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Cervical Stiffness Index as predictor of preterm birth in women with threatened preterm labor

医学 早产 早产 产科 索引(排版) 濒危物种 早产 早产 妇科 横断面研究
作者
Dario Colacurci,Gabriele Saccone,Alessandra Ammendola,Giorgia Buonomo,Chiara Murolo,M. Locci
出处
期刊:European Journal of Obstetrics & Gynecology and Reproductive Biology [Elsevier BV]
卷期号:318: 114910-114910 被引量:1
标识
DOI:10.1016/j.ejogrb.2025.114910
摘要

OBJECTIVE: To determine the uterine cervix stiffness in patients presenting with threatened preterm labor (PTL) measured with an aspiration-based device (expressed as Cervical Stiffness Index - CSI) and to correlate CSI with pregnancy outcomes. STUDY DESIGN: weeks. Patients underwent a physical examination, ultrasound examination, transvaginal ultrasound cervical length (CL) measurement and cervical stiffness assessment using the Pregnolia System, an aspiration-based device measuring the vacuum required to displace the tissue into the device tip by a fixed distance, a proxy for stiffness (CSI, mbar). Higher CSI indicates stiffer tissue. RESULTS: Between April 2022 and August 2024, 100 patients with signs and symptoms of PTL were recruited. Thirty-five had a PTB, of which 7 delivered < 34 weeks, 5 within 14 days and 11 within 28 days from measurement. CSI and CL were significantly different between patients delivering at term and patients with a PTB. The Area under the Curve of CSI and CL for prediction of delivery ≤ 14 days from measurement were 0.979 (95 % CI, 0.952-1.000) and 0.744 (0.369-1.000), respectively; for delivery ≤ 28 days from measurement, 0.802 (0.612-0.993), and 0.764 (0.579-0.948), respectively; for PTB < 34 weeks, 0.873 (0.729-1.000) and 0.836 (0.563-1.000), respectively; and for PTB < 37 weeks 0.845 (0.763-0.926) and 0.779 (0.680-0.877), respectively. CONCLUSIONS: In patients presenting with threatened PTL, a softer cervix as measured by CSI was associated with an increased risk of preterm birth. These findings suggest that CSI has potential as a predictor of PTB in symptomatic patients, but require confirmation in larger, independent cohorts. CLINICAL TRIAL REGISTRATION: NCT05355649.
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