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不同控制性卵巢过度刺激方案的临床经验研究:关注安全性和有效性。

Study of clinical experience with different approaches to controlled ovarian hyperstimulation: a focus on safety and efficacy.

机构信息

Medical University Sofia, Sofia, Bulgaria

Social Pharmacy, Faculty of Pharmacy, Sofia, Bulgaria.

出版信息

Eur J Hosp Pharm. 2021 Jan;28(1):33-37. doi: 10.1136/ejhpharm-2019-001870. Epub 2019 May 4.

Abstract

OBJECTIVES

Current retrospective cohort study analyses clinical database records of 4792 assisted reproduction procedures to assess the significance of target effectiveness endpoints from a safety perspective.

METHODS

Stimulation protocols with urinary, recombinant or combination of both types gonadotrophin preparations are compared according to the following primary endpoints: incidence of ovarian hyperstimulation syndrome (OHSS), cycle cancellation, follicle count, induced estradiol values, clinical pregnancy achieved and cycles reached embryo transfer/freezing. We have investigated the incidence of cases evaluated as 'risky for OHSS' by secondary efficacy endpoints (exogenous gonadotrophin exposure, luteinising hormone and progesterone values, oocyte yield, eggs with normal maturation). The following statistical methods were applied: descriptive statistics, Mann-Whitney test, Kruskal-Wallis test, Pearson chi-square test, Fisher's exact test, binary logistic regression.

RESULTS

Only 16 cases (0.42%) of moderate and delayed OHSS were established. Three hundred and seven (8.6%) stimulation cycles have been cancelled, principally among urinary protocols. Although the clinical pregnancy rate does not differ significantly in compared groups, punctured follicle count, oocyte yield and progesterone level were higher for recombinant preparations, followed by combined and urinary protocols. Follicle count, mean estradiol and luteinising hormone levels are within the 'safe window' for all investigated groups, associated with minimised risk of stimulation cancellation. The mean follicle-stimulating hormone (FSH) dose was highest in urinary protocols at the same duration of stimulation compared with recombinant products. The younger age, bigger follicle count, oocytes yield, mature oocytes count, percentage of fertilised oocytes, more embryos transferred and the later day of embryo transfer are critical for both assisted reproduction techniques (ART) success rate and the safety profile of sterility treatment.

CONCLUSIONS

Safety surveillance of ART exceeds the incidence of OHSS. Suboptimal effectiveness of stimulation protocols may also jeopardise the well-being of ART patients. Gonadotrophin exposure, induced values of sex hormones, and quantity and quality of extracted oocytes should be considered to minimise any unintended suffering of treated couples.

摘要

目的

本回顾性队列研究分析了 4792 例辅助生殖过程的临床数据库记录,从安全性角度评估了靶向有效性终点的意义。

方法

根据以下主要终点比较尿源性、重组或两者组合的促性腺激素制剂的刺激方案:卵巢过度刺激综合征(OHSS)的发生率、周期取消、卵泡计数、诱导的雌二醇值、临床妊娠率和达到胚胎移植/冷冻的周期数。我们通过次级疗效终点(外源性促性腺激素暴露、黄体生成素和孕酮值、卵母细胞产量、正常成熟的卵子)研究了评估为“OHSS 风险”的病例发生率。应用以下统计方法:描述性统计、Mann-Whitney 检验、Kruskal-Wallis 检验、Pearson χ2 检验、Fisher 确切检验、二项逻辑回归。

结果

仅确定了 16 例(0.42%)中度和迟发性 OHSS。307 例(8.6%)刺激周期被取消,主要发生在尿源性方案中。虽然比较组的临床妊娠率无显著差异,但重组制剂的穿刺卵泡计数、卵母细胞产量和孕酮水平较高,其次是联合和尿源性方案。卵泡计数、平均雌二醇和黄体生成素水平均在所有研究组的“安全窗口”内,与刺激取消的风险最小化相关。与重组产品相比,在相同的刺激持续时间内,尿源性方案的卵泡刺激素(FSH)平均剂量最高。年龄较小、卵泡计数较大、卵母细胞产量、成熟卵母细胞计数、受精卵母细胞百分比、移植胚胎数较多以及胚胎移植日较晚,对辅助生殖技术(ART)成功率和不孕治疗的安全性状况均至关重要。

结论

ART 的安全性监测超过了 OHSS 的发生率。刺激方案效果不理想也可能危及 ART 患者的健康。应考虑促性腺激素暴露、诱导的性激素水平以及提取的卵母细胞的数量和质量,以尽量减少治疗夫妇的任何意外痛苦。

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