Tauranga Urology Research, Tauranga, New Zealand.
Can J Urol. 2020 Feb;27(1):10072-10079.
To compare 3-year efficacy and safety after prostate resection with Aquablation therapy or transurethral resection of the prostate (TURP) for the treatment of lower urinary tract symptoms related to benign prostate hyperplasia (BPH).
One hundred and eighty-one patients assigned to either Aquablation therapy or TURP were followed for 3 years postoperatively. Patients and follow up assessors were blinded to treatment. Assessments included International Prostate Symptom Score (IPSS), Male Sexual Health Questionnaire (MSHQ-EjD), International Index of Erectile Function (IIEF) and uroflow.
Over 3 years of treatment, improvements in IPSS scores were statistically similar across groups. Mean 3-year improvements were 14.4 and 13.9 points in the Aquablation and TURP groups, respectively (difference of 0.6 points, 95% CI -3.3-2.2, p = .6848). Similarly, 3-year improvements in Qmax were 11.6 and 8.2 cc/sec (difference of 3.3 [95% CI -0.5-7.1] cc/sec, p = .0848). At 3 years, PSA was reduced significantly in both groups by 0.9 and 1.1 ng/mL, respectively; the reduction was similar across groups (p = .5983). There were no surgical retreatments for BPH beyond 20 months for either Aquablation or TURP.
Three-year BPH symptom reduction and urinary flow rate improvement were similar after TURP and Aquablation therapy. No subjects required surgical retreatment beyond 20 months postoperatively. (ClinicalTrials.gov number, NCT02505919).
比较前列腺切除术联合 Aquablation 治疗与经尿道前列腺切除术(TURP)治疗良性前列腺增生(BPH)相关下尿路症状的 3 年疗效和安全性。
181 例患者被分配至 Aquablation 治疗或 TURP 组,术后随访 3 年。患者和随访评估者对治疗均不知情。评估包括国际前列腺症状评分(IPSS)、男性性健康问卷(MSHQ-EjD)、国际勃起功能指数(IIEF)和尿流率。
在 3 年的治疗过程中,各组的 IPSS 评分改善情况在统计学上相似。Aquablation 和 TURP 组的平均 3 年改善值分别为 14.4 和 13.9 分(差值为 0.6 分,95%CI -3.3-2.2,p =.6848)。同样,3 年时 Qmax 的改善值分别为 11.6 和 8.2 cc/sec(差值为 3.3 [95%CI -0.5-7.1] cc/sec,p =.0848)。在 3 年时,两组的 PSA 均显著降低,分别为 0.9 和 1.1 ng/mL,两组间降低程度相似(p =.5983)。两组均无患者在术后 20 个月后需要针对 BPH 进行再次手术。
TURP 和 Aquablation 治疗后,3 年 BPH 症状缓解和尿流率改善情况相似。两组患者均无患者在术后 20 个月后需要再次手术。(临床试验注册号:NCT02505919)