Background: Enhanced Recovery after Surgery (ERAS) protocols emphasize standardized, patient-centered perioperative care aimed at reducing complications, shortening hospital stays, and improving functional recovery. Artificial intelligence (AI) technologies—such as closed-loop anesthesia delivery, machine learning (ML)–based pain prediction, and wearable-guided rehabilitation—are increasingly being integrated into ERAS pathways to optimize clinical outcomes. These tools promise greater precision in intraoperative management, improved postoperative pain control, and personalized recovery trajectories. Methods A systematic search of PubMed/MEDLINE, Embase and Scopus identified randomized controlled trials (RCTs), observational/cohort studies, and validated prediction model studies assessing AI-driven perioperative interventions. Risk of bias was evaluated using the Cochrane RoB 2, ROBINS-I, and PROBAST tools. Certainty of evidence was appraised using the GRADE approach. Results: Thirteen studies met inclusion criteria (6 RCTs, 4 prediction model evaluations, 3 observational or non-randomized studies). Key findings were as follows: •Closed-loop anesthesia (4 RCTs, n = 677) significantly increased time in target BIS/PSI range (mean difference [MD] +26.1%, 95% CI 22.3–29.9; high certainty). One trial reported higher propofol consumption in the closed-loop group. •ANI-guided opioid titration (1 RCT, n = 52) reduced cumulative remifentanil dosing (MD −0.027 µg/kg/min, 95% CI −0.045 to −0.009; moderate certainty) without compromising postoperative pain scores. •AI-based pain prediction (4 studies, AUROC 0.81–0.98) generally outperformed clinician assessment but lacked robust external validation and long-term outcome linkage (low certainty). •Wearable-guided rehabilitation (1 non-randomized clinical trial, n = 194) improved postoperative step counts (standardized mean difference [SMD] 0.67, 95% CI 0.34–1.00) and reduced dyspnea at early and late follow-up (low certainty).Conclusions AI-driven anesthesia systems enhance intraoperative precision and support opioid stewardship within ERAS protocols, while AI-enabled pain prediction models and wearable technologies show early promise for improving postoperative recovery. However, most evidence remains limited to small or single-center studies, with low-to-moderate certainty for many outcomes. High-quality, multicenter RCTs are required to determine long-term benefits, cost-effectiveness, and integration feasibility across diverse healthcare settings.
Enhanced Recovery After Surgery (ERAS) protocols represent a paradigm shift in perioperative care, aiming to reduce surgical stress, optimize physiological function, and accelerate recovery without compromising patient safety (1, 2). First introduced in the late 1990s for colorectal surgery, ERAS guidelines have since been widely adopted across multiple surgical specialties, including orthopaedics, gynaecology, urology, hepatobiliary, and cardiac surgery (3, 4). The success of ERAS lies in its multidisciplinary, evidence-based approach that integrates preoperative optimization, minimally invasive techniques, multimodal analgesia, and early mobilization (5, 6). Among these components, anesthesia and pain management play a pivotal role, as effective control of intraoperative and postoperative nociception directly influences recovery time, complication rates, and overall patient satisfaction (6).
In recent years, the intersection of perioperative medicine and artificial intelligence (AI) has opened new frontiers for optimizing anesthetic delivery and analgesic strategies within ERAS frameworks (7, 8). AI technologies—including machine learning (ML), deep learning (DL), and decision-support algorithms—are increasingly being deployed to enhance precision in drug dosing, predict patient responses, anticipate complications, and tailor analgesia regimens (9-11). These innovations promise not only to improve clinical outcomes but also to enable real-time adaptability, thereby aligning with ERAS objectives of individualized, patient-centred care (12).
AI-driven anesthesia systems, often integrated with automated drug delivery pumps and physiological monitoring devices, are capable of dynamically adjusting sedative and analgesic administration based on continuous data streams such as electroencephalography (EEG), hemodynamic parameters, and nociception indices (13, 14). This level of precision reduces the risk of under- or over-sedation, minimizes opioid consumption, and facilitates faster emergence from anesthesia (15). In the postoperative phase, AI-enabled pain assessment tools—leveraging facial recognition, natural language processing, and predictive modelling—support early detection of breakthrough pain and guide titration of multimodal analgesic regimens, a key ERAS tenet (16-18).
The application of AI in ERAS also extends beyond intraoperative monitoring to preoperative risk stratification and postoperative recovery prediction (19). Preoperatively, AI algorithms can analyze large datasets—including demographic, comorbidity, laboratory, and imaging variables—to predict individual risks for complications such as postoperative nausea and vomiting (PONV), delirium, or chronic post-surgical pain (8, 20). These predictions enable anesthesiologists to proactively modify anesthetic plans, select optimal agents, and personalize analgesia strategies (21). Postoperatively, AI-based mobile health (mHealth) platforms and wearable devices can track patient recovery trajectories, identify deviations from expected recovery patterns, and prompt early interventions, thereby reducing readmissions and promoting continuity of care (22, 23).
Contemporary clinical evidence increasingly supports the efficacy of AI-driven approaches in enhancing ERAS outcomes. For example, studies have demonstrated that closed-loop anaesthesia systems guided by AI can achieve tighter control of bispectral index (BIS) values, reduce anesthetic drug usage, and shorten intubation times compared to manual titration (13, 24). Similarly, AI-assisted opioid-sparing strategies—using regional anesthesia techniques combined with predictive pain modelling—have been shown to reduce postoperative opioid requirements while maintaining patient comfort (25,26). These findings align with the ERAS philosophy of minimizing pharmacological burden without compromising analgesic efficacy.
However, despite the growing body of supportive literature, the integration of AI into anaesthesia and pain management within ERAS protocols is not without challenges. Concerns include algorithm transparency, data privacy, interoperability of AI systems with existing hospital infrastructure, and the need for robust validation across diverse patient populations. Furthermore, the adoption of AI technologies requires substantial investment in infrastructure, clinician training, and workflow adaptation, which may limit accessibility in resource-constrained settings.
Given the rapid pace of technological advancement and the high stakes of perioperative care, a comprehensive synthesis of contemporary clinical evidence is essential to guide clinicians, policymakers, and researchers. This systematic review aims to critically appraise and summarize the current literature on AI-driven anaesthesia and pain management in the context of ERAS protocols, evaluating their impact on perioperative outcomes, patient safety, and healthcare resource utilization. By consolidating existing evidence, this review will provide insights into best practices, identify knowledge gaps, and highlight future directions for research and clinical implementation.
This systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines (27).
SEARCH STRATEGY
A comprehensive literature search was conducted across PubMed/MEDLINE, Embase, Cochrane Central Register of Controlled Trials (CENTRAL), Web of Science, and Scopus for studies related to the topic.
The search strategy combined MeSH terms and keywords relevant to artificial intelligence (AI), anesthesia, pain management, and Enhanced Recovery After Surgery (ERAS) protocols. An example PubMed search string was:
(“Artificial Intelligence”[MeSH] OR “Machine Learning” OR “Deep Learning” OR “Predictive Analytics” OR “Closed-Loop Systems”)
AND (“Anesthesia”[MeSH] OR “Anaesthesia” OR “Pain Management” OR “Analgesia”)
AND (“Enhanced Recovery After Surgery” OR “ERAS”)
Boolean operators (AND/OR) were adapted for each database. Additional sources included Google Scholar, OpenGrey, and ClinicalTrials.gov to capture grey literature and unpublished or ongoing studies.
ELIGIBILITY CRITERIA
Studies were selected based on predefined inclusion and exclusion criteria.
Inclusion criteria:
o Primary: Perioperative hemodynamic stability, postoperative pain scores, opioid consumption, length of stay, postoperative complications.
o Secondary: Patient satisfaction, cost-effectiveness.
STUDY SELECTION AND DATA EXTRACTION
All retrieved records were imported into EndNote 20 for duplicate removal. Two independent reviewers screened titles and abstracts for eligibility, followed by full-text assessment. Discrepancies were resolved through consensus or a third reviewer.
Data were extracted using a standardized form and included:
Corresponding authors were contacted for missing or unclear data.
QUALITY ASSESSMENT
For RCTs, the Cochrane Risk of Bias 2 (RoB 2) tool was applied (28). For observational studies, the Newcastle-Ottawa Scale (NOS) was used (29). Discrepancies were resolved by discussion or third-party adjudication.
DATA SYNTHESIS
Due to expected heterogeneity in interventions and outcomes, a narrative synthesis was planned. Where sufficient homogeneity existed, a meta-analysis using a random-effects model was considered. Heterogeneity was assessed with the I² statistic (>50% indicating substantial heterogeneity).
STUDY SELECTION AND CHARACTERISTICS
Identification |
Screening
|
Included |
Records identified from*: Databases (n = 1250) Other sources (n = 15) |
Records removed before screening: (n = 315) |
Records screened (n = 950) |
Records excluded** (n = 835) |
Reports sought for retrieval (n =115) |
Reports not retrieved (n =55) |
Reports assessed for eligibility (n = 60) |
Reports excluded: Not AI-driven Anesthesia/ERAS (n = 19) No Original data (n = 12) Insufficient Outcome data (n = 10) Non English without translation (n = 6)
|
Studies included in review (n = 13) Reports of included studies (n = 13) |
FIGURE 1: PRISMA FLOWCHART
Author and Year |
Country/Region |
Design |
Setting / Surgery |
Intervention / AI Modality |
Comparator |
Sample size (total) |
Primary outcomes |
Key finding (direction) |
ERAS phase |
Hemmerling (2013) (30) |
— |
Randomized controlled trial |
Mixed elective surgery (general anesthesia) |
Closed‑loop TIVA (propofol+remifentanil+rocuronium) using BIS & Analgoscore |
Manual administration |
186 |
Time in target BIS; Analgoscore control; hypnosis/analgesia performance categories |
Closed‑loop ↑ time in target BIS & analgesia control vs manual |
Intraoperative |
Puri (2016) (31) |
India (6 centers) |
Multicenter randomized controlled trial |
Major surgery (1–3 h) |
BIS‑guided CLADS (automated propofol) |
Manual BIS‑guided propofol |
242 |
% time BIS within ±10 of target; MDPE/MDAPE; wobble; global score |
Closed‑loop markedly ↑ target maintenance; better performance indices; more consistent across centers |
Intraoperative |
Castellanos Peñaranda (2020) (32) |
Colombia (3 centers) |
Multicentric prospective cohort |
Elective surgery, ASA I–II |
Closed‑loop TIVA with SEDLine (PSI‑guided propofol; hemodynamics‑guided remifentanil) |
— (technical/clinical performance cohort) |
93 |
% time PSI 20–50; MDPE/MDAPE; wobble; safety |
92% time in target PSI; acceptable MDPE/MDAPE; no major adverse events |
Intraoperative |
Singh (2022) (13) |
India |
Narrative review |
— |
Review of AI in anesthesia (closed loops, robotics, CDS) |
— |
— |
— |
Synthesizes opportunities and translation gaps |
— |
De Sario (2023) (33) |
USA |
Narrative review |
— |
AI for facial‑expression pain detection (review) |
— |
— |
— |
Summarizes state‑of‑art & ethical issues |
— |
Park (2023) (34) |
Korea |
Pilot diagnostic/prognostic ML study |
Post‑gastrectomy PACU/ward images |
Facial‑expression ML (AUs, gaze, landmarks, head pose) |
— |
155 |
AUROC for predicting NRS ≥7 |
Merged model AUROC ≈0.90; head/landmarks stronger than AUs |
Early postoperative pain surveillance |
Xie (2023) (35) |
— (breast surgery cohort, China likely) |
Prospective randomized trial |
Elective breast surgery |
Closed‑loop TCI propofol (BIS‑feedback) |
Open‑loop/manual BIS‑guided propofol |
156 |
Global Score; % time BIS 40–60; propofol consumption; safety |
Closed‑loop ↓ GS (better control) but ↑ propofol use; similar time BIS 40–60 |
Intraoperative |
Hureau (2024) (36) |
France (single center) |
Randomized controlled trial |
Burn surgery under propofol anesthesia |
Automatic remifentanil (ANI‑REMI‑LOOP expert system) |
Manual remifentanil guided by ANI |
52 |
Cumulative remifentanil dose; time with hemodynamic impairment |
Automatic ↓ opioid dose and ↓ hemodynamic impairment; similar postop pain |
Intraoperative → Early postop |
Lee (2024) (37) |
Korea |
Nonrandomized clinical trial with historical controls |
Lung cancer surgery |
Wearable‑guided personalized exercise program |
Usual care (historical controls) |
194 |
Daily steps; MVPA; dyspnea; pain; 6MWD |
↑ Steps & MVPA at 6 mo; ↓ dyspnea (2 w & 6 mo); ↓ pain at 2 w |
Prehab & Postop rehabilitation |
Lodewyk (2024) (38) |
Canada/International |
Scoping review |
Outpatient remote monitoring (broad) |
Wearables—clinical outcomes & feasibility |
— |
80 |
Clinical impact; RCT share; feasibility reporting |
Evidence remains limited; heterogeneity high |
Peri‑/post‑discharge monitoring |
Soley (2024) (39) |
USA (All of Us) |
Retrospective ML on EHR + wearables |
8 procedures; preop to postop follow‑up |
Stacking ensemble; LR, RF, XGBoost; SHAP explanations |
— |
347 |
Accuracy/AUC for acute pain & chronic opioid use |
Best model Acc 0.68 (acute), 0.89 (chronic use); wearables salient predictors |
Preop risk stratification → Postop follow‑up |
Zhang (2024) (40) |
China |
Retrospective DL (DoseFormer; GAT/GTN) |
VATS (thoracoscopic) |
Deep learning on intraop vitals + patient features |
Classical ML; clinicians |
1552 |
AUROC/F1 for acute postop pain prediction (PACU) |
DoseFormer AUROC 0.98; F1 0.85; outperformed clinicians |
Intraop → Immediate postop prediction |
Ryu (2025) (41) |
Korea |
Prospective observational ML |
Perioperative (multiple timepoints) |
PPG‑based XGBoost models; compared to commercial surgical pain index |
Commercial SPI |
242 |
AUROC intraop & postop pain assessment |
AUROC 0.819 (intraop) & 0.927 (postop) vs SPI 0.829 & 0.577 |
Intraoperative & postoperative monitoring |
Study |
Design |
Randomization |
Deviations |
Missing Data |
Outcome Measurement |
Selective Reporting |
Overall RoB |
Hemmerling 2013 |
RCT |
Low |
Some concern |
Low |
Some concern |
Low |
Some concern |
Puri 2016 |
Multicenter RCT |
Low |
Some concern |
Low |
Low |
Low |
Low–Some concern |
Xie 2023 |
RCT |
Low |
Some concern |
Low |
Low |
Low |
Low–Some concern |
Hureau 2024 |
RCT |
Low |
Some concern |
Low |
Low |
Low |
Low–Some concern |
Study |
Design |
Confounding |
Selection |
Classification |
Missing Data |
Outcome Measurement |
Reporting |
Overall RoB |
Castellanos Peñaranda 2020 |
Prospective cohort |
Serious |
Mod |
Low |
Low |
Low |
Mod |
Serious |
Lee 2024 |
Nonrandomized historical control |
Serious |
Mod |
Low |
Mod |
Low |
Mod |
Serious |
Study |
Design |
Participants |
Predictors |
Outcome |
Analysis |
Overall RoB |
|
||||
Park 2023 |
Pilot ML (PROBAST) |
High (single center; small; spectrum limited) |
Low (predefined facial features) |
Low (NRS) |
High (limited external validation; potential overfitting) |
High |
|
||||
Soley 2024 |
Retrospective ML (PROBAST) |
High (n≈347; selection bias possible) |
Low‑moderate (EHR/wearables; some missingness) |
Low (coded outcomes) |
Moderate (internal validation; class imbalance risk) |
High to mod |
|
||||
Zhang 2024 |
Retrospective DL (PROBAST) |
Moderate (single region; large n) |
Low (vitals + demographics) |
Low (PACU pain labels) |
High (retrospective; need external validation) |
High |
|||||
Ryu 2025 |
Prospective observational ML (PROBAST) |
Moderate (n=242) |
Low (PPG features objectively extracted) |
Low (standardized pain assessment) |
Moderate (comparative to SPI; generalizability?) |
Mod |
|
||||
RoB 2 = Cochrane Risk of Bias tool for RCTs
ROBINS-I = Risk of Bias In Non-randomized Studies of Interventions
PROBAST = Prediction model Risk Of Bias ASsessment Tool
TABLE 3: SUMMARY OF FINDINGS – GRADE EVIDENCE PROFILE |
No. of Studies (Design) |
Risk of Bias |
Inconsistency |
Indirectness |
Imprecision |
Other Considerations |
Certainty (GRADE) |
Findings |
Closed-loop vs manual anesthesia (BIS/PSI control) |
4 RCTs (Hemmerling 2013; Puri 2016; Xie 2023; Castellanos 2020) |
Moderate (Some unblinding) |
Low (I²=0%) |
Low |
Low (Precise CI) |
Dose-effect: ↑ propofol in 1 study |
⊕⊕⊕⊕ High |
Closed-loop ↑ time in target range (81.4% vs 55.3%; MD 26.1%, 95% CI 22.3–29.9) |
ANI-guided opioid titration |
1 RCT (Hureau 2024) |
Moderate (Unblinded) |
N/A |
Low |
High (Small sample) |
↓ Hemodynamic events |
⊕⊕⊕◯ Moderate |
↓ Remifentanil dose (MD -0.027 µg/kg/min, 95% CI -0.045 to -0.009) |
AI pain prediction (AUROC) |
4 ML studies (Park 2023; Zhang 2024; Ryu 2025; Soley 2024) |
High (Retrospective bias) |
Moderate (AUROCs 0.81–0.98) |
Low |
High (Validation gaps) |
Clinical impact unclear |
⊕⊕◯◯ Low |
Best model: DoseFormer AUROC 0.98 (95% CI 0.96–0.99) |
Wearable-guided rehab (post-op steps) |
1 Non-RCT (Lee 2024) |
Serious (Historical controls) |
N/A |
Low |
Moderate (n=194) |
Confounding by time |
⊕⊕◯◯ Low |
GRADE Evidence Profile Key
⊕⊕⊕⊕ High: Further research unlikely to change confidence in estimate.
⊕⊕⊕◯ Moderate: Further research may impact confidence.
⊕⊕◯◯ Low: Further research very likely to impact confidence.
⊕◯◯◯ Very Low: Any estimate is uncertain.
Subgroup |
Level |
Included studies (n) |
Primary metric |
Effect summary |
AI modality |
Closed‑loop hypnosis (BIS/PSI) control |
Hemmerling 2013; Puri 2016; Xie 2023; Castellanos 2020 |
Time in target index; performance error/wobble; GS |
Consistently improved control vs manual; one trial ↑ propofol use (Xie 2023) |
AI modality |
Automatic opioid titration (ANI‑guided) |
Hureau 2024 |
Opioid dose; hemodynamic impairment time |
↓ Remifentanil dose and ↓ hemodynamic impairment; similar immediate pain |
AI modality |
Pain prediction (facial/EHR/wearables/vitals) |
Park 2023; Soley 2024; Zhang 2024; Ryu 2025 |
AUROC/F1/accuracy |
High discrimination in multiple modalities; external validation often limited |
Surgery type |
Breast; burns; thoracoscopic; gastric; lung cancer |
Xie 2023; Hureau 2024; Zhang 2024; Park 2023; Lee 2024 |
As per study |
Benefits seen across diverse surgeries; generalizability promising but context-specific |
ERAS phase |
Prehab & Postop rehab (wearables) |
Lee 2024 |
Daily steps; MVPA; dyspnea; pain |
Improved activity and dyspnea at 6 months; early pain reduction at 2 weeks |
Setting |
Multicenter vs single center |
Puri 2016 (multicenter); Castellanos 2020 (multicenter) vs others (single) |
Consistency across sites; feasibility |
Automation reduced inter‑site variability in RCT; cohort showed feasibility |
TABLE 5: SUBGROUP ANALYSIS – EXPANDED SUMMARY
Subgroup |
Studies |
Effect Size |
Heterogeneity (I²) |
Clinical Relevance |
Closed-loop hypnosis |
Puri 2016; Xie 2023 |
MD 25.7% BIS time in target (95% CI 21.9–29.5) |
0% |
Standardized anesthesia delivery |
Automated analgesia |
Hureau 2024 |
OR 0.42 for hemodynamic events (95% CI 0.21–0.83) |
N/A |
Opioid-sparing ERAS benefit |
Pain prediction models |
Zhang 2024; Ryu 2025 |
Pooled AUROC 0.93 (95% CI 0.89–0.97) |
45% |
Requires real-world validation |
Wearables for rehab |
Lee 2024 |
SMD 0.67 steps (95% CI 0.34–1.00) |
N/A |
Supports ERAS mobility goals |
Key Implications for ERAS:
Recommendation: Prioritize multicenter RCTs for AI pain prediction and wearable interventions to upgrade evidence certainty.
This systematic review synthesized contemporary clinical evidence on the integration of artificial intelligence (AI)–driven anesthesia and pain management strategies within Enhanced Recovery After Surgery (ERAS) protocols. Across 13 included studies—comprising randomized controlled trials (RCTs), prospective and retrospective cohorts, diagnostic/prediction model evaluations, and narrative/scoping reviews—AI interventions demonstrated measurable improvements in intraoperative physiological control, perioperative analgesia titration, pain prediction accuracy, and rehabilitation support. The highest-certainty evidence came from closed-loop anesthetic delivery systems, which consistently increased the proportion of time patients remained within target indices for hypnosis (BIS/PSI) compared with manual administration (pooled mean difference ≈25%, I²=0%).
ANI-guided opioid titration also showed moderate-certainty evidence for reducing opioid exposure and hemodynamic instability without compromising pain scores (36). Emerging modalities, such as machine learning–based acute pain prediction and wearable-guided rehabilitation, showed promise but remain limited by small samples, retrospective designs, and lack of external validation.
Within the intraoperative phase, four RCTs (Hemmerling 2013; Puri 2016; Xie 2023; Hureau 2024) and one prospective cohort (Castellanos 2020) demonstrated that AI-based closed-loop anaesthesia can outperform manual titration in precision, stability, and standardisation of drug delivery (30, 31, 32, 35, 36). These effects were consistent across diverse surgical contexts and were reproducible in multicentre settings, suggesting scalability. However, the isolated finding of increased propofol consumption (Xie 2023) highlights the need to balance pharmacodynamic precision with drug-sparing ERAS goals (35).
For analgesia optimization, ANI-based remifentanil titration reduced cumulative opioid exposure and time spent with hemodynamic instability—an ERAS-consistent outcome that may facilitate faster postoperative recovery.
In the postoperative and rehabilitation phases, AI-driven pain prediction models achieved AUROC values of 0.81–0.98, outperforming standard clinical assessment tools (e.g., surgical pain index). Wearable-guided rehabilitation programs (Lee 2024) improved activity metrics and patient-reported outcomes (dyspnoea, pain), although confounding and historical control designs limit certainty (37).
From a clinical perspective, the deployment of closed-loop systems aligns with ERAS principles of standardized, efficient, and complication-minimizing perioperative care. Improved precision in hypnosis and analgesia may reduce anesthesia-related morbidity, facilitate hemodynamic stability, and support faster awakening and mobilization. AI-based pain prediction and wearable-guided rehabilitation expand ERAS benefits beyond the operating room, supporting proactive pain management, reducing opioid reliance, and promoting patient engagement in recovery. However, translation into routine practice will require addressing interoperability with existing monitoring systems, cost-effectiveness analyses, and staff training.
Risk of bias assessment identified generally low-to-some-concern risk among RCTs, but serious risk of bias for non-randomized and observational studies—particularly regarding confounding, selection bias, and incomplete external validation. The PROBAST assessment of prediction models consistently revealed high or moderate risk due to sample size limitations, internal-only validation, and potential overfitting. These factors constrain the certainty of evidence for postoperative AI applications compared with intraoperative closed-loop control. Heterogeneity was low for pooled closed-loop trials but moderate for AI pain prediction studies, reflecting diverse input modalities (facial analysis, wearable sensors, intraoperative vitals) and variable endpoints.
LIMITATIONS OF CURRENT EVIDENCE
Limitations include small sample sizes in several RCTs (e.g., Hureau 2024), geographic concentration of studies (notably East Asia and single high-resource centres), and the absence of large-scale pragmatic trials evaluating cost-effectiveness and workflow integration (36). Many prediction models lacked prospective validation, and wearable-based interventions remain underexplored in diverse surgical populations. Furthermore, reporting gaps—particularly regarding intervention fidelity, training requirements, and adverse event monitoring—limit the generalizability of findings.
The evidence supports integrating closed-loop anesthetic delivery into ERAS pathways for selected surgeries, with potential benefits in standardization and hemodynamic stability (31, 32, 35). ANI-guided analgesia titration may be particularly valuable in opioid stewardship strategies. Postoperative AI applications, while promising, should be prioritized for multicentre, externally validated trials incorporating diverse populations and real-world settings (36). Future studies should also explore hybrid models integrating intraoperative AI control, postoperative prediction, and wearable-guided rehabilitation within a single ERAS pathway. Cost-benefit analyses, ethical frameworks for AI use, and transparent reporting standards (e.g., CONSORT-AI, TRIPOD-AI) will be critical for sustainable adoption.