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Abnormal involuntary movement scale in tardive dyskinesia: Minimal clinically important difference

BACKGROUND: A minimal clinically important difference has not been established for the Abnormal Involuntary Movement Scale in patients with tardive dyskinesia. Valbenazine is a vesicular monoamine transporter 2 inhibitor approved for the treatment of tardive dyskinesia in adults. Efficacy in randomi...

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Autores principales: Stacy, Mark, Sajatovic, Martha, Kane, John M., Cutler, Andrew J., Liang, Grace S., O'Brien, Christopher F., Correll, Christoph U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6772010/
https://www.ncbi.nlm.nih.gov/pubmed/31234240
http://dx.doi.org/10.1002/mds.27769
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author Stacy, Mark
Sajatovic, Martha
Kane, John M.
Cutler, Andrew J.
Liang, Grace S.
O'Brien, Christopher F.
Correll, Christoph U.
author_facet Stacy, Mark
Sajatovic, Martha
Kane, John M.
Cutler, Andrew J.
Liang, Grace S.
O'Brien, Christopher F.
Correll, Christoph U.
author_sort Stacy, Mark
collection PubMed
description BACKGROUND: A minimal clinically important difference has not been established for the Abnormal Involuntary Movement Scale in patients with tardive dyskinesia. Valbenazine is a vesicular monoamine transporter 2 inhibitor approved for the treatment of tardive dyskinesia in adults. Efficacy in randomized, double‐blind, placebo‐controlled trials was defined as the change from baseline in Abnormal Involuntary Movement Scale total score (sum of items 1‐7). OBJECTIVES: To estimate an minimal clinically important difference for the Abnormal Involuntary Movement Scale using valbenazine trial data and an anchor‐based method. METHODS: Data were pooled from three 6‐week double‐blind, placebo‐controlled trials: KINECT (NCT01688037), KINECT 2 (NCT01733121), and KINECT 3 (NCT02274558). Valbenazine doses were pooled for analyses as follows: “low dose,” which includes 40 or 50 mg/day; and “high dose,” which includes 75 or 80 mg/day. Mean changes from baseline in Abnormal Involuntary Movement Scale total score were analyzed in all participants (valbenazine‐ and placebo‐treated) with a Clinical Global Impression of Change‐Tardive Dyskinesia or Patient Global Impression of Change score of 1 (very much improved) to 3 (minimally improved). RESULTS: The least squares mean improvement from baseline to week 6 in Abnormal Involuntary Movement Scale total score was significantly greater with valbenazine (low dose: –2.4; high dose: –3.2; both, P < 0.001) versus placebo (–0.7). An minimal clinically important difference of 2 points was estimated based on least squares mean changes in Abnormal Involuntary Movement Scale total score in participants with a Clinical Global Impression of Change‐Tardive Dyskinesia score ≤3 at week 6 (mean change: –2.2; median change: –2) or Patient Global Impression of Change score ≤3 at week 6 (mean change: –2.0; median change: –2). CONCLUSIONS: Results from an anchor‐based method indicate that a 2‐point decrease in Abnormal Involuntary Movement Scale total score may be considered clinically important. © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
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spelling pubmed-67720102019-10-07 Abnormal involuntary movement scale in tardive dyskinesia: Minimal clinically important difference Stacy, Mark Sajatovic, Martha Kane, John M. Cutler, Andrew J. Liang, Grace S. O'Brien, Christopher F. Correll, Christoph U. Mov Disord Research Articles BACKGROUND: A minimal clinically important difference has not been established for the Abnormal Involuntary Movement Scale in patients with tardive dyskinesia. Valbenazine is a vesicular monoamine transporter 2 inhibitor approved for the treatment of tardive dyskinesia in adults. Efficacy in randomized, double‐blind, placebo‐controlled trials was defined as the change from baseline in Abnormal Involuntary Movement Scale total score (sum of items 1‐7). OBJECTIVES: To estimate an minimal clinically important difference for the Abnormal Involuntary Movement Scale using valbenazine trial data and an anchor‐based method. METHODS: Data were pooled from three 6‐week double‐blind, placebo‐controlled trials: KINECT (NCT01688037), KINECT 2 (NCT01733121), and KINECT 3 (NCT02274558). Valbenazine doses were pooled for analyses as follows: “low dose,” which includes 40 or 50 mg/day; and “high dose,” which includes 75 or 80 mg/day. Mean changes from baseline in Abnormal Involuntary Movement Scale total score were analyzed in all participants (valbenazine‐ and placebo‐treated) with a Clinical Global Impression of Change‐Tardive Dyskinesia or Patient Global Impression of Change score of 1 (very much improved) to 3 (minimally improved). RESULTS: The least squares mean improvement from baseline to week 6 in Abnormal Involuntary Movement Scale total score was significantly greater with valbenazine (low dose: –2.4; high dose: –3.2; both, P < 0.001) versus placebo (–0.7). An minimal clinically important difference of 2 points was estimated based on least squares mean changes in Abnormal Involuntary Movement Scale total score in participants with a Clinical Global Impression of Change‐Tardive Dyskinesia score ≤3 at week 6 (mean change: –2.2; median change: –2) or Patient Global Impression of Change score ≤3 at week 6 (mean change: –2.0; median change: –2). CONCLUSIONS: Results from an anchor‐based method indicate that a 2‐point decrease in Abnormal Involuntary Movement Scale total score may be considered clinically important. © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. John Wiley & Sons, Inc. 2019-06-24 2019-08 /pmc/articles/PMC6772010/ /pubmed/31234240 http://dx.doi.org/10.1002/mds.27769 Text en © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Stacy, Mark
Sajatovic, Martha
Kane, John M.
Cutler, Andrew J.
Liang, Grace S.
O'Brien, Christopher F.
Correll, Christoph U.
Abnormal involuntary movement scale in tardive dyskinesia: Minimal clinically important difference
title Abnormal involuntary movement scale in tardive dyskinesia: Minimal clinically important difference
title_full Abnormal involuntary movement scale in tardive dyskinesia: Minimal clinically important difference
title_fullStr Abnormal involuntary movement scale in tardive dyskinesia: Minimal clinically important difference
title_full_unstemmed Abnormal involuntary movement scale in tardive dyskinesia: Minimal clinically important difference
title_short Abnormal involuntary movement scale in tardive dyskinesia: Minimal clinically important difference
title_sort abnormal involuntary movement scale in tardive dyskinesia: minimal clinically important difference
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6772010/
https://www.ncbi.nlm.nih.gov/pubmed/31234240
http://dx.doi.org/10.1002/mds.27769
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