Department of Urology, Singapore General Hospital, Singapore.
Int J Urol. 2010 Jan;17(1):69-74. doi: 10.1111/j.1442-2042.2009.02409.x. Epub 2009 Nov 16.
To assess intravesical prostatic protrusion (IPP) as a novel predictor of clinical progression in patients with benign prostatic enlargement (BPE).
All patients attending the outpatient clinic at our institution who were being treated for lower urinary tract symptoms (LUTS) secondary to BPE between January 1997 and December 2003 were recruited into the study. International Prostate Symptom Score (IPSS) scores, uroflowmetry parameters, post-void residual urine volume (PVR), IPP and serum prostate-specific antigen (PSA) were collected. IPP was classified into Grade 1, 2 or 3. Patients were stratified to different treatment options including watchful waiting, alpha blockers or 5-alpha reductase inhibitors. Those who developed high post-void residual urine volume (>100 mL), acute urinary retention or a deterioration of at least 4 points in IPSS score were considered to have disease progression. Using the Grade 1 IPP group as a reference, the odds ratio for clinical progression of Grade 2 and Grade 3 IPP were calculated by using multivariate analysis.
A total of 259 patients with a mean age of 63 years (range 50-90 years) and mean follow-up time of 32 months were available for analysis. Fifty-two patients were found to have clinical progression. Odds ratio for progression of a Grade 2 IPP was 5.1 (95% confidence interval [CI] 1.6-16.2) and that of a Grade 3 IPP was 10.4 (95% CI 3.3-33.4).
A higher IPP grade is associated with a higher risk of clinical progression in BPE. IPP is a useful non-invasive predictor for clinical progression in BPE.
评估膀胱内前列腺突出(IPP)作为良性前列腺增生(BPE)患者临床进展的新预测指标。
本研究纳入了 1997 年 1 月至 2003 年 12 月期间因 BPE 导致下尿路症状(LUTS)在我院门诊就诊的所有患者。收集国际前列腺症状评分(IPSS)、尿流率参数、剩余尿量(PVR)、IPP 和血清前列腺特异性抗原(PSA)。IPP 分为 1 级、2 级或 3 级。患者分层为不同的治疗方案,包括观察等待、α受体阻滞剂或 5-α还原酶抑制剂。那些出现高剩余尿量(>100ml)、急性尿潴留或 IPSS 评分至少恶化 4 分的患者被认为有疾病进展。以 1 级 IPP 组为参照,采用多变量分析计算 2 级和 3 级 IPP 的临床进展的比值比。
共有 259 例患者,平均年龄 63 岁(50-90 岁),平均随访时间 32 个月,可用于分析。52 例患者出现临床进展。2 级 IPP 进展的比值比为 5.1(95%置信区间 [CI] 1.6-16.2),3 级 IPP 进展的比值比为 10.4(95% CI 3.3-33.4)。
较高的 IPP 分级与 BPE 临床进展的风险增加相关。IPP 是 BPE 临床进展的一种有用的非侵入性预测指标。