Summary
Prenatal care is the health care provided throughout a pregnancy; it is aimed at optimizing maternal and fetal outcomes. Prenatal visits allow high-risk pregnancies to be identified and are used to monitor maternal health and fetal development. After an initial visit (usually in the first trimester), follow-up prenatal visits generally occur once monthly until 28 weeks' gestation, twice monthly between 28 and 36 weeks, and weekly after 36 weeks. Components of prenatal visits include evaluation of the medical history, physical and gynecological examinations, laboratory testing, and ultrasonography. More frequent assessment may be indicated in pregnancies deemed high-risk for the fetus or pregnant individual. This article covers the general principles of prenatal care, including recommended screening studies, elective prenatal genetic screening, fetal surveillance, and patient education.
For other aspects of peripartum care, see also “Preconception care,” “Normal labor and delivery,” “Abnormal labor and delivery,” and “Postpartum visit.” For prenatal care for transgender and nonbinary individuals, see “Pregnancy in transgender individuals.”
General principles
Diagnosis of pregnancy is covered in “Pregnancy.”
Ethics of prenatal care [1][2]
- Healthcare providers have an ethical obligation to obtain informed consent from patients for prenatal care.
- Patients may refuse recommended screening or procedures.
- Use shared-decision making when discussing treatment options with patients in order to:
- Ensure a safe environment for asking questions and addressing concerns
- Encourage voluntary, informed decisions
- Avoid miscommunication
Because pregnancy outcomes are unpredictable, pregnant individuals should be informed about the potential need for obstetric interventions (e.g., cesarean delivery) and encouraged to discuss any concerns ahead of time. [1]
Legal aspects of prenatal care
- Follow state laws pertaining to induced abortion and mandatory reporting (e.g., of maternal substance use). [3]
- Regardless of state law, EMTALA allows for provision of emergency abortion to stabilize a patient. [4]
- In accordance with EMTALA, patients in active labor cannot be turned away.
- See also “Principles of medical law and ethics.”
Frequency of prenatal visits [1]
- Visit frequency should be tailored to maternal needs and pregnancy risk factors. [1][5]
- Typical timing of routine prenatal visits for an uncomplicated pregnancy:
- Initial visit: usually in the first trimester [5]
- Follow-up visits [1]
- Every 4 weeks: from initial visit to 28 weeks' gestation
- Every 2 weeks: from 28 to 36 weeks' gestation
- Weekly: from 36 weeks' gestation until delivery (see also “Postterm pregnancy”)
High-risk pregnancies generally warrant more than the usual number of follow-up visits for maternal and/or fetal surveillance. [1]
Monitoring fetal growth and wellbeing
General principles [6][7]
- Assess growth via physical examinations and ultrasound (US).
- In high-risk pregnancies or if there is concern for fetal well-being, consider:
- Specialized ultrasound
- Antepartum fetal surveillance
Gestational age and estimated date of delivery [1][8]
- Determination of gestational age and estimated date of delivery is important for:
- Guiding the timing of prenatal screening and fetal monitoring
- Managing postterm pregnancy
- Methods of pregnancy dating include one or both of the following:
-
Naegele rule
- Expected date of delivery (due date) is estimated as the first day of the LMP + 280 days [8][9]
- May be unreliable in patients with uncertain LMP or irregular menstrual cycles
-
Ultrasound: should be performed to estimate gestational age if LMP is unreliable [1][10]
- First-trimester US: estimation is based on crown-rump length
- Second-trimester US: estimation is based on fetal biometric parameters
-
Naegele rule
- For a gestational age discrepancy between ultrasound and LMP, use EDD determined by ultrasound if: [8]
- > 5 days gestational age discrepancy in gestations < 9 weeks
- > 7 days gestational age discrepancy in gestations 9–13 weeks
Symphysis-fundal height measurement [6]
- Measured from the top of the pubic symphysis to the top of the uterus.
- Fundal height can be used to monitor fetal growth or to roughly estimate gestational age in an emergency. [11]
- Screen all patients > 24 weeks' gestation for fetal growth abnormalities using symphysis fundal height. [6]
- From 20 weeks, fundal height in centimeters should roughly approximate the week of gestation. [12]
- If comparison of fundal height and gestational age suggests growth abnormality , perform an ultrasound. [10]
| Fundal height and gestational age[11][13] | |
|---|---|
| Week of pregnancy | Fundal height during pregnancy |
| 12th | Just above the symphysis |
| 16th | Between the symphysis and navel |
| 20– 24th | Navel |
| 32nd | Between the navel and xiphoid |
| 36th | Peak: at the costal arch |
| 40th | Two finger widths below the costal arch |
Prenatal ultrasound
Standard examinations [10]
- First-trimester US is performed to estimate gestational age and assess for complications (e.g., suspected ectopic pregnancy).
- A second-trimester US is recommended between 18–22 weeks to assess fetal anatomy.
- For more information, see “First-trimester ultrasound” and “Second-trimester ultrasound.”
Additional ultrasounds [10][14]
Additional US may be performed for further evaluation of potential pregnancy complications, follow-up of abnormal US, and for imaging guidance during procedures.
-
US-guided procedures
- Genetic testing: guided needle placement in amniocentesis or chorionic villus sampling
- Cervical cerclage placement: in cervical insufficiency
- External cephalic version: to turn a breech baby before labor
- Limited US: imaging of a specific area based on clinical concern
-
Specialized US: detailed US evaluation performed to further evaluate for fetal abnormalities in patients with concerning findings on clinical history and/or examination, laboratory testing, and/or prior ultrasound examination
- Nuchal translucency: as part of prenatal genetic testing
- Fetal echocardiography: in suspected congenital heart disease [15]
- Biophysical profile: if there is concern for fetal well-being
- Transvaginal measurement of cervical length: if there are concerns for preterm labor
- Doppler ultrasound; : for suspected abnormalities in fetal/placental perfusion or suspected fetal deformities [16][17]
| Overview of maternal and fetal vessel doppler ultrasound [7][16] | ||
|---|---|---|
| Vessel | Indication for imaging | Pathological findings |
| Maternal uterine artery |
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| Umbilical artery |
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| Fetal middle cerebral artery |
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Only obtain prenatal ultrasounds when clinically indicated, using the minimum acoustic output necessary as per the As Low As Reasonably Achievable (ALARA) principle. [14][21]
High-risk pregnancies [1][19][22]
- Any pregnancy with risk factors for adverse pregnancy outcomes (e.g., maternal age, preexisting medical and gynecological conditions, fetal-placental factors, pregnancy complications)
- Prenatal care includes:
- Assessment of risk factors for adverse pregnancy outcomes at each visit
- Increased monitoring: e.g., clinical monitoring, antepartum fetal surveillance, prenatal ultrasound
- Referral to specialists (e.g., maternal-fetal medicine, neonatology)
- Development of birth and other care plans (e.g., treatment of medical complications, post-partum care)
- See “Management of high-risk pregnancies” for details.
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Illustration of expected fundal height throughout pregnancy
At 12 weeks' gestation, the fundus is usually just emerging from the pelvic brim. By 20 weeks, it is palpable at the height of the umbilicus. The fundus is highest at 36 weeks' gestation at the costal arch; at 40 weeks' gestation, it usually drops to two finger widths below the costal arch.
© AMBOSS
First-trimester care
General principles
- The goal of the initial prenatal visit is to determine gestational age, identify and manage risk factors, and educate patients. [1]
- The initial prenatal visit usually occurs in the first trimester, unless there has been late entry into prenatal care.
- Components of first-trimester care may occur prior to the initial prenatal visit.
- Some aspects of first-trimester care, e.g., prenatal genetic testing, may require multiple visits.
Initial prenatal visit [1][23]
- Assess patient's feelings about the pregnancy; if the pregnancy was not planned see “Unintended pregnancy”.
- Review prior preconception counseling, if any was given.
- Perform a comprehensive clinical assessment, including history and physical examination.
- Take a medication history; if possible, stop or change medications contraindicated in pregnancy.
- Screen for comorbid physical and mental health conditions.
- Inquire about risk factors for lead exposure and send a lead level if any are present. [1][24]
- Assess for risk factors for adverse pregnancy outcomes; manage as high-risk pregnancy if present.
- Determine estimated date of delivery (EDD) and perform first-trimester ultrasound, if indicated (see “Gestational age and estimated date of delivery”).
- Offer prenatal aneuploidy and genetic carrier screening (see “Prenatal genetic testing”).
- Assess vaccination status and administer vaccines recommended in pregnancy, including: [25]
- Inactivated seasonal influenza vaccine
- COVID-19 vaccine
- Provide prenatal patient education.
- Arrange follow-up visits and referrals as needed.
Live attenuated influenza, varicella, and MMR vaccine are contraindicated during pregnancy; delay administration until after delivery. [25]
History and physical examination [1][5]
- Personal medical history, including obstetric history (e.g., miscarriage, preterm delivery, preeclampsia)
-
Family history: maternal and paternal [26]
- Medical conditions (e.g., early-onset heart disease, cancer)
- Genetic or congenital abnormalities
- Poor obstetrical outcomes (e.g., preeclampsia, preterm delivery)
-
Complete physical examination including: [1][23]
- Height and weight [1][27]
- Blood pressure to screen for hypertensive pregnancy disorders [28]
- Breast examination [23]
- Pelvic examination
- Auscultation of fetal heart tones at > 10 weeks' gestation [23]
- Oral health assessment
Screening for medical comorbidities
The following laboratory studies are recommended during the initial prenatal visit to screen for conditions associated with negative obstetric and fetal outcomes.
All patients
| Recommended initial prenatal screening tests [1][5] | ||
|---|---|---|
| Tests | Management of abnormal results | |
| Complete blood count to screen for anemia and thrombocytopenia [29] |
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| Blood typing (ABO and rhesus) and RBC antibody screening to prevent hemolytic disease of the newborn [31][32][33] |
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| Urine dipstick to screen for proteinuria [1] |
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| Urine culture to screen for asymptomatic bacteriuria [35] |
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| Screening for STIs and bloodborne pathogens | HIV testing [1] |
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| HBV serology |
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| Anti-HCV antibody [37][38][39] |
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| Prenatal syphilis screening [40] |
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HIV screening in pregnancy is opt-out; inform individuals an HIV test will be sent as part of the routine prenatal studies unless they decline testing. [1]
Patients with select indications
| Prenatal screening studies for patients with select indications | ||
|---|---|---|
| Indications | Management of abnormal results | |
| Rubella antibody |
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| Varicella antibody |
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| TSH |
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| Prenatal chlamydia screening (using NAAT) [45][46] |
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Prenatal gonorrhea screening (using NAAT) [45][46] |
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| Pap smear and/or HPV DNA testing |
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| Screening tests for latent TB [1][5] |
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| Hyperglycemia testing [1][47][48] |
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Psychosocial screening
Psychosocial assessments should be performed for all pregnant individuals in the first trimester.
| Recommended prenatal psychosocial screenings [1] | ||||
|---|---|---|---|---|
| Method(s) | Repeat screening | Management of patients with positive screening results | ||
| Peripartum depression [49][50][51] |
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| Anxiety [51] |
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| Bipolar disorder [51] |
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| Intimate partner violence (IPV) [55][56] |
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| Substance use in pregnancy [1] | Nicotine and tobacco [58] |
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| Alcohol [59] |
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| Drugs [61] |
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Social determinants of health [62] |
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This calculator is provided by the third-party QXMD, who is solely responsible for its content and functionality.
Created by: QxMD.
This calculator is provided by the third-party QXMD, who is solely responsible for its content and functionality.
Created by: QxMD.
This calculator is provided by the third-party QXMD, who is solely responsible for its content and functionality.
Created by: QxMD.
This calculator is provided by the third-party QXMD, who is solely responsible for its content and functionality.
Created by: QxMD.
This calculator is provided by the third-party QXMD, who is solely responsible for its content and functionality.
Created by: QxMD.
First-trimester ultrasound
Indications [10][14]
- Confirmation of pregnancy and its location (i.e., exclusion of ectopic pregnancy and gestational trophoblastic disease)
- Determination of EDD
- Evaluation for multiple gestation
- Assessment of fetal cardiac activity
- Evaluation of maternal symptoms (e.g., pelvic pain, vaginal bleeding) or abnormalities on examination (e.g., masses, structural uterine abnormalities)
- Evaluation of for fetal anomalies (e.g., anencephaly)
- Measurement of nuchal translucency as part of aneuploidy screening
- Provision of imaging guidance during procedures (e.g., chorionic villus sampling)
Estimating gestational age via ultrasonography is most accurate when performed in the first trimester. [14]
Modalities [10][14]
- Transvaginal ultrasound
- Transabdominal ultrasound
Components [10][14]
- Visualization of location and contents of gestational sac(s).
- Determination of number of fetuses.
- Evaluation of the embryo or fetus, including:
- Cardiac activity
- Crown-rump length for estimating gestational age [8]
- Anatomy as appropriate for gestational size
- Nuchal translucency in patients desiring aneuploidy screening
- Evaluation of maternal pelvic anatomy (e.g., uterus, adnexa, rectouterine pouch)
Transabdominal ultrasound of a pregnant patient
A dichorionic diamniotic twin pregnancy in the first trimester is seen. The triangular appearance of the chorion insinuating between layers of the intertwin membrane resembles the Greek letter lambda (λ; blue overlay). The lambda sign (also known as the “twin peak sign”) strongly suggests a dichorionic twin pregnancy.
Green overlay: placenta; red overlay: uterus; yellow overlay: fetus
© AMBOSS
Ultrasound pelvis (gravid uterus; CRL measurement)
The crown-rump length (CRL) is measured as 65 mm, which correlates with an estimated gestational age of 12 weeks 6 days.
CRL is the greatest length measured in a straight line from the top of the embryonic or fetal head to the bottom of the torso (yellow markings). CRL excludes the yolk sac and extremities. First trimester CRL is considered the most accurate measurement for determining gestational age. It is used up to a length of 84 mm, beyond which a combination of biometric parameters (biparietal diameter, head circumference, abdominal circumference, femur length) should be employed for ultrasound dating.
Source: “CRL Crown rump length 12 weeks ecografia” by Dr. W. Moroder, Wikimedia Commons, licensed under CC BY-SA 3.0. Modifications: Text at the top has been removed.
Ultrasound pelvis (transvaginal; transverse plane)
A gestational sac (red line) within the uterus contains an embryo with a crown-rump length of 11.7 mm (green overlay), indicating normal development.
Source: © IMPP
Prenatal genetic testing
Approach [65][66]
-
Offer all patients genetic carrier screening and testing for chromosomal abnormalities.
- Screening should preferably be offered at the initial prenatal visit.
- Provide counseling prior to prenatal genetic testing to all patients.
- For patients interested in carrier screening, see “Genetic carrier screening.”
- For patients interested in testing for chromosomal abnormalities, discuss options for both screening and diagnostic testing:
- Noninvasive aneuploidy screening; (e.g., through measurement of maternal serum biomarkers and ultrasound; markers, or cell-free fetal DNA testing)
- Invasive genetic testing (amniocentesis or chorionic villus sampling)
- Offer appropriate follow-up genetic counseling and/or testing depending on results.
Counseling prior to prenatal genetic testing [1][65][67]
- Inform patients that all prenatal genetic testing is voluntary.
- Explain the differences between screening and diagnostic testing
- Discuss the patient's risk factors for fetal genetic abnormalities.
- Discuss the benefits of early identification of disorders: [65]
- Potential for prenatal treatment
- Optimizing outcomes by referral to appropriate specialists and location for delivery
- Possibility of pregnancy termination
- Review all testing options and associated risks and benefits.
- Use shared decision-making to decide whether to perform a test and the specific testing to perform.
- Inform patients about follow-up options for a positive test result.
Inform patients that a negative screening test result for fetal chromosomal abnormalities does not guarantee that a fetus has no genetic abnormalities. [68]
Risk factors associated with fetal genetic abnormalities [65]
- Fetal structural abnormality on ultrasound
- Increased maternal age [65]
- Increased paternal age
- Parental genetic abnormalities
- Previous child with aneuploidy [65]
Noninvasive fetal aneuploidy screening tests [1][66][69]
- For patients who elect to have screening for chromosomal abnormalities, select a screening test based on gestational age and patient preference. [66]
- Communicate results of screening tests to patients and arrange follow-up as necessary.
- No abnormalities on screening: Inform the patient the risk of a genetic abnormality is reduced.
- If screening results are abnormal, offer all of the following:
- Genetic counseling
- Invasive prenatal diagnostic testing (e.g., chorionic villus sampling, amniocentesis) [68]
- Second-trimester ultrasound at 18–22 weeks' gestation
One-step screening tests
| Overview of one-step screening tests for fetal chromosomal abnormalities [66] | |||||
|---|---|---|---|---|---|
| Test | Timing [66] | Components | Interpretation [66] | ||
| Cell-free fetal DNA testing (cffDNA) |
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| Sonographic nuchal translucency (NT screen) [66][70] |
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| First-trimester combined screening |
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| Triple screen test and quad screen test [66] |
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Cell-free fetal DNA testing can be performed in any trimester of pregnancy after ∼ 10 weeks' gestation. [66]
Multi-step screening tests
| Overview of multi-step screening tests for fetal chromosomal abnormalities [66] | ||||
|---|---|---|---|---|
| Test | Timing [66] | Components | Interpretation [66] | |
| Integrated screen [1] |
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| Sequential integrated screening [66] |
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Interpretation of test results
Results of first-trimester combined screening test
| Overview of first-trimester combined screening test results [71][72] | |||
|---|---|---|---|
| Condition | HCG | PAPP-A | Nuchal translucency |
| Trisomy 21 | ↑ | ↓ | ↑ |
| Trisomy 18 | ↓ | ↓ | ↑↑ |
| Trisomy 13 | ↓ | ↓ | ↑ |
On US examination of fetuses with aneuploidy, increased nuchal translucency is usually visible in the first trimester and a thickened nuchal fold is visible in the second trimester. [73]
Results of quad screening and triple screening
| Overview of quad and triple screening test results [71] | ||||
|---|---|---|---|---|
| Condition | HCG | AFP | Estriol | Inhibin A (quad test only) |
| Trisomy 21 | ↑ | ↓ | ↓ | ↑ |
| Trisomy 18 | ↓ | ↓↓ | ↓↓ | ↔︎ or ↓ |
| Neural tube defects | ↔︎ | ↑ | ↔︎ | |
| Abdominal wall defects | ||||
An abnormal maternal serum AFP may be due to inaccurate estimation of fetal gestational age. [74]
Invasive prenatal diagnostic testing [65]
-
Invasive prenatal diagnostic testing is typically performed through chorionic villus sampling (CVS) or amniocentesis.
- CVS is performed in the first trimester, while amniocentesis can be performed in the second or third trimester.
- Cordocentesis to obtain a sample of fetal blood may be performed in select cases.
-
Chromosomal testing of specimens collected through diagnostic procedures may include: [65]
- DNA microarray
- Karyotyping
- Fluorescence in situ hybridization
- Direct detection of specific DNA mutations
| Overview of invasive prenatal diagnostic tests [65] | |||
|---|---|---|---|
| Chorionic villus sampling (CVS) | Amniocentesis | Cordocentesis [75][76] | |
| Timing |
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| Procedure |
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| Indications |
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| Complications [65][75] |
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Ultrasound of a fetal head and neck during the first trimester (sagittal view; nuchal translucency scan)
There is an increased depth of the nuchal translucency (yellow cursors; green overlay). The nasal bone is also absent.
These findings are consistent with Down syndrome.
Source: “Nuchal edema in Down Syndrome Dr. W. Moroder” by Dr. W. Moroder, Wikimedia Commons, licensed under CC BY-SA 3.0. The supplementary image with overlays of relevant areas was adapted from the image mentioned above and licensed under CC BY-SA 3.0.
Ultrasound of a fetal head and neck during the first trimester (sagittal view)
There is an anechoic region of subcutaneous fluid collection in the posterior portion of the neck (green overlay) measuring 1.57 mm.
This value is used to calculate the statistical risk for fetal chromosome disorders. A nuchal translucency measurement >3 mm is considered abnormal.
© AMBOSS
Ultrasound-guided chorionic villus biopsy (left): chorionic tissue is collected with either a needle inserted through the abdominal wall (transabdominal) or via a catheter inserted into the uterus (transvaginal).
Ultrasound-guided amniocentesis (right): a sample of amniotic fluid and sloughed fetal tissue is taken with a needle inserted through the abdominal wall.
© AMBOSS
Second-trimester care
Routine prenatal visits in the second trimester are focused on maternal-fetal surveillance, symptom management, and prevention and management of pregnancy complications.
Components [1][23]
- Routine clinical assessment, including:
- Assessment for symptoms of pregnancy complications
- Focused physical examination
- Obstetric ultrasound for fetal anatomy screening. [10]
- Screening for anemia and gestational diabetes at 24–28 weeks' gestation.
- COVID-19 vaccine and inactivated influenza vaccination, if not administered earlier in pregnancy
- Prenatal counseling, including labor precautions
- Assessment for risk factors for adverse pregnancy outcomes; manage as high-risk pregnancy if present.
In uncomplicated pregnancies dated with a reliable last menstrual period, a single obstetric ultrasound may be performed, preferably at 18–22 weeks' gestation, to evaluate fetal anatomy and the EDD. [66][80]
Routine prenatal clinical assessment [1][23]
- Ask all patients about:
- Signs of pregnancy complications (e.g., vaginal bleeding or contractions, symptoms of preeclampsia, leakage of fluid) [5]
- Awareness of fetal movement [1][5][81]
- Perform physical examination, including:
- Weight
- Blood pressure to screen for hypertensive pregnancy disorders [28]
- Fundal height measurement : to monitor fetal growth after 24 weeks' gestation [5][23]
- Auscultation of fetal heart rate: to confirm fetal heartbeat [1][23]
- Consider urine dipstick analysis. [1][23]
Pregnant individuals often begin to feel fetal movement (i.e., quickening) between 18 and 19 weeks' gestation in the first pregnancy and between 16 and 18 weeks in subsequent pregnancies. [23]
In most cases, the EDD should not be changed in the second or third trimester if the EDD was established by an ultrasound performed in the first trimester. [8]
Second-trimester laboratory studies
Laboratory studies are performed between 24–28 weeks; screening may therefore take place in the second or third trimester.
| Recommended laboratory screening studies at 24–28 weeks' gestation | |||
|---|---|---|---|
| Test | Indication | Purpose | Management of abnormal results |
| CBC [29] |
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| Oral glucose tolerance tests [47][48] |
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Second-trimester ultrasound
Fetal anatomy scan [10][14][82]
General principles
- A scan offered at 18–22 weeks' gestation to all patients to assess for:
- Fetal anomalies, e.g., abnormal growth or anatomic abnormalities [10]
- Estimation of gestational age (if not already performed) [10][78]
- If possible, the anatomy scan should be offered well in advance of the legal limit for pregnancy termination. [82]
Modalities [10][14]
- Transabdominal ultrasound: usually initial modality
- Transvaginal or transperineal ultrasound: if the transabdominal approach is suboptimal for evaluation
Components
- Evaluation of fetus, including:
- Number of fetuses
- Fetal presentation
- Cardiac activity
- Anatomy survey, including assessment for structural abnormalities and sex
-
Fetal biometric parameters ; [14]
- Biparietal diameter
- Fetal femoral length
- Abdominal circumference
- Head circumference
-
Evaluation of amniotic fluid volume
-
Deepest vertical pocket (DVP): preferred over AFI for multiple gestation pregnancies and assessment of oligohydramnios
- Method: The deepest single pocket of fluid with a width of at least 1 cm is measured by ultrasound
- Normal 2–7 cm
- Abnormal: oligohydramnios < 2 cm, polyhydramnios ≥ 8 cm
-
Amniotic fluid index (AFI)
- Method: The uterus is divided into four quadrants, and the DVP measurement in each quadrant is added together to determine the AFI.
- Normal: 8–23 cm
- Abnormal: oligohydramnios < 8 cm, polyhydramnios ≥ 24 cm
-
Deepest vertical pocket (DVP): preferred over AFI for multiple gestation pregnancies and assessment of oligohydramnios
- Evaluation of placenta (e.g., location, appearance, cord insertion)
- Evaluation of maternal pelvic anatomy, including cervix [14][83]
Additional ultrasounds
- Indications include:
- Provide imaging guidance during procedures (e.g., amniocentesis)
- Evaluation of suspected fetal or maternal abnormalities
- Potential obstetric emergencies, e.g., vaginal bleeding or premature rupture of the membranes
- See “Prenatal ultrasound.”
Ultrasound of 21-week fetus (sagittal plane)
A myelomeningocele sac (green overlay) is identified at the lumbar region. The sac contains anechoic fluid and some solid neural elements.
T: thorax
Source: “Spina bifida lombare sagittale” by Dr. W. Moroder, Wikimedia Commons, licensed under CC BY-SA 3.0. The supplementary image with overlays of relevant areas was adapted from the image mentioned above and licensed under CC BY-SA 3.0.
Ultrasound fetal (BPD and HC)
Biparietal diameter (BPD) is measured at the level of the thalami on an axial plane image taken perpendicular to the central axis of the head. The hemispheres should appear symmetric and the cerebellum should not be in the image. Calipers may be placed from the outer cortex of the parietal bone in the near field to the inner cortex of the parietal bone in the far field or from outer cortex to outer cortex; placement will vary with the growth chart used.
Head circumference (HC) is measured around the outer table of the skull.
Created by: Lalash Bexten. Modifications to original image: deleted patient data.
Fetal ultrasound (femur length)
Femur length should be measured with the ultrasound beam perpendicular to the femoral diaphysis, such that shadowing from the bone evenly includes both ends. The measured ends should be blunted to only include the diaphysis; the proximal and distal epiphyses and pointed distal femoral secondary ossification center (when visible) should not be included in the measurement.
Created by: Lalash Bexten. Modifications to original image: patient data deleted.
Ultrasound fetal (abdominal circumference)
Abdominal circumference (AC) is measured by tracing the skin surface on an axial image taken at the level of the liver, with the fetal stomach (S) and umbilical portion (U) of the left portal vein visible. Identification of three ossification centers (green overlay) of the spine helps confirm the correct, cross-sectional plane. The abdomen should appear circular in shape.
Created by: Lalash Bexten. Modifications to original image: deleted patient data.
Illustration of ultrasound fetal (deepest vertical pocket or single deepest pocket method)
A measurement < 2 cm indicates oligohydramnios, while a measurement ≥ 8 cm indicates polyhydramnios.
© AMBOSS
The amniotic fluid index is calculated by dividing the uterus into quadrants and adding together the depth of the deepest vertical pocket of fluid in each quadrant.
© AMBOSS
Third-trimester care
Third-trimester care is focused on monitoring maternal and fetal well-being and preparing for delivery.
Components
- Monitoring of fetal growth with symphysis-fundal height and ultrasounds as indicated
- Assess for risk factors for adverse pregnancy outcomes; manage as high-risk pregnancy if present.
- Screening for hypertensive pregnancy disorders [28]
- Measures to prevent neonatal infection
- Perform third-trimester STI screening, if indicated.
- Offer seasonal influenza vaccination and/or COVID booster, if due.
- 27–36 weeks' gestation: Provide Tdap. [84]
- 32–36 weeks' gestation: Give respiratory syncytial virus vaccine if not given in a prior pregnancy. [85][86]
- 36–37+6 weeks' gestation: Perform Group B streptococcus prenatal screening.
- 36 weeks' gestation: For individuals with a history of genital HSV, start suppressive antivirals for HSV in pregnancy. [45][87]
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Screening for rhesus antibody in Rh-negative nonsensitized individuals [31]
- Perform at 28 weeks' gestation.
- Administer Anti-D immunoglobulin as needed.
- See “Management of rhesus-negative individuals without anti-D antibodies” for further information.
- Screening for anemia and gestational diabetes, if not already performed (see “Second-trimester laboratory studies”).
- Preparation for delivery
- Provide counseling related to peripartum care.
- Assess for indications for antepartum fetal surveillance and perform, if indicated.
- From 36 weeks' gestation, use Leopold maneuvers for assessment of fetal presentation. [23]
- Use ultrasound as needed to confirm fetal lie and placental position (see “Prenatal ultrasound”).
In the third trimester, prenatal visits usually increase in frequency to every 2 weeks between 28–36 weeks and weekly thereafter. [1]
Third-trimester screening for sexually-transmitted infections (STI) [45]
| Indications for third-trimester STI screening [1][45] | ||
|---|---|---|
| STI | Indications for screening | Timing |
| Prenatal chlamydia screening |
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| Prenatal gonorrhea screening | ||
| HIV screening |
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| Prenatal syphilis screening [88] |
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| Hepatitis B screening |
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Leopold maneuvers [23][89]
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The Leopold maneuvers consist of four abdominal palpation maneuvers used to determine fetal lie, fetal presentation, and fetal position in utero.
- Use both hands to palpate the uterine fundus, fetal head, and buttocks to assess:
- Fetal lie (longitudinal/oblique/transverse)
- Fundal height
- Place each hand on either side of the maternal abdomen to determine the location of the fetal back.
-
Grasp the lower maternal abdomen above the symphysis to determine the fetal presenting part and if it is engaged.
- In cephalic presentation, the fetal head is felt as hard, round, and ballottable.
- In breech presentation, the buttocks are felt as a soft, less movable structure.
- Facing the mother's feet, use both hands to determine:
- The cephalic prominence
- Fetal attitude (based on the degree of flexion of the fetus's head)
- Use both hands to palpate the uterine fundus, fetal head, and buttocks to assess:
- If fetal malpresentation is suspected or fetal position cannot be accurately determined, proceed to ultrasound. [90][91]
First maneuver: bimanual examination of the fetal position (longitudinal/oblique/transverse) and fundal height;
Second maneuver: bimanual examination of the location of the fetal back;
Third maneuver: one hand grasps above the symphysis to determine if the presenting part is engaged;
Fourth maneuver: bimanual examination of the location of the fetal brow and the degree of flexion of the fetal head
© AMBOSS
© AMBOSS
This malpresentation is characterized by flexed hips and extended knees. The buttocks of the baby are directed towards the birth canal.
© AMBOSS
One of the baby's legs is flexed while the other one is extended and straight up to its head.
© AMBOSS
Both hips and knees are flexed with the feet close to the buttocks.
© AMBOSS
Antepartum fetal surveillance testing
General principles [1][7]
Antepartum fetal surveillance testing is typically performed in the third trimester (at ≥ 32 weeks' gestation) to assess fetal well-being and reduce the risk of adverse fetal outcomes. [7]
Indications for antepartum fetal surveillance [19]
- High-risk pregnancy (e.g., maternal medical conditions or fetal conditions associated with increased risk of fetal hypoxic injury or death)
- Perceived reduction in fetal movement by mother
Modalities [7]
- Options include:
- Kick counts
- Nonstress test (NST)
- Contraction stress test (CST)
- Biophysical profile (BPP)
- Modified biophysical profile
- Doppler velocimetry of the umbilical artery (for suspected fetal growth restriction)
- A combination of modalities may be utilized. [7]
Results and ongoing management
| Overview of management of antepartum fetal test results [7] | ||
|---|---|---|
| Result of test | Next steps | |
| Normal | Resolved indication for testing |
|
| Ongoing indication for testing |
|
|
| Abnormal | Kick count |
|
| NST or modified biophysical profile |
|
|
| CST or BPP |
|
|
Kick counts [7]
- Maternal counting of the number of fetal movements within a particular time period (e.g., 1 or 2 hours).
- Number of kicks reduced compared to prior assessments: Perform additional antepartum surveillance testing.
- Limitations [7]
- No consensus on the optimal duration of monitoring or abnormal number of counts
- Limited evidence monitoring kick counts affects perinatal adverse outcomes.
Nonstress test (NST) [1][7]
NST is a noninvasive test that measures how fetal heart rate (FHR) responds to fetal movements; a rise in fetal heart rate is expected with fetal movement.
Method [7]
- Perform electronic fetal heart rate monitoring over a minimum of 20 minutes.
- Review the FHR tracing for FHR accelerations and decelerations. [7]
-
If no FHR accelerations are observed within the first 20 minutes:
- Perform vibroacoustic stimulation.
- Continue with the NST for another 20–40 minutes.
Interpretation [1]
-
Reactive nonstress test: a normal NST that shows ≥ 2 FHR accelerations over the course of 20 minutes
- If the indication for testing has resolved, offer reassurance; further testing is not required.
- If the indication persists, repeat the test (usually at weekly intervals).
-
Nonreactive nonstress test: an abnormal NST that shows < 2 FHR accelerations over the course of 20 minutes (after at least 40 minutes of monitoring) [7]
- Causes of a nonreactive NST include:
- Fetal sleep (most common)
- Hypoxemia or acidemia
- Neurologic or cardiac abnormalities
- Fetal immaturity [7]
- Maternal drug use
- Next steps: Perform a BPP or CST. [1]
- Causes of a nonreactive NST include:
- Concerning decelerations : Consider further monitoring or delivery.
Contraction stress test (CST) [1][7]
- CST is a test that measures how FHR responds to uterine contractions.
- Can be safely performed, provided there are no contraindications to labor or vaginal delivery. [1][92]
Method
- Perform cardiotocography to assess both FHR and uterine contractions.
- If < 3 contractions lasting at least 40 seconds are observed over 10 minutes, induce contractions using either:
- Nipple stimulation [93]
- IV oxytocin
CST may induce early labor; consider alternative methods of assessing fetal well-being in patients with contraindications to labor or vaginal delivery. [1]
Interpretation [1][7]
- Negative: absence of late decelerations or significant variable decelerations
- Positive
- Late decelerations after ≥ 50 % of contractions
- Consider repeat testing or delivery.
- Equivocal
- Defined as any of the following:
- Intermittent variable decelerations or late decelerations
- Decelerations occurring with uterine tachysystole
- Repeat in 24 hours.
- Defined as any of the following:
- Unsatisfactory
- Tracing uninterpretable or insufficient number of contractions (< 3 in 10 minutes).
- Repeat with an alternative form of contraction stimulation. [94]
Biophysical profile (BPP) [7]
The BPP is a noninvasive test consisting of fetal ultrasound of four specified parameters and NST.
Method [7]
- An ultrasound examination is performed over 30 minutes to assess the following four parameters:
- Fetal movement
- Fetal tone
- Fetal breathing
- Amniotic fluid volume
- An NST is then performed if any ultrasound parameter is abnormal but may be omitted if all are normal.
- Each parameter of the ultrasound examination and the NST is given a score of either 0 (abnormal) or 2 (normal)
| Biophysical profile scoring criteria [1] | |
|---|---|
| Parameter | Normal results (= 2 points) |
| Fetal movement |
|
| Fetal tone |
|
| Fetal breathing |
|
| Amniotic fluid volume |
|
| Nonstress test |
|
Interpretation [1][7]
- The maximum total score on the biophysical profile is 10 (if NST performed) or 8 (if NST not performed).
- Follow-up recommendations vary based on total score and the presence of oligohydramnios.
| Interpretation and follow-up of biophysical profile results | |||
|---|---|---|---|
| Total score | Interpretation | Follow-up | |
| Oligohydramnios absent | Oligohydramnios present | ||
| ≥ 8 points |
|
|
|
| 6 points |
|
|
|
| ≤ 4 points |
|
|
|
Regardless of total biophysical profile score, delivery or close monitoring may be indicated if oligohydramnios is identified. [7]
Modified biophysical profile [1][7]
- Description: NST plus amniotic fluid measurement by ultrasound [95]
-
Method: Use one of two methods of assessing amniotic fluid volume.
- Measurement of the deepest vertical pocket of amniotic fluid
- Amniotic fluid index
-
Interpretation
- A normal result is a reactive NST plus either: [1]
- Deepest vertical pocket of amniotic fluid > 2 cm
- Amniotic fluid index of ≥ 5 cm
- An abnormal result includes any of the following:
- Nonreactive NST
- Deepest vertical pocket of amniotic fluid ≤ 2 cm
- Amniotic fluid index of < 5 cm
- A normal result is a reactive NST plus either: [1]
- Next steps: For abnormal results, obtain a BPP or CST. [7]
Doppler velocimetry of the umbilical artery [7]
- Used to monitor pregnancies with fetal growth restriction
- Assesses diastolic flow velocity of the umbilical artery
- For more information, see:
- “Overview of maternal and fetal vessel Doppler ultrasound”
- “Fetal growth restriction”
Recording of a fetal nonstress test
There is a baseline heart rate of ∼ 130/min (white dotted line) with four accelerations (1–4) within the recorded window (recording shows 13.5 minutes).
This is a reactive, normal fetal nonstress test.
Source: “Kardiotokogramm” by Mariakeernik, Wikimedia Commons, licensed under CC BY-SA 3.0. Modifications: cropped. The supplementary image with overlays of relevant areas was adapted from the image mentioned above and licensed under CC BY-SA 3.0.
Ultrasound fetal (amniotic fluid index)
Amniotic fluid index (AFI) is part of the fetal biophysical profile. The deepest pocket of amniotic fluid without fetal parts or umbilical cord is measured in centimeters in each quadrant. The AFI is the sum of the four measurements.
Created by: Lalash Bexten. Modifications to original image: deleted patient data.
Ultrasound fetal (amniotic fluid index)
Amniotic fluid index (AFI) is part of the fetal biophysical profile. The deepest pocket of amniotic fluid without fetal parts or umbilical cord is measured in centimeters in each quadrant. The AFI is the sum of the four measurements.
P: placenta
Created by: Lalash Bexten. Modifications to original image: deleted patient data.
Group B streptococcus screening
Routine prenatal GBS screening combined with targeted intrapartum prophylactic antibiotics for GBS has decreased vertical transmission of GBS and the number of early-onset neonatal GBS infections. [96][97]
Indications [96]
-
Routine screening for all women from 36+0 to 37+6 weeks' gestation, regardless of planned delivery method, unless prophylaxis is already indicated, e.g.: [96][98]
- GBS bacteruria during pregnancy
- Prior newborn with early-onset GBS infection
- Urgently: women in labor or with ruptured membranes with unknown GBS culture status
Regardless of whether a cesarean or vaginal delivery is planned, screen all pregnant women with indications for GBS screening in order to guide management if unexpected early labor or rupture of membranes occurs. [96]
Method of collection [96]
- Swab the lower vagina and introitus, followed by the rectum.
- Use a single flocked swab without a speculum. [99]
Laboratory studies
- All patients: GBS culture
- Pregnant individuals with history of severe penicillin reaction: Add reflex clindamycin susceptibility testing. [96]
- For urgent indications: Consider adding a rapid nucleic acid amplification test (NAAT). [96]
Next steps
- Positive GBS culture: See “Prophylaxis for neonatal GBS infection” for intrapartum management.
- Negative GBS culture: Consider repeat testing if the patient is still pregnant in 5 weeks. [96]
Prenatal patient education
-
Beginning in early pregnancy and continuing throughout pregnancy, educate patients on factors related to maternal and fetal health, including: [1]
- Education on common discomforts during pregnancy
- Nutrition and weight gain during pregnancy
- Physical activity during pregnancy
- Dental care, travel, use of medications, and work during pregnancy (see “Other health and safety counseling during pregnancy”).
- In the second and third trimesters, provide counseling related to peripartum care. [1]
Common discomforts during pregnancy
Uncomplicated nausea and vomiting of pregnancy [100][101]
-
Epidemiology [101][102]
- Occurs in 50–80% of pregnancies [100]
- Onset at ∼ 4 weeks' gestation
- Peaks at 9 weeks' gestation
- Usually abates by 16–20 weeks' gestation
-
Clinical features
- Nausea and/or vomiting
- Normal vital signs and physical examination
-
Diagnostics
- Not routinely required for uncomplicated nausea and vomiting; laboratory studies are typically normal.
- Severe or persistent symptoms: Evaluate for laboratory findings in dehydration and other causes of nausea and vomiting.
- CBC, CMP, urinalysis, β-HCG, TSH, amylase [101]
- Ultrasound abdomen and pelvis to evaluate for multifetal gestation or molar pregnancy [103][104]
- See also “Hyperemesis gravidarum.”
- Differential diagnoses: See “Differential diagnosis of nausea and vomiting.”
-
Treatment [100]
- Rehydration (oral hydration is usually sufficient)
- Nonpharmacologic options
- Adapt diet and avoid triggers.
- Ginger tea and/or ginger capsules
- Acupressure , hypnosis
- Replace iron-containing supplements with folate-containing prenatal vitamins.
-
Antiemetic therapy for nausea and vomiting of pregnancy: If the response to an antiemetic from one class is inadequate, add an antiemetic from another class in a stepwise manner, as shown below. [100][101]
-
Pyridoxine (vitamin B6) with or without doxylamine
- Oral pyridoxine (vitamin B6) with or without oral doxylamine [100]
- Oral pyridoxine/doxylamine
-
For refractory symptoms, add one of the following:
- Diphenhydramine
- Dimenhydrinate
- Prochlorperazine
- Promethazine
-
For refractory symptoms despite combination therapy above, add one of the following:
- Metoclopramide
- Ondansetron
- Promethazine
- Consider also:
- Changing from oral to IV dimenhydrinate
- Trimethobenzamide
-
Last resort; : Add chlorpromazine or methylprednisolone.
- Chlorpromazine
- Methylprednisolone
-
Pyridoxine (vitamin B6) with or without doxylamine
- Thiamine repletion (in patients with severe recurrent vomiting)
-
Acute management checklist for uncomplicated nausea and vomiting of pregnancy
- Rule out alternate etiologies (see differential diagnosis of nausea and vomiting).
- Identify and treat dehydration (see IV fluids).
- If dehydration is present, check urine ketones and serum electrolytes to rule out hyperemesis gravidarum.
- Electrolyte and thiamine repletion (in patients with severe recurrent vomiting)
- Trial nonpharmacologic options (e.g., dietary changes, ginger tea/capsules)
- Replace iron-containing supplements with folate-containing prenatal vitamins.
- Start pyridoxine and/or doxylamine.
- For refractory emesis, add antiemetic therapy in a stepwise manner (see above).
- Consider OB/GYN consult.
In pregnant women, a thorough history, examination, and, if necessary, diagnostics are essential to rule out potential causes of nausea and vomiting that are not pregnancy-related.
Because antiemetics are potentially teratogenic, their use should be considered only if nausea and vomiting are refractory to dietary changes and supportive therapy.
Pelvic girdle pain [105]
- Etiology: increased pressure from the uterus, lumbar lordosis, and relaxation of the ligaments supporting the joints of the pelvic girdle
- Epidemiology: common, occurring in 15–25 % of pregnant patients.
-
Clinical features: lower back pain
- Particularly between the posterior iliac crest and the gluteal fold and in the area of the sacroiliac joint
- May radiate to the thighs and hips
- Worsens with weight-bearing
- Diagnosis: positive pelvic pain provocation tests (e.g., posterior pelvic pain provocation test, FABER test, active straight leg raise)
-
Management
- Nonpharmacological: heat therapy, manual therapy (e.g., massage, spinal manipulation), braces, physical therapy
- Pharmacological: acetaminophen
Round ligament pain
- Etiology: stretching of the round ligament of the uterus as the uterus expands
- Epidemiology: one of the most common conditions during pregnancy
-
Clinical features
- Typically manifests in the second and third trimester
- Sharp pain in the lower abdomen and groin area (most often right-sided)
- Triggered by sudden and/or rapid movements (e.g., rolling over in bed, sneezing, vigorous physical activity)
- Diagnosis: based on clinical history
- Management: usually no treatment required; resolves after delivery
Peripheral edema
- Very common, benign finding
- Management
- Exclude alternative diagnoses (e.g., DVT, preeclampsia)
- Expectant management is usually sufficient
Paresthesias
-
Meralgia paresthetica
- Compression at the level of the inguinal ligament (lateral femoral cutaneous nerve), caused by increased intraabdominal pressure during pregnancy → pain and paresthesias on the lateral surface of the anterior thigh
- Pain may worsen as pregnancy progresses but typically resolves after delivery as compression is relieved.
-
Carpal tunnel syndrome in pregnancy
- Caused by peripheral edema
- Usually resolves after delivery
Supine hypotensive syndrome
-
Compression of the vena cava and pelvic veins by the uterus may occur during the third trimester of pregnancy (typically >20 weeks) as a result of the mother lying in a supine position.
- Gravid uterus → compression of the abdominal aorta and IVC → impaired venous return and decrease in cardiac output → placental hypoperfusion → fetal hypoxia → deceleration (CTG)
- After repositioning the mother in the left lateral position, the fetal heart rate recovers.
- In the mother, supine hypotensive syndrome is characterized by tachycardia, dizziness, and nausea, and occasionally causes syncope.
Other symptoms
- Gastroesophageal reflux
- See also “Physiological changes during pregnancy”
Nutrition and weight gain
General principles [27][106]
- Dietary intake during pregnancy should be optimized to meet the demands of both the mother and the fetus. [106]
- Appropriate weight gain and nutrition should be assessed on an individual basis.
- Encourage pregnant women to follow a well-balanced diet and avoid restrictive diet plans.
- A daily multivitamin that includes folic acid is generally recommended for the duration of pregnancy. [106][107]
- For individuals with special dietary needs (e.g., those with diabetes, vegetarians), consider referral to a nutritionist. [1]
- Refer individuals suspected to have an eating disorder to a specialist (e.g., psychiatry) for appropriate diagnosis and management; see also “Anorexia nervosa in pregnancy” and “Overview of eating disorders” as needed. [108]
Recommended dietary intake and supplementation [107][109]
- Calories: Average daily calorie requirements increase in the second and third trimesters.
- Women with a normal pre-pregnancy BMI
- Second trimester: additional 340 calories/day
- Third trimester: additional 452 calories/day
- For women with a pre-pregnancy BMI ≥ 25, tailor calorie recommendations to recommended weight gain during pregnancy.
- Women with a normal pre-pregnancy BMI
- Protein: 71 grams/day is recommended. [109]
- Carbohydrates: 175 grams/day is recommended, including 25–36 grams of fiber per day. [109]
- Fats
- It is recommended that 20–35% of daily calorie intake come from fats. [109]
- Adequate intake of Omega‐3 fatty acids is recommended. [109][110][111]
Micronutrients during pregnancy
Patients considering pregnancy should aim for similar intakes (see “Preconception counseling”).
| Recommended vitamin and mineral supplementation in pregnancy [1][109] | |||
|---|---|---|---|
| Supplementation | Reason for increased demand | Consequences of deficiency | |
| Folic acid [1][112] |
|
|
|
| Vitamin B12 [116] |
|
|
|
| Iron [1] |
|
|
|
| Calcium [118] |
|
|
|
| Iodine [43] |
|
|
|
Excessive consumption of vitamin A during pregnancy may be teratogenic. [1]
Vegetarian mothers are at risk of deficiencies in vitamin D, iron, calcium, vitamin B12, and zinc; consider laboratory evaluation as indicated. [1][107]
Dietary restrictions during pregnancy [117]
- Limit caffeine: to < 200 mg daily (∼ 2 cups of coffee or ∼ 4 cups of caffeinated tea) [124]
- Avoid alcohol use throughout pregnancy. [125]
-
Avoid foods associated with higher risk of foodborne illness, e.g.: [23]
- Raw or undercooked seafood: risk of contamination with parasites and norovirus
- Raw or undercooked meat: risk of Listeria, Brucella, and Toxoplasma contamination
- Deli meats and hot dogs: risk of Listeria contamination
- Raw eggs: risk of Salmonella contamination
- Unwashed fruits and vegetables: risk of Listeria and Toxoplasma contamination
- Unpasteurized dairy products: risk of Listeria, Brucella, and Toxoplasma contamination
- Avoid seafood with possibly high levels of methylmercury: such as tilefish, swordfish, shark, mackerel, and bigeye tuna. [1]
Consumption of raw or undercooked meats, unpasteurized dairy products, and unwashed fruits and vegetables by pregnant women can increase the risk of congenital toxoplasmosis and congenital listeriosis and should be avoided. [23]
Recommended weight gain during pregnancy [1][117]
- Total recommended weight gain is determined by BMI prior to pregnancy. [27]
-
Singleton pregnancies
- BMI < 18.5 (underweight): 28–40 lb (12.7–18.1 kg)
- BMI 18.5–24.9 (normal weight): 25–35 lb (11.3–15.9 kg)
- BMI 25–29.9 (overweight): 15–25 lb (6.8–11.3 kg)
- BMI ≥ 30 (obese): 11–20 lb (5–9.1 kg)
- Twin pregnancies
- BMI 18.5–24.9 (normal weight): 37–54 lb (17–25 kg)
- BMI 25–29.9 (overweight): 31–50 lb (14–23 kg)
- BMI ≥ 30 (obese): 25–42 lb (11–19 kg)
-
Singleton pregnancies
- Both excessive and inadequate gestational weight gain can impact fetal and maternal outcomes. [126]
| Risk factors and outcomes of inadequate or excessive gestational weight gain | ||
|---|---|---|
| Inadequate weight gain | Excessive weight gain | |
| Risk factors |
|
|
| Fetal outcomes [133] |
|
|
| Maternal outcomes [126][134] |
|
|
During the second and third trimesters, recommended weekly weight gain is 0.5 lb/week if pre-pregnancy BMI ≥ 30, 0.6 lb/week if pre-pregnancy BMI 25–29.9, and 1 lb/week if pre-pregnancy BMI < 25. [27]
Physical activity
General principles [136]
- Evaluate all patients for contraindications to aerobic exercise in pregnancy prior to recommending physical activity.
-
Regular physical activity is recommended during most pregnancies.
- Educate patients on safe and unsafe activities and advise activity avoidance or modification as needed. [136][137]
- Patients should aim for ≥ 20–30 minutes of aerobic and/or strength-training exercise most days of the week. [1]
- In the absence of medical or surgical complications, physical activity may resume soon after delivery. [136]
- Consider occupational accommodations for women with jobs requiring high levels of physical effort or potentially unsafe activities. [138]
Contraindications to aerobic exercise in pregnancy [1]
- Restrictive lung disease
- Hemodynamically significant heart disease
- Severe anemia [137]
- Cervical insufficiency
- Premature rupture of membranes or premature labor
- Gestational hypertension or preeclampsia
- Placenta previa or vaginal bleeding
Safe and unsafe sports during pregnancy [136][137]
| Safety of physical activity during pregnancy [1] | ||
|---|---|---|
| Safe activities | High impact training |
|
| Low impact training |
|
|
| Unsafe activities [136][137] |
|
|
Physical activity should be stopped and the patient should notify their provider in the event of any the following: antepartum or postpartum hemorrhage, uterine contractions, amniotic fluid leakage, chest pain, dyspnea before exertion, dizziness, headaches, calf pain/swelling, and/or muscle weakness with impaired balance. [136]
Other health and safety counseling
Dental care during pregnancy [1]
- Poor oral health may be associated with preterm delivery.
- Encourage regular brushing, flossing, and cleanings.
- Educate patients about common dental problems seen in pregnancy.
Travel during pregnancy
- Encourage pregnant individuals to always wear a seatbelt. [139]
- Provide counseling before travel. Discuss: [140][141]
- Avoiding travel if risk factors for adverse pregnancy outcomes are present
-
Infection prevention and control
- Consider if additional vaccinations are required.
- Advise against travel to areas with active Zika virus outbreaks or malaria.
- Recommend strict food hygiene and water hygiene precautions.
- Planned activities (see “Safe and unsafe sports during pregnancy”)
- Risk of VTE with long-haul travel [141][142]
- Airline and cruise ship restrictions on travel in late pregnancy
- Importance of travel insurance and carrying a copy of medical records
Pregnant women should be informed that the most common obstetric emergencies occur in the first and third trimesters and they may, therefore, prefer to restrict travel to the second trimester. [140]
Medications and substance use [1]
- Advise the patient to avoid tobacco, alcohol, and recreational drugs.
- Ensure all prescribing clinicians are aware the patient is pregnant.
- Have the patient check with a healthcare professional before taking over-the-counter medications, supplements, or herbal preparations.
Work during pregnancy [138]
- Educate patients on occupational hazards, e.g.:
- Known hazards: toxic exposures (e.g., heavy metals, pesticides, ionizing radiation)
- Suspected hazards
- Standing/walking for long periods of time (> 3 hours a day)
- Heavy lifting
- Working > 40 hours a week
- Support patients in seeking workplace accommodations where appropriate.
When writing a work accommodation note for pregnant patients, make sure to be specific and outline reasonable limitations to avoid the note being used as grounds for dismissal. [138]
Counseling related to peripartum care
- Inform patients about clinical features of preterm labor and rupture of membranes, and when to seek medical care.
- Review any maternal birth expectations and provide counseling on options, including: [1][143]
- Methods of delivery (spontaneous vaginal delivery, assisted vaginal delivery, cesarean delivery)
- Labor pain management (e.g., epidural anesthesia)
- Umbilical cord blood banking
- Breastfeeding and formula feeding
- If complex delivery is anticipated, discuss options with the patient, e.g.: [1]
- Breech presentation: cesarean delivery, vaginal breech delivery, or external cephalic version
- Previous cesarean section: trial of labor, scheduled cesarean delivery
- Encourage patients and other individuals who will be involved in the childbirth to attend educational classes.
- Discuss neonatal procedures that may be performed prior to hospital discharge, e.g.:
- Hepatitis B immunization
- Routine neonatal ophthalmic antibiotic prophylaxis
- Parenteral vitamin K administration for prevention of VKDB
- Circumcision
- Plan postpartum care. [144]
- Determine who will provide postpartum care (primary care physician or OBGYN).
- Advise patients to find an infant healthcare provider prior to delivery.
- Discuss the plan for infant feeding (see “Infant nutrition and breastfeeding”).
- Provide basic counseling on child safety.
- Offer guidance on contraception in postpartum individuals as some methods can be instigated at time of delivery. [1]
Unintended pregnancy
An unintended pregnancy is a pregnancy that occurs in an individual who does not desire pregnancy at that time or at all. [145][146]
- Use a patient-centered approach to explore the individual's feelings toward the pregnancy. [147]
- Provide unbiased counseling on pregnancy options, including: [147]
- Continuation of pregnancy (with the plan to raise the child themselves or place the child up for adoption)
- Induced abortion
- Refer to appropriate providers, agencies, and/or support groups as indicated. [147]
Clinicians who are unable or unwilling to provide comprehensive counseling on pregnancy options should promptly transfer care to an appropriate provider. [148][149]
Special patient groups
Pregnancy in adolescents [150]
In this section, “adolescent” refers to individuals between 15 and 19 years of age. Prenatal care in adolescents is similar to that in adults. [151]
Epidemiology [150][151]
- Most adolescent pregnancies are unintended. [152]
-
Adolescents are at increased risk for: [150]
- Late entry to prenatal care
- Poor weight gain
- Intimate partner violence and commercial sexual exploitation
- Adverse social determinants of health
- High-risk pregnancy
- Substance use in pregnancy [153]
Management of adolescent pregnancy [150]
- Counsel on pregnancy options. [152]
- Address all prenatal care needs.
- Additional screening and appropriate management should focus on the following: [154][155]
- Proper nutrition and weight gain during pregnancy
- Substance use in pregnancy
- Screening for intimate partner violence and reproductive coercion
- Red flags for human trafficking
- Adverse social determinants of health (e.g., lack of safe housing, food insecurity, and barriers to care)
- Referral to a specialist (maternal-fetal medicine) is indicated for, e.g.:
- High-risk pregnancies
- Age < 15 years
- Maintain confidentiality when possible (laws vary by state). [152][156]
Consult a specialist for pregnancies in individuals < 15 years of age. [157]
Complications in adolescent pregnancy [150]
- Iron deficiency anemia in pregnancy
- Hypertensive pregnancy disorders
- Preterm birth
- Small-for-gestational-age infants
- Low birth weight
- Neonatal mortality
Peripartum care in adolescent pregnancy [150]
- Provide counseling related to peripartum care, especially:
- Clinician follow-up
- Infant nutrition and breastfeeding
- Contraception in postpartum individuals [150]
- Offer wraparound support services (e.g., return-to-school program, social services, home visitation).
- Encourage involvement with the patient's partner, family members, and/or others who will participate in caring for the infant.
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External Resources
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- 2024 WHO recommendation: Screening of Pregnant Women for the Prevention of Early-Onset Group B Streptococcus Disease in Newborns
- 2024 USPSTF Recommendation Statement: Screening and Supplementation for Iron Deficiency and Iron Deficiency Anemia During Pregnancy
- 2023 US Preventive Services Task Force Final Recommendation Statement on Screening for Hypertensive Disorders of Pregnancy
- 2022 ACOG Obstetric Care Consensus No. 11: Pregnancy at Age 35 Years or Older
- 2021 ACOG Practice Bulletin No. 233: Anemia in Pregnancy
- 2021 ACOG Practice Bulletin No. 229: Antepartum Fetal Surveillance
- 2021 ACOG Committee Opinion No. 828:Indications for Outpatient Antenatal Fetal Surveillance
- 2021 ACOG Committee Opinion No. 819: Informed Consent and Shared Decision Making in Obstetrics and Gynecology
- 2021 ACOG Practice Bulletin No. 227: Fetal Growth Restriction
- 2020 ACOG Committee Opinion No. 804: Physical Activity and Exercise During Pregnancy and the Postpartum Period
- 2020 ACOG Committee Opinion No. 797: Prevention of Group B Streptococcal Early-Onset Disease in Newborns
- 2020 ACOG Practice Bulletin No 226: Screening for Fetal Chromosomal Abnormalities url::
- 2018 ACOG Practice Bulletin No. 190: Gestational Diabetes Mellitus
- 2018 AIUM/ACR/ACOG/SMFM/SRU Practice Parameter for the Performance of Obstetric Ultrasound Examinations
- 2017 ACOG/AAP Guidelines for Perinatal Care
- 2017 ACOG Committee Opinion No. 700: Methods for Estimating the Due Date
- 2016 WHO Recommendations on Antenatal Care for a Positive Pregnancy Experience
- 2016 ACOG Practice Bulletin No. 175: Ultrasound in Pregnancy
- 2016 ACOG Practice Bulletin No. 162: Prenatal Diagnostic Testing for Genetic Disorders
- 2013 ACOG Committee Opinion No. 548: Weight Gain During Pregnancy
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