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Accurately identifying patients who are excellent candidates or unsuitable for a medication: a novel approach
OBJECTIVE: The objective of the study was to determine whether a unique analytic approach – as a proof of concept – could identify individual depressed outpatients (using 30 baseline clinical and demographic variables) who are very likely (75% certain) to not benefit (NB) or to remit (R), accepting...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735989/ https://www.ncbi.nlm.nih.gov/pubmed/29290685 http://dx.doi.org/10.2147/NDT.S139577 |
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author | South, Charles Rush, A John Carmody, Thomas J Jha, Manish K Trivedi, Madhukar H |
author_facet | South, Charles Rush, A John Carmody, Thomas J Jha, Manish K Trivedi, Madhukar H |
author_sort | South, Charles |
collection | PubMed |
description | OBJECTIVE: The objective of the study was to determine whether a unique analytic approach – as a proof of concept – could identify individual depressed outpatients (using 30 baseline clinical and demographic variables) who are very likely (75% certain) to not benefit (NB) or to remit (R), accepting that without sufficient certainty, no prediction (NP) would be made. METHODS: Patients from the Combining Medications to Enhance Depression Outcomes trial treated with escitalopram (S-CIT) + placebo (n=212) or S-CIT + bupropion-SR (n=206) were analyzed separately to assess replicability. For each treatment, the elastic net was used to identify subsets of predictive baseline measures for R and NB, separately. Two different equations that estimate the likelihood of remission and no benefit were developed for each patient. The ratio of these two numbers characterized likely outcomes for each patient. RESULTS: The two treatment cells had comparable rates of remission (40%) and no benefit (22%). In S-CIT + bupropion-SR, 11 were predicted NB of which 82% were correct; 26 were predicted R – 85% correct (169 had NP). For S-CIT + placebo, 13 were predicted NB – 69% correct; 44 were predicted R – 75% correct (155 were NP). Overall, 94/418 (22%) patients were identified with a meaningful degree of certainty (69%–85% correct). Different variable sets with some overlap were predictive of remission and no benefit within and across treatments, despite comparable outcomes. CONCLUSION: In two separate analyses with two different treatments, this analytic approach – which is also applicable to pretreatment laboratory tests – identified a meaningful proportion (over 20%) of depressed patients for whom a treatment outcome was predicted with sufficient certainty that the clinician can elect to strongly recommend for or choose to avoid a particular treatment. Different persons seem to be remitting or not benefiting with these two different treatments. |
format | Online Article Text |
id | pubmed-5735989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57359892017-12-29 Accurately identifying patients who are excellent candidates or unsuitable for a medication: a novel approach South, Charles Rush, A John Carmody, Thomas J Jha, Manish K Trivedi, Madhukar H Neuropsychiatr Dis Treat Original Research OBJECTIVE: The objective of the study was to determine whether a unique analytic approach – as a proof of concept – could identify individual depressed outpatients (using 30 baseline clinical and demographic variables) who are very likely (75% certain) to not benefit (NB) or to remit (R), accepting that without sufficient certainty, no prediction (NP) would be made. METHODS: Patients from the Combining Medications to Enhance Depression Outcomes trial treated with escitalopram (S-CIT) + placebo (n=212) or S-CIT + bupropion-SR (n=206) were analyzed separately to assess replicability. For each treatment, the elastic net was used to identify subsets of predictive baseline measures for R and NB, separately. Two different equations that estimate the likelihood of remission and no benefit were developed for each patient. The ratio of these two numbers characterized likely outcomes for each patient. RESULTS: The two treatment cells had comparable rates of remission (40%) and no benefit (22%). In S-CIT + bupropion-SR, 11 were predicted NB of which 82% were correct; 26 were predicted R – 85% correct (169 had NP). For S-CIT + placebo, 13 were predicted NB – 69% correct; 44 were predicted R – 75% correct (155 were NP). Overall, 94/418 (22%) patients were identified with a meaningful degree of certainty (69%–85% correct). Different variable sets with some overlap were predictive of remission and no benefit within and across treatments, despite comparable outcomes. CONCLUSION: In two separate analyses with two different treatments, this analytic approach – which is also applicable to pretreatment laboratory tests – identified a meaningful proportion (over 20%) of depressed patients for whom a treatment outcome was predicted with sufficient certainty that the clinician can elect to strongly recommend for or choose to avoid a particular treatment. Different persons seem to be remitting or not benefiting with these two different treatments. Dove Medical Press 2017-12-15 /pmc/articles/PMC5735989/ /pubmed/29290685 http://dx.doi.org/10.2147/NDT.S139577 Text en © 2017 South et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research South, Charles Rush, A John Carmody, Thomas J Jha, Manish K Trivedi, Madhukar H Accurately identifying patients who are excellent candidates or unsuitable for a medication: a novel approach |
title | Accurately identifying patients who are excellent candidates or unsuitable for a medication: a novel approach |
title_full | Accurately identifying patients who are excellent candidates or unsuitable for a medication: a novel approach |
title_fullStr | Accurately identifying patients who are excellent candidates or unsuitable for a medication: a novel approach |
title_full_unstemmed | Accurately identifying patients who are excellent candidates or unsuitable for a medication: a novel approach |
title_short | Accurately identifying patients who are excellent candidates or unsuitable for a medication: a novel approach |
title_sort | accurately identifying patients who are excellent candidates or unsuitable for a medication: a novel approach |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735989/ https://www.ncbi.nlm.nih.gov/pubmed/29290685 http://dx.doi.org/10.2147/NDT.S139577 |
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