TY - GEN
T1 - MARAS
T2 - 23rd ACM SIGKDD International Conference on Knowledge Discovery and Data Mining, KDD 2017
AU - Qin, Xiao
AU - Kakar, Tabassum
AU - Wunnava, Susmitha
AU - Rundensteiner, Elke A.
AU - Cao, Lei
N1 - Publisher Copyright:
© 2017 ACM.
PY - 2017/8/13
Y1 - 2017/8/13
N2 - There is a growing need for computing-supported methods that facilitate the automated signaling of Adverse Drug Reactions (ADRs) otherwise left undiscovered from the exploding amount of ADR reports tiled by patients, medical professionals and drug manufacturers. In this research, we design a Multi-Drug Adverse Reaction Analytics Strategy, called MARAS, to signal severe unknown ADRs triggered by the usage of a combination of drugs, also known as Multi-Drug Adverse Reactions (MDAR). First, MARAS features an efficient signal generation algorithm based on association rule learning that extracts non-spurious MDAR associations. Second, MARAS incorporates contextual information to detect drug combinations that are strongly associated with a set of ADRs. It groups related associations into Contextual Association Clusters (CACs) that then avail contextual information to evaluate the significance of the discovered MDAR Associations. Lastly, we use this contextual significance to rank discoveries by their notion of interestingness to signal the most compelling MDARs. To demonstrate the utility of MARAS, it is compared with state-of-the-art techniques and evaluated via case studies on datasets collected by U.S. Food and Drug Administration Adverse Event Reporting System (FAERS).
AB - There is a growing need for computing-supported methods that facilitate the automated signaling of Adverse Drug Reactions (ADRs) otherwise left undiscovered from the exploding amount of ADR reports tiled by patients, medical professionals and drug manufacturers. In this research, we design a Multi-Drug Adverse Reaction Analytics Strategy, called MARAS, to signal severe unknown ADRs triggered by the usage of a combination of drugs, also known as Multi-Drug Adverse Reactions (MDAR). First, MARAS features an efficient signal generation algorithm based on association rule learning that extracts non-spurious MDAR associations. Second, MARAS incorporates contextual information to detect drug combinations that are strongly associated with a set of ADRs. It groups related associations into Contextual Association Clusters (CACs) that then avail contextual information to evaluate the significance of the discovered MDAR Associations. Lastly, we use this contextual significance to rank discoveries by their notion of interestingness to signal the most compelling MDARs. To demonstrate the utility of MARAS, it is compared with state-of-the-art techniques and evaluated via case studies on datasets collected by U.S. Food and Drug Administration Adverse Event Reporting System (FAERS).
KW - Adverse drug reaction
KW - Association rule learning
KW - Interestingness of association
KW - Public health surveillance
UR - https://www.scopus.com/pages/publications/85029037804
UR - https://www.scopus.com/pages/publications/85029037804#tab=citedBy
U2 - 10.1145/3097983.3097986
DO - 10.1145/3097983.3097986
M3 - Conference contribution
AN - SCOPUS:85029037804
T3 - Proceedings of the ACM SIGKDD International Conference on Knowledge Discovery and Data Mining
SP - 1615
EP - 1623
BT - KDD 2017 - Proceedings of the 23rd ACM SIGKDD International Conference on Knowledge Discovery and Data Mining
PB - Association for Computing Machinery
Y2 - 13 August 2017 through 17 August 2017
ER -