Overactive Bladder Prescribing Considerations: The Role of Polypharmacy, Anticholinergic Burden, and CYP2D6 Drug‒Drug Interactions.

Overactive bladder (OAB) is a common disorder in the general population, and the prevalence increases with age. Adults with OAB typically have a greater number of comorbid conditions, such as hypertension, depression, and dementia, compared with adults without OAB. Subsequent to an increased number of comorbidities, adults with OAB take a greater number of concomitant medications, which may increase the risk of potentially harmful drug‒drug interactions. There are two important considerations for many of the medications approved for the treatment of OAB in the USA: anticholinergic burden and potential for drug‒drug interactions, notably related to cytochrome P450 (CYP) 2D6, which is responsible for the metabolism of approximately 25% of all drugs. A substantial number of drugs used for the treatment of OAB and comorbid conditions (e.g., cardiovascular and neurologic disorders) are CYP2D6 substrates or inhibitors. Furthermore, a substantial number of drugs with CYP2D6 properties also have strong anticholinergic properties. Here, we review polypharmacy associated with OAB and its common comorbidities, identify drugs with reported anticholinergic properties, and provide an overview of clinically relevant drug‒drug interactions in the treatment of OAB as they relate to CYP2D6 metabolism. This review aims to provide clinicians with essential information necessary for making treatment decisions when managing OAB.

Key Points

Introduction

An estimated 23% of Americans ≥ 40 years old have bothersome symptoms of overactive bladder (OAB) [1], and the proportion of adults who report urgency or urgency urinary incontinence increases with age in both men and women [1, 2]. Among residents of long-term care (LTC) facilities who are ≥ 65 years old, approximately 65–70% report urinary incontinence [3, 4], which is the second-leading cause for the placement of older adults into care facilities [5]. Compared to individuals without OAB, adults with OAB have a significantly higher prevalence of comorbid medical conditions, particularly cardiovascular and central nervous system (CNS) comorbidities [6, 7]. This holds true for older adults, as those ≥ 65 years old with OAB continue to experience a greater number of comorbid medical conditions than age-matched cohorts without OAB; among adults with OAB, those ≥ 75 years old have a greater number of comorbidities than those 65–74 years old [8].

The 2019 American Urological Association/Society of Urodynamics, Female Pelvic Medicine and Urogenital Reconstruction guidelines for the treatment of OAB (Table 1) recommend behavioral therapy as first-line treatment, which may be combined with pharmacotherapy; second-line treatment includes oral anticholinergics or β3-adrenergic agonists [9]. Treatment with anticholinergics, however, is associated with well-known side effects such as dry mouth, blurred vision, and constipation [10] and, perhaps more importantly, is associated with an increased risk of falls [11] and incident dementia [12-14]. Therefore, patients should be monitored for adverse drug reactions while taking anticholinergic treatments, and doses or treatments should be modified as necessary [9]. Furthermore, the American Geriatrics Society Beers Criteria® for Potentially Inappropriate Medication Use in Older Adults provides guidance regarding safety and dosing considerations in older adults for not only anticholinergics (e.g., strongly anticholinergic drugs such as chlorpheniramine, diphenhydramine, and amitriptyline are considered inappropriate), but also for other drug classes (e.g., antidepressants, skeletal muscle relaxants, and peripheral α1-blockers are considered inappropriate) [15].

Table 1

American Urological Association/Society of Urodynamics, Female Pelvic Medicine and Urogenital Reconstruction guidelines for the treatment of overactive bladder (adapted from [9])

Strategy	Treatment	Notes
First line	Behavioral therapy consisting of bladder training, bladder control strategies, pelvic floor muscle training, and fluid management	May be combined with pharmacologic treatment
Second line	Pharmacologic management consisting of oral anticholinergics (darifenacin, fesoterodine, oxybutynin, solifenacin, tolterodine, trospium) and/or β3-adrenergic receptor agonists (mirabegron, vibegron)	Extended-release formulations are preferable; transdermal formulations may be offered; consider dose modification or alternate medication if patients do not respond to initial treatment
Third line	Intradetrusor onabotulinumtoxinA or nerve stimulation (peripheral nerve stimulation or sacral neuromodulation)	Patient populations should be carefully selected, and patients must be thoroughly counseled
Fourth line	Augmentation cystoplasty or urinary diversion	Consider for severe, refractory, or complicated patients

Given the greater number of comorbid conditions experienced by adults with OAB and the subsequently greater number of pharmacologic treatments prescribed [6-8], there is an increased risk of potentially clinically relevant drug‒drug interactions (DDIs) in this population. Furthermore, a substantial number of drugs used to treat OAB and comorbid conditions, such as cardiovascular, neurologic, and psychiatric disorders, are CYP2D6 substrates or inhibitors. Drugs that inhibit CYP2D6 lead to increased plasma concentrations of drugs that are substrates of the enzyme, increasing the possibility of experiencing adverse events and toxicity. While not a focus of this review, other liver-based metabolic pathways, including CYP3A4 and CYP2B6, should also be considered [16].

Computerized physician order entry (CPOE) and prescribing systems are widely used with the goal of simplifying the prescribing process and identifying potential DDIs to minimize the risk of adverse effects. However, some CPOE systems remain problematic and may increase the risk of certain types of unforeseen prescribing errors, revealing new opportunities for error reduction [17]. Electronic health record (EHR) databases, which allow clinicians to track the potential benefits and risks of medical treatments, have been implemented by a substantial percentage of physician offices, and by 2014, approximately 74% of office-based physicians had implemented certified EHRs [18]. Electronic health records can provide decision-making support and can also alert clinicians of potential DDIs, similar to CPOE systems. However, while certified EHRs do exist, such databases are not regulated or standardized, and safety performance varies among the different EHR vendors [19]. As such, it is necessary for healthcare providers who treat patients with OAB to be aware of relevant DDIs so as not to rely solely on CPOE systems or EHRs to determine contraindications and the potential for clinically meaningful DDIs.

The aim of this review is to evaluate polypharmacy associated with OAB comorbidities and the implications relating to anticholinergic burden. The potential for clinically relevant CYP2D6-related DDIs is also explored to provide essential information for clinicians treating patients with OAB.

Comorbidities and Polypharmacy in Patients with OAB

Overall, adults with OAB experience a greater number of comorbidities compared with those without OAB [6, 20, 21]. Prevalence of comorbidities in older adults is substantial, with one database analysis reporting that adults 65–74 years old may experience an average of 16 comorbid medical conditions in a 12-month period, whereas adults ≥ 75 years old may experience an average of 20 [8]. Cardiovascular and neuropsychiatric comorbidities among adults with OAB are of particular interest given that the mainstays of pharmacologic treatment of OAB are anticholinergic medications, including oxybutynin, tolterodine, fesoterodine, and solifenacin, among others, that have well-known cardiovascular and neurologic side effects [22, 23]. Indeed, adults with OAB have a greater number of pre-existing neuropsychiatric disorders, including psychosis, nonpsychotic mental disorders, and dementia, compared with individuals without OAB; they also have a greater number of cardiovascular comorbidities such as hypertension and cardiac conduction disorders [6, 7].

Subsequent to a greater number of comorbid conditions, older adults with OAB are more likely to be taking a greater number of concomitant medications, particularly those used to treat cardiovascular and psychiatric conditions, than older adults without OAB [8]. Furthermore, adults with OAB have significantly increased use of anticholinergic medications than individuals without OAB [6], which has the potential to increase adverse effects or toxicity. A pooled analysis of ten clinical trials of fesoterodine for the treatment of OAB in participants ≥ 65 years old showed that the probability of experiencing a treatment-emergent adverse event significantly increased with increasing baseline concomitant diseases and medications [24].

In LTC facilities, the prevalence of OAB and/or urinary incontinence is high, with reports of 65–70% [3, 4]. Approximately 89% of nursing home residents need assistance with toileting, and 92% need assistance with walking or locomotion [25]. Consistent with the general population, residents of LTC facilities with urinary incontinence and/or OAB have a significantly higher prevalence of comorbidities such as hypertension, hyperlipidemia, dementia, depression, and anxiety disorders than residents without OAB [4]. Additionally, rates of frailty in LTC facilities are high, with one report suggesting that approximately 85% of LTC residents are frail [26], which may be related to comorbidities. Polypharmacy, a term with a broad range of definitions in the literature but commonly defined as taking five or more medications [27], in residents of LTC facilities is also high overall, with a recent systematic reviewing suggesting that 91% and 65% of LTC residents are taking more than five or more than ten medications, respectively [28]. Residents in LTC facilities with OAB have high rates of use of anticholinergic medications [29] and have significantly greater concomitant medication use, including use of diuretics, anxiolytics, and antipsychotics, compared with their age-matched cohorts [4]. In addition to highlighting challenges with polypharmacy, these obstacles to pharmacologic treatment highlight a need for behavioral treatments, which can be beneficial in this population.

Healthcare Burden of Polypharmacy

Management of OAB in older adults can be challenging given the high prevalence of polypharmacy [4, 8, 28, 29], which can lead to safety concerns and an increased risk of DDIs, potentially increasing healthcare resource utilization and costs. Indeed, current methods for treating patients with OAB has been shown to increase the healthcare burden and costs, typically because of the high prevalence of comorbid conditions [20, 21, 30]. Drug–drug interactions experienced by patients receiving polypharmacy can compound the economic burden because DDIs are associated with increased costs of hospitalization [31]. Additionally, the increased need for assistance with toileting and walking/locomotion [25] can place an extra burden on LTC staff that could be further encumbered when coupled with managing DDIs and adverse events from anticholinergics. Low persistence of treatment with anticholinergics for OAB [32] may also contribute to the burden and increase the safety risk for patients who abruptly stop OAB medications after drug regimens have been adjusted to account for DDIs. The potential for clinically relevant DDIs should be monitored for all patients, and DDIs should be carefully considered in high-risk populations such as patients ≥ 65 years old [33].

Many hospital admissions of older adults for drug toxicity occur after administration of a drug known to cause DDIs [34]. Although continuous monitoring for DDIs and adjustment of medications require diligence on the part of treating clinicians to ensure patient safety, studies have shown that evaluating polypharmacy and DDIs and updating treatment plans accordingly is associated with decreased healthcare and medication costs [35, 36]. Furthermore, deprescribing of medications should be considered for patients with OAB who are receiving polypharmacy; in such cases, it may be necessary for providers to carefully consider baseline medication use, prioritize medications, and discontinue or change medications (e.g., from anticholinergics for OAB to adrenergic agonists) to optimize clinical outcomes [27]. Use of a validated method to identify older patients at risk of adverse drug reactions, such as the GerontoNet ADR risk score, may facilitate this process [37].

Drug Safety: Anticholinergic Burden Including Drugs for OAB

Guidelines for the Safe Prescribing of Medications

A number of guidelines are available for clinicians to aid in clinical decision making, and many guidelines are geared toward use in older adults. The American Geriatrics Society Beers Criteria for Potentially Inappropriate Medication Use is arguably one of the most widely used guidelines in clinical practice and research. In 2019, the American Geriatrics Society published an update to the Beers Criteria [15], which aims to provide guidance to healthcare providers regarding the safe prescribing of medications in older adults. Additional guidelines include the screening tool of older people’s prescriptions (STOPP) and the screening tool to alert to the right treatment (START), which were first published in 2008 and most recently updated in 2015 [38]. The goals of the STOPP and START criteria are to provide clinicians with information necessary to minimize inappropriate prescribing in older adults, including defining medications significantly associated with adverse drug reactions. Applying STOPP and START criteria has been shown to significantly improve the appropriateness of medication and reduce adverse drug reactions [38]. The Medication Appropriateness Index is another tool developed to serve as a sensitive measure in prescribing quality due to intervention by a pharmacist [39, 40]. As a whole, the numerous available guidelines aim to provide clinicians with the necessary information to effectively treat patients while minimizing unsafe and harmful prescribing practices.

Guidelines for Anticholinergic Use

Appropriate anticholinergic prescribing is particularly important in adults with OAB because anticholinergics are one of the primary pharmacologic treatments and are intended for long-term use. The 2019 Beers Criteria update includes > 50 drugs with strong anticholinergic properties, many of which are recommended to avoid in older adults owing to an increased risk of confusion, dry mouth, constipation, and other common anticholinergic effects [15]. The Beers Criteria also recommends cautious use and monitoring of sodium levels for some anticholinergics, such as antipsychotics, selective-serotonin reuptake inhibitors, selective-norepinephrine reuptake inhibitor, and tricyclic antidepressants. High anticholinergic burden (ACB), which is the cumulative effect of taking one or more medications with anticholinergic activity, is associated with falls/fractures, cognitive decline, and increased mortality risk [11, 12, 41]. With alternatives to anticholinergics available for at-risk populations, prescribing of multiple anticholinergics should be avoided owing to DDIs and the increased risk of cognitive decline [42].

Despite this guidance, adults with OAB are commonly prescribed medications with high ACB. A database analysis of residents of US nursing homes showed that approximately 71% of residents with OAB or urinary incontinence were receiving anticholinergic agents; of those treated with anticholinergics for OAB, 77% were receiving additional medications with anticholinergic properties [29]. An analysis of patients (age range 65‒97 years) receiving trospium for the treatment for OAB, which is generally considered to have the lowest risk of DDIs of the anticholinergics for OAB, showed that approximately 28% of patients had an ACB score of ≥ 2 at baseline [43]. Use of anticholinergic medications is associated with an increased risk of incident dementia [12]; thus, treatment with anticholinergics in older adults and adults with dementia should be carefully considered. In a cross-sectional analysis of community-dwelling adults ≥ 65 years old, approximately 5% took an OAB-related anticholinergic medication, and adults with impaired cognition (e.g., mild cognitive impairment, dementia) were more likely to take anticholinergics than those without cognitive impairment [44]. Furthermore, 41% of adults who were taking anticholinergics were also taking cholinesterase inhibitors [44], which may not only cause both drugs to lose efficacy but is also likely to cause harm. Dual use of anticholinergics with cholinesterase inhibitors has been shown to lead to a faster rate of functional decline in activities of daily living [45].

Considerations When Prescribing OAB Anticholinergics

Clinicians should use caution when prescribing anticholinergics for the treatment of OAB, especially in frail older adult patients and when patients are taking other medications with anticholinergic properties [9]. Anticholinergics are also contraindicated in patients receiving solid oral potassium supplements because of reduced gastric motility caused by anticholinergics [9]. Further, owing to the high percentage of adults with OAB who also have comorbid cardiovascular and/or neuropsychiatric conditions [6, 7], clinicians should be especially cognizant of cardiovascular and CNS effects. Although adverse cardiovascular events are typically reported at low rates in clinical trials of anticholinergics for OAB, post-marketing experience suggests that anticholinergics are associated with palpitations [46-50] and tachycardia (from anticholinergic effects on the heart) [46-48], as well as QT prolongation (from blockade of hERG channels) [46, 51]. QT prolongation may lead to the development of torsades de pointes (TdP), a potentially fatal ventricular arrhythmia. Drugs with a risk of TdP are categorized as (1) known risk of TdP; (2) possible risk of TdP; or (3) conditional risk of TdP [52]. With regard to effects on the CNS, oxybutynin, trospium, darifenacin, and solifenacin are associated with hallucinations, confusion, and somnolence [46, 48, 49, 51], and tolterodine is associated with disorientation and memory impairment [47]. Although CNS effects are not included within the US Food and Drug Administration-approved label for fesoterodine, consideration should be given to the potential for more general anticholinergic effects.

Drug–Drug Interactions

General Considerations with Polypharmacy

In populations with a high prevalence of comorbid medical conditions and polypharmacy, use of anticholinergics and drugs that are substrates of CYP2D6 is particularly concerning, as each additional medication leads to a greater risk of DDIs, adverse events, and potentially life-threatening situations. Further, a number of medications are known to cause QTc prolongation, which makes medication management difficult for patients who may be at higher risk for cardiac arrythmias. Assuming a 22% likelihood of a drug being metabolized by CYP2D6, the probability of a patient taking at least one medication that is a substrate for CYP2D6 rapidly increases with the number of medications prescribed (Fig. 1), ultimately increasing the probability of a patient experiencing a clinically relevant DDI. In a recent retrospective analysis, residents of LTC facilities with OAB were taking a median of nine medications [53]. Using the above estimated likelihood, each resident receiving nine medications would therefore have an 89% probability of receiving at least one CYP2D6 substrate. Indeed, residents of LTCs with OAB have a greater overall use of medications that are substrates of CYP2D6 compared with residents without OAB (74% vs 67%, respectively), including significantly increased use of antidepressants (54% vs 46%); they also had significantly increased use of medications known to cause QTc prolongation (39% vs 29%) [53].

Fig. 1

Probability of a patient receiving a cytochrome P450 2D6 substrate. Probabilities are based on the assumption of a binomial distribution in which each drug prescribed is considered an independent event and the probability of each drug being a cytochrome P450 2D6 substrate is 22%

Drugs with Clinically Significant CYP2D6 Metabolism

As approximately one-quarter of currently used drugs are metabolized by CYP2D6, inhibition of CYP2D6, which leads to reduced enzyme activity and increased concentration of CYP2D6 substrates, is an important consideration for patients who are receiving polypharmacy. Thus, to identify clinically relevant CYP2D6 substrates in the treatment of OAB, we searched the following four drug databases and references: (1) Drug Interactions: Flockhart Table™ [54]; (2) Drug Interaction Solutions: In Vivo CYP2D6 Substrates [55]; (3) Lexicomp Facts & Comparisons Searchable Drug Information Database [56]; and (4) The Top 100 Drug Interactions: A Guide to Patient Management [57]. Review of four DDI databases or references indicates that 108 drugs approved for use in the USA are clinically relevant substrates of CYP2D6 (Table 2). These medications include common treatments for psychiatric disorders (e.g., depression, schizophrenia), cardiovascular disorders (e.g., hypertension, high cholesterol), and gastrointestinal disorders. A substantial number of these CYP2D6 substrates are also commonly used for the treatment of comorbidities often associated with OAB. Of the CYP2D6 substrates, 33 drugs are some of the most commonly prescribed drugs in the USA (i.e., included among the top 200 prescribed drugs) [58]. Approximately one-third (33/108) of these CYP2D6 substrates have ACB scores of 2 or 3 per the Anticholinergic Cognitive Burden Scale [59, 60], and 60 have risk of QT prolongation or TdP (Table 2).

Table 2

Therapeutic class, anticholinergic properties, and potential for QT prolongation of clinically relevant CYP2D6 substrates

Therapeutic class
Overactive bladder and lower urinary tract disorders
Darifenacin	Fesoterodine	Tamsulosina	Tolterodineb
Psychiatric disorders
Amitriptylinea,b	Doxepinb	Mirtazapinea,b	Quetiapinea,b
Amoxapine	Duloxetinea	Nefazodone	Risperidonea,b
Aripiprazolea,b	Escitaloprama,b	Nortriptylineb	Sertralinea,b
Asenapineb	Fluoxetinea,b	Olanzapineb	Thioridazineb
Brexpiprazole	Fluphenazine	Paliperidoneb	Trazodonea,b
Cariprazine	Fluvoxamineb	Paroxetinea,b	Trimipramineb
Chlorpromazineb	Haloperidolb	Perphenazineb	Venlafaxinea,b
Citaloprama,b	Iloperidoneb	Pimavanserinb	Vilazodone
Clomipramineb	Imipramineb	Pimozideb	Vortioxetine
Clozapineb	Loxapine	Prochlorperazine
Desipramineb	Maprotilineb	Protriptyline
Cardiovascular disorders
Carvedilola	Metoprolola	Propafenoneb	Timolola
Clonidinea	Mexiletine	Propranolola
Flecainideb	Nebivolola	Ranolazineb
Lovastatina	Procainamideb	Simvastatina
Neurologic disorders
Deutetrabenazineb	Fingolimodb	Tetrabenazineb	Valbenazineb
Donepezila,b	Galantamineb
Supportive care, pain, and gastrointestinal disorders
Almotriptan	Dihydrocodeine	Metaxalone	Oxycodonea
Chlorpheniramine	Diphenhydramineb	Methadoneb	Palonosetronb
Codeine	Dolasetronb	Metoclopramideb	Promethazinea,b
Desloratadine	Hydrocodonea,b	Netupitant	Tramadola,b
Dextromethorphan	Loratadinea	Ondansetrona,b
Antineoplastic
Gefitinib	Ibrutinib	Rucaparibb	Tamoxifenb
Other
Amphetaminea	Dacomitinib	Lofexidineb	Pitolisantb
Atomoxetinea,b	Dextroamphetaminea	Luliconazole	Ponatinib
Cevimeline	Eliglustatb	Methamphetamine	Primaquineb
Chloroquineb	Fenfluramine	Methylphenidatea	Ritonavir
Cinacalcet	Flibanserin	Panobinostatb	Umeclidinium

Drug names in bold have scores of 2 or 3 according to the Anticholinergic Cognitive Burden Scale [59], where 2 = evidence from the literature, prescribing information, or expert opinion of clinical effect and 3 = evidence from the literature, prescribing information, or expert opinion that the medication may cause delirium. Drugs were cross-referenced against reports by Salahudeen et al. [60]

CYP cytochrome P450

aIndicates drug included in top 200 list of prescribed drugs in the USA [58]

bIndicates drug with a risk of QT prolongation and/or causing torsades de pointes [52]

When CYP2D6 substrates are co-administered with a CYP2D6 inhibitor, patients may experience supra-therapeutic levels of the CYP2D6 substrate owing to increased exposure from inhibited metabolism. This in turn leads to an increased risk of adverse events. These adverse effects commonly affect the CNS, leading to neurologic adverse events (e.g., seizures, serotonin toxicity, altered mental status), and are especially relevant for patients being treated for neurologic or psychiatric conditions with the CYP2D6 substrates listed in Table 2 [61, 62]. Similarly, treatment with analgesics (e.g., tramadol) can lead to adverse neurologic effects such as seizures or serotonin toxicity [63-65]. In addition to neurologic adverse effects, patients may experience clinically significant cardiovascular adverse effects such as bradycardia and hypotension when CYP2D6 inhibitors are administered with β-blockers that are CYP2D6 substrates (e.g., metoprolol, carvedilol) [66], which is particularly relevant for patients receiving treatment for heart failure. When it is necessary to prescribe a drug that is a CYP2D6 inhibitor, treating clinicians should be aware of drugs that are CYP2D6 substrates and monitor for adverse events or modify doses accordingly.

Five CYP2D6 substrates have a boxed warning or documented contraindication when co-administered with CYP2D6 inhibitors (Table 3). These drugs should generally not be co-administered with CYP2D6 inhibitors, and alternatives should be considered. Because drugs that are CYP2D6 inhibitors may not contain corresponding boxed warnings for all medications metabolized by CYP2D6, DDIs between newly prescribed CYP2D6 inhibitors and substrates can often be overlooked. The total effect of the concurrent administration of multiple drugs that inhibit CYP2D6 is unknown, and some increase in inhibition is likely. Thus, treating clinicians should carefully review patient treatment plans and revise medication regimens to avoid the administration of multiple CYP2D6 inhibitors. Further, in patients receiving polypharmacy, it is especially important to perform medication reviews at every patient visit to ensure optimal treatment regimens and to determine whether it is appropriate to substitute or stop prescribing certain medications. Clinicians should also encourage medication adherence when counseling patients because nonadherence may be additionally problematic if dose adjustments have been made to account for DDIs.

Table 3

CYP2D6 substrates with a boxed warning or other contraindication when co-administered with a CYP2D6 inhibitor

Drug	Indication	Risk when co-administered with CYP2D6 inhibitor
Codeine	Pain management	Respiratory depression, extreme sleepiness, confusion, shallow breathing [75]
Eliglustat tartrate	Gaucher disease	Prolongation of PR, QTc, and/or QRS interval [76]
Methadone	Opioid use disorder, pain management	Respiratory depression [77]
Thioridazine	Schizophrenia	QTc prolongation, torsades de pointes [78]
Tramadola	Pain management	Seizures, serotonin toxicity (mental status change, autonomic instability, neuromuscular aberrations, gastrointestinal symptoms) [63]

CYP cytochrome P450

aIndicates drug included in the top 200 list of prescribed drugs in the USA [58]

OAB Medications and CYP2D6 Substrates and Inhibitors

The 2019 update to the American Urological Association/Society of Urodynamics, Female Pelvic Medicine and Urogenital Reconstruction guidelines for the management of OAB now recommends the use of combination therapy with anticholinergics and β3-adrenergic agonists for patients refractory to monotherapy [9]. Of the drugs approved for the treatment of OAB or lower urinary tract symptoms, three of the anticholinergics (darifenacin, fesoterodine, tolterodine) and one α1-adrenergic receptor blocker (tamsulosin) are CYP2D6 substrates. Furthermore, darifenacin is also a CYP2D6 inhibitor [57], and in vitro and in vivo results indicate that mirabegron, a β3-adrenergic receptor agonist, is a moderate inhibitor of CYP2D6 [67, 68]. In healthy women, co-administration of mirabegron with tolterodine increased tolterodine peak plasma concentration and area under the curve from 0 to 24 hours approximately two-fold and resulted in a significant QTc prolongation, as measured by an electrocardiogram [69]. Tolterodine and fesoterodine are converted to an active metabolite, 5-hydroxymethyl tolterodine, that is further metabolized by CYP2D6 and CYP3A4 [70]. Altering the metabolism of CYP2D6 and CYP3A4, whether through patient factors (e.g., poor vs extensive metabolizers) or through therapeutics, in individuals receiving fesoterodine results in an increase (2.3- to 2.5-fold) in the area under the curve of the active metabolite [71]. Thus, combination therapy with mirabegron and a CYP2D6 substrate for OAB (e.g., tolterodine, fesoterodine) should be accompanied by careful patient monitoring, particularly in patients taking other drugs that could have DDIs. In the case of CYP2D6 inhibition with mirabegron, patients receiving anticholinergic drugs that are CYP2D6 substrates for common comorbid conditions may experience increased ACB and associated risks, and such use should be avoided [72].

Co-Administration of OAB CYP2D6 Inhibitors and Non-OAB Medications

For adults with OAB who are prescribed or may be receiving a new prescription for mirabegron, careful consideration of co-administered medications should be undertaken. Co-administration of mirabegron with metoprolol, a β-blocker approved for the treatment of hypertension that is a CYP2D6 substrate, has been shown to increase metoprolol peak plasma concentration 1.9-fold and total exposure 3.3-fold [68], which represents a dose three times greater than the intended dosage. Similarly, co-administration of mirabegron with desipramine, a tricyclic antidepressant that is also a CYP2D6 substrate, has been shown to increase desipramine peak plasma concentration 1.8-fold and total exposure 3.4-fold [68]. The effect of mirabegron on the plasma concentration of metoprolol and desipramine is greater than that reported with tolterodine and fesoterodine because CYP2D6 is the primary pathway for metoprolol and desipramine metabolism. Additionally, the magnitude of DDIs observed between mirabegron and CYP2D6 substrates may be explained by the mechanism-based inhibition property of mirabegron or by genetic polymorphisms in CYP2D6 [73]. Although data reporting the effect of mirabegron on CYP2D6 substrates are limited, it is reasonable, based on the data summarized above, to assume an approximately two- to three-fold increase in plasma concentrations of typical CYP2D6 substrates. Careful monitoring of patients receiving CYP2D6 substrates during the initiation and discontinuation of mirabegron is warranted [72]. Alternatively, a β3-adrenergic agonist that does not inhibit CYP2D6 enzymes, such as vibegron [74], could be considered for patients taking CYP2D6 substrates.

Conclusions

Patients with OAB experience a greater number of comorbid medical conditions and have a higher prevalence of polypharmacy compared with patients without OAB. Many drugs used to treat comorbid conditions have clinically relevant anticholinergic properties and/or are CYP2D6 substrates, which may make management of OAB difficult owing to the potential for anticholinergic side effects and an increased risk of potentially harmful DDIs. Current pharmacologic treatments for OAB include anticholinergics and β3-adrenergic agonists; however, four drugs approved for the treatment of OAB or lower urinary tract symptoms are CYP2D6 substrates, and two are CYP2D6 inhibitors. Treating clinicians should carefully consider medications prescribed and refine regimens as necessary to minimize potential harms related to DDIs while maximizing benefit in the treatment of OAB.

Adults with overactive bladder (OAB) have high rates of comorbid medical conditions (e.g., cardiovascular, neurologic, psychiatric) and polypharmacy; many drugs used for the treatment of OAB or for common comorbidities have anticholinergic properties, are substrates of cytochrome P450 (CYP) 2D6, or are both.

When co-administered with treatments for OAB that are CYP2D6 inhibitors, CYP2D6 substrates with anticholinergic properties may lead to effects such as impaired cognition, while exposure to substrates of CYP2D6 may lead to potentially harmful drug‒drug interactions and adverse effects.

Many drugs with clinically significant CYP2D6 metabolism have anticholinergic properties (and thus are associated with an increased risk of dementia and falls) and/or are associated with a variety of safety concerns including the risk of QT prolongation and other boxed warnings or contraindications when co-administered with CYP2D6 inhibitors.