Extensive blinded, published validation data
The Harmony Prenatal Test is broadly studied, including 11 blinded published validation trials.1-11
In blinded prospective published trials including over 22,000 pregnant women from ages 18 to 50, Harmony demonstrated exceptional sensitivity and specificity. 1-2,4,7,11
Combined Harmony Performance Across All Clinical Studies
|Detection Rate||> 99 %|
|Taux de faux positifs||< 0,1 %|
|Taux de faux positifs|
|Taux de faux positifs||<0,1 %|
Harmony is Validated for Pregnant Women of Any Age or Risk Categories† and Trusted by Clinicians Worldwide
Studied extensively in blinded prospective published trials including >22,000 pregnant women. 1-2,4,7,11
Clinicians in more than 100 countries have trusted Harmony to screen more than 500,000 pregnancies.12
†Harmony has been studied extensively in women both under and over age 35, studies have included women ages 18-48.
The Harmony Prenatal Test Shows Clear Difference Between High-Risk and Low-Risk Results12
The below graphs represent data from the blinded prospective head to head comparison study of First Trimester Screening (FTS*) against Harmony. 11-12
Data represent 15,841 patients in a general pregnancy population.12
Harmony provides clear results for trisomy 21 risk, generating a wide separation between high-risk and low-risk values, with only extremely rare (less than 1 in 1000) false-positive results.12
*Serum PAPP-A, total or free ß-hCG & Nuchal Translucency
Valeur positive prédictive (VPP) exceptionnelle
Positive Predictive Value (PPV) is the likelihood that a positive test result is a true-positive. PPV varies by population.
Harmony’s extremely low false-positive rate of less than 0.1% gives it a high PPV for trisomy 21.1,11 Harmony has a PPV for trisomy 21 of 93% in pregnancies in women age 35, where the incidence of fetal trisomy 21 is 1 in 249.1 In contrast, for this same population, the PPV of traditional first trimester screening is 6%.15
Valeur positive prédictive (VPP) et incidence
PPV depends on the incidence of the condition being tested. The rarer the condition, the higher the probability a positive result is a "false positive". 16
Testing for extremely rare conditions (1 in 10,000 incidence rate) in a routine genetic test may:
- Augmenter le taux cumulé de faux positifs de l'ensemble du test
- Diminuer de façon significative la VPP de l'ensemble du test
2. Nicolaides et al. Am J Obstet Gynecol. 2012 Nov;207(5):374.e1-6.
3. Ashoor et al. Ultrasound Obstet Gynecol. 2013 Jan;41(1):21-5.
4. Verweij et al. Prenat Diagn. 2013 Oct;33(10):996-1001.
5. Ashoor et al. Am J Obstet Gynecol. 2012 Apr;206(4):322.e1-5.
6. Sparks et al. Am J Obstet Gynecol. 2012 Apr;206(4):319.e1-9.
7. Gil et al. Fetal Diagn Ther. 2014;35:204-11.
8. Nicolaides et al. Fetal Diagn Ther. 2014;35(1):1-6.
9. Hooks et al. Prenat Diagn. 2014 May;34(5):496-9.
10. Sparks et al. Prenat Diagn. 2012 Jan;32(1):3-9.
11. Norton M, et al, N Engl J Med. 2015 Apr 23;372(17):1589-97.
12. Data on file
13. Juneau et al. Fetal Diagn Ther. 2014;36(4):282-6.
14. Estimate based on an average-risk population with prevalence for T21, T18, and T13 of 1 in 700, 1 in 5000, and 1 in 16000 respectively.