Table 2. Summary of studies on the medication-taking status of overactive bladder patients.
Study | Study design | Drug | No. | Outcome measurement | Length of follow-up | Results |
---|---|---|---|---|---|---|
Abrams et al. [31] | Randomized controlled study | Tolterodine | 150 | Discontinuation rate | 12 Weeks | 11.3% |
Rogers et al. [32] | Randomized controlled study | Tolterodine | 201 | Discontinuation rate | 12 Weeks | 18.9% |
Cardozo et al. [33] | Randomized controlled study | Solifenacin | 576 | Discontinuation rate | 12 Weeks | 7.6% |
Nitti et al. [34] | Randomized controlled study | Fesoterodine | 562 | Discontinuation rate | 12 Weeks | 20.3% |
Drutz et al. [35] | Randomized controlled study | Tolterodine | Tolterodine: 109 | Discontinuation rate | 12 Weeks | Tolterodine: 12.8% |
Oxybutynin | Oxybutynin: 112 | Oxybutynin: 31.3% | ||||
Homma et al. [36] | Randomized controlled study | Tolterodine | Tolterodine: 240 | Discontinuation rate | 12 Weeks | Tolterodine: 10.4% |
Oxybutynin | Oxybutynin: 246 | Oxybutynin: 23.2% | ||||
Armstrong et al. [37] | Randomized controlled study | Tolterodine | Tolterodine: 399 | Discontinuation rate | 12 Weeks | Tolterodine: 10.5% |
Oxybutynin | Oxybutynin: 391 | Oxybutynin: 13.3% | ||||
Chapple et al. [38] | Randomized controlled study | Tolterodine | Tolterodine: 263 | Discontinuation rate | 12 Weeks | Tolterodine: 9.9% |
Solifenacin | Solifenacin: 547 | Solifenacin: 8.6% | ||||
Chapple et al. [39] | Randomized controlled study | Tolterodine | Tolterodine: 599 | Discontinuation rate | 12 Weeks | Tolterodine: 7.3% |
Solifenacin | Solifenacin: 578 | Solifenacin: 5.9% | ||||
Chapple et al. [40] | Randomized controlled study | Tolterodine | Tolterodine: 290 | Discontinuation rate | 12 Weeks | Tolterodine: 12.8% |
Fesoterodine | Fesoterodine: 559 | Fesoterodine: 13.8% | ||||
Giannitsas et al. [41] | Randomized open-label study | Tolterodine | 128 | Discontinuation rate | 6 Weeks | 16.4% |
Oxybutynin | ||||||
Sand et al. [42] | Randomized open-label study | Tolterodine | Tolterodine: 163 | Discontinuation rate | 12 Weeks | Tolterodine: 10.4% |
Oxybutynin | Oxybutynin: 152 | Oxybutynin: 14.5% | ||||
Salvatore et al. [43] | Randomized open-label study | Oxybutynin | 66 | Discontinuation rate | 2 Years | 66.7% |
Abrams et al. [44] | Open-label extension study | Tolterodine | 714 | Discontinuation rate | 52 Weeks | 38.2% |
Yu et al. [16] | Retrospective medical claims study | OAB medication | 2,415 | Discontinuation rate | 52 Weeks | Discontinuation rate: 88.6% |
Compliance rate | Compliance rate : 0.7% | |||||
Shaya et al. [47] | Retrospective medical claims study | Tolterodine or oxybutynin | 1,637 | Persistence rate | 52 Weeks | Tolterodine ER: 9% |
Oxybutynin ER: 6%; Oxybutynin IR: 5% | ||||||
Gomes et al. [48] | Retrospective medical claims study | Tolterodine | Tolterodine: 24,855 | Persistence rate | 52 Weeks | Tolterodine: 27.3% |
Oxybutynin | Oxybutynin: 31,996 | Oxybutynin: 18.9% | ||||
2 Years | Tolterodine: 13.6% | |||||
Oxybutynin: 9.4% | ||||||
Wagg et al. [58] | Retrospective medical claims study | Mirabegron | 1,683 | Persistence rate | 52 Weeks | Persistence rate: 31.7% |
Compliance rate | Compliance rate: 64.5% | |||||
Wagg et al. [49] | Retrospective study | Tolterodine | 4,833 | Persistence rate | 12 Weeks | Tolterodine ER: 47%; Tolterodine IR: 46% |
Solifenacin | Solifenacin: 58% | |||||
Oxybutynin | Oxybutynin ER: 44%; Oxybutynin IR: 40% | |||||
Propiverine | Propiverine: 47% | |||||
Trospium | Trospium: 42% | |||||
Darifenacin | Darifenacin: 52% | |||||
Flavoxate | Flavoxate: 28% | |||||
24 Weeks | Tolterodine ER: 36% Tolterodine IR: 33% | |||||
Solifenacin: 46% | ||||||
Oxybutynin ER: 35%; Oxybutynin IR: 29% | ||||||
Propiverine: 36% | ||||||
Trospium: 33% | ||||||
Darifenacin: 30% | ||||||
Flavoxate: 16% | ||||||
52 Weeks | Tolterodine ER: 28% Tolterodine IR: 24% | |||||
Solifenacin: 35% | ||||||
Oxybutynin ER: 26%; Oxybutynin IR: 22% | ||||||
Propiverine: 27% | ||||||
Trospium: 26% | ||||||
Darifenacin: 17% | ||||||
Flavoxate: 14% | ||||||
Pindoria et al. [57] | Retrospective study | Mirabegron | 197 | Persistence rate | 12 Weeks | 69% |
24 Weeks | 48% | |||||
Diokno et al. [51] | Open-label study | Oxybutynin | 1,067 | Discontinuation rate | 52 Weeks | 53.8% |
Homma et al. [52] | Open-label study | Imidafenacin | 478 | Discontinuation rate | 52 Weeks | 21.3% |
Lee et al. [53] | Prospective, observational study | Solifenacin | 176 | Persistence rate | 12 Weeks | 56.8% |
24 Weeks | 40.9% | |||||
52 Weeks | 25.0% | |||||
Kim et al. [27] | Prospective, observational study | Any antimuscarinics | 952 | Persistence rate Compliance rate | 4 Weeks | Persistence rate: 85.6% |
Compliance rate: 75.6% | ||||||
12 Weeks | Persistence rate: 71.4% | |||||
Compliance rate: 53.8% | ||||||
24 Weeks | Persistence rate: 56.8% | |||||
Compliance rate: 34.3% | ||||||
Kim et al. [54] | Prospective, observational study | Solifenacin | 1018 | Persistence rate | 12 Weeks | Persistence rate: 72.4% |
Compliance rate | ||||||
24 Weeks | Persistence rate: 45.8% | |||||
36 Weeks | Persistence rate: 31.1% | |||||
52 Weeks | Persistence rate: 22.1% | |||||
Compliance rate: 94.1% |
OAB, overactive bladder; ER, extended-release; IR, immediate-release.