we reviewed 42 cases (mean age 48.3±7.6 years, range 30 to 63 years) who underwent the modified Gittes bladder neck suspendsion for female stress urinary incontinenc between January 1990 and May 1995 to evaluate the efficacy of two different
suspension
suture materials and new suspension suture carrier.
Af first we used the No. 1-0 prolene as suspension suture in 24 cases (group I) and secondly no. 1-0 Ethibond in 18 cases 9group II) with Ostucyt bone biopsy needle(r) (Angiomed) as suture carrier.
@ES Following results were obtained.
@EN 1. The patient's ages ranged from 30 to 63 years (mean age 48.3±7.6 years), and most patients were multiparous with an average of 3.3±1.2 deliveries and we classified the patients according to Blaivas classification and there was
statistically no
difference of variables in both groups except the parity.
2. The mean values of operative time, postoperative days on catheter, and postoperative hospitalization were 65.5±11.4 minutes, 6.9±1.6 days, 7.3±1.4 days respectively.
3. the postoperative complications were transient urinary retention 8 cases (2.1%), vaginitis or cystitis 5 cases (11.9%), wound bleeding 1 case (2.4%) and deviation of urinary stream 1 case (2.4%)
4. The success rate was 83.3% in the group I, 94.4% in group II with minimum followup of 12 months (eman 24.6±5.0 months) but the latter wasn't significantly higher than the former statistically. The overall success rate was 88.1%.
5. The Ostycut bone biopsy needle as suspension suture carrier was simple and safe in the bladder neck suspension treatment.
With above results, we recommend the No.1-0 Ethibond as suspension suture material rather than the Prolene in bladder neck suspension and Ostycut bone biopsy needle as suspension suture carrier.
|