Kuo Hann-Chorng, Chancellor Michael B
Department of Urology, Buddhist Tzu Chi General Hospital, and Tzu Chi University, Hualien, Taiwan.
BJU Int. 2009 Sep;104(5):657-61. doi: 10.1111/j.1464-410X.2009.08495.x. Epub 2009 Mar 30.
To compare the clinical effectiveness of botulinum toxin type A (BoNT-A) injections followed by hydrodistention (HD) with HD alone in patients with interstitial cystitis/painful bladder syndrome (IC/PBS).
A prospective, randomized study was performed in a urological referral centre. In all, 67 patients with IC/PBS who had failed conventional treatments were enrolled. Of these, 44 patients received suburothelial injection with 200 U (15) or 100 U (29) of BoNT-A followed by cystoscopic HD 2 weeks later (BoNT-A groups). The control group (23 patients) received the identical HD procedure with no BoNT-A injection. All patients remained on baseline medications of pentosan polysulphate throughout the study. Bladder pain visual analogue scale (VAS), O'Leary-Sant symptom and problem indexes, functional bladder capacity (FBC) and urodynamic variables were measured at baseline and after treatment. Global response assessment was used to evaluate successful treatment response.
The IC/PBS symptom score significantly decreased in all three groups, but VAS reduction, FBC and cystometric bladder capacity increases were significant only in the BoNT-A groups at 3 months. Of the 44 patients in the BoNT-A group 31 (71%) had a successful result at 6 months. A successful result at 12 and 24 months was reported in 24 (55%) and 13 (30%) patients in BoNT-A group, respectively, compared with only six (26%) and four (17%) in the control group (P=0.002).
Intravesical injections of BoNT-A followed by HD produced significantly better clinical results than HD alone in patients with IC/PBS.
比较A型肉毒杆菌毒素(BoNT-A)注射联合膀胱水扩张术(HD)与单纯膀胱水扩张术在间质性膀胱炎/膀胱疼痛综合征(IC/PBS)患者中的临床疗效。
在一家泌尿外科转诊中心进行了一项前瞻性随机研究。总共纳入了67例常规治疗失败的IC/PBS患者。其中,44例患者接受了200 U(15例)或100 U(29例)BoNT-A的黏膜下注射,2周后进行膀胱镜下膀胱水扩张术(BoNT-A组)。对照组(23例患者)接受相同的膀胱水扩张术,但未注射BoNT-A。在整个研究过程中,所有患者均继续使用戊聚糖多硫酸盐作为基线药物。在基线和治疗后测量膀胱疼痛视觉模拟量表(VAS)、奥利里-桑特症状和问题指数、功能性膀胱容量(FBC)和尿动力学变量。采用整体反应评估来评估治疗反应是否成功。
所有三组的IC/PBS症状评分均显著降低,但仅BoNT-A组在3个月时VAS降低、FBC和膀胱容量测量值增加显著。BoNT-A组的44例患者中,31例(71%)在6个月时治疗成功。BoNT-A组分别有24例(55%)和13例(30%)患者在12个月和24个月时治疗成功,而对照组分别只有6例(26%)和4例(17%)患者治疗成功(P=0.002)。
对于IC/PBS患者,膀胱内注射BoNT-A联合膀胱水扩张术比单纯膀胱水扩张术产生的临床效果显著更好。