AssessmentsRoutine prenatal care: Clinical practice
USMLE® Step 1 style questions USMLE
USMLE® Step 2 style questions USMLE
A 35-year-old woman, gravida 2, para 1, at 40 weeks gestation, comes to the hospital in labor. Her past medical history is significant for diabetes, which she has controlled with insulin during this pregnancy. Her pregnancy has been otherwise unremarkable. A baby boy is born via a spontaneous vaginal delivery. Physical examination shows he weighs 4.5-kg (9-lb), pulse is 140/min, respirations are 40/min, and he has good oxygen saturation on room air. His left arm is pronated and medially rotated. He is unable to move it away from his body. The infant’s right arm functions normally and he is able to move his wrists and all 10 digits. Which of the following nerve roots were most likely damaged during delivery?
Content Reviewers:Rishi Desai, MD, MPH
Prenatal care refers to evaluations that can be done during pregnancy, to assess maternal and fetal health, and intervene when possible to ensure the birth of a healthy baby with minimal risk for the mother. Prenatal care also includes preconception counseling, which seeks to identify a spectrum of social, behavioral, environmental, and biomedical risks to a woman's fertility and pregnancy outcome with the goal of reducing these risks through education, counseling, and appropriate intervention. Now, pregnancy consists of three trimesters, the first lasting for the first 12 weeks of pregnancy, the second between weeks 13 and 27, and the third from weeks 28 to 40, and during each of these trimesters, the obstetrical consult focuses on different aspects of maternal and fetal health. Prenatal visits are usually done every 4 weeks until week 28, every two weeks from week 28 to 36, and then weekly until delivery.
So, the initial prenatal visit may occur either when the individual suspects they are pregnant, or because they wish to conceive in the near future. No matter the case, at the initial prenatal visit, the history should be focused on obstetrical history, family history, and identifying any potential risks during pregnancy.
The obstetrical history comprises of gravidity, parity and abortions. Gravidity, or G, means the number of times the individual has been pregnant so far, including the current pregnancy. Parity, or P, refers to the number of times the individual has carried the pregnancy to a viable gestational age - meaning more than 24 weeks. Finally, abortions, or A, refers to the number of pregnancies that were lost for any reason. So, for example, if the individual is currently pregnant, has been pregnant once before, and that pregnancy resulted in a live birth at 38 weeks, you’d say that as Gravida 2, Para1, Abortions0, or G2P1A0. Alternatively, if that previous pregnancy had resulted in a miscarriage at 12 weeks, you’d say that as G2P0A1.
Also, a detailed family history with a focus on genetic conditions should also be obtained. In some individuals, genetic counselling and genetic carrier screening is indicated before conception. For example, when there’s a strong family history of cystic fibrosis, or sickle cell disease, individuals can benefit from genetic testing to see if they and/or their partner have the mutation, and genetic counselling could help them make the best reproductive decision. Genetic counselling is also recommended in inbred families, as autosomal recessive disorders are more frequent in these situations.
The rest of the history focuses on identifying and correcting any potential risks, such as chronic medical problems, like diabetes, hypertension, or epilepsy, mental health disorders, like depression, and use of medications known to be teratogenic, such as valproic acid, isotretinoin, or some dietary supplements. Information about lifestyle factors, like nutrition, exercise, and the use of tobacco, alcohol, or illicit drugs, and environmental concerns, such as mercury, lead or pesticide exposure at home or at work should also be assessed. Finally, social concerns, like the possibility of domestic abuse, as well as other potential barriers to care, like remote living and economic constraints, should be identified and addressed.
Core interventions that can be done to minimize maternal and fetal risk following this step are to stop teratogenic medications, like isotretinoin, or switch to a less harmful alternative in case of chronic health conditions. For example, individuals with hypertension, antihypertensives can be used during pregnancy include labetalol, methyldopa or calcium channel blockers like nifedipine. Seizure control in individuals with epilepsy can be achieved with lamotrigine or levetiracetam, which provide adequate seizure control without teratogenic risk. And in individuals with diabetes, oral medications like glyburide or metformin are indicated, or the individual can switch from oral medications to insulin.
Finally, folic acid supplementation with 0.4 milligrams per day is indicated to prevent neural tube defects, or NTDs, in the fetus. This can be done as early as 3 months preconception, but if the initial prenatal visit occurs when the individual is already pregnant, supplementation should start on the day of the visit, and continue throughout the pregnancy. In individuals who are at higher risk of having a child with NTDs, like those who have had a previous pregnancy with NTDs, a family history of NTDs, or those who are using valproic acid, higher doses, of up to 4 milligrams per day are recommended for the first 12 weeks of pregnancy, and the dose can be lowered to 0.4 milligrams for the rest of the pregnancy.
Next, a physical exam and a laboratory evaluation should be done in both a preconception setting, and if the individual suspects they are pregnant. The body mass index, or BMI, should also be calculated, and weight loss or weight gain should be recommended in individuals with a BMI over 25, or, respectively, under 18.5.
The general physical exam focuses on the heart, breasts, thyroid, lungs and abdomen, as well as blood pressure measurement, to screen some of the most common conditions that can affect pregnancy outcome - like hypertension, thyroid disorders, or genital issues.
The laboratory evaluation comprises of establishing a baseline hemoglobin and hematocrit, determining the individual’s blood group and Rh status, and screening for infections and, in some cases, screening for other diseases that could have an adverse impact on the fetus, like diabetes. Specifically, a blood sample is taken to screen for infections like HIV, syphilis and viral hepatitis, and to document immunity against diseases like rubella and varicella If a sexually transmitted infection is diagnosed, treatment should be initiated immediately. Likewise, if there are low IgG antibody titers against rubella virus and varicella zoster virus, vaccination should be done before pregnancy - that’s because these are live attenuated vaccines, and they may cause adverse effects to the fetus if given during pregnancy. Additionally, pregnancy should be postponed for 1 to 3 months following vaccination. If low antibody titers are found during pregnancy, vaccination is postponed until after the pregnancy.
Finally, screening for diabetes, with a fasting blood glucose level and glycosylated hemoglobin, is recommended in individuals with risk factors for diabetes, like age over 40, a body mass index greater than 25 kg per m2, a previous HbA1c level in the prediabetes range, or a history of dyslipidemia and hypertension.
A urine sample should also be sent for urinalysis and urine culture, to rule out asymptomatic bacteriuria or a urinary tract infection, both of which are common during pregnancy and should be treated if found.
A full pelvic exam should be done, including an ultrasound to look for any anatomic abnormalities, like uterine fibroids, that may complicate pregnancy, as well as a pap smear to screen for cervical cancer, if one hasn’t been done in the past 3 years. Cervical swabs are also taken to screen for chlamydia and gonorrhea. In individuals who suspect they are pregnant, like if they missed their last menstrual period, or they’ve had a positive urine pregnancy test at home, pregnancy should be confirmed with a urine pregnancy test and a transvaginal ultrasound. The earliest visible sign of pregnancy is the presence of an anechoic gestational sac - which looks like a tiny black bubble, and can be detected as early as 3 to 5 weeks after the last missed period.
Then, the estimated date of delivery, or EDD, should be calculated based on the first day of the last menstrual period, or LMP. There are a lot of apps and online calculators that do this for you, but a simple way to calculate it yourself is to use Naegele’s rule, which says that the EDD is the first day of the LMP, plus one year, minus 3 months, plus 7 days. All this math adds up to about 280 days of gestation - so for example, if the first day of the LMP was May 4th 2019, the estimated date of delivery is: May 4th 2019, plus 1 year, so May 4th, 2020, minus 3 months, so February 4th, and plus 7 days. So the EDD is February 11th, 2020. In individuals with irregular menses, or if the first day of the last menstrual period is unknown, the ultrasound can determine the gestational age, based on the crown to rump length - which means how long the embryo is. Then, the gestational age can be used to determine the estimated date of delivery. The ultrasound can also distinguish between single and multiple gestations, and rule out ectopic pregnancy, which is when the fetus implants somewhere other than the uterine cavity, most frequently in the fallopian tube, and a molar pregnancy, which results from errors in normal fertilization, and leads to the formation of an abnormal placenta, and no fetus.
Ok, now, aside from genetic carrier screening, there are other tests that can be done to screen for fetal aneuploidies, which means chromosome number abnormalities. The most common aneuploidies are Down syndrome, Edwards syndrome, and Patau syndrome, which are also called trisomy 21, 18 and 13.
During the first trimester, the combined test can be done, usually between weeks 10 and 13. This test includes an ultrasound nuchal scan, or nuchal translucency scan, which measures the sonographic thickness of the fluid under the fetus’s neck, and measuring serum levels of pregnancy-associated plasma protein A, or PAPP-A levels, for short, and serum levels of free beta hCG. Based on this test, the risk category is established for each of the aneuploidies. When nuchal translucency, or NT, for short, is very large, more than 4 millimeters, and PAPP-A levels are very low, and serum free beta hCG is high, that means high risk for Down syndrome. When nuchal translucency is very increased, PAPP-A levels are very low and free beta hCG is low, that’s high risk for trisomy 18. Finally, when nuchal translucency is increased, but not quite as much as with Down’s, and PAPP-A and free beta hCG levels are very low, and low, respectively, that’s high risk for trisomy 13.
During the second trimester, screening was classically done with the triple test, which measured serum levels of serum alpha-fetoprotein, of AFP, unconjugated estriol, or uE3, and free beta-hCG. Nowadays, the quadruple test is performed, which is the same as the triple test, but also includes inhibin A levels. The quadruple test is usually done between weeks 15 and 18. When AFP and uE3 are decreased, while inhibin A and free beta HCG are increased, that’s high risk for Down syndrome. When AFP is low, uE3 and free beta hCG are very low, and inhibin A levels are unchanged, that’s high risk for trisomy 18. Finally, when all levels are unchanged, that could mean trisomy 13 in the context of high risk first trimester screening results.
Now, an alternative to these classic screening tests is the assessment of cell-free DNA in a maternal blood sample. This is basically fetal DNA from mom’s blood - and can be analyzed as early as 10 weeks of gestation to determine the risk of fetal aneuploidies.
It’s important to note that these tests don’t diagnose an aneuploidy, but rather establish if there’s a high risk for it. Regardless of which screening test was done, an invasive procedure like chorionic villus sampling between weeks 10 and 13, or amniocentesis between weeks 15 and 18, with subsequent fetal karyotyping is considered the gold standard diagnostic test, and it’s recommended for individuals in the high risk group, especially those who are considering termination of pregnancy in case of a positive result. Of note, these invasive procedures come with a risk of fetal loss between 1 in 300 and 1 in 200.
Finally, a special mention regarding screening tests is that high maternal serum AFP levels could suggest a high risk of neural tube defects in the fetus. These include anencephaly, which is when a large part of the brain, skull and scalp doesn’t form during fetal development, encephalocele, which is when the brain and the meninges herniate through an opening in the skull, and spina bifida, which is when the vertebrae and the membranes around the spinal cord don’t close, or close incompletely during fetal development.