This multicenter, cooperative study represents, the initial United Sta
tes experience using an expandable, titanium intraprostatic stent in 6
8 patients (60 to 93 years old). The stents were inserted under direct
vision and expanded to 33F using a balloon catheter. All patients had
a symptom score analysis, and underwent measurement of peak urine flo
w and rate and post-void residual urine volume as part of the initial
evaluation. Patients were seen at approximately 1, 3, 6 and 18 months
after stent insertion (mean followup 16 months). Of the 68 patients 38
presented in urinary retention. The type of anesthesia used included
general anesthesia in 6 patients, spinal or epidural anesthesia in 24,
intravenous sedation in 20 and intraurethral lidocaine only in 18. Al
l patients were able to void spontaneously within 36 hours after stent
insertion. Symptom scores decreased from 16.8 to 3.9, 6.3, 5.0, 5.7 a
nd 3.2 at approximately 1, 3, 6, 12 and 18 months, respectively. Peak
urine flow rate increased from 3.9 to 13.8, 11.5, 11.2, 12.4 and 14.4
ml. per second at approximately 1, 3, 6, 12 and 18 months, respectivel
y. Post-void residual urine volume decreased from 74.4 to 30.1, 29.2,
19.8 and 40.2 ml. at approximately 1, 3, 6 and 12 months, respectively
. Of the initial 68 patients 5 died of the underlying disorder (all vo
iding satisfactorily with the stent in place) and 17 underwent unevent
ful stent removal (10 for technical failure and 7 for treatment failur
e). Technical failures were secondary to either inaccurate positioning
or improper stent sizing. Of the 58 patients with proper placement of
the stent and no technical failures 46 (79%) had improvement in sympt
om scores and urine flow rate. Transient hematuria was noted in 43 pat
ients (63%) and usually resolved within 48 hours. None of the 6 urinar
y tract infections (9%) was recurrent. In conclusion, the titanium int
raprostatic stent, when properly placed, is a promising therapeutic al
ternative to prostatectomy or long-term catheterization in high risk o
bstructed patients or those in urinary retention. Studies are currentl
y in progress to determine the long-term efficacy of this therapeutic
modality.