition:
Implantation is the process by which the blastocyst (early-stage embryo) attaches to and embeds itself into the endometrial lining of the uterus, usually 6–10 days after fertilization.
👉 This marks the true beginning of pregnancy.
When Does Implantation Occur?
Fertilization: Occurs on Day 0 in the ampulla of the fallopian tube.
The zygote undergoes cleavage → morula → blastocyst.
Implantation occurs around Day 6–10 after fertilization, in the uterine cavity.
Site of Implantation:
Most commonly on the posterior wall of the uterus, in the upper part (fundus).
The blastocyst comes into close contact with the endometrium.
2. Adhesion
The blastocyst attaches to the endometrial epithelium using cell adhesion molecules.
3. Invasion
Trophoblast cells (outer layer of blastocyst) invade the endometrial lining.
Trophoblast differentiates into:
Cytotrophoblast
Syncytiotrophoblast – invades deeply and forms placenta.
Role of Hormones in Implantation:
Hormone
Function
Estrogen
Prepares the endometrium (proliferation phase)
Progesterone
Converts endometrium into secretory phase, rich for implantation
hCG (Human Chorionic Gonadotropin)
Secreted by syncytiotrophoblast after implantation; maintains corpus luteum and progesterone secretion
🔍 hCG is the basis of pregnancy tests (detected in blood/urine after implantation).
Changes in Endometrium After Implantation:
The endometrium becomes:
Decidua (maternal part of placenta)
Decidua basalis – under the implanted embryo (forms maternal placenta)
Decidua capsularis – over the embryo
Decidua parietalis – rest of the uterine lining
Signs & Symptoms of Implantation (Sometimes Observed):
Implantation bleeding (light spotting)
Mild cramping
Often goes unnoticed
Clinical Significance:
Clinical Aspect
Importance
Successful implantation
Start of pregnancy
Failure of implantation
Early pregnancy loss
Ectopic implantation
Dangerous – requires emergency treatment
Assisted Reproductive Technology (ART)
Aims to ensure optimal endometrial environment for implantation
hCG detection
Basis for urine pregnancy test (positive ~14 days after fertilization)
Summary Table:
Feature
Description
Time
6–10 days after fertilization
Site
Upper posterior wall of uterus
Structure implanted
Blastocyst
Key cells
Trophoblast (→ placenta)
Hormones involved
Estrogen, Progesterone, hCG
Outcome
Pregnancy begins, placenta formation starts
EMBRYOLOGICAL DEVELOPMENT
(From Fertilization to Fetal Stage)
Definition:
Embryological development is the process through which a zygote (fertilized egg) transforms into a multicellular embryo, then into a fetus, eventually forming a complete human being.
Entire development depends on hormonal support, genetic health, and maternal well-being
🌿 PLACENTAL DEVELOPMENT
(Also known as: Placentogenesis)
✅ Definition:
Placental development refers to the formation and growth of the placenta, a vital organ that connects the developing fetus to the uterine wall, allowing nutrient, gas, and waste exchange, and secreting hormones to maintain pregnancy.
✅ Origin of the Placenta:
Component
Derived From
Fetal part
Trophoblast (from the blastocyst)
Maternal part
Endometrium of uterus (decidua basalis)
✅ Timeline of Placental Development:
Time
Event
Day 6–7
Implantation begins
Day 8–9
Trophoblast differentiates into cytotrophoblast and syncytiotrophoblast
Week 2–3
Chorionic villi form
Week 4–5
Maternal blood begins to flow into intervillous spaces
Week 12
Placenta becomes fully functional
Week 20
Mature placenta is formed
✅ Phases of Placental Development:
🔹 1. Trophoblast Differentiation (Day 6–9)
After implantation, the trophoblast (outer layer of blastocyst) divides into:
Cytotrophoblast – inner layer, mitotically active
Syncytiotrophoblast – outer multinucleated layer that invades endometrium and secretes hCG
🔹 2. Formation of Chorionic Villi (Week 2–3)
Finger-like projections called chorionic villi grow into the endometrium.
These villi become the functional unit of the placenta.
Types:
Primary villi – core of cytotrophoblast
Secondary villi – add mesoderm
Tertiary villi – develop blood vessels
🔹 3. Formation of Placental Circulation (Week 4–5)
Fetal blood vessels form within villi.
Maternal spiral arteries open into intervillous spaces, allowing nutrient/gas exchange without direct blood mixing.
✅ Structure of the Mature Placenta (By 20 Weeks)
🔸 Fetal Surface:
Smooth, shiny, covered with amnion.
Contains umbilical cord (2 arteries + 1 vein).
Supplied by chorionic villi.
🔸 Maternal Surface:
Rough, reddish, and lobulated (cotyledons: 15–20 lobes).
🌿 PLACENTAL FUNCTION: BARRIER ROLE vs BLOOD-BRAIN BARRIER
✅ Placenta as a Barrier (Placental Barrier)
🔹 Definition:
The placental barrier refers to the layers of tissue that separate maternal blood in the intervillous space from fetal blood in the capillaries of chorionic villi, allowing selective exchange of substances.
🔹 Purpose:
To protect the fetus from harmful substances in the maternal circulation.
To allow transport of essential nutrients, gases, and antibodies.
✅ Structure of the Placental Barrier
In early pregnancy, the barrier is thicker and includes:
Syncytiotrophoblast
Cytotrophoblast
Basement membrane
Connective tissue of villus
Endothelium of fetal capillaries
As pregnancy advances, the cytotrophoblast layer disappears, and the barrier thins, improving exchange efficiency.
✅ Substances That CAN Cross the Placental Barrier:
Substance
Mode of Transport
Oxygen & CO₂
Diffusion
Glucose
Facilitated diffusion
Amino acids
Active transport
Fatty acids
Simple diffusion
Vitamins & Minerals
Specific transport systems
Drugs (e.g., alcohol, nicotine, some antibiotics)
Diffusion
Viruses (HIV, rubella, CMV)
Transplacental passage
Maternal IgG antibodies
Active transport (provides fetal immunity)
✅ Substances That CANNOT Cross Easily:
Substance
Reason
Heparin
Large molecule
Insulin
Degraded in placenta
IgM antibodies
Large size prevents crossing
Bacteria (most)
Blocked unless placental integrity is compromised
✅ FUNCTIONAL COMPARISON: Placental Barrier vs Blood-Brain Barrier (BBB)
Feature
Placental Barrier
Blood-Brain Barrier
Location
Between maternal and fetal blood
Between blood and brain tissue
Function
Nutrient exchange, fetal protection
Protects brain from toxins, regulates entry of substances
Permeability
Selectively permeable (more permissive)
Highly selective and restrictive
Allows antibody passage
Yes (IgG)
No large antibodies
Formed by
Trophoblast layers & fetal capillary endothelium
Endothelial cells with tight junctions
Crossed by drugs?
Many drugs can cross
Fewer drugs cross due to tight regulation
Clinical concern
Teratogenic drug exposure
Neurotoxicity from certain drugs or infections
✅ Nursing and Midwifery Implications:
Drug administration in pregnancy must consider whether the drug crosses the placental barrier.
Understanding placental function is key to:
Preventing fetal harm
Supporting fetal development
Educating mothers on teratogens
Maternal infections like rubella, cytomegalovirus (CMV), toxoplasmosis can cross placenta and cause congenital anomalies.
🧠 Summary Points:
The placental barrier protects but does not block all substances.
It is more permissive than the blood-brain barrier.
It allows essential nutrients and antibodies, but also some harmful drugs, alcohol, and infections.
Proper prenatal care and drug screening are essential.
🌿 STRUCTURE AND FUNCTIONS OF THE PLACENTA
✅ Definition:
The placenta is a temporary organ that forms during pregnancy, connecting the developing fetus to the uterine wall to enable exchange of nutrients, gases, waste, and to secrete hormones essential for maintaining pregnancy.
Fetal growth and development refers to the progressive increase in size, structure, function, and complexity of the human fetus from conception to birth.
The process occurs in three trimesters and includes cell division, organogenesis, maturation, and functional development of all body systems.
✅ Phases of Intrauterine Development:
Stage
Duration
Key Features
Pre-embryonic
0–2 weeks
Zygote → blastocyst → implantation
Embryonic
3–8 weeks
Formation of major organs (organogenesis)
Fetal
9 weeks to birth
Growth and maturation of organs and body systems
✅ FETAL DEVELOPMENT BY TRIMESTERS
🟡 FIRST TRIMESTER (Week 1–12)
📅 Week 3–4:
Formation of neural tube (→ brain & spinal cord).
Heart begins to beat (~day 22).
Formation of somites (future vertebrae & muscles).
📅 Week 5–6:
Formation of limb buds.
Eyes, ears, and facial features begin forming.
Primitive gut and early organ systems develop.
📅 Week 7–8:
All major organs are present but immature.
Bones begin to ossify.
Fingers and toes start to appear.
📅 Week 9–12:
Embryo now called fetus.
External genitalia begin to differentiate.
Kidneys start functioning; urine forms part of amniotic fluid.
Fetal movements start (not yet felt by mother).
Length: ~7–8 cm; Weight: ~20 g
🟠 SECOND TRIMESTER (Week 13–26)
📅 Week 13–16:
Fetus grows rapidly in length.
External genitalia visible on ultrasound.
Skeleton continues to ossify.
Lanugo (fine hair) covers the body.
📅 Week 17–20:
Quickening: First fetal movements felt by mother.
Vernix caseosa (waxy coating) forms on skin.
Eyebrows and scalp hair begin to grow.
Length: ~25 cm; Weight: ~300 g
📅 Week 21–24:
Lungs begin to develop alveoli (no surfactant yet).
Taste buds form.
Fetal heartbeat audible with a fetoscope.
Limited viability starts (~23–24 weeks with NICU support).
📅 Week 25–26:
Surfactant production begins in lungs (crucial for breathing post-birth).
Monitor fetal growth via fundal height, ultrasound
Nutrition advice
Encourage protein, iron, folic acid intake
Danger signs
Monitor for IUGR (Intrauterine Growth Restriction), macrosomia, reduced fetal movements
Education
Teach mother about fetal development and what to expect each trimester
🧠 SUMMARY TABLE
Trimester
Key Development
1st (0–12 wk)
Organ formation, heartbeat, basic structure
2nd (13–26 wk)
Growth, movement, gender, viability
3rd (27–40 wk)
Maturation, weight gain, lung development
❤️🩹 FETAL CIRCULATION
(Unique blood circulation system in the unborn fetus)
✅ Definition:
Fetal circulation is the specialized vascular system in the fetus that allows oxygen and nutrient exchange through the placenta, bypassing the lungs and liver (since they are non-functional before birth).
Key Points to Remember:
Lungs are non-functional before birth → blood is shunted to avoid pulmonary circulation.
Oxygenation occurs in the placenta, not in the lungs.
Blood bypasses lungs via foramen ovale and ductus arteriosus.
Blood bypasses liver via ductus venosus.
Structures Involved in Fetal Circulation:
Structure
Function
Umbilical vein (1)
Carries oxygenated blood from placenta to fetus
Ductus venosus
Bypasses liver → connects umbilical vein to inferior vena cava
Foramen ovale
Opening between right and left atria → bypasses lungs
Ductus arteriosus
Connects pulmonary artery to aorta → bypasses lungs
Umbilical arteries (2)
Carry deoxygenated blood from fetus back to placenta
Pathway of Fetal Circulation:
1️⃣ Placenta → 2️⃣ Umbilical vein → 3️⃣ Some blood goes to liver; most bypasses via ductus venosus → 4️⃣ Inferior vena cava → 5️⃣ Right atrium → 6️⃣ Most blood flows through foramen ovale → left atrium → left ventricle → aorta → body 7️⃣ Remaining blood in right atrium → right ventricle → pulmonary artery → 8️⃣ Most bypasses lungs via ductus arteriosus → aorta → body 9️⃣ Deoxygenated blood returns via umbilical arteries → to placenta for oxygenation
Summary of Major Shunts in Fetal Circulation:
Shunt
Location
Purpose
Ductus venosus
Liver
Bypasses liver, directs blood to IVC
Foramen ovale
Between atria
Bypasses pulmonary circulation
Ductus arteriosus
Between pulmonary artery & aorta
Diverts blood from lungs to aorta
Changes After Birth:
At birth, when the baby takes the first breath:
Change
Effect
Lungs expand
↓ Pulmonary resistance, ↑ blood flow to lungs
Umbilical cord clamped
Stops placental blood flow
Ductus venosus closes
Becomes ligamentum venosum
Foramen ovale closes
Becomes fossa ovalis
Ductus arteriosus closes
Becomes ligamentum arteriosum
Umbilical vein and arteries close
Become ligaments in abdomen
Clinical Importance in Nursing & Midwifery:
Relevance
Explanation
Congenital heart defects
May involve persistent fetal shunts (e.g., PDA)
Patent Ductus Arteriosus (PDA)
Common in premature babies, causes abnormal circulation
Antenatal ultrasounds
Check fetal heart structures and flow
Newborn assessment
Heart murmurs or cyanosis may indicate shunt closure failure
Summary Table:
Vessel/Shunt
Function
Postnatal Remnant
Umbilical vein
Oxygenated blood to fetus
Ligamentum teres
Ductus venosus
Bypasses liver
Ligamentum venosum
Foramen ovale
Bypasses lungs
Fossa ovalis
Ductus arteriosus
Bypasses lungs
Ligamentum arteriosum
Umbilical arteries
Return deoxygenated blood
Medial umbilical ligaments
FETAL NUTRITION
(How the fetus receives nourishment during pregnancy)
Definition:
Fetal nutrition is the process by which the developing fetus receives nutrients (such as glucose, amino acids, fatty acids, vitamins, and minerals) from the maternal blood through the placenta to support its growth, development, and survival.