Adherence to Oral Therapy for Urgency Urinary Incontinence: Results from the Anticholinergic Versus Botox Comparison (ABC) Trial

Female Pelvic Med Reconstr Surg. 2016 Jan-Feb;22(1):24-8. doi: 10.1097/SPV.0000000000000215.

Abstract

Objectives: Medication adherence with urgency urinary incontinence (UUI) treatment is challenging and the best assessment methodology is uncertain. We sought to describe adherence with anticholinergic (AC) versus placebo (P) by comparing pill counts and MEMSCAP event data and to identify factors associated with adherence.

Methods: The randomized controlled AC versus Botox Comparison trial of women with moderate to severe idiopathic UUI included 126 participants initiating AC plus P bladder injection and 121 receiving P pills plus Botox injection. Adherence data on 243 participants (124 AC and 119 P) were calculated by pill count and MEMSCAP data for each 2-month interval during the 6-month study that allowed for dose escalation/drug change. Overall composite adherence estimates were calculated using the average of both methods and weighted by the duration of each 2-month interval.

Results: Treatment groups had no significant differences in dosing duration (P = 0.76) or mean adherence (AC, 83.3% [16.8] vs. P, 84.8% [13.8]). Only 53% of women met the dichotomous outcome of more than 80% adherence during all intervals. Correlation between adherence by pill counts versus MEMSCAP decreased over time with pill counts demonstrating higher adherence than MEMSCAP (r = 0.53, 0.50, and 0.36 for each 2-month interval). Lower adherence was associated with higher baseline incontinence severity and better UUI quality of life for the AC group and with current smoking status in both groups.

Conclusions: Adherence using pill counts and MEMSCAP was reasonably correlated and similar in both the AC and P groups. In the AC group, higher baseline incontinence severity and better UUI Quality of Life were associated with decreased adherence. Smokers were less adherent.

Trial registration: ClinicalTrials.gov NCT01166438.

Publication types

  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetylcholine Release Inhibitors / administration & dosage*
  • Administration, Intravesical
  • Administration, Oral
  • Benzilates / administration & dosage*
  • Botulinum Toxins, Type A / administration & dosage*
  • Double-Blind Method
  • Female
  • Humans
  • Medication Adherence
  • Middle Aged
  • Muscarinic Antagonists / administration & dosage*
  • Nortropanes / administration & dosage*
  • Prospective Studies
  • Solifenacin Succinate / administration & dosage*
  • Treatment Outcome
  • Urinary Incontinence, Urge / drug therapy*
  • Urological Agents / administration & dosage

Substances

  • Acetylcholine Release Inhibitors
  • Benzilates
  • Muscarinic Antagonists
  • Nortropanes
  • Urological Agents
  • trospium chloride
  • Botulinum Toxins, Type A
  • Solifenacin Succinate

Associated data

  • ClinicalTrials.gov/NCT01166438