Abstract

BackgroundAlthough a large number of studies have been dedicated to ovarian hyperstimulation syndrome (OHSS) none gave full embryological and clinical outcomes comparing oocyte trigger with human chorionic gonadotrophin (HCG) versus with a gonadotrophin-releasing hormone (GnRH) agonist (Buserelin) in cases with suspicious OHSS. The aim of the present study was thus to analyze 4894 consecutive assisted reproductive treatment cycles to undercover associated risk factors for development of OHSS, and the effects of the use of Buserelin as ovulation trigger on embryological and clinical outcomes.MethodsIn the 51 cases that developed OHSS, ovulation trigger was performed with HCG as indicators were not suspicious for OHSS. These were compared against two types of groups: 71 cases where Buserelin was used for ovulation induction due to suspicious development of OHSS; and those remaining 4772 cases where ovulation trigger was currently performed with HCG (control).ResultsOf the cases treated with Buserelin the oocyte maturation rate and the ongoing pregnancy rate were significantly lower, with higher rates of ectopic pregnancy and newborn malformations, but none developed OHSS. Of the OHSS cases, 23 needed hospitalization, with no major complications.ConclusionsYoung age, lower time of infertility, lower basal follicle stimulating hormone levels, higher number of cases with female factor and polycystic ovarian syndrome, high number of follicles and higher estradiol concentrations were the risk factors found associated with OHSS. Cases with OHSS also presented higher follicle count but the estradiol levels were within the normal range. It thus remains to develop more strict criteria to avoid all cases with OHSS.

Highlights

  • A large number of studies have been dedicated to ovarian hyperstimulation syndrome (OHSS) none gave full embryological and clinical outcomes comparing oocyte trigger with human chorionic gonadotrophin (HCG) versus with a gonadotrophin-releasing hormone (GnRH) agonist (Buserelin) in cases with suspicious OHSS

  • Sousa et al Reproductive Biology and Endocrinology (2015) 13:66 thromboembolism that can be fatal [5,6,7,8,9]. Due to these severe outcomes, the recognition of risk factors for the development of OHSS became crucial. These have been postulated to rely on young age, low body mass index (BMI), presence of polycystic ovarian syndrome (PCOS), high basal anti-Mullerian hormone (AMH) concentrations, high number of antral follicles, development of multiple follicles, number of collected oocytes, high serum estradiol (E2) levels, blood group A, mutations in bone morphogenic protein (BMP) alleles, presence of follicle stimulating hormone (FSH) receptor mutations and polymorphisms, high FSH dosage, high ratio between luteinizing hormone (LH)/ FSH, high human chorionic gonadotrophin (HCG) dosage, high inhibin A and inhibin B values, high vascular endothelial growth factor (VEGF) and other interleukins levels, decreased alpha-2-macroglobulin levels, and allergies [1,2,3,4, 10,11,12]

  • Of the 4894 assisted reproduction technologies (ART) treatments analysed, there were 71/ 4894 (1.5 %) cycles with a suspection for development of OHSS and Buserelin was used for ovulation trigger, and all these cases have not developed OHSS

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Summary

Introduction

A large number of studies have been dedicated to ovarian hyperstimulation syndrome (OHSS) none gave full embryological and clinical outcomes comparing oocyte trigger with human chorionic gonadotrophin (HCG) versus with a gonadotrophin-releasing hormone (GnRH) agonist (Buserelin) in cases with suspicious OHSS. The presence of OHSS is characterized by enlargement of the ovaries associated with ascites due to an increased peritoneal capillary permeability [3] It presents a very broad spectrum of clinical manifestations, with a incidence of 0.2-1 % of all stimulation cycles, from mild to moderate symptoms (about 3-6 % of the ART treatment cycles), which only requires vigilance [2], to more severe symptoms (about 1 % of the treatment cycles) that often requires hospitalization [4]. Sousa et al Reproductive Biology and Endocrinology (2015) 13:66 thromboembolism that can be fatal [5,6,7,8,9] Due to these severe outcomes, the recognition of risk factors for the development of OHSS became crucial. A personalization of the stimulation protocols are of the utmost importance [12]

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