Department of Urology, University of Miami Miller School of Medicine, Miami, Florida, United States of America.
Department of Urology, Wake Forest University, Winston-Salem, North Carolina, United States of America.
Int Braz J Urol. 2024 Jan-Feb;50(1):58-64. doi: 10.1590/S1677-5538.IBJU.2023.0402.
This retrospective study aimed to evaluate the effectiveness of low-dose prednisone as a rescue therapy for patients with deteriorating semen parameters following vasovasostomy.
Electronic medical records were queried at the University of Miami with documented CPT code 55400 (Bilateral Vasovasostomy) between January 2016 and April 2023. Records were then reviewed to identify patients who demonstrated ≥50% decrease in semen parameters, specifically sperm concentration, motility and total motile sperm count. Patients who were treated with 6 weeks of low-dose prednisone were identified, and baseline semen parameters and subsequent changes after prednisone therapy were assessed. A Mann-Whitney U Test was used to compare semen parameter changes before and after prednisone. Adverse effects associated with prednisone were monitored.
A total of 8 patients were identified with deteriorating semen parameters who were treated with 6 weeks of low-dose prednisone. Following prednisone therapy, all patients demonstrated improvements in total motile sperm count (TMSC), with a median improvement of 6 million. The median relative improvement in TMSC was 433%. Sperm concentration and motility also improved compared to post-operative baseline. No adverse effects were reported during the treatment period.
Low-dose prednisone therapy appears to be a safe and effective intervention for managing deteriorating semen parameters following VV. The observed improvements in TMSC suggest the potential of prednisone to rescue patients with delayed failure after VV. Further research with larger sample sizes is warranted to confirm the safety and efficacy of low-dose prednisone as a rescue therapy in this specific patient population. Optimizing VV outcomes is crucial in male infertility, and further exploration of steroid therapy and innovative biotechnologies is warranted.
本回顾性研究旨在评估低剂量泼尼松作为挽救性治疗对行吻合术后精液参数恶化患者的疗效。
在迈阿密大学,通过电子病历系统查询了 2016 年 1 月至 2023 年 4 月间记录的 CPT 代码 55400(双侧吻合术)的患者。然后,回顾记录以确定精液参数,特别是精子浓度、活力和总活动精子数下降≥50%的患者。确定了接受 6 周低剂量泼尼松治疗的患者,并评估了泼尼松治疗前的基础精液参数和随后的变化。采用 Mann-Whitney U 检验比较泼尼松治疗前后精液参数的变化。监测与泼尼松相关的不良反应。
共确定了 8 例因精液参数恶化而行 6 周低剂量泼尼松治疗的患者。泼尼松治疗后,所有患者的总活动精子数(TMSC)均有所改善,中位数增加了 600 万。TMSC 的中位数相对改善率为 433%。与术后基线相比,精子浓度和活力也有所改善。治疗期间未报告不良反应。
低剂量泼尼松治疗似乎是一种安全有效的方法,可用于治疗行吻合术后精液参数恶化的患者。TMSC 的改善表明,泼尼松可能有助于挽救行吻合术后延迟失败的患者。需要更大样本量的进一步研究来确认低剂量泼尼松作为这种特定患者人群的挽救性治疗的安全性和疗效。优化吻合术的结果对于男性不育症至关重要,需要进一步探索类固醇治疗和创新生物技术。