富血小板血浆(PRP)激素治疗阿什曼综合征一项随机临床试验。

Elham Naghshineh, Safoura Rouholamin, Zahra Derakhshandeh
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引用次数: 3

摘要

背景:ashherman综合征是妇产科中一个有争议的问题,对其管理和治疗尚无共识。它的特点是子宫腔内的各种病变,也会导致月经不规则、不孕和胎盘异常。本研究旨在通过评估富血小板血浆(PRP)对改善月经周期和宫内粘连(IUA)阶段的影响,来评估富血小板血浆(PRP)对宫内粘连女性的影响。材料与方法:本临床试验研究将60例阿什曼综合征女性患者分为两组,每组30例。第一组仅行激素治疗,第二组宫腔镜后富血小板血浆激素治疗。在宫腔镜检查后6 ~ 8周评估Asherman综合征的恢复情况和IUA分期,并比较两组间的差异。结果:我们的研究结果显示,两组的人口学资料以及治疗前后两组的月经模式比较,差异均无统计学意义(P > 0.05)。PRP +激素治疗组干预后IUA频次分布I、II、III级分别为73.3%、20%、6.7%,激素治疗组干预后IUA频次分布分别为53.3%、26.7%、20% (P = 0.22)。PRP +激素治疗组和激素治疗组的痛经发生率分别为33.3%和40%,两组间差异无统计学意义(P = 0.71)。结论:与常规手术治疗后单独激素治疗相比,激素治疗联合PRP对IUA的分期、持续时间和月经严重程度无显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hormone Therapy with or without Platelet-Rich Plasma (PRP) for Treatment Asherman Syndrome; A Randomized Clinical Trial.

Hormone Therapy with or without Platelet-Rich Plasma (PRP) for Treatment Asherman Syndrome; A Randomized Clinical Trial.

Background: Asherman syndrome is a controversial issue in obstetrics and gynecology without any consensus on its management and treatment. It is characterized by variable lesions inside the uterine cavity and also causes menstrual irregularities, infertility, and placental abnormalities. The study aimed to assess the platelet-rich plasma (PRP) effect in women with intrauterine adhesions by evaluating the improvement of the menstrual cycle and intrauterine adhesion (IUA) stage.

Materials and methods: This clinical trial study was performed on 60 women with Asherman syndrome in two groups of 30. For the first group, only hormone therapy was performed and for the second group, hormone therapy with platelet-rich plasma after hysteroscopy. Recovery of Asherman syndrome and IUA stage was assessed at 6 to 8 weeks after hysteroscopy and compared between the two groups.

Results: Our results demonstrated that there was no significant difference between demographic data in the two groups as well as the menstrual pattern of both groups before or after treatment (P > 0.05). Frequency distribution of IUA after the intervention in the PRP + hormone therapy group in grade I, II, and III were equal to 73.3%, 20%, and 6.7% and in the hormone therapy group were 53.3%, 26.7%, and 20%, respectively (P = 0.22). In addition, hypo menorrhea was observed in 33.3% of PRP + hormone therapy group and 40% of the hormone therapy group with no significant difference between the two groups (P = 0.71).

Conclusion: Hormone therapy with PRP compared to hormone therapy alone after routine surgical treatment had not a significant effect on the IUA stage, duration, and severity of menstruation.

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