Document details

Randomized Clinical Trial of Balloon Occlusion versus Conventional Microcatheter Prostatic Artery Embolization for Benign Prostatic Hyperplasia

Author(s): Bilhim, T ; Costa, NV ; Torres, D ; Pisco, J ; Carmo, S ; Oliveira, A

Date: 2019

Persistent ID: http://hdl.handle.net/10400.17/3685

Origin: Repositório do Centro Hospitalar de Lisboa Central, EPE

Subject(s): Acrylic Resins; Aged; Embolization, Therapeutic; Equipment Design; Gelatin; Humans; Male; Middle Aged; Miniaturization; Portugal; Prospective Studies; Prostate; Prostatic Hyperplasia; Radiography, Interventional; Regional Blood Flow; Single-Blind Method; Time Factors; Treatment Outcome; Arteries; Balloon Occlusion; Catheters; CHLC IMA


Description

Purpose: To compare balloon occlusion prostatic artery embolization (bPAE) with conventional microcatheter PAE (cPAE). Materials and methods: In this single-center trial, between November 2017 and November 2018, 89 patients with symptomatic benign prostatic hyperplasia were randomly assigned to cPAE (n = 43) or bPAE (n = 46). All patients received embolization with 300-500 μm Embosphere microspheres and were evaluated before and 1 and 6 months after PAE. Primary outcome measure was change from baseline in International Prostate Symptom Score (IPSS). Student t test was used for between-group comparisons of change from baseline, and paired t test was used for within-group comparisons. Results: At baseline, groups were identical (P > .05). Unilateral PAE was performed in 4 patients receiving cPAE and 3 patients receiving bPAE (9.30% and 6.52%, P = .708). Procedural and fluoroscopy times, dose area product, air kerma, embolic volume, and mean prostate-specific antigen (PSA) 24 hours after PAE did not differ between groups (P > .05). Coils were used in 6 patients receiving cPAE and 4 patients receiving bPAE (14.0% and 8.70%, P = .51). Assessments at 6 months after PAE showed mean IPSS reduction was 7.58 ± 6.88 after cPAE and 8.30 ± 8.12 after bPAE (P = .65); mean prostate volume reduction was 21.9 cm3 ± 51.6 (18.2%) after cPAE and 6.15 cm3 ± 14.6 (7.3%) after bPAE (P = .05); mean PSA reduction was 0.9 ng/mL ± 2.22 after cPAE and 0.22 ng/mL ± 1.65 after bPAE (P = .10). Penile skin lesions (n = 3) and rectal bleeding (n = 2) were documented only in patients receiving cPAE (11.9%, P = .01). No major adverse events occurred. Conclusions: bPAE is as effective as cPAE in treating benign prostatic hyperplasia with a potential to reduce nontarget embolization.

Document Type Journal article
Language English
Contributor(s) Repositório da Unidade Local de Saúde São José
facebook logo  linkedin logo  twitter logo 
mendeley logo

Related documents

No related documents