Kotsar Andres, Isotalo Taina, Juuti Hanne, Mikkonen Joonas, Leppiniemi Jenni, Hänninen Venla, Kellomäki Minna, Talja Martti, Tammela Teuvo L J
Department of Biomedical Engineering, Tampere University of Technology, Tampere, Finland.
BJU Int. 2009 Mar;103(5):626-9. doi: 10.1111/j.1464-410X.2008.08111.x. Epub 2008 Oct 16.
To evaluate, in a pilot study, the efficacy and safety of combining a braided poly(lactic-co-glycolic acid) (PLGA, a copolymer of l-lactide and glycolide) urethral stent and dutasteride in the treatment of acute urinary retention (AUR) due to benign prostatic enlargement (BPE).
Ten men with AUR due to BPE were treated as outpatients. A biodegradable braided PLGA urethral stent was inserted into the prostatic urethra, using a specially designed insertion device under visual control. Dutasteride treatment was started and the patients were followed up for 3 months after insertion of the stents.
In all patients the stents were placed successfully with the new insertion device. All men were able to void after inserting the stent. At 1 month five patients voided freely with a low residual urine volume (<150 mL), two voided but had a high residual urine volume and a suprapubic catheter was placed, and three needed a suprapubic or an indwelling catheter before 1 month, due to AUR or comorbidities. At 3 months five patients were voiding with no problems.
We have developed a new and effective insertion device for biodegradable braided prostatic stents. The new braided-pattern stent overcomes the earlier problems of migration and sudden breakage into large particles associated with biodegradable spiral stents. However, the mechanical properties of the new stent need to be improved and tested in a longer follow-up. We consider that this new biodegradable braided-pattern urethral stent could provide a new option in the future treatment of AUR.
在一项初步研究中评估联合使用编织型聚乳酸 - 乙醇酸共聚物(PLGA,左旋丙交酯和乙交酯的共聚物)尿道支架和度他雄胺治疗良性前列腺增生(BPE)所致急性尿潴留(AUR)的疗效和安全性。
10例因BPE导致AUR的男性患者作为门诊患者接受治疗。在可视控制下,使用专门设计的插入装置将可生物降解的编织型PLGA尿道支架插入前列腺尿道。开始度他雄胺治疗,并在支架插入后对患者进行3个月的随访。
使用新的插入装置,所有患者的支架均成功置入。所有男性在插入支架后均能排尿。1个月时,5例患者能自由排尿,残余尿量低(<150 mL),2例能排尿但残余尿量高,遂放置耻骨上导尿管,3例因AUR或合并症在1个月前需要耻骨上或留置导尿管。3个月时,5例患者排尿无问题。
我们开发了一种用于可生物降解编织型前列腺支架的新型有效插入装置。新型编织型支架克服了早期与可生物降解螺旋支架相关的移位和突然破碎成大颗粒的问题。然而,新支架的机械性能需要在更长时间的随访中进行改进和测试。我们认为这种新型可生物降解编织型尿道支架可能为未来AUR的治疗提供一种新选择。