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and safety of AquaBeam were confirmed

[58]

. One-year

results of a prospective single-armmulticentre phase 2 trial

on 21 men supported safety and efficacy of aquablation

[59]

. Duration of the procedure averaged 38 min and mean

aquablation treatment time was 5 min. In 20 patients,

catheters were removed within the 1st 24 h of the

procedure and most patients were discharged 1 d after

the procedure. No cases of urinary incontinence, erectile

dysfunction, or retrograde ejaculation were reported. After

12 mo, IPSS was reduced from 23.0 points at baseline to

6.8 points (

p

<

0.001). An increase from 8.7 ml/s to 18.3 ml/

s in Q

max

was demonstrated (

p

<

0.0001). At 12 mo the

average prostate size showed a reduction from57 cc to 35 cc

(

p

<

0.001). This first clinical experience provided encour-

aging results, but further modifications of the AquaBeam

systemwill be necessary. Anatomical prostatic features like

a prostate volume

>

100 cc and the presence of a large

middle lobe are currently limitations to the technology and

therefore considered relative contraindications. Further

RCTs are underway to evaluate efficacy, durability, and

safety of this innovative approach.

[23_TD$DIFF]

3.9.

Convective water vapour energy (WAVE) ablation: The

Rezu- m system

[24_TD$DIFF]

3.9.1.

Basic principle

Ablation using the Rezu- m system (NxThera, Inc., Maple-

Grove, MN, USA) takes advantage of the thermodynamic

principle of convective energy transfer, which is in contrast

to conductive heat transfer techniques as applied by known

minimally invasive treatment options like transurethral

microwave therapy or transurethral needle ablation. In this

case, radiofrequency power is used to create thermal energy

in the form of water vapor, which in turn deposits the stored

thermal energy when the steam phase shifts to liquid upon

cell contact. The Rezu- m system is composed of a generator

containing a radiofrequency power supply to create water

vapor from sterile water and a single-use transurethral

delivery device. The tip of the delivery device contains an

18-gauge polyether ether ketone needle where 12 small

emitter holes spaced circumferentially at 120

8

intervals

allow for targeted dispersion of water vapor into the tissue.

The injection is performed at approximately 103

8

and

exceeds slightly interstitial pressure. Due to the convective

properties of water vapor the steam disperses rapidly and

homogenously through the tissue interstices and releases

stored thermal energy onto prostatic tissue effecting cell

necrosis. Of note, when the transition zone is treated,

energy deposition is contained within the zonal anatomy of

the prostate. Histologic and imaging studies using Gadolin-

ium-enhanced magnetic resonance imaging after treatment

provided evidence that coalesced thermal lesions were

limited to the transition zone without extension to the

peripheral zone, bladder, rectum or striated urinary

sphincter

[60,61]

. It was shown that 6 mo after treatment

the total prostate volume was reduced by 28.9% and the

resolution of thermal lesions as determined with Gadolini-

um-enhanced magnetic resonance imaging was almost

complete

[61] .

The procedure can be performed in an office

based setting with minimal pain management. Under

cystoscopic guidance, the needle is positioned at 90

8

to

the area of interest and a 9-s injection of water vapor is

achieved. Usually, one to three injections are needed for

each lateral lobe and one to two injections may be delivered

[(Fig._3)TD$FIG]

Fig. 3 – Aquablation – image guided robotic waterjet ablation: AquaBeam. (A) The Aquablation system is composed of three main components: the

console, the robotic hand-piece, and a transrectal ultrasound probe. (B) Tip of the Aquablation probe. The terminal balloon is retracted for sealing of

the bladder neck. The trough enables Aquablation. (C) Graphic control interface.

E U R O P E A N U R O L O G Y 7 2 ( 2 0 1 7 ) 9 8 6 – 9 9 7

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