Dear OBGYN Reader -
 
The PartoSure Test was recently FDA approved.
 
Accurately assessing the risk of preterm birth is a major diagnostic challenge with significant implications. Clinical evaluation alone is limited in its ability to predict imminent delivery among patients with signs of threatened preterm labor (PTL).
 
Around 85% of patients admitted for threatened PTL do not deliver within 7 days (1). A more accurate assessment to identify those truly at risk is needed.
 
PartoSure is a rapid, qualitative test to aid in your risk assessment of spontaneous preterm birth within 7 days. The test is for pregnant women with signs and symptoms of early preterm labor. PartoSure test benefits include (2):
 
Results in 5 minutes
Semen does not interfere with the results
Speculum examination is not required
External reader or calibration is not required
 
 
References
 
1. Alfirevic, Z., Allen-Coward, H., Vinuesa, F. (2007) Targeted therapy for threatened preterm labor based on sonographic measurement of the cervical length: a randomized controlled trial. Ultrasound Obstet Gynecol. 29, 47–50.
2. PartoSure Test Instructions for Use. QIAGEN, 2018.  
 
For contact information, click here.
 
 
For up-to-date licensing information and product-specific disclaimers, see the respective QIAGEN kit handbook or user manual. QIAGEN kit handbooks and user manuals are available at www.qiagen.com or can be requested from QIAGEN Technical Services or your local distributor.
 
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