eFigure. Schematic of Time-Varying Intermittent Exposure to Antithrombotic Medications, Illustrating the Calculation of Incidence Density Rates.
eTable 1. Medications Included in Exposure Definition.
eTable 2. Outcome Definitions.
eTable 3. Validation of Administrative Data Sources.
eTable 4. Medications Included in BPH Medication Exposure.
eTable 5. Sensitivity Analysis: Multivariable Negative Binomial Regression Models Assessing the Association Between Exposure to Antithrombotic Agents (Primary Exposure) and Hematuria-Related Complications, Using a limited definition of Urologic Procedures (Study Interval Between 2002-2014).
eTable 6. Standardized Incidence Ratios (SIR) of Potential Outcomes of Hematuria-Related Investigations (Study Interval Between 2002-2014).
eTable 7. Continuous Length of Time That Patients Spend on Each Drug.
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Wallis CJD, Juvet T, Lee Y, et al. Association Between Use of Antithrombotic Medication and Hematuria-Related Complications. JAMA. 2017;318(13):1260–1271. doi:10.1001/jama.2017.13890
Is there an association between the use of oral antithrombotic agents and hematuria-related complications?
In this cohort study that included 2 518 064 older adults in Ontario, Canada, use of antithrombotic medications, compared with nonuse of these medications, was significantly associated with hematuria-related complications (including emergency department visits, hospitalizations, and urologic procedures).
Use of antithrombotic medications was associated with a significant increase in rates of hematuria-related complications.
Antithrombotic medications are among the most commonly prescribed medications.
To characterize rates of hematuria-related complications among patients taking antithrombotic medications.
Design, Setting, and Participants
Population-based, retrospective cohort study including all citizens in Ontario, Canada, aged 66 years and older between 2002 and 2014. The final follow-up date was December 31, 2014.
Receipt of an oral anticoagulant or antiplatelet medication.
Main Outcomes and Measures
Hematuria-related complications, defined as emergency department visit, hospitalization, or a urologic procedure to investigate or manage gross hematuria.
Among 2 518 064 patients, 808 897 (mean [SD] age, 72.1 [6.8] years; 428 531 [53%] women) received at least 1 prescription for an antithrombotic agent over the study period. Over a median follow-up of 7.3 years, the rates of hematuria-related complications were 123.95 events per 1000 person-years among patients actively exposed to antithrombotic agents vs 80.17 events per 1000 person-years among patients not exposed to these drugs (difference, 43.8; 95% CI, 43.0-44.6; P < .001, and incidence rate ratio [IRR], 1.44; 95% CI, 1.42-1.46). The rates of complications among exposed vs unexposed patients (80.17 events/1000 person-years) were 105.78 for urologic procedures (difference, 33.5; 95% CI, 32.8-34.3; P < .001, and IRR, 1.37; 95% CI, 1.36-1.39), 11.12 for hospitalizations (difference, 5.7; 95% CI, 5.5-5.9; P < .001, and IRR, 2.03; 95% CI, 2.00-2.06), and 7.05 for emergency department visits (difference, 4.5; 95% CI, 4.3-4.7; P < .001, and IRR, 2.80; 95% CI, 2.74-2.86). Compared with patients who were unexposed to thrombotic agents, the rates of hematuria-related complications were 191.61 events per 1000 person-years (difference, 117.3; 95% CI, 112.8-121.8) for those exposed to both an anticoagulant and antiplatelet agent (IRR, 10.48; 95% CI, 8.16-13.45), 140.92 (difference, 57.7; 95% CI, 56.9-58.4) for those exposed to anticoagulants (IRR, 1.55; 95% CI, 1.52-1.59), and 110.72 (difference, 26.5; 95% CI, 25.9-27.0) for those exposed to antiplatelet agents (IRR, 1.31; 95% CI, 1.29-1.33). Patients exposed to antithrombotic agents, compared with patients not exposed to these drugs, were more likely to be diagnosed as having bladder cancer within 6 months (0.70% vs 0.38%; odds ratio, 1.85; 95% CI, 1.79-1.92).
Conclusions and Relevance
Among older adults in Ontario, Canada, use of antithrombotic medications, compared with nonuse of these medications, was significantly associated with higher rates of hematuria-related complications (including emergency department visits, hospitalizations, and urologic procedures to manage gross hematuria).
Antithrombotic agents are among the most commonly prescribed medications for older adults in North America.1 Oral anticoagulants are indicated for primary and secondary prevention of stroke and systemic embolism, as well as treatment of venous thromboembolism.2 Antiplatelet agents are indicated for primary and secondary prevention of cardiovascular disease.3 Despite proven benefits, antithrombotic agents are among the medications most commonly associated with adverse events4 and have contributed to nearly half of all adverse drug events.5 Further, the rates of these adverse events are increasing.4 To date, published randomized clinical trials and observational studies of antithrombotic agents have focused on intracranial hemorrhage, gastrointestinal bleeding, and all-cause bleeding as adverse events.6,7
To our knowledge, a complication that has not been examined as the primary outcome in patients treated with antithrombotic agents is hematuria. While hematuria represents a less life-threatening adverse event than intracranial or gastrointestinal bleeding, it is common and involves diagnostic evaluation including abdominal imaging and invasive testing8,9 and management. The prevalence, severity, and risk factors for hematuria associated with the use of antithrombotic agents are largely unknown. To better characterize this association, this analysis examined rates of gross hematuria-related complications including hospitalization, emergency department visits, and urologic interventions over a 13-year period among patients who received anticoagulant or antiplatelet therapy from a population-based cohort of adults aged 66 years or older in Ontario, Canada.
We conducted a population-based, retrospective cohort study of patients aged 66 years or older in Ontario, Canada, between April 2002 and December 2014 using data from the Institute of Clinical Evaluative Sciences (ICES). In Ontario, medical care is reimbursed by a single, government-operated health insurance system (Ontario Health Insurance Plan). The cost of prescription medications is covered for all patients starting at age 65 years through the Ontario Drug Benefit.
This study was designed and conducted according to the Strengthening the Reporting of Observational Studies in Epidemiology guidelines10 and Reporting of Studies Conducted Using Observational Routinely-Collected Health Data Statement.11 The Sunnybrook Health Sciences Centre Research Ethics Board approved this study. Individual informed consent was waived owing to the anonymous, aggregated nature of the data.
We identified all residents of Ontario born before 1936, who would be aged 66 years or older during the study interval (2002-2014), based on date of birth using unique identifiers (ICES key number). The index date was defined as each person’s 66th birthday. To include only those patients actively receiving medical care in Ontario during the study interval, we excluded individuals who died and those who emigrated prior to the index date. We further excluded patients diagnosed as having a cancer (other than nonmelanomatous skin cancer) prior to the index date and those with prior endoscopic urologic procedures as these are likely to significantly affect a patient’s likelihood of hematuria-related complications. We also excluded patients older than the age of 105 years.
From linked databases, we collected demographic information including patient age at the time of each prescription, geographic location (local health integration networks12), sex, geographically derived socioeconomic status, rurality, and general comorbidity (Johns Hopkins aggregate disease group13). The Johns Hopkins aggregate disease group has better discrimination than the Charlson score in comorbidity assessment.14
The primary exposure was use of any oral antithrombotic agent, including anticoagulant and antiplatelet medications for which the first prescription occurred during the study interval (eTable 1 in the Supplement). We operationalized antithrombotic exposure in an intermittent, time-varying fashion (examples of operationalization of this exposure are in the eFigure in the Supplement). Age 66 years was selected for cohort inclusion to allow for a 1-year look-back to ensure that patients were not exposed to antithrombotic agents prior to study entry.
On the date of filling their first prescription during the study interval, patients were considered “exposed” and remained exposed until 14 days following the prescription end date (washout period). Fifteen days following the prescription end date, patients were considered to be “unexposed.” When the washout period coincided with prescription renewal, patients had continuous, ongoing exposure. When patients discontinued antithrombotic therapy and then restarted after discontinuation, a new exposure period commenced. Similarly, when patients switched medications, exposure and outcome time was allocated to each medication during the prescription period plus the 14-day washout period.
We measured counts of total hematuria-related complications, which was the sum of the counts of 3 specific end points including the occurrence of emergency department visits for gross hematuria, hospital admissions with a primary diagnosis of gross hematuria, or urologic procedures to manage gross hematuria. No other adverse events were included in this total. Specific diagnostic and procedural codes are provided in eTable 2 in the Supplement.
We linked the following validated data sets using patients’ unique ICES key numbers: the Ontario Drug Benefit database, which provides information on all outpatient prescription pharmaceuticals15; the Canadian Institute for Health Information Discharge Abstract Database, which contains records for all hospitalizations16; the Canadian Institute for Health Information National Ambulatory Care Reporting System, which contains records for emergency department visits; the Ontario Health Insurance Plan database, which tracks claims paid for physician billings, laboratories, and out-of-province providers (physicians, allied health, and hospitals)17; the Ontario Cancer Registry, a population-based registry estimated to be 95% or more complete18; and the Registered Persons database for demographic information19 (validation details in eTable 3 in the Supplement).
We measured the total number of complications each individual experienced rather than the first presentation of a complication. Patients contributed data until the date of death or until the last date of follow-up. Patients with missing data were excluded from the multivariate analysis. We calculated incidence density rates of each complication using the total count of the complication as the numerator and number of person-years exposed as the denominator, stratified by exposure to antithrombotic agents. Multivariable negative binomial regression was used to study the association between exposure to antithrombotic agents (operationalized in the time-varying manner described above) and complications due to the skewed nature of health services data.20,21 We expressed this as the incidence rate ratio (IRR), the ratio of incidence density rate during antithrombotic agent exposure to the rate during unexposed periods. Each rate ratio was adjusted for the association of patient age, sex, comorbidity, income quintile, region of residence, and rurality with tests for interaction. We tested for interaction between exposure variables using separate interaction terms in the models (ie, exposure A × exposure B). Where there was statistical significance, we included the interaction term in the final model and expressed the results using the interaction. This only occurred for the interaction between antithrombotic exposure and age at prescription. As a result, we expressed the IRR for antithrombotic exposure in a stratified fashion according to the patient’s age at the time of prescription.
We compared differences in the IRR of hematuria-related complications between medications using pairwise tests for heterogeneity between aspirin and other antiplatelet agents and between each of the 4 anticoagulants. Many patients received more than 1 agent during the study interval, and some received them concurrently. While assessing the association of each medication, concurrent exposures were handled using each medication as an independent exposure variable within the multivariable models such that an effect estimate could be derived for each medication. As concurrent antiplatelet and anticoagulant exposure may have a synergistic effect, the association of combination therapy was also assessed.
We conducted several preplanned subgroup analyses to understand modifying risks, given the known association between hematuria and benign prostatic hypertrophy (BPH)22 and medical kidney disease.23 As a surrogate for BPH, we examined patients’ prescriptions for BPH-related medications. We assessed the association of receipt of BPH-related medications in the year prior to antithrombotic exposure on rates of hematuria-related complications among men (eTable 4 in the Supplement). Then, among all patients, we assessed for the association of medical kidney disease by including consultation with a nephrologist.
We identified patients diagnosed as having bladder cancer within 6 months after an episode of hematuria using the Ontario Cancer Registry. We calculated the standardized incidence ratio (SIR) of bladder cancer among patients receiving antithrombotic agents by identifying the age- and sex-stratified expected number of bladder cancer cases based on the Ontario population. We then calculated the SIR as the ratio of the observed number of bladder cancer cases divided by the expected number of cases. Logistic regression analysis was also performed to calculate the odds ratio for being diagnosed as having cancer between the exposed and unexposed group, as patients are only diagnosed as having cancer once.
Statistical significance was set at P < .05 based on a 2-tailed comparison. All analyses were performed using SAS Enterprise Guide 6.1 (SAS Institute Inc).
We identified 4 184 141 residents of Ontario born before 1936, who would be aged 66 years or older during the study interval (2002-2014). Following exclusion of individuals who died (n = 915 892) and emigrated (n = 317 141) prior to the index date, those diagnosed as having a cancer (other than nonmelanomatous skin cancer) prior to the index date (n = 348 302), those with prior endoscopic urologic procedures (n = 84 674), and those older than the age of 105 years (n = 68), the final cohort comprised 2 518 064 individuals aged 66 years and older. Of these, 607 323 died after the index date, and 208 159 were lost to follow-up: 111 845 had a date of last contact of more than 2 years before the end of the study period, and 96 314 had loss of continuous health insurance coverage.
Of these participants, 808 897 filled at least 1 prescription for an antithrombotic agent, while 1 709 167 were not exposed during the study interval. Patients who filled a prescription for an antithrombotic agent were older (median age, 70 years vs 66 years; P < .001), more likely to be male (47.0% vs 41.9%; P < .001), had a lower level of income (20.8% vs 17.9%; P < .001), and had higher levels of comorbidity (30.6% vs 18.4%; P < .001) (Table 1). Patients exposed to antithrombotic agents were significantly more likely to have been diagnosed as having a relevant medical condition in the 5 years preceding the index date than those who were not exposed (Table 1).
Over a median follow-up of 7.3 years, gross hematuria-related complication rates were higher during active exposure to any antithrombotic agent (123.95 events/1000 person-years) than during unexposed periods (80.17 events/1000 person-years; difference, 43.8; 95% CI, 43.0-44.6; P < .001; Table 2). Of the hematuria-related complications, urologic procedures were the most common (105.78 events/1000 person-years; difference, 33.5; 95% CI, 32.8-34.3; P < .001), followed by hospitalizations (11.12 events/1000 person-years; difference, 5.7; 95% CI, 5.5-5.9; P < .001) and emergency department visits (7.05 events/1000 person-years; difference, 4.5; 95% CI, 4.3-4.7; P < .001; Table 2). The crude rate ratio for the development of hematuria-related complications was 1.44 (95% CI, 1.42-1.46) for exposure to antithrombotic agents compared with unexposed periods. Despite the fact that urologic procedures were the most common complication, the association between antithrombotic agent use and complications, when compared with unexposed periods, was highest for emergency department visits (crude rate ratio, 2.80; 95% CI, 2.74-2.86), followed by hospitalizations (crude rate ratio, 2.03; 95% CI, 2.00-2.06) and urologic procedures (crude rate ratio, 1.37; 95% CI, 1.36-1.39). These associations persisted on multivariable analysis with increasing age, male sex, and increasing comorbidity being significantly associated with rates of hematuria-related complications (Table 3). The highest rate was for emergency visits among adults aged 85 years and older (adjusted rate ratio, 4.74; 95% CI, 4.51-4.99; Table 3).
We then examined each antithrombotic medication individually: 315 639 individuals filled prescriptions for aspirin (dose ≥82 mg), 275 887 for other antiplatelet agents, 15 102 for apixaban, 43 451 for dabigatran, 87 912 for rivaroxaban, and 320 347 for warfarin. Hematuria-related complications were more common during exposure to anticoagulants than antiplatelet agents, and patients experienced the lowest rates of complications during exposure to older medications (aspirin and warfarin; Table 2). Among anticoagulants, in multivariable models, exposure to dabigatran (and not warfarin) was associated with the lowest rate of complications, while rivaroxaban had the highest rate for each age group (Table 4). Other antiplatelet agents, including clopidogrel, prasugrel, tricagrelor, ticlopidine, and dipyridamole, were associated with higher rates of hematuria-related complications than acetylsalicylic acid (≥82-mg dosage; Table 4).
Patients taking a combination of any antiplatelet agent and any anticoagulant experienced significantly increased rates of hematuria-related complications, particularly for hospitalizations (range of rate ratios, 2.68-4.16) and emergency department visits (range of rate ratios, 6.03-10.48) (Table 5).
While clot evacuation, control of bladder bleeding, and cystoscopy are unlikely to be indicated for patients without a history of bladder cancer in the absence of hematuria, urethral catheterization may be indicated owing to urinary retention. Thus, we performed a sensitivity analysis excluding catheterization from the definition of urologic procedures. While the overall event rate was lower, in regression models, the direction and magnitude of association were similar to the primary analysis, with antithrombotic exposure associated with a rate ratio of hematuria-related complications ranging from 1.39 to 2.36, depending on patient age (all P < .001; eTable 5 in the Supplement).
To examine the association of BPH and medical kidney disease on hematuria, we used surrogate measures including prescriptions of BPH medications and consultations with nephrologists. Prescription of a BPH-related medication in the year prior to antithrombotic prescription was also associated with an increased rate of hematuria-related complications (range of adjusted rate ratios, 1.67-1.93; all P < .001). This association persisted across secondary outcomes and individual antithrombotic medication exposures. Similarly, nephrology consultation was significantly associated with an increased risk of hematuria-related complications (range of adjusted rate ratios, 1.88-2.26; all P < .001).
In addition, 12 108 of 425 350 individuals (2.85%; 95% CI, 2.80%-2.90%) who presented with a hematuria-related complication were subsequently diagnosed as having bladder cancer within 6 months. A significantly higher proportion of patients exposed to antithrombotic agents (0.70%) were diagnosed as having bladder cancer than those who were unexposed to these agents (0.38%; unadjusted odds ratio, 1.85; 95% CI, 1.79-1.92). We calculated the standardized incidence ratio of bladder cancer among patients receiving antithrombotic agents, compared with the general Ontario population, with age and sex adjustment. Those receiving antithrombotic prescriptions had significantly more bladder cancer diagnoses than expected (SIR, 2.38; 95% CI, 2.32-2.44). Among women, the SIR was 2.17 (95% CI, 2.06-2.30) and among men it was 2.33 (95% CI, 2.26-2.40). Standardized incidence ratios of other urologist-managed cancers (prostate cancer: SIR, 0.75; 95% CI, 0.73-0.77, and kidney cancer: SIR, 0.64; 95% CI, 0.59-0.68) were not elevated among patients prescribed antithrombotic agents. The unadjusted odds ratio for being diagnosed as having prostate cancer was 1.65 (95% CI, 1.62-1.73) for patients in the exposed group, compared with the unexposed group, and for kidney cancer was 1.50 (95% CI, 1.4-1.6). Specific frequency of cancers and BPH outcomes are detailed in eTable 6 in the Supplement and the distribution of duration of time for each antithrombotic medication are detailed in eTable 7 in the Supplement.
In this population-based cohort study among 2 518 064 older adults in Ontario, Canada, treatment with antithrombotic medications, compared with nonuse of these medications, was significantly associated with increased rates of hematuria-related complications (including emergency department visits, hospitalizations, and urologic procedures to manage gross hematuria). While there was variation between medications, this association was present for all medications examined. Readily identifiable factors, including patient age, male sex, comorbidity, and preexistent urologic disease, were significantly associated with rates of gross hematuria. Patients taking antithrombotic agents were more likely to be diagnosed as having bladder cancer, both compared with unexposed individuals and with the general population. As there is no putative mechanistic linkage, these data suggest that use of antithrombotic agents was likely unmasking otherwise clinically silent bladder cancers.
In 1994, a prospective study of 243 patients receiving oral anticoagulation concluded that there was no association between anticoagulant use and hematuria.8 These data are outdated given the introduction of novel anticoagulant and antiplatelet agents. More recently, observational postmarketing surveillance reports have included other sources of “extracranial bleeding”24,25 but none have explicitly examined the association between hematuria and treatment with antithrombotic agents.
Historically, hematuria, particularly among patients taking antithrombotic agents, was associated with a significant burden of clinically significant, and potentially life-threatening, urologic disease.26,27 This analysis identified an association of asymptomatic bladder cancer among patients undergoing antithrombotic therapy, with an SIR of 2.4, although the absolute rate of bladder cancer remains low. Compared with the control group, in this study, positive associations for being diagnosed as having prostate and kidney cancer were found between the exposed and unexposed groups, but there was no increase in their SIRs. This is because the SIR was based on comparison with the general population, which is more heterogeneous than the control group that was used in the analysis.
A previous population-based study in Ontario showed that randomized clinical trials significantly underestimate rates of hemorrhage associated with warfarin therapy.28 Compared with warfarin, recent studies have shown lower rates of intracranial bleeding for each of the direct oral anticoagulants individually and, when combined, major bleeding is also reduced.29 In contrast, this analysis demonstrated an increased rate of hematuria-related complications associated with rivaroxaban use and comparable rate between warfarin and other newer anticoagulants. A similar result has been observed for gastrointestinal bleeding and abnormal uterine bleeding in menstruating women.30,31 There is no clear biologic explanation why there were observed differences in hematuria complications between different antithrombotic agents. Further study into the exact mechanisms of the causes of hematuria from the urinary tract based on their mechanism of action will be necessary.
Long-term antithrombotic decisions often require complex risk-benefit considerations. Among patients with a clear indication for anticoagulation, these medications are associated with improved survival.2,3 Over time, significant changes in the prescribing of antithrombotic medications have occurred and overall use has significantly expanded.32 Gross hematuria can be significantly distressing to patients33 and may contribute to subsequent poor adherence with antithrombotic therapy,34,35 which has been shown to increase the risk of stroke and death.35 Similarly, antithrombotic discontinuation due to bleeding contributes to increased rates of thrombotic events.36 Thus, the persistent risk of thrombotic events and relative infrequency of hematuria requiring hospitalization suggest that ongoing anticoagulant use is often warranted. Research to produce patient-specific decision aids based on cost-benefit or cost-effectiveness analyses incorporating reductions in thrombotic events, as well as hematuria and other adverse events, would be valuable.
This sample was larger than recent nationwide cohort studies assessing bleeding events from antithrombotic treatment in Denmark25 and France.37 In addition to the large sample size, this study has significant strengths owing to its population-based nature. First, this study was performed in Ontario, Canada, a jurisdiction in which all relevant medications and health services are available free of cost to seniors and are systematically tracked in administrative databases. Second, as all patients older than the age of 66 years in the largest province of Canada were identified, these results are generalizable. Unlike randomized clinical trials with strict inclusion and exclusion criteria or institutional reports representing tertiary care patterns, these results represent the population spectrum of clinical practice. Third, all hospitalizations and emergency department visits occurring anywhere in the province of Ontario were captured. This eliminates recall bias and minimizes selection bias. Thus, the outcome ascertainment is more robust than institutional studies. Fourth, as patients may stop antithrombotic medications owing to adverse events, they may transition from exposed to unexposed states and back. The use of a time-varying exposure used herein allows for accurate attribution of exposure for each patient at the time of each hematuria-related event. For this reason, survival analysis could not be conducted with competing risk analysis with morbidity and mortality, which would cause the exposure to cease.
This study had 5 limitations. First, owing to funding eligibility for prescription medications in Ontario, the cohort was restricted to patients aged 66 years and older. Given the interaction between age and the association of antithrombotic therapies with hematuria-related complications, these results are not directly applicable to younger patients. Second, the databases preclude capture of the use of over-the-counter low-dose aspirin and nonsteroidal anti-inflammatories. Low-dose aspirin has been associated with lower rates of major bleeding compared with higher-dose therapy.38,39 Thus, as high-dose aspirin (≥82 mg) had the lowest rate ratio for hematuria-related complications of all agents examined, low-dose aspirin is unlikely to be associated with a clinically significant risk of hematuria. Low-molecular-weight heparins were not included in the analysis owing to differing indications and their typical short durations of use. Thus, these results should only be applied to oral antithrombotic agents. Third, exposure ascertainment relied on data on prescriptions filled as a surrogate for medication use without verification of medication consumption. Nonadherence estimates have ranged from 25% to 55%40 and would bias these results toward the null. Fourth, the outcome definition was restricted to hospitalizations and emergency department visits, excluding outpatient office physician interactions. Hospitalizations, emergency department visits, and urologic interventions are likely to capture most significant episodes of gross hematuria and the validity of these diagnoses has been well established in Ontario,16 while this is not true for diagnostic fields associated with outpatient consultations. However, the specific diagnoses and procedures examined in this study have not been directly validated. For urological procedures, these were used as surrogates for actual complications without an ability to ascertain the indication for each intervention. While there are alternative indications for urethral catheterization (namely, acute urinary retention), few alternatives exist for cystoscopy, clot removal/irrigation, or control of bladder bleeding in the absence of a history of bladder cancer. A sensitivity analysis removing urethral catheterization from the outcome definition did not substantively change the findings. Fifth, the available data sets lacked information on the doses of antithrombotic medications, cumulative dose exposure, patient weight or body mass index, international normalized ratio values for patients taking warfarin, and alcohol consumption. However, within the study, a proportion of patients served as their own controls for the time they were not taking an antithrombotic medication, which would minimize this bias.
Among older adults in Ontario, Canada, use of antithrombotic medications, compared with nonuse of these medications, was significantly associated with higher rates of hematuria-related complications (including emergency department visits, hospitalizations, and urologic procedures to manage gross hematuria).
Accepted for Publication: September 5, 2017.
Corresponding Author: Robert K. Nam, MD, MSc, Division of Urology, Sunnybrook Health Sciences Centre, Room MG-406, 2075 Bayview Ave, Toronto, ON M4N 3M5, Canada (email@example.com).
Author Contributions: Drs Wallis and Nam had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
Study concept and design: Wallis, Juvet, Narod, Nam.
Acquisition, analysis, or interpretation of data: All authors.
Drafting of the manuscript: Wallis, Herschorn, Narod, Nam.
Critical revision of the manuscript for important intellectual content: All authors.
Statistical analysis: Wallis, Satkunasivam, Nam.
Obtained funding: Nam.
Administrative, technical, or material support: Wallis, Nam.
Study supervision: Lee, Kulkarni, Geerts, Narod, Nam.
Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Herschorn reports grants and/or personal fees from Astellas, Ipsen, Pfizer, and Allergan. Dr Geerts reports personal fees and/or other funding from Bayer, Pfizer, Leo Pharma, Bristol-Myers Squibb, Sanofi, and Janssen. No other disclosures were reported.
Funding/Support: Dr Wallis is supported by the Canadian Institute of Health Research Banting and Best Doctoral Award. Dr Nam is supported by the Ajmera Family Chair in Urologic Oncology. This study was funded by the Ajmera Family Chair in Urologic Oncology and Sunnybrook Foundation. This study used deidentified data from the Institute of Clinical Evaluative Sciences Data Repository, which is managed by the Institute for Clinical Evaluative Sciences with support from its funders and partners: Canada’s Strategy for Patient-Oriented Research (SPOR), the Ontario SPOR Support Unit, the Canadian Institutes of Health Research, and the Government of Ontario.
Role of the Funder/Sponsor: The funding organizations had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Disclaimer: The opinions, results, and conclusions reported are those of the authors. No endorsement by the Institute of Clinical Evaluative Sciences or any of its funders or partners is intended or should be inferred.
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