Evidence map›Paper›PMID 34969114›Full record

ArticleClinical chemistry2021

Applications of Digital Microscopy and Densely Connected Convolutional Neural Networks for Automated Quantification of Babesia-Infected Erythrocytes.

Thomas J S Durant, Sarah N Dudgeon, Jacob McPadden, Anisia Simpson, Nathan Price, Wade L Schulz, Richard Torres, Eben M Olson

Abstract read
In one paragraph

Article in Clinical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Research progress on diagnostic techniques for differentFrontiers in cellular and infection microbiology · 2025
    Review
  5. Article
  6. Review
  7. Building the Model.Archives of pathology & laboratory medicine · 2023
    Review
  8. Deep learning for microscopic examination of protozoan parasites.Computational and structural biotechnology journal · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Thomas J S DurantDepartment of Laboratory Medicine, Yale School of Medicine, New Haven, CT, USA.
Sarah N DudgeonCenter for Outcomes Research and Evaluation, Yale New Haven Hospital, New Haven, CT, USA.
Jacob McPaddenDepartment of Pediatrics, Yale School of Medicine, New Haven, CT, USA.
Anisia SimpsonDepartment of Laboratory Medicine, Yale New Haven Hospital, New Haven, CT, USA.
Nathan PriceCenter for Computational Health, Yale New Haven Hospital, New Haven, CT, USA.
Wade L SchulzDepartment of Laboratory Medicine, Yale School of Medicine, New Haven, CT, USA.
Richard TorresDepartment of Laboratory Medicine, Yale School of Medicine, New Haven, CT, USA.
Eben M OlsonDepartment of Laboratory Medicine, Yale School of Medicine, New Haven, CT, USA.

Funding

IMMUNOHEMATOLOGY/TRANSFUSION MEDICINE RESEARCH TRAININGT32HL007974 · NHLBI · YALE UNIVERSITY · PI JEANNE E HENDRICKSON, Diane S Krause · 2001 to 2026
$8.1M
Academy of Clinical Laboratory Physicians and Scientists: Paul E. Strandjord Young Investigator Research GrantNHLBI NIH HHS T32 HL007974
6 · The paper itself

Abstract

backgroundClinical babesiosis is diagnosed, and parasite burden is determined, by microscopic inspection of a thick or thin Giemsa-stained peripheral blood smear. However, quantitative analysis by manual microscopy is subject to error. As such, methods for the automated measurement of percent parasitemia in digital microscopic images of peripheral blood smears could improve clinical accuracy, relative to the predicate method.

methodsIndividual erythrocyte images were manually labeled as "parasite" or "normal" and were used to train a model for binary image classification. The best model was then used to calculate percent parasitemia from a clinical validation dataset, and values were compared to a clinical reference value. Lastly, model interpretability was examined using an integrated gradient to identify pixels most likely to influence classification decisions.

resultsThe precision and recall of the model during development testing were 0.92 and 1.00, respectively. In clinical validation, the model returned increasing positive signal with increasing mean reference value. However, there were 2 highly erroneous false positive values returned by the model. Further, the model incorrectly assessed 3 cases well above the clinical threshold of 10%. The integrated gradient suggested potential sources of false positives including rouleaux formations, cell boundaries, and precipitate as deterministic factors in negative erythrocyte images.

conclusionsWhile the model demonstrated highly accurate single cell classification and correctly assessed most slides, several false positives were highly incorrect. This project highlights the need for integrated testing of machine learning-based models, even when models in the development phase perform well.

Indexed as

BabesiaParasitemiaErythrocytesHumansMicroscopyNeural Networks, Computerbabesiaconvolutional neural networkserythrocyteimage analysismachine learningperipheral blood smear

Identifiers

PMID34969114
PMCPMC12928752

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.