Hilab System Device in an Oncological Hospital: A New Clinical Approach for Point of Care CBC Test, Supported by the Internet of Things and Machine Learning

Author:

Gasparin Aléxia Thamara1,Araujo Claudiane Isabel Franco1ORCID,Cardoso Mônica Ribas1ORCID,Schmitt Patricia1,Godoy Juliana Beker1ORCID,Reichert Eduarda Silva1,Pimenta Maria Eduarda1,Gonçalves Caroline Bretas1,Santiago Erika Bergamo1,Silva Ivan Lucas Reis1,Gaideski Bruno de Paula1,Cardoso Milena Andreuzo1,Silva Fernanda D’Amico1ORCID,Sommer Viviane da Rosa1,Hartmann Luis Felipe1ORCID,Perazzoli Carolina Rodrigues de Araujo1,Farias João Samuel de Holanda2,Beltrame Olair Carlos2,Winter Nicole2,Nicollete Diego Rinaldi Pavesi1ORCID,Lopes Silvia Nathalia Bueno1,Predebon João Victor1,Almeida Bernardo Montesanti Machado de1ORCID,Rogal Júnior Sérgio Renato1,Figueredo Marcus Vinícius Mazega1

Affiliation:

1. Department of Research and Development, Hilab, Jose Altair Possebom, 800, Curitiba 81270-185, PR, Brazil

2. Erasto Gaertner Hospital, Curitiba 81520-060, PR, Brazil

Abstract

The complete blood count (CBC) is a highly requested test that is generally restricted to centralized laboratories, which are limited by high cost, being maintenance-demanding, and requiring costly equipment. The Hilab System (HS) is a small, handheld hematological platform that uses microscopy and chromatography techniques, combined with machine learning (ML) and artificial intelligence (AI), to perform a CBC test. This platform uses ML and AI techniques to add higher accuracy and reliability to the results besides allowing for faster reporting. For clinical and flagging capability evaluation of the handheld device, the study analyzed 550 blood samples of patients from a reference institution for oncological diseases. The clinical analysis encompassed the data comparison between the Hilab System and a conventional hematological analyzer (Sysmex XE-2100) for all CBC analytes. The flagging capability study compared the microscopic findings from the Hilab System and the standard blood smear evaluation method. The study also assessed the sample collection source (venous or capillary) influences. The Pearson correlation, Student t-test, Bland–Altman, and Passing–Bablok plot of analytes were calculated and are shown. Data from both methodologies were similar (p > 0.05; r ≥ 0.9 for most parameters) for all CBC analytes and flagging parameters. Venous and capillary samples did not differ statistically (p > 0.05). The study indicates that the Hilab System provides humanized blood collection associated with fast and accurate data, essential features for patient wellbeing and quick physician decision making.

Funder

Hi Technologies

Publisher

MDPI AG

Subject

Clinical Biochemistry

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