Search Results (1,033)

Background/Objectives: Peripheral pulsed radiofrequency (PRF) is a minimally invasive option for trigeminal neuralgia (TN) with a favorable safety profile compared with neurorestorative techniques, but its durability and recurrence patterns remain uncertain. This study evaluated the early effectiveness, durability, recurrence-free survival, and safety of peripheral PRF in refractory classical or idiopathic TN. Methods: This retrospective single-center cohort study assessed procedure-level outcomes of peripheral PRF targeting the ophthalmic, maxillary, and mandibular branches. Pain intensity and clinical status were evaluated using the Numeric Rating Scale (NRS) and Barrow Neurological Institute (BNI) pain score. Early effectiveness was defined as clinically meaningful pain relief sustained for at least 1 month, and sustained effectiveness as NRS ≤ 3 at 6 months. Recurrence-free survival was analyzed using Kaplan–Meier methods. Results: A total of 68 procedures in 57 patients were analyzed. Early effectiveness at 1 month was achieved in 85.3% of procedures. Median NRS decreased from 9 (IQR 8–9) at baseline to 2 (0–4) at 1 month and 0 (0–2) at 3 and 6 months (p < 0.001). In a worst-case analysis, 6-month sustained effectiveness was 72.1%. Recurrence occurred in 61.8% of procedures, with a median recurrence-free survival of 11 months. Among procedures with recurrence, repeat peripheral PRF was performed in 45.2%. Medication requirements decreased in 66.2% of procedures, and no major complications occurred. Conclusions: Peripheral PRF provides rapid and meaningful early pain relief in TN, but durability is limited. These findings support peripheral PRF as a safe, repeatable neuromodulatory intervention within a staged treatment strategy rather than a definitive therapy. Full article

Background/Objectives: Hemodynamic disturbances in sepsis and septic shock arise from the vasoactive effects of inflammatory mediators involved in the immune response. Relaxin-1 is a pleiotropic hormone associated with inflammation, angiogenesis, tissue repair, and vasodilation. This study aimed to investigate the changes in relaxin-1 levels in septic shock and to evaluate their association with mortality. Methods: This prospective observational study was conducted in a Level II intensive care unit. Demographic characteristics, vital signs, APACHE II and SOFA scores, comorbidities, and routine laboratory parameters were recorded at admission and at 48 h. Serum relaxin-1 levels were measured at both time points and analyzed in relation to survival status. Binary logistic regression was additionally performed to evaluate variables associated with mortality in a multivariable framework. Results: A total of 48 patients with sepsis and septic shock were included (54.2% female; mean age 73.4 ± 14.7 years). Overall mortality was 33.3%. Relaxin-1 levels significantly increased from baseline (11.25 ± 4.85 pg/mL) to 48 h (12.64 ± 4.81 pg/mL) (p = 0.047). Baseline relaxin-1 levels were significantly higher in non-survivors compared to survivors (14.62 ± 4.47 pg/mL vs. 11.65 ± 4.73 pg/mL, p = 0.043). Conclusions: Elevated Relaxin-1 levels were associated with mortality in patients with sepsis and septic shock. The observed increase in Relaxin-1 during early follow-up suggests a potential link with the underlying pathophysiological processes. Although Relaxin-1 was associated with mortality, its independent prognostic value could not be established in multivariable analysis due to the limited sample size. Larger, adequately powered multicenter studies are required to confirm these findings. Full article

Introduction. Chronic non-cancer pain is highly prevalent and profoundly diminishes quality of life. While pharmacological and interventional treatments are central, its psychosocial and spiritual dimensions remain under-addressed. This pilot study assessed the feasibility of a therapist-led support group intervention for patients with chronic non-cancer pain and explored preliminary psychospiritual outcomes. Methods. A two-arm, non-randomized pilot feasibility study was conducted among 58 outpatients of a university pain management clinic in Poland. Feasibility was assessed through recruitment, retention, attendance, and safety, while preliminary psychological and spiritual outcomes were evaluated using validated self-report instruments. The intervention group (n = 29) participated in eight group sessions combining psychoeducation, mindfulness-based techniques, and supportive dialogue inspired by the Simonton Method. The control group (n = 29) received standard care. Participants completed the Numeric Rating Scale to measure pain intensity, the Satisfaction with Life Scale, the Positive and Negative Affect Schedule, the WHOQOL-BREF, the Spiritual Well-Being Scale, the Generalized Anxiety Disorder Scale, and the Patient Health Questionnaire-9. Results. The intervention was feasible in terms of physician workload; however, patients adherence varied significantly. At baseline, the control group showed a significantly higher positive affect and existential well-being than did the intervention group. In exploratory within-group analyses, participants in the intervention group showed improved positive affect and reduced anxiety (p < 0.05), whereas existential well-being showed a trend toward improvement (p < 0.06). However, the self-selection design limits causal inferences. Nevertheless, participants reported social connectedness, meaning-making, and enhanced vitality. Discussion. This pilot feasibility study provides preliminary evidence that a therapist-led support group intervention integrating psychoeducation, mindfulness, and supportive components is practicable within multidisciplinary pain management. Further research in a larger, randomized trial is needed to evaluate adherence and safety, as well as clinical effects, more rigorously. Full article

Background/Objectives: Strict hemodynamic stability is critical during supratentorial craniotomy. This systematic review and meta-analysis aimed to evaluate the efficacy of magnesium sulfate (MgSO₄) as a multimodal adjuvant on intraoperative hemodynamics, opioid consumption, and biomarker outcomes in this setting. Methods: We systematically searched PubMed, Scopus, EBSCO, and the Cochrane Library for randomized controlled trials (RCTs) comparing perioperative MgSO₄ administration to placebo or standard care in adult patients undergoing elective supratentorial craniotomy. Results: Meta-analysis of nine included RCTs using a random-effects model demonstrated that MgSO₄ significantly reduced intraoperative mean arterial pressure (mean difference [MD]: −4.65 mmHg; 95% confidence interval [CI]: −7.76 to −1.55; p = 0.0033; I² = 73.6%). Furthermore, MgSO₄ administration significantly lowered postoperative serum S100B levels (standardized MD [SMD]: −0.81; 95% CI: −1.24 to −0.38; p = 0.0002, I² = 0.0%), indicating mitigated cellular neural damage, and decreased perioperative fentanyl consumption (standardized MD: −1.01; 95% CI: −1.45 to −0.57; p < 0.0001; I² = 0.0%). Intraoperative blood loss volume did not differ significantly between groups (MD: −85.03 mL; 95% CI: −331.42 to 161.37; p = 0.4952; I² = 92.5%). Conclusions: MgSO₄ is a safe and effective multimodal adjuvant for supratentorial craniotomy, providing significant hemodynamic stability, opioid-sparing effects, and preliminary biochemical evidence suggestive of neuroprotection without compromising intraoperative hemostasis. Full article

Objectives: This randomized, single-blind study aimed to compare the effects of ultrasound-guided erector spinae plane block (ESPB), thoracic paravertebral block (TPVB) and intravenous (IV) analgesia on postoperative pain, opioid consumption and quality of recovery in patients undergoing laparoscopic cholecystectomy (LC). Methods: A total of 120 adult patients (ASA I-III) scheduled for elective LC were randomized into three groups: ESPB (GI), TPVB (GII) and IV analgesia (GIII). Bilateral ESPB or TPVB was performed preoperatively; then all patients received standardized general anesthesia and postoperative analgesia including paracetamol, tenoxicam and IV tramadol via patient-controlled analgesia. The primary outcome was 24 h tramadol consumption. Secondary outcomes included pain scores, rescue analgesia requirement, patient satisfaction, postoperative nausea and vomiting, time to first ambulation, length of hospital stay and Quality of Recovery-15 (QoR-15) scores. Results: Twenty-four-hour tramadol consumption was significantly higher in GIII (135.78 ± 22.73 mg) compared with GI (101.05 ± 26.99 mg) and GII (95.67 ± 31.49 mg) (p < 0.001), with no difference between GI and GII. Both static and dynamic pain scores were lower in GI and GII compared with GIII at most time points. Rescue analgesia requirement and patient dissatisfaction were significantly higher in GIII. QoR-15 scores were significantly improved in GI and GII compared with GIII (p < 0.001), while no difference was observed between the regional techniques. Block performance time was shorter with ESPB than TPVB (p < 0.001). No complications were reported. Conclusions: ESPB and TPVB provided effective analgesia and improved recovery after LC compared with IV analgesia alone. Both regional techniques may be considered as components of multimodal analgesia after LC. Full article

Background: Cognitive changes after minor surgery may affect patient safety, functional recovery, and readiness for hospital discharge, even after low-risk procedures with early discharge protocols. In this regard, patients require neuropsychological assessment at discharge, which may have important clinical implications for return to daily activities and postoperative decision-making. Our study investigated postoperative cognitive changes after minor surgery under general anesthesia using a neuropsychological assessment and a non-surgical group. Methods: Patients undergoing laparoscopic cholecystectomy received propofol or sevoflurane anesthesia. A non-surgical control group was included. Cognitive performance was assessed at baseline and discharge using the Computerized Visual Attention Test (CVAT), the controlled oral word association test (COWAT), and the symbol digit modalities test (SDMT). Relative change scores were calculated as ((baseline − postoperative performance)/baseline). Group differences were analyzed using two-tailed multivariate analysis of variance (MANOVA), followed by ANOVAs and Bonferroni-adjusted pairwise comparisons. Results: A total of 105 participants were included (37 non-surgical, 34 propofol, 34 sevoflurane). MANOVA showed a significant group effect (Pillai’s trace = 0.332, p < 0.001, η² = 0.196). The ANOVAs revealed significant differences in sustained attention (CVAT), verbal fluency (COWAT) and executive function (SDMT). The propofol group showed evident decline in sustained attention compared to non-surgical. In verbal fluency, non-surgical improved at day after, whereas both surgical groups showed no improvement, indicating worse performance. In SDMT the sevoflurane group had worse performance. Conclusions: Minor surgery under general anesthesia may lead to transient impairments in attention and learning at discharge, supporting the need for postoperative cognitive monitoring and individualized discharge decisions. Full article

Background/Objectives: Opioid-free anesthesia (OFA) has emerged as a potential alternative to opioid-based anesthesia (OBA) to reduce opioid-related adverse effects. This meta-analysis compares OFA and OBA with respect to postoperative pain and opioid consumption. Methods: PubMed, Cochrane, and Embase libraries were searched for OFA studies published through 12 June 2025. Randomized controlled trials (RCTs) conducted on adult humans were selected; observational studies, studies including neuraxial anesthesia, and RCTs currently awaiting approval were excluded. A forest plot was used to summarize findings of a random-effects meta-analysis to compare OFA (treatment) and OBA (control). Results: Of 1446 citations found, twenty-nine articles met our inclusion criteria. Twenty-six studies reported pain scores with a 0–10 scale. OFA was associated with lower postoperative pain scores (Hedges’ g = –0.34; 95% CI –0.55 to –0.13; p < 0.001; I² = 84%) but with high heterogeneity, limiting clinical significance or strong interpretation of results. Eleven trials were analyzed for opioid use, showing a small reduction with OFA (Hedges’ g = –0.55; 95% CI –1.10 to –0.005; p = 0.048; I² = 96.22%). Subgroup outcomes favored OFA, with an overall reduction in pain found specifically in endoscopic abdominal surgeries. Some secondary outcomes also indicated potential improved recovery profiles through OFA for certain surgeries. Conclusions: OFA was associated with statistically significant lower postoperative pain scores, along with opioid consumption, but with a small effect size and high heterogeneity when compared to OBA. This is potentially comparable in pain control and opioid consumption with limited clinical significance. Overall, outcomes support the continued controlled study of OFA as an alternative to conventional analgesia. Full article

Background: Accurate endotracheal tube (ETT) insertion depth is critical in infants and young children, where tracheal malposition carries significant risk. Formula-based depth estimation is widely used at the bedside, but the performance of published formulas in children under two years of age admitted to a general PICU remains poorly characterized. Methods: A retrospective, single-center study was conducted at the PICU of King Saud Medical City, Riyadh. A total of 115 patients aged 1–24 months requiring orotracheal intubation were included. ETT depth was predicted using five established formulas: height-based [(H/10)+5], weight-based [W+6], ETT size-based [ETT×3], Lee weight-based [5.5+0.5W], and Lee height-based [3+0.1H]. Agreement between predicted and radiographically confirmed insertion depth was assessed using Lin’s concordance correlation coefficient (CCC), Bland–Altman analysis, and clinical classification of predictions. Results: None of the five formulas achieved acceptable concordance (CCC < 0.75 for all). The height-based formula performed best among published formulas, with negligible bias and the highest proportion of clinically acceptable predictions. Both Lee formulas showed near-universal systematic underestimation and are not suitable for this age group. Over half of all intubations resulted in non-ideal ETT position on the first post-intubation chest X-ray. Novel cohort-derived regression equations outperformed all published formulas, with the weight-based equation (Depth = 0.385 × Weight + 9.145) emerging as the strongest predictor of insertion depth. Conclusions: No published formula achieved reliable concordance with radiographic ETT depth in children aged 1–24 months. The cohort-derived weight-based formula represents a more accurate bedside tool for this population and warrants prospective external validation. Post-intubation radiographic verification remains essential. Full article

Background: Chronic pain is the leading cause of years lived with disability worldwide, with low back pain representing the most prevalent and disabling condition. Spinal cord stimulation (SCS) and intrathecal drug delivery (IDD) systems are established neuromodulation techniques for refractory chronic pain. However, a subset of patients experiences partial or declining benefit with either modality alone. In such cases, combined therapy may represent a rescue strategy. Methods: retrospective case series at a single center, including patients previously implanted with SCS who subsequently required IDD due to loss of efficacy or inadequate pain coverage. Pain intensity, opioid consumption, health-related quality of life, and patient satisfaction were assessed using validated instruments. Results: Twelve patients were included. Persistent low back pain with mixed nociceptive–neuropathic features was the most common indication. Combined therapy was observed in association with a mean reduction of 3.5 points on the Numeric Rating Scale, corresponding to an approximate 40% decrease in pain intensity. More than half of the patients discontinued systemic opioids. Complications occurred in seven patients (58.3%), mostly hardware-related and manageable with surgical revision; only one patient developed a device-related infection. Conclusions: In this case series, combined SCS and IDD therapy was observed in association with clinically meaningful pain reduction, decreased opioid use, and high patient-reported satisfaction. Although quality-of-life scores remained below population norms, patients consistently reported subjective improvement. Combined neuromodulation may represent a valid rescue option in selected patients with insufficient response to SCS alone. Full article

Background: Total knee arthroplasty is associated with significant postoperative pain. The erector spinae plane block (ESPB) is increasingly used as part of multimodal analgesia, but its duration may be limited. Adjuvants such as dexamethasone and dexmedetomidine may enhance analgesic efficacy; however, direct comparisons between these agents in ESPB remain limited. Methods: In this prospective, randomized, double-blind trial, 90 patients undergoing total knee arthroplasty were allocated to receive ESPB with ropivacaine alone (control), with ropivacaine plus dexamethasone (DEX), or with ropivacaine plus dexmedetomidine (DEM) (n = 30 per group). The primary outcome was time-to-first opioid requirement within 48 h. Secondary outcomes included total opioid consumption, postoperative pain intensity (NRS), and adverse events. Time-to-event analysis was performed using Kaplan–Meier and Cox regression. Results: Time-to-first opioid requirement was significantly prolonged in both DEX and DEM groups compared with control (log-rank p < 0.0001). Median time was 7.85 h (95% CI 7.40–8.50) in control, 13.70 h (12.80–14.50) in DEX, and 12.40 h (11.20–14.30) in DEM. Both DEX (HR 0.036, 95% CI 0.017–0.079) and DEM (HR 0.058, 95% CI 0.028–0.121) significantly reduced the hazard of opioid requirement (p < 0.0001). Total opioid consumption was significantly lower in the DEX group compared with both control and DEM (p < 0.0001), while no difference was observed between DEM and control. Pain scores were lower in the DEX group in the early postoperative period. No statistically significant differences in adverse events were observed between groups. Conclusions: Both dexamethasone and dexmedetomidine prolong ESPB analgesia in total knee arthroplasty. However, dexamethasone provides superior analgesic efficacy without increasing adverse events. Full article

Background: Surgical site infection (SSI) is a common complication that increases morbidity, prolongs hospital stays, and raises healthcare costs. Perioperative hypothermia may contribute to its development by altering tissue perfusion, oxygenation, and the immune response. Objective: To evaluate the association between perioperative hypothermia and the risk of SSI in adult patients. Methods: A scoping review was conducted following the methodological framework of Arksey and O’Malley, expanded by Levac, the recommendations of the Joanna Briggs Institute, and the PRISMA-ScR guidelines. A systematic search was performed in PubMed and Scopus through 30 April 2026. We included observational studies and clinical trials in adults undergoing surgery that evaluated the association between perioperative or intraoperative hypothermia and the occurrence of SSI or other postoperative infectious complications. Results: A total of 28 studies were included. Retrospective observational studies were the most common design, comprising 19/28 studies (67.9%), followed by 6/28 prospective cohorts (21.4%) and 4/28 randomized clinical trials (14.3%). The studies were conducted across 12 countries, with the United States contributing the largest proportion (14/28, 50%), followed by China, Turkey, and Japan with two studies each (7.1% per country). Regarding the main findings, 14 studies (50%) reported a positive association between perioperative hypothermia and an increased risk of SSI or other postoperative infections, whereas 11 studies (39.3%) found no statistically significant association. Most studies (15/28, 53.6%) used a fixed temperature threshold of <36 °C, while a smaller proportion applied lower cutoffs such as <35–35.5 °C (3/28, 10.7%); in the remaining studies (10/28, 35.7%), the threshold was not clearly specified. Temperature measurement methods were frequently underreported (21/28, 75.0%). Among studies that did report them, approaches included repeated measurements (3/28, 10.7%), continuous monitoring (2/28, 7.1%), mean intraoperative temperature (1/28, 3.6%), nadir temperature (1/28, 3.6%), and single-point measurements (1/28, 3.6%). Conclusions: Perioperative hypothermia may be associated with an increased risk of SSI; however, the available evidence is inconsistent across surgical settings. Rather than indicating a clear independent effect, the findings suggest that hypothermia could play a context-dependent role within a broader set of perioperative factors influencing infection risk. Full article

Background/Objectives: Postoperative nausea and vomiting (PONV) remain frequent after breast surgery despite prophylaxis. This single-center, parallel-group randomized controlled trial evaluated whether intraoperative opioid-sparing anesthesia using dexmedetomidine and lidocaine reduced 48 h PONV compared with opioid-based anesthesia. Methods: Adult women undergoing elective breast surgery were randomized 1:1 to opioid-sparing anesthesia with dexmedetomidine and lidocaine or conventional opioid-based anesthesia with remifentanil. Participants and postoperative outcome assessors were blinded to group allocation; attending anesthesiologists were not blinded. All patients received standardized sevoflurane anesthesia, dexamethasone, ramosetron, quantitative neuromuscular monitoring, and postoperative fentanyl patient-controlled analgesia. The primary outcome was PONV within 48 h after surgery. Results: Among 68 randomized patients, 67 were analyzed (opioid-sparing group, n = 33; control group, n = 34). PONV within 48 h occurred in 8 patients (24.2%) in the opioid-sparing group and 28 patients (82.4%) in the control group (risk ratio, 0.29; 95% confidence interval, 0.16–0.55; p < 0.001; absolute risk reduction, 58.1%; number needed to treat, 1.7). Rescue antiemetic use was lower in the opioid-sparing group in the postanesthesia care unit and at 1 h postoperatively. Pain scores and cumulative opioid consumption were comparable. No Clavien–Dindo grade III or higher complications occurred. Conclusions: Intraoperative opioid-sparing anesthesia was associated with lower 48 h PONV after breast surgery without apparent compromise in analgesia. These single-center findings, from a trial registered after enrollment of one participant, require confirmation in larger prospectively registered multicenter trials. Trial Registration: Clinical Research Information Service (CRIS), KCT0009829. Registered on 10 October 2024. Full article

Objectives: Oocyte pick-up (OPU) is commonly performed under propofol-based sedation during in vitro fertilization (IVF). However, considerable interindividual variability in propofol requirement has been observed. Controlled ovarian hyperstimulation results in supraphysiological levels of ovarian steroid hormones, which may influence anesthetic sensitivity. This study aimed to evaluate the relationship between preprocedural serum estradiol and progesterone levels and propofol requirement during OPU performed under bispectral index (BIS)-guided sedation. Methods: In this prospective observational study, 96 women undergoing OPU were included. Serum estradiol and progesterone levels measured on the day of the procedure were recorded. Sedation was performed using a standardized protocol with midazolam, fentanyl, and propofol titrated to maintain BIS values between 40 and 60. Propofol consumption was normalized to body weight (mg/kg) and procedure duration (μg/kg/min). Correlation analyses and multivariable linear regression models were used to evaluate associations. Results: Mean propofol consumption was 157.3 ± 53.1 mg (2.41 ± 0.83 mg/kg), corresponding to an infusion rate of 125.7 ± 69.6 μg/kg/min. In multivariable analysis, estradiol levels were independently associated with propofol requirement (β = 0.238, p = 0.014), whereas progesterone levels were not significantly associated with anesthetic dosing after adjustment. BMI (β = −0.305, p = 0.002) and procedure duration (β = 0.224, p = 0.021) were also identified as independent predictors. Conclusions: Estradiol levels were associated with propofol requirement during OPU performed under BIS-guided sedation. However, given the observational design and the modest magnitude of the observed associations, these findings should be interpreted cautiously. BMI and procedure duration appeared to be more consistent predictors of propofol administration. Full article

Background: Perioperative assessment of hemostasis remains challenging, particularly in non-cardiac surgery, where the incidence of clinically significant bleeding is relatively low. Viscoelastic testing enables real-time evaluation of whole-blood coagulation, but its perioperative dynamics and agreement with conventional assays require further characterization. Methods: In this prospective single-center observational study, 53 patients undergoing major non-cardiac surgery were included in the final analysis. Hemostatic parameters were assessed preoperatively, intraoperatively at two-hour intervals, and 24 h postoperatively using ROTEM (EXTEM, INTEM, and FIBTEM) and conventional coagulation assays. Longitudinal changes and correlations between fibrinogen concentration according to Clauss and ROTEM-derived parameters were analyzed. Results: Fifty-three patients undergoing major hepatopancreatobiliary surgery completed longitudinal perioperative monitoring. Pancreaticoduodenectomy and liver resection accounted for 60.7% and 39.3% of procedures, respectively. Serial perioperative ROTEM and laboratory assessments demonstrated time-dependent changes in coagulation parameters, including decreased intraoperative fibrinogen and antithrombin III levels and shortening of INTEM clotting time. Clinically significant bleeding was infrequent, with severe intraoperative bleeding observed in 7.4% of patients. Strong correlations were confirmed between fibrinogen concentration according to Clauss and FIBTEM-derived parameters, particularly FIBTEM MCF (r = 0.811, p < 0.001), whereas the correlation with FIBTEM A10 was moderate (r = 0.574, p < 0.001). No significant association was observed between preoperative fibrinogen concentration and perioperative blood loss. Conclusions: This study provides a longitudinal characterization of perioperative coagulation dynamics and demonstrates strong agreement between fibrinogen concentration according to Clauss and ROTEM-derived parameters. The findings are primarily descriptive and highlight the methodological consistency between viscoelastic and conventional fibrinogen assessment. Further studies are required to determine their clinical relevance in perioperative management. These findings suggest that ROTEM-derived parameters may provide a rapid functional estimate of fibrinogen status in the perioperative setting, potentially supporting clinical assessment, although their role in guiding management requires further validation. Full article

Background: The American Society of Anesthesiologists Physical Status (ASA-PS) classification is widely used for perioperative risk stratification but is subject to inter-rater variability. The 2024 South Korean medical crisis abruptly shifted preoperative ASA-PS assessment from resident-led to specialist-centered care, providing a natural opportunity to examine how this transition affected ASA-PS distribution and prognostic performance. Methods: In this single-center retrospective cohort study, surgical patients during the pre-crisis (January 2022–December 2023) and crisis (March 2024–August 2025) periods were matched 1:2 by propensity score on age, sex, Charlson Comorbidity Index, surgical specialty, emergency status, and anesthesia type. The primary outcome was 30-day mortality; secondary outcomes were postoperative intensive care unit (ICU) admission and length of stay. ASA-PS discrimination was compared between periods using DeLong’s test, and ASA × crisis interaction terms were assessed by the likelihood ratio test. Results: A total of 53,895 cases (35,930 pre-crisis; 17,965 crisis) were matched, with all post-matching standardized mean differences below 0.1. ASA-PS demonstrated higher discrimination for 30-day mortality during the crisis than the pre-crisis period (area under the curve [AUC], 0.891 [0.863–0.919] vs. 0.827 [0.803–0.851]; ΔAUC = 0.064, p < 0.001). The ASA-PS × crisis interaction remained significant after adjustment (p = 0.014). Discrimination for ICU admission was similar between periods. Conclusions: ASA-PS classifications assigned during the crisis period were associated with higher discrimination for 30-day mortality than those from the pre-crisis period, suggesting that the operational performance of perioperative risk-assessment tools may vary with evaluator context and broader healthcare system conditions. Full article