Obstetrics



Obstetrics







5 What routine tests should be obtained for all pregnant patients?


Pap smear: If the patient is due for a pap smear. Pregnancy does not change the frequency of screening.


Urinalysis: At the first visit and every visit thereafter (to screen for proteinuria, preeclampsia, and bacteriuria; not a good screen for diabetes).


Urine culture: Obtained at 12 to 16 weeks to screen for asymptomatic bacteriuria.


Hemoglobin and hematocrit: At the first visit to determine whether the patient is anemic (because pregnancy may worsen anemia); repeat in the third trimester.


Blood type, rhesus (Rh) type, and antibody screen: At first visit (for identification of possible isoimmunization).


Syphilis test: At first visit (mandated in most states) and subsequent visits (for high-risk patients).


Rubella antibody screen: If the patient is found to be nonimmune, counsel her to get postpartum immunization. Rubella vaccine should not be given during pregnancy.


Glucose screen for gestational diabetes: At first visit in patients with risk factors for diabetes mellitus (obesity, positive family history, or age older than 30 years); otherwise, screen at 24 to 28 weeks. Use fasting serum glucose and serum glucose levels 1 or 2 hours after an oral glucose load (oral glucose tolerance test).


Serum alpha-fetoprotein: Performed at 15 to 20 weeks, primarily to detect open spina bifida and anencephaly.


Hepatitis B antigen testing: To prevent perinatal transmission.


Varicella: All pregnant women should be tested for immunity to varicella.


Thyroid function: Maternal hypothyroidism may affect fetal neurologic development. Maternal hyperthyroidism can lead to fetal and maternal complications.


HIV test: The American College of Obstetrics and Gynecology (ACOG) advocates an “opt-out” approach to screening rather than an “opt-in” approach to increase screening.


Chlamydia screening: The Centers for Disease Control and Prevention (CDC) and ACOG advocate testing all pregnant women at the first prenatal visit.


Down syndrome screening: Should be offered to all pregnant patients. There are multiple ways to screen. See questions 21 to 27.


Group B beta-hemolytic streptococcus (GBS): Screen at 35 to 37 weeks with a swab of the lower vagina and rectum.


Others: Tuberculosis skin test for women at higher risk. Testing for gonorrhea for women at higher risk of infection. Testing for toxoplasmosis is controversial. If asked, you should do chlamydia and gonorrhea cultures for any pregnant teenager. Testing for sexually transmitted infections should be repeated in the third trimester for women who continue to be at risk or for women who acquire a risk factor during pregnancy.



6 On every prenatal visit, listen to fetal heart tones and evaluate uterine size. When can these factors first be noticed? What constitutes a size/date discrepancy?


Fetal heart tones can be heard with Doppler ultrasound at 10 to 12 weeks and with a normal stethoscope at 16 to 20 weeks. At 12 weeks of gestation, the uterus enters the abdomen and is palpable at the symphysis pubis; at roughly 20 weeks, it reaches the umbilicus. Uterine size is evaluated by measuring the distance from the symphysis pubis to the top of the fundus in centimeters. At roughly 20 to 35 weeks, the measurement in centimeters should equal the number of weeks of gestation. A discrepancy greater than 2 to 3 cm is called a size/date discrepancy. Ultrasound should be done for further evaluation (e.g., intrauterine growth retardation, multiple gestations).








12 How is fetal well-being evaluated?


A nonstress test is the easiest initial screen. It is performed with the mother at rest. A fetal heart rate tracing is obtained for 20 minutes. A normal strip has at least 2 accelerations of heart rate, each at least 15 beats per minute above baseline and lasting at least 15 seconds.


A biophysical profile is slightly more involved and includes a nonstress test as well as a measure of amniotic fluid (to determine whether oligohydramnios or polyhydramnios is present), a measure of fetal breathing movements, and a measure of general fetal movements.


If the fetus scores poorly on the biophysical profile, the next test is the contraction stress test, which looks for uteroplacental dysfunction. Oxytocin is given, and a fetal heart strip is monitored. If late decelerations are seen on the fetal heart strip with each contraction, the test is positive. In most cases of a positive contraction stress test, a cesarean section is performed.





15 Define postterm pregnancy. Why is it a major concern? How is it treated?


Postterm pregnancy is defined as more than 42 weeks of gestation. Both prematurity and postmaturity increase perinatal morbidity and mortality rates. With postmaturity, dystocia (or difficult delivery) becomes more common because of the increased size of the infant.


In general, if the gestational age is known to be accurate and the cervix is favorable, labor is induced (e.g., with oxytocin). If the cervix is not favorable or the dates are uncertain, twice-weekly biophysical profiles are done. At 41 weeks, most obstetricians advise induction of labor. A 2012 meta-analysis demonstrated that routine labor induction at greater than 41 weeks compared with expectant management resulted in lower perinatal mortality and a lower rate of meconium aspiration syndrome.














27 What is a maternal plasma-based test?


This is the newest option that is just becoming widely available and may someday make many of these other tests obsolete. This test, also called cell-free fetal DNA testing, detects fetal DNA in the circulation and has a detection rate more than 98% and a false-positive rate of less than 0.5% for Down syndrome and Edward syndrome (trisomy 18). It is used after 10 weeks of gestation. Cell-free fetal DNA testing is not yet validated in low-risk women, but can be used in higher risk women (i.e., women who will be older than 35 at the time of delivery; presence of sonographic findings associated with fetal aneuploidy; history of previous pregnancy with fetal trisomy; or positive screening results on tests such as the first trimester combined test, the integrated test, or the quadruple test).






31 Cover the right-hand column and specify the effects of the following classic teratogens on an exposed fetus









36 What are the TORCH syndromes? What do they cause?


TORCH is an acronym for several maternal infections that can cross the placenta and can cause intrauterine fetal infections that may result in birth defects. Most TORCH infections can cause mental retardation, microcephaly, hydrocephalus, hepatosplenomegaly, jaundice, anemia, low birth weight, and IUGR.


T = Toxoplasma gondii: Look for exposure to cats. Specific defects include intracranial calcifications and chorioretinitis.


O = Other: Varicella-zoster causes limb hypoplasia and scarring of the skin. Syphilis causes rhinitis, saber shins, Hutchinson teeth, interstitial keratitis, and skin lesions.


R = Rubella: Worst in the first trimester (some recommend abortion if the mother has rubella in the first trimester). Always check antibody status on the first visit in patients with a poor immunization history. Look for cardiovascular defects, deafness, cataracts, and microphthalmia.


C = Cytomegalovirus: Most common infection of the TORCH group. Look for deafness, cerebral calcifications, and microphthalmia.


H = Herpes: Look for vesicular skin lesions (with positive Tzanck smears) and history of maternal herpes lesions.




38 Describe therapy to reduce HIV transmission from an infected mother to the fetus. When should an infant born to an HIV-infected mother be tested?


In untreated HIV-positive patients, HIV is transmitted to the fetus in roughly 25% of cases. When three-drug therapy is given to the mother prenatally and zidovudine is given to the infant for 6 weeks after birth, HIV transmission is reduced to roughly 2%. A noninfected infant may still have a positive HIV antibody test at birth because maternal antibodies can cross the placenta. Within 6 to 18 months, however, the test reverts to negative. This is why infants of infected mothers are tested using a direct HIV DNA PCR (polymerase chain reaction) test at birth, at 4 to 6 weeks of age, and 2 months after the second test. Babies who have these three negative tests should have an HIV antibody test at 12 and 18 months of age. Cesarean section may reduce HIV transmission to the child.




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Apr 8, 2017 | Posted by in NURSING | Comments Off on Obstetrics

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