TY - JOUR
T1 - Post-void residual urine volume is not a good predictor of the need for invasive therapy among patients with benign prostatic hyperplasia
AU - Mochtar, Chaidir Arif
AU - Kiemeney, L. A.L.M.
AU - Van Riemsdijk, M. M.
AU - Laguna, M. P.
AU - Debruyne, F. M.J.
AU - De La Rosette, J. J.M.C.H.
N1 - Funding Information:
Supported by an unrestricted educational grant from GlaxoSmithKline Corp.
PY - 2006/1
Y1 - 2006/1
N2 - Purpose: We assessed the value of baseline PVR as predictor of the need for invasive therapy during long-term followup of patients with clinical BPH treated initially with α1-blockers or WW. Materials and Methods: The records of a cohort of 942 patients with BPH treated with α1- blockers or WW were reviewed. Baseline I-PSS scores, PSA, prostate volume, uroflowmetry, pressure flow parameters and followup data were collected prospectively. Correlations between PVR and other baseline parameters were calculated. The 5-year cumulative risks of invasive therapy were calculated with the Kaplan-Meier method. After stratification of PVR by various cutoff levels (50, 100 and 300 ml), rate ratios between large and small PVRs were calculated using proportional hazards analyses. Results: PVR has weak (-0.2<R <0.2) correlations with other baseline parameters. With increasing PVR cutoff levels, the 5-year cumulative risk of invasive therapy for the large PVR subgroup, increases from 45% to 64% and from 15% to 21% in the α1-blockers and WW group, respectively. Large PVR yields a significant 2-fold up to a 4-fold increased risk of invasive therapy compared to small PVR in both treatment groups. In multivariate models these significant risk differences largely disappear, although a statistically not significant higher risk remains for the large PVR (greater than 300 ml) patients. Conclusions: In general, baseline PVR has little prognostic value for the risk of BPH related invasive therapy in patients on α1-blocker and WW. Only patients with large PVR have a 2-fold increased risk of invasive therapy compared to patients with smaller PVR.
AB - Purpose: We assessed the value of baseline PVR as predictor of the need for invasive therapy during long-term followup of patients with clinical BPH treated initially with α1-blockers or WW. Materials and Methods: The records of a cohort of 942 patients with BPH treated with α1- blockers or WW were reviewed. Baseline I-PSS scores, PSA, prostate volume, uroflowmetry, pressure flow parameters and followup data were collected prospectively. Correlations between PVR and other baseline parameters were calculated. The 5-year cumulative risks of invasive therapy were calculated with the Kaplan-Meier method. After stratification of PVR by various cutoff levels (50, 100 and 300 ml), rate ratios between large and small PVRs were calculated using proportional hazards analyses. Results: PVR has weak (-0.2<R <0.2) correlations with other baseline parameters. With increasing PVR cutoff levels, the 5-year cumulative risk of invasive therapy for the large PVR subgroup, increases from 45% to 64% and from 15% to 21% in the α1-blockers and WW group, respectively. Large PVR yields a significant 2-fold up to a 4-fold increased risk of invasive therapy compared to small PVR in both treatment groups. In multivariate models these significant risk differences largely disappear, although a statistically not significant higher risk remains for the large PVR (greater than 300 ml) patients. Conclusions: In general, baseline PVR has little prognostic value for the risk of BPH related invasive therapy in patients on α1-blocker and WW. Only patients with large PVR have a 2-fold increased risk of invasive therapy compared to patients with smaller PVR.
KW - Adrenergic alpha-antagonists
KW - Prostatic hyperplasia
KW - Treatment outcome
UR - http://www.scopus.com/inward/record.url?scp=29144445966&partnerID=8YFLogxK
U2 - 10.1016/S0022-5347(05)00038-8
DO - 10.1016/S0022-5347(05)00038-8
M3 - Article
C2 - 16406914
AN - SCOPUS:29144445966
VL - 175
SP - 213
EP - 216
JO - Investigative Urology
JF - Investigative Urology
SN - 0022-5347
IS - 1
ER -