EVICOSCREEN - EVIDENCE BASED COMPREHENSIVE PRENATAL SCREENING REPORT
Hospital ID:
Patient DOB:
City:
Patient Name:
Ethnicity:
INTERPRETATION
SUGGESTIONS AND OTHER FINDINGS
Sample ID LI190024863
Patient ID LI190246491
Received on 11-03-2019 18:48
Registered on 11-03-2019 18:48
Reported on 12-03-2019 15:49
Dr. Kanchan Divekar
Sonography by
Referred by
To: Dandekar Clinic
Agri Samaj Mandir Road, Old Panvel
Panvel Navi Mumbai - 410206
Maharashtra
Contact: 022-27452194
Report Of: APARNA AMIT PATIL
Pt. Contact: 8454060799
Sample Type: Serum
Method: Time-resolved Fluroimmunoassay
Risk Assessment: Risk Assessment software accredited by Fetal Medicine
Foundation (UK)
Lilac Insights Pvt. Ltd. 301-302, Building A-1, Rupa Solitaire Millennium Business Park, MIDC Industrial Area, Sector-1, Navi Mumbai, Maharashtra 400710.
Phone: +91 22 41841438; Website: www.lilacinsights.com; For queries or complaints, please email: info@lilacinsights.com
Verified by
Mr. Pradip Kadam
Incharge Biochemistry
Verified by
Dr. Suresh Bhanushali
MD (Path), Consultant Pathologist
MULTIPLE OF
MEDIAN (MOM)
Free ß-hCG
AFP
2.0
1.0
uE3
1.0
Inhibin-A
1.0
T21 (Down syndrome) 1: Low Risk
T18 (Edwards’ syndrome) 1: Low Risk
Neural tube/ 1: Low Risk
Abdominal wall defect
RISK ASSESSMENT
LOW HIGH
LOW HIGH
LOW HIGH
is an evidence based prenatal screening program curated by Lilac Insights in accordance with the international guidelines
for prenatal screening to determine the probability of most common chromosomal aneuploidies in a pregnancy. It utilizes:
• Hormonal values from the pregnancy measured on Fetal Medicine foundation (UK) accredited analyzers and reagents
• Robust indigenous medians from over 5 lac+ pregnancies for different gestation ages
• Risk calculations from evidence based algorithms validated through large international studies
• External audit of the prenatal screening program by United Kingdom National External Quality Assessment Service (UKNEQAS)
scheme and Randox International Quality Assessment Scheme (RIQAS)
Lilac Insights Pvt. Ltd. 301-302, Building A-1, Rupa Solitaire Millennium Business Park, MIDC Industrial Area, Sector-1, Navi Mumbai, Maharashtra 400710.
Phone: +91 22 41841438; Website: www.lilacinsights.com; For queries or complaints, please email: info@lilacinsights.com
SPECIMEN DETAILS
Sample ID: : Li190024863
Collection Date : 11-03-2019
Scan Date : 11-03-2019
GA at Coll Date : 12 Weeks 6 Days
GA at Scan Date : 12 Weeks 6 Days
Received on : 11-03-2019
CRL : 64.9 mm
CRL2 : 64.9 mm
BPD : 64.9 mm
BPD2 : 64.9 mm
HC : 164.90 mm
HC2 : 164.90 mm
Test Name
Conc.
Unit
Corr. MoM
AFP 66.68 ng/mL 1.74
free-ß-hCG 66.68 ng/mL 1.74
uE3 8710.00 mU/L 1.85
Inhibin A 94.00 mmhg 1.07
RISKS
Disorder: Down Syndrome
Result: Low Risk
Final risk: 1:24365 Age risk: 1:1226
Cutoff: 1:250 Risk type: Risk At Term
Disorder: Edwards' Syndrome
Result: Low Risk
Final risk: 1:100000 Age risk: 1:11028
Cutoff: 1:100 Risk type: Risk At Term
Neural tube / Abdominal wall defect Result: Low Risk
Final risk: 1:100000 Age risk: 1:11028
Cutoff: 1:100 Risk type: Risk At Term
Down syndrome
Edwards' syndrome
Patau syndrome
NTD syndrome
Assisted Reproduction: Donor Egg
Transfer Date: 17-11-2018
Extraction Date: 17-11-2018
Donor DOB: 17-11-2018
Note! Age at term is calculated from the Donor DOB
EDD: Estimated Due Date | GA: Gestation Age | LMP: Last Menstrual Period | FHR: Fetal Heart Rate | NTD: Neural Tube Defect | PE: Pre-eclampsia | DOB: Date of Birth
PE in previous pregnancy
Pat. mother had PE
Insulin dependent diabetes
Chronic hypertension
PREGNANCY DETAILS
No. of Fetuses : 2 Monochorionic, monoamniotic
GA is Based on : CRL 64.9 mm on 11-03-2019
EDD : 17-09-2019
LMP Date : 17-11-2018
Height : 160 cm
Age at Term : 27 Years
LMP Certainty : Irregular Cycle
Weight : 50.70 kg
Smoking: None
Parity: Nulliparous
FHR:
Pre-eclampsia history
Other findings
Previous pregnancy history
GA: Gestation Age | CRL: Crown Rump Length | BPD: Bi-parietal Diameter | HC: Head Circumference | free--hCG: free-Beta Human Chorionic Gonadotropin
AFP: Alpha-Fetoprotein | uE3: Unconjugated Estriol
PRENATAL SCREENING BACKGROUND
• Every pregnant woman carry a certain degree of risk that her fetus/baby may have certain chromosomal defect/ abnormalities. Diagnosis
of these fetal chromosomal abnormalities requires confirmatory testing by thorough analysis post amniocentesis or Chorionic Villous
Sampling (CVS).
• However, amniocentesis and CVS procedures carry some degree of risk for miscarriage or other pregnancy complications (Tabor and
Alfirevic, 2010).
• Therefore in routine practice, prenatal screening tests are offered to a pregnant woman to provide her a personalized risk for the most
common chromosomal abnormalities (T21-Down syndrome, T18- Edwards' syndrome, T13- Patau syndrome) using her peripheral blood
sample. Based on this risk assessment, if the risk is high or intermediate, you can take informed decision of opting for invasive procedure
such as amniocentesis or CVS followed by confirmatory diagnostic test(s), as per discussion with your clinician.
Lilac Insights Pvt. Ltd. 301-302, Building A-1, Rupa Solitaire Millennium Business Park, MIDC Industrial Area, Sector-1, Navi Mumbai, Maharashtra 400710.
Phone: +91 22 41841438; Website: www.lilacinsights.com; For queries or complaints, please email: info@lilacinsights.com
END OF REPORT
Note:
• Quality of the Down’s Syndrome & ONTD screening program (Biochemical values, MoMs and Risk assessments) monitored by UKNEQAS on an ongoing basis.
• This interpretation assumes that patient and specimen details are accurate and correct.
• Lilac Insights does not bear responsibility for the Ultra sound measurements.
• “This is a risk estimation test and not a diagnostic test. An increased risk result does not mean that the fetus is affected and a low risk result does not mean that
the fetus is unaffected. Reported risks should be correlated and adjusted according to the absence/presence of sonographic markers observed in the
anomaly/malformation scan.”
• The above risk has been calculated based on Biochemistry values alone.
• This interpretation assumes that patient and specimen details are accurate and correct. In all cases where an assessment of increased risk is based on LMP
dates, the gestational age must be by ultrasound before further action is taken.
• It must be clearly understood that the results represent risk and not diagnostic outcomes. Increased risk does not mean that the baby is affected and further
tests must be performed before a firm diagnosis can be made. A low risk result does not exclude the possibility of Down's Syndrome or other abnormalities, as
the risk assessment does not detect all affected pregnancies.
• Lilac Insights does not bear the responsibility for the NT result. The company strongly recommends that only NT value from qualified experts (for example,
clinicians certified by the Fetal Medicine Foundation) is utilized to provide a first trimester risk.
DISCLAIMERS
Limitations of the Test:
As prenatal screening tests are not confirmatory diagnostic tests, the possibility of false positive or false negative results can not be denied. The
results issued for this test does not eliminate the possibility that this pregnancy may be associated with other chromosomal or sub-
chromosomal abnormalities, birth defects and other complications.
Nuchal Translucency is the most prominent marker in screening for Trisomy 13, 18, 21 in the first trimester and should be measured in
accordance with the Fetal Medicine Foundation (UK) guidelines. Nuchal Translucency or Crown Rump Length measurement, if not performed
as per FMF (UK) imaging guidelines may lead to erroneous risk assessments and Lilac Insights bears no responsibility for errors arising due to
sonography measurements not performed as per these criteria defined by international bodies such as FMF (UK), ISUOG.
It is assumed that the details provided along with the sample are correct. The manner in which this information is used to guide patient care is
the responsibility of the healthcare provider, including advising for the need for genetic counselling or additional diagnostic testing like
amniocentesis or Chorionic Villus Sampling. Any diagnostic test should be interpreted in the context of all available clinical findings.
As with any medical test, there is always a chance of failure or error in sample analysis though extensive measures are taken to avoid these
errors.
PRENATAL SCREENING TESTS ARE NOT CONFIRMATORY TESTS AND THEY PROVIDE RISK ASSESSMENT RESULT AS
High risk or screen positive report- which does not mean that the pregnancy is affected with these conditions. It means
that you have a higher chance of having a baby with one of these conditions as compared to the chances of miscarriage
that you have, if you opt for an invasive procedure.
High Risk
Low Risk
Low risk or screen negative report- which does not mean that the pregnancy is not affected with these conditions. It
means that you have a lower chance of having a baby with one of these conditions as compared to the chances of
miscarriage that you have, if you opt for an invasive procedure.
Based on a comparison of two risks (i.e. risk reported by screening test vs. risk of miscarriage associated with invasive procedure), the patient,
guided by her clinician can decide on opting or rejecting definitive invasive testing.
SIGNIFICANCE OF MULTIPLE OF MEDIAN (MOM) VALUES OF HORMONES
Prenatal screening tests analyze the levels of fetoplacental hormones (hormones released by placenta or fetus) found in mother's blood
sample. Their raised or grossly reduced levels not only provides indication for common chromosomal abnormalities like Down syndrome,
Edwards' syndrome or Patau syndrome but also provide indication for placental insufficiency that can in some cases lead to late pregnancy
complications such as Pre-eclampsia or Fetal Growth Restriction. This necessitates observation of the levels of hormones (MoMs) reported in
the prenatal screening report besides looking at the reported risk estimates for holistic interpretation and clinical decision making.
