Evidence map›Paper›PMID 35187469›Full record

ArticleFrontiers in artificial intelligence2021

Development and Validation of Manually Modified and Supervised Machine Learning Clinical Assessment Algorithms for Malaria in Nigerian Children.

Megan McLaughlin, Karell G Pellé, Samuel V Scarpino, Aisha Giwa, Ezra Mount-Finette, Nada Haidar, Fatima Adamu, Nirmal Ravi, Adam Thompson, Barry Heath and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in artificial intelligence, 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
1.0field-weighted citation impact, top 21% of its field
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, 7 citations in OpenAlex.

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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

12 authors at 3 institutions in 2 countries.

Megan McLaughlinTHINKMD, Burlington, VT, United States.
Karell G PelléFIND, Geneva, Switzerland.
Samuel V ScarpinoNetwork Science Institute, Northeastern University, Boston, MA, United States.
Aisha GiwaeHealth Africa, Kano, Nigeria.
Ezra Mount-FinetteTHINKMD, Burlington, VT, United States.
Nada HaidareHealth Africa, Kano, Nigeria.
Fatima AdamueHealth Africa, Kano, Nigeria.
Nirmal RavieHealth Africa, Kano, Nigeria.
Adam ThompsoneHealth Africa, Kano, Nigeria.
Barry HeathTHINKMD, Burlington, VT, United States.
Sabine DittrichFIND, Geneva, Switzerland.
Barry FinetteTHINKMD, Burlington, VT, United States.
Foundation for Innovative New Diagnostics · CHUniversity of Vermont · USNortheastern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is currently estimated that 67% of malaria deaths occur in children under-five years (WHO, 2020). To improve the identification of children at clinical risk for malaria, the WHO developed community (iCCM) and clinic-based (IMCI) protocols for frontline health workers using paper-based forms or digital mobile health (mHealth) platforms. To investigate improving the accuracy of these point-of-care clinical risk assessment protocols for malaria in febrile children, we embedded a malaria rapid diagnostic test (mRDT) workflow into THINKMD's (IMCI) mHealth clinical risk assessment platform. This allowed us to perform a comparative analysis of THINKMD-generated malaria risk assessments with mRDT truth data to guide modification of THINKMD algorithms, as well as develop new supervised machine learning (ML) malaria risk algorithms. We utilized paired clinical data and malaria risk assessments acquired from over 555 children presenting to five health clinics in Kano, Nigeria to train ML algorithms to identify malaria cases using symptom and location data, as well as confirmatory mRDT results. Supervised ML random forest algorithms were generated using 80% of our field-based data as the ML training set and 20% to test our new ML logic. New ML-based malaria algorithms showed an increased sensitivity and specificity of 60 and 79%, and PPV and NPV of 76 and 65%, respectively over THINKD initial IMCI-based algorithms. These results demonstrate that combining mRDT "truth" data with digital mHealth platform clinical assessments and clinical data can improve identification of children with malaria/non-malaria attributable febrile illnesses.

Indexed as

digital healthfebrile illnessIMCImachine learningrapid diagnostic test

Identifiers

PMID35187469
PMCPMC8851346
OpenAlexW4210664948

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.