恶性肿瘤妇女在控制卵巢过度刺激以保持生育能力后接受长效促性腺激素释放激素激动剂治疗卵巢过度刺激综合征的风险:系统综述。

IF 3.1 Q1 OBSTETRICS & GYNECOLOGY Therapeutic advances in reproductive health Pub Date : 2023-01-01 DOI:10.1177/26334941231196545
Caroline Ingold, Paula Andrea Navarro, Renato de Oliveira, Caio Parente Barbosa, Giuliano Bedoschi
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引用次数: 1

摘要

背景:生育能力保存是育龄妇女接受促性腺毒素治疗的一个重要的生活质量问题。为了减少易受化疗影响的卵泡数量,从而降低卵巢损伤的风险,一些国际社会的指导方针考虑了给予长效促性腺激素释放激素激动剂(GnRHa)辅助治疗的可能性,特别是在某些癌症,如乳腺癌中。目前,在控制性卵巢过度刺激(COH)后给予长效GnRHa以冷冻保存卵母细胞或胚胎的生育能力被越来越多地使用。然而,有报道称,COH后使用长效GnRHa保存生育能力后出现卵巢过度刺激综合征(OHSS),这表明这种治疗方法的潜在不良影响有待进一步研究。目的:本系统综述的目的是全面描述COH保留生育能力后使用长效GnRHa治疗后发生OHSS的患者。方法:全面检索截至2023年1月的主要电子数据库。报告了COH后使用长效GnRHa保存生育能力和发展OHSS的研究。偏倚风险采用改良版的纽卡斯尔-渥太华量表进行评估。结果进行了定性合成。结果:3项研究5例患者符合入选标准。大多数患者诊断为乳腺癌,所有患者均行COH卵母细胞冷冻保存。所有患者在给予长效GnRHa后均发生OHSS。排卵诱导与长效GnRHa用药之间的间隔为3 ~ 5天。所有患者均经保守治疗,康复无并发症。结论:目前的证据表明,COH后使用长效GnRHa保存生育能力可能与OHSS有关。在做出决定之前,医疗保健提供者应该与患者彻底讨论这种干预的好处和风险。需要进一步的研究来充分阐明长效GnRHa和OHSS之间的因果关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Risk of ovarian hyperstimulation syndrome in women with malignancies undergoing treatment with long-acting gonadotropin-releasing hormone agonist after controlled ovarian hyperstimulation for fertility preservation: a systematic review.

Background: Fertility preservation is an important quality of life issue for women of reproductive age undergoing gonadotoxic treatment. The possibility of administering an adjuvant long-acting gonadotropin-releasing hormone agonist (GnRHa) with the aim of reducing the number of follicles susceptible to the effects of chemotherapy and thus reducing the risk of ovarian damage is considered in some international society guidelines, particularly in certain cancers such as breast cancer. Nowadays, the administration of long-acting GnRHa after controlled ovarian hyperstimulation (COH) for fertility preservation by cryopreservation of oocytes or embryos is increasingly used. However, cases of ovarian hyperstimulation syndrome (OHSS) have been reported following the use of long-acting GnRHa after COH for fertility preservation, indicating that the potential adverse effects of this treatment need to be further investigated.

Objectives: The aim of this systematic review was to comprehensively characterize patients who developed OHSS after treatment with long-acting GnRHa following COH for fertility preservation.

Methods: A comprehensive search of major electronic databases through January 2023 was performed. Studies reporting the use of long-acting GnRHa after COH for fertility preservation and the development of OHSS were included. Risk of bias was assessed using a modified version of the Newcastle-Ottawa scale. Results were synthesized qualitatively.

Results: Three studies with five patients met the eligibility criteria. The majority of patients were diagnosed with breast cancer and all patients underwent COH for oocyte cryopreservation. OHSS occurred in all patients after administration of long-acting GnRHa. The interval between ovulation induction and administration of long-acting GnRHa thereafter ranged from 3 to 5 days. All patients were treated conservatively and recovered without complications.

Conclusion: Current evidence suggests that the use of long-acting GnRHa after COH for fertility preservation may be associated with OHSS. Healthcare providers should thoroughly discuss the benefits and risks of this intervention with their patients before making a decision. Further studies are needed to fully elucidate the causal relationship between long-acting GnRHa and OHSS in this population.

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