Defining the minimal clinically important difference (MCID) of the Heinrichs-carpenter quality of life scale (QLS)
To determine the Minimal Clinically Important Difference (MCID) of the Heinrichs–Carpenter Quality of Life Scale (QLS). Data from the “Schizophrenia Trial of Aripiprazole” (STAR) study were used in this analysis. The MCID value of the QLS total score was estimated using the anchor‐based method. Thes...
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Published in | International journal of methods in psychiatric research Vol. 25; no. 2; pp. 101 - 111 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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United States
Blackwell Publishing Ltd
01.06.2016
John Wiley & Sons, Inc John Wiley and Sons Inc |
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Abstract | To determine the Minimal Clinically Important Difference (MCID) of the Heinrichs–Carpenter Quality of Life Scale (QLS). Data from the “Schizophrenia Trial of Aripiprazole” (STAR) study were used in this analysis. The MCID value of the QLS total score was estimated using the anchor‐based method. These findings were substantiated/validated by comparing the MCID estimate to other measurements collected in the study. Half of the patients (49%) showed improvement in Clinical Global Impressions of Severity (CGI‐S) during the trial. The estimated MCID of the QLS total score was 5.30 (standard error: 2.60; 95% confidence interval: [0.16; 10.43]; p < 0.05). Patients were divided into two groups: “QLS improvers” (QLS total score increased ≥ six points) and “non‐improvers”. The QLS improvers had significantly better effectiveness and reported significantly higher levels of preference for their current medications. There was a statistically significant difference between the two groups in the change in two of the four domains of QLS; “Interpersonal relations” and “Intrapsychic foundations” domains during the study. These findings support the value of the estimated MCID for the QLS and may be a useful tool in evaluating antipsychotic treatment effects and improving long‐term patient outcomes in schizophrenia. Copyright © 2015 John Wiley & Sons, Ltd. |
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AbstractList | To determine the Minimal Clinically Important Difference (MCID) of the Heinrichs-Carpenter Quality of Life Scale (QLS). Data from the "Schizophrenia Trial of Aripiprazole" (STAR) study were used in this analysis. The MCID value of the QLS total score was estimated using the anchor-based method. These findings were substantiated/validated by comparing the MCID estimate to other measurements collected in the study. Half of the patients (49%) showed improvement in Clinical Global Impressions of Severity (CGI-S) during the trial. The estimated MCID of the QLS total score was 5.30 (standard error: 2.60; 95% confidence interval: [0.16; 10.43]; p < 0.05). Patients were divided into two groups: "QLS improvers" (QLS total score increased ≥ six points) and "non-improvers". The QLS improvers had significantly better effectiveness and reported significantly higher levels of preference for their current medications. There was a statistically significant difference between the two groups in the change in two of the four domains of QLS; "Interpersonal relations" and "Intrapsychic foundations" domains during the study. These findings support the value of the estimated MCID for the QLS and may be a useful tool in evaluating antipsychotic treatment effects and improving long-term patient outcomes in schizophrenia. Copyright © 2015 John Wiley & Sons, Ltd. To determine the Minimal Clinically Important Difference (MCID) of the Heinrichs-Carpenter Quality of Life Scale (QLS). Data from the "Schizophrenia Trial of Aripiprazole" (STAR) study were used in this analysis. The MCID value of the QLS total score was estimated using the anchor-based method. These findings were substantiated/validated by comparing the MCID estimate to other measurements collected in the study. Half of the patients (49%) showed improvement in Clinical Global Impressions of Severity (CGI-S) during the trial. The estimated MCID of the QLS total score was 5.30 (standard error: 2.60; 95% confidence interval: [0.16; 10.43]; p < 0.05). Patients were divided into two groups: "QLS improvers" (QLS total score increased greater than or equal to six points) and "non-improvers". The QLS improvers had significantly better effectiveness and reported significantly higher levels of preference for their current medications. There was a statistically significant difference between the two groups in the change in two of the four domains of QLS; "Interpersonal relations" and "Intrapsychic foundations" domains during the study. These findings support the value of the estimated MCID for the QLS and may be a useful tool in evaluating antipsychotic treatment effects and improving long-term patient outcomes in schizophrenia. To determine the Minimal Clinically Important Difference (MCID) of the Heinrichs–Carpenter Quality of Life Scale (QLS). Data from the “Schizophrenia Trial of Aripiprazole” (STAR) study were used in this analysis. The MCID value of the QLS total score was estimated using the anchor‐based method. These findings were substantiated/validated by comparing the MCID estimate to other measurements collected in the study. Half of the patients (49%) showed improvement in Clinical Global Impressions of Severity (CGI‐S) during the trial. The estimated MCID of the QLS total score was 5.30 (standard error: 2.60; 95% confidence interval: [0.16; 10.43]; p < 0.05). Patients were divided into two groups: “QLS improvers” (QLS total score increased ≥ six points) and “non‐improvers”. The QLS improvers had significantly better effectiveness and reported significantly higher levels of preference for their current medications. There was a statistically significant difference between the two groups in the change in two of the four domains of QLS; “Interpersonal relations” and “Intrapsychic foundations” domains during the study. These findings support the value of the estimated MCID for the QLS and may be a useful tool in evaluating antipsychotic treatment effects and improving long‐term patient outcomes in schizophrenia. Copyright © 2015 John Wiley & Sons, Ltd. |
Author | Hansen, Karina Loze, Jean-Yves Sapin, Christophe Falissard, Bruno Landsberg, Wally |
AuthorAffiliation | 4 Otsuka Pharmaceutical Europe Ltd London UK 1 INSERM U669 Université Paris‐Sud and Université Paris‐Descartes, APHP Paris France 2 Global Analytics Lundbeck SAS Issy‐les‐Moulineaux France 5 Global Health Economics and Epidemiology Lundbeck SAS Issy‐les‐Moulineaux France 3 Otsuka Pharmaceutical Europe Ltd Paris France |
AuthorAffiliation_xml | – name: 1 INSERM U669 Université Paris‐Sud and Université Paris‐Descartes, APHP Paris France – name: 5 Global Health Economics and Epidemiology Lundbeck SAS Issy‐les‐Moulineaux France – name: 3 Otsuka Pharmaceutical Europe Ltd Paris France – name: 2 Global Analytics Lundbeck SAS Issy‐les‐Moulineaux France – name: 4 Otsuka Pharmaceutical Europe Ltd London UK |
Author_xml | – sequence: 1 givenname: Bruno surname: Falissard fullname: Falissard, Bruno email: bruno.falissard@gmail.com organization: INSERM U669, Université Paris-Sud and Université Paris-Descartes, APHP, Paris, France – sequence: 2 givenname: Christophe surname: Sapin fullname: Sapin, Christophe organization: Global Analytics, Lundbeck SAS, Issy-les-Moulineaux, France – sequence: 3 givenname: Jean-Yves surname: Loze fullname: Loze, Jean-Yves organization: Otsuka Pharmaceutical Europe Ltd, Paris, France – sequence: 4 givenname: Wally surname: Landsberg fullname: Landsberg, Wally organization: Otsuka Pharmaceutical Europe Ltd, London, UK – sequence: 5 givenname: Karina surname: Hansen fullname: Hansen, Karina organization: Lundbeck SAS, Global Health Economics and Epidemiology, Issy-les-Moulineaux, France |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26238598$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s12325_017_0507_x crossref_primary_10_1371_journal_pone_0183475 crossref_primary_10_1097_YIC_0000000000000177 crossref_primary_10_1038_s41598_022_16130_5 crossref_primary_10_1016_j_jpsychires_2023_02_008 crossref_primary_10_1017_S2045796020000566 crossref_primary_10_3389_fpsyt_2022_951376 crossref_primary_10_1016_j_amjsurg_2021_06_018 crossref_primary_10_1016_j_schres_2017_04_013 crossref_primary_10_1016_j_eurpsy_2015_11_007 crossref_primary_10_1016_S0013_7006_17_30052_0 crossref_primary_10_1093_schbul_sbac053 crossref_primary_10_3389_fpsyt_2022_816339 crossref_primary_10_1016_j_cct_2020_105965 crossref_primary_10_1080_03007995_2023_2287612 crossref_primary_10_1371_journal_pone_0290290 |
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Copyright | Copyright © 2015 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd. |
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Snippet | To determine the Minimal Clinically Important Difference (MCID) of the Heinrichs–Carpenter Quality of Life Scale (QLS). Data from the “Schizophrenia Trial of... To determine the Minimal Clinically Important Difference (MCID) of the Heinrichs-Carpenter Quality of Life Scale (QLS). Data from the "Schizophrenia Trial of... |
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SubjectTerms | Adult Antipsychotic Agents - pharmacology Aripiprazole - pharmacology Confidence intervals Female Humans Male Middle Aged Minimal Clinically Important Difference Original Psychiatric Status Rating Scales Quality of Life Quality of Life Scale Schizophrenia Schizophrenia - drug therapy |
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Title | Defining the minimal clinically important difference (MCID) of the Heinrichs-carpenter quality of life scale (QLS) |
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