Evidence map›Paper›PMID 42441703›Full record

ArticleOnline journal of public health informatics2026

AI-Based Diagnostic Platform Capabilities With Lyme Disease as a Use Case: Integrative Exploration.

Sarah P Maxwell, Connie L McNeely, Abdollah Zeraatpisheh, Chris Brooks, Claire Maxwell, Kevin C Thomas

Abstract read
In one paragraph

Article in Online journal of public health informatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Sarah P MaxwellPublic Health, Public Management, and Public Policy, School of Economic, Political and Policy Sciences, The University of Texas at Dallas, 800 W Cambell, Richardson, TX, 75080, United States, 1 972-883-6469.ORCID http://orcid.org/0000-0003-2452-6114
Connie L McNeelySchar School of Policy and Government, George Mason University, Fairfax, VA, United States.ORCID http://orcid.org/0000-0002-4292-8195
Abdollah ZeraatpishehPublic and Non-Profit Management, School of Economic, Political and Policy Sciences, The University of Texas at Dallas, Richardson, TX, United States.ORCID http://orcid.org/0009-0001-0139-2910
Chris BrooksSchool of Biological Sciences, University of Oklahoma, Norman, OK, United States.ORCID http://orcid.org/0000-0002-9511-5390
Claire MaxwellO'Donnell School of Public Health, The University of Texas Southwestern Medical Center, Dallas, TX, United States.ORCID http://orcid.org/0000-0002-1266-8011
Kevin C ThomasLaboratory for Human Neurobiology, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA, United States.ORCID http://orcid.org/0000-0003-3463-5832

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lyme disease (LD) is the most common vector-borne disease in the United States. It is difficult to diagnose because it can mimic numerous other conditions, and testing protocols may not be sufficient. Although the Centers for Disease Control and Prevention (CDC) recommend a 2-tiered serologic testing approach for LD diagnosis, many patients are diagnosed clinically based on criteria such as the erythema migrans rash and, particularly when the rash is not present, various symptom patterns, exposure history, other information, and clinician observations. Against this backdrop, online symptom checkers, using artificial intelligence (AI) processing techniques, are increasingly used to obtain diagnostic information and resources. With LD as a use case, this research applied a modified capabilities approach to explore the relative effectiveness and utility of AI-based tools in application and comparison to serologically (CDC+) and clinically based diagnoses. Objective: The overarching goal of this research was to provide a baseline exploration of AI-assisted diagnostic tools relative to more traditional medical assessment approaches in detecting complex infectious diseases. To assess the potential diagnostic utility (DU) of online symptom checker platforms with LD as a use case, this study aimed to (1) evaluate platform performance in identifying LD across different diagnostic cohorts; (2) compare symptom patterns and severity distributions among online LD diagnoses; and (3) identify the most frequently co-occurring conditions potentially misclassified as LD or vice versa. Methods: Data were drawn from a limited structured survey of patients with confirmed or probable LD, including diagnostic pathways (CDC+ and/or clinical), symptom profiles and severity, treatment history, and time to diagnosis. These patient cases were then entered into 3 leading AI-based symptom checker platforms-MediFind, Isabel, and WebMD-to examine diagnostic performance. Descriptive analytics, logistic regressions, and postestimation analyses were used to identify patterns of DU and interaction effects among cohort type, symptom severity, and AI-based platforms. This survey-based research was not intended to serve as an experiment or clinical trial. Results: DU varied significantly across platforms and symptom severity thresholds. DU improved at higher symptom severity thresholds (≥3; P<.001) and was slightly higher among clinically diagnosed cohorts compared to CDC+ cohorts (P=.21). Marginal analyses revealed that clinically diagnosed respondents were more sensitive to changes in severity, but with different levels of platform consistency across conditions. Note that DU was analyzed principally for exploratory purposes. Conclusions: This research serves as a preliminary and directive step for expanded data collection and a larger, more comprehensive study. The findings suggest that AI-based symptom checkers may supplement early diagnostic reasoning in complex conditions such as LD, particularly when symptom severity is high. Inconsistency across platforms and diagnostic categories highlights the need for algorithmic refinement and standardized validation frameworks to enhance diagnostic reliability in AI-based tools.

Indexed as

clinical diagnosisdiagnostic accuracyLyme diseaseserologic testingsymptom checker

Identifiers

PMID42441703
PMCPMC13361615

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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.