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The use of a decremental dose regimen in patients treated with a chronic low-dose step-up protocol for WHO Group II anovulation: a prospective randomized multicentre study

机译:减少剂量的方案在接受慢性小剂量递增方案治疗世卫组织II组无排卵的患者中的应用:一项前瞻性随机多中心研究

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BACKGROUND: In women with chronic anovulation, the choice of the FSH starting dose and the modality of subsequent dose adjustments are critical in controlling the risk of overstimulation. The aim of this prospective randomized study was to assess the efficacy and safety of a decremental FSH dose regimen applied once the leading follicle was 10–13 mm in diameter in women treated for WHO Group II anovulation according to a chronic low-dose (CLD; 75 IU FSH for 14 days with 37.5 IU increment) step-up protocol. METHODS: Two hundred and nine subfertile women were treated with recombinant human FSH (r-hFSH) (Gonal-f) for ovulation induction according to a CLD step-up regimen. When the leading follicle reached a diameter of 10–13 mm, 158 participants were randomized by means of a computer-generated list to receive either the same FSH dose required to achieve the threshold for follicular development (CLD regimen) or half of this FSH dose [sequential (SQ) regimen]. HCG was administered only if not more than three follicles ≥16 mm in diameter were present and/or serum estradiol (E2) values were <1200 pg/ml. The primary outcome measure was the number of follicles ≥16 mm in size at the time of hCG administration. RESULTS: Clinical characteristics and ovarian parameters at the time of randomization were similar in the two groups. Both CLD and SQ protocols achieved similar follicular growth as regards the total number of follicles and medium-sized or mature follicles (≥16 mm: 1.5 ± 0.9 versus 1.4 ± 0.7, respectively). Furthermore, serum E2 levels were equivalent in the two groups at the time of hCG administration (441 ± 360 versus 425 ± 480 pg/ml for CLD and SQ protocols, respectively). The rate of mono-follicular development was identical as well as the percentage of patients who ovulated and achieved pregnancy. CONCLUSIONS: The results show that the CLD step-up regimen for FSH administration is efficacious and safe for promoting mono-follicular ovulation in women with WHO Group II anovulation. This study confirms that maintaining the same FSH starting dose for 14 days before increasing the dose in step-up regimen is critical to adequately control the risk of over-response. Strict application of CLD regimen should be recommended in women with WHO Group II anovulation.
机译:背景:在患有慢性无排卵的女性中,FSH起始剂量的选择和后续剂量调整的方式对于控制过度刺激的风险至关重要。这项前瞻性随机研究的目的是评估按照慢性低剂量(CLD; WHO II组无排卵治疗)的情况,一旦前卵泡直径为10-13 mm,采用FSH递减剂量方案的疗效和安全性。 75 IU FSH持续14天,增量协议为37.5 IU)。方法:按照CLD递增方案,用重组人FSH(r-hFSH)(Gonal-f)治疗了209名不育女性。当前卵泡直径达到10–13 mm时,通过计算机生成的列表将158名参与者随机分配,以达到达到卵泡发育阈值(CLD方案)所需的相同FSH剂量或该FSH剂量的一半[顺序(SQ)方案]。仅当存在不超过三个直径≥16 mm的卵泡和/或血清雌二醇(E 2 )值<1200 pg / ml时才施用HCG。主要结果指标是给予hCG时卵泡大小≥16 mm。结果:随机分组时,两组的临床特征和卵巢参数相似。就卵泡总数和中型或成熟卵泡总数而言,CLD和SQ方案均实现了相似的卵泡生长(≥16 mm:分别为1.5±0.9和1.4±0.7)。此外,hCG给药时两组的血清E 2 水平相同(CLD和SQ方案分别为441±360和425±480 pg / ml)。单卵泡发育的速度以及排卵并获得妊娠的患者的百分比相同。结论:结果显示,FSH给药的CLD升压方案对于促进WHO II组无排卵妇女的单卵排卵是有效和安全的。这项研究证实,在升压方案中增加剂量之前,保持14天相同的FSH起始剂量对于充分控制过度反应的风险至关重要。应建议世卫组织II级无排卵妇女严格应用CLD方案。

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