Physician perception of clinical improvement in children with attention-deficit/hyperactivity disorder: a post hoc comparison of lisdexamfetamine dimesylate and mixed amphetamine salts extended release in a crossover analog classroom study
Frank A López1, Brian Scheckner2, Ann C Childress31Children's Developmental Center, Winter Park, FL, USA; 2Clinical Development and Medical Affairs, Shire Development Inc., Wayne, PA, USA; 3Center for Psychiatry and Behavioral Medicine, Las Vegas, NV, USA Trial Registry: N...
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doaj-fabf07d2d6b04f57bc36dedda425ff952020-11-25T01:46:07ZengDove Medical PressNeuropsychiatric Disease and Treatment1176-63281178-20212011-05-012011Issue 1267273Physician perception of clinical improvement in children with attention-deficit/hyperactivity disorder: a post hoc comparison of lisdexamfetamine dimesylate and mixed amphetamine salts extended release in a crossover analog classroom studyLópez FScheckner BChildress AFrank A López1, Brian Scheckner2, Ann C Childress31Children's Developmental Center, Winter Park, FL, USA; 2Clinical Development and Medical Affairs, Shire Development Inc., Wayne, PA, USA; 3Center for Psychiatry and Behavioral Medicine, Las Vegas, NV, USA Trial Registry: NCT00557011Objective: To assess effects of lisdexamfetamine dimesylate (LDX) and mixed amphetamine salts extended release (MAS XR) on symptom improvement in children with attention-deficit/hyperactivity disorder (ADHD).Methods: Post hoc analysis of a randomized, double-blind, placebo-controlled, crossover analog-classroom environment was conducted. The primary efficacy outcome was the deportment subscale of the Swanson, Kotkin, Agler, M-Flynn, and Pelham (SKAMP-D) rating scale. The secondary efficacy outcome was the investigator-rated Clinical Global Impressions-Improvement (CGI-I), a 7-point scale ranging from 1 (very much improved) to 7 (very much worse), which assesses improvement over time from baseline. McNemar test was used to compare participants' responses to LDX and MAS XR on CGI-I scores dichotomized into 1 (very much improved) vs all other response scores (2 to 7) in a 2 × 2 table.Results: Fifty-two children (aged 6 to 12 years) were enrolled, titrated, and randomized; 50 completed the study. Investigators rated 74% of LDX participants as either very much improved or much improved on the CGI-I scale relative to 72% of MAS XR participants and 18% of placebo participants. Of the 50 children who completed the study, 32% of LDX participants were very much improved vs 16% of MAS XR, and 2% of placebo participants relative to baseline. McNemar test indicated that 10 participants were very much improved with LDX, but not MAS XR; 2 participants were very much improved with MAS XR, but not LDX; 6 participants were very much improved with both, while 32 were not very much improved with either. Analysis showed that LDX had a significantly higher number of children with a very much improved score on the CGI-I than MAS XR (P = 0.0386).Conclusion: Treatment of children with LDX resulted in a higher number of participants with a very much improved score on the CGI-I than treatment with MAS XR or placebo.Keywords: lisdexamfetamine dimesylate, LDX, Vyvanse, mixed amphetamine salts, extended release, ADHD, CGI-Ihttp://www.dovepress.com/physician-perception-of-clinical-improvement-in-children-with-attentio-a7351 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
López F Scheckner B Childress A |
spellingShingle |
López F Scheckner B Childress A Physician perception of clinical improvement in children with attention-deficit/hyperactivity disorder: a post hoc comparison of lisdexamfetamine dimesylate and mixed amphetamine salts extended release in a crossover analog classroom study Neuropsychiatric Disease and Treatment |
author_facet |
López F Scheckner B Childress A |
author_sort |
López F |
title |
Physician perception of clinical improvement in children with attention-deficit/hyperactivity disorder: a post hoc comparison of lisdexamfetamine dimesylate and mixed amphetamine salts extended release in a crossover analog classroom study |
title_short |
Physician perception of clinical improvement in children with attention-deficit/hyperactivity disorder: a post hoc comparison of lisdexamfetamine dimesylate and mixed amphetamine salts extended release in a crossover analog classroom study |
title_full |
Physician perception of clinical improvement in children with attention-deficit/hyperactivity disorder: a post hoc comparison of lisdexamfetamine dimesylate and mixed amphetamine salts extended release in a crossover analog classroom study |
title_fullStr |
Physician perception of clinical improvement in children with attention-deficit/hyperactivity disorder: a post hoc comparison of lisdexamfetamine dimesylate and mixed amphetamine salts extended release in a crossover analog classroom study |
title_full_unstemmed |
Physician perception of clinical improvement in children with attention-deficit/hyperactivity disorder: a post hoc comparison of lisdexamfetamine dimesylate and mixed amphetamine salts extended release in a crossover analog classroom study |
title_sort |
physician perception of clinical improvement in children with attention-deficit/hyperactivity disorder: a post hoc comparison of lisdexamfetamine dimesylate and mixed amphetamine salts extended release in a crossover analog classroom study |
publisher |
Dove Medical Press |
series |
Neuropsychiatric Disease and Treatment |
issn |
1176-6328 1178-2021 |
publishDate |
2011-05-01 |
description |
Frank A López1, Brian Scheckner2, Ann C Childress31Children's Developmental Center, Winter Park, FL, USA; 2Clinical Development and Medical Affairs, Shire Development Inc., Wayne, PA, USA; 3Center for Psychiatry and Behavioral Medicine, Las Vegas, NV, USA Trial Registry: NCT00557011Objective: To assess effects of lisdexamfetamine dimesylate (LDX) and mixed amphetamine salts extended release (MAS XR) on symptom improvement in children with attention-deficit/hyperactivity disorder (ADHD).Methods: Post hoc analysis of a randomized, double-blind, placebo-controlled, crossover analog-classroom environment was conducted. The primary efficacy outcome was the deportment subscale of the Swanson, Kotkin, Agler, M-Flynn, and Pelham (SKAMP-D) rating scale. The secondary efficacy outcome was the investigator-rated Clinical Global Impressions-Improvement (CGI-I), a 7-point scale ranging from 1 (very much improved) to 7 (very much worse), which assesses improvement over time from baseline. McNemar test was used to compare participants' responses to LDX and MAS XR on CGI-I scores dichotomized into 1 (very much improved) vs all other response scores (2 to 7) in a 2 × 2 table.Results: Fifty-two children (aged 6 to 12 years) were enrolled, titrated, and randomized; 50 completed the study. Investigators rated 74% of LDX participants as either very much improved or much improved on the CGI-I scale relative to 72% of MAS XR participants and 18% of placebo participants. Of the 50 children who completed the study, 32% of LDX participants were very much improved vs 16% of MAS XR, and 2% of placebo participants relative to baseline. McNemar test indicated that 10 participants were very much improved with LDX, but not MAS XR; 2 participants were very much improved with MAS XR, but not LDX; 6 participants were very much improved with both, while 32 were not very much improved with either. Analysis showed that LDX had a significantly higher number of children with a very much improved score on the CGI-I than MAS XR (P = 0.0386).Conclusion: Treatment of children with LDX resulted in a higher number of participants with a very much improved score on the CGI-I than treatment with MAS XR or placebo.Keywords: lisdexamfetamine dimesylate, LDX, Vyvanse, mixed amphetamine salts, extended release, ADHD, CGI-I |
url |
http://www.dovepress.com/physician-perception-of-clinical-improvement-in-children-with-attentio-a7351 |
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