Applications of machine learning in decision analysis for dose management for dofetilide

被引:24
|
作者
Levy, Andrew E. [1 ]
Biswas, Minakshi [1 ]
Weber, Rachel [2 ]
Tarakji, Khaldoun [3 ]
Chung, Mina [3 ]
Noseworthy, Peter A. [4 ]
Newton-Cheh, Christopher [5 ,6 ]
Rosenberg, Michael A. [1 ,7 ]
机构
[1] Univ Colorado, Div Cardiol, Anschutz Med Campus, Aurora, CO 80045 USA
[2] Colorado Sch Publ Hlth, Div Biostat & Informat, Aurora, CO USA
[3] Cleveland Clin Fdn, Ctr Atrial Fibrillat, Sect Cardiac Pacing & Electrophysiol, 9500 Euclid Ave, Cleveland, OH 44195 USA
[4] Mayo Clin, Robert D & Patricia E Kern Ctr Sci Hlth Care Deli, Rochester, MN USA
[5] Massachusetts Gen Hosp, Dept Med, Cardiovasc Res Ctr, Boston, MA 02114 USA
[6] Harvard Med Sch, Boston, MA 02115 USA
[7] Univ Colorado, Colorado Ctr Personalized Med, Anschutz Med Campus, Aurora, CO 80045 USA
来源
PLOS ONE | 2019年 / 14卷 / 12期
关键词
ARTIFICIAL-INTELLIGENCE; REINFORCEMENT; GAME; GO;
D O I
10.1371/journal.pone.0227324
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Initiation of the antiarrhythmic medication dofetilide requires an FDA-mandated 3 days of telemetry monitoring due to heightened risk of toxicity within this time period. Although a recommended dose management algorithm for dofetilide exists, there is a range of real-world approaches to dosing the medication. Methods and results In this multicenter investigation, clinical data from the Antiarrhythmic Drug Genetic (AAD-G EN) study was examined for 354 patients undergoing dofetilide initiation. Univariate logistic regression identified a starting dofetilide dose of 500 mcg (OR 5.0, 95%CI 2.5-10.0, p<0.001) and sinus rhythm at the start of dofetilide loading (OR 2.8, 95%CI 1.8-4.2, p<0.001) as strong positive predictors of successful loading. Any dose-adjustment during loading (OR 0.19, 95%CI 0.12-0.31, p<0.001) and a history coronary artery disease (OR 0.33, 95%CI 0.19-0.59, p<0.001) were strong negative predictors of successful dofetilide loading. Based on the observation that any dose adjustment was a significant negative predictor of successful initiation, we applied multiple supervised approaches to attempt to predict the dose adjustment decision, but none of these approaches identified dose adjustments better than a probabilistic guess. Principal component analysis and cluster analysis identified 8 clusters as a reasonable data reduction method. These 8 clusters were then used to define patient states in a tabular reinforcement learning model trained on 80% of dosing decisions. Testing of this model on the remaining 20% of dosing decisions revealed good accuracy of the reinforcement learning model, with only 16/410 (3.9%) instances of disagreement. Conclusions Dose adjustments are a strong determinant of whether patients are able to successfully initiate dofetilide. A reinforcement learning algorithm informed by unsupervised learning was able to predict dosing decisions with 96.1% accuracy. Future studies will apply this algorithm prospectively as a data-driven decision aid.
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页数:13
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