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HoLEP 与 ThuFLEP 术后刺激性症状严重程度的随机前瞻性试验。

Randomized prospective trial of the severity of irritative symptoms after HoLEP vs ThuFLEP.

机构信息

Institute for Urology and Reproductive Health, Sechenov University, Bolshaya Pirogovskaya str. 2 bld. 1, Moscow, Russia, 119991.

Institute for Clinical Medicine, Sechenov University, Moscow, Russia.

出版信息

World J Urol. 2022 Aug;40(8):2047-2053. doi: 10.1007/s00345-022-04046-8. Epub 2022 Jun 12.

Abstract

PURPOSE

To compare the short-term postoperative functional outcomes and severity of irritative symptoms following holmium and thulium fiber laser enucleation (HoLEP and ThuFLEP).

METHODS

This prospective randomized single-blinded study was performed in accordance with CONSORT. The inclusion criteria were IPSS > 20 or Qmax < 10 ml/s. Patients were randomized between HoLEP and ThuFLEP. Demographics, objective data (PSA, prostate volume, etc.), data on urinary and sexual function (IPSS, IIEF, QoL, QUID, Qmax, ICIQ-MLUTS) were collected. Detailed perioperative information and postoperative data on functional outcomes at 1, 2, 3, 4, 6, 8, 10, 12 weeks and 6 months were collected.

RESULTS

Data on 163 participants were included (77-HoLEP, 86-ThuFLEP). No differences were found in surgery duration; number of postoperative complications (Clavien-Dindo I-III), catheterization time and hospital stay. Functional outcomes up to 6 months didn't differ between the groups (IPPS, IIEF, QoL, QUID, ICIQ-MLUTS, Qmax, p > 0.05). Total ICIQ-MLUTS, bother and voiding scores at 1 and 3 months significantly increased compared with the baseline in both groups (p < 0.05). No difference between the groups were observed. In HoLEP the SUI series rate was 1.3% and 1.3% after 3 and 6 months following the procedure; in ThuFLEP: it was 3.5% and 2.3% respectively (p = 0.35 and p = 0.54).

CONCLUSION

The preliminary results of the study showed no apparent differences in functional outcomes (IPSS, Qmax), rate of SUI or irritative symptoms. Both ThuFLEP and HoLEP are efficient ways of treating benign prostatic obstruction. Both surgeries are comparable in terms of duration and postoperative complication rates.

摘要

目的

比较钬激光前列腺剜除术(HoLEP)和铥激光前列腺剜除术(ThuFLEP)术后短期的功能结局和刺激性症状的严重程度。

方法

本前瞻性随机单盲研究符合 CONSORT 标准。纳入标准为国际前列腺症状评分(IPSS)>20 或最大尿流率(Qmax)<10ml/s。患者被随机分为 HoLEP 组和 ThuFLEP 组。收集人口统计学资料、客观数据(PSA、前列腺体积等)、尿功能和性功能数据(IPSS、勃起功能国际指数、生活质量评分、尿流率测定、Qmax、国际前列腺症状评分简表、最大尿流率、尿失禁困扰问卷、男性下尿路症状评分)。收集详细的围手术期信息和术后 1、2、3、4、6、8、10、12 周及 6 个月的功能结局数据。

结果

共纳入 163 名参与者(77 名 HoLEP 组,86 名 ThuFLEP 组)。手术时间、术后并发症(Clavien-Dindo I-III 级)数量、导尿管留置时间和住院时间无差异。两组术后 6 个月的功能结局(IPSS、勃起功能国际指数、生活质量评分、尿流率测定、国际前列腺症状评分简表、最大尿流率、尿失禁困扰问卷、男性下尿路症状评分)无差异(p>0.05)。两组术后 1 个月和 3 个月的总尿失禁困扰问卷、困扰和排尿评分均较基线显著增加(p<0.05)。两组间无差异。HoLEP 组术后 3 个月和 6 个月的尿失禁发生率分别为 1.3%和 1.3%,ThuFLEP 组分别为 3.5%和 2.3%(p=0.35 和 p=0.54)。

结论

研究的初步结果显示,在功能结局(IPSS、Qmax)、尿失禁发生率或刺激性症状方面,无明显差异。ThuFLEP 和 HoLEP 都是治疗良性前列腺增生的有效方法。两种手术在手术时间和术后并发症发生率方面相当。

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