Evidence map›Paper›PMID 42018985›Full record

ArticleJMIR human factors2026

Near Miss Reporting and Organizational Learning in Health Care: Conceptual Framework Development Study.

Mohammed As'ad

Abstract read
In one paragraph

Article in JMIR human factors, 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

1 author.

Mohammed As'adDr Sulaiman Al Habib Medical Group, Corporate QPS, Headquarters, Al Awsat Valley S, Al Olaya, Riyadh, 12241, Saudi Arabia, 966 11525999.ORCID 0000-0003-2179-4375

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Near miss events can reveal system problems before patients are harmed, but current reviews are inconsistent and often rely on simple counts that are distorted by patient volume and reporting culture. Consequently, leaders cannot tell whether a rise in reports means that safety is getting worse or that staff are reporting more, and current systems are not strong enough to clearly separate real safety risks from random variation. Objective: This study developed a 3-level near miss framework (NM³), a conceptual framework that converts descriptive near miss data into decision-grade intelligence through a structured, evidence-based process, including baseline measurement and advanced interpretation and governance. Methods: NM³ was developed to provide decision-grade analytics for acute inpatient hospital settings. The framework was designed as a maturity model, progressing from baseline measurement to advanced interpretation. It integrates standardized definitions, rate calculations, statistical process control, severity weighting, and learning metrics. Results: Level 1 establishes an organizational baseline through near miss rates per 1000 patient-days and near miss-to-harm ratios monitored with control charts. Level 2 introduces domain-specific denominators and unit-level charts to detect local variation. Level 3 applies severity weighting to generate a Near Miss Index; incorporates learning yields at 90 and 180 days; and triangulates near miss trends with harm events, exposure, reporting volume, and culture measures. A synthetic example demonstrates how the framework converts raw reports into stable rates, weighted indices, and learning metrics. Conclusions: NM³ provides a structured pathway for organizations to strengthen near miss analytics. By progressing through maturity levels, leaders can improve the interpretation of safety signals, prioritize high-consequence risks, and integrate near miss reporting into governance.

Indexed as

Delivery of Health CareNear Miss, HealthcarePatient SafetyRisk ManagementHumansacute carehospitalnear misspatient safetyquality improvementsafety culturestatistical process control

Identifiers

PMID42018985
PMCPMC13102322

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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.