Probably the most proven cell-free DNA-based non-invasive prenatal test (NIPT) 1

Probably the most proven cell-free DNA-based non-invasive prenatal test (NIPT) 1

Email Address

Pose a question to your maternity care provider for the Harmony test. You may also contact our customer solutions team.

Phone: 1-855-927-4672 (Toll-Free) Call: 1-925-854-6246

What’s NIPT?

Non-invasive testing that is prenatalNIPT) uses cell-free DNA (cfDNA) based on the pregnancy to evaluate feasible chromosomal conditions in a maternity. NIPT is really a prenatal assessment test which can be done as early as 10 months of being pregnant utilizing a blood draw that is single. Prenatal diagnostic tests such as amniocentesis and CVS diagnose the current presence of chromosomal conditions. They truly are typically done later on in maternity and so are connected with a little threat of maternity loss.

Why display for chromosomal conditions?

Chromosomal conditions such as for example Down problem can impact handling of your maternity and distribution besides the ongoing wellness of one’s newborn.

These conditions sometimes happens in almost any pregnancy- even though there’s absolutely no family history- since they typically aren’t inherited. They happen by “chance”, and though the chance increases with mother’s age, many infants with chromosomal conditions are created to females under 35 years of age. 1

That’s why the United states College of Obstetricians and Gynecologists (ACOG) advises that most expecting mothers be provided assessment and diagnostic tests for chromosomal conditions. 2 And because NIPT is considered the most screening that is sensitive for trisomies 21, 18, and 13, the Global Society for Prenatal Diagnosis (ISPD) supports offering NIPT to any or all expectant mothers. 3

Your prenatal screening results can offer both you and your physician with information particular to your maternity so you can do have more informed conversations regarding the prenatal care.

  1. The California Prenatal Screening Program. March 2009. Company Handbook 2009.
  2. ACOG Practice Bulletin 163 Obstet Gynecol. 2016 May;127(5):e123-37.
  3. Benn et al. Prenat Diagn 2015; 35: 725–734.

For the baby’s health insurance and your satisfaction

The Harmony® prenatal test is really a style of NIPT, that could additionally be called NIPS (non-invasive prenatal testing). It appears to be at fragments of the baby’s DNA in your bloodstream to give information that is accurate the chance for the most frequent chromosomal conditions as soon as 10 months. It may determine the intercourse of one’s child.

Why display screen for chromosomal conditions?

Chromosomal conditions such as for example Down problem can affect handling of your pregnancy and distribution besides the health of the newborn.

These conditions sometimes happens in every pregnancy- even if there isn’t any family members history- since they typically aren’t inherited. They happen by “chance”, and though the chance increases with mom’s age, many children with chromosomal conditions are created to females under 35 years. 1

That’s why the United states College of Obstetricians and Gynecologists (ACOG) advises that every expecting women be provided assessment and diagnostic tests for chromosomal conditions. 2 And since NIPT is one of sensitive and painful testing choice for trisomies 21, 18, and 13, the Global Society for Prenatal Diagnosis (ISPD) supports offering NIPT to all or any expecting mothers. 3

Your prenatal screening results can offer you and your medical professional with information certain to your maternity in order to do have more informed conversations regarding the prenatal care.

  1. The California Prenatal Screening Program. March 2009. Company Handbook 2009.
  2. ACOG Practice Bulletin 163 Obstet Gynecol. 2016 May;127(5):e123-37.
  3. Benn et al. Prenat Diagn 2015; 35: 725–734.

For a variety of conditions

Chromosomal conditions can happen in every maternity. The Harmony test that is prenatal for the most typical ones, including:

  • Trisomy 21 (Down syndrome), trisomy 18 and trisomy 13
  • 22q11.2 microdeletion
  • Monosomy X
  • Sex chromosome aneuploidies (SCA)

For three reasons that are good

Clear responses to your concerns

More accurate than old-fashioned testing 2

Less alarms that are false

Lower false positive rates * than conventional testing tests 2 *Reports a large probability for the condition when it’s NOT actually present.

Successful by clinical ev >

Evaluated in peer-reviewed magazines involving >148,000 pregnancies in females both under and over age 35 1

Clear responses to your concerns

More accurate than old-fashioned assessment 2

Less false alarms

Lower false positive rates * than conventional testing tests 2 *Reports a big probability for a condition if it is NOT actually present.

Tested by clinical ev >

Evaluated in peer-reviewed magazines involving >148,000 pregnancies in women both under and over age 35 1

Private stories of three moms and their journeys

Melissa’s Personal Story

I will be the caretaker of two kiddies, a child and a son. A boy at the age of 40, I became pregnant with my second child. My spouce and I knew through the outset I would personally decide to go through a non-invasive test that is prenatalNIPT). We’d skilled a miscarriage with my very first maternity, so that it ended up being vital that you be equipped with because much information as feasible in regards to the health of our infant. We wished to additionally be prepared if our infant encountered any possible chromosomal conditions.

We had been proactive about going for a NIPT and I also decided to use the Harmony® Prenatal Test, that we discovered from my research, through buddies and my medical practitioner, can be performed because early as 10 months of maternity. NIPT appeared like such a much better choice than many other screenings which were open to me personally formerly. The test would offer a far more accurate outcome for Down problem compared to older assessment tests.

I’ve supported friends who’d false positives with other prenatal testing practices, therefore precision had been important. I’d an experience that is wonderful the Harmony test. It absolutely was effortlessly administered, so we received the total outcomes, which came ultimately back normal, quickly. I think that collecting information during one’s pregnancy is very important. This screening offered the given information we desired.

Barbara’s Personal tale

I will be a mother to 3 children that are beautiful two on the planet plus one angel whom watches over us.

We became expecting with my very very first youngster last year and, at that time, non-invasive testing that is prenatalNIPT) wasn’t available. From the this obviously when I discovered of the chromosomal that is possible during my child from a routine ultrasound and bloodstream test during my 2nd trimester. My spouce and I confirmed through amniocentesis which our unborn daughter, Joan, had trisomy 18.

We learned that trisomy 18 is just a uncommon condition that causes severe variations in development – so serious that many infants with trisomy 18 perish during delivery or briefly a short while later. Our physician talked about our choices we chose to continue our pregnancy with Joan, knowing the difficult challenges we faced with us, and.

We have experienced two more young ones since Joan’s delivery and death. During those pregnancies, we utilized the Harmony® test that is prenatal. Provided our experience losing our child to trisomy 18, we had been thinking about NIPT for many different reasons.

The NIPT had been appealing it can be done in the first trimester as it’s a simple blood draw – quick, relatively painless, with no risk to the pregnancy- and. We knew that when the NIPT outcome had shown a top chance for the chromosomal condition, it would have allowed us additional time to organize for the young child’s unique requirements in addition to road ahead.

We additionally knew that individuals didn’t wish to have invasive evaluating unless a problem ended up being suspected. Both in situations, our Harmony test result revealed that our youngsters had been not likely to possess three of the most extremely chromosome that is common: trisomy 21, trisomy 18 and trisomy 13. Having NIPT into the trimester that is first relieve our anxiety through the entire final two pregnancies. It aided provide us with some satisfaction.

Jean’s Personal tale

I’m sure firsthand essential a noninvasive test that is prenatalNIPT) are in assisting parents prepare for their children. While expecting with my 2nd son we had accepted blood testing having a translucency that is nuchal, therefore the outcomes revealed that my child had a higher possibility of being created with Down problem. I became worried to the point of sickness, and wanted more details. The follow-up choices presented to my hubby and me are not satisfying to us.

I consequently found out that the Harmony test has an increased precision compared to older assessment tests, therefore I asked my medical practitioner for this. I quickly received the outcome, which indicated that my infant had an extremely chance that is low of Down problem, along with other two conditions tested.

I’m happy to report our young boy happens to be three-years-old and doing great. I will be therefore happy that We made a decision to simply take the Harmony test. Harmony NIPT to our experience ended up being a good one. I’m glad We took the effort for more information on prenatal assessment choices and I also would encourage other expectant mothers to accomplish exactly asianwifes the same in their trimester that is first to very very very early responses.

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