Psychomotor functioning and alertness with guanfacine extended release in subjects with attention-deficit/hyperactivity disorder
To determine whether treatment with guanfacine extended release (GXR) in subjects with attention-deficit/hyperactivity disorder (ADHD) disrupted psychomotor functioning and alertness, or impacted daytime sleepiness. This was a randomized, double-blind, placebo-controlled, multicenter, phase 2, dose-...
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Veröffentlicht in: | Journal of child and adolescent psychopharmacology 2011-04, Vol.21 (2), p.111-120 |
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creator | Kollins, Scott H López, Frank A Vince, Bradley D Turnbow, John M Farrand, Kimberly Lyne, Andrew Wigal, Sharon B Roth, Thomas |
description | To determine whether treatment with guanfacine extended release (GXR) in subjects with attention-deficit/hyperactivity disorder (ADHD) disrupted psychomotor functioning and alertness, or impacted daytime sleepiness.
This was a randomized, double-blind, placebo-controlled, multicenter, phase 2, dose-optimization, noninferiority, laboratory classroom study of GXR (1, 2, and 3 mg/day) in 182 subjects aged 6 to 17 years with ADHD. Psychomotor functioning and alertness were assessed through several measures, including the Choice Reaction Time (CRT) test from the Cambridge Neuropsychological Test Automated Battery. Sedative effects were examined via spontaneously reported adverse events of sedation, somnolence, and hypersomnia as well as fatigue and lethargy, and with two validated subject- and observer-rated sleepiness scales. Standard efficacy measures for ADHD also were included. Cardiovascular and laboratory parameters were assessed.
There were no significant differences between the GXR and placebo groups on measures of psychomotor functioning or alertness from the CRT at endpoint (least-square mean difference: 2.5 [95% confidence interval (CI): -22.9, 28.0], p = 0.8 for CRT; 2.5 [95% CI: -21.5, 26.4], p = 0.84 for correct responses; 15.5 [95% CI: -45.1, 14.1], p = 0.30 for movement time; and -8.2 [95% CI: -54.1, 37.6] p = 0.72 for total time). Most sedative adverse events were mild to moderate, occurred during dose titration, decreased with dose maintenance, and resolved during the study period. One subject in the GXR group discontinued due to fatigue and somnolence. GXR was not associated with increased daytime sleepiness. GXR treatment was associated with significant improvement in ADHD symptoms (6.3 [95% CI: 2.7, 9.8], p = 0.001 for ADHD Rating Scale IV total scores at endpoint).
At doses that resulted in significant improvement in ADHD symptoms, impairment on cognitive tasks was not observed. Daytime sleepiness did not differ with GXR compared with placebo. Results suggest that the beneficial effects of GXR on ADHD symptoms are independent of sedation. |
doi_str_mv | 10.1089/cap.2010.0064 |
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This was a randomized, double-blind, placebo-controlled, multicenter, phase 2, dose-optimization, noninferiority, laboratory classroom study of GXR (1, 2, and 3 mg/day) in 182 subjects aged 6 to 17 years with ADHD. Psychomotor functioning and alertness were assessed through several measures, including the Choice Reaction Time (CRT) test from the Cambridge Neuropsychological Test Automated Battery. Sedative effects were examined via spontaneously reported adverse events of sedation, somnolence, and hypersomnia as well as fatigue and lethargy, and with two validated subject- and observer-rated sleepiness scales. Standard efficacy measures for ADHD also were included. Cardiovascular and laboratory parameters were assessed.
There were no significant differences between the GXR and placebo groups on measures of psychomotor functioning or alertness from the CRT at endpoint (least-square mean difference: 2.5 [95% confidence interval (CI): -22.9, 28.0], p = 0.8 for CRT; 2.5 [95% CI: -21.5, 26.4], p = 0.84 for correct responses; 15.5 [95% CI: -45.1, 14.1], p = 0.30 for movement time; and -8.2 [95% CI: -54.1, 37.6] p = 0.72 for total time). Most sedative adverse events were mild to moderate, occurred during dose titration, decreased with dose maintenance, and resolved during the study period. One subject in the GXR group discontinued due to fatigue and somnolence. GXR was not associated with increased daytime sleepiness. GXR treatment was associated with significant improvement in ADHD symptoms (6.3 [95% CI: 2.7, 9.8], p = 0.001 for ADHD Rating Scale IV total scores at endpoint).
At doses that resulted in significant improvement in ADHD symptoms, impairment on cognitive tasks was not observed. Daytime sleepiness did not differ with GXR compared with placebo. Results suggest that the beneficial effects of GXR on ADHD symptoms are independent of sedation.</description><identifier>ISSN: 1044-5463</identifier><identifier>EISSN: 1557-8992</identifier><identifier>DOI: 10.1089/cap.2010.0064</identifier><identifier>PMID: 21476931</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Adolescent ; Adrenergic alpha-2 Receptor Agonists - administration & dosage ; Adrenergic alpha-2 Receptor Agonists - adverse effects ; Adrenergic alpha-2 Receptor Agonists - therapeutic use ; Alertness (Psychology) ; Attention Deficit Disorder with Hyperactivity - drug therapy ; Attention Deficit Disorder with Hyperactivity - psychology ; Attention deficit hyperactivity disorder ; Child ; Children & youth ; Clinical trials ; Delayed-Action Preparations ; Disorders of Excessive Somnolence - chemically induced ; Disorders of Excessive Somnolence - drug therapy ; Dosage and administration ; Dose-Response Relationship, Drug ; Double-Blind Method ; Drug Administration Schedule ; Drug therapy ; Evaluation ; Fatigue - chemically induced ; Fatigue - drug therapy ; Female ; Guanfacine ; Guanfacine - administration & dosage ; Guanfacine - adverse effects ; Guanfacine - therapeutic use ; Humans ; Male ; Patient outcomes ; Placebos ; Psychiatric Status Rating Scales ; Psychomotor Performance - drug effects ; Treatment Outcome</subject><ispartof>Journal of child and adolescent psychopharmacology, 2011-04, Vol.21 (2), p.111-120</ispartof><rights>COPYRIGHT 2011 Mary Ann Liebert, Inc.</rights><rights>(©) Copyright 2011, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-2fd67d0106e6c71a7f390546805970ef7585233842c8bce09eaa103f7eb905383</citedby><cites>FETCH-LOGICAL-c386t-2fd67d0106e6c71a7f390546805970ef7585233842c8bce09eaa103f7eb905383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21476931$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kollins, Scott H</creatorcontrib><creatorcontrib>López, Frank A</creatorcontrib><creatorcontrib>Vince, Bradley D</creatorcontrib><creatorcontrib>Turnbow, John M</creatorcontrib><creatorcontrib>Farrand, Kimberly</creatorcontrib><creatorcontrib>Lyne, Andrew</creatorcontrib><creatorcontrib>Wigal, Sharon B</creatorcontrib><creatorcontrib>Roth, Thomas</creatorcontrib><title>Psychomotor functioning and alertness with guanfacine extended release in subjects with attention-deficit/hyperactivity disorder</title><title>Journal of child and adolescent psychopharmacology</title><addtitle>J Child Adolesc Psychopharmacol</addtitle><description>To determine whether treatment with guanfacine extended release (GXR) in subjects with attention-deficit/hyperactivity disorder (ADHD) disrupted psychomotor functioning and alertness, or impacted daytime sleepiness.
This was a randomized, double-blind, placebo-controlled, multicenter, phase 2, dose-optimization, noninferiority, laboratory classroom study of GXR (1, 2, and 3 mg/day) in 182 subjects aged 6 to 17 years with ADHD. Psychomotor functioning and alertness were assessed through several measures, including the Choice Reaction Time (CRT) test from the Cambridge Neuropsychological Test Automated Battery. Sedative effects were examined via spontaneously reported adverse events of sedation, somnolence, and hypersomnia as well as fatigue and lethargy, and with two validated subject- and observer-rated sleepiness scales. Standard efficacy measures for ADHD also were included. Cardiovascular and laboratory parameters were assessed.
There were no significant differences between the GXR and placebo groups on measures of psychomotor functioning or alertness from the CRT at endpoint (least-square mean difference: 2.5 [95% confidence interval (CI): -22.9, 28.0], p = 0.8 for CRT; 2.5 [95% CI: -21.5, 26.4], p = 0.84 for correct responses; 15.5 [95% CI: -45.1, 14.1], p = 0.30 for movement time; and -8.2 [95% CI: -54.1, 37.6] p = 0.72 for total time). Most sedative adverse events were mild to moderate, occurred during dose titration, decreased with dose maintenance, and resolved during the study period. One subject in the GXR group discontinued due to fatigue and somnolence. GXR was not associated with increased daytime sleepiness. GXR treatment was associated with significant improvement in ADHD symptoms (6.3 [95% CI: 2.7, 9.8], p = 0.001 for ADHD Rating Scale IV total scores at endpoint).
At doses that resulted in significant improvement in ADHD symptoms, impairment on cognitive tasks was not observed. Daytime sleepiness did not differ with GXR compared with placebo. Results suggest that the beneficial effects of GXR on ADHD symptoms are independent of sedation.</description><subject>Adolescent</subject><subject>Adrenergic alpha-2 Receptor Agonists - administration & dosage</subject><subject>Adrenergic alpha-2 Receptor Agonists - adverse effects</subject><subject>Adrenergic alpha-2 Receptor Agonists - therapeutic use</subject><subject>Alertness (Psychology)</subject><subject>Attention Deficit Disorder with Hyperactivity - drug therapy</subject><subject>Attention Deficit Disorder with Hyperactivity - psychology</subject><subject>Attention deficit hyperactivity disorder</subject><subject>Child</subject><subject>Children & youth</subject><subject>Clinical trials</subject><subject>Delayed-Action Preparations</subject><subject>Disorders of Excessive Somnolence - chemically induced</subject><subject>Disorders of Excessive Somnolence - drug therapy</subject><subject>Dosage and administration</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Drug Administration Schedule</subject><subject>Drug therapy</subject><subject>Evaluation</subject><subject>Fatigue - chemically induced</subject><subject>Fatigue - drug therapy</subject><subject>Female</subject><subject>Guanfacine</subject><subject>Guanfacine - administration & dosage</subject><subject>Guanfacine - adverse effects</subject><subject>Guanfacine - therapeutic use</subject><subject>Humans</subject><subject>Male</subject><subject>Patient outcomes</subject><subject>Placebos</subject><subject>Psychiatric Status Rating Scales</subject><subject>Psychomotor Performance - drug effects</subject><subject>Treatment Outcome</subject><issn>1044-5463</issn><issn>1557-8992</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkUtvEzEUhUcIREthyRZZdMFqUnv8nGVVUUCqBAtYW459nTia2MH2ANnx0_EoAQmEvPBD3z2-556ue0nwimA13lhzWA243TAW7FF3STiXvRrH4XE7Y8Z6zgS96J6VssOYUIHF0-5iIEyKkZLL7uencrTbtE81ZeTnaGtIMcQNMtEhM0GuEUpB30Pdos1sojc2REDwo0J04FCGCUwBFCIq83oHtp5hUxuxiPUOfLCh3myPB8imffAt1CNyoaTsID_vnngzFXhx3q-6L_dvP9-97x8-vvtwd_vQW6pE7QfvhHTNpwBhJTHS0xE3awrzUWLwkis-UKrYYNXaAh7BGIKpl7BuHFX0qntz0j3k9HWGUvU-FAvTZCKkuWglKCOKU9nI1_-QuzTn2Jpr0MBGJThr0PUJ2rQh6RB9qs3bIqlvB84bwiRu1Oo_VFsO9sGm2CbT3v8q6E8FNqdSMnh9yGFv8lETrJe8dctbL3nrJe_Gvzr3Oq_34P7QvwOmvwDc7abG</recordid><startdate>201104</startdate><enddate>201104</enddate><creator>Kollins, Scott H</creator><creator>López, Frank A</creator><creator>Vince, Bradley D</creator><creator>Turnbow, John M</creator><creator>Farrand, Kimberly</creator><creator>Lyne, Andrew</creator><creator>Wigal, Sharon B</creator><creator>Roth, Thomas</creator><general>Mary Ann Liebert, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7RV</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>201104</creationdate><title>Psychomotor functioning and alertness with guanfacine extended release in subjects with attention-deficit/hyperactivity disorder</title><author>Kollins, Scott H ; López, Frank A ; Vince, Bradley D ; Turnbow, John M ; Farrand, Kimberly ; Lyne, Andrew ; Wigal, Sharon B ; Roth, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-2fd67d0106e6c71a7f390546805970ef7585233842c8bce09eaa103f7eb905383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Adrenergic alpha-2 Receptor Agonists - administration & dosage</topic><topic>Adrenergic alpha-2 Receptor Agonists - adverse effects</topic><topic>Adrenergic alpha-2 Receptor Agonists - therapeutic use</topic><topic>Alertness (Psychology)</topic><topic>Attention Deficit Disorder with Hyperactivity - drug therapy</topic><topic>Attention Deficit Disorder with Hyperactivity - psychology</topic><topic>Attention deficit hyperactivity disorder</topic><topic>Child</topic><topic>Children & youth</topic><topic>Clinical trials</topic><topic>Delayed-Action Preparations</topic><topic>Disorders of Excessive Somnolence - chemically induced</topic><topic>Disorders of Excessive Somnolence - drug therapy</topic><topic>Dosage and administration</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>Drug Administration Schedule</topic><topic>Drug therapy</topic><topic>Evaluation</topic><topic>Fatigue - chemically induced</topic><topic>Fatigue - drug therapy</topic><topic>Female</topic><topic>Guanfacine</topic><topic>Guanfacine - administration & dosage</topic><topic>Guanfacine - adverse effects</topic><topic>Guanfacine - therapeutic use</topic><topic>Humans</topic><topic>Male</topic><topic>Patient outcomes</topic><topic>Placebos</topic><topic>Psychiatric Status Rating Scales</topic><topic>Psychomotor Performance - drug effects</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kollins, Scott H</creatorcontrib><creatorcontrib>López, Frank A</creatorcontrib><creatorcontrib>Vince, Bradley D</creatorcontrib><creatorcontrib>Turnbow, John M</creatorcontrib><creatorcontrib>Farrand, Kimberly</creatorcontrib><creatorcontrib>Lyne, Andrew</creatorcontrib><creatorcontrib>Wigal, Sharon B</creatorcontrib><creatorcontrib>Roth, Thomas</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of child and adolescent psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kollins, Scott H</au><au>López, Frank A</au><au>Vince, Bradley D</au><au>Turnbow, John M</au><au>Farrand, Kimberly</au><au>Lyne, Andrew</au><au>Wigal, Sharon B</au><au>Roth, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Psychomotor functioning and alertness with guanfacine extended release in subjects with attention-deficit/hyperactivity disorder</atitle><jtitle>Journal of child and adolescent psychopharmacology</jtitle><addtitle>J Child Adolesc Psychopharmacol</addtitle><date>2011-04</date><risdate>2011</risdate><volume>21</volume><issue>2</issue><spage>111</spage><epage>120</epage><pages>111-120</pages><issn>1044-5463</issn><eissn>1557-8992</eissn><abstract>To determine whether treatment with guanfacine extended release (GXR) in subjects with attention-deficit/hyperactivity disorder (ADHD) disrupted psychomotor functioning and alertness, or impacted daytime sleepiness.
This was a randomized, double-blind, placebo-controlled, multicenter, phase 2, dose-optimization, noninferiority, laboratory classroom study of GXR (1, 2, and 3 mg/day) in 182 subjects aged 6 to 17 years with ADHD. Psychomotor functioning and alertness were assessed through several measures, including the Choice Reaction Time (CRT) test from the Cambridge Neuropsychological Test Automated Battery. Sedative effects were examined via spontaneously reported adverse events of sedation, somnolence, and hypersomnia as well as fatigue and lethargy, and with two validated subject- and observer-rated sleepiness scales. Standard efficacy measures for ADHD also were included. Cardiovascular and laboratory parameters were assessed.
There were no significant differences between the GXR and placebo groups on measures of psychomotor functioning or alertness from the CRT at endpoint (least-square mean difference: 2.5 [95% confidence interval (CI): -22.9, 28.0], p = 0.8 for CRT; 2.5 [95% CI: -21.5, 26.4], p = 0.84 for correct responses; 15.5 [95% CI: -45.1, 14.1], p = 0.30 for movement time; and -8.2 [95% CI: -54.1, 37.6] p = 0.72 for total time). Most sedative adverse events were mild to moderate, occurred during dose titration, decreased with dose maintenance, and resolved during the study period. One subject in the GXR group discontinued due to fatigue and somnolence. GXR was not associated with increased daytime sleepiness. GXR treatment was associated with significant improvement in ADHD symptoms (6.3 [95% CI: 2.7, 9.8], p = 0.001 for ADHD Rating Scale IV total scores at endpoint).
At doses that resulted in significant improvement in ADHD symptoms, impairment on cognitive tasks was not observed. Daytime sleepiness did not differ with GXR compared with placebo. Results suggest that the beneficial effects of GXR on ADHD symptoms are independent of sedation.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>21476931</pmid><doi>10.1089/cap.2010.0064</doi><tpages>10</tpages></addata></record> |
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subjects | Adolescent Adrenergic alpha-2 Receptor Agonists - administration & dosage Adrenergic alpha-2 Receptor Agonists - adverse effects Adrenergic alpha-2 Receptor Agonists - therapeutic use Alertness (Psychology) Attention Deficit Disorder with Hyperactivity - drug therapy Attention Deficit Disorder with Hyperactivity - psychology Attention deficit hyperactivity disorder Child Children & youth Clinical trials Delayed-Action Preparations Disorders of Excessive Somnolence - chemically induced Disorders of Excessive Somnolence - drug therapy Dosage and administration Dose-Response Relationship, Drug Double-Blind Method Drug Administration Schedule Drug therapy Evaluation Fatigue - chemically induced Fatigue - drug therapy Female Guanfacine Guanfacine - administration & dosage Guanfacine - adverse effects Guanfacine - therapeutic use Humans Male Patient outcomes Placebos Psychiatric Status Rating Scales Psychomotor Performance - drug effects Treatment Outcome |
title | Psychomotor functioning and alertness with guanfacine extended release in subjects with attention-deficit/hyperactivity disorder |
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