Traceable machine learning real-time quality control based on patient data

Author:

Zhou Rui12,Wang Wei3,Padoan Andrea4ORCID,Wang Zhe5,Feng Xiang5,Han Zewen5,Chen Chao6,Liang Yufang1,Wang Tingting7,Cui Weiqun7,Plebani Mario4ORCID,Wang Qingtao12

Affiliation:

1. Department of Laboratory Medicine , Beijing Chao-yang Hospital, Capital Medical University , Beijing , P.R. China

2. Beijing Center for Clinical Laboratories , Beijing , P.R. China

3. Department of Blood Transfusion , Beijing Ditan Hospital, Capital Medical University , Beijing , P.R. China

4. Department of Medicine-DIMED , University of Padova , Padova , Italy

5. Inner Mongolia Wesure Date Technology Co., Ltd , Inner Mongolia , P.R. China

6. Beijing Jinfeng Yitong Technology Co., Ltd , Beijing , P.R. China

7. Center for Metrology Scientific Data and Energy Metrology , National Institute of Metrology , Beijing , P.R. China

Abstract

Abstract Objectives Patient-based real-time quality control (PBRTQC) has gained attention as an alternative/integrative tool for internal quality control (iQC). However, it is still doubted for its performance and its application in real clinical settings. We aim to generate a newly and easy-to-access patient-based real-time QC by machine learning (ML) traceable to standard reference data with assigned values by National Institute of Metrology of China (NIM), and to compare it with PBRTQC for clinical validity evaluation. Methods For five representative biochemistry analytes, 1,195 000 patient testing results each were collected. After data processing, independent training and test sets were divided. Machine learning internal quality control (MLiQC) was set up by Random Forest in ML and was validated by way of both metrology algorithm traceability and 4 PBRTQC methods recommended by IFCC analytical working group. Results MLiQC were established. As an example of albumin (ALB) at the critical bias, the uncertainty of MLiQC was 0.14%, which was evaluated by standard reference data produced by NIM. Compared with four optimal PBRTQC methods at critical bias, the average of the number of patient samples from a bias introduced until detected (ANPed) of MLiQC averagely decreased from 600 to 20. The median and 95 quantiles of NPeds (MNPed and 95NPed) of MLiQC were superior to all optimal PBRTQCs above 90% for all test items. Conclusions MLiQC is highly superior to PBRTQC and well-suited in real settings. The validation of the model from two aspects of algorithm traceability and clinical effectiveness confirms its satisfactory performance.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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