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Interpretation
---------------------------------------------------
| WEEKS OF |AFP MEDIANS|HCG MEDIANS|ESTRIOL FREE, |
| GESTATION| (ng/ml) |(mIU/ml) |MEDIANS (ng/ml) |
|----------|-----------|-----------|----------------|
| 14 | 27.20 | 40370 | 0.37 |
|----------|-----------|-----------|----------------|
| 15 | 32.01 | 32200 | 0.55 |
|----------|-----------|-----------|----------------|
| 16 | 37.67 | 25690 | 0.76 |
| ---------|-----------|-----------|----------------|
| 17 | 44.33 | 20490 | 1.00 |
| ---------|-----------|-----------|----------------|
| 18 | 52.16 | 16340 | 1.25 |
| ---------|-----------|-----------|----------------|
| 19 | 61.38 | 13040 | 1.50 |
|----------|-----------|-----------|----------------|
| 20 | 72.33 | 10400 | 1.76 |
| ---------|-----------|-----------|----------------|
| 21 | 85.00 | 8295 | 1.99 |
|----------|-----------|-----------|----------------|
| 22 | 100.02 | 6620 | 2.30 |
---------------------------------------------------
---------------------------------------------------------
|ABNORMALITY |CUT OFF | DETECTION RATE|FALSE POSITIVE |
| | | IN % | RATE IN % |
|------------|-----------|---------------|----------------|
| Neural tube| | | |
| defects | >=2.5 MoM | 70-75 | 2-4 |
|------------|-----------|---------------|----------------|
| Trisomy 21 | | | |
| (Down) | 1:250 | 65 | 5 |
|------------|-----------|---------------|----------------|
| Trisomy 18 | 1:100 | 60 | 0.3 |
-----------|-----------|--------------------------------
Note
· Statistical evaluation has been done using CE marked PRISCA 5 software
PatientReportSCSuperPanel.GENERAL_PANEL_ANALYTE_SC (Version: 6)
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Comments
Second trimester screening for Prenatal disorders (Trisomy 21 & 18 and Open Neural Tube defects) is
essential to identify those women at sufficient risk for a congenital anomaly in the fetus to warrant further
evaluation and followup. These are screening procedures which cannot discriminate all affected pregnancies
from all unaffected pregnancies. Screening cutoffs are established by using MoM values that maximize the
detection rate and minimize false positives.
PatientReportSCSuperPanel.GENERAL_PANEL_ANALYTE_SC (Version: 6)
*147793619*
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*Test results released pertain to the specimen submitted .*All test results are dependent on the quality of the sample received by the Laboratory .
*Laboratory investigations are only a tool to facilitate in arriving at a diagnosis and should be clinically correlated by the Referring Physician .*Sample
repeats are accepted on request of Referring Physician within 7 days post reporting.*Report delivery may be delayed due to unforeseen
circumstances. Inconvenience is regretted.*Certain tests may require further testing at additional cost for derivation of exact value. Kindly submit
request within 72 hours post reporting.*Test results may show interlaboratory variations .*The Courts/Forum at Delhi shall have exclusive
jurisdiction in all disputes/claims concerning the test(s) & or results of test(s).*Test results are not valid for medico legal purposes. * Contact
customer care Tel No. +91-11-39885050 for all queries related to test results.
(#) Sample drawn from outside source.
PatientReportSCSuperPanel.GENERAL_PANEL_ANALYTE_SC (Version: 6)
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1:100
Trisomy 18 Risk
<1:10000
1:250 Cut off
Neural Tube
1:1000 Defects Risk
<1:10000
1:10000
13 15 17 19 21 23 25 27 29 31 33 35 37 39 41 43 45 47 49 Age Risk
Age 1:984
NEURAL TUBE DEFECTS SCREENING TRISOMY 21 SCREENING
SCREEN NEGATIVE SCREEN NEGATIVE
The calculated risk for spina bifida is <1:10000. The calculated risk for Trisomy 21 is below the cut
There is no statistical indication for spina bifida. off which represents a low risk.
Anencephaly has been excluded by ultrasound. It is expected that among 570 women with the same
data, there is one woman with a trisomy 21 pregnancy
and 569 women with normal pregnancies.
The calculated risk by PRISCA depends on the
accuracy of the information provided by the referring
TRISOMY 18 SCREENING physician.
SCREEN NEGATIVE Please note that Risk calculations are statistical
The calculated risk for trisomy 18 is <1:10000. approaches and have limited diagnostics value.
There is no statistical indication for trisomy 18
risk
COMMENTS
DR. NIMMI KANSAL
AUTHORIZED BY
Report Printing Date: 13. May 2019 PRISCA 5.1.0.17 Dr. Lal Pathlabs Pvt. Ltd.
below cut off Below Cut Off, but above Age Risk above cut off
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