Does Polyvinyl Alcohol Particle Size Change the Outcome of Prostatic Arterial Embolization for Benign Prostatic Hyperplasia? Results from a Single-Center Randomized Prospective Study

被引:94
作者
Bilhim, Tiago [1 ,2 ,4 ]
Pisco, Joao [4 ]
Pinheiro, Luis Campos [3 ,5 ]
Tinto, Hugo Rio [2 ,4 ]
Fernandes, Lacia [2 ,4 ]
Pereira, Jose A. [2 ,4 ]
Duarte, Marisa [4 ]
Oliveira, Antonio G. [6 ]
机构
[1] Univ Nova Lisboa, Fac Ciencias Med, Univ Dept Anat, P-1200 Lisbon, Portugal
[2] Univ Nova Lisboa, Fac Ciencias Med, Univ Dept Radiol, P-1200 Lisbon, Portugal
[3] Univ Nova Lisboa, Fac Ciencias Med, Univ Dept Urol, P-1200 Lisbon, Portugal
[4] Hosp St Louis, Dept Intervent Radiol, P-1200249 Lisbon, Portugal
[5] Ctr Hosp Lisboa Cent, Hosp Sao Jose, Dept Urol, Lisbon, Portugal
[6] Univ Fed Rio Grande do Norte, Dept Pharm, BR-59072970 Natal, RN, Brazil
关键词
SYMPTOMS;
D O I
10.1016/j.jvir.2013.06.003
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: To evaluate whether different polyvinyl alcohol (PVA) particle sizes change the outcome of prostatic arterial embolization (PAE) for benign prostatic hyperplasia (BPH). Materials and Methods: A randomized prospective study was undertaken in 80 patients (mean age, 63.9 y; range, 48-81 y) with symptomatic BPH undergoing PAE between May and December 2011. Forty patients underwent PAE with 100-mu m (group A.), and 200-mu m PVA particles (group B). Visual analog scales were used to measure pain, and rates of adverse events were recorded. PAE outcomes were evaluated based on International Prostate Symptom Score (IPSS) and quality-of-life (QoL) questionnaires, prostate volume (PV), prostate-specific antigen (PSA) levels, and peak flow rate measurements at baseline and 6 months. Results: No differences between groups regarding baseline data, procedural details, or adverse events were noted. Mean pain scores were as follows: during embolization, 3.2 +/- 2.97 (group A) versus 2.93 +/- 3.28 (group B); after embolization, 0.10 +/- 0.50 (group A) versus 0 (group B; P = .20); and the week after PAE, 0.85 +/- 1.65 (group A) versus 0.87 +/- 1.35 (group B; P = .96). Patients in group B had greater decreases in IPSS (3.64 points; P = .052) and QoL (0.57 points; P = .07). Patients in group A had a greater decrease in PV (8,75 cm(3); P = .13) and PSA level (2.09 ng/mL; P < .001). Conclusions: No significant differences were found in pain scores and adverse events between groups. Whereas PSA level and PV showed greater reductions after PAE with 100-mu m PVA particles, clinical outcome was better with 200-mu m particles.
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收藏
页码:1595 / 1602
页数:8
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