![Qiagen/AmniSure ROM Test (Rupture of [fetal] Membranes test)/For the detection of PAMG-1 in the amniotic fluid found in vaginal discharge of pregnant women/ASSK100](https://www.ebiomall.cn/images/Qiagen/2_8.jpeg)
For the detection of PAMG-1 in the amniotic fluid found in vaginal discharge of pregnant women
/ASSK100AmniSure ROM Test (Rupture of [fetal] Membranes test)
For the detection of PAMG-1 in amniotic fluid found in vaginal discharge of pregnant women
- 99% sensitive and 98% specific to support accuracy of negative and positive ROM clinical results
- No gestational age limit
- Not affected by urine, semen, vaginal infections and trace amounts of blood on the swab (1)
The AmniSure ROM (Rupture Of [fetal] Membranes) Test is a rapid, non-instrumented, qualitative immunochromatographic test for the in vitro detection of amniotic fluid in vaginal discharge of pregnant women. The AmniSure ROM Test uses amniotic fluid test strips to detect the PAMG-1 protein marker of the amniotic fluid in vaginal discharge. The amniotic fluidtest isused by health care professionalsto aid in the detection of ROM in pregnant women reporting signs, symptoms, or complaints suggestive of ROM. Want to try this solution for the first time? Request a quote for a trial kit.
Watch the AmniSure training video here.
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Cat No./ID:ASSK100 AmniSure Test Starter Kit Inquire For the detection of PAMG-1 in the amniotic fluid found in vaginal discharge of pregnant women. |
Cat No./ID:ASSKCP100 AmniSure ROM Test CAP Starter Kit Inquire For the detection of PAMG-1 in the amniotic fluid found in vaginal discharge of pregnant women. |
Cat No./ID:ASSKNE100 AmniSure ROM Test ExtStarter Kit Inquire For the detection of PAMG-1 in the amniotic fluid found in vaginal discharge of pregnant women. |
Cat No./ID:ASVC020 AmniSure Solution with Cap and Vial (20) Inquire For the detection of PAMG-1 in the amniotic fluid found in vaginal discharge of pregnant women. |
Cat No./ID:FMRT-1-10-US AmniSure ROM Test (10) Inquire For the detection of PAMG-1 in the amniotic fluid found in vaginal discharge of pregnant women |
Cat No./ID:FMRT-1-25-US AmniSure ROM Test (25) $1,499.00 For the detection of PAMG-1 in the amniotic fluid found in vaginal discharge of pregnant women |
The AmniSure ROM Test (Rupture of [fetal] Membranes test) are intended for in vitro diagnostic use.
- AmniSure ROM (Rupture of [fetal] Membranes) Test Instructions for Use. QIAGEN, 2015.
- Cousins LM et al. AmniSure placental alpha microglobulin-1 rapiimmunoassay versus standard diagnostic methods for detection of rupture of membranes. Am J Perinatol. 2005 Aug; 22(6): 317-20.
- Lockwood CJ et al. Fetal membrane rupture is associated with the presence of insulin-like growth factor-binding protein-1 in vaginal secretions. Am. J. Obstet. Gynecol. 1994 Jul;171(1):146-50.
- Caughey AB et al. Contemporary diagnosis and management of preterm premature rupture of membranes. Rev Obstet Gynecol. 2008 Winter; 1(1): 11-22.
Product Details
Premature rupture of fetal membranes (PROM) occurs in about 10% of pregnancies and poses one of the most important therapeutic dilemmas in current obstetric practice (2). Management of patients with PROM and pPROM (pre-term PROM, occurring before 37 weeks gestation) is expensive and remains an important perinatal dilemma as the clinician attempts to balance the risk of prolonging gestation against the risks of infection (2).
Risks of PROM at term are related to serious neonatal consequences such as pre-term delivery, fetal distress, prolapsed cord, abruptio placentae and infection (2). pPROM accounts for 20% to 40% of PROM cases, and is associated with 20% to 50% of premature births. Complications of pPROM include infectious morbidity in the mother and fetus, pulmonary hypoplasia of the fetus, prolapse of the umbilical cord, development of fetal deformities, and postnatal endometritis (2). All of these consequences significantly increase risk of fetal and maternal morbidity and mortality.
The AmniSure ROM Test kit is a self-contained system that can serve as part of your overall clinical evaluation of PROM, which is crucial to ensure appropriate obstetric measures are taken in the event of a rupture. Failure to identify patients with ROM can result in the failure to intervene appropriately.
Conversely, the false diagnosis of ROM can lead to inappropriate interventions (e.g., hospitalization or induction of labor). Therefore the correct and timely diagnosis of ROM is of crucial importance for the clinician (2). Accurate diagnosis of [fetal] membranes rupture, however, remains a frequent clinical problem in obstetrics (2-4).
Other available tests have limitations or are in some degree invasive (2). The AmniSure ROM Test is a rapid, non-invasive, amniotic fluidtest that can aid in the detection of ROM, providing rapid, easy-to-interpret and timely results. As an alternative to conventional methods of ROM detection, the AmniSure test has a 99% sensitivity and 98% specificity to support accuracy of negative and positive ROM clinical results.The simple 4-step test procedure* detects placental alpha microglobulin-1 (PAMG-1) a protein found in high concentrations in amniotic fluid and low concentration in cervicovaginal fluid (4).
- Collect sample of vaginal discharge with sterile collection swab (no speculum required).
- Rinse specimen swab in solvent vial. Discard swab.
- Insert amniotic fluidtest strip into vial and remove if 2 lines are visible, or at 10 minutes sharp.
- Results are observed and recorded.
*Please refer to package insert for complete instructions for use.
The AmniSure test is for use by healthcare professionals to aid in the detection of fetal membranes rupture in pregnant women when they report signs, symptoms, or complaints suggestive of such a rupture.
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