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any patient. The median time to urinary catheter removal

was 5.5 d and the median hospital stay was 6 d. For the

continence endpoint, we used two measures. For conti-

nence defined as 0 pads/d, 21.9% of patients in the ARVUS

group and 5.9% in the control group were continent at 24 h

after catheter removal. At the later time points, continence

rates for the ARVUS versus control groups were 43.8%

versus 11.8% at 2 wk (

p

= 0.005), 62.5% versus 14.7% at 4 wk

(

p

<

0.001), 68.8% versus 20.6% at 8 wk (

p

<

0.001), 75.0%

versus 44.1% at 6 mo (

p

= 0.013), and 86.66% versus 61.29%

at 12 mo (

p

= 0.04), respectively

( Table 2 )

. A significant

improvement in continence was evident from the time of

catheter removal and at the 8-wk visit. We also evaluated

continence using the ICIQ-SF

( Table 2 )

. The median ICIQ-SF

score at 24 h after catheter removal was 8.5 for the ARVUS

group and 13 for the control group (

p

= 0.008). At 2, 4, and

8 wk after catheter removal, the median scores were 7, 4.5,

and 4 for the ARVUS group, and 11, 10, and 8.5, respectively,

for the control group (

p

<

0.001 for all time points). Median

ICIQ-SF scores at 6 and 12 mo were 3 and 1 in the ARVUS

group, and 5.5 and 4, respectively, in the control group.

At 12 mo, six patients were still incontinent. For these

patients, further investigations included a 1-h standardised

pad test, a micturition diary, and a urodynamics study. One

patient in the ARVUS group had mixed stress and urge

incontinence. In the control group, two patients had stress

Table 2 – Continence data at various time points

Time

Patients achieving continence,

n

(%

) a

p

value

Median ICIQ-SF score (5th–95th percentile)

p

value

Control group (

n

= 34)

ARVUS (

n

= 32)

Control group (

n

= 34)

ARVUS (

n

= 32)

24 h

2 (5.9)

7 (21.9)

0.079

13.0 (9.0–16.0)

8.5 (3.00–14.00)

0.008

2 wk

4 (11.8)

14 (43.8)

0.005

11.0 (8.0–14.0)

7.0 (3.00–9.00)

<

0.001

4 wk

5 (14.7)

20 (62.5)

<

0.001

10.0 (6.0–14.0)

4.5 (1.00–7.00)

<

0.001

8 wk

7 (20.6)

22 (68.8)

<

0.001

8.5 (4.0–12.0)

4.0 (1.00–7.00)

<

0.001

6 mo

15 (44.1)

24 (75.0)

0.013

5.5 (0.0–15.35)

3.0 (0.0–8.0)

<

0.001

12 mo

19 (61.3)

26 (86.7)

0.040

4.0 (0.0–16.0)

1.0 (0.00–9.00)

<

0.035

ICIQ-SF = International Consortium on Incontinence Questionnaire, short form; ARVUS = advanced reconstruction of vesicourethral support.

a

Continence defined as 0 pads/d.

Table 1 – Patient characteristics, perioperative data, and pathologic outcomes

Control group (

n

= 34)

ARVUS (

n

= 32)

p

value

Age (yr)

62.5 (61.0–68.0)

64.5 (56.0–67.0)

0.695

Body mass index (kg/m

2

)

28.0 (25.4–31.4)

27.7 (25.7–33.2)

0.959

ASA score

2.0 (1.0–2.0)

2.0 (1.0–2.0)

0.873

TRUS prostate volume (cm

3

)

32.5 (22.0–52.0)

35.0 (30.0–55.0)

0.397

Preoperative PSA (ng/ml)

5.7 (3.6–12.0)

7.3 (5.2–11.2)

0.060

D’Amico risk group

Low risk

15 (44.1)

13 (40.62)

0.999

Intermediate risk

12 (35.3)

12 (37.5)

High risk

7 (20.6)

7 (21.9)

IPSS score

5.0 (2.8–14.0)

5.5 (2.0–9.3)

0.374

IIEF-5 score

17.0 (13.3–21.0)

19.0 (13.5–21.0)

0.777

Console time (min)

76.5 (48.0–130.0)

78.0 (63.0–126.0)

0.559

Blood loss (ml)

140.0 (80.0–294.0)

145.0 (85.5–234.5)

0.146

Prostate size (g)

51.0 (42.0–64.0)

53.5 (48.0–64.0)

0.362

Middle lobe

2 (5.9)

2 (6.3)

0.999

Nerve sparing

Bilateral

23 (67.6)

20 (62.5)

0.647

Unilateral

5 (14.7)

6 (18.75)

None

6 (17.6)

6 (18.75)

Lymph node dissection

8 (23.52)

7 (21.9)

0.7661

Postoperative complications

Clavien grade 2

2 (5.8)

1 (3.1)

Clavien grade 3

0

1 (3.1)

Pathologic stage

pT2

23 (67.6)

20 (62.5)

0.797

pT3a

8 (23.52)

10 (31.25)

pT3b

3 (8.82)

2 (6.25)

Pathologic Gleason score

>

6

27 (79.4)

26 (81.3)

0.999

Positive surgical margins

5 (14.7)

4 (12.5)

0.999

Pathologic node-positive cancer

2 (5.9)

0 (0.0)

0.009

ARVUS = advanced reconstruction of vesicourethral support. ASA = American Society of Anesthesiologists; TRUS = transrectal ultrasound; PSA =

prostate-specific antigen; IPSS = International Prostate Symptom Score; IIEF = International Index of Erectile Function.

Data are presented as median (5th–95th percentile) for continuous variables and

n

(%) for categorical variables.

E U R O P E A N U R O L O G Y 7 1 ( 2 0 1 7 ) 8 2 2 – 8 3 0

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