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IDENTIFYING CLIENTS AT RISK • Some risk factors may later appear and are

 Assessment of risk factors detected at subsequent visits.


 Screening procedures • The cases are also reassessed near term and again
 Diagnostic tests and laboratory exams in labor for any new risk factors.

Introduction Risk approach (according to WHO)


 All pregnancies and deliveries are potentially at risk. • The main objective of the risk approach is the
However, there are certain categories of optimal use of existing resources for the benefit of
pregnancies where the mother, the fetus or the the majority. It attempts to ensure a minimum of
neonate is in a state of increased jeopardy. care for all while providing guidelines for the
 About 20 to 30 percent pregnancies belong to this diversion of limited resources to those who most
category. need them.
 Though all mothers and children are vulnerable to • Inherent in this approach is maximum utilization of
disease or disability, there are certain mothers and all resources, including some human resources,
infants who are at increased or special risk of that are not conventionally involved in such care
complications of pregnancy/labor or both. If we e.g.,- TBA, women’s group.
desire to improve obstetric results, this group must
be identified and given extra care. High Risk cases (according to WHO)
During Pregnancy
Definition • Elderly primigravida (≥30 years) & Elderly grand
• “A risk factor is defined as any ascertainable multiparas
characteristic or circumstance of a person (or group • Short statured primi (≤ 140 cm)
of such persons) known to be associated with an • Threatened abortion and APH
abnormal risk of developing or being adversely • Malpresentations & Malpositions
affected by a morbid process” -(WHO, 1973). • Pregnancy associated with medical diseases (like
• High risk pregnancy is defined as one which is PIH, metabolic disorders, and/or any systemic co-
complicated by factor or factors that adversely morbidities)
affects the pregnancy outcome –maternal or • Twins and hydramnios
perinatal or both. • Previous still birth, IUD, manual removal of
placenta
Assessment, Screening and Risk Approach • Prolonged pregnancy
• Assessment- is a process for defining the nature of • History of previous caesarean section and
that problem, determining a diagnosis, and instrumental delivery
developing specific treatment recommendations. During labor
• Screening- is a process of identifying apparently • PROM
healthy people who may be at increased risk of a • Prolonged labor
disease or condition. • Hand, feet or cord prolapse
-They can then be offered information, • Placenta retained more than half an hour
further tests and appropriate treatment to reduce their • PPH
risk and/or any complications arising from the disease • Puerperal fever and sepsis.
or condition. Course of the present pregnancy
• The cases should be reassessed at each antenatal
Screening of high risk cases- visit to detect any abnormality that might have
• The cases are assessed at the initial antenatal arisen later.
examination, preferably in the first trimester of • Few examples are- pre-eclampsia, anemias, Rh-
pregnancy. isoimmunization, high fever, pyelonephritis,
• This examination may be performed in a big hemorrhage, diabetes mellitus, large uterus, lack
institution (teaching or non-teaching) or in a public of uterine growth, post maturity, abnormal
health centers.
presentation, twins and history of exposure to • multiple pregnancy (maternal side)
drugs or radiation, acute surgical problems. • congenital malformation.
Complications of labor Diagnostic Tests
 Anemia, pre-eclampsia or eclampsia - premature - Are tests done to establish the presence (or absence)
labor of disease as a basis for treatment decisions in
 PROM - Abnormal FHR symptomatic or screen positive individuals
 Amnionitis – admitted with prolonged labor (confirmatory test).
 Abnormal presentation and position - Obstructed
labor Diagnostic Tests for High Risk Pregnancy
 Disproportion, floating head in labor - Rupture Non-invasive diagnostic tests
uterus  Fetal ultrasound or ultrasonic testing
 Multiple pregnancy – having induction or  Cardiotocography(CTG)
acceleration of labor  Non-stress test (NST)
Certain complications may arise during labour and  Contraction stress test (CST)
place the mother or baby at risk
• Intrapartum fetal distress Invasive diagnostic tests
• Difficult forceps or breech delivery  Chorionic villus sampling
• Prolonged interval from the diagnosis of fetal  Amniocentesis
distress to delivery.  Embryoscopy
• PPH or retained placenta  Fetoscopy
• Postpartum complications  Percutaneous umbilical cord blood sampling.
uneventful labour may suddenly turn into an abnormal
one in the form of Non-Invasive Diagnostic Tests
• PPH 1. Ultrasonography
• Retained placenta  -which measures the response of sound waves
• Shock against solid objects, is a much-used tool in modern
• Inversion obstetrics, although the recommendations for its
• Sepsis may develop later on use are being questioned because of unproven
SCREENING/ASSESSMENT benefits in the face of added expense (Neilson,
• Initial screening History 2009). It can be used to:
• Maternal age  Diagnose pregnancy as early as 6 weeks’ gestation
• Reproductive history  Confirm the presence, size, and location of the
• Pre-eclampsia, eclampsia placenta and amniotic fluid
• Anemia  Establish that a fetus is growing and has no gross
• Third stage abnormality anomalies, such as hydrocephalus, anencephaly, or
• Previous infant with Rh-isoimmunization or ABO spinal cord, heart, kidney, and bladder defects
incompatibility  Establish sex if a penis is revealed
• Medical or surgical disorders  Establish the presentation and position of the fetus
• Psychiatric illness  Predict maturity by measurement of the biparietal
• Cardiac disease diameter of the head
• Viral hepatitis  can also be used to discover complications of
• Previous operations pregnancy, such as the presence of an intrauterine
• Myomectomy device, hydramnios or oligohydramnios, ectopic
• Repair of complete perineal tear pregnancy, missed miscarriage, abdominal
• Repair of vesico-vaginal fistula pregnancy, placenta previa, premature separation
Family History of the placenta, coexisting uterine tumors, multiple
• Socio-economic status pregnancy, or genetic disorders such as Down
• Family history of diabetes syndrome.
• hypertension
 fetal anomalies such as neural tube disorders,  -uterine contractions (-toco-)
diaphragmatic hernia, or urethral stenosis also can  -during pregnancy, typically in the third
be diagnosed.  trimester. The machine used to perform
 fetal death can be revealed by a lack of heartbeat the monitoring is called a cardiotocograph, more
and respiratory movement. commonly known as an electronic fetal monitor (EFM).
 after birth, an ultrasound may be used to detect a
retained placenta or poor uterine involution in the FETAL HEART RATE AND UTERINE
new mother. CONTRACTION RECORDS
 intermittent sound waves of high frequency (above  monitors trace both the FHR and the duration and
the audible range) are projected toward the uterus interval of uterine contractions onto an
by a transducer placed on the abdomen or in the oscilloscope screen and produce a permanent
vagina record on paper rolls.
 sound frequencies that bounce back can be Fetal Heart Rate Patterns:
displayed on an oscilloscope screen as a visual  Baseline Fetal Heart Rate
image  Variability
 frequencies returning from tissues of various  Periodic Changes
thicknesses and properties present distinct Accelerations.
appearances Accelerations.
 a video or photograph can be made of the scan Late Decelerations.
 B-mode scanning- gray-scale imaging Prolonged Decelerations.
 Real-time mode- whole fetal imaging in real-time Variable Decelerations.
 Sinusoidal Fetal Heart Rate Pattern
1st- trimester fetal ultrasound is done to:

 Determine how pregnancy is progressing. Baseline Fetal Heart Rate- determined by analyzing the
 Find out if female is pregnant with more than 1 range of fetal heartbeats recorded on a 10-minute
fetus. tracing that was obtained between contractions.
 Estimate the age of the fetus (gestational age). o normal rate is 120 to 160 bpm
 Estimate the risk of a chromosome defect, such as o fluctuates slightly (5 to 15 bpm) when a fetus
Down syndrome. moves or sleeps
 Check for birth defects that affect the brain or o abnormal patterns in the baseline rate include
spinal cord. fetal bradycardia and fetal tachycardia
o - moderate bradycardia of 100 to 119bpm is not
2nd-trimester fetal ultrasound is done to:
considered serious and is probably
 Estimate the age of the fetus (gestational age).
because of a vagal response elicited by
 Look at the size and position of the fetus, placenta,
compression of the fetal head during labor
and amniotic fluid.
o marked bradycardia (less than 100 bpm) is a sign
 Determine the position of the fetus, umbilical cord,
of possible hypoxia and is potentially dangerous
and the placenta during a procedure, such as an
o moderate tachycardia is 161 to 180 bpm
amniocentesis, camera.gif or umbilical cord blood
o marked fetal tachycardia may be caused by fetal
sampling.
hypoxia, maternal fever, drugs, fetal arrhythmia,
 Detect major birth defects, such as a neural tube
or maternal anemia or hyperthyroidism
defect or heart problems.
Variability- the variation or differing rhythmicity in the
3rd-trimester fetal ultrasound is done to:
heart rate over time and is reflected on the FHR tracing
 Make sure that a fetus is alive and moving.
as a slight irregularity or “jitter” to the wave
 Look at the size and position of the fetus, placenta,
and amniotic fluid. Periodic Changes

CARDIOTOCOGRAPHY(CTG) Accelerations-Nonperiodic accelerations are temporary


 -recording (-graphy), normal increases in FHR caused by fetal movement
 -fetal heartbeat (cardio-)
change in maternal position, or administration of an CHORIONIC VILLI SAMPLING
analgesic.  Chorionic villi are small structures in the
Early Decelerations- are normal periodic placenta that act like blood vessels.
decreases in FHR resulting from pressure on the fetal  These structures contain cells from the
head during contractions developing fetus. A test that removes a sample
of these cells through a needle is called
Late Decelerations- are delayed until 30 to 40 seconds
chorionic villus sampling (CVS).
after the onset of a contraction and continue beyond
 CVS is a form of prenatal diagnosis to determine
the end of a contraction
chromosomal or genetic disorders in the fetus.
Prolonged Decelerations- are decelerations that last AMNIOCENTESIS
longer than 2 to 3 minutes but less than 10 minutes  a test that can be done during pregnancy to
look for birth defects and genetic problems in
Variable Decelerations- refers to decelerations that the developing baby
occur at unpredictable times in relation to contractions  the withdrawal of amniotic fluid through the
Sinusoidal Fetal Heart Rate Pattern abdominal wall for analysis at the 14th to 16th
-a fetus who is severely anemic or hypoxic, central week of pregnancy (Alfirevic, Mujezinovic, &
nervous system control of heart pacing may be so Sunberg, 2009)
impaired that the FHR pattern resembles a frequently  removes a small amount of fluid (200mL) from
undulating wave the sac around the baby in the womb (uterus).
NON-STRESS TEST(NST)  most often offered to women who are at
• A nonstress test is a common prenatal test used to increased risk for bearing a child with birth
check on a baby's health. During a nonstress test, also defects.
known as fetal heart rate monitoring, a baby's heart  has the advantage over CVS of carrying only a
rate is monitored to see how it responds to the baby's 0.5% risk of spontaneous miscarriage
movements.  Women with an Rh-negative blood type need
• Typically, a nonstress test is recommended for women Rh immune globulin administration after the
at increased risk of fetal death. A nonstress test is procedure to protect against isoimmunisation in
usually the fetus
done after week 26 of pregnancy. Certain nonstress test  women need to be observed for about 30
results might indicate that client and baby need further minutes after the procedure to be certain that
monitoring, testing or special care. labor contractions are not beginning and that
CONTRACTION STRESS TEST(CST) the fetal heart rate remains within normal limits
 It is performed near the end of pregnancy to PERCUTANEOUS UMBILICAL BLOOD SAMPLING (PUBS)
determine how well the fetus will cope with the  or cordocentesis, is the removal of blood from
contractions of childbirth. the fetal umbilical cord at about 17 weeks using
 The aim is to induce contractions and monitor the an amniocentesis technique
fetus to check for heart rate abnormalities using a  allows analysis of blood components as well as
cardiotocograph. more rapid karyotyping than is possible when
 Rarely used today only skin cells are remove
 Measures the response of FHR to contraction FETOSCOPY
 The test requires 3 contractions in 10 minutes  is the insertion of a fiberoptic fetoscope
 A positive or abnormal test results in decelerations through a small incision in the mother’s
in more than half of the contractions abdomen into the uterus and membranes to
 Negative result: no deceleration with the visually inspect the fetus
contractions  can be used to confirm an ultrasound finding, to
 Contraindication: any case where labour is not remove skin cells for DNA analysis, or to
allowed perform surgery for a congenital disorder such
as a stenosed urethra.
Invasive Diagnostic test

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