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DEFINITION
High
risk pregnancy is defined as one which is complicated by factor or factors that adversely affects the pregnancy outcome- maternal or perinatal or both.
General consideration
Mother ,fetus,or newborn increased risk of morbidity or mortality during,or after delivery
At
Before,
Obstetric
Prematurity
Postterm pregnancy
Preeclampsia-eclampsia
Polyhydramnios
Oligohydramnios
Growth restriction
Chromosomal abnormalities
Leading
Thromboembolic disease
Hypertensive disease
Hemorrhage Infection Ectopic pregnancy
Preterm labor
age below 16 or over 35 years Low socioecomonic status Maternal weight below 50Kg Poor nutrition Previous preterm birth Incomplete cervix Uterine anomalies Smoking Drug addiction and alcohol abuse Pyelonephritis, pneumonia Multiple gestation Anemia Abnormal fetal presentation Preterm rupture of membranes Placental abnormalities infection
Polyhydramnios
Diabetes mellitus Mutiple gestation Fetal congenital abnormalities Isoimmunization(Rh or ABO) Nonimmune hydrops Abnormal fetal presentation
Oligohydramnios
Renal agenesis Prolonged rupture of membranes
Intrauterine growth
restriction Intrauterine fetal
demise
PRECONCEPTIONAL EVALUATION
Preconceptional
evaluation and counseling of women of reproductive age Issues of potential consequence to a pregnancy such as medical problems, lifestyle, or genetic issues should be investigated and interventions devised prior to pregnancy.
screening
oMaternal age oModality of conception oEthic background oPast obstetric history
History :
oParental karyotype
oCervical and uterine anomalies oConnective tissue disease
oHormonal abnormalities
oAcquired and inherited thrombophilias
o drugs
oInfectious agents oradiation
Reproductive history
Grand
multiparity
Third
Previous surgery
Myomectomy Repair
of complete perineal tear Repair of vesico- vaginal fistula Repair of stress incontinence Previous Caesarian section or hysterectomy
Family history
Socio-economic
status- patients belonging to low socio- economic status have a higher incidence of anaemia, preterm labour, growth retarded babies. Family history of diabetes, hypertension or multiple pregnancy and congenital malformation.
RISK APPROACH
During pregnancy Elderly primi ( 30 years) Short statured primi ( 140 cm) Threatened abortion and APH Malpresentations Pre-eclampsia and eclampsia Anaemia Elderly grand multiparas Twins and hydroamnios Previous still birth, IUD, manual removal of placenta Prolonged pregnancy History of previous Caesarean section and instrumental delivery Pregnancy associated with medical diseases.
During labour
PROM Prolonged
labour Hand, feet or cord prolapsed Placenta retained more than half an hour PPH Puerperal fever and sepsis
Antepartum course
Prenatal
visits
o Fever(>100.4,even >)
o Urinary ,pulmonary ,hematological
Vital signs
A
sources; chorioamnionitis o Preterm labor;adverse effect on fetus and mother o Amniocentesis for microscopy and culture o Antipyretics, antibiotics
Pulse B
oTachycardia(>100bpm) oInfection, anemia, heart disease,et. oMild:follow-up; Severe: ECG , hemogram
Blood pressue C
o >140/90mmHg >30/15mmHg oPIH, chronic hypertention,
urinalysis
Blood test Haemoglobin Blood type and Rh grouping with antibody screening Rubella titres Syphillis screen Hepetitis B screen HIVscreen Pap Smear Gonorrhea and Chlamydia culture Test for toxoplasmosis and antiphospholipid antibodies Post prandial blood glucose and glucose tolerance test
EXAMINATION
General
physical examination Height: Below 150 cm particularly, Below 145 cm in our country. Weight: Overweight or underweight, Body Mass Index (BMI): Weight/( height)2 BMI: 20- 24 is accepted as normal
Pelvic Examination Uterine size and fundal heightdisproportionately smaller or bigger Abdominal girth Genital prolapse Lacerations or dilatations of the cervix Associated tumors Pelvic inadequacy
PRENATAL SCREENING
Maternal Serum Alpha Fetoprotein
AFP-
is a fetal protein- yolk sac and fetal liver in fetal serum & amniotic fluid by 6 weeks
Present Peak
Neural Blood
Elevated in
Wrong NTD
gestational age
Multiple
IUFD
pregnancy
Abdominal
Renal IUGR
wall defects
anomalies
Pre-eclampsia
Low in
Trisomy GTN
Triple test
Triple
screen, the Kettering test or the Bart's test multiple-marker screening test MSAFP, hCG, UE3
hCG
Maximum:
days
Fall
Remains Peaks
at 32 week onwards
Oestriol
Detectable
30
ng/ml at term
Triple test
Detect
downs syndrome
nad UE3 is low
MSAFP hCG
Performed Confirm
by amniocentesis
AcetylCholine
Inhibin
Mother counts the fetal movements from 9 am Stops as soon as 10 movements are perceived Report if:
<10 movement in 12 hrs on 2 successive days
No movements even after 12 hrs in a single day
DFMC
Less
Ultrasonography
Fetal indications
Diagnosis
Assessment Diagnosis
pregnancy
Diagnosis
Assess
IUGR
Utero placental
Localization Diagnosis
of placenta
of liquor amnii
size
Maternal
Pelvic
mass diagnosis
fetal therapy
Basic:
Comprehensive:
Procedure
Explain Ensure Supine Gel
the procedure
Transducer
Transvaginal ultrasound
Lie
down on a table with knees bent Place transducer, into the vagina The probe is covered with a condom and a gel. The probe sends out sound waves, which reflect off body structures. A computer receives these waves and uses them to create a picture. See the picture on a nearby TV monitor.
Abnormal findings on a physical exam, such as cysts, fibroid tumors, or other growths Abnormal vaginal bleeding and menstrual problems Ectopic pregnancy Pelvic pain
Transvaginal ultrasound is also used during pregnancy to: Evaluate cases of threatened miscarriage Listen to the unborn baby's heartbeat Look at the placenta Look for the cause of bleeding Monitor the growth of the embryo or fetus early in the prgnancy See if the cervix is changing or opening up when labor is starting early
Amnioscopy
Visual
amnioscope.
The
staining
Carries
pocket is measured.
AFI
20 weeks and more: divide into 4 quadrants Vertical diameter of the largest pocket of fluid in each quadrant is checked
4 values are added Between 28-40 weeks- average AFI is 15cm 20-24 cms indicate hydramnios 5-6 cm indicates oligohydramnios
Fetoscopy
Fetoscope-
Uses
Intactness of spinal cord can be confirmed Biopsies of fetal tissue and fetal blood
samples
Performed
Prepared
Local Minor
as for amniocentesis
inserted
Risks
Premature
Amnionitis Leakage Injury
labour
of fluid
to the fetus
of prenatal diagnosis to
Indications
Abnormal first trimester screen results Increased nuchal translucency Family history of a chromosomal abnormality or other genetic disorder
Transcervically:
10-12 weeks
10 weeks to term
Transabdominally:
Ultrasonic guidance Long malleable polythene catheter Safe between 10-12 weeks Anti D immunoglobulin 50 mcg IM
Risks
Risk Risk Risk
deformities
bleeding
Amniocentesis
Amniocentesis is a procedure used in prenatal diagnosis of chromosomal abnormalities and fetal infections, in which a small amount of amniotic fluid, which contains fetal tissues, is extracted from the amnion or amniotic sac surrounding a
Diagnostic
Early
Therapeutic
First
amnioinfusion
Empty bladder- dorsal position Ultrasonic guidance- local anesthetic a 18-20 gauze needle (4) is inserted through the mother's abdominal wall into the amniotic sac. puncture the sac & extract approximately 30 ml of amniotic fluid.
After the amniotic fluid is extracted, the fetal cells are separated from the sample.
The cells are grown in a culture medium, then fixed and stained.
Site
Early
Later
presenting part
Precautions
Prior
sonographic localization
of 100 mcg of anti D
Administration
immunoglobulin
Hazards
Maternal:
infection, hemorrhage,
hemorrhage, oligohydramnios
USE
Cytogenetic
turners syndrome
DNA
sachs disease
Percutaneous umbilical
Ultrasound guidance
Punctures the umbilical vein app. From 1-2 cm
INDICATION
Hematological:
anemia, bleeding
disorders
Infection:
Fetal
Fetal
therapy
Risks
Abortion
Preterm
labour
IUD-
Definition
Cardiotocograph
is an electronic fetal
monitor which records graphically the fetal heart activity (cardio) and uterine contractions (toco).Both can be recorded simultaneously and continuously.
Indications
Oligo hydramnios
Hypertension.
Abnormal FHR detected
Mal presentation
GDM
Multiple Gestation.
Previous CS. Abdominal Trauma. Prolonged ROM. Meconium Liquor
Parts of tocograph
movement
Accelerations
Accelerations
increases in FHR due to fetal movement or compression of the umbilical vein during contraction.
Deceleration
They
Early Decelerations
Early deceleration follows the pattern of contractions, beginning when the contraction begins & ending when the contraction ends.
The waveform of FHR is inverse to the contraction wave form.
The
rate rarely falls below 100 BPM & returns quickly between 120-160 BPM.
It occurs late in labour. If they occur early in labour before the head has descended, it could be the result of cephalo pelvic disproportion.
Late decelerations
Late decelerations are those that are delayed until 30-40 seconds after the onset of contraction and continue beyond the end of contraction.
It suggests uteroplacental insufficiency or decreased blood flow through the intervillous spaces during contractions.
The
peak.
Changing the womans position from supine to lateral may help in relieving the pressure on the aorta & vena cava & to supply more blood to the uterus.
Variable decelerations:
It
occurs during unpredictable times during the contractions & indicates compression of the cord. Changing the womans position from supine to lateral or to a trendelenburg position may help in relieving the pressure on the cord. Administering oxygen to the mother is also helpful.
10 minutes or more
Baseline Bradycardia
Baseline
Baseline Tachycardia
It
means baaseline FHR>160 beats per minute Causes: Maternal fever dehydration drugs(beta sympatho mimetics)
Baseline acceleration
These
are abrupt increase in FHR above baseline, their onset to peak is <30 seconds. If the increase lasts for 2-10 minutes it is called prolonged acceleration
Types of cardiotocograph
1.
2.
non stress test is used to assess the integrity of the fetal central nervous system.
This test is based on the theory that an intact nervous system and responsive cardiovascular system results in transient acceleration of fetal heart rate in response to fetal activity
NST-meaning
When it is done in labour it is called intra partum fetal monitoring or contraction stress test
Advantage of NST:
Easy
Non
invasive procedure
Procedure:
Explain the purpose and function of external electronic fetal monitoring to the women Turn on the monitor and press the test button . confirm the paper speed, switch on the back of the monitor is set i.e. 1cm /mts, 3cm/mts Record complete patient identification , information at the beginning of the strip. Record the date and time
perform Leopold maneuver to determine fetal position and the location of the fetal back Place monitor belts under the womens back . position the women in semi fowlers or lateral tilt position. The supine position is avoided to prevent the compression of maternal blood vessels supine hypertension
Connect ultra sound transducer and toco transducer to the fetal monitor. Apply gel to the transducers. Gel is needed to improve conduction
Place the toco transducer on the fundus of the uterus. since normal uterine contraction are dominant in fundal region Evaluate the tracing for baseline rate ; long term variability, acceleration and deceleration and uterine contraction frequency, duration and return to resting tonus between contraction
Interpretation
Reactive
NST:- it is defined as two or more accelerations of fetal heart rate with amplitude at least 15beats /mts and duration of at least 15seconds during a 20mts period
Non-reactive
NST:- this test result shows no acceleration or acceleration less than 15beats/mts or less than 15 seconds in duration for a 40 mts observation
test is also called oxytocin challenge test ( OCT ). This test is based on experimental evidence showing that utero placental blood flow decreases markedly or ceases during uterine contraction . Therefore uterine contraction cause a hypoxic stress that a normal healthy fetus can tolerate without difficulty.
A fetus with a chronic or acute problem will not be able to tolerate such a decrease in oxygen supply and will demonstrate this by late deceleration of fetal heart rate following the contraction
Procedure
It is same as that of NST except start intravenous oxytocin administration using pump at 0.5-1 mu/mts . Double the rate every 15 to 20 mts until the mother gets 3 contraction lasting for 40 to 60 seconds with in
Negative CST
No
late decelerations with a minimum of three uterine contractions lasting 40 to 60 seconds within a10 minute period. This indicates fetal well being
Positive
Contraindication
Threatened
preterm labour Placenta previa Hydramnios Multifetal pregnancy Rupture of membrane Previous preterm labour Previous classical c.birth
Contraindication
Threatened
preterm labour Placenta previa Hydramnios Multifetal pregnancy Rupture of membrane Previous preterm labour Previous classical c.birth
This technique provides an accurate appraisal of fetal wellbeing during labour. For this method, membranes must be ruptured and the cervix must be sufficiently dilated. A small electrode attached to the presenting part yields a continuous fetal heart rate monitoring. A solid or fluid filled catheter is introduced in to the uterine cavity to monitor uterine activity. This technique carries much complications, so it is clinically not so significant in Indian setup
Findings
Baseline fetal heart rate is the fetal heart rate between the uterine contraction. A rate more rapid than 160 beats per minute is termed as baseline tachycardia
This
The causes of baseline tachycardia are: Prematurirty Mild fetal hypoxia Maternal fever Parasympatholytic drugs(atropine) Beta sympathomimetics(ritrodrine, isoxupirine) Amnionitis Maternal anemia Fetal infection Fetal cardiac problems
rate slower than 110 beats per minute is baseline bradicardia. causes are
The
Fetal
hypoxia Maternal hypotension Prolonged cord compression Fetal congenital heart blocks
Baseline variability
Electrical
activity in the fetal heart results in minute variations in the length of each beat.
This causes the tracing to appear as a jagged rather than a smooth line.
The baseline rate should vary by at least 5 beats over a period of one minute.
Loss
but
Period of fetal sleep "also causes a reduction in variability and commonly last for 20-30 minute even in advanced labour.
Nursing management
Notify
the physian Late deceleration: change the position Stop the oxytocin in case of hyper stimulation Oxygen administration start IV fluids Tachy cardia-maternal pyrexia: antipyretics
Fetal Assessment
1. Vibroacoustic stimulation o burst of sound to stimulate fetus o when NST is nonreactive
C Ancillary tests
o anoxia
2.fetal scalp stimulation o stimulate fetal vertex
o anoxia
Foetal
CONCLUSION
Aim at: Recognize the risk beginning as early as possible. Just by: Preconceptual counseling. Early and frequent prenatal care And try to: Optimize outcome both of fetus and mother Maximize therapeutic treatment
BIBLIOGRAPHY
Dutta DC, Text Book of Obstetric, 6th edi. New Central Company,Calcutta, 2004. Pillitteri A. Maternal and Child Health Nursing .4th ed 2010. Perry L. Maternity and Womens Health Care.9th edi. Mosby publications 2009. Boback J. Maternity and Gynecological Care, the nurse and the family.4th ed. Mosby company publication. USA.1989. Jenson.D.M., Benson.C.R, Bobak.M.I. Maternity care of nurse and family, First edition, St LouiseC.V. MosbyCompany, 1977 Elizabeth.M. Midwifery for Nurses, First edition , New Delhi: CBI Publishers, 2010. Cooper.A.M, Diane.M.F, Myles textbook for Nidwifes, 14th edi, Churchill livingstone Edinburgh 2003 American college of obstetricians and gynacologists; Ante partum fetal surveillance. ACOG practice Bulletin no 9, 1999
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