Literature DB >> 24919793

Likelihood ratio based tests for longitudinal drug safety data.

Lan Huang1, Jyoti Zalkikar, Ram Tiwari.   

Abstract

This article presents longitudinal likelihood ratio test (LongLRT) methods for large databases with exposure information. These methods are applied to a pooled large longitudinal clinical trial dataset for drugs treating osteoporosis with concomitant use of proton pump inhibitors (PPIs). When the interest is in the evaluation of a signal of an adverse event for a particular drug compared with placebo or a comparator, the special case of the LongLRT, referred to as sequential LRT (SeqLRT), is also presented. The results show that there is some possible evidence of concomitant use of PPIs leading to more adverse events associated with osteoporosis. The performance of the proposed LongLRT and SeqLRT methods is evaluated using simulated datasets and shown to be good in terms of (conditional) power and control of type I error over time. The proposed methods can also be applied to large observational databases with exposure information under the US Food and Drug Administration Sentinel Initiative for active surveillance. Published 2014. This article is a US Government work and is in the public domain in the USA. Published 2014. This article is a US Government work and is in the public domain in the USA.

Entities:  

Keywords:  active surveillance; drug exposure; longitudinal method; safety surveillance; sequential method

Mesh:

Substances:

Year:  2014        PMID: 24919793     DOI: 10.1002/sim.6103

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  6 in total

1.  Data Mining for Adverse Drug Events With a Propensity Score-matched Tree-based Scan Statistic.

Authors:  Shirley V Wang; Judith C Maro; Elande Baro; Rima Izem; Inna Dashevsky; James R Rogers; Michael Nguyen; Joshua J Gagne; Elisabetta Patorno; Krista F Huybrechts; Jacqueline M Major; Esther Zhou; Megan Reidy; Austin Cosgrove; Sebastian Schneeweiss; Martin Kulldorff
Journal:  Epidemiology       Date:  2018-11       Impact factor: 4.822

2.  Mixture drug-count response model for the high-dimensional drug combinatory effect on myopathy.

Authors:  Xueying Wang; Pengyue Zhang; Chien-Wei Chiang; Hengyi Wu; Li Shen; Xia Ning; Donglin Zeng; Lei Wang; Sara K Quinney; Weixing Feng; Lang Li
Journal:  Stat Med       Date:  2017-11-23       Impact factor: 2.373

3.  Efficient methods for signal detection from correlated adverse events in clinical trials.

Authors:  Guoqing Diao; Guanghan F Liu; Donglin Zeng; William Wang; Xianming Tan; Joseph F Heyse; Joseph G Ibrahim
Journal:  Biometrics       Date:  2019-03-29       Impact factor: 2.571

Review 4.  Sources of Safety Data and Statistical Strategies for Design and Analysis: Postmarket Surveillance.

Authors:  Rima Izem; Matilde Sanchez-Kam; Haijun Ma; Richard Zink; Yueqin Zhao
Journal:  Ther Innov Regul Sci       Date:  2018-01-08       Impact factor: 1.778

Review 5.  Statistical methods for the analysis of adverse event data in randomised controlled trials: a scoping review and taxonomy.

Authors:  Rachel Phillips; Odile Sauzet; Victoria Cornelius
Journal:  BMC Med Res Methodol       Date:  2020-11-30       Impact factor: 4.615

6.  A tree-based scan statistic for zero-inflated count data in post-market drug safety surveillance.

Authors:  Goeun Park; Inkyung Jung
Journal:  Sci Rep       Date:  2022-09-29       Impact factor: 4.996

  6 in total

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