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Health economics perspective of fesoterodine, tolterodine or solifenacin as first-time therapy for overactive bladder syndrome in the primary care setting in Spain
© Sicras-Mainar et al.; licensee BioMed Central Ltd. 2013
Received: 25 June 2013
Accepted: 11 October 2013
Published: 21 October 2013
Overactive bladder (OAB) is associated with high healthcare costs, which may be partially driven by drug treatment. There is little comparative data on antimuscarinic drugs with respect to resource use and costs. This study was conducted to address this gap and the growing need for naturalistic studies comparing health economics outcomes in adult patients with OAB syndrome initiating treatment with different antimuscarinic drugs in a primary care setting in Spain.
Medical records from the databases of primary healthcare centres in three locations in Spain were assessed retrospectively. Men and women ≥18 years of age who initiated treatment with fesoterodine, tolterodine or solifenacin for OAB between 2008 and 2010 were followed for 52 weeks. Healthcare resource utilization and related costs in the Spanish National Health System were compared. Comparisons among drugs were made using multivariate general linear models adjusted for location, age, sex, time since diagnosis, Charlson comorbidity index, and medication possession ratio.
A total of 1,971 medical records of patients (58.3% women; mean age, 70.1 [SD:10.6] years) initiating treatment with fesoterodine (n = 302), solifenacin (n = 952) or tolterodine (n = 717) were examined. Annual mean cost per patient was €1798 (95% CI: €1745; €1848). Adjusted mean (95% bootstrap CI) healthcare costs were significantly lower in patients receiving fesoterodine (€1639 [1542; 1725]) compared with solifenacin (€1780 [€1699; €1854], P = 0.022) or tolterodine (€1893 [€1815; €1969], P = 0.001). Cost differences occurred because of significantly fewer medical visits, and less use of absorbent products and OAB-related concomitant medication in the fesoterodine group.
Compared with solifenacin and tolterodine, fesoterodine was a cost-saving therapy for treatment of OAB in the primary care setting in Spain.
Overactive bladder (OAB) is a syndrome characterized by symptoms of urinary urgency, with or without urge incontinence, often accompanied by daytime frequency and nocturia. It is caused by an overactive detrusor muscle and may be accompanied by neurological dysfunction [1–3]. The prevalence in adults ranges between 10% and 20% and increases with age [4–6]. In Europe the prevalence in the general population >18 years of age is 11.8% and is similar for men and women [4, 7, 8]. In Spain the population-based EPICC study estimated the prevalence of OAB to be 21.5% in adults ≥40 years of age and 38.5% in institutionalized people ≥65 years of age [9, 10]. OAB has a negative effect on quality of life in affected individuals, which results from both the characteristic symptoms of OAB syndrome as well as the coping strategies frequently adopted to reduce symptom impact [11, 12]. People often take extreme measures to reduce urinary frequency and episodes of incontinence, which significantly impacts their physical health, vitality, social life, emotional state and functionality [13–15]. Many individuals do not seek professional help for OAB symptoms and only a quarter receive treatment [5, 16, 17].
Pharmacological treatment of OAB aims to decrease involuntary contractions of the detrusor muscle of the bladder by blocking the bladder receptors with antimuscarinic drugs [18–21]. Efficacy, safety, and tolerability [22–26] as well as improved health-related quality of life  have been demonstrated in clinical studies for the antimuscarinics fesoterodine, tolterodine and solifenacin. However little is known about how these findings from clinical trials extrapolate to the heterogeneous populations seen in primary practice. Several studies indicate that real-world adherence is low and is typically attributed to a perceived lack of efficacy or tolerability issues [28, 29].
OAB is associated with high direct healthcare costs [30–32]. Factors contributing to the cost of OAB include drug treatment, physician visits, hospitalizations and laboratory tests. Evidence comparing antimuscarinic drugs with respect to resource use and costs is limited, and totally lacking from a Spanish National Health System (NHS) perspective. To address this gap and the growing need for naturalistic multicenter studies, this study was conducted to compare healthcare resource utilization and related costs in patients initiating treatment with fesoterodine, tolterodine, or solifenacin for the treatment of OAB syndrome in the primary care setting in a representative sample of the Spanish NHS.
Design and objectives
In this observational, multicenter, post-marketing, longitudinal, retrospective study, existing medical records (computerized databases with de-identified data) of outpatients and inpatients with a diagnostic code of OAB in three different locations in Spain were extracted and reviewed.
The main objectives of the study were to compare healthcare resource utilization related to the clinical management of OAB syndrome and corresponding costs in patients treated with fesoterodine, tolterodine, or solifenacin for the first time in the primary care setting in Spain’s NHS.
The study population consisted of patients from three geographical areas of two autonomous regions (Catalonia [Badalona and Barcelona locations] and the Balearic Islands [Mallorca]). These regions were selected because of the existence of available healthcare provider databases and because one region (Catalonia) is continental and large while the other (the Balearic Islands) is insular and small, meaning that the varied geographical composition of the country is reflected in the study and thus may be considered representative of Primary Care settings in Spain. Eighteen primary health care centres (PHC), 7 in Badalona, 2 in Barcelona and 9 in Mallorca, and their corresponding referral hospitals (three) participated in the study. The population assigned to these centres is mostly urban and industrial and low- to middle-class socioeconomic status. The follow-up period was 52 weeks from the initiation date of antimuscarinic treatment (index date).
Eligible men and women were ≥18 years of age who had not received any antimuscarinic therapy for ≥1 year before the index date; who sought medical care and initiated treatment with fesoterodine, tolterodine or solifenacin during the recruitment period (1 January 2008 to 31 December 2010); who received treatment within the designated healthcare system area; who were followed up regularly as demonstrated by ≥2 computerized health records in the corresponding health area; and who participated in a prescription drug program. Patients who transferred to other primary care centres, regions, or health areas; who were treated simultaneously with ≥2 antimuscarinic drugs during the study period; or who were permanently institutionalized were excluded. Sampling of medical records was exhaustive without reposition among those meeting eligibility criteria for the study.
Clinical data on patients treated with fesoterodine, tolterodine or solifenacin (Anatomical Therapeutic Chemical Classification System ) were obtained from claim databases using the same informatics system for filing and handle health data (ONMI-AP software). These databases are owned by Badalona Serveis Assistencials (BSA), a healthcare provider in Badalona (Barcelona), Sagrada Familia Primary Care Health Centre in Barcelona Spain, and the Primary Health Care Directorate of ib-Salut, the healthcare provider for Mallorca. The choice of specific medicine and dose was determined by the patients’ physicians as part of routine primary care. Data on prescribed doses of fesoterodine (4 and 8 mg), solifenacin (5 and 10 mg) and tolterodine (2 and 4 mg) and treatment time (in weeks) during follow-up were recorded in the database.
Compliance, as defined by the International Society for Pharmacoeconomics and Outcomes Research working group, was computed using the medication possession ratio (MPR) . The MPR is measured from first to last prescription and represents the number of days of medication supplied divided by number of days the patient was followed (starting with the index date) . The MPR is viewed as a proxy of compliance because compliance may be overestimated by simply summing the number of days’ supply; patients may refill medication before finishing the current fill.
Definition of overactive bladder and co-morbidities included in the study
The diagnosis of OAB was confirmed in enrolled patients using the International Classification of Primary Care (ICPC-2), component 7; diseases and health problems  (U13), and hospital and emergency room discharge coding, according to the International Classification of Diseases, 9th Revision, Clinical Modification, ICD-9-CM (596.51). The main study variables were: age (continuous and ranges), sex, occupational status (active, retired), time from diagnosis until treatment initiation and personal history (ICPC-2) of hypertension (K86, K87), diabetes mellitus (T89, T90), dyslipidemia (T93), obesity (T82), smoking (P17), alcoholism (P15, P16), all types of organ failure (cardiac, hepatic and renal), cerebrovascular accident (K90, K91, K93), chronic obstructive pulmonary disease (R95, chronic airflow obstruction), bronchial asthma (R96), dementia or memory disorders (P70, P20), neurological diseases: (Parkinson’s disease [N87], epilepsy [N88], multiple sclerosis [N86] and other neurological diseases [N99]), depressive syndrome (P76) and malignant neoplasms (all types, A79, B72-75, D74-78, F75, H75, K72, L71, L97, N74-76, R84-86, T71-73 , U75-79, W72-73, X75-81, Y77-79). The Charlson comorbidity index  was used to summarize each patient’s comorbidity status as well as the number of chronic co-morbidities.
Resource use and cost analysis
Unit costs of resources utilized
Health and non-health resources
2011 Unit costs (€)
Hospitalization (one day in a general ward)
Data confidentiality and ethics statement
This was a retrospective observational study using existing data on patients included in a claim database. Data confidentiality was respected at all times by means of de-identification thus ensuring anonymity according to Spanish Organic Law (Law 15/1999 of 13 December on the Protection of Personal Data). Thus no data which could reveal patient identity was extracted. The database was then prepared and closed for statistical analysis, not allowing further manipulation of data. The study, its design and procedures was classified by the Spanish Medicines Agency (AEMPS) as a Post-Authorisation Study – Other Designs (EPA-OD) trial type and was subsequently approved by the Clinical Research Ethics Committee of Hospital Clinic I Provincial of Barcelona. Based on its design, it was exempt under Spanish law from requiring written informed consent (Law 29/2006 of 26 July and Royal Decree 1344/2007 of 11 October; see http://www.aemps.gob.es/investigacionClinica/medicamentos/estudiosPostautorizacion.htm).
In this population-based study, the sample size was calculated according to an expected prevalence of OAB of 15% in the country, assuming a random error of 5% and an estimated precision of 2%. The study required medical records in a 1:2:2 proportion for fesoterodine, solifenacin and tolterodine, respectively, to match the expected distribution of use of these drugs on the Spanish market. A minimum of 300:600:600 medical records (one record per patient) were necessary to be able to detect a difference in healthcare costs of €260 (standard error, 71) between two drugs with an α level of <0.05 (with degree of freedom corrected after applying a Bonferroni adjustment for multiple comparisons) and a minimum power of 80%.
Computerized medical records were assessed for frequency distributions as well as possible errors in registration or coding. Descriptive univariate statistical analyses were performed, using the mean, median, standard deviation and 95% confidence intervals (CI) for parametric variables and the median and interquartile ranges (25 and 75 percentiles of the distribution) for non-parametric variables, after verifying the normality of the distribution with the Kolmogorov-Smirnov test. Two-sample comparisons were performed for all variables with location as a grouping variable to confirm homogeneity of data across study locations (Badalona, Barcelona and Mallorca). Although no clinically relevant differences were noted, location was included as a covariate in all subsequent analyses. Persistence with antimuscarinic treatment was initially analyzed descriptively by calculating the proportion of patients who remained on treatment during the 52-week period following the index date.
Resource utilization and costs were compared using robust analysis of variance (ANOVA) tests (Welch test and Brown-Forsythe test with a subsequent pairing of contrasts using the Games-Howell test) and the chi-square test, and depending on the distribution of the data, a bivariate analysis, without controlling for possible confounding variables. Resource utilization and the associated costs were compared according to the recommendations of Thompson and Barber , using a multivariate general linear model controlling for the following covariates: location, age, sex, MPR, time since diagnosis and disease burden. Disease burden included the number of comorbid diagnoses and the Charlson comorbidity index. Pairwise comparisons were adjusted using the procedure for estimating marginal means, applying the Bonferroni correction to estimate the P value of statistical significance. The data are presented as adjusted mean differences between treatments with corresponding 95% CIs calculated using re-sampling techniques (bootstrapping) corrected for bias, given the non-normal distributions of the variables with respect to resource utilization and costs. The analysis was performed using the statistical package SPSS for Windows version 19. Statistical significance was established as P < 0.05, all tests were 2-sided.
Unit drug costs were obtained from prices listed at the time of prescription, which is an approximation because drug prices may have varied during follow-up. We performed a secondary analysis by applying a 40% reduction in the cost of tolterodine and 7.5% reduction in the costs of solifenacin and fesoterodine. The 40% reduction in the price of tolterodine is justified by the recent (3rd quarter 2012) loss of exclusivity of this drug; the reduction was applied to the price at the time described above. The 7.5% reduction in the price of fesoterodine and solifenacin is justified by the discount applicable to these active principles set in Royal Decree RD 8/2010 of 20 May.
Demographic and clinical characteristics by type of antimuscarinic drug
(n = 302)
(n = 952)
(n = 717)
Mean age, years (SD)
Female, n (%)
Retired, n (%)
Burden of comorbidity
Associated diagnoses, n (%)
Charlson comorbidity index, mean (SD)
Score, n (%)
Associated co-morbidities, n (%)
Ischemic heart disease
Dementia (all types)
Treatment duration and dose, mean (SD)
Time since OAB diagnosis, years
Observed treatment duration, weeks
Medication possession ratio, %
Number of antimuscarinics‖
Antimuscarinic dose, n (%)
No statistically significant differences were found in pre-treatment costs among treatment groups. Costs for outpatient visits, analytical tests, radiology, laboratory tests, hospitalization days and absorbent products used were not significantly different by antimuscarinic group prior to the study.
Percentage of patients using OAB-related concomitant medications during follow-up by antimuscarinic drug
(n = 302)
(n = 952)
(n = 717)
(N = 1971)
Use of healthcare resources per patient per year according to antimuscarinic treatment in adjusted analysis*
Resource, mean (95% CI†)
(n = 302)
(n = 952)
(n = 717)
Medical visits, n
13.2 (12.3; 14.1)
15.1 (14.5; 15.9)‡
16.4 (15.5; 17.5)‡§
11.6 (10.8; 12.5)
12.9 (12.2; 13.7)‖
14.2 (13.2; 15.3)‡
1.5 (1.4; 1.6)
2.0 (2.0; 2.1)‡
2.0 (1.9; 2.0)‡
0.1 (0.1; 0.1)
0.2 (0.2; 0.2)‡
0.3 (0.3; 0.3)‡¶
Analytical tests, n
0.8 (0.7; 0.9)
0.7 (0.7; 0.8)
0.7 (0.6; 0.8)
0.3 (0.3; 0.4)
0.4 (0.3; 0.4)
0.4 (0.4; 0.5)
Complementary tests, n
0.2 (0.1; 0.3)
0.2 (0.1; 0.2)
0.2 (0.1; 0.3)
Hospital stays, days
0.1 (0.1; 0.2)
0.2 (0.1; 0.2)
0.2 (0.1; 0.2)
Adjusted* healthcare cost (€) per patient per year by antimuscarinic drug
Resource, mean (95% CI†)
(n = 302)
(n = 952)
(n = 717)
433 (411; 457)
533 (515; 552)‡
563 (539; 585)‡§
268 (249; 290)
300 (284; 319)‖
329 (305; 353)‡§
152 (144; 162)
212 (208; 216)‡
204 (200; 207)§¶
12 (10; 16)
21 (19; 24)‡
30 (27; 33)§¶
18 (15; 20)
17 (15; 18)
16 (14; 18)
6 (5; 8)
7 (6; 7)
8 (7; 9)
7 (5; 10)
7 (5; 8)
8 (5; 10)
35 (19; 59)
46 (33; 63)
53 (41; 70)
740 (690; 796)
626 (602; 652)‡
624 (597; 650)‡
216 (180; 258)
305 (274; 338)‡
335 (306; 366)‡
187 (135; 244)
243 (201; 290)
289 (237; 344)‖
Total healthcare costs
1780 (1699; 1854)‖
1893 (1815; 1969)‡§
Discussion and conclusion
There are few reports detailing healthcare resource utilization and corresponding costs in routine clinical practice with antimuscarinics. This study indicates that fesoterodine treatment for OAB was associated with lower healthcare resource use than solifenacin or tolterodine treatment, and therefore lower average costs per patient, in routine clinical practice in the Spanish NHS. The treatment groups were comparable at baseline, as indicated by burden of comorbidity and duration of antimuscarinic treatment. There were no significant differences in resource use and costs incurred during the year preceding the index date; baseline costs per patient were lower because no antimuscarinics were prescribed and patients were not actively followed for OAB. This study included a large sample of medical records from three different geographic regions of Spain. Our findings did not vary by location and thus are likely generalizable throughout Spain.
Antimuscarinic cost was higher in patients treated with fesoterodine because a greater proportion of patients received the higher dose and had a longer duration of use compared with patients treated with solifenacin and tolterodine. The additional pharmacy costs found in fesoterodine-treated patients were offset by overall lower healthcare use, mostly driven by reductions in medical visits (of all types) and OAB-related concomitant medications compared with solifenacin and tolterodine. After controlling for confounding variables, fesoterodine-treated patients had a significantly lower total annual healthcare cost per patient. This represents an annual per-patient savings of approximately €141 to the Spanish NHS when compared with solifenacin and approximately €254 versus tolterodine. From a healthcare decision-making perspective, these savings are substantial in view of the number of patients with OAB in the NHS. In a secondary analysis, the total annual per-patient costs for fesoterodine were similar to those of tolterodine when the price of tolterodine was reduced by 40% to reflect current prices subsequent to the loss of patent protection in Spain. Both fesoterodine and tolterodine showed significantly lower total healthcare costs than solifenacin.
The cost advantage of fesoterodine over tolterodine may be explained by its greater efficacy, which may result from pharmacokinetic differences. Fesoterodine has greater bioavailability and therefore a greater possibility of exerting therapeutic effects. The improved efficacy of the higher fesoterodine dose (8 mg) has been established in clinical trials [22, 25, 39] and primary medical practice ; this dose was used by 57% of patients taking fesoterodine in our study.
In contrast, titration of solifenacin to the higher dose (10 mg) has not been shown to be associated with increased efficacy [41, 42]; in our study, 13% of patients taking solifenacin used the 10-mg dose. A 4-mg dose of tolterodine ER is the only commercially available formulation; 12% of patients taking tolterodine received a 2-mg twice daily standard (i.e. not extended release) dose. Therefore it is possible that patients taking solifenacin and tolterodine may have received an ineffective dosage in our study. However our results under real-world conditions appear to be consistent with those observed in head-to-head comparative clinical trials. The Fesoterodine Assessment and Comparison Versus Tolterodine (FACT) trials showed that fesoterodine 8 mg is superior in efficacy to tolterodine ER 4 mg, with significantly greater reductions in episodes of urgency and urgency with incontinence and a significantly higher proportion of “dry” patients [24, 25, 39]. Likewise, comparative clinical trials of solifenacin versus tolterodine showed these two drugs to be similar in efficacy for the treatment of symptomatic OAB .
There are several limitations to this study. Some patients with OAB may have been excluded because of disease miscoding/misclassification, and some patients diagnosed as having OAB may not have the disease. The risk of disease misclassification was minimized in this study because physicians in participating locations were well trained in medical data recording and the computerized system includes regular quality control testing. Under-recording of healthcare resource use, whether an oversight by healthcare professionals or due to resource use outside of the geographical areas of interest, may have led to an underestimation of total costs. In all cases these potential biases are likely to have affected the three study drugs equally. Direct non-health costs (i.e. out-of-pocket costs paid by the patient that are not funded by the NHS) could not be assessed, because none of the three databases analyzed accounts for these costs. Out-of-pocket costs of OAB can be substantial, particularly for non-funded absorbent products. Because only 10% of the records analyzed were on occupationally active patients, an economic analysis that considers effects on productivity could not be performed. Furthermore it was not possible to assess OAB severity among patients for any of the antimuscarinic drugs prescribed; significant differences among groups could have influenced outcomes. However the fact that no significant differences in resource use and/or healthcare costs were found in the year prior to the index date suggests that symptom severity was similar among treatment groups.
This study demonstrated that in primary clinical practice in Spain, treatment of OAB with fesoterodine was a cost-saving therapy compared with solifenacin or tolterodine in the NHS system, and that the higher cost of fesoterodine therapy could be offset by lower overall healthcare resource use. Fesoterodine was associated with decreased healthcare resource utilization, including medical visits of all types as well as concomitant medications; this reduced utilization translated into significantly lower total annual healthcare costs per patient. Future studies in other healthcare settings are needed to confirm these findings.
We thank the BSA healthcare professionals who aided this study.
- Haylen BT, de Ridder D, Freeman RM, Swift SE, Berghmans B, Lee J, Monga A, Petri E, Rizk DE, Sand PK, Schaer GN: An International Urogynecological Association (IUGA)/International Continence Society (ICS) joint report on the terminology for female pelvic floor dysfunction. Neurourol Urodyn. 2010, 29: 4-20.PubMedGoogle Scholar
- Kirby M, Artibani W, Cardozo L, Chapple C, Diaz DC, De Ridder D, Espuna-Pons M, Haab F, Kelleher C, Milsom I, Van Kerrebroeck P, Vierhout M, Wagg A: Overactive bladder: the importance of new guidance. Int J Clin Pract. 2006, 60: 1263-1271. 10.1111/j.1742-1241.2006.01127.x.View ArticlePubMedGoogle Scholar
- Latini JM, Giannantoni A: Pharmacotherapy of overactive bladder: epidemiology and pathophysiology of overactive bladder. Expert Opin Pharmacother. 2011, 12: 1017-1027. 10.1517/14656566.2011.554396.View ArticlePubMedGoogle Scholar
- Irwin DE, Milsom I, Hunskaar S, Reilly K, Kopp Z, Herschorn S, Coyne K, Kelleher C, Hampel C, Artibani W, Abrams P: Population-based survey of urinary incontinence, overactive bladder, and other lower urinary tract symptoms in five countries: results of the EPIC study. Eur Urol. 2006, 50: 1306-1315. 10.1016/j.eururo.2006.09.019.View ArticlePubMedGoogle Scholar
- Milsom I, Abrams P, Cardozo L, Roberts RG, Thuroff J, Wein AJ: How widespread are the symptoms of an overactive bladder and how are they managed? A population-based prevalence study. BJU Int. 2001, 87: 760-766.View ArticlePubMedGoogle Scholar
- Stewart WF, Van Rooyen JB, Cundiff GW, Abrams P, Herzog AR, Corey R, Hunt TL, Wein AJ: Prevalence and burden of overactive bladder in the United States. World J Urol. 2003, 20: 327-336.PubMedGoogle Scholar
- Odeyemi IA, Dakin HA, O’Donnell RA, Warner J, Jacobs A, Dasgupta P: Epidemiology, prescribing patterns and resource use associated with overactive bladder in UK primary care. Int J Clin Pract. 2006, 60: 949-958. 10.1111/j.1742-1241.2006.01057.x.View ArticlePubMedGoogle Scholar
- Tikkinen KA, Tammela TL, Rissanen AM, Valpas A, Huhtala H, Auvinen A: Is the prevalence of overactive bladder overestimated? A population-based study in Finland. PLoS ONE. 2007, 2: e195-10.1371/journal.pone.0000195.View ArticlePubMedPubMed CentralGoogle Scholar
- Castro D, Espuna M, Prieto M, Badia X: Prevalence of overactive bladder in Spain: a population-based study. Arch Esp Urol. 2005, 58: 131-138.View ArticlePubMedGoogle Scholar
- Martinez Agullo E, Ruiz Cerda JL, Gomez Perez L, Ramírez Backhaus M, Delgado Oliva F, Rebollo P, González-Segura Alsina D, Arumi D: Prevalence of urinary incontinence and hyperactive bladder in the Spanish population: results of the EPICC study. Actas Urol Esp. 2009, 33: 159-166. 10.1016/S0210-4806(09)74117-8.View ArticlePubMedGoogle Scholar
- Sexton CC, Coyne KS, Thompson C, Bavendam T, Chen CI, Markland A: Prevalence and effect on health-related quality of life of overactive bladder in older americans: results from the epidemiology of lower urinary tract symptoms study. J Am Geriatr Soc. 2011, 59: 1465-1470. 10.1111/j.1532-5415.2011.03492.x.View ArticlePubMedGoogle Scholar
- Vaughan CP, Johnson TM, Ala-Lipasti MA, Cartwright R, Tammela TL, Taari K, Auvinen A, Tikkinen KA: The prevalence of clinically meaningful overactive bladder: bother and quality of life results from the population-based FINNO study. Eur Urol. 2011, 59: 629-636. 10.1016/j.eururo.2011.01.031.View ArticlePubMedGoogle Scholar
- Yoo ES, Kim BS, Kim DY, Oh SJ, Kim JC: The impact of overactive bladder on health-related quality of life, sexual life and psychological health in Korea. Int Neurourol J. 2011, 15: 143-151. 10.5213/inj.2011.15.3.143.View ArticlePubMedPubMed CentralGoogle Scholar
- Martinez Agullo E, Ruiz Cerda JL, Gomez Perez L, Rebollo P, Perez M, Chaves J: Impact of urinary incontinence and overactive bladder syndrome on health-related quality of life of working middle-aged patients and institutionalized elderly patients. Actas Urol Esp. 2010, 34: 242-250.PubMedGoogle Scholar
- Bartoli S, Aguzzi G, Tarricone R: Impact on quality of life of urinary incontinence and overactive bladder: a systematic literature review. Urology. 2010, 75: 491-500. 10.1016/j.urology.2009.07.1325.View ArticlePubMedGoogle Scholar
- Irwin DE, Milsom I, Kopp Z, Abrams P: Symptom bother and health care-seeking behavior among individuals with overactive bladder. Eur Urol. 2008, 53: 1029-1037. 10.1016/j.eururo.2008.01.027.View ArticlePubMedGoogle Scholar
- Benner JS, Becker R, Fanning K, Jumadilova Z, Bavendam T, Brubaker L: Bother related to bladder control and health care seeking behavior in adults in the United States. J Urol. 2009, 181: 2591-2598. 10.1016/j.juro.2009.02.018.View ArticlePubMedGoogle Scholar
- Andersson KE: Antimuscarinic mechanisms and the overactive detrusor: an update. Eur Urol. 2011, 59: 377-386. 10.1016/j.eururo.2010.11.040.View ArticlePubMedGoogle Scholar
- Hunter KF, Wagg A, Kerridge T, Chick H, Chambers T: Falls risk reduction and treatment of overactive bladder symptoms with antimuscarinic agents: a scoping review. Neurourol Urodyn. 2011, 30: 490-494. 10.1002/nau.21051.View ArticlePubMedGoogle Scholar
- Swinburn P, Lloyd A, Ali S, Hashmi N, Newal D, Najib H: Preferences for antimuscarinic therapy for overactive bladder. BJU Int. 2011, 108: 868-873.PubMedGoogle Scholar
- Dobrek L, Juszczak K, Wyczolkowski M, Thor PJ: Current management and future perspectives of overactive bladder (OAB) pharmacotherapy. Acta Pol Pharm. 2011, 68: 807-821.PubMedGoogle Scholar
- Chapple C, Van Kerrebroeck P, Juenemann K, Wang J, Brodsky M: Comparison of fesoterodine and tolterodine in subjects with overactive bladder. BJU Int. 2008, 102: 1128-1132. 10.1111/j.1464-410X.2008.07907.x.View ArticlePubMedGoogle Scholar
- Chapple C, Van Kerrebroeck P, Tubaro A, Haag-Molkenteller C, Forst HT, Massow U, Wang J, Brodsky M: Clinical efficacy, safety, and tolerability of once-daily fesoterodine in subjects with overactive bladder. Eur Urol. 2007, 52: 1204-1212. 10.1016/j.eururo.2007.07.009.View ArticlePubMedGoogle Scholar
- Corcos J, Angulo JC, Garely AD, Carlsson M, Gong J, Guan Z: Effect of fesoterodine 4 mg on bladder diary and patient-reported outcomes during the first week of treatment in subjects with overactive bladder. Curr Med Res Opin. 2011, 27: 1059-1065. 10.1185/03007995.2011.565044.View ArticlePubMedGoogle Scholar
- Herschorn S, Swift S, Guan Z, Carlsson M, Morrow JD, Brodsky M, Gong J: Comparison of fesoterodine and tolterodine extended release for the treatment of overactive bladder: a head-to-head placebo-controlled trial. BJU Int. 2010, 105: 58-66. 10.1111/j.1464-410X.2009.09086.x.View ArticlePubMedGoogle Scholar
- Nitti VW, Dmochowski R, Sand PK, Forst HT, Haag-Molkenteller C, Massow U, Wang J, Brodsky M, Bavendam T: Efficacy, safety and tolerability of fesoterodine for overactive bladder syndrome. J Urol. 2007, 178: 2488-2494. 10.1016/j.juro.2007.08.033.View ArticlePubMedGoogle Scholar
- Kelleher CJ, Tubaro A, Wang JT, Kopp Z: Impact of fesoterodine on quality of life: pooled data from two randomized trials. BJU Int. 2008, 102: 56-61. 10.1111/j.1464-410X.2008.07710.x.View ArticlePubMedGoogle Scholar
- Sexton CC, Notte SM, Maroulis C, Dmochowski RR, Cardozo L, Subramanian D, Coyne KS: Persistence and adherence in the treatment of overactive bladder syndrome with anticholinergic therapy: a systematic review of the literature. Int J Clin Pract. 2011, 65: 567-585. 10.1111/j.1742-1241.2010.02626.x.View ArticlePubMedGoogle Scholar
- Benner JS, Nichol MB, Rovner ES, Jumadilova Z, Alvir J, Hussein M, Fanning K, Trocio JN, Brubaker L: Patient-reported reasons for discontinuing overactive bladder medication. BJU Int. 2010, 105: 1276-1282. 10.1111/j.1464-410X.2009.09036.x.View ArticlePubMedGoogle Scholar
- Watanabe JH, Campbell JD, Ravelo A, Chancellor MB, Kowalski J, Sullivan SD: Cost analysis of interventions for antimuscarinic refractory patients with overactive bladder. Urology. 2010, 76: 835-840. 10.1016/j.urology.2010.01.080.View ArticlePubMedGoogle Scholar
- Reeves P, Irwin D, Kelleher C, Milsom I, Kopp Z, Calvert N, Lloyd A: The current and future burden and cost of overactive bladder in five European countries. Eur Urol. 2006, 50: 1050-1057. 10.1016/j.eururo.2006.04.018.View ArticlePubMedGoogle Scholar
- Mullins CD, Subak LL: New perspectives on overactive bladder: quality of life impact, medication persistency, and treatment costs. Am J Manag Care. 2005, 11 (4 Suppl): S101-S102.PubMedGoogle Scholar
- WHO Collaborating Centre for Drug Statistics Methodology: Anatomic Therapeutic Chemical classification system: structure and principles. Available at: http://www.whocc.no/atc/structure_and_principles/#structure. Accessed: March 13, 2013,
- Steiner JF, Prochazka AV: The assessment of refill compliance using pharmacy records: methods, validity, and applications. J Clin Epidemiol. 1997, 50: 105-116. 10.1016/S0895-4356(96)00268-5.View ArticlePubMedGoogle Scholar
- Benner JS, Glynn RJ, Mogun H, Neumann PJ, Weinstein MC, Avorn J: Long-term persistence in use of statin therapy in elderly patients. JAMA. 2002, 288: 455-461. 10.1001/jama.288.4.455.View ArticlePubMedGoogle Scholar
- The International Classification of Primary Care in the European Community: With a Multi-language Layer. 1993, Oxford: Oxford Medical PublicationsGoogle Scholar
- Charlson ME, Pompei P, Ales KL, MacKenzie CR: A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987, 40: 373-383. 10.1016/0021-9681(87)90171-8.View ArticlePubMedGoogle Scholar
- Thompson SG, Barber JA: How should cost data in pragmatic randomised trials be analysed?. BMJ. 2000, 320: 1197-1200. 10.1136/bmj.320.7243.1197.View ArticlePubMedPubMed CentralGoogle Scholar
- Kaplan SA, Schneider T, Foote JE, Guan Z, Carlsson M, Gong J: Superior efficacy of fesoterodine over tolterodine extended release with rapid onset: a prospective, head-to-head, placebo-controlled trial. BJU Int. 2011, 107: 1432-1440. 10.1111/j.1464-410X.2010.09640.x.View ArticlePubMedGoogle Scholar
- Castro-Diaz D, Miranda P, Sanchez-Ballester F, Lizarraga I, Arumi D, Rejas J: Dose and aging effect on patients reported treatment benefit switching from the first overactive bladder therapy with tolterodine Er to fesoterodine: post-hoc analysis from an observational and retrospective study. BMC Urol. 2012, 12: 19-10.1186/1471-2490-12-19.View ArticlePubMedPubMed CentralGoogle Scholar
- Cardozo L, Lisec M, Millard R, van Vierssen TO, Kuzmin I, Drogendijk TE, Huang M, Ridder AM: Randomized, double-blind placebo controlled trial of the once daily antimuscarinic agent solifenacin succinate in patients with overactive bladder. J Urol. 2004, 172: 1919-1924. 10.1097/01.ju.0000140729.07840.16.View ArticlePubMedGoogle Scholar
- Chapple CR, Rechberger T, Al-Shukri S, Meffan P, Everaert K, Huang M, Ridder A: Randomized, double-blind placebo- and tolterodine-controlled trial of the once-daily antimuscarinic agent solifenacin in patients with symptomatic overactive bladder. BJU Int. 2004, 93: 303-310. 10.1111/j.1464-410X.2004.04606.x.View ArticlePubMedGoogle Scholar
- Chapple CR, Martinez-Garcia R, Selvaggi L, Toozs-Hobson P, Warnack W, Drogendijk T, Wright DM, Bolodeoku J: A comparison of the efficacy and tolerability of solifenacin succinate and extended release tolterodine at treating overactive bladder syndrome: results of the STAR trial. Eur Urol. 2005, 48: 464-470. 10.1016/j.eururo.2005.05.015.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2490/13/51/prepub
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