Amniotic Fluid Physiology PDF
Document Details
Uploaded by ConstructiveLawrencium
Tags
Summary
This document provides a comprehensive overview of amniotic fluid physiology, focusing on various aspects including its presence, functions, volume, and sources. It also details methods of collection and testing, and how these applications are used in prenatal care. The information is likely intended for medical professionals or students in a related field.
Full Transcript
# Amniotic Fluid Physiology * Amniotic fluid is present in the amnion. * A membranous sac that surrounds the fetus. * Is involved in the exchange of water and chemicals between the fluid, fetus, and maternal circulation ## Functions of Amniotic Fluids * Provide a protective cushion for...
# Amniotic Fluid Physiology * Amniotic fluid is present in the amnion. * A membranous sac that surrounds the fetus. * Is involved in the exchange of water and chemicals between the fluid, fetus, and maternal circulation ## Functions of Amniotic Fluids * Provide a protective cushion for the fetus * Allow fetal movement * Stabilize the temperature to protect the fetus from extreme temperature changes. * Permit proper lung development. ## Amniotic Fluid Volume ### Sources * During 1st trimester: 35mL of amniotic fluid is derived from maternal circulation * After the 1st trimester: fetal urine becomes the major contributor to the amniotic fluid volume. * When fetal urine production occurs, fetal swallowing of amniotic fluid begins. * The amount of amniotic fluid increases in quantity throughout pregnancy. * Peaks to 800-1200 ml during the 3rd trimester, and then gradually decreases prior to delivery. ### Variation In Amniotic Fluid Volume | | | | | | :-------------------- | :-------------------------------------------------------------- | :-------------------- | :----------------------------------------------------------------- | | **Polyhydramnios** | ↑ amniotic fluid volume (>1200 ml) | **Oligohydramnios** | ↓ amniotic fluid volume (<800 ml) | | **Causes:** | | **Causes:** | | | ✓ Decrease fetal swallowing of urine | | ✓ Increase fetal swallowing of urine | | | * Neural Tube Defect | | ✓ Membrane leakage | | | | | | ✓ Urinary Tract deformities | ## Specimen Collection and Handling ### Method of Collection: Amniocentesis * Up to 30 ml is collected in a sterile syringe. * The first 2 or 3 mL collected can be contaminated by maternal blood, tissue fluid, and are discarded. * 2nd trimester collection * To assess genetic defects (Trisomy 21 or Down Syndrome) * 3rd trimester collection * Fetal Lung Maturity (FML), Fetal Hemolytic Disease (HDN) ### Table 13-2 **Indications for Performing Amniocentesis** Amniocentesis may be indicated at 15 to 18 weeks' gestation for the following conditions to determine early treatment or intervention: * Mother's age of 35 or older at delivery * Family history of chromosome abnormalities, such as trisomy 21 (Down syndrome) * Parents carry an abnormal chromosome rearrangement * Earlier pregnancy or child with birth defect * Parent is a carrier of a metabolic disorder * Family history of genetic diseases such a sickle cell disease, Tay-Sachs disease, hemophilia, muscular dystrophy, sickle cell anemia, Huntington chorea, and cystic fibrosis * Elevated maternal serum alpha-fetoprotein * Abnormal triple marker screening test * Previous child with a neural tube disorder such as spina bifida, or ventral wall defects (gastroschisis) * Three or more miscarriages **Amniocentesis is indicated later in the pregnancy (20 to 42 weeks) to evaluate:** * Fetal lung maturity * Fetal distress * HDN caused by Rh blood type incompatibility * Infection ## Amniotic Fluid Vs. Maternal Urine * Necessary to determine possible premature membrane rupture or accidental puncture of the bladder during specimen collection. | Test | Amniotic Fluid | Maternal Urine | | :---------- | :------------- | :-------------- | | Creatinine | <3.5 mg/dl | up to 10 mg/dl | | Urea | <30 mg/dl | up to 300 mg/dl | **\*Less reliable tes: Glucose and Protein: Higher in amniotic fluid than maternal urine** ## Fern Test * Use to evaluate premature rupture of membrane * Specimen: Vaginal Fluid → Slide (Air Dry) → (+) Fern-like crystals * Detect early pregnancy ## Specimen Handling and Storage: * **Fetal Lung Maturity Test:** placed in ice for delivery and kept refrigerated. * Filtration is recommended to prevent the lost of phospholipids. * **Bilirubin Test:** protected from light at all times * **Cytogenetics and Microbial studies:** Kept at room temperature or body temperature (37°C) prior to analysis to prolong the life of the cells needed for analysis. # Laboratory Examination of Amniotic Fluids ## Color and Appearance | Amniotic Fluid Color | Clinical Significance | | :--------------------- | :--------------------------------------------------------------------------------------------------- | | Colorless | Normal | | Blood-streaked | Traumatic tap, abdominal trauma, and intra-amniotic hemorrhage | | Yellow | Hemolytic disease of the newborn ( ↑ Bilirubin ) | | Dark green * | Meconium - Newborn's first bowel movement | | Dark red-brown | Fetal death | ## I. Test for Hemolytic Disease of the Newborn * Measured by spectrophotometric analysis * Bilirubin causes a rise in OD at 450 nm. * Oxyhemoglobin will peak at 410 nm and may interfere thus specimen contaminated with blood are not accepted. * Specimen with meconium will cause false low value and are not accepted. * O.D. 450 nm - Normal Absorbance * Reported with Liley graph. * Zone 1 = non-affected/mildly affected fetus * Zone 2 = moderately affected (requires close monitoring) * Zone 3 = Severely affected (requires intervention) ## II. Test for Neural Tube Defect * Neural tube defects (NTD) are one of the most common birth defects in the United States. It can be detected by maternal serum alpha-fetoprotein (MSAFP) blood test, high-resolution ultrasound, and amniocentesis. * Common Neural Tube Defects: * Spina bifida, slit-spine (incomplete closing of spine and backbone) * Anencephaly (absence of major part of the brain) * Screening Test: Alpha-fetoprotein * ↑ in NTD * ↓ in Down Syndrome * Confirmatory Test: Acetylcholinesterase ## III. Test for Fetal Lung Maturity * Respiratory Distress Syndrome (RDS) * Most frequent complication of early delivery * 7th most common cause of morbidity and mortality in premature infant * Caused by insufficiency of lung surfactant production and structural immaturity of fetal lungs. * **a.** Lecithin-Sphingomyelin (L/S ratio) (REFERENCE METHOD) * **Lecithin** = Primary surfactant; for alveolar stability * **Sphingomyelin** = Serves as a control (contrast production) * ✓ L/S RATIO of >2.0 = Mature Lungs * Reject specimens contaminated with blood and meconium * **b.** Amniostat-FLM – immunologic test for Phosphatidylglycerol (PG) -surfactant * Replaces L/S Ratio; Not affected by blood and meconium * Production of PG is delayed in diabetic mother * Low or High Positive: Mature Lungs * Negative: Immature lungs * **c.** Foam Stability (Foam Shake Test) * Amniotic fluid + 95% ethanol → Vigorous shaking for 15 seconds * Stand for 15 minutes * (+) Continuous line of bubble/ foam = Mature Lungs * **d.** Microviscosity – presence of phospholipids decrease microviscosity * **e.** Lamellar Body Count (LBC) – Lamellar Bodies * Type II Pneumocytes - Responsible for the production of alveolar surfactants. * 32,000/ UL lamellar body count = Adequate FLM * **f.** OD 0.150 at 650 nm - Presence of Lamellar Bodies = ↑ Optical Density * OD of ≥ 0.15 = L/S ratio >2.0 * (+) Phosphatidylglycerol ## IV. Test for Fetal Age * **a.** Creatinine * 1.5 to 2.0 mg/dl = prior to 36 weeks of gestation * >2.0 mg/dl = Fetal age is over 36 weeks of gestation