<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v2.0 20040830//EN" "journalpublishing.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="2.0" xml:lang="en" article-type="research-article"><front><journal-meta><journal-id journal-id-type="nlm-ta">JMIR Pediatr Parent</journal-id><journal-id journal-id-type="publisher-id">pediatrics</journal-id><journal-id journal-id-type="index">30</journal-id><journal-title>JMIR Pediatrics and Parenting</journal-title><abbrev-journal-title>JMIR Pediatr Parent</abbrev-journal-title><issn pub-type="epub">2561-6722</issn><publisher><publisher-name>JMIR Publications</publisher-name><publisher-loc>Toronto, Canada</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">v8i1e74964</article-id><article-id pub-id-type="doi">10.2196/74964</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Paper</subject></subj-group></article-categories><title-group><article-title>Evaluation of the Use of a Novel Intelligent Diagnosis and Cost Control System on Pediatric Bronchopneumonia Outcomes: Retrospective Cohort Study</article-title></title-group><contrib-group><contrib contrib-type="author"><name name-style="western"><surname>Wu</surname><given-names>Yanjun</given-names></name><degrees>MM</degrees><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="aff" rid="aff2">2</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Liu</surname><given-names>Kaijie</given-names></name><degrees>MAM</degrees><xref ref-type="aff" rid="aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Mao</surname><given-names>Xinli</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="aff3">3</xref></contrib><contrib contrib-type="author" equal-contrib="yes"><name name-style="western"><surname>Wu</surname><given-names>Danjie</given-names></name><degrees>MM</degrees><xref ref-type="aff" rid="aff4">4</xref><xref ref-type="fn" rid="equal-contrib1">*</xref></contrib><contrib contrib-type="author" corresp="yes" equal-contrib="yes"><name name-style="western"><surname>Zhu</surname><given-names>Feng</given-names></name><degrees>BAM</degrees><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="fn" rid="equal-contrib1">*</xref></contrib></contrib-group><aff id="aff1"><institution>Department of Medical Affairs, Taizhou Hospital of Zhejiang Province</institution><addr-line>150 Ximen Street</addr-line><addr-line>Linhai City</addr-line><country>China</country></aff><aff id="aff2"><institution>Department of Pediatrics, Taizhou Hospital of Zhejiang Province</institution><addr-line>Linhai City</addr-line><addr-line>Zhejiang Province</addr-line><country>China</country></aff><aff id="aff3"><institution>Department of Gastroenterology, Taizhou Hospital of Zhejiang Province</institution><addr-line>Linhai City</addr-line><addr-line>Zhejiang Province</addr-line><country>China</country></aff><aff id="aff4"><institution>Department of Stomatology, Taizhou Hospital of Zhejiang Province</institution><addr-line>Linhai City</addr-line><addr-line>Zhejiang Province</addr-line><country>China</country></aff><contrib-group><contrib contrib-type="editor"><name name-style="western"><surname>Badawy</surname><given-names>Sherif</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="reviewer"><name name-style="western"><surname>Poddighe</surname><given-names>Dimitri</given-names></name></contrib><contrib contrib-type="reviewer"><name name-style="western"><surname>Dezfouli</surname><given-names>Sepehr Abbasi</given-names></name></contrib></contrib-group><author-notes><corresp>Correspondence to Feng Zhu, BAM, Department of Medical Affairs, Taizhou Hospital of Zhejiang Province, 150 Ximen Street, Linhai City, 317000, China, 86 0576-85120120; <email>zhuf@enzemed.com</email></corresp><fn fn-type="equal" id="equal-contrib1"><label>*</label><p>these authors contributed equally</p></fn></author-notes><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>15</day><month>10</month><year>2025</year></pub-date><volume>8</volume><elocation-id>e74964</elocation-id><history><date date-type="received"><day>26</day><month>03</month><year>2025</year></date><date date-type="rev-recd"><day>12</day><month>09</month><year>2025</year></date><date date-type="accepted"><day>20</day><month>09</month><year>2025</year></date></history><copyright-statement>&#x00A9; Yanjun Wu, Kaijie Liu, Xinli Mao, Danjie Wu, Feng Zhu. Originally published in JMIR Pediatrics and Parenting (<ext-link ext-link-type="uri" xlink:href="https://pediatrics.jmir.org">https://pediatrics.jmir.org</ext-link>), 15.10.2025. </copyright-statement><copyright-year>2025</copyright-year><license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Pediatrics and Parenting, is properly cited. The complete bibliographic information, a link to the original publication on <ext-link ext-link-type="uri" xlink:href="https://pediatrics.jmir.org">https://pediatrics.jmir.org</ext-link>, as well as this copyright and license information must be included.</p></license><self-uri xlink:type="simple" xlink:href="https://pediatrics.jmir.org/2025/1/e74964"/><abstract><sec><title>Background</title><p>Health care systems face challenges of inconsistent quality, inefficiency, and rising costs. Fragmented applications of clinical decision support systems (CDSSs), clinical pathways (CPs), and diagnosis-related group (DRG) payment systems have limited their synergistic potential.</p></sec><sec><title>Objective</title><p>This study proposed a CDSS-CP-DRG closed-loop model enabled by digital health technologies; specifically, the CDSS optimized CP execution through real-time data, the CP standardized workflows to support DRG cost control, and DRG payment pressures drove iterative improvements in both technology and processes. This research aimed to validate the model&#x2019;s effectiveness in clinical efficacy, cost control, and standardized diagnosis and treatment of bronchopneumonia in children and provide evidence for value-based health care transformation.</p></sec><sec sec-type="methods"><title>Methods</title><p>A total of 4543 children with bronchopneumonia were selected and divided into the experimental or control group based on whether the intelligent diagnosis and cost control system was used in the diagnostic process. Chi-square test, 1-way analysis of variance, paired <italic>t</italic> test, multiple regression analysis, and other mathematical statistical methods were used to verify the difference between the outcomes of the two groups of patients.</p></sec><sec sec-type="results"><title>Results</title><p>This study demonstrated comparably high cure rates in both groups (<italic>P</italic>&#x003E;.05). However, the experimental group exhibited a 0.4-day reduction in average length of stay, 12.3% lower total hospitalization costs, RMB 135.3 (US $19) higher medical insurance reimbursement surplus, and a reduction of 0.16 defined daily doses of antibiotic use intensity versus the control group (<italic>P</italic>&#x003C;.05 for all significant differences).</p></sec><sec sec-type="conclusions"><title>Conclusions</title><p>The novel intelligent diagnosis and cost control system demonstrated significant improvement in clinical effect, cost control, and standardized treatment for pediatric bronchopneumonia, but the CP for pediatric pneumonia requiring intensive care still needs further attention and adjustment.</p></sec></abstract><kwd-group><kwd>intelligent diagnosis and cost control system</kwd><kwd>clinical decision support system</kwd><kwd>clinical pathway</kwd><kwd>diagnosis-related group</kwd><kwd>pediatric bronchopneumonia</kwd><kwd>evaluation</kwd><kwd>medical expenses</kwd><kwd>treatment outcomes</kwd></kwd-group></article-meta></front><body><sec id="s1" sec-type="intro"><title>Introduction</title><sec id="s1-1"><title>Background</title><p>Bronchopneumonia, a prevalent lower respiratory tract infection, exhibits high incidence in children globally [<xref ref-type="bibr" rid="ref1">1</xref>], with approximately 150 million annual cases among those aged 0&#x2010;5 years. Severe cases requiring hospitalization account for 12.82% of affected children [<xref ref-type="bibr" rid="ref2">2</xref>,<xref ref-type="bibr" rid="ref3">3</xref>], imposing substantial health burdens and socioeconomic costs [<xref ref-type="bibr" rid="ref4">4</xref>].</p><p>Clinical decision support systems (CDSSs) integrate patient-specific data with computerized knowledge bases to generate evidence-based recommendations through software algorithms, representing a pivotal advancement in health informatics [<xref ref-type="bibr" rid="ref5">5</xref>,<xref ref-type="bibr" rid="ref6">6</xref>]. Pediatric applications demonstrate the capacity of CDSSs to enhance diagnostic accuracy, reduce errors, and improve workflow efficiency via intelligent alerts [<xref ref-type="bibr" rid="ref7">7</xref>]. In addition, standardization of treatment through the use of clinical pathways (CPs) has proven to be an effective way to streamline care in a way that minimizes errors and cost while improving outcomes [<xref ref-type="bibr" rid="ref8">8</xref>].</p><p>Although these information-based systems hold transformative potential for global health care digitalization, rigorous economic evaluations and real-world effectiveness analyses remain scarce, with most evidence derived from narrative reviews rather than empirical data.</p></sec><sec id="s1-2"><title>The Design and Implementation Path of a Novel Intelligent Diagnosis and Cost Control System</title><p>As shown in <xref ref-type="fig" rid="figure1">Figure 1</xref>, the artificial intelligence (AI)&#x2013;driven CP optimization and cost containment system uses generalizable identification mechanisms and data-intelligent decision-making, integrating natural language processing, data mining, and machine learning technologies. It is integrated with core hospital information systems including electronic medical records, the laboratory information system, and the picture archiving and communication system. The system constructs disease-specific smart CPs that synchronize treatment quality assurance with expenditure control. This machine learning&#x2013;powered architecture enables granular diagnosis-related group (DRG) adaptation, achieving precision treatment protocols (dynamic pathway optimization based on real-time patient status monitoring), intelligent cost governance (automated detection of billing deviations through natural language processing&#x2013;based charge item analysis), and quality-cost balance (continuous learning from multisource clinical data to maintain care standards while reducing low-value services).</p><fig position="float" id="figure1"><label>Figure 1.</label><caption><p>Closed-loop management framework of the intelligent decision and cost control system. DRG: diagnosis-related group.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="pediatrics_v8i1e74964_fig01.png"/></fig></sec><sec id="s1-3"><title>Implementation Pathway and Core Functions</title><p>The intelligent diagnosis and cost control system (IDCCS) operates through a streamlined workflow, integrating multisource data from hospital systems (eg, hospital information system, laboratory information system, picture archiving and communication system, electronic medical records), followed by automated data cleaning and standardization. It features customizable CPs with DRG-based treatment branches and preimplementation cost simulations using historical data. The system establishes baselines through retrospective data analysis, then automatically enrolls eligible patients into pathways. During treatment, it provides real-time clinical decision support with deviation alerts requiring clinician confirmation, while monitoring prescription appropriateness and forecasting costs with early warnings. Posttreatment multidimensional analytics evaluate pathway efficacy, supporting continuous optimization.</p></sec><sec id="s1-4"><title>Study Goal</title><p>This retrospective study analyzed the clinical outcomes, cost containment, and treatment standardization metrics of children with bronchopneumonia in a tertiary hospital in Eastern China (May 2023 to November 2024) and compared the difference of using or not using the IDCCS on these treatment outcome indicators. The findings provided empirical evidence for developing specialized and systematic intelligent CDSSs integrating cost-effective quality control in pediatric respiratory treatment.</p></sec></sec><sec id="s2" sec-type="methods"><title>Methods</title><sec id="s2-1"><title>Study Design</title><p>We designed a retrospective cohort study to analyze the differences in the results of 3 dimensions of treatment outcomes of hospitalized children with pneumonia for whom the IDCCS was used or was not used. The specific indicators of the 3 dimensions were as follows. The indicator of clinical efficacy was whether the disease improved. The economic indicators included length of hospital stay, total hospitalization expenses, proportion of drugs and consumables in expenses, and medical insurance settlement balance. The standardized diagnosis and treatment index was the volume of antibiotics dispensed (defined daily dose [DDD]).</p><p>Antibiotic therapy remains pivotal in pediatric pneumonia management [<xref ref-type="bibr" rid="ref9">9</xref>]. The selection of DDD for evaluating antibiotic therapy compliance and normative treatment aligns with international guidelines [<xref ref-type="bibr" rid="ref10">10</xref>,<xref ref-type="bibr" rid="ref11">11</xref>]. This metric demonstrates superior validity in quantifying adherence to evidence-based protocols while balancing clinical relevance, operational feasibility, and comparability across multicenter studies [<xref ref-type="bibr" rid="ref12">12</xref>]. The quantitative indicators including length of stay and health care costs can serve as economic end points to further validate the IDCCS&#x2019;s beneficial effects on treatment outcomes through cost analysis and resource utilization evaluation. These metrics&#x2019; integration with CDSSs enables real-time feedback.</p></sec><sec id="s2-2"><title>IDCCS Evaluation</title><sec id="s2-2-1"><title>Participants and Setting</title><p>This study was carried out at a tertiary hospital in Eastern China. The deployment of the IDCCS in December 2023 served as a natural intervention. Accordingly, patients retrospectively enrolled from the preimplementation phase (January to November 2023) comprised the control group. Conversely, patients from the postimplementation phase (the corresponding period in 2024) comprised the experimental group.</p><p>Information was collected for patients admitted to the hospital with the diagnosis of &#x201C;bronchial pneumonia&#x201D; and aged &#x003C;14 years. The experimental group consisted of patients for whom the IDCCS was used (n=1658), and the control group consisted of patients for whom the IDCCS was not used (n=2885).</p><p>Cases were excluded if their medical records had home pages with incomplete information or important fields missing, home pages with errors, hospitalization expenses with outliers, hospitalization expenses below 100 yuan (US $13.95), hospitalization days below 0.1 days; ultimately, records for 4543 children were retained.</p></sec><sec id="s2-2-2"><title>Data Collection</title><p>All the data were extracted from the hospital&#x2019;s internal database. To describe the population included in the study, the following variables were extracted at baseline: age, sex, diagnosis, with coinfection or not, and treatment result.</p></sec></sec><sec id="s2-3"><title>Statistical Analysis</title><p>Statistical analyses were conducted using SPSS for Windows (version 23.0; IBM Corp). Categorical data were denoted in numbers and percentages, while continuous variables were represented as means and SDs. Data normality and homoscedasticity were preliminarily verified before executing each statistical analysis.</p><p>The <italic>&#x03C7;</italic><sup>2</sup> test was used to compare the differences in categorical variable indicators between the experimental group and the control group (gender, diagnosis results of disease severity, concurrent infections, treatment outcomes). Paired <italic>t</italic> test and 1-way ANOVA were used to test the differences in continuous variables of the research subjects (length of hospital stay, total hospitalization cost, proportion of drug and consumable costs in the total cost, balance of medical insurance settlement, DDD).</p><p>For all tests, a <italic>P</italic> value &#x2264;.05 was considered statistically significant.</p><p>Furthermore, in the comparison of treatment outcome differences, we not only conducted the analysis of the overall experimental group and intervention group, but also further divided the patients based on whether they required intensive care and whether they had severe complications or comorbidities, and then conducted further analysis separately.</p></sec><sec id="s2-4"><title>Ethical Considerations</title><p>This study, conducted in accordance with the Declaration of Helsinki, received approval from the institutional review board of Taizhou Hospital of Zhejiang Province (K20250873). As it was a retrospective study involving the analysis of existing, anonymized data, the requirement for informed consent was waived by the ethics committee. To ensure data security and patient confidentiality, all personally identifiable information was removed prior to analysis. The data were accessed strictly for research purposes and stored on secure, password-protected hospital servers [<xref ref-type="bibr" rid="ref13">13</xref>].</p></sec></sec><sec id="s3" sec-type="results"><title>Results</title><sec id="s3-1"><title>Overview</title><p>Among the 4543 patients included in the study, 1658 were in the IDCCS-used (experimental) group, and 2885 were in the IDCCS-without (control) group. Data on demographic characteristics, discharge diagnosis, coinfection with or without, and treatment outcomes of the patients are provided in <xref ref-type="table" rid="table1">Table 1</xref>. No statistically significant differences were observed in age or sex distribution between the experimental and control groups (<italic>P&#x003E;</italic>.05).</p><table-wrap id="t1" position="float"><label>Table 1.</label><caption><p>Characteristics of participants in the study sample (N=4543).</p></caption><table id="table1" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom" colspan="2">Characteristics</td><td align="left" valign="bottom">Control (n=2885)</td><td align="left" valign="bottom">Experimental (n=1658)</td><td align="left" valign="bottom">Total missing, n (%)</td><td align="left" valign="bottom"><italic>F</italic> test/chi-square (<italic>df</italic>)</td></tr></thead><tbody><tr><td align="left" valign="top"/><td align="left" valign="top">Age (years), mean (SD)</td><td align="left" valign="top">4.17 (3.16)</td><td align="left" valign="top">3.54 (3.12)</td><td align="left" valign="top">0 (0)</td><td align="left" valign="top">1.9 (1, 4543)<sup><xref ref-type="table-fn" rid="table1fn1">a</xref></sup></td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Sex (female), n (%)</td><td align="left" valign="top">772 (46.6)</td><td align="left" valign="top">596 (48)</td><td align="left" valign="top">1643 (36.2)</td><td align="left" valign="top">0.4 (1, 1368)<sup><xref ref-type="table-fn" rid="table1fn2">b</xref></sup></td></tr><tr><td align="left" valign="top" colspan="2">Discharge diagnosis</td><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia</td><td align="left" valign="top">2577 (89.3)</td><td align="left" valign="top">1648 (99.4)</td><td align="left" valign="top">0 (0)</td><td align="left" valign="top">165.0<sup><xref ref-type="table-fn" rid="table1fn3">c</xref></sup> (2, 4413)<sup><xref ref-type="table-fn" rid="table1fn2">b</xref></sup></td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia requiring intensive care</td><td align="left" valign="top">178 (6.2)</td><td align="left" valign="top">10 (0.6)</td><td align="left" valign="top"/><td align="left" valign="top"/></tr><tr><td align="left" valign="top" colspan="2">Coinfection</td><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Without</td><td align="left" valign="top">2324 (80.6)</td><td align="left" valign="top">1067 (64.4)</td><td align="left" valign="top">0 (0)</td><td align="left" valign="top">146.0<sup><xref ref-type="table-fn" rid="table1fn3">c</xref></sup> (2, 4543)<sup><xref ref-type="table-fn" rid="table1fn2">b</xref></sup></td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">With</td><td align="left" valign="top">561 (19.4)</td><td align="left" valign="top">591 (35.6)</td><td align="left" valign="top"/><td align="left" valign="top"/></tr><tr><td align="left" valign="top" colspan="2">Treatment outcome</td><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Improved</td><td align="left" valign="top">2840 (99.27)</td><td align="left" valign="top">1647 (99.34)</td><td align="left" valign="top">24 (0.5)</td><td align="left" valign="top">2.5 (2, 4159)<sup><xref ref-type="table-fn" rid="table1fn2">b</xref></sup></td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Unresolved</td><td align="left" valign="top">22 (0.77)</td><td align="left" valign="top">9 (0.54)</td><td align="left" valign="top"/><td align="left" valign="top"/></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Death</td><td align="left" valign="top">0 (0)</td><td align="left" valign="top">1 (0.06)</td><td align="left" valign="top"/><td align="left" valign="top"/></tr></tbody></table><table-wrap-foot><fn id="table1fn1"><p><sup>a</sup><italic>F</italic> test.</p></fn><fn id="table1fn2"><p><sup>b</sup>Chi-square test.</p></fn><fn id="table1fn3"><p><sup>c</sup><italic>P</italic>&#x003C;.001.</p></fn></table-wrap-foot></table-wrap></sec><sec id="s3-2"><title>Clinical Efficacy</title><p>Participants were stratified into 3 diagnostic subgroups: pediatric pneumonia, pediatric pneumonia requiring intensive care, and pediatric pneumonia with severe comorbidities and complications. Statistical analysis revealed no significant differences in treatment outcomes between the intervention and control groups across these subgroups (<italic>P</italic>&#x003E;.05) (<xref ref-type="table" rid="table2">Table 2</xref>).</p><table-wrap id="t2" position="float"><label>Table 2.</label><caption><p>The differences in treatment outcomes among participants in different diagnostic subgroups.</p></caption><table id="table2" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom" colspan="2"/><td align="left" valign="bottom">Control (n=2554)</td><td align="left" valign="bottom">Experimental (n=1647)</td><td align="left" valign="bottom">Chi-square (<italic>df</italic>)</td></tr></thead><tbody><tr><td align="left" valign="top" colspan="5">Pediatric pneumonia</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Improved</td><td align="left" valign="top">2534 (99.2)</td><td align="left" valign="top">1637 (99.4)</td><td align="left" valign="top">2.4 (2)</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Unresolved</td><td align="left" valign="top">20 (69)</td><td align="left" valign="top">9 (31)</td><td align="left" valign="top"/></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Death</td><td align="left" valign="top">0 (0)</td><td align="left" valign="top">1 (0.1)</td><td align="left" valign="top"/></tr><tr><td align="left" valign="top" colspan="5">Pediatric pneumonia requiring intensive care</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Improved</td><td align="left" valign="top">176 (98.9)</td><td align="left" valign="top">10 (100)</td><td align="left" valign="top">0.1 (1)</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Unresolved</td><td align="left" valign="top">2 (1.1)</td><td align="left" valign="top">0 (0)</td><td align="left" valign="top"/></tr><tr><td align="left" valign="top" colspan="5">Pediatric pneumonia with severe comorbidities and complications</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Improved</td><td align="left" valign="top">130 (100)</td><td align="left" valign="top">&#x2014;<sup><xref ref-type="table-fn" rid="table2fn1">a</xref></sup></td><td align="left" valign="top"/></tr></tbody></table><table-wrap-foot><fn id="table2fn1"><p><sup>a</sup>Not applicable.</p></fn></table-wrap-foot></table-wrap></sec><sec id="s3-3"><title>Economic Indicators</title><p>As shown in the analytical data in <xref ref-type="table" rid="table3">Table 3</xref>, following the implementation of the IDCCS, the experimental groups demonstrated a statistically significant reduction in the length of stay by 0.4 days (<italic>P</italic>&#x003C;.001), with total hospitalization expenses decreasing by 12.2% (RMB 508.56 [US $71.43]) and medical insurance settlement balance increasing by RMB 135.3 (US $19; both <italic>P</italic>&#x003C;.001).</p><p>Further group analysis found that the previously mentioned indicators of patients with pneumonia in the experimental group were improved. However, no significant differences were observed in the pediatric pneumonia subgroup requiring intensive care (<italic>P</italic>&#x003E;.05).</p><table-wrap id="t3" position="float"><label>Table 3.</label><caption><p>Differences in economic indicators of all participants.</p></caption><table id="table3" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom" colspan="2"/><td align="left" valign="bottom" colspan="3">Control (n=2885)</td><td align="left" valign="bottom" colspan="3">Experimental (n=1658)</td><td align="left" valign="bottom"/><td align="left" valign="bottom"/></tr><tr><td align="left" valign="top" colspan="2"/><td align="left" valign="top">Mean</td><td align="left" valign="top">SD</td><td align="left" valign="top">95% CI</td><td align="left" valign="top">Mean</td><td align="left" valign="top">SD</td><td align="left" valign="top">95% CI</td><td align="left" valign="top"><italic>F</italic> test (<italic>df</italic>)</td><td align="left" valign="top"><italic>P</italic> value</td></tr></thead><tbody><tr><td align="left" valign="top" colspan="2">Length of hospital stay</td><td align="left" valign="top">6.5</td><td align="left" valign="top">0.0</td><td align="left" valign="top">6.4 to 6.6</td><td align="left" valign="top">6.1</td><td align="left" valign="top">0.0</td><td align="left" valign="top">6.0 to 6.2</td><td align="left" valign="top">32.7 (1)</td><td align="left" valign="top">&#x003C;.001</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia</td><td align="left" valign="top">6.3</td><td align="left" valign="top">0.0</td><td align="left" valign="top">6.2 to 6.4</td><td align="left" valign="top">6.1</td><td align="left" valign="top">0.0</td><td align="left" valign="top">6.0 to 6.2</td><td align="left" valign="top">10.2 (1)</td><td align="left" valign="top">.001</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia requiring intensive care</td><td align="left" valign="top">7.9</td><td align="left" valign="top">0.0</td><td align="left" valign="top">7.5 to 8.3</td><td align="left" valign="top">8.9</td><td align="left" valign="top">0.0</td><td align="left" valign="top">7.7 to 10.4</td><td align="left" valign="top">1.4 (1)</td><td align="left" valign="top">.24</td></tr><tr><td align="left" valign="top" colspan="2">Total hospitalization expenses</td><td align="left" valign="top">4153.9</td><td align="left" valign="top">0.2</td><td align="left" valign="top">4086.2 to 4225.9</td><td align="left" valign="top">3645.4</td><td align="left" valign="top">1.1</td><td align="left" valign="top">3588.8 to 3711.6</td><td align="left" valign="top">104.5 (1)</td><td align="left" valign="top">&#x003C;.001</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia</td><td align="left" valign="top">3824.4</td><td align="left" valign="top">&#x2013;0.3</td><td align="left" valign="top">3770.5 to 3884.0</td><td align="left" valign="top">3610.4</td><td align="left" valign="top">&#x2013;0.7</td><td align="left" valign="top">3559.0 to 3663.5</td><td align="left" valign="top">28.9 (1)</td><td align="left" valign="top">&#x003C;.001</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia requiring intensive care</td><td align="left" valign="top">7266.5</td><td align="left" valign="top">&#x2013;3.0</td><td align="left" valign="top">6829.9 to 7748.0</td><td align="left" valign="top">9410.2</td><td align="left" valign="top">20.89</td><td align="left" valign="top">7578.5 to 11,828.3</td><td align="left" valign="top">4.5 (1)</td><td align="left" valign="top">.04</td></tr><tr><td align="left" valign="top" colspan="2">Proportion of drugs and consumables in expenses</td><td align="left" valign="top">0.1</td><td align="left" valign="top">0.0</td><td align="left" valign="top">0.1 to 0.1</td><td align="left" valign="top">0.1</td><td align="left" valign="top">0.0</td><td align="left" valign="top">0.1 to 0.1</td><td align="left" valign="top">0.5 (1)</td><td align="left" valign="top">.49</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia</td><td align="left" valign="top">0.1</td><td align="left" valign="top">0.0</td><td align="left" valign="top">0.1 to 0.1</td><td align="left" valign="top">0.1</td><td align="left" valign="top">0.0</td><td align="left" valign="top">0.1 to 0.1</td><td align="left" valign="top">4.0 (1)</td><td align="left" valign="top">.046</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia requiring intensive care</td><td align="left" valign="top">0.1</td><td align="left" valign="top">0.0</td><td align="left" valign="top">0.1 to 0.2</td><td align="left" valign="top">0.1</td><td align="left" valign="top">0.0</td><td align="left" valign="top">0.1 to 0.2</td><td align="left" valign="top">1.3 (1)</td><td align="left" valign="top">.25</td></tr><tr><td align="left" valign="top" colspan="2">Medical insurance settlement balance</td><td align="left" valign="top">&#x2013;457.0</td><td align="left" valign="top">&#x2013;0.4</td><td align="left" valign="top">&#x2013;508.6 to &#x2013;405.1</td><td align="left" valign="top">&#x2212;321.7</td><td align="left" valign="top">&#x2212;1.7</td><td align="left" valign="top">&#x2013;377.0 to &#x2013;272.0</td><td align="left" valign="top">11.8 (1)</td><td align="left" valign="top">&#x003C;.001</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia</td><td align="left" valign="top">&#x2013;533.7</td><td align="left" valign="top">&#x2013;0.7</td><td align="left" valign="top">&#x2013;581.7 to &#x2013;485.4</td><td align="left" valign="top">193.6</td><td align="left" valign="top">1.0</td><td align="left" valign="top">&#x2013;390.8 to &#x2013;290.1</td><td align="left" valign="top">28.3 (1)</td><td align="left" valign="top">&#x003C;.001</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Pediatric pneumonia requiring intensive care</td><td align="left" valign="top">715.0</td><td align="left" valign="top">&#x2013;5.0</td><td align="left" valign="top">381.6 to 1052.1</td><td align="left" valign="top">2704.7</td><td align="left" valign="top">12.4</td><td align="left" valign="top">135.8 to 5335.7</td><td align="left" valign="top">6.1 (1)</td><td align="left" valign="top">.01</td></tr></tbody></table></table-wrap></sec><sec id="s3-4"><title>Standardized Diagnosis and Treatment</title><p><xref ref-type="table" rid="table4">Table 4</xref> demonstrates that while the experimental group showed a modest reduction in mean antibiotic prescribing intensity (&#x2212;0.1 DDD) compared to the control group, this system-wide effect was not statistically significant (<italic>P</italic>=.21). However, in the pediatric pneumonia subgroup that leveraged the clinical decision support features of the IDCCS, we observed a statistically and clinically meaningful reduction in antimicrobial exposure intensity (&#x2212;0.2 DDD; <italic>P</italic>=.002), representing a 6.8% decrease compared to the control group.</p><table-wrap id="t4" position="float"><label>Table 4.</label><caption><p>Differences in antibiotic use intensity among participants.</p></caption><table id="table4" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom" colspan="2"/><td align="left" valign="bottom" colspan="3">Control (n=2588)</td><td align="left" valign="bottom" colspan="3">Experimental (n=1613)</td><td align="left" valign="bottom"/><td align="left" valign="bottom"/></tr><tr><td align="left" valign="top" colspan="2"/><td align="left" valign="top">Mean</td><td align="left" valign="top">SD</td><td align="left" valign="top">95% CI</td><td align="left" valign="top">Mean</td><td align="left" valign="top">SD</td><td align="left" valign="top">95% CI</td><td align="left" valign="top"><italic>F</italic> test (<italic>df</italic>)</td><td align="left" valign="top"><italic>P</italic> value</td></tr></thead><tbody><tr><td align="left" valign="top" colspan="2">All participants</td><td align="left" valign="top">2.3</td><td align="left" valign="top">0.0002</td><td align="left" valign="top">2.3 to 2.4</td><td align="left" valign="top">2.3</td><td align="left" valign="top">&#x2212;0.0006</td><td align="left" valign="top">2.2 to 2.4</td><td align="left" valign="top">1.6 (1)</td><td align="left" valign="top">.21</td></tr><tr><td align="left" valign="top" colspan="2">Discharge diagnosis</td><td align="left" valign="top">2.3</td><td align="left" valign="top">&#x2212;0.0004</td><td align="left" valign="top">2.2 to 2.3</td><td align="left" valign="top">2.3</td><td align="left" valign="top">&#x2212;0.0010</td><td align="left" valign="top">2.2 to 2.3</td><td align="left" valign="top">0.0 (1)</td><td align="left" valign="top">.97</td></tr><tr><td align="left" valign="top" rowspan="2"/><td align="left" valign="top">Pediatric pneumonia</td><td align="left" valign="top">2.3</td><td align="left" valign="top">0.0020</td><td align="left" valign="top">2.1 to 2.6</td><td align="left" valign="top">2.2</td><td align="left" valign="top">&#x2212;0.0132</td><td align="left" valign="top">2.0 to 2.3</td><td align="left" valign="top">9.8 (1)</td><td align="left" valign="top">.002</td></tr><tr><td align="left" valign="top">Pediatric pneumonia requiring intensive care</td><td align="left" valign="top">2.4</td><td align="left" valign="top">0.0010</td><td align="left" valign="top">2.3 to 2.5</td><td align="left" valign="top">2.3</td><td align="left" valign="top">0.0004</td><td align="left" valign="top">2.2 to 2.4</td><td align="left" valign="top">1.7 (1)</td><td align="left" valign="top">.19</td></tr><tr><td align="left" valign="top" colspan="2">Coinfection</td><td align="left" valign="top">2.1</td><td align="left" valign="top">0.0029</td><td align="left" valign="top">1.9 to 2.3</td><td align="left" valign="top">2.2</td><td align="left" valign="top">&#x2212;0.0021</td><td align="left" valign="top">2.1 to 2.3</td><td align="left" valign="top">1.1 (1)</td><td align="left" valign="top">.30</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">Without</td><td align="left" valign="top">2.3</td><td align="left" valign="top">0.0002</td><td align="left" valign="top">2.3 to 2.4</td><td align="left" valign="top">2.3</td><td align="left" valign="top">&#x2212;0.0006</td><td align="left" valign="top">2.2 to 2.4</td><td align="left" valign="top">1.6 (1)</td><td align="left" valign="top">.21</td></tr><tr><td align="left" valign="top"/><td align="left" valign="top">With</td><td align="left" valign="top">2.3</td><td align="left" valign="top">&#x2212;0.0004</td><td align="left" valign="top">2.2 to 2.3</td><td align="left" valign="top">2.3</td><td align="left" valign="top">&#x2212;0.0010</td><td align="left" valign="top">2.2 to 2.3</td><td align="left" valign="top">0.0 (1)</td><td align="left" valign="top">.97</td></tr></tbody></table></table-wrap></sec></sec><sec id="s4" sec-type="discussion"><title>Discussion</title><sec id="s4-1"><title>Principal Results</title><p>Our findings demonstrate that implementing the IDCCS CDSS significantly reduced treatment costs and improved standardized treatment in pediatric pneumonia management [<xref ref-type="bibr" rid="ref14">14</xref>]. The digital intervention was associated with a reduction in the length of stay, a decrease in total hospitalization expenses, an increase in the medical insurance settlement balance, and a reduction in antibiotic prescribing volumes [<xref ref-type="bibr" rid="ref15">15</xref>].</p><p>These results highlight the dual benefits of AI-driven decision support in enhancing value-based treatment while maintaining normative treatment quality.</p><p>However, within our study, in the pediatric pneumonia subgroup requiring intensive care, the aforementioned outcome metrics demonstrated no statistically significant improvement, suggesting that the current CP algorithms in the intelligent diagnosis assistance system require further optimization for use in critically ill patient populations.</p></sec><sec id="s4-2"><title>Interpretation and Comparison With Prior Work</title><p>Extensive international research demonstrates that health information technology, characterized by accessibility, feasibility, and efficiency, significantly reduces antibiotic resistance rates, antimicrobial therapy mortality, and health care costs [<xref ref-type="bibr" rid="ref16">16</xref>-<xref ref-type="bibr" rid="ref19">19</xref>].</p><p>Christensen et al [<xref ref-type="bibr" rid="ref20">20</xref>] put forward that CDSSs were designed according to the &#x201C;Five Rights&#x201D; principle: delivering the right information to the right recipient at the right time, through the right channel, in the right format. As a tool for auxiliary diagnosis, CDSS can improve the quality and efficiency of diagnosis. D&#x00FC;vel et al [<xref ref-type="bibr" rid="ref21">21</xref>] demonstrated in a qualitative study that CDSS holds promise for optimizing antibiotic stewardship, while current systems lack AI technology integration.</p><p>Umoh et al [<xref ref-type="bibr" rid="ref22">22</xref>] proposed the future development of CDSS in clinical treatment and management; a comprehensive tool that is precise and user-friendly would improve clinical decisions and efficiency.</p><p>Farkas et al [<xref ref-type="bibr" rid="ref23">23</xref>] revealed that the use of CPs could reduce unnecessary diagnostic testing in hospitalized patients, which is consistent with the conclusion of our study. Jaafar et al [<xref ref-type="bibr" rid="ref24">24</xref>] found that the implementation of DRG policy and CPs significantly enhanced health care resource utilization. However, evidence evaluating the effectiveness of CPs using real-world data remains limited in current literature. As noted by Bakel et al [<xref ref-type="bibr" rid="ref25">25</xref>], most hospitals were unable to measure their pathway outcomes or demonstrate improvement in care.</p><p>In these prior studies, CDSS, CP, and DRG payment systems were mostly applied and evaluated separately, and the fragmented application greatly limited their synergy potential. Current literature lacks real-world data studies investigating the integration of CDSSs with CPs.</p><p>This study innovatively proposed a CDSS-CP-DRG closed-loop model enabled by digital health technologies, where CDSS optimized CP execution through real-time data, CPs standardized workflows to support DRG cost control, and DRG payment pressures drove iterative improvements in both technology and processes. Their integration promoted evidence-based practice, reduced clinical variation, and curbed overutilization, particularly in resource-sensitive pediatric settings.</p></sec><sec id="s4-3"><title>Strengths and Limitations</title><p>DRG is a well-known type of hospital payment system that aims to establish the reference interval of medical expenses. It can effectively reduce costs, decrease the difficulty of standardized management of the medical diagnosis and treatment, and facilitate the macroprediction and control of medical expenses.</p><p>The ultimate goal of the DRG cost pathway is to achieve optimal medical value [<xref ref-type="bibr" rid="ref26">26</xref>]. In this study, we integrated CDSS with CP systems using AI technology to develop the IDCCS, and the framework established a closed-loop quality and cost control process spanning preimplementation DRG-based deficit analysis and CP optimization, intraimplementation execution with real-time alerts, and postimplementation statistical analytics. This system ensures standardized diagnosis and treatment while managing and controlling health care costs for hospitalized patients through the establishment of defined insurance payment quotas. As a result, hospitals are incentivized to reduce medical costs proactively, shorten hospital stays, and minimize unnecessary expenditures in pursuit of economic profitability. This approach facilitates cost control and promotes the rational and standardized use of medical resources [<xref ref-type="bibr" rid="ref27">27</xref>]. Ultimately, it aims to achieve low-cost, high-quality, efficient, and health-oriented value-based treatment [<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref29">29</xref>].</p></sec><sec id="s4-4"><title>Conclusion</title><p>This study innovatively integrated a CDSS with CPs to optimize DRG-based case management. An AI-driven CDSS-CP framework was developed for pediatric pneumonia, demonstrating scalability for diverse clinical contexts. AI-optimized CPs enhanced cost-effectiveness (ie, reduced medical expenditures) and care standardization, further validating its role in health care system reform. The model contributed to evidence-based global health care practices and population health improvement. However, CPs for critical cases or other diseases require continuous optimization and adaptation to enhance health care resource utilization and standardize clinical practices.</p></sec></sec></body><back><ack><p>Our heartfelt thanks to all the reviewers for reviewing the manuscript. This research was supported by the Scientific Research Program of Zhejiang Health Information Society (2024XHZN-Y01), Taizhou Science and Technology Plan Project (Category B, grant number 24ywb10), the Enze Medical Center (Group) Scientific Research Fund (grant number 2025EZAI09), and the Enze Hospital Management Research (Youth) Fund (grant number ENHM2020024). This article did not receive sponsorship.</p></ack><notes><sec><title>Data Availability</title><p>All the data are accessible and available from the corresponding author upon request.</p></sec></notes><fn-group><fn fn-type="con"><p>All authors contributed to the design, execution, and writing of this manuscript and approved the submitted version. YW and KL designed the study, performed experiments, and wrote the manuscript. FZ and DW supervised the project, analyzed data, revised the manuscript, and coordinated revisions. XM participated in the research design, project support, and paper revision. YW and KL contributed equally to this work as co-first authors. FZ and DW contributed equally to this work as co-corresponding authors. Danjie Wu can be reached at wudj10039@enzemed.com and 17857149701. All authors approved the final version.</p></fn><fn fn-type="conflict"><p>None declared.</p></fn></fn-group><glossary><title>Abbreviations</title><def-list><def-item><term id="abb1">AI</term><def><p>artificial intelligence</p></def></def-item><def-item><term id="abb2">CDSS</term><def><p>clinical decision support system</p></def></def-item><def-item><term id="abb3">CP</term><def><p>clinical pathway</p></def></def-item><def-item><term id="abb4">DDD</term><def><p>defined daily dose</p></def></def-item><def-item><term id="abb5">DRG</term><def><p>diagnosis-related group</p></def></def-item><def-item><term id="abb6">IDCCS</term><def><p>intelligent decision and cost control system</p></def></def-item></def-list></glossary><ref-list><title>References</title><ref id="ref1"><label>1</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Rudan</surname><given-names>I</given-names> </name><name 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