PMID- 25284747 OWN - NLM STAT- MEDLINE DCOM- 20160607 LR - 20181202 IS - 1742-1241 (Electronic) IS - 1368-5031 (Linking) VI - 68 IP - 12 DP - 2014 Dec TI - Persistence with solifenacin add-on therapy in men with benign prostate obstruction and residual symptoms of overactive bladder after tamsulosin monotherapy. PG - 1496-502 LID - 10.1111/ijcp.12483 [doi] AB - AIMS: In spite of the reported efficacy and safety of antimuscarinics in men with OAB (overactive bladder) and BPO (benign prostatic obstruction), many patients do not persist with the treatment. We aimed to evaluate persistence and the reasons for the discontinuation of solifenacin add-on therapy in men with residual symptoms of OAB after tamsulosin monotherapy for BPO in a real clinical environment. METHODS: Men aged >/= 45 years with IPSS >/= 12 and symptoms of OAB (OAB-V8 >/= 8, micturition >/= 8/24 h, urgency >/= 2/24 h) were prescribed tamsulosin 0.2 mg. After 4 weeks, men who had residual symptoms of OAB (OAB-V8 >/= 8, micturition >/= 8/24 h, urgency >/= 1/24 h) and reported that they were 'dissatisfied' or 'a little satisfied' with the therapy were enrolled and prescribed solifenacin 5 mg in combination with tamsulosin. After 52 weeks, persistence and the reasons for the discontinuation of solifenacin were evaluated. Factors related to persistence were analysed. RESULTS: Of the 305 men who had been treated with tamsulosin, 176 were prescribed solifenacin. After 52 weeks, 44 (25%) remained on solifenacin therapy. Of the 132 who discontinued solifenacin, 85 were evaluated on the reason for discontinuation. The three most common reasons for discontinuation were adverse events (AEs) (35%), lack of efficacy (33%), and improvement in symptoms (16%). The aggravation of voiding symptoms was the most common AE leading to discontinuation. Retention was observed in 11 men. None of the demographical or clinical characteristics were significantly related to persistence. CONCLUSIONS: Only 25% men with OAB and BPO remained on antimuscarinic add-on therapy after 1 year, mostly because of AEs and lack of efficacy. Realistic data should be added to what is already known about antimuscarinic treatment in men by including patients who were excluded or who dropped out of well-designed clinical trials. CI - (c) 2014 John Wiley & Sons Ltd. FAU - Lee, Y-S AU - Lee YS AD - Department of Urology, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea. FAU - Lee, K-S AU - Lee KS FAU - Kim, J C AU - Kim JC FAU - Hong, S AU - Hong S FAU - Chung, B H AU - Chung BH FAU - Kim, C-S AU - Kim CS FAU - Lee, J G AU - Lee JG FAU - Kim, D K AU - Kim DK FAU - Park, C H AU - Park CH FAU - Park, J K AU - Park JK LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20141006 PL - India TA - Int J Clin Pract JT - International journal of clinical practice JID - 9712381 RN - 0 (Muscarinic Antagonists) RN - 0 (Quinuclidines) RN - 0 (Sulfonamides) RN - 0 (Tetrahydroisoquinolines) RN - G3P28OML5I (Tamsulosin) RN - KKA5DLD701 (Solifenacin Succinate) SB - IM MH - *Drug Therapy, Combination MH - Humans MH - Male MH - Muscarinic Antagonists/adverse effects/*therapeutic use MH - Prostatic Hyperplasia/*drug therapy MH - Quinuclidines/administration & dosage MH - Solifenacin Succinate/pharmacology/therapeutic use MH - Sulfonamides/pharmacology/therapeutic use MH - Tamsulosin MH - Tetrahydroisoquinolines/administration & dosage MH - Urinary Bladder, Overactive/*drug therapy EDAT- 2014/10/07 06:00 MHDA- 2016/06/09 06:00 CRDT- 2014/10/07 06:00 PHST- 2014/10/07 06:00 [entrez] PHST- 2014/10/07 06:00 [pubmed] PHST- 2016/06/09 06:00 [medline] AID - 10.1111/ijcp.12483 [doi] PST - ppublish SO - Int J Clin Pract. 2014 Dec;68(12):1496-502. doi: 10.1111/ijcp.12483. Epub 2014 Oct 6.