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Benetech PRA
prenatal risk assessment software offers
first and second trimester screening for Down syndrome and Trisomy 18, calculating
risk based on some or all of these markers:
| First Trimester |
Second Trimester |
| PAPP-A |
AFP |
| Free beta hCG |
Free beta hCG |
| Total hCG |
Total hCG |
| Dimeric Inhibin A |
Dimeric Inhibin A |
| Nucal Translucency |
uE3 |
| Nasal Bone |
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Using one of several internationally recognized algorithms including SURUSS, or one of
your own specification.
Second trimester screening for Open Spina Bifida (OSB) calculating risk based on AFP MoM's.
Multiple marker screening for SLOS may also be calculated.
Features
- The ability to define various standard test panels to enable fully automated batch processing.
Each panel can have its own cutoffs, markers, etc.
- Integrated, sequential and contingent screening
(in countries where patent applies, a licence must be obtained from the patent holder)
- User definable races and sub-populations with choice of race-specific medians or factors
- IVF data entry and risk adjustment
- Support for Wald/Rish algorithm for twins
- Extensive new NT quality reports
- Median adjustment for Insulin Dependant Diabetes, Smoking and Rh negative sub-populations
- Real-time interpretive engine that links to LIS
- Full support for traditional and simplified Chinese character set
- PRA can be installed locally, or you can use our web-enabled PRA from any web browser
- Pre-defined user-amendable interpretive comments
- Enterprise version - allows sharing of multiple databases over several
sites each of which maintains its own data set of patient records, medians
and physicians with central or individual site statistical and QA reporting
Benetech PRA
benefits our clients by providing
- a state-of-the-art software that satisfies the stringent and ever-changing
requirements of prenatal screening practice, and conforms to CAP and
ACOG guidelines
- multi-level security to protect confidential patient and clinical
information
- quick and easy access to patient and sample data
- flexibility so the user can tailor the program to local populations
and clinical practices
- a variety of clear interpretive reports
- audit trails to track changes
- statistical, administrative and QC reports for
monitoring the effectiveness of the program
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