LabCorp and its Specialty Testing Group, a fully integrated portfolio of specialty and esoteric testing laboratories.

Your patients deserve more, so you should expect more from an NIPT

New MaterniT collection kit

New MaterniT specimen collection kit

Introducing the upgraded MaterniT specimen collection kit, featuring new branding for better kit identification and fewer components – including one 10 mL Streck tube instead of two – for improved ease-of-use.

When your current NIPT is not enough, use MaterniT 21 PLUS, the most clinically complete NIPT solution.1-4

Time, experience and confidence are valuable resources in any practice. MaterniT 21 PLUS performs in key areas that ensure your time is spent wisely, delivering fast, reliable, and effective prenatal screening results.

Integrated Genetics has run over 1 million non-invasive prenatal tests (NIPT) since pioneering the technology in 2011, including more than 30,000 twins and more than 50,000 genome-wide tests;5 the depth of experience you should expect from an NIPT.

Now offering more screening options and flexibility than other NIPTs,1-4 including GENOME-Flex – the first NIPT high risk pathway – MaterniT 21 PLUS will deliver more value to your practice, and more service to your patients.

Each of the new features is designed to deliver a tangible positive benefit to you and your patients, while improving the service levels you should expect from an NIPT laboratory.

Maternit 21 Plus - New Features

Genome-Flex: the first NIPT high risk pathwayGenome-Flex: the first NIPT high risk pathway
Clear results with PPV and FFClear results with PPV and FF

Clear results with PPV and FFClear results with PPV and FF

MaterniT 21 PLUS now features Positive Predictive Value (PPV) in addition to Fetal Fraction (FF) on all positive lab reports, and Positive / Negative reporting to help you reduce time spent interpreting complicated patient reports. MaterniT 21 PLUS also allows for EMR and online interface ordering and reporting.

Click here to view a sample MaterniT 21 PLUS report.

Services

Patient Engagement ProgramPatient Engagement Program

Patient Engagement Program Genetics IconGenetics is complex; understanding pricing options doesn’t need to be

We work directly with your patients to make our pricing options transparent

With our new Patient Engagement Program, your choice of a genetic testing partner is clear

New cost estimator plus rapid, proactive support from our expert Every Mom Pledge team

Patient responsibility was $0 for over 74% of patients6

New program provides $299 price for MaterniT® 21 PLUS, informaSeq® and Inheritest® NGS for qualifying patients

Send your patients to integratedgenetics.com/transparency or call 844.799.3243

SOCIETY GUIDELINES Professional societies like ACOG, ACMG, and SMFM endorse and/or recognize NIPT as a screening option for all pregnant women
MaterniT® GENOME MaterniT® 21 Plus Other NIPTs**
Trisomy 13, 18, 21
Trisomy 13, 18, 21
Fetal sex
Fetal sex
Sex chromosome aneuploidies
Sex chromosome aneuploidies
Microdeletions
Microdeletions
Trisomy 16, 22
Trisomy 16, 22
GENOME-Flex high risk pathway
GENOME-Flex high risk pathway
Genome-wide with subchromosomal CNVs
Genome-wide with subchromosomal CNVs

*Optional feature. **Panorama® Prenatal Screen3 by Natera, PreludeTM Prenatal Screen4 by Counsyl, InnatalTM Prenatal Screen5 by Progenity, Harmony® Prenatal Test5 by Roche

30 years genetics

MaterniT® 21 PLUS customizable screening options and capabilities

MaterniT 21 PLUS also offers choice with four panels: Core; Core + ESS (enhanced sequencing series); Core + SCA (sex chromosome aneuploidies); and Core + ESS + SCA. With choice in panels— and fetal sex optional— MaterniT 21 PLUS is the most flexible and customizable commercial NIPT available.

Compare versions in the table below.

  MaterniT 21 PLUS Core MaterniT 21 PLUS + SCA MaterniT 21 PLUS + ESS MaterniT 21 PLUS + SCA + ESS GENOME-Flex (Add On) GENOME-Flex (Add On) Redraw
Fetal sex (optional)            
Trisomy 21 (Down syndrome)            
Trisomy 18 (Edwards syndrome)            
Trisomy 13 (Patau syndrome)            
Sex chromosome aneuploidies
45,X (Turner syndrome)            
47,XXY (Klinefelter syndrome)            
47,XXX (Triple X syndrome)            
47,XYY (XYY syndrome)            
ENHANCED SEQUENCING SERIES (CLINICALLY RELEVANT MICRODELETIONS AND ANEUPLOIDIES)
22q (DiGeorge syndrome)            
5p (Cri-du-chat syndrome)            
1p36 deletion syndrome            
15q (Prader-Willi syndrome)            
15q (Angelman syndrome)            
11q (Jacobsen syndrome)            
8q (Langer-Giedion syndrome)            
4p (Wolf-Hirschhorn syndrome)            
Trisomy 16            
Trisomy 22            

Do you have patients who have not had a test and have questions about costs or coverage? Send them to our estimator.

Do you have patients who have already had a test performed and are wondering when their results will be in? We can help.

Patients with questions about their test results who need schedule an appointment with a counselor can do so online.

References

  1. Illumina. https://www.illumina.com/clinical/illumina_clinical_laboratory/verifi-pr.... Accessed August 15, 2018.
  2. Natera. https://www.natera.com/panorama-test/clinical-information. Accessed August 15, 2018.
  3. Counsyl. https://www.counsyl.com/services/prelude/clinical-info. Accessed August 15, 2018.
  4. Progenity. https://progenity.com/tests/innatal. Accessed August 15, 2018.
  5. Harmony. https://www.harmonytestusa.com/healthcare-professionals/providing-harmony. Accessed August 15, 2018.
  6. Internal data
  7. Internal data
  8. Palomaki GE, Deciu C, Lambert-Messerlian GM, et al. DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study. Genet Med. 2011;13(11):913-920.
  9. Wardrop J, McCullough R, Boomer T, et al. Maternal weight – impact on noninvasive prenatal testing (NIPT). Clinical poster presented at ACMG annual meeting, Florida 2016.