Methods for constructing treatment episodes and impact on exposure-outcome associations.


Journal

European journal of clinical pharmacology
ISSN: 1432-1041
Titre abrégé: Eur J Clin Pharmacol
Pays: Germany
ID NLM: 1256165

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 22 03 2019
accepted: 10 10 2019
pubmed: 24 11 2019
medline: 2 10 2020
entrez: 24 11 2019
Statut: ppublish

Résumé

To assess the impact on exposure time and outcome misclassifications, and consequent impact on exposure-outcome associations from treatment episode construction. We investigated the dosage assumptions of 1 unit per day, and 1 DDD per day, versus actual prescribed dosage under different handling of gaps and overlaps of prescriptions. Data on mirtazapine and citalopram exposure (years 2006-2014) from the Swedish Prescribed Drug register were used. Via a within individuals design we compared method A, based on actual dosage, with methods B and C based on 1 unit of drug per day and 1 DDD per day assumptions, respectively, including consideration of gaps and overlaps. Four outcomes were used, hospitalizations and outpatient visits for all and for psychiatric causes. Relative to method A, both alternative methods lead to misclassification of exposure time. With regard to outcome misclassifications, method B overestimates the effect of the exposure on the outcome in 77% and 100% of exposure definition comparisons for mirtazapine and citalopram respectively, while 23% of the comparisons for mirtazapine results in underestimation of exposure-outcome associations. Conversely, treatment episodes based on DDD (method C) result in underestimation of the exposure-outcome association in 100% and 87.5% of exposure definition comparisons for mirtazapine and citalopram respectively, while 12.5% of the comparisons for citalopram results in overestimation of the exposure-outcome associations. The study provides results that have consistent clinical relevance. We have showed that a non-accurate construction of exposure time may lead to errors on outcome detection during exposed time, and consequently affect conclusions on safety or efficacy profile of a treatment.

Identifiants

pubmed: 31758215
doi: 10.1007/s00228-019-02780-4
pii: 10.1007/s00228-019-02780-4
doi:

Substances chimiques

Antidepressive Agents 0
Citalopram 0DHU5B8D6V
Mirtazapine A051Q2099Q

Types de publication

Comparative Study Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

267-275

Subventions

Organisme : public-private real world evidence collaboration between Karolinska Institutet and Janssen Pharmaceuticals
ID : 5-63/2015
Organisme : Novo Nordisk Foundation
ID : NNF15SA0018404

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Auteurs

Laura Pazzagli (L)

Centre for Pharmacoepidemiology, Department of Medicine Solna, Karolinska Institutet, S-171 76, Stockholm, Sweden. laura.pazzagli@ki.se.

Lena Brandt (L)

Centre for Pharmacoepidemiology, Department of Medicine Solna, Karolinska Institutet, S-171 76, Stockholm, Sweden.

Marie Linder (M)

Centre for Pharmacoepidemiology, Department of Medicine Solna, Karolinska Institutet, S-171 76, Stockholm, Sweden.

David Myers (D)

The Janssen Pharmaceutical Companies of Johnson & Johnson, Janssen Cilag AB, Stockholm, Sweden.

Panagiotis Mavros (P)

Janssen Scientific Affairs, Titusville, NJ, USA.

Morten Andersen (M)

Centre for Pharmacoepidemiology, Department of Medicine Solna, Karolinska Institutet, S-171 76, Stockholm, Sweden.
Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.

Shahram Bahmanyar (S)

Centre for Pharmacoepidemiology, Department of Medicine Solna, Karolinska Institutet, S-171 76, Stockholm, Sweden.
The Center for Psychiatry Research, Karolinska Institutet, Stockholm, Sweden.

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Classifications MeSH