Clin Drug Investig. 2013 Jan;33(1):71-91. doi: 10.1007/s40261-012-0046-9.
Propiverine is a well established antimuscarinic agent with a mixed mode of action in the treatment of symptoms associated with overactive bladder (OAB). As well as blocking muscarinic receptors in the detrusor muscle, the drug also inhibits cellular calcium influx, thereby diminishing muscle spasm. In patients with symptoms of OAB resulting from idiopathic detrusor overactivity (IDO) or neurogenic detrusor overactivity (NDO), propiverine demonstrated dose-dependent efficacy and tolerability, with adverse events consistent with those associated with all antimuscarinic agents. In adults with IDO, propiverine demonstrated similar efficacy to that of other antimuscarinic agents (including solifenacin, tolterodine, oxybutynin and imidafenacin) and, in adults with NDO, propiverine and oxybutynin demonstrated similar efficacy. Propiverine was generally well tolerated in these patient populations, with a lower incidence of dry mouth than that associated with oxybutynin. In men with lower urinary tract symptoms (LUTS), and in whom the presence of benign prostatic enlargement (BPE) was implicated, propiverine administered as add-on therapy to an α(1)-adrenoceptor antagonist demonstrated similar or superior efficacy to that achieved with an α(1)-adrenoceptor antagonist alone, and combination therapy was particularly effective in patients with urinary storage symptoms. Combination therapy was generally well tolerated, but was associated with a higher incidence of adverse events than an α(1)-adrenoceptor antagonist alone. In children and adolescents with IDO/OAB or NDO, propiverine was generally more effective and better tolerated than oxybutynin. In conclusion, propiverine provides a valuable option for the treatment of adults and children with OAB associated with IDO or NDO, and in men with storage LUTS.
丙哌维林是一种成熟的抗毒蕈碱药物,具有混合作用模式,可用于治疗膀胱过度活动症(OAB)相关症状。除了阻断逼尿肌中的毒蕈碱受体外,该药物还抑制细胞内钙流入,从而减少肌肉痉挛。在因特发性逼尿肌过度活动(IDO)或神经源性逼尿肌过度活动(NDO)而出现 OAB 症状的患者中,丙哌维林表现出剂量依赖性疗效和耐受性,不良反应与所有抗毒蕈碱药物一致。在 IDO 成人患者中,丙哌维林的疗效与其他抗毒蕈碱药物(包括索利那新、托特罗定、奥昔布宁和依美福汀)相似,而在 NDO 成人患者中,丙哌维林和奥昔布宁的疗效相似。在这些患者人群中,丙哌维林通常具有良好的耐受性,口干的发生率低于奥昔布宁。在患有下尿路症状(LUTS)的男性中,BPE 的存在被认为与 LUTS 有关,丙哌维林作为α1-肾上腺素受体拮抗剂的附加治疗药物,其疗效与单独使用α1-肾上腺素受体拮抗剂相似,联合治疗对有储尿症状的患者尤其有效。联合治疗通常具有良好的耐受性,但与单独使用α1-肾上腺素受体拮抗剂相比,不良反应的发生率更高。在 IDO/OAB 或 NDO 的儿童和青少年中,丙哌维林通常比奥昔布宁更有效且耐受性更好。总之,丙哌维林为治疗 IDO 或 NDO 相关 OAB 以及有储尿症状的男性患者提供了一种有价值的选择。