Skip to main content
Top
Published in: BMC Medical Research Methodology 1/2014

Open Access 01-12-2014 | Research article

The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study

Authors: Nicole L Pratt, Jenni Ilomäki, Chris Raymond, Elizabeth E Roughead

Published in: BMC Medical Research Methodology | Issue 1/2014

Login to get access

Abstract

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.
Appendix
Available only for authorised users
Literature
1.
go back to reference Wahab IA, Pratt NL, Wiese MD, Kalisch LM, Roughead EE: The validity of sequence symmetry analysis (SSA) for adverse drug reaction signal detection. Pharmacoepidemiol Drug Saf. 2013, 22: 496-502. 10.1002/pds.3417.CrossRefPubMed Wahab IA, Pratt NL, Wiese MD, Kalisch LM, Roughead EE: The validity of sequence symmetry analysis (SSA) for adverse drug reaction signal detection. Pharmacoepidemiol Drug Saf. 2013, 22: 496-502. 10.1002/pds.3417.CrossRefPubMed
2.
go back to reference Hallas J: Evidence of depression provoked by cardiovascular medication: a prescription sequence symmetry analysis. Epidemiology. 1996, 7: 478-484. 10.1097/00001648-199609000-00004.CrossRefPubMed Hallas J: Evidence of depression provoked by cardiovascular medication: a prescription sequence symmetry analysis. Epidemiology. 1996, 7: 478-484. 10.1097/00001648-199609000-00004.CrossRefPubMed
3.
go back to reference Vegter S, Berg LT DJ-vd: Misdiagnosis and mistreatment of a common side-effect–angiotensin-converting enzyme inhibitor-induced cough. Br J Clin Pharmacol. 2010, 69: 200-203. 10.1111/j.1365-2125.2009.03571.x.CrossRefPubMedPubMedCentral Vegter S, Berg LT DJ-vd: Misdiagnosis and mistreatment of a common side-effect–angiotensin-converting enzyme inhibitor-induced cough. Br J Clin Pharmacol. 2010, 69: 200-203. 10.1111/j.1365-2125.2009.03571.x.CrossRefPubMedPubMedCentral
4.
go back to reference Vegter S, De Boer P, Van Dijk KW, Visser S, Berg LT DJ-vd: The effects of antitussive treatment of ACE inhibitor-induced cough on therapy compliance: a prescription sequence symmetry analysis. Drug Saf. 2013, 36: 435-439. 10.1007/s40264-013-0024-z.CrossRefPubMed Vegter S, De Boer P, Van Dijk KW, Visser S, Berg LT DJ-vd: The effects of antitussive treatment of ACE inhibitor-induced cough on therapy compliance: a prescription sequence symmetry analysis. Drug Saf. 2013, 36: 435-439. 10.1007/s40264-013-0024-z.CrossRefPubMed
5.
go back to reference Van Boven JF, Berg LT DJ-vd, Vegter S: Inhaled corticosteroids and the occurrence of oral candidiasis: a prescription sequence symmetry analysis. Drug Saf. 2013, 36: 231-236. 10.1007/s40264-013-0029-7.CrossRefPubMed Van Boven JF, Berg LT DJ-vd, Vegter S: Inhaled corticosteroids and the occurrence of oral candidiasis: a prescription sequence symmetry analysis. Drug Saf. 2013, 36: 231-236. 10.1007/s40264-013-0029-7.CrossRefPubMed
6.
go back to reference Caughey GE, Roughead EE, Pratt N, Killer G, Gilbert AL: Stroke risk and NSAIDs: an Australian population-based study. Med J Aust. 2011, 195: 525-529. 10.5694/mja11.10055.CrossRefPubMed Caughey GE, Roughead EE, Pratt N, Killer G, Gilbert AL: Stroke risk and NSAIDs: an Australian population-based study. Med J Aust. 2011, 195: 525-529. 10.5694/mja11.10055.CrossRefPubMed
7.
go back to reference Hersom K, Neary MP, Levaux HP, Klaskala W, Strauss JS: Isotretinoin and antidepressant pharmacotherapy: a prescription sequence symmetry analysis. J Am Acad Dermatol. 2003, 49: 424-432. 10.1067/S0190-9622(03)02087-5.CrossRefPubMed Hersom K, Neary MP, Levaux HP, Klaskala W, Strauss JS: Isotretinoin and antidepressant pharmacotherapy: a prescription sequence symmetry analysis. J Am Acad Dermatol. 2003, 49: 424-432. 10.1067/S0190-9622(03)02087-5.CrossRefPubMed
8.
go back to reference Tsiropoulos I, Andersen M, Hallas J: Adverse events with use of antiepileptic drugs: a prescription and event symmetry analysis. Pharmacoepidemiol Drug Saf. 2009, 18: 483-491. 10.1002/pds.1736.CrossRefPubMed Tsiropoulos I, Andersen M, Hallas J: Adverse events with use of antiepileptic drugs: a prescription and event symmetry analysis. Pharmacoepidemiol Drug Saf. 2009, 18: 483-491. 10.1002/pds.1736.CrossRefPubMed
9.
go back to reference Birkett DJ, McManus P: Modelling the market uptake of new drugs following listing for subsidy in Australia. A report from the Drug Utilisation Subcommittee of the Australian Pharmaceutical Benefits Advisory Committee. Br J Clin Pharmacol. 1995, 40: 407-410. 10.1111/j.1365-2125.1995.tb04565.x.CrossRefPubMedPubMedCentral Birkett DJ, McManus P: Modelling the market uptake of new drugs following listing for subsidy in Australia. A report from the Drug Utilisation Subcommittee of the Australian Pharmaceutical Benefits Advisory Committee. Br J Clin Pharmacol. 1995, 40: 407-410. 10.1111/j.1365-2125.1995.tb04565.x.CrossRefPubMedPubMedCentral
10.
go back to reference Pratt N, Andersen M, Bergman U, Choi NK, Gerhard T, Huang C, Kimura M, Kimura T, Kubota K, Lai CC, Ooba N, Osby U, Park BJ, Sato T, Shin JY, Sundström A, Yang YHK, Roughead EE: Multi-country rapid adverse drug event assessment: the Asian Pharmacoepidemiology Network (AsPEN) antipsychotic and acute hyperglycaemia study. Pharmacoepidemiol Drug Saf. 2013, 22: 915-924.PubMed Pratt N, Andersen M, Bergman U, Choi NK, Gerhard T, Huang C, Kimura M, Kimura T, Kubota K, Lai CC, Ooba N, Osby U, Park BJ, Sato T, Shin JY, Sundström A, Yang YHK, Roughead EE: Multi-country rapid adverse drug event assessment: the Asian Pharmacoepidemiology Network (AsPEN) antipsychotic and acute hyperglycaemia study. Pharmacoepidemiol Drug Saf. 2013, 22: 915-924.PubMed
Metadata
Title
The performance of sequence symmetry analysis as a tool for post-market surveillance of newly marketed medicines: a simulation study
Authors
Nicole L Pratt
Jenni Ilomäki
Chris Raymond
Elizabeth E Roughead
Publication date
01-12-2014
Publisher
BioMed Central
Published in
BMC Medical Research Methodology / Issue 1/2014
Electronic ISSN: 1471-2288
DOI
https://doi.org/10.1186/1471-2288-14-66

Other articles of this Issue 1/2014

BMC Medical Research Methodology 1/2014 Go to the issue