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Clinical Trials Increase Off-Study Drug Use: A Segmented Time-Series Analysis
BACKGROUND: The effect of participation in a clinical trial on concomitant off-study investigational drug use has not been described. We sought to determine if participation in the Daptomycin as Adjunctive Therapy for Staphylococcus aureus bacteremia (DASH) trial increased overall daptomycin prescri...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7651655/ https://www.ncbi.nlm.nih.gov/pubmed/33209948 http://dx.doi.org/10.1093/ofid/ofaa449 |
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author | Butler-Laporte, Guillaume Cheng, Matthew P Thirion, Daniel J G De L’Étoile-Morel, Samuel Frenette, Charles Paquette, Katryn Lawandi, Alexander McDonald, Emily G Lee, Todd C |
author_facet | Butler-Laporte, Guillaume Cheng, Matthew P Thirion, Daniel J G De L’Étoile-Morel, Samuel Frenette, Charles Paquette, Katryn Lawandi, Alexander McDonald, Emily G Lee, Todd C |
author_sort | Butler-Laporte, Guillaume |
collection | PubMed |
description | BACKGROUND: The effect of participation in a clinical trial on concomitant off-study investigational drug use has not been described. We sought to determine if participation in the Daptomycin as Adjunctive Therapy for Staphylococcus aureus bacteremia (DASH) trial increased overall daptomycin prescribing at study sites. METHODS: We retrospectively analyzed daptomycin use for 8 years preceding the trial, off-study daptomycin use during the trial itself (31 months), and daptomycin use for 6 fiscal months after trial completion. We used a segmented linear regression analysis of an interrupted time series to analyze changes in each drug’s defined daily doses (DDD) per 1000 patient-days. As a control, we analyzed use of linezolid over these periods and also accounted for rates of methicillin-resistant S. aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) infections. RESULTS: For 1.5 years before the DASH trial, daptomycin use was decreasing by –0.30 DDD per 1000 patient-days per fiscal period (95% CI, –0.52 to –0.07). Following the initiation of the study, there was a statistically significant increase in daptomycin use of 0.28 DDD per 1000 patient-days per fiscal period (95% CI, 0.03 to 0.52), despite low, stable rates of MRSA and VRE infections. Following trial completion, daptomycin use decreased back toward prestudy rates. Use of linezolid remained stable throughout. CONCLUSIONS: Despite the DASH trial being a negative study, it impacted the prescribing habits of local clinicians during recruitment. Trialists should be aware of potential off-target study effects, and prescribers should be wary of early uptake of interventions before definitive study results. |
format | Online Article Text |
id | pubmed-7651655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76516552020-11-17 Clinical Trials Increase Off-Study Drug Use: A Segmented Time-Series Analysis Butler-Laporte, Guillaume Cheng, Matthew P Thirion, Daniel J G De L’Étoile-Morel, Samuel Frenette, Charles Paquette, Katryn Lawandi, Alexander McDonald, Emily G Lee, Todd C Open Forum Infect Dis Major Articles BACKGROUND: The effect of participation in a clinical trial on concomitant off-study investigational drug use has not been described. We sought to determine if participation in the Daptomycin as Adjunctive Therapy for Staphylococcus aureus bacteremia (DASH) trial increased overall daptomycin prescribing at study sites. METHODS: We retrospectively analyzed daptomycin use for 8 years preceding the trial, off-study daptomycin use during the trial itself (31 months), and daptomycin use for 6 fiscal months after trial completion. We used a segmented linear regression analysis of an interrupted time series to analyze changes in each drug’s defined daily doses (DDD) per 1000 patient-days. As a control, we analyzed use of linezolid over these periods and also accounted for rates of methicillin-resistant S. aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) infections. RESULTS: For 1.5 years before the DASH trial, daptomycin use was decreasing by –0.30 DDD per 1000 patient-days per fiscal period (95% CI, –0.52 to –0.07). Following the initiation of the study, there was a statistically significant increase in daptomycin use of 0.28 DDD per 1000 patient-days per fiscal period (95% CI, 0.03 to 0.52), despite low, stable rates of MRSA and VRE infections. Following trial completion, daptomycin use decreased back toward prestudy rates. Use of linezolid remained stable throughout. CONCLUSIONS: Despite the DASH trial being a negative study, it impacted the prescribing habits of local clinicians during recruitment. Trialists should be aware of potential off-target study effects, and prescribers should be wary of early uptake of interventions before definitive study results. Oxford University Press 2020-09-24 /pmc/articles/PMC7651655/ /pubmed/33209948 http://dx.doi.org/10.1093/ofid/ofaa449 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Major Articles Butler-Laporte, Guillaume Cheng, Matthew P Thirion, Daniel J G De L’Étoile-Morel, Samuel Frenette, Charles Paquette, Katryn Lawandi, Alexander McDonald, Emily G Lee, Todd C Clinical Trials Increase Off-Study Drug Use: A Segmented Time-Series Analysis |
title | Clinical Trials Increase Off-Study Drug Use: A Segmented Time-Series Analysis |
title_full | Clinical Trials Increase Off-Study Drug Use: A Segmented Time-Series Analysis |
title_fullStr | Clinical Trials Increase Off-Study Drug Use: A Segmented Time-Series Analysis |
title_full_unstemmed | Clinical Trials Increase Off-Study Drug Use: A Segmented Time-Series Analysis |
title_short | Clinical Trials Increase Off-Study Drug Use: A Segmented Time-Series Analysis |
title_sort | clinical trials increase off-study drug use: a segmented time-series analysis |
topic | Major Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7651655/ https://www.ncbi.nlm.nih.gov/pubmed/33209948 http://dx.doi.org/10.1093/ofid/ofaa449 |
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