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The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study
BACKGROUND: Sequence symmetry analysis (SSA) is a potential tool for rapid detection of adverse drug events (ADRs) associated with newly marketed medicines utilizing computerized claims data. SSA is robust to patient specific confounders but it is sensitive to the underlying utilization trends in th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4035856/ https://www.ncbi.nlm.nih.gov/pubmed/24886247 http://dx.doi.org/10.1186/1471-2288-14-66 |
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author | Pratt, Nicole L Ilomäki, Jenni Raymond, Chris Roughead, Elizabeth E |
author_facet | Pratt, Nicole L Ilomäki, Jenni Raymond, Chris Roughead, Elizabeth E |
author_sort | Pratt, Nicole L |
collection | PubMed |
description | BACKGROUND: Sequence symmetry analysis (SSA) is a potential tool for rapid detection of adverse drug events (ADRs) associated with newly marketed medicines utilizing computerized claims data. SSA is robust to patient specific confounders but it is sensitive to the underlying utilization trends in the medicines of interest. Methods to adjust for utilisation trends have been developed, however, there has been no systematic investigation to assess the performance of SSA when variable prescribing trends occur. The objective of this study was to evaluate the validity of SSA as a signal detection tool for newly marketed medicines. METHODS: Randomly simulated prescription supplies for a population of 1 million were generated for two medicines, DrugA (medicine of interest) and DrugB (medicine indicative of an adverse event). Scenarios were created by varying medicine utilization trends for a newly marketed medicine (DrugA). In addition, the magnitude of association between DrugA and DrugB was varied. For each scenario 1000 simulations were generated. Average Adjusted Sequence Ratios (ASR), bootstrapped 95% confidence intervals (CIs), percentage of CI's which covered the expected ASR and percent relative bias were calculated. RESULTS: When no association was simulated between DrugA and DrugB, over 95% of SSA CI's covered the expected ASR (ASR = 1) and relative bias was 1% or less irrespective of medicine utilization trends. In scenarios where DrugA and DrugB were associated (ASR = 2), unadjusted SR's were underestimated by between 11.7 and 15.3%. After adjustment for trend, ASR estimates were close to expected with relative bias less than 1%. Power was over 80% in all scenarios except for one scenario in which medicine uptake was gradual and the effect of interest was weak (ASR = 1.2). CONCLUSIONS: Adjustment for underlying medicine utilization patterns effectively overcomes potential under-ascertainment bias in SSA analyses. SSA may be effectively applied as a safety signal detection tool for newly marketed medicines where sufficiently large health claim data are available. |
format | Online Article Text |
id | pubmed-4035856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40358562014-05-29 The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study Pratt, Nicole L Ilomäki, Jenni Raymond, Chris Roughead, Elizabeth E BMC Med Res Methodol Research Article BACKGROUND: Sequence symmetry analysis (SSA) is a potential tool for rapid detection of adverse drug events (ADRs) associated with newly marketed medicines utilizing computerized claims data. SSA is robust to patient specific confounders but it is sensitive to the underlying utilization trends in the medicines of interest. Methods to adjust for utilisation trends have been developed, however, there has been no systematic investigation to assess the performance of SSA when variable prescribing trends occur. The objective of this study was to evaluate the validity of SSA as a signal detection tool for newly marketed medicines. METHODS: Randomly simulated prescription supplies for a population of 1 million were generated for two medicines, DrugA (medicine of interest) and DrugB (medicine indicative of an adverse event). Scenarios were created by varying medicine utilization trends for a newly marketed medicine (DrugA). In addition, the magnitude of association between DrugA and DrugB was varied. For each scenario 1000 simulations were generated. Average Adjusted Sequence Ratios (ASR), bootstrapped 95% confidence intervals (CIs), percentage of CI's which covered the expected ASR and percent relative bias were calculated. RESULTS: When no association was simulated between DrugA and DrugB, over 95% of SSA CI's covered the expected ASR (ASR = 1) and relative bias was 1% or less irrespective of medicine utilization trends. In scenarios where DrugA and DrugB were associated (ASR = 2), unadjusted SR's were underestimated by between 11.7 and 15.3%. After adjustment for trend, ASR estimates were close to expected with relative bias less than 1%. Power was over 80% in all scenarios except for one scenario in which medicine uptake was gradual and the effect of interest was weak (ASR = 1.2). CONCLUSIONS: Adjustment for underlying medicine utilization patterns effectively overcomes potential under-ascertainment bias in SSA analyses. SSA may be effectively applied as a safety signal detection tool for newly marketed medicines where sufficiently large health claim data are available. BioMed Central 2014-05-15 /pmc/articles/PMC4035856/ /pubmed/24886247 http://dx.doi.org/10.1186/1471-2288-14-66 Text en Copyright © 2014 Pratt et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Pratt, Nicole L Ilomäki, Jenni Raymond, Chris Roughead, Elizabeth E The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study |
title | The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study |
title_full | The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study |
title_fullStr | The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study |
title_full_unstemmed | The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study |
title_short | The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study |
title_sort | performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4035856/ https://www.ncbi.nlm.nih.gov/pubmed/24886247 http://dx.doi.org/10.1186/1471-2288-14-66 |
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