Abstract

Objective: To assess treatment patterns, health care resource utilization, and health care costs associated with use of atypical antipsychotics (AAPs) or the nonstimulant guanfacine extended release (GXR) after stimulant therapy for attention-deficit/hyperactivity disorder (ADHD). In Canada, GXR is approved as a monotherapy for children and adolescents with ADHD or as an adjunct to stimulants, and AAPs are commonly used off-label as an adjunct to stimulants.Methods: Health care claims data (January 1, 2007 to March 31, 2016) from Quebec's provincial health plan were assessed for individuals with ADHD, 6–17 years of age, who received ≥1 stimulant followed by a first AAP or GXR prescription (index medication), without a diagnosis for which AAPs are indicated.Results: Overall, 1327 individuals were included (AAPs, 1098; GXR, 229). Rates of discontinuation, augmentation, or switching of the index medication did not differ between AAPs and GXR during the first follow-up year. Discontinuation rates were significantly lower with GXR than with AAPs during the second year (22.0% vs. 35.9%; p = 0.03). GXR and AAPs resulted in similar increases in total health care cost. In GXR users, the increase in prescription drug cost after 6 months was higher than in AAP users, whereas the increase in overall medical cost was higher with AAPs than GXR, owing to more psychiatric department visits.Conclusions: In children and adolescents with ADHD who used AAPs or GXR after stimulants, secondary treatment changes were similar with both treatments after 1 year, but discontinuation rates were significantly lower with GXR than with AAPs in the second year. The greater increase in prescription cost with GXR was balanced by a greater increase in overall medical costs with AAPs, resulting in no overall difference in total health care cost between the two treatments.

Highlights

  • Attention-deficit/hyperactivity disorder (ADHD) is a common pediatric disorder associated with a considerable economic burden

  • In children and adolescents with attention-deficit/ hyperactivity disorder (ADHD) who used atypical antipsychotics (AAPs) or guanfacine extended release (GXR) after stimulants, secondary treatment changes were similar with both treatments after 1 year, but discontinuation rates were significantly lower with GXR than with AAPs in the second year

  • The type of stimulant most frequently used before the index treatment was MPH in the AAP group, and extended release (ER) amphetamine in the GXR group (Supplementary Table S1)

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Summary

Introduction

Attention-deficit/hyperactivity disorder (ADHD) is a common pediatric disorder associated with a considerable economic burden. Attention Deficit Hyperactivity Disorder Resource Alliance [CADDRA] 2011); a considerable proportion of patients receiving stimulants change their regimen, owing to an inadequate response, dose-limiting side effects, comorbid disorders, or personal preferences (Arnold 2000; Stockl et al 2003; Elvanse Prescribing Information 2014; Equasym Prescribing Information 2014). Claims database studies from Canada and the USA have demonstrated that, among stimulant-treated children and adolescents with ADHD, the 1-year prevalence of medication switching or augmentation is 19%–23% (Ben Amor et al 2014; Betts et al 2014). Not approved for the treatment of ADHD, clonidine and atypical antipsychotics (AAPs) are commonly used off-label in ADHD, especially when stimulants fail

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