Reproductive Medicine Center, Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China (mainland).
Department of Urology, Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China (mainland).
Med Sci Monit. 2018 Mar 7;24:1379-1386. doi: 10.12659/msm.909026.
BACKGROUND As a safety and efficacy protocol, oocyte vitrification has been widely used in IVF treatment. The aim of this study was to evaluate the outcome of ICSI-ET utilizing vitrified oocytes with sperm obtained from non-obstructive azoospermia (NOA) patients via micro-TESE. MATERIAL AND METHODS A total of 150 NOA patients underwent micro-TESE. Ten patients were unable to ejaculate and refused to accept TESA at the time of oocyte retrieval; later, these patients underwent TESA. A total of 174 obstructive azoospermia (OA) patients underwent TESA. Vitrified oocytes were used with micro-TESE in 35 cycles (group 1), and TESA in 10 cycles (group 2). Fresh oocytes were used with micro-TESE in 38 cycles (group 3) and TESA in 174 cycles (group 4). RESULTS The overall sperm retrieval rate of the 150 NOA patients was 48.7% (73/150). A total of 257 cycles of ICSI-ET were conducted with testicular spermatozoa; 212 cycles utilized fresh oocytes and 45 cycles utilized vitrified oocytes. No differences were observed with fertilization (73.8%, 77.2%,72.8%, 73.6%), implantation (33.3%, 34.7%, 33.8%, 37.5%), or clinical pregnancy rates (51.4%, 60%, 52.6%, 51.7%) for groups 1 through 4, respectively (P>0.05). Developmental competence was greatest among couples using sperm obtained via TESA rather than micro-TESE, not dependent on whether vitrified or fresh oocytes were utilized. Fertilization, implantation, and clinical pregnancy rates did not differ between using fresh vs. vitrified oocytes, nor did they differ between using testicular sperm derived from men with NOA vs. men with OA. CONCLUSIONS Vitrified oocytes combined with micro-TESE showed similar clinical efficacy when compared with fresh oocytes.
作为一种安全有效的方案,卵母细胞玻璃化已广泛应用于体外受精治疗中。本研究旨在评估通过 micro-TESE 从非梗阻性无精子症(NOA)患者中获取精子进行 ICSI-ET 的结果。
共有 150 名 NOA 患者接受了 micro-TESE。10 名患者无法射精,在取卵时拒绝接受 TESA;后来,这些患者接受了 TESA。174 名梗阻性无精子症(OA)患者接受了 TESA。35 个周期(第 1 组)使用 micro-TESE 与玻璃化的卵母细胞,10 个周期(第 2 组)使用 TESA。38 个周期(第 3 组)使用 micro-TESE 与新鲜卵母细胞,174 个周期(第 4 组)使用 TESA。
150 名 NOA 患者的总精子获取率为 48.7%(73/150)。共进行了 257 个 ICSI-ET 周期,其中 212 个周期使用新鲜卵母细胞,45 个周期使用玻璃化卵母细胞。第 1 至 4 组的受精率(73.8%、77.2%、72.8%、73.6%)、着床率(33.3%、34.7%、33.8%、37.5%)和临床妊娠率(51.4%、60%、52.6%、51.7%)均无差异(P>0.05)。使用 TESA 而不是 micro-TESE 获得的精子的夫妇,其胚胎发育能力最强,而与使用新鲜或玻璃化的卵母细胞无关。受精率、着床率和临床妊娠率在使用新鲜卵母细胞与玻璃化卵母细胞之间没有差异,在使用来自 NOA 患者和 OA 患者的睾丸精子之间也没有差异。
与新鲜卵母细胞相比,玻璃化卵母细胞与 micro-TESE 结合显示出相似的临床疗效。