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27 Cards in this Set

  • Front
  • Back
Amniocentesis
Surgical puncture of the amniotic sac to obtain a sample of amniotic fluid from which it can be determined whether the fetus has Down syndrome, neural tube defects, Tay-Sachs disease, or other genetic defects
Blood groupings
Determines blood types A, B, AB and O.
Cerclage
Suturing an incompetent cervix to keep it from dilating prematurely during pregnancy
Cesarean section
Delivery of the fetus by means of an incision through the abdominal cavity and then into the uterus
Complete blood count.
Test for anemia, infection, or cell abnormalities.
Cordocentesis
Process of obtaining a sample of blood from the umbilical cord while the fetus is in utero
CVS/Chorionic villus sampling
Determines chromosomal abnormalities and biochemical disorders (Down syndrome, Tay-Sachs disease, and cystic fibrosis).
Diagnostic ultrasound 3
Use of extremely high-frequency sound waves for diagnosing genetic defects and hydrocephalic conditions in the unborn fetus.
Doppler ultrasound
Procedure using an audio transformation of high-frequency sounds to monitor the fetal heartbeat
Electronic fetal monitor
Electronic instrument used to record fetal heartbeat and contractions of the mother’s uterus during labor
Episiotomy
Surgical procedure performed during labor to prevent tearing of the perineum and to facilitate delivery of the fetus
Group B streptococcus
Type of bacterium commonly found in the vagina and intestinal tract, it is found in 10% to 25% of all pregnant women; can cause life-threatening infections in the newborn
Hematocrit
Test for Anemia during pregnancy. Blood test that separates solids from plasma in the blood by centrifuging the blood sample
Hemoglobin
Test for Anemia during pregnancy. Blood protein; the iron-containing pigment of red blood cells that carries oxygen from the lungs to the tissues
Hepatitis B screen
Test to identify carriers of hepatitis.
HIV/Human immunodeficiency virus
Test to identify HIV infection.
Hydatidiform mole
Intrauterine condition with multiple cysts of grapelike, enlarged chorionic villi that occurs in 1/1500 pregnancies in the USA; also called hydatid mole or hydatiform. Signs include a fundal height higher than gestational age, absence of fetal heart sounds, dark brown or bright red vaginal discharge or bleeding, expulsion of cystic vesicles, edema, and hypertension.
Maternal blood glucose.
Test to screen for gestational diabetes. If level of glucose is moderately elevated, a more conclusive glucose tolerance test (GTT) can be ordered.
NST/Nonstress test
Identifies fetal compromise in conditions with poor placental function, such as hypertension, diabetes mellitus, or postterm gestation (pregnancy lasts beyond 42 weeks).
Pelvimetry
Measurement of the expectant mother’s pelvic dimensions to determine whether it will be possible to deliver a fetus through the normal vaginal route
Quad marker screen (AFP, hCG, Ue, AND INHIBIN-a)
Test to assess probabilities of potential genetic disorders by measuring high and low levels of alpha-fetoprotein (AFP) a protein produced by the baby's liver; abnormal levels of human chorionic gonadotropin (hCG) a hormone produced by placenta; unconjugated estriol (UE), a hormone produced in placenta and in baby's liver; and inhibin; a hormone produced by placenta.
Rh factor (+ve or -ve).
Test to determine risk for maternal-fetal blood incompatibility.
Rubella (German measles) titer.
Test determines immunity to rubella.
TORCH panel (Test screens for toxoplasmosis, rubella, cytomegalovirus (CMV) and herpes simplex virus (HSV).
Toxoplasmosis screen
Test to determine toxoplasmosis infection.
Urinalysis.
Test that checks for infection, renal disease, or diabetes.
VDRL/Venereal Disease Research Laboratory
Test to screen for syphilis. Also used to screen for syphilis is RPR (rapid plasma reagin).