Joshi Devashree P, Desai Devang, Fuziwara Seichi, Raveenthiran Sheliyan, Nafea Mohammed, Kulkarni Sanjay B
Kulkarni Reconstructive Urology Center, Pune, India.
Turk J Urol. 2021 Jul;47(4):319-324. doi: 10.5152/tud.2021.21065.
To define the role of tadalafil in improving outcomes of redo urethroplasty for pelvic fracture urethral injury (PFUI). PFUI is common in developing countries, invariably as a result of road traffic trauma. Repair is complex, and redo cases are even more challenging.
This was a longitudinal prospective nonrandomized study between 2017 and 2019. Men undergoing redo-urethroplasty were nonrandomized into two groups. Group 1 received tadalafil 5 mg the next day after surgery and continued for 3 months, and group 2 did not receive tadalafil. Inclusion criteria were patients undergoing redo-urethroplasty willing to trial low-dose tadalafil post-operatively. Exclusion criteria were <18 years, females, primary cases, and complex cases such as recto-urethral fistula. Average follow-up was 19.5 months.
Sixty patients were enrolled (29 in group 1 and 31 in group 2). Mean age was 31 years. These patients had 1-3 prior failed urethroplasties. Most required step 3 anastomotic urethroplasty (68.3%). Success was defined as absence of symptoms and no need for surgical intervention. Failure was defined as redo urethroplasty or >1 endoscopic intervention. Primary success was 83.3%. Success with tadalafil was 96.6%, compared to 71.0% in the non-Tadalafil group (P ¼ .0008). Only one patient on tadalafil failed, compared with nine in the non-tadalafil group. Secondary success rate was defined as the need for a single subsequent endoscopic intervention and was 93.3%.
In our series, there was improved outcome with using tadalafil in patients having redo urethroplasty for PFUI. Further trials should be done to evaluate the use in all PFUI cases.
明确他达拉非在改善骨盆骨折后尿道损伤(PFUI)再次尿道成形术效果中的作用。PFUI在发展中国家很常见,多因道路交通创伤所致。修复手术复杂,再次手术的病例更具挑战性。
这是一项2017年至2019年的纵向前瞻性非随机研究。接受再次尿道成形术的男性被非随机分为两组。第1组在术后第二天开始服用5毫克他达拉非,并持续3个月,第2组未服用他达拉非。纳入标准为愿意在术后试用低剂量他达拉非的再次尿道成形术患者。排除标准为年龄<18岁、女性、初次病例以及直肠尿道瘘等复杂病例。平均随访时间为19.5个月。
共纳入60例患者(第1组29例,第2组31例)。平均年龄为31岁。这些患者之前有1 - 3次尿道成形术失败经历。大多数患者需要进行3级吻合性尿道成形术(68.3%)。成功定义为无症状且无需手术干预。失败定义为再次尿道成形术或>1次内镜干预。初次成功率为83.3%。他达拉非组的成功率为96.6%,非他达拉非组为71.0%(P = 0.0008)。他达拉非组仅有1例失败,而非他达拉非组有9例。二次成功率定义为后续仅需进行1次内镜干预,为93.3%。
在我们的系列研究中,对于因PFUI接受再次尿道成形术的患者,使用他达拉非可改善手术效果。应进行进一步试验以评估其在所有PFUI病例中的应用。