Van Kerrebroeck Philip E V, Kelleher Con J, Coyne Karin S, Kopp Zoe, Brodsky Marina, Wang Joseph T
Department of Urology, University Hospital Maastricht, Maastricht, The Netherlands.
Health Qual Life Outcomes. 2009 Feb 18;7:13. doi: 10.1186/1477-7525-7-13.
Previous studies demonstrate that tolterodine extended release (ER) significantly improves urgency urinary incontinence (UUI) episodes. Instruments that measure patient-reported outcomes (PROs) provide additional information that is valuable for assessing whether clinical improvements are meaningful to the patient. This study determined the correlation of changes in bladder diary variables and other PROs in subjects with overactive bladder (OAB).
Subjects with OAB, urinary frequency, and UUI were treated with 4 mg once-daily tolterodine ER or placebo for 12 weeks. Subjects completed 7-day bladder diaries, the Patient Perception of Bladder Condition (PPBC), and the King's Health Questionnaire (KHQ) at baseline and week 12. Only subjects who reported at least some minor bladder-related problems at baseline (PPBC score > or = 3) were included in this analysis.
Reductions in UUI episodes per week were significantly greater in the tolterodine ER group (n = 500) compared with the placebo group (n = 487) at week 12 (-71% vs -33%, P < 0.0001). A significantly greater percentage of subjects in the tolterodine ER group reported improvement on the PPBC versus placebo (58% vs 45%, P < 0.0001), and 7 of 10 KHQ domains were significantly improved versus placebo (all P < 0.05). Significant correlations were found for median percentage changes in UUI episodes with changes in PPBC scores (r = 0.35,P < 0.0001) and the 7 improved KHQ domains (r = 0.16-0.32, P < or = 0.0011). Changes in PPBC scores and all KHQ domains were significantly correlated (r = 0.13-0.38, P < or = 0.009) in the tolterodine ER group. Correlations among endpoints in the placebo group were similar to those observed in the tolterodine ER group.
Improvement in UUI episodes after 12 weeks of treatment with tolterodine ER or placebo was correlated with improvements in patients' perception of their bladder-related problems and health-related quality of life. Correlations were moderate in magnitude but statistically significant, suggesting that PROs are important and relevant measures for evaluating OAB treatment.
既往研究表明,托特罗定缓释剂(ER)可显著改善急迫性尿失禁(UUI)发作次数。测量患者报告结局(PRO)的工具可提供额外信息,这对于评估临床改善对患者是否有意义很有价值。本研究确定了膀胱过度活动症(OAB)患者膀胱日记变量变化与其他PRO之间的相关性。
OAB、尿频和UUI患者接受4 mg每日一次的托特罗定ER或安慰剂治疗12周。患者在基线和第12周完成7天膀胱日记、患者膀胱状况感知(PPBC)和国王健康问卷(KHQ)。本分析仅纳入基线时报告至少一些轻微膀胱相关问题(PPBC评分≥3)的患者。
在第12周时,托特罗定ER组(n = 500)每周UUI发作次数的减少显著大于安慰剂组(n = 487)(-71%对-33%,P < 0.0001)。与安慰剂相比,托特罗定ER组报告PPBC改善的患者比例显著更高(58%对45%,P < 0.0001),并且与安慰剂相比,KHQ的10个领域中有7个显著改善(所有P < 0.05)。发现UUI发作次数的中位数百分比变化与PPBC评分变化(r = 0.35,P < 0.0001)和7个改善的KHQ领域(r = 0.16 - 0.32,P≤0.0011)之间存在显著相关性。在托特罗定ER组中,PPBC评分变化与所有KHQ领域均显著相关(r = 0.13 - 0.38,P≤0.009)。安慰剂组终点之间的相关性与托特罗定ER组中观察到的相似。
托特罗定ER或安慰剂治疗12周后UUI发作次数的改善与患者对膀胱相关问题的感知及健康相关生活质量的改善相关。相关性强度中等但具有统计学意义,表明PRO是评估OAB治疗的重要且相关的指标。