Suspension Suture Materials and Suture Carrier in Modified Gittes Bladder Neck Suspension.
- Author:
Jeong Yeol KIM
1
;
Tae Gyun KWON
;
Sung Kwang CHUNG
;
Yoon Kyu PARK
Author Information
1. Department of Urology, Kyungpook National University, Taegu, Korea.
- Publication Type:Original Article
- Keywords:
bladder neck suspension;
stress urinary incontinence;
suture materials;
bone biopsy needle
- MeSH:
Biopsy;
Catheters;
Classification;
Cystitis;
Female;
Follow-Up Studies;
Hemorrhage;
Hospitalization;
Humans;
Neck*;
Needles;
Operative Time;
Parity;
Polypropylenes;
Postoperative Complications;
Steam;
Sutures*;
Urinary Bladder*;
Urinary Incontinence;
Urinary Retention;
Vaginitis;
Wounds and Injuries
- From:Korean Journal of Urology
1996;37(11):1283-1288
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
We reviewed 42 cases (mean age 48.3+/-7.6 years, range 30 to 63 years) who underwent the modified Gittes bladder neck suspension for female stress urinary incontinence between January 1990 and May 1995 to evaluate the efficacy of two different suspension suture materials and new suspension suture carrier. At 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 (group II) with Ostycut bone biopsy needle (Angiomed) as suture carrier Following results were obtained. 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 (21.1%), vaginitis or cystitis 5 cases (11.9%), wound bleeding 1 case (2.4%) and deviation of urinary steam 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 (mean 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.
