Daily Anesthesiology Research Analysis
Analyzed 132 papers and selected 3 impactful papers.
Summary
An RCT shows ultrasound-guided in-plane subclavian venous access reduces a composite complication risk and arterial punctures compared with a landmark technique, at the cost of a modestly longer procedure. A meta-analysis of randomized trials finds that Hypotension Prediction Index–guided management does not reduce postoperative AKI and yields a non-robust signal for reduced myocardial injury. Translational work links monocyte transmigration to remifentanil-induced hyperalgesia and demonstrates attenuation with flurbiprofen axetil in a small RCT.
Research Themes
- Vascular access safety and ultrasound guidance
- AI-guided hemodynamic management and patient-centered outcomes
- Mechanisms and mitigation of opioid-induced hyperalgesia
Selected Articles
1. Ultrasound-Guided In-Plane Subclavian Vein Puncture versus Prior Ultrasound and Landmark Technique: A Randomized Controlled Trial.
In 101 surgical patients, ultrasound-guided in-plane subclavian venous access reduced a composite complication risk and arterial punctures versus a landmark approach, with higher overall success. The trade-off was a roughly 5-minute longer procedure time.
Impact: This RCT directly informs a common high-stakes procedure, demonstrating that a specific ultrasound technique meaningfully reduces complications.
Clinical Implications: Adopting microconvex in-plane ultrasound for subclavian CVC can improve safety by reducing arterial puncture and overall procedural risk, accepting a modest time increase and emphasizing operator training.
Key Findings
- Composite risk score significantly lower with MISP versus landmark (mean diff 5.21; P = .028).
- Higher as-treated overall success with MISP (86% vs 71%; P = .046).
- Arterial punctures reduced with MISP (1.9% vs 12%; P = .047).
- Procedure time ~5 minutes longer with MISP (P < .001); pneumothorax occurred once in each group.
Methodological Strengths
- Prospective randomized controlled trial with an a priori composite primary endpoint
- Predefined statistical analysis with multiple clinically relevant secondary outcomes
Limitations
- Single-center study with a modest sample size (n=101)
- As-treated success rates reported; operator experience and learning curve not fully explored
Future Directions: Multicenter trials to confirm generalizability, assess learning curves, and evaluate implementation strategies for standardizing MISP in diverse settings.
BACKGROUND: Central venous catheterization (CVC) of the subclavian vein is a standard procedure in medicine. Ultrasound guidance is increasingly recommended to improve the success rates and reduce complications. This study compared the success rates and complications of ultrasound-guided microconvex in-plane subclavian puncture (MISP) with those of the landmark technique. METHODS: In this randomized controlled trial, 101 patients scheduled for elective surgery were enrolled and randomly assigned to either the group MISP or the control group using the landmark technique after ultrasound prescan. The primary end point was an a priori defined composite risk score including puncture attempts, required time, posterior venous wall injury, arterial punctures, hematoma formation, hemo-, pneumothorax, and catheter mispositioning. The secondary and exploratory end points included success rates, complication rates, and procedural times. Comparisons between groups were performed using Student t test, χ2 test, and Mann-Whitney U test with a significance level of 0.05. Data are mean ± standard deviation [SD], frequencies (%) or 95% confidence interval [CI] [lower limit-upper limit]). RESULTS: The mean ± SD composite risk score was significantly lower in the MISP group compared to control (6.4 ± 5.9 vs 11.6 ± 10.8; mean diff 5.21 [95% CI, 1.71-8.71], P = .028). The MISP technique demonstrated significantly higher as-treated overall success rates (86% [95% CI, 74.6%-93.9%] vs 71% [95% CI, 56.2%-82.5%], P = .046) and significantly reduced the risk of arterial punctures (1.9% [95% CI, 0.05%-10.45%] vs 12% [4.5%-24.3%], number needed to harm: 10 punctures, P = .047). One pneumothorax was noted in both groups (2% each). The mean procedural time was 5 minutes longer in the MISP group (P < .001). CONCLUSIONS: Compared with the landmark technique, the ultrasound-guided MISP technique significantly reduced the risk of complications. The extended procedural time may be justified by lower complication rates. Further studies should evaluate the implementation of the MISP technique as a standard approach for subclavian vein catheterization.
2. Monocyte Transmigration Involves in Remifentanil Induced Mechanical Hyperalgesia in Animal Models and a Randomized Controlled Clinical Trial.
Across animal models and a 44-patient randomized trial, monocyte trafficking was implicated in remifentanil-induced hyperalgesia, and perioperative flurbiprofen axetil attenuated hyperalgesia at 2 and 24 hours. Mechanistic markers (circulating monocytes, CCL3/G-CSF) were favorably modulated.
Impact: This study bridges mechanism and practice by identifying a leukocyte-driven pathway for opioid-induced hyperalgesia and testing a practical mitigation strategy.
Clinical Implications: Consider perioperative NSAID strategies (e.g., flurbiprofen axetil) to mitigate remifentanil-induced hyperalgesia, especially when remifentanil is used at higher rates; mechanistic biomarkers may guide future risk stratification.
Key Findings
- In mice, remifentanil induced sustained mechanical hyperalgesia with transient monocytopenia and macrophage infiltration; monocyte depletion attenuated RIH.
- In a randomized trial (n=44), flurbiprofen axetil (1 mg/kg) reduced hyperalgesia at 2 h and 24 h postoperatively under sevoflurane-remifentanil anesthesia.
- Flurbiprofen axetil prevented reductions in circulating monocytes and suppressed plasma CCL3 and G-CSF elevations.
- Remifentanil directly promoted PBMC migration in vitro without affecting cell viability.
Methodological Strengths
- Translational design combining mechanistic animal/in vitro data with a randomized clinical trial
- Use of biological markers (monocytes, CCL3, G-CSF) to support mechanistic interpretation
Limitations
- Small single-center RCT with short (24 h) clinical follow-up
- Generalizability limited to sevoflurane-remifentanil regimens and minor surgery populations
Future Directions: Larger multicenter RCTs with longer follow-up to evaluate functional outcomes and dosing; exploration of monocyte-targeted strategies and biomarker-guided personalization.
Remifentanil-induced hyperalgesia (RIH) complicates postoperative pain management under total intravenous anesthesia. Although monocyte transmigration contributes to neuropathic pain, its role in RIH remains undefined. Here, we investigated monocyte dynamics in RIH through preclinical and clinical studies. In male mice, intraperitoneal remifentanil infusion (4 μg/kg/min, 1 h) induced sustained mechanical hyperalgesia (reduced paw withdrawal thresholds, PWTs) over 48 hours, paralleled by a transient decline in circulating monocytes (3 h post-infusion) and increased macrophage infiltration in paw tissues. Critically, monocyte depletion significantly attenuated RIH, implicating monocytes in its pathogenesis. Translating these findings, a randomized trial of 44 patients undergoing minor surgery under sevoflurane-remifentanil anesthesia (0.3 μg/kg/min) revealed that perioperative flurbiprofen axetil (1 mg/kg) attenuated remifentanil-induced mechanical hyperalgesia (peri-incisional and upper limb regions) at 2 h and 24 h postoperatively (p < 0.05). Mechanistically, flurbiprofen axetil prevented remifentanil-driven reductions in circulating monocytes and suppressed plasma CCL3/G-CSF elevations (p < 0.05), despite unchanged monocytic COX-2 expression. In vitro, remifentanil (1000 ng/mL) directly promoted peripheral blood mononuclear cell migration (p < 0.05) without affecting viability. Collectively, monocyte transmigration underlies RIH in both animal models and humans, while flurbiprofen axetil counteracts hyperalgesia by retaining monocytes in circulation and modulating chemokine signaling. These translational insights highlight monocyte-targeted strategies as a therapeutic avenue for RIH. In this study, we demonstrated that extravascular migration of circulating monocytes is involved in remifentanil-induced hyperalgesia. Flurbiprofen axetil attenuates remifentanil-induced hyperalgesia, possibly by suppressing monocyte extravasation.
3. Hypotension Prediction Index-Guided Hemodynamic Management on Postoperative Organ Outcome: A Systematic Review and Meta-Analysis of Randomized Clinical Trials.
Across 14 RCTs (N=2030), HPI-guided hemodynamic management did not reduce postoperative AKI and showed a non-robust reduction in myocardial injury; no improvements were seen in other complications, LOS, or mortality.
Impact: This synthesis challenges assumptions that predictive hypotension control translates into better organ outcomes, recalibrating expectations and guiding future trial designs.
Clinical Implications: Clinicians should not assume HPI-guided protocols improve hard postoperative outcomes despite reducing IOH exposure; adoption should be coupled with outcome-focused protocols and rigorous evaluation.
Key Findings
- Meta-analysis of 14 RCTs (N=2030) found no significant reduction in postoperative AKI with HPI-guided management (RR 0.87, 95% CI 0.71–1.07).
- Postoperative myocardial injury was reduced (RR 0.61, 95% CI 0.39–0.96), but this effect was not robust in sensitivity analyses.
- No significant differences were observed for LOS, arrhythmia, stroke, cognitive dysfunction/delirium, SSI, pneumonia, or mortality.
Methodological Strengths
- Inclusion of only randomized controlled trials with Cochrane risk-of-bias assessment
- Prospective comprehensive database search and random-effects pooling
Limitations
- Heterogeneity in populations, surgical types, standard care, and outcome reporting across trials
- Potential underpowering for relatively infrequent patient-centered outcomes
Future Directions: Large pragmatic RCTs powered for clinical endpoints, standardized co-interventions, and patient-level meta-analyses to clarify which patients, surgeries, and thresholds benefit from prediction-guided therapy.
Intraoperative hypotension (IOH) is a frequent occurrence during noncardiac surgery. Hypotensive episodes can compromise tissue perfusion, and cumulative exposure has been associated with adverse outcomes such as acute kidney injury (AKI), myocardial injury, and increased mortality. The Hypotension Prediction Index (HPI) is an artificial intelligence tool designed to predict hypotensive events before they occur, allowing clinicians to intervene proactively to prevent or mitigate hypotension. Although randomized trials and pooled analyses have shown its effectiveness in reducing both the incidence and duration of IOH, its impact on patient-centered outcomes remains unclear. From 1946 to August 8, 2025, we prospectively queried MEDLINE (PubMed), Embase, Cochrane Library, and Web of Science. We included randomized controlled trials in adult surgical patients with invasive arterial monitoring, comparing HPI-guided perioperative hemodynamic management to standard care. Primary outcome was postoperative AKI, and secondary outcomes were postoperative myocardial injury, pneumonia, arrhythmia, stroke, postoperative cognitive dysfunction, including delirium, surgical site infection, length of hospital stay, and mortality. Two authors independently evaluated the risk of bias according to the methods described in the Cochrane Handbook for Systematic Reviews of Interventions. A meta-analysis was performed using RevMan 5.4.1 software. Dichotomous data were presented as risk ratio, 95% confidence interval [CI]; continuous data were presented as mean difference, 95% CI. All results were pooled using random-effects models. Of 883 imported references, 14 studies (N = 2030) were included for final analysis. No significant difference in incidence of postoperative AKI was observed between HPI-guided management and standard care, RR = 0.87, 95% CI (0.71-1.07). Postoperative myocardial injury was significantly reduced in HPI-guided management group, RR = 0.61, 95% CI (0.39-0.96), although exclusion-based sensitivity analysis suggests that this finding may not be robust. No other significant differences were observed for hospital length of stay, arrhythmia, stroke, cognitive dysfunction (including delirium), surgical site infection, pneumonia, or mortality. Although HPI-guided management is associated with a reduction in postoperative myocardial injury, its significance does not withstand sensitivity analysis. All other postoperative complications, including AKI incidence, are not reduced in the intervention groups. This study has limitations inherent to the heterogeneity of included patient populations, surgical interventions performed, standard of care practices, and reporting of postoperative outcomes.