Imperatore Vittorio, Creta Massimiliano, Di Meo Sergio, Buonopane Roberto, Longo Nicola, Fusco Ferdinando, Spirito Lorenzo, Imbimbo Ciro, Mirone Vincenzo
Unità Operativa di Urologia, Ospedale Buon Consiglio - Fatebenefratelli, Napoli.
Arch Ital Urol Androl. 2018 Mar 31;90(1):11-14. doi: 10.4081/aiua.2018.1.11.
We investigated the efficacy of intravesical instillations of combined hyaluronic acid (HA) and chondroitin sulphate (CS) in patients with bacillus Calmette-Guérin (BCG)-induced chemical cystitis unresponsive to first-line therapies.
We retrospectively reviewed the clinical records of patients with grade 2 BCG-induced chemical cystitis unresponsive to first line therapeutic options performed according to the International Bladder Cancer Group guidelines who underwent intravesical instillations of HA/CS. Bladder pain, urinary urgency, voiding volume and number of voids/24 hours recorded prior to treatment, at the end of the treatment, at six months and at one-year follow-up were recorded and analyzed.
The records of 20 patients were identified. All patients underwent eight weekly instillations of HA/CS. Mean baseline visual analogue scale (VAS) scores ± Standard Deviation (SD) for urinary urgency and bladder pain were 7.8 ± 0.5 and 7.2 ± 1.0, respectively. Mean number of voids/24 hours ± SD was 15.4 ± 2.3 and mean urine volume per void ± SD was 85.8 ± 21.0 mL. At the end of the treatment, mean VAS scores ± SD for urgency and pain significantly decreased to 4.7 ± 1.1 and 4.2 ± 0.9, respectively (p < 0.05 in both cases). Mean number of voids/24 hours ± SD decreased to 9.6 ± 1.4 (p < 0.05) and mean urine volume per void ± SD significantly increased to 194.1 ± 59.5 mL (p < 0.05). At six months and one-year followup, all outcome measures remained stable.
Bladder instillations of HA/CS provide significant and durable improvement of bladder pain, urinary urgency, urinary volume per void and urinary frequency in patients with refractory BCG-induced chemical cystitis.
我们研究了联合透明质酸(HA)和硫酸软骨素(CS)膀胱灌注对卡介苗(BCG)诱导的化学性膀胱炎患者的疗效,这些患者对一线治疗无反应。
我们回顾性分析了根据国际膀胱癌小组指南进行HA/CS膀胱灌注的2级BCG诱导的化学性膀胱炎患者的临床记录,这些患者对一线治疗方案无反应。记录并分析治疗前、治疗结束时、6个月和1年随访时的膀胱疼痛、尿急、排尿量和24小时排尿次数。
确定了20例患者的记录。所有患者均接受了为期8周的HA/CS灌注。尿急和膀胱疼痛的平均基线视觉模拟量表(VAS)评分±标准差(SD)分别为7.8±0.5和7.2±1.0。24小时平均排尿次数±SD为15.4±2.3,每次排尿平均尿量±SD为85.8±21.0 mL。治疗结束时,尿急和疼痛的平均VAS评分±SD显著降至4.7±1.1和4.2±0.9(两者p均<0.05)。24小时平均排尿次数±SD降至9.6±1.4(p<0.05),每次排尿平均尿量±SD显著增至194.1±59.5 mL(p<0.05)。在6个月和1年随访时,所有结果指标均保持稳定。
HA/CS膀胱灌注可显著且持久地改善难治性BCG诱导的化学性膀胱炎患者的膀胱疼痛、尿急、每次尿量和尿频。