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期待治疗的未足月胎膜早破病例中潜伏期的影响。

The effects of latency period in PPROM cases managed expectantly.

作者信息

Baser Emre, Aydogan Kirmizi Demet, Ulubas Isik Dilek, Ozdemirci Safak, Onat Taylan, Serdar Yalvac Ethem, Demirel Nihal, Moraloglu Tekin Ozlem

机构信息

Department of Obstetrics and Gynecology, Faculty of Medicine, Yozgat Bozok University, Yozgat, Turkey.

Department of Neonatology, Etlik Zubeyde Hanim Women's Health Training and Research Hospital, Health Science University, Ankara, Turkey.

出版信息

J Matern Fetal Neonatal Med. 2020 Jul;33(13):2274-2283. doi: 10.1080/14767058.2020.1731465. Epub 2020 Feb 23.

Abstract

Preterm premature rupture of membranes (PPROM), associated with prematurity, is an important obstetric complication that may cause neonatal mortality and morbidity. The optimal delivery time is controversial in cases with the expectant approach. The fetal effects of long-term exposure to PPROM are unknown. This study aimed to evaluate the maternal and fetal outcomes of expectantly-managed PPROM cases with different latency periods at 24-34weeks of gestation. The study group consisted of 206 patients at 24-34weeks of gestation who met the inclusion criteria. Patients were divided into three groups according to their weeks of PPROM diagnosis as 24-28, 29-31, and 32-34. The period from membrane rupture to delivery was defined as the latency period and divided into three subgroups as 3-7 days, 8-13 days and ≥14 days. In addition to the demographic characteristics of the patients, maternal and obstetric complications, primary and secondary neonatal outcomes were compared between the groups. Primary neonatal outcomes were determined in terms of pathological Apgar scores (<5 at minute 1, <7 at minute 5), requiring resuscitation, admission to Neonatal Intensive Care Unit (NICU) and NICU length of stay. Secondary neonatal outcomes were determined in terms of respiratory distress syndrome, bronchopulmonary dysplasia, intraventricular hemorrhage, retinopathy of prematurity, necrotizing enterocolitis, patent ductus arteriosus, periventricular leukomalacia, and neonatal sepsis. In addition, for the prediction of morbidity and mortality, newborns were evaluated by SNAPPE II (Score for Neonatal Acute Physiology with Perinatal extension-II) consisting of the combination of biochemical and physiological parameters, using the parameters including mean blood pressure (mm/Hg), corporal temperature (°C), PO/FiO ratio, lowest serum pH, multiple seizures, urine output (ml/kg/hr), Apgar score, birth weight, and small for gestational age. The higher the score of SNAPPE II, the higher the morbidity and mortality risk of neonates. For the statistical analysis, the Kruskal Wallis and one-way ANOVA tests were utilized for the numerical data. Categorical data were compared using the chi-square test. The receiver operating characteristic (ROC) test was used to determine the threshold value of the data affecting neonatal morbidity. The mean PPROM week was found to be 29.7 ± 3.0 weeks and the mean delivery week was 31.8 ± 2.5 weeks. The mean latency period for all the patients was 15.1 ± 13.8 days. Clinic chorioamnionitis was observed in 17% of the cases. The lowest chorioamnionitis rate (8.6%) was in the 3-7-day latency period group. Total complications were significantly lower in the 29-31week PPROM group in which the latency period was ≥14 days, compared to those in 3-7 days and 8-13 days ( = .001). Total complications were lower in the < 32 weeks PPROM groups in which the latency period was ≥14 days compared to those obtained in 3-7 days and 8-13 days. There was no significant difference between the latency period and total complications after 32 weeks ( = .422). The best discriminative cutoff value of SNAPPE-II for neonatal morbidity was 11.0 (sensitivity 82%, specificity 80%). In the present study, the optimal latency period for the best neonatal outcomes was found to be 34.5 days (sensitivity 70% and specificity 84%) between weeks 24-28, and 11.0 days between weeks 29-31 (sensitivity 68% and specificity 85%). Our findings indicated that a long latency period did not increase neonatal morbidity and there was no increase in neonatal complications after 32 weeks of the gestational period compared to those obtained before 32 weeks.

摘要

胎膜早破(PPROM)与早产相关,是一种重要的产科并发症,可能导致新生儿死亡和发病。在采用期待疗法的情况下,最佳分娩时间存在争议。长期暴露于PPROM对胎儿的影响尚不清楚。本研究旨在评估妊娠24 - 34周采用期待疗法管理的不同潜伏期PPROM病例的母婴结局。研究组由206例妊娠24 - 34周符合纳入标准的患者组成。根据PPROM诊断孕周将患者分为三组,即24 - 28周、29 - 31周和32 - 34周。从胎膜破裂到分娩的时间定义为潜伏期,并分为三个亚组,即3 - 7天、8 - 13天和≥14天。除患者的人口统计学特征外,还比较了各组间的母体和产科并发症、新生儿主要和次要结局。新生儿主要结局根据病理阿氏评分(1分钟时<5分,5分钟时<7分)、需要复苏、入住新生儿重症监护病房(NICU)及NICU住院时间来确定。新生儿次要结局根据呼吸窘迫综合征、支气管肺发育不良、脑室内出血、早产儿视网膜病变、坏死性小肠结肠炎、动脉导管未闭、脑室周围白质软化和新生儿败血症来确定。此外,为预测发病率和死亡率,采用由生化和生理参数组合而成的SNAPPE II(新生儿急性生理学及围生期扩展-II评分)对新生儿进行评估,使用的参数包括平均血压(mmHg)、体温(℃)、PO/FiO比值、最低血清pH值、多次惊厥、尿量(ml/kg/hr)、阿氏评分、出生体重和小于胎龄。SNAPPE II评分越高,新生儿发病和死亡风险越高。对于统计分析,数值数据采用Kruskal Wallis检验和单因素方差分析。分类数据采用卡方检验进行比较。采用受试者工作特征(ROC)检验确定影响新生儿发病的数据阈值。发现PPROM的平均孕周为29.7±3.0周,平均分娩孕周为31.8±2.5周。所有患者的平均潜伏期为15.1±13.8天。17%的病例观察到临床绒毛膜羊膜炎。最低绒毛膜羊膜炎发生率(8.6%)出现在潜伏期为3 - 7天的组。与潜伏期为3 - 7天和8 - 13天的组相比,潜伏期≥14天的29 - 31周PPROM组的总并发症显著更低(P = 0.001)。潜伏期≥14天的<32周PPROM组的总并发症低于潜伏期为3 - 7天和8 - 13天的组。32周后潜伏期与总并发症之间无显著差异(P = 0.422)。SNAPPE-II对新生儿发病的最佳判别临界值为11.0(敏感性82%,特异性80%)。在本研究中,发现24 - 28周之间最佳新生儿结局的最佳潜伏期为34.5天(敏感性70%,特异性84%),29 - 31周之间为11.0天(敏感性68%,特异性85%)。我们的研究结果表明,较长的潜伏期不会增加新生儿发病率,与32周前相比,妊娠32周后新生儿并发症也没有增加。

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