Still got some questions about EVITA TEST COMPLETE?
Below are the most common frequently asked questions.
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Frequently asked questions
When in pregnancy can an EVITA TEST COMPLETE blood sample be taken?
You can have blood samples taken for both the tests at gestational age 10+0 to 14+6.
Where can the blood sample for the test be taken?
The blood sample for the test is taken at one of our partner clinics in Denmark. Contact one of our partner clinics, here, and book an appointment.
I do not live in Denmark. Can I still get an EVITA TEST?
Yes, you can. Please contact one of our partner clinics in Denmark or contact us at contact@evitatest.com and we can guide you to where the nearest partner clinic is.
Getting the test
When in pregnancy can an EVITA TEST COMPLETE blood sample be taken?
You can have blood samples taken for both the tests at gestational age 10+0 to 14+6.
Where can the blood sample for the test be taken?
The blood sample for the test is taken at one of our partner clinics in Denmark. Contact one of our partner clinics, here, and book an appointment.
I do not live in Denmark. Can I still get an EVITA TEST?
Yes, you can. Please contact one of our partner clinics in Denmark or contact us at contact@evitatest.com and we can guide you to where the nearest partner clinic is.
How much does an EVITA TEST cost?
Please visit our partner clinics’ websites for EVITA TEST prices or contact one of our partner clinics directly to inquire about price.
Can my doctor take an EVITA TEST blood sample and send it to you?
No, the blood sample must be taken at one of our partner clinics, which are distributed throughout Denmark.
Results
How long does it take before I get the answer to the EVITA TEST COMPLETE test?
In most of the cases within 12 working days, you will receive the result of the test via a telephone call and a short report from the clinic where the test was taken.
How do I get the answer from my EVITA TEST?
The result of your EVITA TEST will be sent directly to the clinic where you have had the blood sample taken. The clinic will then communicate the results to you.
What does a negative EVITA TEST COMPLETE answer mean?
A negative EVITA TEST COMPLETE result indicates that the fetus has normal genetics, which means that there is a very low risk that the fetus will have chromosomal abnormalities.
What do I do if a high risk of chromosomal aberrations is detected in my fetus?
In case of a positive EVITA TEST COMPLETE result (with a high risk of chromosomal aberration in the fetus), it is recommended that you contact your general practitioner or the hospital where you plan to give birth, to arrange the further course of invasive diagnostics and medical advice.
Alternatives
How is EVITA TEST COMPLETE different from other NIPT tests?
In EVITA TEST COMPLETE, whole and intact fetal cells are isolated from the blood sample from the pregnant woman. That makes it possible to analyze the complete genome of the fetus. Conventional NIPTs, on the other hand, analyze fragments of DNA from broken cells from the fetus that circulate in the pregnant woman’s blood.
With DNA from intact fetal cells, which are isolated in EVITA TEST COMPLETE, it is therefore possible to analyze all the chromosomes of the fetus and not just a few chromosomes, which other NIPTs do.
Can I find out the sex of the fetus from an EVITA TEST COMPLETE?
Yes, you can. When you have given the sample for the test in one of our partner clinics, simply tick off your wish regarding the result of the sex of the fetus on the consent form.
Details of the test
Can EVITA TEST COMPLETE be equated with a chorionic villus sampling?
No, EVITA TEST COMPLETE is a screening test performed on a blood sample, while chorionic villus sampling (CVS) is a diagnostic analysis performed on a placental biopsy.
EVITA TEST COMPLETE is a safe and non-invasive method, whereas CVS is an invasive method that carries a small risk (0.5%) of procedure related miscarriage.
EVITA TEST COMPLETE can find deletions down to at least 1 Mb, whereas CVS can detect genetic changes down to 0.1 Mb. However, the majority of the known disease-causing deletion/duplication syndromes are larger than 1 Mb.
CVS can detect if there is a mixture between genetically normal and abnormal cells (mosaicism), which EVITA TEST COMPLETE has a lower sensitivity for. However, only a small amount of these mosaic findings is found in the fetus, whereas the majority are confined to the placenta.
If chromosomal abnormalities are found upon EVITA TEST COMPLETE, it is always recommended to follow up with invasive tests such as CVS to verify the findings.
Can EVITA TEST COMPLETE be equated with the combined first trimester screening (cFTS) based on my age, a blood test (double test) and measurement of the nuchal translucency performed at ultrasound scan?
No, the risk indications that can be obtained from the combined first trimester screening can detect other pregnancy-relevant factors, which EVITA TEST COMPLETE does not investigate. EVITA TEST COMPLETE exclusively examines the entire fetal genome for chromosomal aberrations down to 1 million DNA base pairs in size.
The combined first trimester screening, based on my age, a blood test (double test) and measurement of the nuchal translucency at the first trimester scan, has shown that I am in the low-risk group. Can I still benefit from an EVITA TEST COMPLETE?
Yes, the combined first trimester screening is a risk assessment, of the fetus carrying one of the most common trisomies, especially trisomy 21 (Down syndrome). Even for pregnant women in the low-risk group, the examinations do not give a guarantee that the fetus does not have a chromosomal aberration. Other, and especially minor deviations in the fetal genome, may go undetected in the combined first trimester screening.
EVITA TEST COMPLETE analyzes the entire fetal genome and can detect changes on all chromosomes. The test identifies both larger deletion and and extra copies (duplications) of DNA down to 1 Mb across the whole genome.
Additionally, the resolution is extended to ~0.4 Mb for well-characterized microdeletion syndromes, i.e., those registered in Decipher’s international database (grade 1). In this way, EVITA TEST can identify unexpected and undescribed changes and, with particular care, review already known microdeletions.
All findings from the analysis of the fetal genome, which are considered clinically relevant by a geneticist, will be communicated to you.
What is the risk of finding a deviation with an EVITA TEST COMPLETE that cannot be explained?
All results are analyzed by a geneticist with many years of experience in analyzing genetic results from fetal cells. All findings which are considered clinically relevant, will be communicated to you.
Other
What does 1 million DNA base pairs mean?
The length of a genome is given in number of DNA base pairs. Thus, 1 million DNA base pairs is the size of a piece of the genome that counts 1 million DNA base pairs from start to end on that chromosome.
An entire human genome is about 3 billion DNA base pairs long, which is distributed across the 23 chromosome pairs that make up a normal human genome. The chromosomes vary in size from 47-250 million DNA base pairs, and 1 million DNA base pairs is thus a relatively small size of the entire genome.
Do you have more questions about EVITA TEST COMPLETE?
If you cannot find the answer to your questions above, please feel free to call our EVITA TEST COMPLETE service line on +45 93 96 00 00. We are open from 9am until 11:30am every weekday. Our experts will be ready to answer your questions.
Alternatively, please pop your question in the contact form. We strive to respond within 24 hours (Monday – Friday).