A clinical deep learning framework for continually learning from cardiac signals across diseases, time, modalities, and institutions.
A clinical deep learning framework for continually learning from cardiac signals across diseases, time, modalities, and institutions.
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DOI:
10.1038/s41467-021-24483-0
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发表时间:
2021-07-09
影响因子:
16.6
通讯作者:
Clifton D
中科院分区:
文献类型:
--
作者:
Kiyasseh D;Zhu T;Clifton D
Deep learning algorithms trained on instances that violate the assumption of being independent and identically distributed (i.i.d.) are known to experience destructive interference, a phenomenon characterized by a degradation in performance. Such a violation, however, is ubiquitous in clinical settings where data are streamed temporally from different clinical sites and from a multitude of physiological sensors. To mitigate this interference, we propose a continual learning strategy, entitled CLOPS, that employs a replay buffer. To guide the storage of instances into the buffer, we propose end-to-end trainable parameters, termed task-instance parameters, that quantify the difficulty with which data points are classified by a deep-learning system. We validate the interpretation of these parameters via clinical domain knowledge. To replay instances from the buffer, we exploit uncertainty-based acquisition functions. In three of the four continual learning scenarios, reflecting transitions across diseases, time, data modalities, and healthcare institutions, we show that CLOPS outperforms the state-of-the-art methods, GEM and MIR. We also conduct extensive ablation studies to demonstrate the necessity of the various components of our proposed strategy. Our framework has the potential to pave the way for diagnostic systems that remain robust over time. Deep learning algorithms trained on data streamed temporally from different clinical sites and from a multitude of physiological sensors are generally affected by a degradation in performance. To mitigate this, the authors propose a continual learning strategy that employs a replay buffer.
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影响因子:
82.9
作者:
Hannun, Awni Y.;Rajpurkar, Pranav;Ng, Andrew Y.
通讯作者:
Ng, Andrew Y.
DOI:
10.22489/cinc.2017.065-469
发表时间:
2017-09
期刊:
Computing in cardiology
影响因子:
--
作者:
Clifford GD;Liu C;Moody B;Lehman LH;Silva I;Li Q;Johnson AE;Mark RG
通讯作者:
Mark RG
影响因子:
9.8
作者:
Martinez-Sancho, Elisabet;Slamova, Lenka;Fonti, Patrick
通讯作者:
Fonti, Patrick
影响因子:
--
作者:
Dwork, Cynthia;Roth, Aaron
通讯作者:
Roth, Aaron