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首页> 外文期刊>BMC Women s Health >Sequential E2 levels not ovarian maximal diameter estimates were correlated with outcome of cetrotide therapy for management of women at high-risk of ovarian hyperstimulation syndrome: a randomized controlled study
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Sequential E2 levels not ovarian maximal diameter estimates were correlated with outcome of cetrotide therapy for management of women at high-risk of ovarian hyperstimulation syndrome: a randomized controlled study

机译:序贯E2水平而非卵巢最大直径估计值与西妥替肽治疗卵巢过度刺激综合征高危女性的治疗效果相关:一项随机对照研究

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Ovarian hyperstimulation syndrome (OHSS) is an important condition with considerable morbidity and a small risk of mortality and most commonly results as an iatrogenic condition following follicular stimulation of the ovaries. We aimed to evaluate safety and efficacy of 3-day cetrotide therapy started on day of oocyte retrieval (Day-0) in women at high-risk for development of ovarian hyperstimulation syndrome (OHSS) after GnRH agonist induction protocol. Forty-eight women fulfilling inclusion criteria underwent ultrasound scanning for maximal ovarian diameter (MOD) estimation and ascites grading. Patients underwent embryo freezing, but the study group received 3-day Cetrotide sc injection (0.25?mg/day) started on Day-0. Serum E2, pain scores and MOD were checked daily. Hematocrite value (Ht%), total leucocytic count (TLC), gastrointestinal (GI) manifestations and ascites grading were re-evaluated on Day-3, 6 and 8. Sequential serum E2 levels decreased significantly in both groups with significantly lower levels in the study group. Sequential MOD estimates showed non-significant difference between the two groups and versus Day-0 estimates. On Day-2, pain scores showed progressive significant decrease compared to Day-0 scores in both groups with significantly lower scores in the study group. On Day-3; four control patients still had vomiting and by Day-6, 6 of the control patients still had GI manifestations with significant difference versus the study group. Compared to Day-0 estimates, Ht% and TLC were significantly lower on Day-3, 6 and 8 in the study group, but only on Day-8 in the control group. Day-3 and Day-8 ascites grading in both groups was significantly lower compared to respective Day-0 grading with significant difference in favor of the study group. Six patients required hospitalization, but without mortalities. Day-3 E2 levels in the study group showed positive significant correlation with clinical and other laboratory data and ascites grading, while the correlation was non-significant with MOD. The 3-day cetrotide therapy starting after oocyte retrieval with embryo transfer freezing could be an appropriate management policy for women received GnHR-agonist induction protocol and were at high-risk for OHSS. Sequential E2 serum levels could predict outcome more perfectly than sequential MOD estimates. Trial registration ( clinicaltrial.gov registration) NCT02823080 (retrospective) Initial Release 21–6-2016 Last Release 3–1-2017 Unique Protocol ID: Benha U Secondary IDs: kmsalama.
机译:卵巢过度刺激综合症(OHSS)是一种重要的疾病,发病率高,死亡风险小,最常见的结果是卵泡刺激卵巢后引起的医源性疾病。我们旨在评估在GnRH激动剂诱导方案后发生卵巢过度刺激综合征(OHSS)的高危女性中,从卵母细胞摘除日(第0天)开始的为期3天的十六肽治疗的安全性和有效性。符合纳入标准的48名妇女接受了超声扫描,以评估最大卵巢直径(MOD)和腹水等级。患者进行了胚胎冷冻,但研究组在第0天开始接受为期3天的塞罗肽皮下注射(0.25?mg /天)。每天检查血清E2,疼痛评分和MOD。在第3天,第6天和第8天重新评估了血细胞计数值(Ht%),总白细胞计数(TLC),胃肠道(GI)表现和腹水等级。学习小组。顺序MOD估算显示两组之间的差异无统计学意义,与Day-0估算相比无显着差异。在第2天,疼痛评分显示出与两组的Day-0评分相比逐渐降低,而研究组的评分显着降低。第3天; 4名对照患者仍在呕吐,到第6天,仍有6名对照患者的GI表现与研究组有显着差异。与第0天的估算值相比,研究组的第3天,第6天和第8天的Ht%和TLC显着降低,而对照组只有第8天。两组的第3天和第8天腹水评分明显低于相应的第0天评分,对研究组有利。六名患者需要住院治疗,但没有死亡。研究组的第3天E2水平与临床和其他实验室数据以及腹水分级呈正相关,而与MOD无关。对于接受了GnHR激动剂诱导方案并且处于OHSS高危状态的女性,从卵母细胞取出并进行胚胎移植冻结后开始的为期3天的鲸蜡肽疗法可能是合适的管理策略。顺序的E2血清水平比顺序的MOD估计更能预测结果。试用注册(Clinicaltrial.gov注册)NCT02823080(追溯性)初始版本21-6-2016最新版本3-1-2017唯一协议ID:Benha U次要ID:kmsalama。

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