Popov S V, Orlov I N, Martov A G, Malevich S M, Sushina I V, Grin E A, Obidnyak V M, Dovganskiy D V, Topuzov T M
SPb GBUZ City Hospital Saint Luka, Saint Petersburg, Russia.
Department of Hospital Surgery of Medical Faculty of SPbGU, Saint Petersburg, Russia.
Urologiia. 2019 Jul(3):80-83.
The aim of our study was to evaluate efficiency of thulium laser enucleation of the prostate (ThuLEP) for the treatment of benign prostatic hyperplasia (BPH).
A retrospective analysis of 112 patients with BPH who underwent ThuLEP (n=60) or holmium laser enucleation of the prostate (HoLEP) (n=52) at our institution from January 2017 to June 2017 was carried out. The perioperative data and complication rate were assessed. Severity of lower urinary tract symptom (LUTS) was evaluated after 1, 6 and 12 months using International Prostate Symptom Score [I-PSS], quality-of-life [QoL] score and maximum flow rate [Qmax]. To shorten learning curve, we modified the technique and simplified the intervention. To reduce noise during surgery, we performed ThuLEP using Vela XL.
There were significant differences in pre- and perioperative parameters, including operative time (113.15+/-12.14 vs. 118.08+/-15.76 min, p=0.46), decrease in serum sodium concentration (3.49+/-0.83 vs. 3.48+/-0.84 mmol/L, P=0.97), hemoglobin drop (1.37+/-0.18 vs. 1.43+/-0.38 g/dL, p=0.65), catheterization time (2.15+/-0.38 vs. 2.27+/-0.39 days, p=0.52) and hospital stay (6.95+/-0.82 vs 7.56+/-1.36 days, p=0.25) between the two groups (ThuLEP and HoLEP). Compared with the HoLEP group, intraoperative noise was lower in ThuLEP group (47.22+/-10.31 vs. 59.45+/-9.65 db, p<0.05). At 1-, 6- and 12 months follow-up, the LUTS severity (I-PSS, QoL score and Qmax) were significantly improved in both groups in comparison with the baseline values. Furthermore, there was no difference in LUTS severity between two groups (p>0.05).
ThuLEP is comparable to the holmium laser in terms of efficiency, safety and indications and represent minimally invasive treatment option for patients with LUTS secondary to BPH.
本研究旨在评估铥激光前列腺剜除术(ThuLEP)治疗良性前列腺增生(BPH)的疗效。
对2017年1月至2017年6月在我院接受ThuLEP(n = 60)或钬激光前列腺剜除术(HoLEP)(n = 52)的112例BPH患者进行回顾性分析。评估围手术期数据和并发症发生率。在术后1、6和12个月,使用国际前列腺症状评分(I-PSS)、生活质量(QoL)评分和最大尿流率(Qmax)评估下尿路症状(LUTS)的严重程度。为缩短学习曲线,我们改进了技术并简化了操作。为减少手术过程中的噪音,我们使用Vela XL进行ThuLEP。
两组(ThuLEP和HoLEP)在术前和围手术期参数方面存在显著差异,包括手术时间(113.15±12.14 vs. 118.08±15.76分钟,p = 0.46)、血清钠浓度下降(3.49±0.83 vs. 3.48±0.84 mmol/L,P = 0.97)、血红蛋白下降(1.37±0.18 vs. 1.43±0.38 g/dL,p = 0.65)、导尿时间(2.15±0.38 vs. 2.27±0.39天,p = 0.52)和住院时间(6.95±0.82 vs 7.56±1.36天,p = 0.25)。与HoLEP组相比,ThuLEP组术中噪音更低(47.22±10.31 vs. 59.45±9.65分贝,p < 0.05)。在1、6和12个月的随访中,两组的LUTS严重程度(I-PSS、QoL评分和Qmax)与基线值相比均有显著改善。此外,两组之间的LUTS严重程度无差异(p > 0.05)。
ThuLEP在疗效、安全性和适应症方面与钬激光相当,是继发于BPH的LUTS患者的微创治疗选择。