Peters K M, Diokno A C, Steinert B W, Gonzalez J A
Department of Urology, William Beaumont Hospital, Royal Oak, Michigan, USA.
J Urol. 1998 May;159(5):1483-6; discussion 1486-7. doi: 10.1097/00005392-199805000-00019.
Interstitial cystitis is a severe debilitating bladder disease characterized by unrelenting pelvic pain and urinary frequency. A prospective, double-blind, placebo controlled study of the use of intravesical bacillus Calmette-Guerin (BCG) in the treatment of interstitial cystitis was recently completed with a mean followup of 8 months. Results demonstrated a 60% BCG response rate, compared to a 27% placebo response rate. We now report the long-term followup results of those patients who received intravesical BCG.
Subjects randomized to receive BCG were followed at routine intervals with questionnaires and voiding diaries identical to those in the blinded study. Adverse events were closely monitored in the treatment and followup phases of the study. Subject baseline values were compared to followup data.
Of the BCG responders mean followup was 27 months (range 24 to 33), and 8 of 9 (89%) continue to have an excellent response in all parameters measured. The global interstitial cystitis survey improved 70%, daily voids decreased 31%, nocturia improved 54%, mean voided volume increased 61%, pelvic pain decreased 81%, vaginal pain decreased 71%, urgency decreased 71% and dysuria decreased 82%. Overall well-being improved 54% and the Rand-36 quality of life survey overall improved 64%. In 86% of the patients (6 of 7) dyspareunia resolved. Of the initial BCG nonresponders there was no significant difference in interstitial cystitis symptomatology from baseline to last followup, suggesting that BCG does not worsen interstitial cystitis symptoms. No long-term adverse events from BCG were noted.
Intravesical Tice BCG is safe, effective and durable in the treatment of interstitial cystitis. Of those patients who received only 6 weekly treatments and responded favorably 89% continue to have an excellent response with followup ranging from 24 to 33 months.
间质性膀胱炎是一种严重的使人衰弱的膀胱疾病,其特征为持续的盆腔疼痛和尿频。最近完成了一项关于膀胱内灌注卡介苗(BCG)治疗间质性膀胱炎的前瞻性、双盲、安慰剂对照研究,平均随访8个月。结果显示BCG的有效率为60%,而安慰剂的有效率为27%。我们现在报告那些接受膀胱内BCG治疗患者的长期随访结果。
随机接受BCG治疗的受试者按常规间隔进行随访,使用与盲法研究中相同的问卷和排尿日记。在研究的治疗和随访阶段密切监测不良事件。将受试者的基线值与随访数据进行比较。
BCG治疗有效的患者平均随访27个月(范围24至33个月),9例中有8例(89%)在所有测量参数方面继续有良好反应。间质性膀胱炎总体调查改善了70%,每日排尿次数减少31%,夜尿改善54%,平均排尿量增加61%,盆腔疼痛减少81%,阴道疼痛减少71%,尿急减少71%,尿痛减少82%。总体健康状况改善了54%,兰德36项生活质量调查总体改善了64%。86%的患者(7例中的6例)性交困难得到缓解。最初对BCG无反应的患者,从基线到最后随访,间质性膀胱炎症状无显著差异,这表明BCG不会使间质性膀胱炎症状恶化。未发现BCG引起的长期不良事件。
膀胱内灌注蒂氏BCG治疗间质性膀胱炎安全、有效且持久。那些仅接受6周治疗且反应良好的患者中,89%在24至33个月的随访中继续有良好反应。