Evidence map›Paper›PMID 42114005›Full record

Observational studyJournal of medical Internet research2026

Combining Machine Learning Models and Screening to Enhance Suicide Risk Identification for American Indian Patients: Retrospective Cohort Study.

Novalene Alsenay Goklish, Emily E Haroz, Rohan R Dayal, Valentín Q Sierra, Roy Adams, Francene Larzelere Sinquah, Paul Rebman, Jacob L Taylor

Abstract readObservational Study
In one paragraph

Observational study in Journal of medical Internet research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

8 authors.

Novalene Alsenay Goklish *Department of International Health, Center for Indigenous Health, Johns Hopkins Bloomberg School of Public Health, 415 N. Washington St, Baltimore, MD, 21205, United States, 1 410-955-0011.ORCID 0000-0001-8478-4604
Emily E Haroz *Department of International Health, Center for Indigenous Health, Johns Hopkins Bloomberg School of Public Health, 415 N. Washington St, Baltimore, MD, 21205, United States, 1 410-955-0011.ORCID 0000-0003-1833-4925
Rohan R DayalDepartment of International Health, Center for Indigenous Health, Johns Hopkins Bloomberg School of Public Health, 415 N. Washington St, Baltimore, MD, 21205, United States, 1 410-955-0011.ORCID 0009-0009-0538-7615
Valentín Q SierraDepartment of International Health, Center for Indigenous Health, Johns Hopkins Bloomberg School of Public Health, 415 N. Washington St, Baltimore, MD, 21205, United States, 1 410-955-0011.ORCID 0000-0002-9035-8094
Roy AdamsDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, United States.ORCID 0000-0001-6859-3007
Francene Larzelere SinquahDepartment of International Health, Center for Indigenous Health, Johns Hopkins Bloomberg School of Public Health, 415 N. Washington St, Baltimore, MD, 21205, United States, 1 410-955-0011.ORCID 0009-0006-5739-3126
Paul RebmanDepartment of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.ORCID 0000-0003-2961-5407
Jacob L TaylorDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, United States.ORCID 0009-0001-8620-9432

Funding

NATIVE RISE-Risk Identification for Suicide and Enhanced care for Native AmericansR01MH128518 · NIMH · JOHNS HOPKINS UNIVERSITY · PI Emily Haroz · 2023 to 2026
$2.4M
Computational Social Science Training ProgramT32HD101364 · NICHD · UNIVERSITY OF CALIFORNIA BERKELEY · PI Jennifer Ahern, PATRICK T BRADSHAW · 2020 to 2026
$1.7M
Preparing Indigenous Scientists to Lead Innovative Substance Use Research: The Native Children's Research Exchange Scholars ProgramR25DA061492 · NIDA · UNIVERSITY OF COLORADO DENVER · PI Jerreed Dean Ivanich, Michelle C Sarche · 2024 to 2026
$804k
NICHD NIH HHS T32 HD101364NIDA NIH HHS R25 DA061492NIMH NIH HHS R01 MH128518
6 · The paper itself

Abstract

Background: American Indian and Alaska Native communities experience disproportionately high suicide rates. While machine learning (ML) models leveraging electronic health records have emerged as promising tools for suicide risk identification, the optimal integration of these models with existing screening practices remains unclear. Objective: The objective of this study was to compare parallel and serial testing strategies that combine an ML suicide risk model and the Ask Suicide-Screening Questions (ASQ) against using the ASQ alone. To achieve this, we conducted a retrospective secondary analysis of electronic health record data. The cohort consisted of adult emergency department visits at an Indian Health Service facility between October 1, 2019, and October 2, 2021. Methods: Sensitivity, specificity, predictive values, and 95% CIs were averaged across 10 cross-validated patient-level folds. The final sample included 7897 American Indian patients with 26,896 visits, 824 (3.1%) of which had a positive ASQ result and 102 (0.4%) of which had the outcome of suicide attempt or death within 90 days of the visit. The logistic regression ML model previously developed using Indian Health Service-specific data was operationalized at the 95th and 75th percentiles to evaluate high-risk and medium-risk thresholds, respectively. A sensitivity analysis was performed to evaluate identification approaches across all emergency department visits during this period. Results: The ML medium-risk threshold alone identified the most true positives (sensitivity: 0.782, 95% CI 0.648-0.915; specificity: 0.751, 95% CI 0.725-0.777; positive predictive value [PPV]: 0.012, 95% CI 0.009-0.014; negative predictive value [NPV]: 0.999, 95% CI 0.998-0.999) in comparison to the ML high-risk threshold alone (sensitivity: 0.429, 95% CI 0.287-0.572; specificity: 0.955, 95% CI 0.948-0.961; PPV: 0.035, 95% CI 0.022-0.048; NPV: 0.998, 95% CI 0.997-0.999) or the ASQ alone (sensitivity: 0.178, 95% CI 0.073-0.282; specificity: 0.970, 95% CI 0.968-0.971; PPV: 0.022, 95% CI 0.010-0.034; NPV: 0.997, 95% CI 0.996-0.998). Combining the ML high-risk threshold with the ASQ in series yielded the greatest positive predictive ability (PPV: 0.050, 95% CI 0.014-0.086) at the cost of reduced sensitivity (0.129, 95% CI 0.036-0.221). Finally, the parallel testing approach using the ML medium-risk threshold yielded the greatest sensitivity (0.795, 95% CI 0.671-0.920; specificity: 0.742, 95% CI 0.716-0.767; PPV: 0.012, 95% CI 0.009-0.014; NPV: 0.999, 95% CI 0.998-0.999) without missing any cases identified through screening. Conclusions: Unlike existing studies that evaluate ML and screening tools in isolation, this study innovates by assessing combined parallel and serial testing strategies in a real-world setting. We demonstrated that, while serial testing maximizes predictive accuracy, it is often infeasible. Instead, parallel testing brings value as a clinical "safety net" to catch at-risk patients missed by standard practices. Ultimately, integrating ML in suicide prevention requires balancing statistical accuracy with setting-specific, real-world workflows.

Indexed as

Indians, North AmericanPredictive Learning ModelsSuicideSuicide PreventionAdultElectronic Health RecordsFemaleHumansMaleMiddle AgedRetrospective StudiesRisk AssessmentUnited StatesAmerican Indian and Alaska Nativeelectronic health recordsmachine learningpredictive modelingscreeningsuicide preventionsuicide risk identification

Identifiers

PMID42114005
PMCPMC13160258

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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.