Modified Foam Stability Test (Fs-50) as Predictor of Fetal Lung Maturity in Preterm Premature Rupture of Membrane Patients Given Dexamethasone Therapy

Olivia Listiowati Prawoto, Tjokorda Gde, Agung Suwardewa, Putu Made Darmayasa, Doster Mahayasa, I. Nyoman, Bayu Mahendra, Evert Solomon, P. D. Mahayasa, Solomon Pangkahila
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Abstract

This study aims to determine the ability of the Modified Foam Stability (FS-50) test to predict fetal lung maturity in preterm premature rupture of membranes treated with Dexamethasone. The study sample included pregnant women with PROM at a gestational age of 24 to less than 34 weeks in the ER and Obstetrics Ward of Sanglah Central General Hospital, Denpasar. The patient underwent a vaginal speculum examination to collect fluid pooled in the vagina or from the outer cervical opening. Fluids are checked with the Modified Foam Stability (FS-50) test and graded from 0 to +4 to estimate fetal lung maturity. The first test was performed before Dexamethasone, followed by serial examinations at 12-hour intervals for 48 hours. Before dexamethasone injection, all patients got 0 scores as a baseline. There were statistically significant differences in FS-50 values before and after injection of the first, second, third, and fourth doses of Dexamethasone in PPROM patients. Fetal lung maturity was reached after the third dose of dexamethasone injection (36 hours after the first injection), characterized by an FS-50 value of > +3 and no asphyxia in the newborn. Spearman's rank analysis showed a significant correlation (p=0.005) between infants' maximum FS-50 value and asphyxia status. The FS-50 value > +3 is associated with the absence of asphyxia in infants born to PPROM patients who were given Dexamethasone for lung maturation. FS-50 can predict fetal lung maturity in preterm premature rupture of membranes given dexamethasone therapy.
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改良泡沫稳定性试验(Fs-50)在给予地塞米松治疗的胎膜早破患者中作为胎儿肺成熟度的预测指标
本研究旨在确定改良泡沫稳定性(FS-50)试验对地塞米松治疗的早产儿胎膜早破胎儿肺成熟度的预测能力。研究样本包括登巴萨Sanglah Central General Hospital急诊室和产科病房24至34周的胎龄为早舞会的孕妇。患者行阴道窥镜检查,收集阴道内或宫颈外开口积液。用改良泡沫稳定性(FS-50)测试检查液体,并从0到+4分级,以估计胎儿肺成熟度。在使用地塞米松之前进行第一次检查,随后每隔12小时进行连续检查,持续48小时。注射地塞米松前,所有患者均以0分为基线。PPROM患者注射第1、2、3、4次地塞米松前后FS-50值差异有统计学意义。第三次地塞米松注射后(第一次注射后36 h)胎儿肺成熟,FS-50值> +3,新生儿无窒息。Spearman秩次分析显示,婴儿最大FS-50值与窒息状态之间存在显著相关(p=0.005)。FS-50值> +3与给予地塞米松促进肺成熟的PPROM患者所生婴儿无窒息相关。FS-50可以预测地塞米松治疗的早产胎膜早破胎儿肺成熟度。
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