Laparoscopic ovarian drilling vs. step-up gonadotropin therapy in infertile anovulatory polycystic ovary syndrome women resistant to sequential letrozole and gonadotropin-based ovulation induction cycles: a randomized controlled trial.

H V Bhavana, Reeta Mahey, Aarthi K Jayraj, Ashish Datt Upadhyay, Archana Kumari, Garima Kachhawa, Ayushi Negi, Khushbu Bashir, Srikar Yedlapalli
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Abstract

Objective: To study the effect of laparoscopic ovarian drilling (LOD) vs. step-up gonadotropin therapy on follicular response in infertile anovulatory polycystic ovary syndrome (PCOS) women resistant to sequential letrozole + human menopausal gonadotropin (HMG)-based ovulation induction (OVI) cycles DESIGN: Open-labeled, pilot, randomized controlled trial SUBJECTS: Infertile anovulatory PCOS women (diagnosed according to modified Rotterdam criteria), resistant to sequential letrozole 5 mg + HMG-based OVI cycle (no dominant follicle >10 mm after 14 days of stimulation). Other inclusion criteria were: age 19-38 years; body mass index ≤35 kg/m2; patent fallopian tubes documented on either hysterosalpingography/saline infusion sonography or laparoscopy; antimüllerian hormone (AMH) levels >6 ng/mL. Exclusion criteria were AMH ≤6 ng/mL; moderate to severe male factor infertility and endometriosis.

Intervention: Participants in group 1 (N = 35) underwent LOD, after which OVI cycles were started with letrozole 5 mg from the following menses. Gonadotropin were added in a sequential manner if required as per the follicular response. Women in group 2 (N = 35) were administered injection of HMG (75 IU) from day 2 of menses and dose increments were done from day 9 onward as per response.

Main outcome measures: Primary outcome was follicular response (dominant follicle >16 mm). Secondary objectives were gonadotropin requirement per cycle, duration of stimulation, time to conception (months), clinical pregnancy rate and ongoing pregnancy rate (>12 weeks). The study also compared the effect of LOD on hormonal parameters (AMH, serum testosterone) and metabolic parameters (fasting insulin, fasting blood glucose, lipid profile, homeostasis model assessment of insulin resistance) after 1-2 months of procedure.

Results: Majority of the study participants (82.85%) belonged to PCOS phenotype A. The baseline clinical, hormonal, and metabolic characteristics and phenotype distribution were comparable in both groups. The follicular response was significantly higher in the LOD group (93.25%; 83/89) compared with step-up gonadotropin group (28.20%; 11/39). With four spontaneous conceptions, the median time to conception in LOD group was 3.9 (0-8.4) months. The clinical pregnancy rate per patient was significantly higher in LOD group [54.28% (19/35)] as compared with step-up gonadotropin group [8.57% (3/35)]. The ongoing pregnancy rate in the LOD group was 45.71% (16/35) vs. 0% (0/35) in the gonadotropin group. There was a significant fall in the AMH levels from 15.2 ± 2.7 ng/mL to 10.2 ± 4.4 ng/mL after LOD. Although statistically insignificant, the levels of luteinizing hormone/follicle-stimulating hormone ratio, testosterone, fasting insulin, fasting glucose and homeostasis model assessment of insulin resistance levels were also lowered.

Conclusion: Laparoscopic ovarian drilling significantly improves the follicular response compared with step-up gonadotropin-based ovulation induction and results in higher clinical and ongoing pregnancy rates along with a significant reduction in gonadotropin requirement. The procedure may be considered for PCOS women resistant to sequential letrozole + HMG-based ovulation induction, especially phenotype A with high AMH and high follicle number per ovary.

腹腔镜卵巢钻孔(LOD)与促性腺激素强化治疗对序贯来曲唑和促性腺激素促排卵周期有抗性的不育性无排卵性多囊卵巢综合征(PCOS):一项随机对照试验。
目的:研究腹腔镜卵巢钻孔(LOD)与促性腺激素强化治疗对序贯来曲唑+ HMG(人类绝经期促性腺激素)促排卵(OVI)周期耐药的不孕症无排卵性多囊卵巢综合征(PCOS)患者卵泡反应的影响。不孕症无排卵性多囊卵巢综合征妇女(根据修改的鹿特丹标准诊断)对序列来曲唑5mg + HMG为基础的OVI周期有耐药性(刺激14天后无显性卵泡bbb10mm)。其他入选标准为:年龄19-38岁;BMI≤35kg/m2;经子宫输卵管造影/生理盐水输注超声检查或腹腔镜检查证实输卵管未通畅;AMH水平60 - 6ng/ml。排除标准为AMH≤6 ng/ml;中度至重度男性因素不孕和子宫内膜异位症。干预:第1组(N=35)接受LOD治疗,并在随后的月经周期中使用来曲唑5mg开始OVI周期。如果需要,按卵泡反应顺序添加促性腺激素。第2组(N=35)妇女从月经第2天开始注射HMG (75 IU),从第9天开始根据反应增加剂量。主要结局指标:主要结局是卵泡反应(显性卵泡直径16mm)。次要目标是每个周期的促性腺激素需要量、刺激持续时间、受孕时间(月)、临床妊娠率和持续妊娠率(bb0 - 12周)。该研究还比较了LOD在1-2个月后对激素参数(AMH、血清睾酮)和代谢参数(空腹胰岛素、空腹血糖、血脂、HOMA-IR)的影响。结果:绝大多数研究参与者(82.85%)属于PCOS a型,两组的基线临床、激素和代谢特征以及表型分布具有可比性。LOD组卵泡反应明显高于对照组(93.25%;83/89)与促性腺激素增强组相比(28.20%;结论:与基于促性腺激素的促排卵诱导相比,腹腔镜卵巢钻孔(LOD)显著改善了卵泡反应,导致更高的临床和持续妊娠率,同时显著降低了促性腺激素的需求。对于对序贯来曲唑+ hmg促排卵有抵抗的PCOS女性,特别是具有高AMH和高每卵巢卵泡数(FNPO)的表型A型患者,可考虑采用该方法。
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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来源期刊
F&S science
F&S science Endocrinology, Diabetes and Metabolism, Obstetrics, Gynecology and Women's Health, Urology
CiteScore
2.00
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0.00%
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审稿时长
51 days
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