Mercy Hospital for Women, Melbourne, Australia.
Monash Health, Melbourne, Australia.
Int Urogynecol J. 2021 May;32(5):1177-1183. doi: 10.1007/s00192-020-04652-3. Epub 2021 Jan 16.
Clorpactin is an antibacterial agent with limited evidence for its use as instillation therapy in patients with bladder pain syndrome/interstitial cystitis (BPS/IC). This was a multi-centre, single-blinded randomized controlled trial to investigate whether Clorpactin instillation results in symptom improvement in patients with refractory BPS/IC.
Fifty women with refractory BPS/IC were randomized to undergo cystoscopy/hydrodistension (25) or instillation of Clorpactin 0.4% solution (25) under general anaesthesia. Primary outcome was based on Global Response Assessment (GRA) at 3 months; secondary outcomes were based on O'Leary Sant Symptom (OLSI) and Problem (OLPI) questionnaire scores, visual analogue scale (VAS) score for pain and bladder diary parameters.
Complete follow-up data were available on 22 in the hydrodistension group and 16 in the Clorpactin group. GRA improvement was 4.5% for hydrodistension and 56% for Clorpactin (p = 0.001) at 3 months. Reduction in mean total scores for OLSI (14.1 to 9.1; p = 0.004) and OLPI (12.6 to 7.4; p = 0.001) was seen in the Clorpactin group only. VAS pain scores were reduced in the Clorpactin group only (7.4 to 3.3; p < 0.001). Post-treatment VAS pain scores did not differ between groups although 6/25 (24%) women in the Clorpactin group required admission for pain compared to 1/25 (4%) in the hydrodistension group.
Clorpactin treatment results in significant improvement in BPS/IC symptoms, bother and pain based on the GRA, OLSI/OLPI and VAS pain scores at 3 months post-treatment compared to cystoscopy/hydrodistension. These conclusions are limited by the high loss to follow-up in both groups.
氯膦酸二钠是一种具有有限证据支持的抗菌剂,用于膀胱疼痛综合征/间质性膀胱炎(BPS/IC)患者的灌注治疗。这是一项多中心、单盲、随机对照试验,旨在研究氯膦酸二钠灌注是否能改善难治性 BPS/IC 患者的症状。
50 名难治性 BPS/IC 女性患者随机分为行膀胱镜检查/水扩张组(25 例)或全身麻醉下氯膦酸二钠 0.4%溶液灌注组(25 例)。主要结局基于 3 个月时的总体反应评估(GRA);次要结局基于 O'Leary Sant 症状(OLSI)和问题(OLPI)问卷评分、视觉模拟评分(VAS)疼痛评分和膀胱日记参数。
水扩张组和氯膦酸二钠组完全随访数据分别为 22 例和 16 例。3 个月时,水扩张组的 GRA 改善率为 4.5%,氯膦酸二钠组为 56%(p=0.001)。氯膦酸二钠组的 OLSI 总评分(14.1 降至 9.1;p=0.004)和 OLPI 总评分(12.6 降至 7.4;p=0.001)均显著降低。仅氯膦酸二钠组的 VAS 疼痛评分显著降低(7.4 降至 3.3;p<0.001)。虽然氯膦酸二钠组 6/25(24%)女性因疼痛需要住院治疗,但与水扩张组 1/25(4%)相比,两组治疗后 VAS 疼痛评分无差异。
与膀胱镜检查/水扩张相比,氯膦酸二钠治疗在 3 个月时可显著改善 BPS/IC 症状、困扰和疼痛,基于 GRA、OLSI/OLPI 和 VAS 疼痛评分。这些结论受到两组高失访率的限制。