OBJECTIVE: To evaluate the cumulative singleton live birth rate after classic ovulation induction in women with anovulatory polycystic ovary syndrome and to validate a previously developed prediction model. DESIGN: Prospective follow-up study. SETTING: Tertiary infertility unit. PATIENT(S): Validation cohort of 108 treatment-naïve anovulatory PCOS patients. INTERVENTION(S): Conventional ovulation induction, applying clomiphene citrate as first-line treatment, followed by exogenous gonadotropins as second-line intervention. MAIN OUTCOME MEASURE(S): Singleton live birth prediction. Model calibration and discrimination were assessed for the initial model (variables included age, duration of infertility, and insulin/glucose ratio) and a second model in which the insulin/glucose ratio was replaced by body mass index. RESULT(S): The cumulative singleton live birth rate after 12 and 24 months was 60% and 78%, respectively. Overall, the observed rates were higher than predicted: hazard ratio 1.21 (95% confidence interval [CI] 0.89, 1.64), first model and 1.25 (95% CI 1.20, 1.30), second model. However, the predictive capacity of the model variables was reliable, with calibration slopes of 0.79 (95% CI -0.04, 1.63) and 1.06 (95% CI 0.95, 1.18), respectively. CONCLUSION(S): The present study confirms the previously reported good treatment prognosis for women with PCOS undergoing classic ovulation induction. Women with a poor prognosis, for whom alternative treatment options may be considered, can best be identified by a prediction model including age, duration of infertility, and body mass index. CLINICAL TRIAL REGISTRATION NUMBER: NCT00821379.
OBJECTIVE: To evaluate the cumulative singleton live birth rate after classic ovulation induction in women with anovulatory polycystic ovary syndrome and to validate a previously developed prediction model. DESIGN: Prospective follow-up study. SETTING: Tertiary infertility unit. PATIENT(S): Validation cohort of 108 treatment-naïve anovulatory PCOSpatients. INTERVENTION(S): Conventional ovulation induction, applying clomiphene citrate as first-line treatment, followed by exogenous gonadotropins as second-line intervention. MAIN OUTCOME MEASURE(S): Singleton live birth prediction. Model calibration and discrimination were assessed for the initial model (variables included age, duration of infertility, and insulin/glucose ratio) and a second model in which the insulin/glucose ratio was replaced by body mass index. RESULT(S): The cumulative singleton live birth rate after 12 and 24 months was 60% and 78%, respectively. Overall, the observed rates were higher than predicted: hazard ratio 1.21 (95% confidence interval [CI] 0.89, 1.64), first model and 1.25 (95% CI 1.20, 1.30), second model. However, the predictive capacity of the model variables was reliable, with calibration slopes of 0.79 (95% CI -0.04, 1.63) and 1.06 (95% CI 0.95, 1.18), respectively. CONCLUSION(S): The present study confirms the previously reported good treatment prognosis for women with PCOS undergoing classic ovulation induction. Women with a poor prognosis, for whom alternative treatment options may be considered, can best be identified by a prediction model including age, duration of infertility, and body mass index. CLINICAL TRIAL REGISTRATION NUMBER: NCT00821379.
Authors: Hongying Kuang; Susan Jin; Karl R Hansen; Michael P Diamond; Christos Coutifaris; Peter Casson; Gregory Christman; Ruben Alvero; Hao Huang; G Wright Bates; Rebecca Usadi; Scott Lucidi; Valerie Baker; Nanette Santoro; Esther Eisenberg; Richard S Legro; Heping Zhang Journal: Hum Reprod Date: 2015-07-22 Impact factor: 6.918