Amer S A, Li T C, Metwally M, Emarh M, Ledger W L
Department of Obstetrics and Gynaecology, University of Nottingham, Derby City General Hospital, Derby DE22 3NE, UK.
Hum Reprod. 2009 Jan;24(1):219-25. doi: 10.1093/humrep/den325. Epub 2008 Sep 14.
Laparoscopic ovarian diathermy (LOD) is currently accepted as a successful second-line treatment for ovulation induction (OI) in clomiphene citrate (CC)-resistant women with polycystic ovary syndrome (PCOS). The aim of this study was to test the hypothesis that LOD may be superior to CC as a first-line treatment.
The study included 72 anovulatory women with PCOS who were randomized to LOD (n = 36) or CC (n = 36). Women who remained anovulatory after LOD were offered CC. Similarly, women receiving CC who failed to ovulate or conceive were offered LOD. Pregnancy rates were compared between the two groups using chi(2) and odds ratio with 95% confidence interval (OR, 95% CI).
After randomization, six women conceived before starting treatment and another patient postponed treatment. The remaining 65 women received the treatment (33 underwent LOD and 32 received CC). After the primary treatment, more pregnancies (44%) occurred in women receiving CC than in those undergoing LOD (27%), although the difference did not reach statistical significance [P = 0.13, OR 2.1 (0.7 - 5.8)]. After adding the second treatment, the pregnancy rate was still higher, but to a less extent, in the CC group [63% versus 52%, P = 0.2, OR 1.6 (0.6 - 4.2)].
LOD is not superior to CC as a first-line method of OI in women with PCOS. The trial is registered with ClinicalTrials.gov with an identifier number NCT00220545.
腹腔镜卵巢打孔术(LOD)目前被认为是多囊卵巢综合征(PCOS)中对枸橼酸氯米芬(CC)耐药的女性进行促排卵(OI)的一种成功的二线治疗方法。本研究的目的是检验LOD作为一线治疗可能优于CC这一假设。
该研究纳入了72例无排卵的PCOS女性,她们被随机分为LOD组(n = 36)或CC组(n = 36)。LOD后仍无排卵的女性给予CC治疗。同样,接受CC治疗但未排卵或未受孕的女性给予LOD治疗。使用卡方检验和95%置信区间的比值比(OR,95%CI)比较两组的妊娠率。
随机分组后,6名女性在开始治疗前受孕,另一名患者推迟治疗。其余65名女性接受了治疗(33例行LOD,32例接受CC治疗)。初始治疗后,接受CC治疗的女性妊娠率(44%)高于接受LOD治疗的女性(27%),尽管差异无统计学意义[P = 0.13,OR 2.1(0.7 - 5.8)]。在增加二线治疗后,CC组的妊娠率仍然较高,但程度较小[63%对52%,P = 0.2,OR 1.6(0.6 - 4.2)]。
对于PCOS女性,LOD作为OI的一线方法并不优于CC。该试验已在ClinicalTrials.gov注册,标识符为NCT00220545。