Gestational Age & Due Date

VBAC Success Calculator

Trial of Labor After Cesarean — induction success probability

yr
Enter values to estimate
VBAC success probability

Bishop Score

Cervical favorability before induction of labor

Bishop Score
0 / 13

Intrauterine Transfusion

Packed-RBC volume for fetal anemia (IVT / IUT)

g
Pre-transfusion fetal sample
%

%
Packed RBCs, usually 75–85%
%
Enter fetal weight and
observed hematocrit

Cerebroplacental Ratio

CPR = MCA-PI ÷ UA-PI

Enter MCA and UA
pulsatility indices

Fetal Analgesia during IUT / Procedures

Paralysis & analgesia by estimated fetal weight

g
Enter estimated fetal weight

sFlt-1 / PlGF Ratio

Preeclampsia interpretation & clinical implications

Enter ratio and
gestational age

≤ 38Any GA · Rule out PET for 1 week (NPV 99.3%)
39–84<34 wk · High risk of PET within 4 weeks (PPV 36.7%)
39–109≥34 wk · High risk of PET within 4 weeks (PPV 36.7%)
≥ 85<34 wk · PET / placental insufficiency likely
≥ 110≥34 wk · PET / placental insufficiency likely

Gestational Age & Due Date Calculator

Calculate from LMP, ultrasound date, or IVF transfer

CCAM Volume Ratio (CVR) Calculator

Congenital Pulmonary Airway Malformation — Hydrops Risk Assessment

cm
cm
cm

Measured at same scan as the lesion
cm

Enter measurements to see results
CVR Score
Lesion Volume (ellipsoid)

Risk Thresholds

CVRDominant CystHydrops Risk
< 1.6AbsentLow (<3%)
≥ 1.6AbsentHigh (~75%)
< 1.6PresentIntermediate
≥ 1.6PresentHigh

Dominant cyst note: Stocker type I / macrocystic lesions (≥2 cm dominant cyst) may be amenable to thoracoamniotic shunting and carry a different natural history than solid/microcystic lesions even at the same CVR.

MCA Peak Systolic Velocity (PSV) Calculator

Middle Cerebral Artery Doppler — Fetal Anemia Assessment (Mari 2000)


Angle of insonation must be <20° — preferably 0°
cm/s

Enter gestational age and
MCA PSV to see results
MoM (Multiples of Median)
Median MCA PSV for GA
1.5 MoM threshold for GA

Centile chart

Interpretation Thresholds

MoMInterpretationAction
< 1.29NormalRoutine follow-up
1.29 – 1.49BorderlineRepeat in 1–2 wk
≥ 1.50Moderate–severe anemiaConsider FBS / IUT

Anti-Kell alloimmunization

Anti-Kell suppresses erythropoiesis. MCA PSV thresholds still apply, but anemia may occur at lower MoM. Lower threshold for FBS is appropriate. Standard MoM cutoffs may underestimate risk.

Technique note: Sample near the origin of the MCA from the circle of Willis. Angle of insonation <20° (ideally 0°). Avoid fetal breathing movements. Use the highest measurable PSV from at least three consecutive waveforms.

Fetal Head Circumference — Microcephaly & Macrocephaly Screening

SD-based assessment using Chervenak 1984 normative chart (20–42 weeks)


Outer-to-outer, at the level of the thalami and cavum septi pellucidi
mm
Enter gestational age and
HC measurement to assess
SD Score (z-score)
Mean HC for GA
+2 SD threshold (macrocephaly)
−2 SD threshold (microcephaly)
−3 SD threshold (severe)
−5 SD−3 SD−2 SD0+2 SD+3 SD
Extreme (<−5)
Severe (−3 to −5)
Microcephaly (−2 to −3)
Normal (−2 to +2)
Macrocephaly (>+2)

Centile chart

Classification Thresholds

SD ScoreClassificationAction
> +2 SDMacrocephalyDetailed anatomy
−2 to +2 SDNormalRoutine care
−2 to −3 SDMicrocephalyFull workup
−3 to −5 SDSevere microcephalyUrgent MRI + genetics
< −5 SDExtreme microcephalyMultidisciplinary

Workup Checklist

When HC < −2 SD (Microcephaly), consider:
• Fetal MRI brain (best after 28–30 wks)
• TORCH serology (CMV, Toxo, Rubella, Zika)
• Chromosomal microarray / exome if indicated
• Detailed anatomy scan (associated anomalies)
• Serial growth scans q3–4 weeks
• Fetal neurology / genetics referral
When HC > +2 SD (Macrocephaly), consider:
• Detailed neurosonography (ventriculomegaly, arachnoid cyst)
• Fetal MRI brain (best after 28–30 wks)
• Rule out hydrocephalus, megalencephaly, storage disorders
• Chromosomal microarray
• Serial head growth monitoring
• Pediatric neurology consultation

Important caveat: HC must be interpreted with overall fetal growth context. Isolated mild reduction (−2 to −2.5 SD) with normal biometry and anatomy may represent a constitutional variant. Severe or progressive microcephaly (<−3 SD) warrants comprehensive workup regardless of associated findings.

Lung-to-Head Ratio (LHR) & O/E LHR Calculator

Congenital Diaphragmatic Hernia — Pulmonary Hypoplasia Severity (Jani 2007 / TOTAL Trial)



Measure at 4-chamber view — longest diameter and its perpendicular
mm
mm
mm

Enter GA, lung diameters &
HC to calculate O/E LHR
O/E LHR
Lung area (D1 × D2)
Observed LHR
Expected LHR for GA
0%25%35%45%100%
SevereModerateMildExpected

Severity & Survival (Left CDH, Liver-up)

O/E LHRSeveritySurvival
< 15%Extreme<5%
15–24.9%Severe~10–25%
25–34.9%Moderate~30–60%
35–44.9%Mild~60–80%
≥ 45%Expected normal>80%

TOTAL Trial — FETO Eligibility

GroupCriteriaFETO window
SevereO/E LHR <25% + liver-up22–24 wks
ModerateO/E LHR 25–34.9% + liver-up27–29 wks
Not eligibleLiver-down or O/E LHR ≥35%
Right CDH: Generally 10–15% worse survival at equivalent O/E LHR. Standard thresholds still applied but prognosis more guarded.

Technique: Measure the contralateral (unaffected) lung at the 4-chamber view. 2D method: longest diameter × perpendicular (Jani 2007). Tracing method: planimetry trace of the lung outline — more reproducible, ~45% smaller area than 2D (Peralta 2005). AP method: anteroposterior diameter × perpendicular at its midpoint. HC from standard biometry. O/E LHR corrects for gestational age; expected values differ by method (Jani 2007 / Peralta 2005).

Skeletal Survey

Z-scores + pattern-based dysplasia screening

1 Gestational Age
2 Biometry (mm — tap field to enter)
Head
HC
BPD
Upper Limbs
Humerus
Radius
Ulna
Lower Limbs
Femur
Tibia
Fibula
Trunk & Foot
Thor. Circ.
Card. Circ.
Abd. Circ.
Foot
AP Mandible
3 Pattern Screens

Lethality Quick Reference

ConditionKey US CluesThoraxLethalityGene(s)
Thanatophoric dysplasiaSevere micromelia; telephone-receiver femurs; macrocephaly; ± cloverleafNarrowLethalFGFR3
OI type IIHypomineralization; fractures/callus; compressible skull; beaded ribsHypoplasticLethalCOL1A1/COL1A2
AchondrogenesisExtreme micromelia; poor ossification; large head; hydropsVery smallLethalCOL2A1; SLC26A2
HypophosphatasiaHypomineralization; short/bowed bones; fracturesSmallLethalALPL
Campomelic dysplasiaBowed long bones esp. tibiae; ambiguous genitaliaOften smallOften lethalSOX9
Short-rib polydactylyShort ribs; narrow thorax; polydactyly; renal/cardiacSevere restrictionOften lethalDYNC2H1, IFT140…
Jeune (ATD)Narrow thorax; short ribs; variable limb shorteningVariableVariableIFT140, DYNC2H1…
Achondroplasia (het.)Rhizomelia 21–27w; macrocephaly; frontal bossing; trident handAdequateSurvivableFGFR3
Achondroplasia (hom.)Earlier rhizomelia; macrocephaly; severe chest narrowingSevereLethalFGFR3
Diastrophic dysplasiaShort limbs; hitchhiker thumbs; clubfeet; joint contracturesAdequateSurvivableSLC26A2
Ellis-van CreveldShort limbs; postaxial polydactyly; congenital heart diseaseAdequateSurvivableEVC, EVC2
Chondrodysplasia punctataEpiphyseal stippling; limb shortening; variable featuresVariableVariableARSE, EBP, PEX7

Cardiothoracic Ratio (CTR)

Fetal cardiac size — normal CTR ≤ 0.50

Trace the outer edge of the heart (epicardium)
mm
Trace the outer edge of the bony thorax (ribs only) — exclude skin and subcutaneous fat
mm

CTR Classification

CTRInterpretationAction
≤ 0.50NormalRoutine
0.51–0.57BorderlineRepeat + echo
> 0.57CardiomegalyEcho + MFM

Causes of Elevated CTR

Structural
CHD — AVSD, Ebstein anomaly, HLHS, TOF
Functional
Cardiomyopathy, arrhythmia, SVT
Volume Overload
Fetal anemia, AVM, twin-to-twin transfusion
Extrinsic
CDH (mediastinal shift), pleural effusion
Other
Hydrops fetalis, pericardial effusion

Technique and Measurement
Should be performed on a four-chamber view of the heart at the end of diastole (just before contraction).

Obtain a transverse (axial) plane of the fetal chest that clearly shows a complete rib on each side.

Clear visualization of cardiac structures and thoracic boundaries is required.

Umbilical Artery Pulsatility Index

GA-specific percentiles — INTERGROWTH-21st (Drukker 2020)

INTERGROWTH-21st (Drukker 2020) · 24–40 weeks · Z-score & centile


Leave blank to see reference values only
Enter gestational age to view
UA PI reference values
UA Pulsatility Index Percentile
Observed PI
50th centile (median)
95th centile (upper normal)
050th75th95th>95th

Clinical Interpretation

PercentileInterpretationAction
< 95thNormalRoutine surveillance
≥ 95thElevated — investigateRepeat + growth scan

Clinical Notes

Normal trend: UA PI decreases progressively with advancing gestation as placental villous vascularity increases and resistance falls.

Elevated PI: Suggests increased placental resistance. In FGR, up to 25% show elevated UA PI. Progressive worsening indicates deterioration.

MFM Referral Criteria

NGH institutional criteria — Fetal & Medical Disorders Clinics

Direct MFM referral (stay in MFM)
Consult & may return to original MRP
Group A — Direct MFM Referral (Remain under MFM Care)
Multiple Fetal Anomalies
Documented multiple fetal anomalies on ultrasound
Fetal Arrhythmias
Any fetal arrhythmia requiring evaluation and monitoring
Rh Isoimmunization
Rh isoimmunization or fetuses at risk for isoimmunization with positive blood group antibodies
Fetal Hydrops
History of previous or current fetal hydrops (immune or non-immune)
Monochorionic Twin
All monochorionic (MCDA and MCMA) twin pregnancies — serial TTTS and TAPS surveillance
Triplet Gestation and Above
Higher-order multiples regardless of chorionicity
DCDA Twins with Complications
Dichorionic/Diamniotic twins with IUGR, OR oligohydramnios (largest amniotic pocket ≤2 cm), OR growth discordance >20%
Early-Onset IUGR (<24 weeks)
Fetal growth restriction identified before 24 weeks of gestation
Severe IUGR
AC or EFW <3rd percentile at <37 weeks — OR — AC or EFW <10th percentile + oligohydramnios and/or abnormal umbilical artery Doppler at <34 weeks
Abnormal Fetal Doppler ± IUGR (<37 weeks)
Any abnormal umbilical artery, MCA, or ductus venosus Doppler waveform with or without growth restriction before 37 weeks
Severe Amniotic Fluid Abnormality (<37 weeks)
Severe polyhydramnios (AFI >35 cm) OR oligohydramnios (AFI <3 cm) at gestational age <37 weeks
Dilated Fetal Renal Pelvis >15 mm
Renal pelviectasis >15 mm at any gestational age
Group B — MFM Consultation (May Return to Original MRP After Counselling)
Previous History of Fetal Anomalies
Prior pregnancy with fetal anomaly — counselling and risk assessment for current pregnancy
Family History of Genetic Disease
After counselling ± antenatal genetic testing if needed; may return if test result is normal
Teratogenic Medication Exposure
Pregnant patient who used teratogenic medication — after normal detailed scan and counselling
Isolated Fetal Anomalies (Selected)
Cleft lip/palate · Familial clubfoot · Mild renal pelvis dilatation 7–15 mm · Isolated cardiac anomalies (e.g., VSD, vascular ring)
DIDA Twins with One IUFD
Dichorionic/Diamniotic twin gestation with single intrauterine fetal demise
AC or EFW <10th Percentile (34–37 weeks)
Fetal growth at <10th percentile between 34 and 37 weeks of gestation
Non-Specific Positive Blood Group Antibodies
Positive antibodies not known to cause fetal/neonatal anemia
Mild–Moderate Amniotic Fluid Abnormality (<37 weeks)
Polyhydramnios (AFI 24–35 cm) OR oligohydramnios (AFI 3–10 cm) at <37 weeks
CVS / Amniocentesis Timing
Next available Sunday or Tuesday at 12w (CVS) and 15w (Amnio)

Twins Calculators

EFW Discordance & TAPS (Mo/Di) assessment

Ultrasound EFW only
Twin 1
Larger
g
Twin 2
Smaller
g
(Larger EFW − Smaller EFW) ÷ Larger EFW × 100
Enter both EFW values above
Select Date
DayMonthYear