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Drug Treatment Choice in Older Adults with Urinary Incontinence

Drug Treatment Choice in Older Adults with Urinary Incontinence. Catherine E. DuBeau, MD Professor of Medicine Director, Geriatric Continence Clinic Co-Director, Urology Resident Geriatric Education Program. Disclosures. Pfizer Astellas Novartis. Factors in Management - Ease of Use.

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Drug Treatment Choice in Older Adults with Urinary Incontinence

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  1. Drug Treatment Choice in Older Adults with Urinary Incontinence Catherine E. DuBeau, MD Professor of Medicine Director, Geriatric Continence Clinic Co-Director, Urology Resident Geriatric Education Program

  2. Disclosures Pfizer Astellas Novartis

  3. Factors in Management - Ease of Use Tolerability Drug Choice for UI in Older Adults Efficacy Pathophysiology

  4. Drug Choice for UI in Older Adults Factors in Management - Ease of Use Efficacy Tolerability Aging Comorbidity Pathophysiology Pathophysiology

  5. Homogeneity of Youth Punk rockers, 1978

  6. Heterogeneity of Age Punk rockers, 2008

  7. Aging effects on UI drug effects • Pharmacokinetics • Pharmacodynamics • Age-related changes in micturition • Structure • Function • Receptors • Impact of comorbidity on voiding and toileting

  8. Pharmacokinetics in Older Persons - 1 Absorption • Healthy: No change • Neuro & GI disease: impaired swallowing • Diabetes, anticholinergics: delayed gastric emptying • Frail: decreased subcutaneous fat affecting topical absorption Distribution • Healthy: No change • Inactive, frail: low muscle, higher fat mass • Longer half life of lipophilic agents • Higher serum concentration of water soluable agents • CNS penetration..?

  9. Water soluble agents Lipophilic agents Plasma proteins Drugs Cationization Efflux pumps Tight junction Transport proteins Metabolism Neuwelt EA. Neurosurgery 2004; 54:131-142

  10. Blood-Brain Barrier in Age & Aging-related Diseases • Data from studies using CSF/serum albumin ratio (C/s) as indication of BBB dysfunction • C/s increases with age • C/s correlates with severity of white matter signal abnormalities (WMSA) on CT in pts with and without dementia • WMSA also associated with vascular risk factors (HTN, DM, hyperlipidemia • WMSA associated with urgency severity Blennow et al, Eur Neurol 1993; Wallin et al, Eur Neurol 2000: Kuchel GA et al, AGS 2008

  11. Pharmacokinetics in Older Persons - 2 Metabolism • Healthy • No change in hepatic glycosylation • No definite change in P450 enzymes •  Hepatic mass and blood flow: less first-pass effect and increased serum levels of un-metabolized drug • Comorbid disease • Further decrease in hepatic mass and blood flow • Polypharmacy - medications that induce or inhibit P450 enzymes Clearance • Healthy • Renal: small decrease in GFR • Comorbid disease • Renal: Significant decrease in GFR, under-estimated by serum creatinine • GI: decreased transit time

  12. Pharmacodynamics • Age-related changes in detrusor muscarinic receptors • Normal contraction: M3 > M2 effect • With age: Decrease in M3 but not M2 mRNA • Age-related decrease in M receptor number in men (aging vs obstruction effect?) • Decrease in muscarinic-mediated contraction • Extrapolation to clinical data uncertain Mansfield KJ. et al. Brit J Pharmacol 2005,144:1089 Andersson KE. Schroder A. Urologe (Ausg. A) 2004,43:552

  13. Impact of Comorbidity: Polypharmacy Polypharmacy is the norm for older patients • Average number of meds = 5 • Among older women reporting medication use in previous week, 57% took > 5 agents • Current disease guidelines promote polypharmacy • Recommended regimen for 74 yo woman with HTN, DM, CHF, arthritis, osteoporosis = 12 meds, taken at 4 different times during the day • Leads to burden and cost disincentives to adding another drug Boyd CM et al. JAMA 2005, 294:716 Kaufman DW et al. JAMA. 2002, 287:337 Ernst ME. Iyer SS, Doucette WR. Value in Health. 2003, 6:51

  14. Impact of Drugs on Continence and LUTS in Older Persons Mentation Sedative hypnotics Benzos Anticholinergics Nocturia Nifedipine “Glitazones” NSAIDs/COX2 Gabapentin Pregabalin Stress UI ACE inhibitors Constipation Calcium blockers Anticholinergics Narcotics • LUT function • Decrease contractility • Anticholinergics • Calcium blockers •  Sphincter tone • Alpha agonist • Sphincter tone Alpha blocker Diuretics Mobility Antipsychotics

  15. Common Drugs for Common Conditions Mentation Sedative hypnotics Benzos Anticholinergics Nocturia Nifedipine “Glitazones” NSAIDs/COX2 Gabapentin Pregabalin Stress UI ACE inhibitors Constipation Calcium blockers Anticholinergics Narcotics • LUT function • Decrease contractility • Anticholinergics • Calcium blockers •  Sphincter tone • Alpha agonists • Sphincter tone Alpha blockers Diuretics Mobility Antipsychotics

  16. Use of Medications Affecting Continence in Women (median age 80) Attending a Geriatric Continence Clinic DuBeau and Shanti, Am Geriatr Soc Annual Meeting, 2006

  17. The Prescribing Cascade 77 yo woman with urgency; gets nifedipine for HTN Edema, constipation, impaired bladder emptying Nocturia,  urgency, some UI OAB! Add antimuscarinic  constipation Add laxative....

  18. The Prescribing Cascade 77 yo woman with urgency; gets nifedipine for HTN Edema, constipation, impaired bladder emptying Nocturia,  urgency, some UI OAB! Add antimuscarinic  constipation Add laxative....

  19. Efficacy “Do urge UI drugs work in older persons?”

  20. Oxytolfesosolidaritros in Patients Aged > 65 yr Analysis of pooled phase III fixed dose clinical data

  21. Oxytolfesosolidaritros in Patients Aged > 65 yr Analysis of pooled phase III fixed dose clinical data Placebo 2.7 mg Placebo 5.4 mg Median % Change UI QoL Perception † †

  22. “Older patients” in trials often much healthier than those in primary care Placebo OAB Drug A <65 y >65 y

  23. OAB Drug A OAB Drug B  UIE <65 y >65 y

  24. Problems with existing efficacy studies • Inadequate heterogeneity of study population • Lack of racial-ethnic and SES diversity • Include only cognitively and functionally intact • Exclusion of comorbidities known to affect micturition and continence • Limited to patients with high daytime frequency (>8 times daily) • Failure to include older- and oldest-old • Failure to include or assess whether patients have age-related detrusor underactivity (“DHIC”)

  25. Problems with existing efficacy studies • Little to no stratification by age group • No stratification by comorbidity • Little stratification by previous treatment No multivariate analyses despite large N’s If you control for age, you can’t evaluate it

  26. Efficacy: Are we looking at the right outcomes? • Patient perception: interaction with expectations? • Patient (and family) concerns about adverse drug effects • Marginal trade-off: drug benefit vs polypharmacy and cost • Dissatisfaction with previous inadequate treatment • Previous encounters with ageist providers • Nocturia: never normalized to hours in bed/sleeping • QoL and Bother • Few scales derived using patient-based data from older persons • Floor effects regarding “social” and “role” functions • None validated in oldest old, cognitively +/- functionally impaired • Alternative measures: in nursing home residents, prevalent and especially incident UI have negative impact on social interactions • DuBeau et al, J Am Geriatr Soc 2006 • DuBeau et al, J Am Geriatr Soc 1998

  27. Urgency and Nocturia Treatment, months What do older persons want from treatment? • Variance in Limitation in Daily Life from OAB • Bother - 42% • UI - 17% • Urgency/Frequency - 12% • Nocturia - 11% Michel MC et al, Neurourol Urodynam 2007

  28. Functional capacity Minimum function needed (eg, GFR >20) Age/Disease  ADE Risk in Older Patients • Not due to chronological age • Important factors vary by individual • Pharmacokinetic changes • Pharmacodynamic changes • Physiologic • Age-related changes in organ systems • Comorbidity and associated medications • Decreased functional reserve: “homeostenosis” Gurwitz and Avorn, Ann Int Med 1991

  29. Takes only 2 more pts to see harm Safety of OAB Drugs in Older Persons Consider number needed to harm (NNH) - inverse of attributable risk • Typical antimuscarinic • Decrease in urge UI: drug 70%, placebo 44% • Dry mouth: drug 28%, placebo 10% • NNT = 1/.26 = 3.8 • NNH = 1/.18 = 5.6

  30. Cognitive Impairment from Antimuscarinics? • Case reports • RCTs using non-standard cognitive measures • Oxybutynin “worse than Benadryl” (Katz, JAGS 1998) • Quantitative EEG studies: oxybutynin worse than tolterodine, trospium (Todorova, J Clin Pharmacol 2001) • Epidemiological studies • Prescription-event monitoring: more hallucinations with tolterodine than 10 non-antimuscarinic, non-CNS active drugs, RR = 4.85 (95% CI, 2.72-8.66) (Layton, Drug Safety 2001) use of • 372 elderly in France: anticholinergics associated with impairments in multiple domains of a cognitive battery (Ancelin, BMJ 2006)

  31. Evidence for Cognitive Impairment from Antimuscarinics • RCTs using standard cognitive batteries • Nursing home residents: oxybutynin ER 5 mg daily did not increase incidence of delirium (measured by CAM) over placebo (Lackner, JAGS 2008) • Older healthy patients: in 3-period crossover trial, variable doses of darifenacin no different than placebo on computerized cognitive battery; however, no intrapatient comparisons, only half of eligible patients randomized (Lipton, J Urol 2005) • Older healthy patients: oxybutynin ER did and darifenacin did not cause more impairment in delayed recall than placebo (Kay, Eur Urology 2006)

  32. 3 week RCT Comparing Darifenacin, Oxybutynin ER and Placebo Delayed Name-Face Association Test (lower score = worse) 7 6 5 * * † † Darifenacin (n=46) 4 Oxybutynin ER (n=49) Placebo (n=50) 0 Baseline Week 1 Week 2 Week 3 Kay G et al, Eur Urol 2006

  33. High starting dose Different titration schedule Very high end dose Are other commonly-used drugs even worse? Was the Study Design Biased? 7.5 mg 10 mg 7.5 mg 15 mg 15 mg 20 mg 7 6 5 * * † † Darifenacin (n=46) 4 Oxybutynin ER (n=49) Placebo (n=50) 0 Baseline Week 1 Week 2 Week 3 Kay G et al, Eur Urol 2006

  34. 3 week RCT Comparing Darifenacin, Oxybutynin ER and Placebo • No differences between darifenacin, oxybutynin ER, and placebo on other tests of delayed recall, immediate recall, visual attention, psychomotor reaction time, information processing speed, or self-rated memory. • In the French community study, anticholinergics were not associated with impairment in delayed recall Kay G et al, Eur Urol 2006; Ancelin, BMJ 2006

  35. Drug-Drug Interactions • Agents utilizing CY2D6 and 34A ubiquitous in primary care • Highly protein-bound drugs (eg, trospium) can compete with digoxin, increasing digoxin serum levels • Toxic digoxin level lower in elderly (> 0.8) • Antimuscarinics may add to pre-existing anticholinergic burden • Implications • Accept and acknowledge drug-drug interactions as fact of life • Use of electronic tools/EMR for checks and alerts

  36. Drug-Disease Interactions: The Example of Diabetes • Renal impairment: drug clearance • Slowed gastric motility: drug absorption • Constipation:  ADE risk and impact • Cognitive impairment:  ADE risk and impact • Glycosuria: masks antimuscarinic efficacy • DM medications • “Glitazones”: CHF; pedal edema causing nocturia • Metformin: competes for clearance with trospium • ACE inhibitors: cough exacerbates mixed UI • Gabapentin, pregabalin: edema causing nocturia • Tricyclics:  PVR , constipation

  37. Drug Choice for UI in Older Adults Factors in Management - Ease of Use Efficacy Tolerability Aging Comorbidity Pathophysiology Pathophysiology

  38. Choosing an Antimuscarinic • Cost (variable) • Dose size and escalation (start Detrol LA 2 mg; Ditropan XL widest range) • Once daily vs other dosing (extended release forms best) • Timing with other meds, meals (trospium: empty stomach) • Drug-drug interactions (CYP 2D6 – SSRIs; 3A4 - antifungals, macrolides) • Drug-disease interactions (trospium – renal clearance) • Dry mouth: oxybutynin worst • Constipation: darifenacin, solifenacin worst • Least: Oxytrol patch (but rash in 15%) No Differences All decrease UI ~70%, ~25% cure rate Tolerability Adverse effects Efficacy 4th International Consultation on Incontinence, 2008 Chapple C et al, Eur Urol 2005 Shamliyan TA et al, Ann Int Med 2008

  39. Research Agenda for Oxytolfesosolidaritros in Older Patients • Efficacy & tolerability • Assess across a spectrum of comorbidity and impairment • Predictors of response • With and without behavioral interventions • Absolute benefits and risk, NNT and NNH • Patient-based treatment utilities • Outcome measures specific to the spectrum of disease/disability and patient preferences

  40. The Example of Dry Mouth • 30% of older people already have it • Most already take at least one drug that causes it • Morbidity: dental caries, problems chewing, poorly fitting dentures, dysphagia, nutritional problems, sleeping difficulty, poor QoL Ship JA et al J Amer Geriatr Soc 2002 Fonda D et al. Frail Elderly, 3rd ICI

  41. Age and Physiology • Inter- and intra-individual variability increases • Chronological age poor marker of health status • “Age-associated” vs “age -related” • Both phenomena may be independent of function and symptoms

  42. Antimuscarinic Drug Trials in Older Patients • Tolterodine • At 4 weeks, urge UI episodes greater in pts 75 yr (P <0.02) • Reduction in voiding frequency similar in both age groups • No differences in efficacy in pts </> 65 years • No differences in dry mouth by age Malone-Lee et al, JAGS 2001;49:700 Malone-Lee et al, J Urol 2001;165:1452

  43. What is the “placebo effect”? “Perceived” placebo effect • Natural history • Maximum expected improvement 42% at 1 yr (6% at 8 wk) • Regression to mean, esp with severe symptoms at entry • MERIT population 3 UI episodes/day, but 45% sx > 5yr • Time effects related to pts • Early improvement leads to hope for good outcome • Unintended parallel interventions • Earlier improvers may be more likely to perform/continue other behavioral modifications (eg, decrease fluids)

  44. What is the “placebo effect”? “True” placebo effect • Conditioning • No difference in previous treatment or its efficacy • Impact of informed consent: improvement is “reasonably expected”; listing of potential side effects • Study participation • Amplification of placebo response by increased hope of good outcomes simply by entering a trial • Outcome measure • If overly sensitive, placebo effect increased • Bladder diary valid/reliable, but subjective/QoL measures?

  45. Preserved Plasticity • Systems can continue to adapt and change “despite” advanced age • Weight training increases muscle mass and strength in 90 year olds • Persons who stay intellectually engaged have improved quality of life • New evidence that CNS plasticity preserved

  46. What Increases ADE Risk? • Not chronological age • The important factors vary by individual • Pharmacokinetic changes • Pharmacodynamic changes • Physiologic: both co-morbidity (and meds to treat it) and decreased reserve • Functional characteristics Gurwitz and Avorn, Ann Int Med 1991

  47. The Example of Dry Mouth • 30% of older people already have it • Most already take at least one drug that causes it • Morbidity: dental caries, problems chewing, poorly fitting dentures, dysphagia, nutritional problems, sleeping difficulty, poor QoL Ship JA et al J Amer Geriatr Soc 2002 Fonda D et al. Frail Elderly, 3rd ICI

  48. Adverse Drug Effects • Common with all drugs in older persons (prevalence 35-66%) • Changes placing elderly at higher risk for anticholinergic AEs: • Altered cholinergic receptor number and distribution • Age and disease effects on blood-brain barrier (BBB) • Drug metabolism, drug-drug interactions • Pre-existing dry mouth and constipation • Impaired visual accomodation

  49. The Confusion around Confusion • Incidence unclear • Ditropan XL: “confusion” rate 2 to <5% in all studies • Detrol LA: “confusion” not listed; hallucinations in UK post-marketing survey, 4.5% rate/1000 pt-yrs (95% CI 2.9 – 6.8) • Case reports: “The addled nonagenarian” • Definition unclear • Is it worsening memory? Delirium? Both? • What are the best measures? Do proxy measures (eg, EEG) correlate clinically? US Ditropan XL prescribing information US Detrol LA prescribing information Layton et al, Drug Safety 2001; 24:703 Shader and Oesterheld, J Clin Psychopharm 1995; 15:378

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