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Prescriber preference for a particular tumour necrosis factor antagonist drug and treatment discontinuation: population-based cohort

OBJECTIVE: To assess the effect of physician preference for a particular tumour necrosis factor α (TNF) antagonist on the risk of treatment discontinuation in rheumatoid arthritis. DESIGN: Population-based cohort study. SETTING: British Columbia administrative health data (inpatients, outpatients an...

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Autores principales: Fisher, Anat, Bassett, Ken, Wright, James M, Brookhart, M Alan, Freeman, Hugh J, Dormuth, Colin R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4179420/
https://www.ncbi.nlm.nih.gov/pubmed/25270855
http://dx.doi.org/10.1136/bmjopen-2014-005532
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author Fisher, Anat
Bassett, Ken
Wright, James M
Brookhart, M Alan
Freeman, Hugh J
Dormuth, Colin R
author_facet Fisher, Anat
Bassett, Ken
Wright, James M
Brookhart, M Alan
Freeman, Hugh J
Dormuth, Colin R
author_sort Fisher, Anat
collection PubMed
description OBJECTIVE: To assess the effect of physician preference for a particular tumour necrosis factor α (TNF) antagonist on the risk of treatment discontinuation in rheumatoid arthritis. DESIGN: Population-based cohort study. SETTING: British Columbia administrative health data (inpatients, outpatients and pharmacy). PARTICIPANTS: 2742 British Columbia residents who initiated a first course of a TNF antagonist between 2001 and December 2008, had been diagnosed with rheumatoid arthritis, and were treated by 1 of 58 medium-volume to high-volume prescribers. INDEPENDENT VARIABLE: A level of physician preference for the drug (higher or lower) was assigned based on preceding prescribing records of the care-providing physician. Higher preference was defined as at least 60% of TNF antagonist courses initiated in the preceding year. Sensitivity analysis was conducted with different thresholds for higher preference. MAIN OUTCOME MEASURE: Drug discontinuation was defined as a drug-free interval of 180 days or switching to another TNF antagonist, anakinra, rituximab or abatacept. The risk of discontinuation was compared between different levels of physician preference using survival analysis. RESULTS: Higher preference for the prescribed TNF antagonist was associated with improved persistence with the drug (4.28 years (95% CI 3.70 to 4.90) vs 3.27 (2.84 to 3.84), with log rank test p value of 0.017). The adjusted HR for discontinuation was significantly lower in courses of drugs with higher preference (0.85 (0.76 to 0.96)). The results were robust in a sensitivity analysis. CONCLUSIONS: Higher physician preference was associated with decreased risk of discontinuing TNF antagonists in patients with rheumatoid arthritis. This finding suggests that physicians who strongly prefer a specific treatment help their patients to stay on treatment for a longer duration. Similar research on other treatments is warranted.
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spelling pubmed-41794202014-10-02 Prescriber preference for a particular tumour necrosis factor antagonist drug and treatment discontinuation: population-based cohort Fisher, Anat Bassett, Ken Wright, James M Brookhart, M Alan Freeman, Hugh J Dormuth, Colin R BMJ Open Epidemiology OBJECTIVE: To assess the effect of physician preference for a particular tumour necrosis factor α (TNF) antagonist on the risk of treatment discontinuation in rheumatoid arthritis. DESIGN: Population-based cohort study. SETTING: British Columbia administrative health data (inpatients, outpatients and pharmacy). PARTICIPANTS: 2742 British Columbia residents who initiated a first course of a TNF antagonist between 2001 and December 2008, had been diagnosed with rheumatoid arthritis, and were treated by 1 of 58 medium-volume to high-volume prescribers. INDEPENDENT VARIABLE: A level of physician preference for the drug (higher or lower) was assigned based on preceding prescribing records of the care-providing physician. Higher preference was defined as at least 60% of TNF antagonist courses initiated in the preceding year. Sensitivity analysis was conducted with different thresholds for higher preference. MAIN OUTCOME MEASURE: Drug discontinuation was defined as a drug-free interval of 180 days or switching to another TNF antagonist, anakinra, rituximab or abatacept. The risk of discontinuation was compared between different levels of physician preference using survival analysis. RESULTS: Higher preference for the prescribed TNF antagonist was associated with improved persistence with the drug (4.28 years (95% CI 3.70 to 4.90) vs 3.27 (2.84 to 3.84), with log rank test p value of 0.017). The adjusted HR for discontinuation was significantly lower in courses of drugs with higher preference (0.85 (0.76 to 0.96)). The results were robust in a sensitivity analysis. CONCLUSIONS: Higher physician preference was associated with decreased risk of discontinuing TNF antagonists in patients with rheumatoid arthritis. This finding suggests that physicians who strongly prefer a specific treatment help their patients to stay on treatment for a longer duration. Similar research on other treatments is warranted. BMJ Publishing Group 2014-09-30 /pmc/articles/PMC4179420/ /pubmed/25270855 http://dx.doi.org/10.1136/bmjopen-2014-005532 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Epidemiology
Fisher, Anat
Bassett, Ken
Wright, James M
Brookhart, M Alan
Freeman, Hugh J
Dormuth, Colin R
Prescriber preference for a particular tumour necrosis factor antagonist drug and treatment discontinuation: population-based cohort
title Prescriber preference for a particular tumour necrosis factor antagonist drug and treatment discontinuation: population-based cohort
title_full Prescriber preference for a particular tumour necrosis factor antagonist drug and treatment discontinuation: population-based cohort
title_fullStr Prescriber preference for a particular tumour necrosis factor antagonist drug and treatment discontinuation: population-based cohort
title_full_unstemmed Prescriber preference for a particular tumour necrosis factor antagonist drug and treatment discontinuation: population-based cohort
title_short Prescriber preference for a particular tumour necrosis factor antagonist drug and treatment discontinuation: population-based cohort
title_sort prescriber preference for a particular tumour necrosis factor antagonist drug and treatment discontinuation: population-based cohort
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4179420/
https://www.ncbi.nlm.nih.gov/pubmed/25270855
http://dx.doi.org/10.1136/bmjopen-2014-005532
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