DIVA: Exploration and Validation of Hypothesized Drug-Drug Interactions

被引:6
|
作者
Kakar, T. [1 ,2 ]
Qin, X. [1 ,2 ]
Rundensteiner, E. A. [1 ]
Harrison, L. [1 ]
Sahoo, S. K. [2 ]
Dee, S. [2 ]
机构
[1] Worcester Polytech Inst, Comp Sci Dept, Worcester, MA 01609 USA
[2] US FDA, Ctr Drug Evaluat & Res, Rockville, MD 20857 USA
关键词
PATTERN-RECOGNITION; NETWORK ANALYSIS; TOOL; VISUALIZATION; SYSTEM;
D O I
10.1111/cgf.13674
中图分类号
TP31 [计算机软件];
学科分类号
081202 ; 0835 ;
摘要
Adverse reactions caused by drug-drug interactions are a major public health concern. Currently, adverse reaction signals are detected through a tedious manual process in which drug safety analysts review a large number of reports collected through post-marketing drug surveillance. While computational techniques in support of this signal analysis are necessary, alone they are not sufficient. In particular, when machine learning techniques are applied to extract candidate signals from reports, the resulting set is (1) too large in size, i.e., exponential to the number of unique drugs and reactions in reports, (2) disconnected from the underlying reports that serve as evidence and context, and (3) ultimately requires human intervention to be validated in the domain context as a true signal warranting action. In this work, we address these challenges though a visual analytics system, DIVA, designed to align with the drug safety analysis workflow by supporting the detection, screening, and verification of candidate drug interaction signals. DTVA's abstractions and encodings are informed by formative interviews with drug safety analysts. DIVA's coordinated visualizations realize a proposed novel augmented interaction data model (AIM) which links signals generated by machine learning techniques with domain-specific metadata critical for signal analysis. DIVA's alignment with the drug review process allows an analyst to interactively screen for important signals, triage signals for in-depth investigation, and validate signals by reviewing the underlying reports that serve as evidence. The evaluation of DIVA encompasses case-studies and interviews by drug analysts at the US Food and Drug Administration - both of which confirm that DIVA indeed is effective in supporting analysts in the critical task of exploring and verifying dangerous drug-drug interactions.
引用
收藏
页码:95 / 106
页数:12
相关论文
共 50 条
  • [31] Drug-drug interactions of empagliflozin and dapagliflozin
    Stoellberger, C.
    Finsterer, J.
    Schneider, B.
    EUROPEAN HEART JOURNAL, 2024, 45
  • [32] Six patterns of drug-drug interactions
    Armstrong, SC
    Cozza, KL
    Sandson, NB
    PSYCHOSOMATICS, 2003, 44 (03) : 255 - 258
  • [33] THE REGULATORY VIEW ON DRUG-DRUG INTERACTIONS
    MULLER, HJ
    GUNDERTREMY, U
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 1994, 32 (06) : 269 - 273
  • [34] Anti hypertensive drug-drug interactions
    Morales-Olivas, FJ
    Estañ, L
    MEDICINA CLINICA, 2005, 124 (20): : 782 - 789
  • [35] An overview of psychotropic drug-drug interactions
    Sandson, NB
    Armstrong, SC
    Cozza, KL
    PSYCHOSOMATICS, 2005, 46 (05) : 464 - 494
  • [36] Editorial: Drug-drug interactions in pharmacology
    Pichini, Simona
    Di Trana, Annagiulia
    Garcia-Algar, Oscar
    Busardo, Francesco Paolo
    FRONTIERS IN PHARMACOLOGY, 2023, 14
  • [37] DRUG-DRUG INTERACTIONS OF FLUOXETINE WITH TRICYCLICS
    CAVANAUGH, SV
    PSYCHOSOMATICS, 1990, 31 (03) : 273 - 276
  • [38] Antiretroviral and Statin Drug-Drug Interactions
    Ray, Gretchen M.
    CARDIOLOGY IN REVIEW, 2009, 17 (01) : 44 - 47
  • [39] Improvement in the handling of drug-drug interactions
    Fuhr, Uwe
    EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 64 (02) : 167 - 171