URINALYSIS AND BODY FLUIDS (AMNIOTIC FLUID) LECTURE - PowerPoint PPT Presentation

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URINALYSIS AND BODY FLUIDS (AMNIOTIC FLUID) LECTURE

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Title: URINALYSIS AND BODY FLUIDS (AMNIOTIC FLUID) LECTURE


1
URINALYSIS AND BODY FLUIDS (AMNIOTIC
FLUID)LECTURE
  • Dr. Essam H. Jiffri

2
  • Amniotic fluid is found in the membranous sac
    that surrounds the fetus and provides a cushion
    to protect the fetus

3
Amniotic Fluid
  • - The Fluid formed from the metabolism of fetal
    cells, transfer of water across the placental
    membrane, and, in later stage of development, by
    fetal urine.
  • - By the time production of fetal urine occurs,
    the fetus begins swallowing the amniotic fluid in
    an amount approximately equal to the urine
    output.

4
Amniotic Fluid
  • - The buildup of amniotic fluid to a total volume
    of 500 to 2500 ml at term is produced primarily
    by increased cell metabolism and placental water
    exchanges.
  • - In ability of the fetus to swallow is a
    critical sign and is indicated by an abnormal
    increase in amniotic fluid.

5
Amniotic Fluid
  • - Fluid for analysis obtained by needle
    aspiration into the amniotic sac, a procedure
    called amniocentesis.
  • - The procedure is relatively safe and can be
    performed on an outpatient basis.

6
Amniotic Fluid
  • - Specimens should be protected from light.
  • - Special precautions must be taken with
    specimens for cytogenetic analysis because cells
    in the fluid must be kept alive for culturing by
    the laboratory.

7
Amniotic Fluid
  • - Cytogenetic analysis has become an important
    predictor of birth defects.

8
FETAL DISTRESS
  • - Clinical analysis of amniotic fluid assesses
    both fetal well being and maturation.
  • - Because amniotic fluid is a product of fetal
    metabolism, the constituents that are present in
    the fluid provide information about the metabolic
    processes taking place and the progress of fetal
    maturation.

9
FETAL DISTRESS
  • - The oldest routinely performed laboratory test
    on amniotic fluid evaluates the severity of the
    fetal anemia produced by hemolytic disease of the
    newborn.
  • - Those infants are referred to as (R h babies).

10
FETAL DISTRESS
  • - The incidence of this disease has been
    decreasing rapidly since the development of
    methods to prevent anti-R h antibody production.
  • - The destruction of fetal red blood cells by
    antibodies that are present in the maternal
    circulation results in the appearance of the red
    blood cell degradation product, bilirubin, in the
    amniotic fluid.

11
FETAL DISTRESS
  • - By measuring the amount of bilirubin present in
    the fluid, it is possible to determine the degree
    of hemolysis taking place and to assess the
    danger of this anemia presents to the fetus.
  • In cases of premature or prolonged rupture of
    the amniotic membranes there is concern over
    possible infection of the mother and fetus.

12
FETAL DISTRESS
  • - Testing of the fluid with the leukocyte
    esterase reagent strip for the presence of white
    blood cells is shown to be a good indicator of
    infection and is more rapid and cost effective
    than Gram stains and cultures.

13
FETAL MATURITY
  • - Fetal distress, whether caused by hemolytic
    disease of the newborn or other conditions,
    forces the obstetrician to consider a preterm
    delivery, therefore, it becomes necessary to
    assess fetal maturity.
  • - Respiratory distress is the most frequent
    complication of early delivery.

14
FETAL MATURITY
  • - Laboratory tests are performed to determine the
    overall fetal maturity.
  • - The laboratory procedure routinely used to
    measure fetal lung maturity is the
  • lecithin ratio (L/S ratio).
  • - Lecithin is the primary component of the
    phospholipids that make up the majority of the
    alveolar lining and a count for alveolar
    stability.

15
FETAL MATURITY
  • - Lecithin is produced at a relatively low and
    constant rate until the 35th week of gestation,
    at which time a noticeable increase in its
    production occurs, resulting in the stabilization
    of the fetal lung alveoli.
  • - Sphingomyelin is a lipid that is produced at a
    constant rate throughout fetal gestation
    therefore, it can serve as a control on which to
    base the rise in lecithin.

16
FETAL MATURITY
  • - Prior to 35 weeks of gestation, the L/S ratio
    is usually less than 1.6 and it will rise to 2.0
    or higher when lecithin production increases.
  • - When the L/S ratio reaches 2.0 a preterm
    delivery is usually considered to be a relatively
    safe procedure.

17
FETAL MATURITY
  • - Measurement of lecithin and sphingomyelin is
    performed using thin-layer chromatography.
  • - Absence of phosphatidylglycerol in the presence
    of a normal L/S ratio is seen in children of
    diabetic mothers

18
FETAL MATURITY
  • - At about 36 weeks of gestation, urine from the
    fetal kidney begins appearing in the amniotic
    fluid therefore, creatinine concentration above
    2.0 mg per dl indicates a fetal age of
    approximately 36 weeks.

19
FETAL MATURITY
  • - The measurement of alpha fetal protein levels
    and acetylcholinesterase activity is being used
    to provide early detection of neural tube
    disorders, such as spina bifida.

20
Summary of the routine chemical tests performed
on amniotic fluid
  • Tests for the Well-being and Maturity
  • __________________________________________________
    ________
  • Test Normal values at term
    Significance
  • __________________________________________________
    ________
  • Bilirubin scan 0.025 mg/dl Hemolytic
    disease of the newborn
  • L/S ratio 2.0 Fetal lung maturity
  • Phosphatidyl- Present Fetal lung maturity
  • Glycerol
  • Creatinine 1.3 4.0 mg/dl Fetal age
  • Alpha fetal protein 4.0 mg/dl Neural tube
    disorders
  • __________________________________________________
    ________
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