Metrics to guide development of machine learning algorithms for malaria diagnosis
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Abstract (arXiv)
Automated malaria diagnosis is a difficult but high-value target for machine learning (ML), and effective algorithms could save many thousands of children's lives. However, current ML efforts largely neglect crucial use case constraints and are thus not clinically useful. Two factors in particular are crucial to developing algorithms translatable to clinical field settings: (i) Clear understanding of the clinical needs that ML solutions must accommodate; and (ii) task-relevant metrics for guiding and evaluating ML models. Neglect of these factors has seriously hampered past ML work on malaria, because the resulting algorithms do not align with clinical needs. In this paper we address these two issues in the context of automated malaria diagnosis via microscopy on Giemsa-stained blood films. First, we describe why domain expertise is crucial to effectively apply ML to malaria, and list technical documents and other resources that provide this domain knowledge. Second, we detail performance metrics tailored to the clinical requirements of malaria diagnosis, to guide development of ML models and evaluate model performance through the lens of clinical needs (versus a generic ML lens). We highlight the importance of a patient-level perspective, interpatient variability, false positive rates, limit of detection, and different types of error. We also discuss reasons why ROC curves, AUC, and F1, as commonly used in ML work, are poorly suited to this context. These findings also apply to other diseases involving parasite loads, including neglected tropical diseases (NTDs) such as schistosomiasis.
Key facts. Cited by 4 papers in the map (data through 14 Oct 2026). Builds on 1 of its 56 references that are in the map. First posted on arXiv 14 Sep 2022.
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1 of 56 references.
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Citing papers per year: 2024: 1; 2025: 0; 2026: 3.
4 papers.
- 2024Driving down Poisson error can offset classification error in clinical taskscited by 0
- 2026Beyond validation loss: Clinically-tailored optimization metrics improve a model's clinical performancecited by 0
- 2026SGMCE: Segment-Grounded Morphological Concept Explanation for Malaria Parasite Species Identification in Thick Blood Smearscited by 0
- 2026CoSWA-YOLOv12: Scale-Invariant Tiny Object Detection and Segmentation of Malaria Parasitescited by 0
- 2026CoSWA-YOLOv12: Scale-Invariant Tiny Object Detection and Segmentation of Malaria Parasites25 Aug 2026
- 2026SGMCE: Segment-Grounded Morphological Concept Explanation for Malaria Parasite Species Identification in Thick Blood Smears15 Jul 2026
- 2026Beyond validation loss: Clinically-tailored optimization metrics improve a model's clinical performance22 Jan 2026
- 2024Driving down Poisson error can offset classification error in clinical tasks9 May 2024