Green light top-firing sharp enucleation of prostate versus photoselective vaporisation of prostate for benign prostatic hyperplasia: a randomized controlled trial
Clinical Medicine|更新时间:2026-01-09
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Green light top-firing sharp enucleation of prostate versus photoselective vaporisation of prostate for benign prostatic hyperplasia: a randomized controlled trial
Journal of Third Military Medical UniversityVol. 42, Issue 5, Pages: 511-516(2020)
作者机构:
400038 重庆,陆军军医大学(第三军医大学)第一附属医院泌尿外科
作者简介:
基金信息:
the Project of Technology Innovation Plan in Major Fields of the First Affiliated Hospital of Army Medical University(SWH2016ZDCX2008);the General Program of Technology Innovation and Application Demonstration of Chongqing(CSTC2018jscx-msyb0682)
Zhengchao LIU, Tao JIANG, Zhipeng CHEN, et al. Green light top-firing sharp enucleation of prostate versus photoselective vaporisation of prostate for benign prostatic hyperplasia: a randomized controlled trial[J]. Journal of Third Military Medical University, 2020, 42(5): 511-516.
DOI:
Zhengchao LIU, Tao JIANG, Zhipeng CHEN, et al. Green light top-firing sharp enucleation of prostate versus photoselective vaporisation of prostate for benign prostatic hyperplasia: a randomized controlled trial[J]. Journal of Third Military Medical University, 2020, 42(5): 511-516. DOI: 10.16016/j.1000-5404.201911198.
Green light top-firing sharp enucleation of prostate versus photoselective vaporisation of prostate for benign prostatic hyperplasia: a randomized controlled trial
To compare the efficacy and safety of a novel procedure
green light top-firing
sharp enucleation of the prostate (GTSEP) and the traditional procedure
photoselective vaporisation of the prostate (PVP) in the treatment of benign prostatic hyperplasia (BPH).
Methods
2
A total of 154 patients diagnosed with BPH admitted in our hospital from June 2018 to April 2019 were recruited in this study
and then randomly divided into GTSEP group (
n
=77) and PVP group (
n
=77). All patients were assessed preoperatively an
d followed at 1 and 6 month postoperatively. International prostate symptom score (IPSS)
quality of life score (QoLs)
post-void residual urine (PVR)
maximum urine flow rate (Qmax)
prostate volume (PV)
prostate-specific antigen (PSA) and complications were recorded and compared between the 2 groups.
Results
2
There were 74 patients in each group completing the follow-up. No significant differences were found in baseline data between the 2 groups. At 1 and 6 months after surgery
both groups had their lower urinary tract symptoms significantly improved
but there were no significant differences in IPSS
QoLs
PVR
Qmax and PSA between the 2 groups. However
the GTSEP group had significantly shorter operation time (41.0±16.4
vs
50.1±18.1 min
P
=0.001)
and smaller prostate volume at 6 months after surgery (22.4±2.4
vs
23.3±1.9 mL
P
=0.011) when compared with the PVP group. No notable differences were seen in the incidence of intraoperative and postoperative complications between the 2 groups.
Conclusion
2
Both GTSEP and PVP achieve good efficacy and safety in BPH treatment. GTSEP can remove larger hyperplastic tissue than PVP
and is superior to PVP in operation efficacy.
关键词
Keywords
references
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