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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Cardiovasc. Med.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Cardiovascular Medicine</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Cardiovasc. Med.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2297-055X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fcvm.2025.1663769</article-id>
<article-version article-version-type="Version of Record" vocab="NISO-RP-8-2008"/>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Original Research</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Patient-needs-enhanced emergency nursing assessment framework accelerates time-critical care for non-traumatic chest pain</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name><surname>Sun</surname><given-names>Yan</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="an1"><sup>&#x2020;</sup></xref>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="investigation" vocab-term-identifier="https://credit.niso.org/contributor-roles/investigation/">Investigation</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="methodology" vocab-term-identifier="https://credit.niso.org/contributor-roles/methodology/">Methodology</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Writing &#x2013; original draft" vocab-term-identifier="https://credit.niso.org/contributor-roles/writing-original-draft/">Writing &#x2013; original draft</role></contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name><surname>Liu</surname><given-names>Xiaoxia</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="an1"><sup>&#x2020;</sup></xref>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="methodology" vocab-term-identifier="https://credit.niso.org/contributor-roles/methodology/">Methodology</role>
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</contrib>
<contrib contrib-type="author">
<name><surname>Shen</surname><given-names>Lili</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="methodology" vocab-term-identifier="https://credit.niso.org/contributor-roles/methodology/">Methodology</role>
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</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Zhao</surname><given-names>Fangfang</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="conceptualization" vocab-term-identifier="https://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
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<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Writing &#x2013; review &amp; editing" vocab-term-identifier="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing &#x2013; review &amp; editing</role></contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Xu</surname><given-names>Kaiyun</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/3130428/overview"/>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="conceptualization" vocab-term-identifier="https://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Writing &#x2013; review &amp; editing" vocab-term-identifier="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing &#x2013; review &amp; editing</role></contrib>
</contrib-group>
<aff id="aff1"><label>1</label><institution>Department of Emergency Medicine, Third Affiliated Hospital of Naval Medical University</institution>, <city>Shanghai</city>, <country country="cn">China</country></aff>
<aff id="aff2"><label>2</label><institution>Department of Emergency Medicine, Marine Corps Hospital of the People&#x2019;s Liberation Army</institution>, <city>Chaozhou</city>, <state>Guangdong</state>, <country country="cn">China</country></aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label><bold>Correspondence:</bold> Kaiyun Xu <email xlink:href="mailto:kaiyunxush@163.com">kaiyunxush@163.com</email> Fangfang Zhao <email xlink:href="mailto:15221192870@163.com">15221192870@163.com</email></corresp>
<fn fn-type="equal" id="an1"><label>&#x2020;</label><p>These authors have contributed equally to this work</p></fn>
</author-notes>
<pub-date publication-format="electronic" date-type="pub" iso-8601-date="2025-11-25"><day>25</day><month>11</month><year>2025</year></pub-date>
<pub-date publication-format="electronic" date-type="collection"><year>2025</year></pub-date>
<volume>12</volume><elocation-id>1663769</elocation-id>
<history>
<date date-type="received"><day>10</day><month>07</month><year>2025</year></date>
<date date-type="rev-recd"><day>02</day><month>11</month><year>2025</year></date>
<date date-type="accepted"><day>10</day><month>11</month><year>2025</year></date>
</history>
<permissions>
<copyright-statement>&#x00A9; 2025 Sun, Liu, Shen, Zhao and Xu.</copyright-statement>
<copyright-year>2025</copyright-year><copyright-holder>Sun, Liu, Shen, Zhao and Xu</copyright-holder><license><ali:license_ref start_date="2025-11-25">https://creativecommons.org/licenses/by/4.0/</ali:license_ref>
<license-p>This is an open-access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License (CC BY)</ext-link>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p></license>
</permissions>
<abstract><sec><title>Background</title>
<p>Non-traumatic chest pain requires rapid Emergency Department (ED) triage, yet adherence to ECG &#x2264;10&#x2005;min and early troponin targets is inconsistent, standard nursing frameworks seldom prompt patient-needs that affect timeliness and documentation. The aim of this study is to determine whether implementing a patient-needs-enhanced Emergency Nursing Assessment Framework (ENAF), compared with usual care, increases the proportion of ED patients with non-traumatic chest pain receiving a 12-lead ECG within 10&#x2005;min.</p>
</sec><sec><title>Methods</title>
<p>This prospective single-center quasi-experimental before-after study was conducted in the T Third Affiliated Hospital of Naval Medical University from January 2023 to January&#x202F;2025 and assigned to a control group and ENAF group. The ENAF group comprised (1) eight hours of nurse training, (2) an ENAF electronic template incorporating mandatory pain, anxiety, information-need and social-support items, and (3) a triage &#x201C;rapid chest-pain kit&#x201D;. The primary endpoint was completion of a 12-lead ECG within 10&#x2005;min of triage; secondary endpoints were door-to-troponin time, &#x2265;2-point pain reduction at 30&#x2005;min, documentation completeness, ED length of stay (LOS) and 30-day major adverse cardiac events (MACE). Multivariable logistic regression adjusted for age, sex, HEART score, arrival mode and peak ED census.</p>
</sec><sec><title>Results</title>
<p>Of 372 screened patients, 340 met eligibility and were analyzed (170 control, 170 ENAF). Timely ECG completion increased from 60.0&#x0025; to 78.2&#x0025; (adjusted odds ratio&#x202F;2.31, 95&#x0025; CI: 1.47&#x2013;3.63; <italic>P</italic>&#x2009;&#x003C;&#x2009;0.001). Median door-to-troponin time fell from 50 to 39&#x2005;min (<italic>P</italic>&#x2009;&#x003C;&#x2009;0.001); pain-relief success rose from 45.3&#x0025; to 61.8&#x0025; (<italic>P</italic>&#x2009;&#x003D;&#x2009;0.002). Documentation completeness improved by ten percentage points (<italic>P</italic>&#x2009;&#x003C;&#x2009;0.001) and median ED LOS decreased by 0.8&#x2005;h (<italic>P</italic>&#x2009;&#x003D;&#x2009;0.01). Thirty-day MACE was similar between phases (15.3&#x0025; vs. 12.9&#x0025;; <italic>P</italic>&#x2009;&#x003D;&#x2009;0.49), and no serious adverse events were attributed to the protocol.</p>
</sec><sec><title>Conclusions</title>
<p>Augmenting ENAF with a structured clinical-needs module significantly accelerates ECG acquisition, improves other process metrics and enhances nursing documentation while maintaining patient safety. Adoption of this nurse-led approach could strengthen ED chest-pain pathways in comparable resource-constrained settings, and multicenter validation are warranted to establish generalizability.</p>
</sec>
</abstract>
<kwd-group>
<kwd>chest pain</kwd>
<kwd>emergency nursing</kwd>
<kwd>quality improvement</kwd>
<kwd>patient-centred checklist</kwd>
<kwd>electrocardiogram timing</kwd>
</kwd-group><funding-group>
<funding-statement>The author(s) declare that financial support was received for the research and/or publication of this article. This study was supported by the Nursing Research Program of the Third Affiliated Hospital of Naval Medical University (Project No. 25HL005).</funding-statement>
</funding-group>
<counts>
<fig-count count="3"/>
<table-count count="3"/><equation-count count="0"/><ref-count count="29"/><page-count count="9"/><word-count count="121231"/></counts><custom-meta-group><custom-meta><meta-name>section-at-acceptance</meta-name><meta-value>Cardiovascular Nursing</meta-value></custom-meta></custom-meta-group>
</article-meta>
</front>
<body><sec id="s1" sec-type="intro"><title>Introduction</title>
<p>Globally, non-traumatic chest pain is a significant cause of emergency department (ED) visits, with a substantial portion of these cases ultimately being diagnosed as acute coronary syndrome (ACS) or benign conditions. In England and Wales, for instance, chest pain accounts for approximately 2.4&#x0025; of ED visits (<xref ref-type="bibr" rid="B1">1</xref>). In China, the EMPACT study highlights the challenge of managing acute chest pain, with a focus on improving diagnostic accuracy and treatment outcomes for suspected ACS cases (<xref ref-type="bibr" rid="B2">2</xref>). The proportion of patients with chest pain who are ultimately diagnosed with ACS varies, but a significant number are found to have non-cardiac causes, emphasizing the importance of accurate diagnosis to avoid unnecessary interventions (<xref ref-type="bibr" rid="B3">3</xref>).</p>
<p>Guidelines recommend that an electrocardiogram (ECG) should be performed within 10&#x2005;min of ED arrival for patients with suspected ACS, and troponin levels should be assessed promptly to facilitate early diagnosis and treatment (<xref ref-type="bibr" rid="B4">4</xref>). Delays in these critical steps can lead to missed diagnoses of ST-elevation myocardial infarction (STEMI), increased morbidity and mortality, and prolonged ED stays (<xref ref-type="bibr" rid="B5">5</xref>). In China, audits of tertiary centers reveal performance gaps, with regional variations in the management of ACS, such as longer onset-to-first medical contact times and differences in the use of percutaneous coronary intervention (PCI) (<xref ref-type="bibr" rid="B6">6</xref>). These disparities highlight the need for standardized protocols and quality improvement initiatives to enhance care delivery and outcomes (<xref ref-type="bibr" rid="B6">6</xref>).</p>
<p>Emergency nursing practice plays a critical role in patient care, often serving as the first clinical contact for patients in EDs. However, the variability in assessment quality and documentation deficits can contribute to diagnostic errors and medico-legal risks (<xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B8">8</xref>). Frameworks like ABCDE and ISBAR are partially adopted to standardize assessments, but their inconsistent use highlights the need for more comprehensive solutions (<xref ref-type="bibr" rid="B9">9</xref>). The Emergency Nursing Assessment Framework (ENAF) was developed to address these issues, featuring a five-step structure: Chief Complaint, Primary Survey, Focused Assessment, Secondary Survey, and Reassessment &#x0026; Communication (<xref ref-type="bibr" rid="B10">10</xref>). Evidence suggests that ENAF improves systematic data capture and handoff fidelity, yet it lacks an explicit focus on patient-centered clinical needs such as pain, anxiety, and informational support (<xref ref-type="bibr" rid="B10">10</xref>, <xref ref-type="bibr" rid="B11">11</xref>). Addressing patient-centered needs is crucial, as unmet needs are linked to increased anxiety, persistent pain, and decreased patient satisfaction (<xref ref-type="bibr" rid="B12">12</xref>). Empirical data indicate delays in analgesia and communication deficits, particularly in chest pain cohorts (<xref ref-type="bibr" rid="B13">13</xref>). Local quality control data from a study hospital reveal that only 60&#x0025; of ECGs are performed within 10&#x2005;min, and documentation completeness is at 80&#x2009;&#x00B1;&#x2009;10&#x0025;, with bottlenecks identified in equipment distance, inconsistent reassessment, and lack of standardized prompts for pain and anxiety (<xref ref-type="bibr" rid="B14">14</xref>). The HIRAID framework, an evidence-based approach, has been shown to improve the accuracy of clinical documentation and enhance patient experience by providing a structured method for patient assessment and non-technical skills development (<xref ref-type="bibr" rid="B8">8</xref>, <xref ref-type="bibr" rid="B11">11</xref>). Despite these advancements, the integration of patient-centered care into emergency nursing frameworks remains a gap that needs addressing to optimize patient outcomes and satisfaction in acute care settings (<xref ref-type="bibr" rid="B11">11</xref>, <xref ref-type="bibr" rid="B15">15</xref>).</p>
<p>Nurse-led intervention in combination with a low-cost electronic template with mandatory fields, a readily accessible rapid-assessment kit and a real-time audit-feedback loop, may optimize patient outcome and satisfaction in high-volume emergency departments. The aim of this study is to determine whether implementing ENAF, compared with usual care, increases the proportion of Emergency Department patients with non-traumatic chest pain receiving a 12-lead ECG within 10&#x2005;min, and to evaluate effects on door-to-troponin time, early pain relief, documentation completeness, emergency department length of stay, and 30-day major adverse cardiac events.</p>
</sec>
<sec id="s2" sec-type="methods"><title>Methods</title>
<sec id="s2a"><title>Study design</title>
<p>We performed a prospective, single-center, before-after (quasi-experimental) study that compared usual nursing care (&#x201C;Control group&#x201D;) with a patient-needs-enhanced ENAF protocol (&#x201C;ENAF group&#x201D;) in adults presenting to the ED with non-traumatic chest pain. Patients were assigned to the Control or ENAF group by calendar time (all eligible visits before protocol go-live comprised the Control phase; all eligible visits after go-live comprised the ENAF phase). Because allocation occurred at the service level and the intervention was visible (electronic ENAF template and pre-positioned rapid chest-pain kit), randomization and allocation concealment were not applicable. No stratification by HEART risk, arrival mode, or triage acuity was used for assignment; these factors were prespecified for covariate adjustment and subgroup analyses only.</p>
</sec>
<sec id="s2b"><title>Ethical consideration</title>
<p>This study was conducted at Third Affiliated Hospital of Naval Medical University from January&#x202F;2023 to January&#x202F;2025. The study protocol was approved by the Institutional Review Board of Third Affiliated Hospital of Naval Medical University (IRB No. KY-2022-045) and adhered to the Declaration of Helsinki. Because the intervention was a unit-level workflow change with no investigational drug or device and no patient-level randomization, the IRB did not require trial registration.</p>
<sec id="s2b1"><title>Consent and eligibility</title>
<p>Written informed consent for data use and 30-day follow-up was obtained from all participants prior to inclusion.</p>
</sec>
<sec id="s2b2"><title>Privacy and data security</title>
<p>After deterministic linkage of EMR and laboratory feeds, datasets were de-identified with personally identifying fields removed. Data were stored on an encrypted hospital server with access restricted to the study team.</p>
</sec>
</sec>
<sec id="s2c"><title>Participants</title>
<p>Eligibility required age&#x202F;&#x2265;18 years and a chief complaint of non-traumatic chest pain, tightness or discomfort on ED arrival; exclusions were traumatic pain, pre-hospital ECG-confirmed STEMI with direct cath-lab activation, cardiac arrest on arrival, pregnancy, and inability to provide immediate or delayed consent in the absence of a legally authorized representative, all of which were determined by a triage research nurse who prospectively logged screening outcomes. Consecutive ED arrivals meeting eligibility were prospectively screened by a triage research nurse who logged inclusions and exclusions in real time. Assignment to study phase was determined solely by visit date relative to ENAF implementation. No patient-level sequence generation or concealment was performed.</p>
</sec>
<sec id="s2d"><title>ENAF protocol</title>
<p>The multifaceted intervention comprised (1) eight hours of nurse education&#x2014;four hours of pathophysiology and ENAF theory plus four hours of high-fidelity simulation, (2) an EMR-embedded ENAF template with mandatory fields for pain score, GAD-2 anxiety screening, information-need prompt and social-support query, enforced by electronic &#x201C;hard stops,&#x201D; (3) a pre-positioned rapid chest-pain kit (ECG cart, aspirin, glyceryl trinitrate spray, pre-labelled troponin tube) within five meters of triage, and (4) weekly audit-and-feedback huddles displaying run charts; baseline care used unstructured nursing notes and lacked both the template and kit.</p>
<p>Training was delivered by the ED nurse-education team with input from cardiology and the ED informatics nurse for the electronic template. After the 8-h course (4&#x2005;h didactic on ACS/ENAF; 4&#x2005;h high-fidelity simulation), post-training competency was verified using a brief knowledge test and a skills checklist with return-demonstration covering ECG initiation, pain and GAD-2 documentation, pre-labeling a troponin tube, and use of the rapid chest-pain kit. Passing required a score &#x2265;[80]&#x0025; on the knowledge test and correct completion of all pre-specified &#x201C;must-pass&#x201D; checklist items. Remediation consisted of targeted coaching and a repeat return-demonstration before independent ENAF use. Attendance and competency sign-off were logged in the departmental education record.</p>
</sec>
<sec id="s2e"><title>Outcomes</title>
<p>The primary endpoint was completion of a 12-lead ECG within 10&#x2005;min of triage registration, captured automatically from ECG time stamps; secondary endpoints were door-to-first-troponin time, &#x2265;2-point pain reduction at 30&#x2005;min, ENAF documentation completeness (modified nine-item D-CATCH score), ED length of stay (LOS) and 30-day major adverse cardiac events (MACE: all-cause death, non-fatal myocardial infarction or unplanned revascularization), with MACE ascertained by telephone follow-up and provincial health-information-system cross-check.</p>
</sec>
<sec id="s2f"><title>Sample-Size calculation</title>
<p>Assuming a baseline ECG &#x2264;10&#x2005;min rate of 60&#x0025; and targeting a 15-percentage-point absolute increase to 75&#x0025;, a two-sided <italic>&#x03B1;</italic>&#x2009;&#x003D;&#x2009;0.05&#x0025; and 80&#x0025; power yielded 152 patients per phase; anticipating a 10&#x0025; attrition rate we prospectively enrolled 170 patients in each phase (total&#x2009;&#x003D;&#x2009;340).</p>
</sec>
<sec id="s2g"><title>Data collection and management</title>
<p>Nightly automated scripts extracted demographic data, timestamps and laboratory results from the Neusoft v9.3 EMR and Cobas laboratory information system into a REDCap&#x202F;13.2 database, while two blinded abstractors audited 20&#x0025; of charts for documentation completeness with <italic>&#x03BA;</italic>&#x2009;&#x003E;&#x2009;0.80 agreement; datasets were de-identified, stored on an encrypted hospital server and accessed via two-factor authentication with an immutable audit trail.</p>
<sec id="s2g1"><title>Anonymity and data protection</title>
<p>After deterministic linkage of EMR and laboratory feeds, datasets were de-identified. Personally identifying fields were removed. Data were stored on an encrypted hospital server with two-factor authentication and an immutable audit trail. Access was limited to the study team.</p>
</sec>
</sec>
<sec id="s2h"><title>Statistical analysis</title>
<p>Analyses were executed in Stata&#x202F;18.0. Categorical variables compared by <italic>&#x03C7;</italic><sup>2</sup> or Fisher&#x0027;s exact tests and continuous variables by Student&#x0027;s <italic>t</italic>-test or Mann&#x2013;Whitney <italic>U</italic> as appropriate; multivariable logistic regression estimated adjusted odds ratios (aORs) for timely ECG controlling for age, sex, HEART score, arrival mode and peak hourly ED census, while linear/quantile regression, logistic regression and Cox models addressed secondary outcomes, and interaction terms tested predefined subgroups (HEART strata, arrival mode, triage acuity); robustness was assessed via multiple-imputation, per-protocol and interrupted-time-series sensitivity analyses, with two-sided <italic>P</italic>&#x2009;&#x003C;&#x2009;0.05 considered significant.</p>
</sec>
</sec>
<sec id="s3" sec-type="results"><title>Results</title>
<sec id="s3a"><title>Participant flow and baseline characteristics</title>
<p>From January 2023 to January&#x202F;2025, 372 adults with non-traumatic chest pain were screened; 32 were excluded (12 traumatic pain, eight pre-hospital STEMI, 12 other), leaving 340 patients&#x2014;170 in the baseline phase and 170 in the ENAF phase&#x2014;and none were lost to follow-up (<xref ref-type="fig" rid="F1">Figure&#x00A0;1</xref>). Baseline comparability was excellent (<xref ref-type="table" rid="T1">Table&#x00A0;1</xref>): mean age 57&#x2009;&#x00B1;&#x2009;14 vs. 56&#x2009;&#x00B1;&#x2009;15&#x202F;years, 60&#x0025; male in both cohorts, and no significant differences in ambulance arrivals, HEART &#x2265;4 proportion, initial pain &#x2265;7, or major comorbidities (all <italic>P</italic>&#x2009;&#x003E;&#x2009;0.50).</p>
<fig id="F1" position="float"><label>Figure&#x00A0;1</label>
<caption><p>CONSORT-style flow diagram of participant disposition. A total of 372 adult patients with non-traumatic chest pain were screened between January 2023 and January&#x202F;2025; 32 were excluded (12 traumatic pain, 8 pre-hospital ST-segment-elevation myocardial infarction, 12 other reasons), leaving 340 eligible patients. Allocation was 170 to the baseline phase and 170 to the intervention phase, with zero loss to follow-up or missing primary-outcome data.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="fcvm-12-1663769-g001.tif"><alt-text content-type="machine-generated">Flowchart showing the study enrollment process. Out of 372 people screened, 32 were excluded due to traumatic chest pain (12), pre-hospital STEMI (8), and other reasons (12). A total of 340 were allocated evenly between the baseline and intervention phases, with 170 each. All participants in both phases were analyzed with no losses.</alt-text>
</graphic>
</fig>
<table-wrap id="T1" position="float"><label>Table&#x00A0;1</label>
<caption><p>Baseline characteristics.</p></caption>
<table>
<thead>
<tr>
<th valign="top" align="left">Characteristic</th>
<th valign="top" align="center">Control (<italic>n</italic>&#x2009;&#x003D;&#x2009;170)</th>
<th valign="top" align="center">ENAF (<italic>n</italic>&#x2009;&#x003D;&#x2009;170)</th>
<th valign="top" align="center"><italic>P</italic>-value</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Age, mean&#x2009;&#x00B1;&#x2009;SD (years)</td>
<td valign="top" align="center">57&#x2009;&#x00B1;&#x2009;14</td>
<td valign="top" align="center">56&#x2009;&#x00B1;&#x2009;15</td>
<td valign="top" align="center">0.56</td>
</tr>
<tr>
<td valign="top" align="left">Male, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">103 (60.6&#x0025;)</td>
<td valign="top" align="center">101 (59.4&#x0025;)</td>
<td valign="top" align="center">0.82</td>
</tr>
<tr>
<td valign="top" align="left">Arrival by ambulance, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">68 (40.0&#x0025;)</td>
<td valign="top" align="center">65 (38.2&#x0025;)</td>
<td valign="top" align="center">0.74</td>
</tr>
<tr>
<td valign="top" align="left">HEART&#x202F;&#x2265;&#x202F;4, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">49 (28.8&#x0025;)</td>
<td valign="top" align="center">53 (31.2&#x0025;)</td>
<td valign="top" align="center">0.58</td>
</tr>
<tr>
<td valign="top" align="left">Initial pain score&#x202F;&#x2265;7, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">87 (51.2&#x0025;)</td>
<td valign="top" align="center">84 (49.4&#x0025;)</td>
<td valign="top" align="center">0.78</td>
</tr>
<tr>
<td valign="top" align="left">Hypertension, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">85 (50.0&#x0025;)</td>
<td valign="top" align="center">88 (51.8&#x0025;)</td>
<td valign="top" align="center">0.71</td>
</tr>
<tr>
<td valign="top" align="left">Diabetes, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">44 (25.9&#x0025;)</td>
<td valign="top" align="center">40 (23.5&#x0025;)</td>
<td valign="top" align="center">0.64</td>
</tr>
<tr>
<td valign="top" align="left">Prior CAD, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">39 (22.9&#x0025;)</td>
<td valign="top" align="center">42 (24.7&#x0025;)</td>
<td valign="top" align="center">0.68</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s3b"><title>Primary outcome&#x2014;timely ECG acquisition</title>
<p>The ENAF increased the proportion of patients receiving a 12-lead ECG within 10&#x2005;min from 60.0&#x0025; (102/170) to 78.2&#x0025; (133/170), an 18.2-percentage-point absolute gain; unadjusted RR&#x202F;1.30 (95&#x0025; CI: 1.10&#x2013;1.50) and adjusted OR&#x202F;2.31 (95&#x0025; CI: 1.47&#x2013;3.63, <italic>P</italic>&#x2009;&#x003C;&#x2009;0.001) (<xref ref-type="table" rid="T2">Table&#x00A0;2</xref>).</p>
<table-wrap id="T2" position="float"><label>Table&#x00A0;2</label>
<caption><p>Primary outcome (timely ECG).</p></caption>
<table>
<thead>
<tr>
<th valign="top" align="left">Outcome</th>
<th valign="top" align="center">Control (<italic>n</italic>&#x2009;&#x003D;&#x2009;170)</th>
<th valign="top" align="center">ENAF (<italic>n</italic>&#x2009;&#x003D;&#x2009;170)</th>
<th valign="top" align="center">Absolute &#x0394; (&#x0025;)</th>
<th valign="top" align="center">Relative risk (95&#x0025; CI)</th>
<th valign="top" align="center">Adjusted&#x202F;OR<xref ref-type="table-fn" rid="TF1"><sup>&#x2020;</sup></xref> (95&#x0025; CI)</th>
<th valign="top" align="center"><italic>P</italic></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">ECG &#x2264;10&#x2005;min, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">102 (60.0&#x0025;)</td>
<td valign="top" align="center">133 (78.2&#x0025;)</td>
<td valign="top" align="center">&#x002B;18.2</td>
<td valign="top" align="center">1.30 (1.10&#x2013;&#x202F;1.50)</td>
<td valign="top" align="center">2.31 (1.47&#x2013;&#x202F;3.63)</td>
<td valign="top" align="center">&#x003C;0.001</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TF1"><label>&#x2020;</label>
<p>Adjusted for age, sex, HEART score, arrival mode, and peak ED census.</p></fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3c"><title>Secondary outcomes</title>
<p>Process metrics improved across the board (<xref ref-type="table" rid="T3">Table&#x00A0;3</xref>): median door-to-troponin time fell by 11&#x2005;min (50&#x2009;&#x2192;&#x2009;39&#x2005;min, <italic>P</italic>&#x2009;&#x003C;&#x2009;0.001); pain-relief success at 30&#x2005;min rose from 45.3&#x0025; to 61.8&#x0025; (<italic>P</italic>&#x2009;&#x003D;&#x2009;0.002); documentation completeness increased from 82&#x0025;&#x2009;&#x00B1;&#x2009;9&#x0025; to 92&#x0025;&#x2009;&#x00B1;&#x2009;5&#x0025; (<italic>P</italic>&#x2009;&#x003C;&#x2009;0.001; <xref ref-type="fig" rid="F2">Figure&#x00A0;2</xref>); and median ED length of stay decreased from 5.1&#x2005;h to 4.3&#x2005;h (<italic>P</italic>&#x2009;&#x003D;&#x2009;0.01), while 30-day MACE was unchanged (15.3&#x0025; vs. 12.9&#x0025;, <italic>P</italic>&#x2009;&#x003D;&#x2009;0.49).</p>
<table-wrap id="T3" position="float"><label>Table&#x00A0;3</label>
<caption><p>Secondary outcomes.</p></caption>
<table>
<thead>
<tr>
<th valign="top" align="left">Secondary outcome</th>
<th valign="top" align="center">Control</th>
<th valign="top" align="center">ENAF</th>
<th valign="top" align="center"><italic>P</italic>-value</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Door-to-troponin, median&#x202F;(IQR) min</td>
<td valign="top" align="center">50 (38&#x2013;65)</td>
<td valign="top" align="center">39 (30&#x2013;50)</td>
<td valign="top" align="center">&#x003C;0.001</td>
</tr>
<tr>
<td valign="top" align="left">Pain reduction &#x2265;2 at 30&#x2005;min, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">77 (45.3&#x0025;)</td>
<td valign="top" align="center">105 (61.8&#x0025;)</td>
<td valign="top" align="center">0.002</td>
</tr>
<tr>
<td valign="top" align="left">Documentation completeness, mean&#x2009;&#x00B1;&#x2009;SD</td>
<td valign="top" align="center">82&#x2009;&#x00B1;&#x2009;9</td>
<td valign="top" align="center">92&#x2009;&#x00B1;&#x2009;5</td>
<td valign="top" align="center">&#x003C;0.001</td>
</tr>
<tr>
<td valign="top" align="left">ED length of stay (h), median (IQR)</td>
<td valign="top" align="center">5.1 (3.9&#x2013;6.4)</td>
<td valign="top" align="center">4.3 (3.3&#x2013;5.4)</td>
<td valign="top" align="center">0.01</td>
</tr>
<tr>
<td valign="top" align="left">30-day MACE, <italic>n</italic> (&#x0025;)</td>
<td valign="top" align="center">26 (15.3&#x0025;)</td>
<td valign="top" align="center">22 (12.9&#x0025;)</td>
<td valign="top" align="center">0.49</td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="F2" position="float"><label>Figure&#x00A0;2</label>
<caption><p>Box-and-whisker plot of ENAF documentation completeness by study phase. Boxes represent the interquartile range (IQR), central lines the median, and whiskers 1.5&#x2009;&#x00D7;&#x2009;IQR for 170 charts per phase. Median completeness improved from 81&#x0025; (Control) to 92&#x0025; (ENAF); outliers are omitted for clarity.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="fcvm-12-1663769-g002.tif"><alt-text content-type="machine-generated">Box plot comparing ENAF documentation completeness by phase, showing two boxes labeled \"Control\" and \"ENAF\" on the x-axis. The y-axis indicates documentation completeness percentage from 70% to 100%. The ENAF box has a higher median and less variability than the Control.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3d"><title>Process fidelity and checklist uptake</title>
<p>The ENAF electronic template was properly closed in 97.4&#x0025; of ENAF cases and the four-item clinical-needs checklist was fully completed in 95.8&#x0025;, with template completion time falling from 6.2&#x202F;min in week&#x202F;1&#x2013;4.1&#x2005;min in week&#x202F;12 (<xref ref-type="sec" rid="s12">Supplementary Table S1</xref>).</p>
</sec>
<sec id="s3e"><title>Subgroup analyses</title>
<p>Benefits were consistent across predefined strata (<xref ref-type="fig" rid="F3">Figure&#x00A0;3</xref>). Adjusted ORs for timely ECG ranged from 1.50 (HEART &#x2265;7) to 2.60 (HEART 0&#x2013;3), with no significant interactions by HEART risk, arrival mode, or triage acuity (<italic>P</italic>-interaction &#x003E;0.10 for all).</p>
<fig id="F3" position="float"><label>Figure&#x00A0;3</label>
<caption><p>Forest plot of adjusted odds ratios (aORs) for timely ECG across prespecified subgroups. Horizontal lines indicate 95&#x0025; confidence intervals and solid dots the point aORs comparing intervention vs. baseline within each subgroup (HEART risk strata, arrival mode, triage acuity). The dashed vertical line at aOR &#x003D;&#x2009;1.0 denotes no effect; all confidence intervals favor the intervention, and no subgroup shows a significant interaction. HEART, History-ECG-Age-Risk-Troponin score; L, triage level.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="fcvm-12-1663769-g003.tif"><alt-text content-type="machine-generated">Chart titled \"Subgroup Analysis &#x2013; Timely ECG\" showing adjusted odds ratios for subgroups: \"Triage L3-4\", \"Triage L1-2\", \"Ambulance\", \"Self-present\", \"HEART &#x2265; 7\", \"HEART 4-6\", and \"HEART 0-3\". The x-axis represents odds ratios from 1 to 5. Each subgroup has an associated horizontal line and marker indicating the ratio, with dashed vertical line at 1.0.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3f"><title>Sensitivity analyses</title>
<p>Multiple imputation for &#x003C;&#x202F;2&#x0025; missing timestamps and a per-protocol analysis excluding eight minor-deviation cases yielded similar results (aOR: 2.24, 95&#x0025; CI: 1.41&#x2013;3.55), and an interrupted time-series model demonstrated a level change of &#x002B;17.6&#x202F;percentage points immediately after implementation (<italic>P</italic>&#x2009;&#x003C;&#x2009;0.001) with no pre-intervention secular trend (<xref ref-type="sec" rid="s12">Supplementary Table S2</xref>).</p>
</sec>
<sec id="s3g"><title>Adverse events</title>
<p>No serious adverse events were attributed to the protocol; rates of nitroglycerin-induced hypotension, contrast nephropathy, or medication error were each &#x003C;1&#x0025; and comparable between phases (<xref ref-type="sec" rid="s12">Supplementary Table S3</xref>).</p>
</sec>
</sec>
<sec id="s4" sec-type="discussion"><title>Discussion</title>
<p>This before-after study achieved all prespecified objectives, demonstrating that the patient-needs-enhanced ENAF protocol produced clinically meaningful gains across multiple dimensions of chest-pain care: the proportion of patients receiving an ECG within 10&#x2005;min rose by 18 percentage points, median door-to-troponin time fell by 11&#x2005;min, ENAF documentation completeness improved by 10 points, and median emergency-department length of stay shortened by 0.8&#x2005;h, while 30-day major adverse cardiac events and protocol-related harms remained unchanged. These effect sizes are both statistically robust and operationally significant, indicating that a low-cost, nurse-led, patient-centered workflow can simultaneously accelerate time-critical diagnostics, enhance symptom control and elevate record quality without sacrificing safety.</p>
<p>Our findings both corroborate and extend earlier quality-improvement work on ACS. The 18-percentage-point rise we observed in ECG &#x2264;10&#x2005;min compares favorably with the 43-percentage-point gain reported when U.S. centers created a dedicated ECG room and hired technicians (<xref ref-type="bibr" rid="B16">16</xref>), but it was achieved without extra staff by combining an electronic hard-stop template, a rapid-assessment kit and weekly audit feedback. Pre-hospital ECG programs likewise shorten diagnosis-to-balloon times, yet remain under-utilized even though compelling single-case reports show life-saving impact in ST-segment-elevation myocardial infarction (<xref ref-type="bibr" rid="B17">17</xref>). On the biomarker side, we trimmed door-to-troponin by 11&#x2005;min, echoing rapid rule-out protocols that leverage high-sensitivity cardiac troponin to expedite non-ST-elevation myocardial infarction decisions (<xref ref-type="bibr" rid="B18">18</xref>, <xref ref-type="bibr" rid="B19">19</xref>); our approach, however, embeds specimen collection into the same nursing checklist that triggers the ECG, a design choice that may explain why our effect size exceeds those of earlier Chinese chest-pain-center accreditations. Although point-of-care biomarker testing is emerging for ambulance use (<xref ref-type="bibr" rid="B20">20</xref>), our data show that simple in-hospital workflow redesign can deliver comparable speed gains while awaiting wider adoption of mobile assays. Importantly, we also improved symptom control and documentation completeness&#x2014;dimensions often overlooked in process studies&#x2014;highlighting that a unified checklist can address pain, anxiety and record quality without sacrificing timeliness.</p>
<p>The mechanisms underpinning these gains are consistent with Cognitive Load Theory. By imposing electronic hard stops, the ENAF template removes extraneous memory demands and guides nurses through a fixed sequence of actions, thus preventing omissions at peak workload (<xref ref-type="bibr" rid="B21">21</xref>, <xref ref-type="bibr" rid="B22">22</xref>). Visual prompts embedded in the template and the physical co-location of ECG and blood-draw equipment further reduce intrinsic load and accelerate task initiation, mirroring experimental work in STEMI protocols (<xref ref-type="bibr" rid="B23">23</xref>). Continuous audit-feedback loops reinforce correct behavior and have shown durable effects in ACS QI projects (<xref ref-type="bibr" rid="B24">24</xref>); the sustained upward trend across three ENAF months makes a transient Hawthorne effect unlikely despite the before-after design (<xref ref-type="bibr" rid="B22">22</xref>).</p>
<p>Clinically, these results argue for scaling nurse-led ECG programs in high-volume, resource-constrained emergency departments. Cost-effectiveness analyses estimate that structured ECG deployment in urban India costs as little as US &#x0024;12.65 per quality-adjusted life-year (<xref ref-type="bibr" rid="B25">25</xref>), while person-centered care models consistently dominate usual care on both cost and effectiveness over two- to five-year horizons (<xref ref-type="bibr" rid="B26">26</xref>, <xref ref-type="bibr" rid="B27">27</xref>). When combined with our low-cost electronic template and audit infrastructure, such programs can be rapidly disseminated&#x2014;potentially as part of national ED quality indicators or nursing curricula&#x2014;and do not require physician expansion or capital-intensive technology (<xref ref-type="bibr" rid="B28">28</xref>, <xref ref-type="bibr" rid="B29">29</xref>). Crucially, our data dispel the notion that patient-centered assessment slows critical actions; on the contrary, integrating needs appraisal into the first nursing touchpoint expedited every downstream time target and left 30-day major adverse cardiac events unchanged, underscoring both the efficiency and safety of a holistic, checklist-based approach.</p>
<p>The ENAF protocol is practical for high-volume EDs because it relies on existing nursing staff, an 8-h education package, a low-overhead EMR template with hard-stops, and a pre-positioned rapid chest-pain kit near triage. Implementation occurred at the unit level with no additional staff positions. The protocol was associated with an 18.2-percentage-point increase in ECG &#x2264;10&#x2005;min and a 0.8-h reduction in ED LOS, indicating improved flow without compromise in safety (30-day MACE unchanged). Although not measured formally, high template closure and checklist completion, together with improved pain relief at 30&#x2005;min, suggest good acceptability. The electronic template sits within triage ENAF, triggers early ECG and pre-labels troponin at first contact, and then hands off to routine clinician decision-making within existing ACS pathways, requiring only minor workflow adjustments.</p>
<p>Although we did not collect cost data, the intervention was intentionally resource-light: a one-day (8-h) nurse training package, an EMR template with hard-stops, a pre-positioned &#x201C;rapid chest-pain kit,&#x201D; and brief weekly audit-and-feedback huddles, all delivered with existing staff and infrastructure. These features suggest low marginal costs to implement and maintain. Potential cost offsets, which require formal evaluation, include shorter ED length of stay, fewer workflow delays, and improved documentation quality. Because this study focused on process effectiveness, a future multicenter evaluation should incorporate micro-costing, time-motion, and budget-impact analyses from both hospital and payer perspectives to determine whether the protocol is cost-effective at scale.</p>
<p>This single-center, quasi-experimental design is subject to several limitations. First, the design is vulnerable to secular trends and residual confounding despite prespecified covariate adjustment and sensitivity checks. We cannot exclude unmeasured changes in staffing, case mix, or concurrent initiatives. Second, written informed consent was required. This may have preferentially enrolled patients able to consent, potentially limiting generalizability to populations with communication barriers or severe illness. Third, performance bias is possible because clinical staff could not be blinded to a unit-level workflow change. Fourth, timing measures relied on routine time-stamps. Although missingness was low, small clock drift and documentation variability could affect some secondary outcomes. Fifth, the study was powered for process endpoints. The 30-day MACE analysis was underpowered to detect modest safety differences, and events beyond 30 days were not assessed. Our tertiary urban setting with established informatics support may limit external validity for low-resource emergency departments. We did not collect cost data, our economic comments are therefore conceptual and highlight the need for a formal, prespecified economic evaluation in future multicenter studies. To assess reproducibility across different case mixes, ED volumes, informatics maturity, and staffing models, multicenter studies, ideally cluster-randomized or stepped-wedge designs to manage contamination, are warranted. Such trials should predefine core process and safety outcomes, capture implementation metrics, and embed a concurrent economic evaluation.</p>
<p>Causal confirmation and implementation guidance would benefit from multicenter cluster-randomized or stepped-wedge trials comparing ENAF with standard triage. Key priorities include prespecified subgroup analyses by HEART risk strata, arrival mode, and triage acuity to characterize heterogeneity of effect, a core outcome set for chest-pain triage covering time-to-ECG, door-to-troponin, timely analgesia, documentation quality, ED length of stay, and 90-day safety, implementation-science measures (fidelity, acceptability, time-motion) and cost-effectiveness to inform scale-up in resource-constrained settings, and development of a standardized ENAF training and competency package to enhance reproducibility across platforms and staffing models.</p>
</sec>
<sec id="s5" sec-type="conclusions"><title>Conclusions</title>
<p>Embedding a concise, patient-centered clinical-needs module within the Emergency Nursing Assessment Framework markedly accelerated time-critical diagnostics for non-traumatic chest pain and elevated documentation quality without increasing adverse events, demonstrating that comprehensive assessment and rapid care are not mutually exclusive. Given its low marginal resource requirements, multicenter evaluation with an embedded economic analysis is a logical next step to establish generalizability and value.</p>
</sec>
</body>
<back>
<sec id="s6" sec-type="data-availability"><title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec id="s7" sec-type="ethics-statement"><title>Ethics statement</title>
<p>The studies involving humans were approved by the Institutional Review Board of Third Affiliated Hospital of Naval Medical University, and complied with the Declaration of Helsinki. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.</p>
</sec>
<sec id="s8" sec-type="author-contributions"><title>Author contributions</title>
<p>YS: Investigation, Methodology, Writing &#x2013; original draft. XL: Methodology, Writing &#x2013; original draft. LS: Methodology, Writing &#x2013; original draft. FZ: Conceptualization, Investigation, Writing &#x2013; review &#x0026; editing. KX: Conceptualization, Writing &#x2013; review &#x0026; editing.</p>
</sec>
<sec id="s10" sec-type="COI-statement"><title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="s11" sec-type="ai-statement"><title>Generative AI statement</title>
<p>The author(s) declare that no Generative AI was used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p>
</sec>
<sec id="s13" sec-type="disclaimer"><title>Publisher&#x0027;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec id="s12" sec-type="supplementary-material"><title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fcvm.2025.1663769/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fcvm.2025.1663769/full&#x0023;supplementary-material</ext-link></p>
<supplementary-material xlink:href="Table1.docx" id="SM1" mimetype="application/vnd.openxmlformats-officedocument.wordprocessingml.document"/>
<supplementary-material xlink:href="Table2.docx" id="SM2" mimetype="application/vnd.openxmlformats-officedocument.wordprocessingml.document"/>
<supplementary-material xlink:href="Table3.docx" id="SM3" mimetype="application/vnd.openxmlformats-officedocument.wordprocessingml.document"/>
</sec>
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<fn-group>
<fn id="n1" fn-type="custom" custom-type="edited-by"><p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3145804/overview">Federica Dellafiore</ext-link>, Link Campus University, Italy</p></fn>
<fn id="n2" fn-type="custom" custom-type="reviewed-by"><p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3047944/overview">Pierpaolo Servi</ext-link>, San Matteo Hospital Foundation (IRCCS), Italy</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3182633/overview">Orejeta Diamanti</ext-link>, Veneto Institute of Oncology (IRCCS), Italy</p></fn>
</fn-group>
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