Dating scan in obg

Reading File
Reading File
Finding Sources
Searching PubMed

pregnancy ultrasound gestational age

Searching the Web

NHS dating scan 8 to 14 weeks crown rump length due date

A dating scan is a first-trimester obstetric ultrasound used to establish the gestational age and estimated due date (EDD).
Usual timing
  • Often performed at 11 to 13 weeks + 6 days as part of first-trimester assessment.
  • It may be done earlier, around 6 to 10 weeks, if there is pain, bleeding, uncertain menstrual dates, or a need to confirm viability/location.
What it assesses
  1. Viability: fetal cardiac activity.
  2. Location: confirms an intrauterine pregnancy and helps exclude ectopic pregnancy.
  3. Number of fetuses: singleton or multiple pregnancy, with chorionicity assessment in twins.
  4. Gestational age and EDD: primarily by crown-rump length (CRL).
  5. Early fetal anatomy: a limited review for major obvious abnormalities.
  6. At 11-13+6 weeks, it can be combined with nuchal translucency measurement for aneuploidy screening.
Dating measurement
  • CRL is measured from the top of the fetal head (crown) to the buttocks (rump).
  • Up to 13 weeks + 6 days, CRL is the most accurate ultrasound parameter for dating, generally within about 5-7 days.
  • If the scan estimate differs substantially from dates calculated using the last menstrual period, the ultrasound-based EDD is generally preferred because early embryonic growth is relatively uniform.
Approach
  • Transabdominal ultrasound is commonly sufficient later in the first trimester.
  • Transvaginal ultrasound provides better detail in very early pregnancy or when the abdominal scan is unclear.
In short: a dating scan confirms where the pregnancy is, whether it is viable, how many fetuses are present, and how far along the pregnancy is.

Congenital rubella syndrome

Reading File
Finding Sources
Searching PubMed

congenital rubella syndrome

Searching the Web

CDC congenital rubella syndrome clinical features prevention vaccination pregnancy

Finding Sources
Reading Web Page

https://www.cdc.gov/surv-manual/php/table-of-contents/chapte…

Congenital rubella syndrome (CRS)

CRS is a group of fetal and neonatal abnormalities caused by transplacental rubella-virus infection, particularly when the mother acquires rubella in the first trimester. Viral damage results from impaired fetal cell division and persistent fetal infection.

Risk by gestation

  • Highest during the first 12 weeks of pregnancy.
  • Risk falls progressively thereafter.
  • Major structural anomalies are uncommon after 20 weeks, although sensorineural hearing loss can still occur.

Classical triad

  1. Eye defects
    • Cataract, often bilateral
    • Congenital glaucoma
    • Pigmentary retinopathy, microphthalmia
  2. Cardiac defects
    • Patent ductus arteriosus (PDA) is classic
    • Peripheral pulmonary artery stenosis
    • May have ventricular septal defect
  3. Sensorineural deafness
    • The commonest and sometimes the only late manifestation.

Other manifestations

  • Intrauterine growth restriction and low birth weight
  • Microcephaly, developmental delay, meningoencephalitis
  • Hepatosplenomegaly and hepatitis
  • Thrombocytopenic purpura with petechiae, producing “blueberry muffin” lesions due to extramedullary hematopoiesis
  • Jaundice, anemia
  • Interstitial pneumonitis
  • Radiolucent bone lesions
The typical combination is cataract, deafness, and congenital heart disease. - Sherris & Ryan's Medical Microbiology, p. 2005

Diagnosis

In a suspected infant:
  • Rubella-specific IgM in serum supports congenital infection because maternal IgM does not cross the placenta.
  • Rubella virus detection by RT-PCR or viral culture from nasopharyngeal/throat swab, urine, blood, or CSF may confirm infection.
  • Evaluate hearing, eyes, heart, growth, blood count, liver function, and neurodevelopment.
The CDC CRS surveillance guidance advises laboratory confirmation in every suspected case.

Prevention

  • Prevention is by rubella-containing vaccine, usually MMR, given before pregnancy.
  • MMR is a live attenuated vaccine and is not administered during pregnancy.
  • A nonimmune pregnant woman should receive MMR postpartum.
  • Maternal exposure or a rubella-like illness in pregnancy needs urgent obstetric and infectious-disease assessment, with rubella IgG, IgM, and where appropriate IgG avidity testing.
The CDC rubella guidance notes that prevention of CRS is the principal aim of rubella immunization programs.

Screening test for gdm

Reading File
Finding Sources
Searching PubMed

gestational diabetes screening

Searching the Web

ACOG gestational diabetes screening 24 28 weeks 50 g glucose challenge test 2024

Screening test for gestational diabetes mellitus (GDM):

Two-step approach

Done routinely at 24-28 weeks of gestation.
  1. 50-g oral glucose challenge test (GCT)
    • No fasting required.
    • Measure venous plasma glucose 1 hour after 50 g oral glucose.
    • A value of ≥140 mg/dL (7.8 mmol/L) is commonly considered screen-positive. Some centers use 130 or 135 mg/dL to increase sensitivity.
  2. If screen-positive: 100-g, 3-hour oral glucose tolerance test (OGTT)
    • This is the confirmatory diagnostic test, done fasting.
    • GDM is usually diagnosed when 2 or more values are abnormal using the selected criteria.

One-step alternative

  • 75-g, 2-hour OGTT, performed fasting at 24-28 weeks.
  • This is used in many guidelines/settings as both screening and diagnosis.
Exam answer:
The usual screening test is the non-fasting 50-g glucose challenge test with a 1-hour plasma glucose measurement, followed by a 100-g 3-hour OGTT if positive.
Women with high risk for pre-existing diabetes should be assessed at the first antenatal visit; if normal, repeat GDM screening at 24-28 weeks. Creasy & Resnik’s Maternal-Fetal Medicine, p. 1563-1570.

Why done after 24 weeks

Reading File
Finding Sources
Searching PubMed

gestational diabetes insulin resistance placental hormones

Searching the Web

gestational diabetes screen 24 28 weeks placental hormones insulin resistance guideline

GDM screening is done after 24 weeks, usually at 24-28 weeks, because this is when pregnancy produces significant insulin resistance.
As the placenta grows in the second half of pregnancy, placental hormones, especially human placental lactogen, along with progesterone, estrogen, cortisol, and placental growth hormone, have an anti-insulin effect. Maternal insulin requirements rise. If the maternal pancreas cannot compensate by increasing insulin secretion, blood glucose rises and GDM becomes detectable.
Before 24 weeks, this placental hormone effect is usually not strong enough, so routine screening may miss GDM. Hyperglycemia detected very early in pregnancy more often suggests previously unrecognized pre-existing type 2 diabetes, rather than typical GDM.
One-line exam answer:
GDM screening is done at 24-28 weeks because placental diabetogenic hormones cause maximal maternal insulin resistance in the late second and third trimesters, unmasking glucose intolerance.
Katzung’s Basic and Clinical Pharmacology, p. 3628.
This is a shared conversation. Sign in to Orris to start your own chat.