Professional Documents
Culture Documents
LECTURE
( Arellano University)
24
3.Estrogen
- stimulates development of uterine and
breast tissues in the mother
- increases vascularity and vasodilation in
the villous capillaries
25
4. Progesterone
- after 11 weeks of pregnancy, placenta takes over
the production of progesterone from the corpus
luteum
26
- THE BLASTOCELE OR EMBRYONIC DISC GIVES
RISE TO THE THREE PRIMARY GERM LAYERS:
ECTODERM, MESODERM, ENDODERM.
PRIMARY GERM LAYERS
TISSUE LAYER BODY PORTIONS FORMED
ECTODERM NERVOUS SYSTEM, SKIN, HAIR
( OUTER LAYER) NAILS, SENSE ORGANS, MUCUS
MEMBRANES OF NOSE & MOUTH
NO MAJOR CONSEQUENCE IN UTERO, BUT COULD LEAD TO A GREATER CHANCE FOR CORD
TRAUMA
* 4. Battledore insertion
The cord is inserted
marginally rather than
centrally
The cord is inserted at
the edge of the placenta
Cord Abnormalities
Knots of the Cord – fetal movements may
cause knots in the cord which could lead to
perinatal loss. Its incidence is high in
monoamniotic twinning. Normal false knots
results from kinking to accommodate cord
length.
Loops of the Cord- the cord may coil around
the fetal body and neck. When cord coil is in
the neck, it is called nuchal cord.
Umbilical knot
PLACENTA
54
2 sides of placenta:
55
FUNCTIONS OF THE PLACENTA
Umbilical cord
length:55 cm at term
1 vein (carries oxygenated blood to the fetus)
2 arteries (carry deoxygenated blood from fetus to
placenta)
Wharton’s jelly, gelatinous substance
Cord extends from the fetal surface of the placenta to the
fetal umbilicus
Placenta succenturiata
Placenta has 1 or
more accessory
lobes connected to
the main placenta
by blood vessels
Placenta circumvallata
Ordinarily, chorion
membrane begins at the
edge of the placenta; no
chorion covers the fetal
side of the placenta
This kind- the fetal side
of the placenta is covered
with chorion
Abnormal Placental
Implantation
Placenta Acreta – invasion of the placenta
deep into the endometrium
Placeta increta- invasion of the placenta into
the myometrium
Placenta percreta – penetration of the
placenta through the myometrium to the serosa
Vasa previa – placental vessels crossing the
cervical os
The Growing Fetus
STAGES OF FETAL GROWTH AND
DEVELOPMENT
32 WEEKS
SUBCUTANEOUS FAT BEGINS TO BE
DEPOSITED ( THE FORMER “ STRINGY” OLD MAN
APPEARANCE IS LOST); FETUS IS AWARE OF SOUNDS
32 weeks
OUTSIDE THE MOTHERS BODY; ACTIVE MORO
REFLEX PRESENT, BIRTH POSITION( VERTEX OR
BREECH) MAY BE ASSUMED; IRON STORES
THAT PROVIDE IRON FOR THE TIME THAT THE
NEONATE WILL INGEST ONLY MILK AFTER BIRTH ARE
BEGINNING TO BE DEVELOPED; FINGERNAILS GROW
TO REACH END OF FINGERTIPS.
36 WEEKS ADDITIONAL AMOUNTS OF SUBCATANEOUS
FATS ARE DEPOSITED; SOLE OF THE FOOT HAS
ONLY ONE OR TWO CRISSCROSS CREASES;
LANUGO BEGINS TO DIMINISH; MOST BABIES TURN
INTO A VERTEX OR HEAD-DOWN PRESENTATION
DURING THIS MONTH
121
Laboratory screening
Initially and at routine visits, urine dipstick for
glucose, protein (pregnancy induced hypertension
and UTI), CBC, rubella IgG antibody
Maternal serum alpha-fetoprotein (AFP) at 16-18 wk
to identify risk of neural tube defect in fetus
Glucose screening between 24-28 wk to detect
gestational diabetes
Repeat CBC at 24 –28 wk
Rh antibody titers for Rh(-) woman at 24, 28, 32, and
40 wks
ultrasound
122
Laboratory Tests
Urinalysis
1.Collect urinary specimen by midstream or clean catch
technique
2. Benedict’s test to detect glycosuria
3. Heat & acetic acid to detect proteinuria
4. Urinalysis in the first trimester is also performed to
detect asymptomatic bacteuria. Bacteuria can lead to
abortion early in pregnancy & can cause premature
labor late in pregnancy.
Blood Tests
Hematocrit & Hemoglobin – count at initial
clinic visit & repeated at 28-32 weeks to detect
anemia.
Normal Hemoglobin level is between 12-16 mg/dl
Normal Hematocrit count is between 37-47%
VDRL and Kahn & Wassaerman test to detect
Syphilis
Gonorrhea Culture
Rubella Antibody Titer – to detect degree of
protection against german measles. A test result of 1:8
or less indicates that the mother is at risk of acquiring
the infection during pregnancy. A titer more than 1:8
means that the mother has immunity against german
measles
Assessment of Fetal Growth
Assessing fetal well-being
Fetal movement
Maternal serum alpha-
fetoprotein
Fetal heart rate
Triple screening (AFP,
Ultrasound estriol and hCG)
Nonstress Test Chorionic villi sampling
Amniocentesis
Percutaneous umbilical
blood sampling
Biophysical profile
126
Fetal movement
Fetal movement that can be felt by the mother :
QUICKENING begins at approximately 18 – 20
weeks of pregnancy; peaks at 28-38 weeks
Primigravid- quickening:20 weeks ( 5 months)
Multigravid- 16 weeks ( 4 months)
Ask the mother to observe fetal movement.
A healthy fetus moves at least 10x a day.
127
Fetal heart rate
FHR should be 120-160
beats per minute
128
LOCATING FETAL HEART SOUNDS BY FETAL POSITION
FHT – heard best at the FETAL BACK
Ultrasound
Response of sound waves
against objects
Allows visualization of the
uterine content
Transabdominal UTZ
- full bladder
- client lies on her back
Transvaginal UTZ
134
An external ultrasound transducer and the
tocodynamometer are applied to the mother and
a tracing of at least 20 minutes’ duration is
obtained so that the FHR and the uterine activity
can be observed.
Obtain baseline blood pressure and monitor
blood pressure frequently.
Position mother in semi-fowler’s or side- lying
position or left lateral position to avoid vena cava
compression.
The mother may be asked to press a button every
time she feels fetal movement; the monitor
records a mark at each point of fetal movement,
which is used as a reference point to assess FHR
response. 135
RESULTS OF NST:
REACTIVE NONSTRESS TEST:Normal/Negative
136
Contraction Stress Test (CST)or
Oxytocin Challenge Test ( OCT)
Assesses placental oxygenation and function
Determines fetal ability to tolerate labor and
determines fetal well-being
Fetus is exposed to the stressor of
contractions to assess the adequacy of
placental perfusion under simulated labor
conditions.
137
External fetal monitor is applied to the
mother, and a 20 to 30 minute baseline
strip is recorded.
The uterus is stimulated to contract by
the administration of a dilute dose of
oxytocin or by having the mother use
nipple stimulation until 3 palpable
contractions with a duration of 40
seconds or more in a 10 minute period
have been achieved.
Frequent maternal BP readings are done,
and the mother is monitored closely while
increasing doses of oxytocin are given.
138
RESULTS OF CST:
NEGATIVE CST/ NORMAL
- no late or variable decelerations of FHR
139
Fetal Heart Rate Patterns Indicative of… Intervention
Tachycardia (>160 bpm) Maternal or fetal infection Depends on the cause
Fetal hypoxia (ominous sign)
Bradycardia (<120 bpm) Fetal hypoxia or stress Place client on her left side
Maternal hypotension after epidural Increase fluids to counteract
initiation hypotension
Stop oxytocin (Pitocin) if in use
144
Chorionic villus sampling (CVS)
146
Percutaneous umbilical blood sampling
(PUBS)Cordocentesis/Funicentesis
147
Lecithin/ Sphingomyelin ratio (2:1)
148
Biophysical profile (BPS)
Assesses 4 to 6 parameters (fetal breathing
movement, fetal body movement, fetal tone, amniotic
fluid volume, placental grading, and fetal heart
reactivity/ reactive NST)
Each item has a potential for scoring a 2; 12 highest
possible score
BPS 8 – 10: fetus is doing well
BPS 6: fetus is in jeopardy; worrisome
BPS 4 or less is Ominous. The doctor may decide to
deliver the baby if the score is 6 or below
149
Criteria in BPS:
1. Fetal Breathing Movements ( FBM)
Normal: At least one episode of FBM of at least 30
sec duration in 30 mins of observation
Abnormal: Absent FBM o no episode of more than
30 sec in 30 mins
2. Gross Body Movement
Normal: at least 3 discrete body/limb movements in
30 mins w/ episodes of activity
Abnormal: 2 or fewer episodes of body/limb
movements in 30 mins
3. Fetal Tone
Normal: the fetus must extend and then flex the
extremities or spine at least once in 30 minutes
4. Amniotic fluid volume
Normal: a pocket of amniotic fluid
measuring more than 1 cm in vertical
diameter must be present
5. Placental grade
Normal: grade 3 ( grading is based on structure
and amount of calcium present)
Placental Grading
Determines the amount of calcium deposits on
the base of the placenta
0 = 12 to 24 weeks
1 = 30 to 32 weeks
2 = 36 weeks
3 = 38 weeks ( mature)
Amniotic Fluid Volume Assessment
Maternal Serum
Alphafetoprotein
Involves drawing a small amount of BLOOD from
the mother to check for the level of
alphafetoprotein
AFP is produced by the fetal liver & is excreted
thru placenta into the mother’s blood ( usually
tested at 15 & 17 wks)
High amount: Neural Tube defect ( NTD) such as
spina bifida (open spine)or anencephaly ( absence
of brain)
Low amount: Indicative of Trisomy 21
Best results are obtained if taken between 16-18
wks
TESTS DONE:
Between 16-18 weeks
Maternal serum Alphafetoprotein
Between 26-28 weeks
Diabetic screening for all pregnant women
Repeat Hgb & Hct
Repeat Antibody for unsensitized Rh negative women
Between 32-36 weeks
Ultrasound
Testing for STD
BASELINE VITAL SIGNS = TEMPERATURE, PULSE
AND RESPIRATORY RATES ARE IMPORTANT
ESPECIALLY DURING THE INITIAL PHASE OF THE
PRENATAL VISIT . BUT CERTAINLY MORE
IMPORTANT ARE THE WEIGHT & BLOOD
PRESSURE AS BASELINE DATA TO DETERMINE
ANY SIGNIFICANT INCREASE.
WEIGHT
*DURING THE FIRST TRIMESTER, WEIGHT GAIN
OF 1.5-3LBS.( 1lb per month)
*ON THE 2ND AND 3RD TRIMESTERS, WEIGHT GAIN
OF 10-11 POUNDS PER TRIMESTER IS
RECOMMENDED.( 1 lb per week)
*TOTAL ALLOWABLE WEIGHT GAIN DURING THE
ENTIRE PERIOD OF PREGNANCY IS 20-25 LBS.
( 10-12 KGS.). MORE THAN 30 LBS OF WEIGHT
GAIN IS A DANGER SIGN = POSSIBLE
PREECLAMPSIA.
DISTRIBUTION OF WEIGHT GAIN DURING
PREGNANCY:
FETUS 7 LBS
PLACENTA 1 LB
AMNIOTIC FLUID 11/2 LBS
INCREASED WT. OF UTERUS 2 LBS
INCREASED BLOOD VOLUME 1 LB
INCREASED WT. OF THE BREASTS11/2-3 LBS
WT. OF ADDITIONAL FLUID 2 LBS
FAT & FLUID ACCUMULATION 4-6 LBS.
TOTAL 25 LBS
3.POST – CONSULTATION PHASE = HEALTH
TEACHINGS
Schedule of clinic visits
Exercises
Dental hygiene
Clothing
Traveling
Bathing
Employment
Sexual relation
Immunization
A.PRENATAL CARE:
SCHEDULE OF PRENATAL VISIT:
A. ONCE EVERY 4 WEEKS , UP TO 32 WEEKS
B. EVERY 2 WEEKS FROM 32 – 37 WEEKS
( MORE FREQUENTLY IF PROBLEM
EXISTS)
C. EVERY WEEK FROM 37 – 40 WEEKS
*** To monitor VS, Weight, FHT, Fundal height and
Outline
BATHING:
FOOD SOURCES:
** PROTEIN RICH FOODS = MEAT, FISH, EGGS,
MILK, POULTRY, CHEESE, BEANS, MONGO
** VIT. A = EGGS, CARROTS, SQUASH, CHEESE,
BEANS, VEGETABLES
** VIT. D = FISH, LIVER, EGGS, MILK ( EXCESS
VIT.D DURING PREGNANCY CAN LEAD TO FETAL
CARDIAC PROBLEMS)
**VITAMIN E = GREEN LEAFY VEGETABLES, FISH
**VITAMIN C= TOMATOES, GUAVA, PAPAYA
**VITAMIN B= PROTEIN RICH FOODS
**CALCIUM/PHOSPHORUS=MILK, CHEESE
**IRON= ESPECIALLY IMPORTANT DURING THE
LAST TRIMESTER WHEN THE PREGNANT WOMAN
IS GOING TO TRANSFER HER IRON STORES FROM
HERSELF TO HER FETUS SO THAT THE BABY HAS
ENOUGH IRON STORES DURING THE 1ST 3
MONTHS OF LIFE WHEN ALL HE TAKES IS
MILK(WHICH IS DEFICIENT IN IRON). IRON HAS A
VERY LOW ABSORPTION RATE: ONLY 10% OF THE
IRON INTAKE CAN BE ABSORBED BY THE BODY.
THUS, FOR OPTIMUM ABSORPTION, GIVE VITAMIN
C.
IRON SHOULD BE GIVEN AFTER MEALS BECAUSE
IT IS IRRITATING TO THE GASTRIC MUCOSA.
January 31 days
February 28 Total = 243 days
March 31 AOG = 243
April 30 7
May 31 34 to 35 weeks
June 30
July 31
August 31
2. MC DONALD’S RULE = ( ESTIMATION OF
AOG IN MONTHS & WEEKS BY FUNDIC HEIGHT
MEASUREMENT)=
FORMULA :
FUNDIC HEIGHT IN CMS X 2/7 OR 8/7
EXAMPLE:
FUNDIC HEIGHT IS 21 CMS
21 CMS X 2 =42
42/ 7 = 6 ( AOG IN MONTHS)
6 MONTHS X 4 = 24 ( AOG IN WEEKS)
Fundic Height
McDonald’s Rule – determines during midpregnancy,
that the fetus is growing in utero by measuring the
fundal (uterine) height
CA – herpes virus
Droplet transmission from person to person
Effects on the infant includes:
Neurological challenge ( hydrocephalus,
microcephalus, spasticity, ) with eye damage
( optic atrophy, deafness, liver disease
No tx
Herpes Simplex Virus
( Genital Herpes Infection)
Systemic involvement ( Viremia) and crosses
the placenta to the fetus.
1st tri- severe congenital anomalies or
spontaneous miscarriage
2nd tri & 3rd tri- premature birth, IUG
retardation and continuing infection of the
newborn at birth
Tx; IV or oral Acyclovir (Zovirax) during
pregnancy
Terminologies
High risk pregnancy – is one in which a
concurrent disorder, pregnancy related
complication, or external factor jeopardizes the
health of the mother, the fetus or both.
Isoimmunization – the production of
antibodies against Rh(+) blood by the
immunologic system
Tocolytic – a drug that halts labor ( stops
uterine contractions by relaxing smooth
muscles)
Risk Factors Associated with
Pregnancy
Parity
First pregnancy – is the period of highest risk
Second / Third and Fourth pregnancy – the risk of
death for the mother is at its lowest
Fifth pregnancy – marked increase especially when
the pregnant mother is over 40 years of age.
COMPLICATIONS OF PREGNANCY
A.FIRST TRIMESTER BLEEDING:
1. ABORTION
- THE EXPULSION OF THE
PRODUCTS OF CONCEPTION BEFORE
THE AGE OF VIABILITY ( FETUS CAN
SURVIVE EXTRAUTERINE LIFE)
- FETUS IS LESS THAN 20 WEEKS ( 24
weeks in the US) OR LESS THAN 500
GRAMS
CAUSES OF ABORTION:
1. ABNORMALITY IN THE GERM PLASMA
2.ABNORMALITY IN THE IMPLANTATION PROCESS
3. TRAUMA – PSYCHOLOGICAL,
PHYSICAL
4. HORMONAL IMBALANCE ( LOW
PROGESTERONE)
5. INTAKE OF DRUGS – QUININE, ASPIRIN
6. INFECTIOUS DISEASES – GERMAN
MEASLES, PTB, HERPES
7. PRESENCE OF VENEREAL DISEASES
8. ABNORMALITY IN THE REPRODUCTIVE
SYSTEM
8. SEVERE MALNUTRITION
EARLY ABORTION – HAPPENS BEFORE 16 WEEKS
LATE ABORTION – HAPPENS BETWEEN 16 – 20 WEEKS
Types of Abortion:
• SPONTANEOUS = UNINTENDED
TERMINATION OF PREGNANCY AT ANY
TIME BEFORE THE FETUS HAS
ATTAINED VIABILITY.
THREATENED – POSSIBLE LOSS OF THE
PRODUCTS OF CONCEPTION
S/SX: SLIGHT BLEEDING; MILD UTERINE
CRAMPING BUT NO CERVICAL
DILATATION ON VAGINAL
EXAMINATION;NO PASSAGE OF TISSUE
INEVITABLE OR IMMINENT
ABORTION - is a loss of pregnancy
that cannot be prevented.
Clinical Manifestations:
Moderate to profuse Bleeding
Moderate to severe uterine cramping
Cervix dilated
Membranes rupture
TYPES OF INEVITABLE ABORTION:
Open cervix
Passage of tissue
S/Sx:
- Foul smelling vaginal dischrage
- Uterine cramping
- Fever
Management:
- Treat abortion
- Antibiotics
HABITUAL OR RECURRENT PREGNANCY
LOSS –SPONTANEOUS ABORTION IN
THREE OR MORE SUCCESSIVE
PREGNANCIES USUALLY DUE TO
INCOMPETENT CERVIX.
B. Induced Abortion – is an intentional loss of
pregnancy through direct stimulation either
by chemical or mechanical means.
Types of induced abortion:
1) Therapeutic abortion – to preserve the life
of the mother
2) Elective abortion
2. ECTOPIC PREGNANCY
- ANY PREGNANCY THAT OCCURS
OUTSIDE THE UTERINE CAVITY.
---SECOND LEADING CAUSE OF
BLEEDING IN EARLY PREGNANCY.
TYPES:
1.AMPULAR 4. CERVICAL
2. INTESTINAL 5. ABDOMINAL
3. OVARIAN
Predisposing causes:
Salpingitis or PID
Previous ectopic pregnancy
Tumors that distort the tubes
Previous mole
Uterine tumor
Scarring from previous previous CS
Decreased vascularity of upper uterine
segment
Past uterine D&C
Signs and Sxs:
Painless, bright red vaginal bleeding
during the 3rd trimester
Abdomen soft, non tender
Ultrasound reveals placenta previa
NURSING MANAGEMENT:
1. MONITOR VITAL SIGNS & BLEEDING
( WEIGH UNUSED PERINEAL PAD, THEN
WEIGH PERINEAL PAD SOAKED IN
BLOOD, THEN SUBTRACT. THE
DIFFERENCE IS THE WEIGHT OF THE
BLOOD LOSS.)
2.PROVIDE STRICT BED REST TO MINIMIZE THE
RISK TO FETUS.( CBR without BRP’s )
3.OBSERVE FOR FURTHER BLEEDING
EPISODES.( PREPARE FOR BT) ( Hgb & Hct)
4. AVOID VAGINAL EXAMINATIONS ( NO IE). IF
IE IS INDICATED, IT SHOULD BE DONE IN A
DOUBLE SET-UP ENVIRONMENT. ( MEANING:
the DR is prepared for vaginal exam and for
cesarean birth in case the examination
precipitates profuse bleeding) WHEREIN THE
PATIENT HAS ALREADY SIGNED A CONSENT
FORM, PRE-OP
MEDS HAVE BEEN GIVEN, ABDOMINAL
PREP HAS BEEN DONE SO THAT IF THE
PLACENTA IS ACCIDENTALLY DETACHED
BECAUSE OF MANIPULATIONS, CS CAN
BE DONE IMMEDIATELY.
5. ASSESS FETAL LUNG MATURITY
6. OBSRVE STRICT ASEPTIC TECHNIQUE
7. OBSERVE PP HEMORRHAGE
8. PROVIDE EMOTIONAL SUPPORT
DURING THE GRIEVING PROCESS.
**** CLASSICAL CESARIAN SECTION
(UTERUS IS INCISED IN THE VERTICAL
SEGMENT) IS DONE IN CASE OF SEVERE
BLEEDING.**
MEDICATIONS:
>IRON SUPPLEMENTATION TO PREVENT ANEMIA
>DIGITALIS TO STRENGTHEN MYOCARDIAL
CONTRACTION AND SLOW DOWN HEART RATE
>NITROGLYCERINE TO RELIEVE CHEST PAIN
>ANTIBIOTICS TO PREVENT AND TREAT
INFECTION
>DIURETICS MAY BE PRESCRIBED IN CASE OF
HEART FAILURE
INTRAPARTAL CARE
1.EARLY HOSPITALIZATION- WOMAN IS HOSPITALIZED
BEFORE LABOR BEGINS TO PROMOTE REST, FOR
CLOSER SUPERVISION AND PREVENT INFECTION
2.WOMAN LABOR’S IN SEMI-FOWLER’S POSITION OR
LEFT LATERAL RECUMBENT POSITION. NO LITHOMY
POSITION.
3.VITAL SIGNS- VITAL SIGNS ARE MONITORED
CONTINUOUSLY. TACHYCARDIA AND RESPIRATORY
RATE MORE THAN 24 ARE SIGNS OF IMPENDING
CARDIAC DECOMPENSATION. DURING THE FIRST
STAGE, MONITOR VITAL SIGNS EVERY 15 MINUTES
AND MORE FREQUENTLY DURING THE SECOND STAGE
4.EPIDURAL ANESTHESIA- IS INSTITUTED FOR
PAINLESS AND PUSHLESS DELIVERY. FORCEPS IS
USED TO SHORTEN THE SECOND STAGE. PUSHING IS
CONTRAINDICATED
5. WOMEN WITH HEART DISEASE ARE POOR
CANDIDATE FOR CS DUE TO INCREASED RISK FOR
HEMORRHAGE, *INFECTION AND
THROMBOEMBOLISM
POSTPARTUM CARE
1. THE MOST DANGEROUS PERIOD IS THE IMMEDIATE
POSTPARTUM BECAUSE OF THE SUDDEN INCREASE
IN CIRCULATORY BLOOD VOLUME.
2. MONITOR VITAL SIGNS.
3. PROMOTE REST- RESTRICT VISITORS TO ALLOW
PATIENT TO REST, THE WOMAN STAYS IN THE
HOSPITAL LONGER, UNTIL CARDIAC STATUS HAS
STABILIZED.
4. EARLY BUT GRADUAL AMBULATION TO PREVENT
THROMBOPHLEBITIS.
5. MEDICATIONS
*ANTIBIOTICS
*STOOL SOFTENERS TO PREVENT STRAINING AT
STOOL CAUSED BY CONSTIPATION. SEDATIVES MAY BE
ORDERED TO PROMOTE REST.
6. BREASTFEEDING IS ALLOWED IF THERE ARE NO
SIGNS OF CARDIAC DECOMPENSATION DURING
PREGNANCY, LABOR AND PUEPERIUM.
Hemolytic Disease:
ISOIMMUNIZATION / RH INCOMPATIBILITY
- OCCURS WHEN AN RH-NEGATIVE MOTHER IS
CARRYING AN RH-POSITIVE FETUS.
- FOR SUCH A SITUATION TO OCCUR, THE
FATHER OF THE CHILD MUST EITHER BE A
HOMOZYGOUS ( DD) OR HETEROZYGOUS ( Dd) RH
POSITIVE.
- IF THE FATHER OF THE CHILD IS
HOMOZYGOUS (DD), 100% OF THE COUPLE’S
CHILDREN WILL BE RH (+).
-PEOPLE WHO HAVE RH (+) BLOOD HAVE A
PROTEIN FACTOR ( D ANTIGEN) THAT RH (-)
PEOPLE DO NOT.
- WHEN AN RH(+) FETUS BEGINS TO GROW
INSIDE AN RH (-) MOTHER, IT IS THOUGH HER
BODY IS BEING INVADED BY FOREIGN AGENT, OR
ANTIGEN.
- THEORETICALLY, THERE IS NO CONNECTION
BETWEEN FETAL BLOOD & MATERNAL BLOOD
DURING PREGNANCY BUT
BUT SOMETIMES ACCIDENTAL BREAKS IN THE
PLACENTAL VILLI RESULTS IN FETAL BLOOD
ENTERING THE MATERNAL BLOODSTREAM. (ex:
AMNIOCENTESIS , PUBS, ABORTION).
- ONLY A FEW ANTIBODIES ARE FORMED THIS
WAY SO THAT IT DOES NOT AFFECT THE FIRST
INFANT.
- DURING PLACENTAL SEPARATION AND
DELIVERY, A GREAT AMOUNT OF MATERNAL &
FETAL BLOOD ARE MIXED, CAUSING THE MOTHER
TO PRODUCE LARGE AMOUNTS OF ANTIBODIES
DURING THE FIRST 72 HOURS AFTER PLACENTAL
DELIVERY.
- IF THE FETUS IN SUBSEQUENT PREGNANCIES
IS RH (+), THE ANTIBODIES ALREADY PRESENT IN
THE BLOODSTREAM WILL CROSS THE PLACENTA,
ATTACK & DESTROY THE FETAL RED BLOOD CELLS
( HEMOLYSIS). THE FETUS BECOMES SO
DEFICIENT IN RBC’S THAT SUFFICIENT O2
TRANSPORT TO BODY CELLS CANNOT BE
MAINTAINED. THIS CONDITION IS TERMED “
HEMOLYTIC DISEASE OF THE NEWBORN” OR
ERYTHROBLASTOSIS FETALIS.
DX:
1. INDIRECT COOMB’S TEST – TEST TO CHECK
FOR THE PRESENCE OF ANTIBODIES IN
MATERNAL SERUM.
2. DIRECT COOMB’S TEST –TEST TO CHECK THE
PRESENCE OF ANTIBODIES IN FETAL CORD
BLOOD.
Prevention:
Administration of Rh ( anti D) globulin (Rhogam)
at 28 weeks gestation and within the first 72 hours
after delivery to a woman who:
Have delivered Rh positive fetus
Have had untypeable pregnancies such as ectopic
pregnancies, stillbirth & abortion
Have received ABO compatible Rh positive blood
Have had invasive diagnostic procedure such as
amniocentesis, PUBS ( cordocentesis)
ABO INCOMPATIBILITY
The problem occurs when the maternal blood enters fetal
circulation.
Most common: mother is Type O and the fetus is either
Type A, B, or AB
The mother’s plasma naturally contains anti-A and anti B
antibodies
With weaker hemolytic effect than Rh antibodies and
only affect mature RBC’s
Number of antibodies is limited to the amount of
maternal blood that entered circulation
May affect fetus of the 1st pregnancy
Affected newborn will become jaundiced in the first 3
days of life
Possible combinations for
ABO INCOMPATIBILITY
MOTHER FETUS
A B
B A
O A, B, AB
MX of HEMOLYTIC DISEASE:
1. SUSPENSION OF BREASTFEEDING DURING THE
FIRST 24 HOURS TO PREVENT PREGNANEDIOL
(BREAKDOWN PRODUCT OF PROGESTERONE
EXCRETED IN BREASTMILK) FROM INTERFERING
WITH THE CONJUGATION OF INDIRECT
BILIRUBIN TO DIRECT BILIRUBIN.
2. PHOTOTHERAPY – DESTRUCTION OF RBC’S
RESULTS IN THE FORMATION OF INDIRECT
BILIRUBIN. INDIRECT BILIRUBIN MUST FIRST BE
CONVERTED TO DIRECT BILIRUBIN BY THE LIVER
CELLS BEFORE IT CAN BE EXCRETED IN THE
BODY. THE LIVER IS IMMATURE AT BIRTH SO IT
CANNOT CONVERT LARGE AMOUNTS OF
BILIRUBIN FORMED DURING HEMOLYSIS OF RBC.
a. USES BILI OR FLUORESCENT LIGHTS
POSITIONED 18 – 20 INCHES ( 12-30) ABOVE
THE INFANT.
NURSING CARE DURING PHOTOTHERAPY:
1. COVER EYES WITH DRESSING
2. COVER GENITALS TO PREVENT PRIAPISM.
3. EXPECT THE STOOL TO BE LOOSE & BRIGHT
GREEN FROM EXCESSIVE BILIRUBIN EXCRETION
& THE SKIN TO BE DARK BROWN ( BRONZE
BABY SYNDROME).
4. PROVIDE GOOD SKIN CARE BECAUSE STOOL
CAN BE IRRITATING TO THE SKIN.
5. EXPECT THE URINE TO BE DARK COLORED
BECAUSE OF UROBILINOGEN FORMATION.
6. ASSESS FOR DEHYDRATION ( I & O ; SKIN
TURGOR). FLUID LOSS THROUGH INSENSIBLE
WATER LOSS MAY OCCUR BECAUSE OF THE HEAT
FROM THE FLUORESCENT LIGHT ABOVE THE
INFANT.
7. OFFER GLUCOSE WATER EVERY 3 HOURS TO
PREVENT DEHYDRATION.
8. MAINTAIN BODY TEMP BETWEEN 36C & 37C.
EXCHANGE TRANSFUSION:
1. INTRAUTERINE TRANSFUSION:
- DONE BY INJECTING RBC’S DIRECTLY INTO A
VESSEL IN THE FETAL CORD OR DEPOSITING
THEM IN THE FETAL ABDOMEN USING
AMNIOCENTESIS TECHNIQUE.
- BLOOD USED FOR TRANSFUSION IS EITHER
THE FETUS’ OWN TYPE OR GROUP O NEGATVE
IF THE FETAL BLOOD TYPE IS UNKNOWN.
-FROM 75 TO 150 ML OF WASHED RBC’S WILL
BE USED, DEPENDING ON THE AGE OF THE
FETUS.
NOTE:
ADMINISTER RhoGAM TO ALL Rh (-) MOTHERS
DURING PREGNANCY ( AT 28 WEEKS GESTATION)
AND WITHIN 72 HOURS OF DELIVERY OR
ABORTION OF AN Rh (+) FETUS **
- AFTER BIRTH, THE INFANT MAY REQUIRE AN
EXCHANGE TRANSFUSION TO REMOVE
HEMOLYZED BLOOD CELLS & REPLACE THEM
WITH HEALTHY ONES.
Notify your healthcare provider if your baby has
any of the following s/s after returning home:
> Fever
> Jaundice
> Poor appetite or poor weight gain
> Excessive crying that does not stop when the
baby is held.
Signs in the newborn:
Paleness
Jaundice that begins within 24 hours after
delivery ( pathologic jaundice)
Unexplained bruising or blood spots under the
skin
Tissue swelling ( edema)
Seizures
Lack of normal movement
Poor reflex response
Gestational Diabetes Mellitus
-is a hereditary endocrine disorder due to
inadequate or lack of insulin production that
results in impaired glucose absorption &
metabolism.
- all women appear to develop an insulin
resistance as pregnancy progresses ( insulin does
not seem normally effective during pregnancy) a
phenomenon that is probably caused by the
presence of the hormone Human Placental
Lactogen (HPL)
SSx:
1. Hyperglycemia – pancreas does not produce
enough insulin , thus glucose is unable to enter
the cells & accumulates in the bloodstream
resulting in hyperglycemia
2. Glycosuria –when blood glucose levels goes
beyond the renal threshold for sugar, glucose spills on
the urine.
3. Polyuria – glucose attracts water so that when it is
excreted in the kidney, it brings along with it large
amounts of water resulting in the woman excreting
large amounts of urine, a condition called, POLYURIA.
4. Polydipsia – the excretion of large amounts of fluid
from the body leads to dehydration. Excessive thirst or
polydipsia is an important symptom of dehydration.
Effects of Diabetes:
Mother:
1. Increased tendency to pre-eclampsia &
eclampsia, UTI, & candidiasis
2. Increased risk for postpartum hemorrhage d/t
overdistention of the uterus.
3. Maternal mortality
4. Preterm delivery
Infant:
1. Macrosomia
2. Hydramnios
3. Prematurity
4. Hypoglycemia ( lowered serum glucose levels)
5. Predisposition to diabetes mellitus later in life as
the disease is hereditary
Complications:
1. Macrosomia – Infants of women with poorly
controlled diabetes tend to be large ( more than
10 lbs) because glucose can cross the placental
barrier, it acts acts as a growth stimulant. The
increased glucose adds subcutaneous fat
deposits. All the nutrients that the fetus receives
comes directly from the mother’s blood.
2. Birth Injury – may occur due to the baby’s large
size and difficulty being born.( may cause CPD
which may necessitate being born by CS)
3. HYPOGLYCEMIA – refers to low blood sugar in
the baby immediately after delivery. This
problem occurs if the mother’s blood sugar
levels have been consistently high, causing the
fetus to have a high level of insulin in its
circulation. After delivery, the baby continues to
have a high insulin level, but no longer has the
high level of sugar from its mother, resulting in
the newborn’s blood sugar level becoming very
low. The baby’s blood sugar level is checked
after birth, and if the level is too low, it may be
necessary to give the baby glucose
intravenously
4. Respiratory distress (difficulty breathing) –
too much insulin or too much glucose in a
baby’s system may delay lung maturation
and cause respiratory difficulties in babies.
This is more likely if they are born before
37 weeks of pregnancy.
Prenatal Management:
1. Diagnosis; Suspect DM in a woman
a. With family history of DM
b. With history of unexplained repeated
abortions and stillbirth
c. With glycosuria
d. Who are obese
e. Who have history of giving birth to large
infants, over 10 lbs. and infants with
congenital anomaly
2. Screening tests
a. Universal screening- 50 gram oral glucose
tolerance test ( OGTT) between 24-28
weeks gestation irregardless of the time of
the day and meals taken for all pregnant
women. If the plasma value is more than
140 mg/dl after one hour, 100 gram three
hour oral glucose tolerance test is performed
to confirm if the woman is having
hypergycemia.
Criteria of 100 gram Oral Glucose Tolerance Test-
(Instruct not to eat after midnight)
Time of Test Venous Level Plasma Level
Fasting 90mg/dl 105mg/dl
= ACTUAL DIAMETER
OF THE PELVIC INLET
THROUGH WHICH THE FETAL HEAD MUST PASS
b. MIDPELVIS/ PELVIC CAVITY/ PELVIC
CANAL = THE SPACE BETWEEN THE INLET &
THE OUTLET. THIS IS NOT A STRAIGHT LINE
BUT A CURVED PASSAGE.THE CURVATURE IS
SO DESIGNED BY NATURE TO CONTROL THE
SPEED OF DESCENT OF THE FETAL HEAD.
RAPID FETAL DESCENT CAN RESULT TO
RUPTURE OF CEREBRAL ARTERIES DUE TO
THE SUDDEN CHANGE OF PRESSURE.
Interspinous ( smallest diameter of the pelvis ) 10
cm
AP diameter at level of ischial spines = 11.5 cm
Posterior saggital diameter – 4.5 cm
3. PELVIC OUTLET = THE INFERIOR
PORTION OF THE PELVIS. THE MOST
IMPORTANT DIAMETER OF THE OUTLET
IS ITS TRANSVERSE OR BI-ISCHIAL
DIAMETER( DISTANCE BET THE TWO
ISCHIAL TUBEROSITIES) WHICH IS
ABOUT 11.5 CM
> AP DIAMETER 9.5 TO 11.5 CM
C. ISCHIAL TUBEROSITY DIAMETER
Distance between the ischial tuberosities or the
transverse diameter of the outlet ( the narrowest
diameter at that level) or the one apt to cause misfit.
A pelvimeter is generally used but a ruler can be
used or clenched fist measurement.
Adequate: 11 cm ( because it will allow the widest
diameter of the fetal head or 9 cm to pass freely.
Obstetric conjugate
Shortest anteroposterior diameter between the
sacral promontory and the symphysis pubis
Can only be measured radiographically
Normal > 10 cm
423
** CONTRACTED PELVIS – A PELVIS WITH A
MEASUREMENT OF LESS THAN 1.5 TO 2 CM IN ANY
OF ITS IMPORTANT DIAMETERS THUS MAKING
VAGINAL DELIVERY OF THE FETUS NOT POSSIBLE “
Nursing Responsibility:
Coach woman on breathing & relaxation
techniques. Abdominal breathing is recommended
during the latent phase & active phase
Breathing Techniques during Labor
.
Begin the Breathing Technique:
This technique is done only during contractions. Rest and
sleep between contractions is important. Instruct the
laboring woman to do the following:
Assume a comfortable position.
Try to maintain a relaxed state throughout the contraction.
Close her eyes or
Concentrate on a focal point while doing the breathing (e.g.,
a pretty picture, a button on someone's shirt).
Infection – Endometritis
Uterine tumors
SSx:
Enlarged & boggy uterus
Prolonged lochial discharge – persistent lochia rubra
Backache
Management:
Methergin to stimulate uterine contractions .2 mg
4x/day for 3 days
Antibiotics to prevent or treat infection
D & C if there are retained fragments
Instruct woman to report the following signs – fever,
vaginal bleeding, passage of tissue
Hematomas
This is due to injury to blood vessels during
delivery or during repair of episiotomy
resulting in blood escaping to the connective
tissue under the skin.
Causes:
1. Vulvar varicosities
2. Precipitate labor
3. Forceps delivery
4. Inadequate suturing of episiotomy or
lacerations
Signs and Symptoms:
Perineal pain
Swelling
Discoloration of skin over the swollen
area
Feeling of pressure over the vagina
Management: