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Second Trimester Doctor Visits
From Your Baby Today
Step right up
Throughout your second trimester, you'll continue to visit your doctor once a
month -- as long as your pregnancy is progressing normally. Each appointment
probably will begin with you stepping on the scale.
Monitoring your weight gain
During your fourth, fifth, and sixth months, you should be gaining one-half
to three-quarters of a pound a week. By tracking your weight, your doctor can
estimate your baby's growth and watch for signs of preeclampsia.
Doctors stress that you should try hard to stay within a 25- to 35-pound
weight gain. Straying too far from this guideline can lead to problems.
By gaining too much weight:
- You put extra stress on your heart, which already is working overtime to
pump your increased blood volume.
- You put additional stress on your joints, which pregnancy hormones have
loosened and made lax.
- You increase your risk of developing preeclampsia, a serious condition
that can be life-threatening.
- You'll be more likely to develop aches in your lower back.
- You may make labor and delivery more difficult because your baby will be big.
Second-trimester tests
- Urinalysis. This test, performed at each doctor's visit, measures the
protein and sugar in your urine. It will detect excess protein, which can be
a warning sign of preeclampsia. Urinalysis also may be used to detect the
presence of drugs or bladder infection.
- Triple marker test. This blood screening usually is performed between the
fifteenth and eighteenth weeks of pregnancy. Part of the test measures a
specific protein, alpha-fetoprotein or AFP, in your blood. If the AFP levels
are high it may identify a neural tube defect; if AFP levels are low
(combined with abnormalities found in two other tests) this may identify Down
Syndrome.
- Rhesus (Rh)-antibody-level test (a blood test) for rhesus negative women.
Most people have a specific protein in their blood called the Rh factor.
Those who don't are Rh-negative. If a woman tests Rh-negative, the father of
the child also must be tested for his Rh factor because problems arise when
an Rh-negative woman conceives a baby with an Rh-positive man. The tests are
done about halfway through the pregnancy, or at once if the woman has a
bleeding problem.
An Rh-positive baby's blood factor, also called an antigen, can stimulate an
intense immune response in his mother. The problem isn't so great with a
first pregnancy, where the mother's body hasn't yet built a strong immune
defense against her child's blood. But a second pregnancy can be tragic. The
mother's antibodies can cross the placenta and terminate the pregnancy.
Fortunately, a substance called Rh-immune globulin, injected into the mother,
can protect the baby.
- Ultrasound. This test uses high-frequency sound waves to visualize the
unborn baby. It's been used for more than 25 years, and it appears to be safe
for both the mother and fetus.
Some of today's obstetricians even have the capability of performing
ultrasound tests right in their offices. The doctor will coat your abdomen
with mineral oil or gel to minimize the loss of ultrasound waves where the
transducer meets the skin. Then she will move the transducer gently and
smoothly over your stomach, allowing the sound waves to pass through into
your abdominal cavity. The waves will bounce back to the transducer, forming
an image that's displayed as a picture on a monitor.
With a vaginal ultrasound, the transducer is placed in the vagina to let the
doctor see the early pregnancy sac and detect any
abnormalities.
An ultrasound examination can detect a pregnancy as early as six weeks after
your last menstrual period and show the baby's movements at approximately 12
weeks of gestational age.
Extra test for older moms-to-be
- Amniocentesis. This test of the fluid that surrounds your baby detects
chromosomal and other genetic disorders, such as Down syndrome, hemophilia,
and sickle-cell anemia. It usually is performed on women over 35 when they're
15 to 16 weeks pregnant, and on women who have an abnormal triple-screen
result. The procedure is done by inserting a long, thin needle through the
abdominal wall to remove a sample of amniotic fluid. This fluid then is
genetically studied in the laboratory.
Also see:
- First Trimester Doctor Visit
- Third Trimester Doctor Visit
- Prenatal Genetic Testing
©Studio One Networks
The content on these pages is provided as general information only and should not be substituted for the advice of your physician.
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