Graduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Department of Urology, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Kaohsiung J Med Sci. 2024 Nov;40(11):1020-1028. doi: 10.1002/kjm2.12899. Epub 2024 Oct 9.
This study investigates predictors of unsatisfactory outcomes in female overactive bladder (OAB) patients treated with oral monotherapy by analyzing skin sympathetic nerve activity (SKNA) using a novel "neuECG" method. The study included 55 newly diagnosed female patients with idiopathic OAB, autonomic function was evaluated using neuECG before treatment initiation, and validated OAB questionnaires and urodynamic studies were administered. Initial monotherapy was administered for the first 4 weeks, with non-responders defined as patients not achieving satisfactory symptom relief and requiring further treatment. Responders (n = 32) and non-responders (n = 23) had no significant differences in baseline characteristics or urodynamic parameters; however, non-responders exhibited significantly higher baseline average SKNA (aSKNA) (1.36 ± 0.49 vs. 0.97 ± 0.29 μV, p = 0.001), higher recovery aSKNA (1.28 ± 0.46 vs. 0.97 ± 0.35 μV, p = 0.007), and a lower stress/baseline ratio of aSKNA (1.05 ± 0.42 vs. 1.26 ± 0.26, p = 0.029). Baseline aSKNA had the highest predictive value for monotherapy refractoriness in OAB (AUROC = 0.759, p = 0.001), with an optimal cut-off point of >1.032 μV. These findings suggest that elevated pre-treatment aSKNA can predict resistance to oral monotherapy in OAB, warranting close monitoring and proactive treatment strategies for patients with high aSKNA.
本研究通过使用新型“neuECG”方法分析皮肤交感神经活动(SKNA),来分析接受口服单药治疗的女性膀胱过度活动症(OAB)患者不良结局的预测因素。该研究纳入了 55 例新诊断的特发性 OAB 女性患者,在开始治疗前使用 neuECG 评估自主神经功能,并进行了经过验证的 OAB 问卷和尿动力学研究。最初的单药治疗持续了前 4 周,无应答者定义为未达到满意症状缓解且需要进一步治疗的患者。应答者(n=32)和无应答者(n=23)在基线特征或尿动力学参数方面无显著差异;然而,无应答者的基线平均 SKNA(aSKNA)明显更高(1.36±0.49 vs. 0.97±0.29 μV,p=0.001),恢复的 aSKNA 更高(1.28±0.46 vs. 0.97±0.35 μV,p=0.007),SKNA 的应激/基线比值更低(1.05±0.42 vs. 1.26±0.26,p=0.029)。基线 aSKNA 对 OAB 单药治疗抵抗具有最高的预测价值(AUROC=0.759,p=0.001),最佳截断点为>1.032 μV。这些发现表明,治疗前 aSKNA 升高可预测 OAB 对口服单药治疗的耐药性,对于 aSKNA 较高的患者需要密切监测并采取积极的治疗策略。