Influence of transvaginal ultrasound examination on quantitative vaginal fibronectin measurements: a prospective evaluation study
-
Michaela Golic
, Jan-Peter Siedentopf
, Franziska Pauly , Larry Hinkson , Wolfgang Henrich and Elisabeth Tucher
Abstract
Objective:
The most important parameter in prediction of preterm birth is the cervical length measured by transvaginal ultrasound. In cases with mid-range cervical length (10–30 mm), prediction of preterm birth is difficult. In these cases, testing for cervicovaginal fluid fetal fibronectin (fFN) can improve prediction. However, it is unclear whether transvaginal ultrasound itself influences the fFN result. The purpose of this study was to evaluate this issue independent of gestational age and cervical length.
Methods:
A prospective evaluation study with 96 cases of pregnant women at 20–41 weeks of gestation was conducted in a tertiary perinatal center. A comparison of cervicovaginal fFN samples before and immediately after transvaginal ultrasound was performed. Fetal fibronectin was measured using the Hologic Rapid fFN 10Q system. It was analyzed quantitatively and qualitatively with ≥50 ng/mL as threshold for “positive”. Changes in fFN values following transvaginal ultrasound were measured.
Results:
Ninety-six percent (69/72) of women with a fFN concentration of <26 ng/mL before ultrasound had a corresponding fFN value <26 ng/mL after ultrasound. Ninety-three percent (13/14) of women with a fFN concentration of ≥100 ng/mL before ultrasound had a corresponding fFN value ≥100 ng/mL after ultrasound. In 80% (4/5) of women with a positive fFN sample but with a value <100 ng/mL, it turned negative (<50 ng/mL) after ultrasound. For fFN concentrations ≥100 ng/mL, there are high random fluctuations in the measurement results.
Conclusions:
Fetal fibronectin values of <26 ng/mL (for “negative”) and ≥100 ng/mL (for “positive”) from samples taken after ultrasound provide the same qualitative information as when sampled before ultrasound. For the correct interpretation however, quantitative analysis is necessary.
Acknowledgment:
We thank Dr. Andreas Busjahn (HealthTwiSt GmbH, Berlin, Germany) for providing excellent statistical analysis.
Conflict of interest statement: Hologic, Inc. provided us with free fetal fibronectin specimen collecting kits and the fFN 10Q analyzing system including the positive and negative controls. Wolfgang Henrich is member of the European advisory board on fetal fibronectin, which is sponsored by Hologic, Inc.
References
[1] International classification of diseases and related health problems. 10th revision. Geneva: World Health Organization. 1992.Search in Google Scholar
[2] Huddy CL, Johnson A, Hope PL. Educational and behavioural problems in babies of 32-35 weeks gestation. Arch Dis Child Fetal Neonatal Ed. 2001;85:F23–8.10.1136/fn.85.1.F23Search in Google Scholar
[3] Wang ML, Dorer DJ, Fleming MP, Catlin EA. Clinical outcomes of near-term infants. Pediatrics. 2004;114:372–6.10.1542/peds.114.2.372Search in Google Scholar
[4] Petrou S. The economic consequences of preterm birth during the first 10 years of life. Br J Obstet Gynaecol. 2005;112(Suppl 1):10–5.10.1111/j.1471-0528.2005.00577.xSearch in Google Scholar
[5] Petrou S, Mehta Z, Hockley C, Cook-Mozaffari P, Henderson J, Goldacre M. The impact of preterm birth on hospital inpatient admissions and costs during the first 5 years of life. Pediatrics. 2003;112(6 Pt 1):1290–7.10.1542/peds.112.6.1290Search in Google Scholar
[6] Blencowe H, Cousens S, Oestergaard MZ, Chou D, Moller AB, Narwal R, et al. National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications. Lancet. 2012;379:2162–72.10.1097/01.aoa.0000432360.25014.c3Search in Google Scholar
[7] Goldenberg RL, Culhane JF, Iams JD, Romero R. Epidemiology and causes of preterm birth. Lancet. 2008;371:75–84.10.1016/S0140-6736(08)60074-4Search in Google Scholar
[8] Matsuura H, Hakomori S. The oncofetal domain of fibronectin defined by monoclonal antibody FDC-6: its presence in fibronectins from fetal and tumor tissues and its absence in those from normal adult tissues and plasma. Proc Natl Acad Sci USA. 1985;82:6517–21.10.1073/pnas.82.19.6517Search in Google Scholar PubMed PubMed Central
[9] Lockwood CJ, Senyei AE, Dische MR, Casal D, Shah KD, Thung SN, et al. Fetal fibronectin in cervical and vaginal secretions as a predictor of preterm delivery. N Engl J Med. 1991;325:669–74.10.1056/NEJM199109053251001Search in Google Scholar PubMed
[10] Shennan A, Jones G, Hawken J, Crawshaw S, Judah J, Senior V, et al. Fetal fibronectin test predicts delivery before 30 weeks of gestation in high risk women, but increases anxiety. Br J Obstet Gynaecol. 2005;112:293–8.10.1111/j.1471-0528.2004.00420.xSearch in Google Scholar PubMed
[11] Liong S, Di Quinzio M, Fleming G, Permezel M, Rice G, Georgiou H. New biomarkers for the prediction of spontaneous preterm labour in symptomatic pregnant women: a comparison with fetal fibronectin. Br J Obstet Gynaecol. 2015;122:370–9.10.1111/1471-0528.12993Search in Google Scholar PubMed
[12] Fell DB, Sprague AE, Grimshaw JM, Yasseen AS 3rd, Coyle D, Dunn SI, et al. Evaluation of the impact of fetal fibronectin test implementation on hospital admissions for preterm labour in Ontario: a multiple baseline time-series design. Br J Obstet Gynaecol. 2014;121:438–46.10.1111/1471-0528.12511Search in Google Scholar
[13] Gomez R, Romero R, Medina L, Nien JK, Chaiworapongsa T, Carstens M, et al. Cervicovaginal fibronectin improves the prediction of preterm delivery based on sonographic cervical length in patients with preterm uterine contractions and intact membranes. Am J Obstet Gynecol. 2005;192:350–9.10.1016/j.ajog.2004.09.034Search in Google Scholar
[14] Goldenberg RL, Iams JD, Mercer BM, Meis PJ, Moawad AH, Copper RL, et al. The preterm prediction study: the value of new vs standard risk factors in predicting early and all spontaneous preterm births. NICHD MFMU Network. Am J Public Health. 1998;88:233–8.10.2105/AJPH.88.2.233Search in Google Scholar
[15] Rizzo G, Capponi A, Arduini D, Lorido C, Romanini C. The value of fetal fibronectin in cervical and vaginal secretions and of ultrasonographic examination of the uterine cervix in predicting premature delivery for patients with preterm labor and intact membranes. Am J Obstet Gynecol. 1996;175:1146–51.10.1016/S0002-9378(96)70020-0Search in Google Scholar
[16] Defranco EA, Lewis DF, Odibo AO. Improving the screening accuracy for preterm labor: is the combination of fetal fibronectin and cervical length in symptomatic patients a useful predictor of preterm birth? A systematic review. Am J Obstet Gynecol. 2013;208:233.e1–6.10.1016/j.ajog.2012.12.015Search in Google Scholar
[17] Kurtzman J, Chandiramani M, Briley A, Poston L, Das A, Shennan A. Quantitative fetal fibronectin screening in asymptomatic high-risk patients and the spectrum of risk for recurrent preterm delivery. Am J Obstet Gynecol. 2009;200:263.e1–6.10.1016/j.ajog.2009.01.018Search in Google Scholar
[18] Abbott DS, Radford SK, Seed PT, Tribe RM, Shennan AH. Evaluation of a quantitative fetal fibronectin test for spontaneous preterm birth in symptomatic women. Am J Obstet Gynecol. 2013;208:122.e1–6.10.1016/j.ajog.2012.10.890Search in Google Scholar
[19] Iams JD, Casal D, McGregor JA, Goodwin TM, Kreaden US, Lowensohn R, et al. Fetal fibronectin improves the accuracy of diagnosis of preterm labor. Am J Obstet Gynecol. 1995;173:141–5.10.1016/0002-9378(95)90182-5Search in Google Scholar
[20] Peaceman AM, Andrews WW, Thorp JM, Cliver SP, Lukes A, Iams JD, et al. Fetal fibronectin as a predictor of preterm birth in patients with symptoms: a multicentre trial. Am J Obstet Gynecol. 1997;177:13–8.10.1016/S0002-9378(97)70431-9Search in Google Scholar
[21] van Baaren GJ, Vis JY, Grobman WA, Bossuyt PM, Opmeer BC, Mol BW. Cost-effectiveness analysis of cervical length measurement and fibronectin testing in women with threatened preterm labor. Am J Obstet Gynecol. 2013;209:436.e1–8.10.1016/j.ajog.2013.06.029Search in Google Scholar PubMed
[22] Ben-Haroush A, Poran E, Yogev Y, Glezerman M. Vaginal fetal fibronectin evaluation before and immediately after ultrasonographic vaginal cervical length measurements in symptomatic women at risk of preterm birth: a pilot study. J Matern Fetal Neonatal Med. 2010;23:854–6.10.3109/14767050903300977Search in Google Scholar PubMed
Supplemental Material:
The online version of this article (DOI: 10.1515/jpm-2015-0270) offers supplementary material, available to authorized users.
©2017 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
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- Editorial
- What’s new in preterm birth prediction and prevention?
- Academy’s Corner
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- Biomarkers of spontaneous preterm birth: a systematic review of studies using multiplex analysis
- Influence of transvaginal ultrasound examination on quantitative vaginal fibronectin measurements: a prospective evaluation study
- Evaluation of quantitative fFn test in predicting the risk of preterm birth
- The value of ultrasound measurement of cervical length and parity in prediction of cesarean section risk in term premature rupture of membranes and unfavorable cervix
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- Congress Calendar
- Congress Calendar
Articles in the same Issue
- Frontmatter
- Editorial
- What’s new in preterm birth prediction and prevention?
- Academy’s Corner
- Antenatal corticosteroids: current controversies
- Review articles
- The safety of progestogen in the prevention of preterm birth: meta-analysis of neonatal mortality
- Cervical pessary for the prevention of preterm birth: is it of any use?
- Maternal and neonatal outcomes following expectant management of preterm prelabour rupture of membranes before viability
- Highlight articles
- Placental malperfusion as a possible mechanism of preterm birth in patients with Müllerian anomalies
- Nifedipine increases fetoplacental perfusion
- Effect of sleep disorders on threatened premature delivery
- Risk of recurrent preterm birth among women according to change in partner
- Biomarkers of spontaneous preterm birth: a systematic review of studies using multiplex analysis
- Influence of transvaginal ultrasound examination on quantitative vaginal fibronectin measurements: a prospective evaluation study
- Evaluation of quantitative fFn test in predicting the risk of preterm birth
- The value of ultrasound measurement of cervical length and parity in prediction of cesarean section risk in term premature rupture of membranes and unfavorable cervix
- Comparison of the duo of insulin-like growth factor binding protein-1/alpha fetoprotein (Amnioquick duo+®) and traditional clinical assessment for diagnosing premature rupture of fetal membranes
- Efficacy of a prospective community-based intervention to prevent preterm birth
- Maternal complications in settings where two-thirds of extremely preterm births are delivered by cesarean section
- The risk of neonatal respiratory morbidity according to the etiology of late preterm delivery
- Thyroid dysfunction in preterm neonates exposed to iodine
- Congress Calendar
- Congress Calendar