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Daily Report

Daily Anesthesiology Research Analysis

02/23/2026
3 papers selected
100 analyzed

Analyzed 100 papers and selected 3 impactful papers.

Summary

Three high-impact anesthesiology studies stand out today: a multicenter factorial RCT shows ultrasound-guided recruitment maneuvers reduce early postoperative atelectasis and pulmonary complications after abdominal surgery; a meta-analysis of 13 RCTs suggests esketamine lowers postoperative delirium in older adults but increases perioperative hypertension; and a multicenter RCT demonstrates SEEKflex-assisted double-lumen tube intubation reduces airway injuries versus a stylet.

Research Themes

  • Perioperative lung protection and respiratory outcomes
  • Delirium prevention pharmacotherapy in older adults
  • Airway device innovation and safety in thoracic anesthesia

Selected Articles

1. Effect of recruitment maneuver strategy on early postoperative atelectasis among intermediate- to high-risk patients undergoing abdominal surgery: A multicenter, 2 × 2 factorial, randomized clinical trial.

79.5Level IRCT
Journal of clinical anesthesia · 2026PMID: 41724004

In a multicenter 2×2 factorial RCT of 353 abdominal surgery patients, ultrasound-guided recruitment maneuvers reduced early postoperative atelectasis (41.9% vs 61.5%; RR 0.67) compared with conventional technique. Ultrasound guidance also lowered hypoxemia and 7-day pulmonary complications and improved oxygenation, with no difference between stepwise versus sustained inflation patterns.

Impact: This well-powered multicenter RCT provides actionable evidence that ultrasound-guided recruitment maneuvers improve immediate postoperative pulmonary outcomes, supporting a practical, scalable enhancement to lung-protective ventilation strategies.

Clinical Implications: Consider adopting ultrasound-guided recruitment maneuvers at the end of abdominal surgery to reduce early atelectasis and hypoxemia and lower short-term pulmonary complications, regardless of inflation pattern.

Key Findings

  • Ultrasound-guided recruitment reduced early postoperative atelectasis versus conventional technique (41.9% vs 61.5%; RR 0.67; P<0.001).
  • Lower incidence of hypoxemia and improved oxygenation index (median +21.7 mmHg) with ultrasound guidance.
  • Reduced 7-day postoperative pulmonary complications (RR 0.78) and lower hospitalization cost; no difference between stepwise and sustained inflation.

Methodological Strengths

  • Multicenter randomized 2×2 factorial design with prespecified outcomes
  • Standardized lung ultrasound assessment and lung-protective ventilation protocol

Limitations

  • Blinding of operators to ultrasound guidance was not feasible
  • Conducted in tertiary centers in China; generalizability to other settings requires confirmation

Future Directions: Evaluate long-term outcomes, cost-effectiveness across health systems, and implementation strategies; assess generalizability to other surgeries and patient risk strata.

STUDY OBJECTIVE: Recruitment maneuver is pivotal for reducing the development of atelectasis but the optimal strategy is far from being established. This study hypothesized that the recruitment maneuver under ultrasound guidance compared with conventional technique, and that stepwise lung inflation compared with sustained inflation would reduce early postoperative atelectasis among intermediate- to high-risk patients undergoing abdominal surgery. DESIGN: A multicenter, 2 × 2 factorial, randomized clinical trial. SETTING: Six tertiary hospitals in China. PATIENTS: Adult patients who had an intermediate to high risk of pulmonary complications scheduled for abdominal surgery with an anticipated duration of 2 h or longer. INTERVENTIONS: Using a factorial design, patients receiving recruitment maneuver at end of surgery were allocated to ultrasound guidance or conventional technique without ultrasound guidance, combined with one of two lung inflation patterns (stepwise or sustained). All patients received lung-protective ventilation. MEASUREMENTS: The primary outcome was the incidence of early postoperative atelectasis, as assessed with lung ultrasound at 30 min after tracheal extubation. MAIN RESULTS: Between April 2024 and October 2024, 353 patients were enrolled and randomly assigned. The ultrasound guidance group had a significantly lower incidence of early postoperative atelectasis compared with conventional technique group (75 [41.9%] vs 107 [61.5%]; RR 0.67 [95% CI 0.53 to 0.83]; P < 0.001). There were significant differences favoring ultrasound guidance versus conventional technique for 5 prespecified secondary outcomes: early postoperative lung ultrasound score (median difference - 1 [95% CI -2 to 0]), incidence of hypoxemia (RR, 0.72; 95% CI, 0.58 to 0.88), oxygenation index (median difference 21.7 mmHg [95% CI 0.5 to 42.1]), incidence of pulmonary complications within 7 days postoperatively (RR 0.78 [95% CI 0.63 to 0.97]), and hospitalization cost (median difference - 3586 yuan [95% CI -7084 to -313]). For stepwise versus sustained inflation, there were no significant differences in primary and secondary outcomes. CONCLUSIONS: Among intermediate- to high-risk patients undergoing abdominal surgery, recruitment maneuver under ultrasound guidance significantly reduced early postoperative atelectasis versus conventional technique, while both stepwise and sustained lung inflation can be used alternatively for achieving a recruitment maneuver.

2. A comprehensive review and meta-analysis on the safety and efficacy of esketamine for emerging delirium in elderly patients.

75.5Level ISystematic Review/Meta-analysis
Frontiers in medicine · 2026PMID: 41728597

This PROSPERO-registered meta-analysis of 13 RCTs (n=1,581) found esketamine reduced postoperative delirium in older adults (RR 0.58), postoperative nausea/vomiting, perioperative hypotension, and intra-induction opioid consumption. However, it increased dizziness and perioperative hypertension, with heterogeneity across outcomes, tempering routine adoption.

Impact: By synthesizing randomized evidence specific to older adults, this review elevates esketamine as a candidate for delirium prevention while transparently flagging cardiovascular risks that must inform perioperative protocols.

Clinical Implications: Consider esketamine as an adjunct for high-risk elderly patients where delirium prevention is prioritized, with vigilant blood pressure monitoring and cardiovascular risk mitigation; further high-quality trials are needed before routine use.

Key Findings

  • Esketamine reduced postoperative delirium (RR 0.58, 95% CI 0.43–0.79) in older surgical patients.
  • Lower PONV (RR 0.57) and perioperative hypotension (RR 0.47), and reduced opioid use during induction (SMD -0.43).
  • Increased dizziness (RR 1.29) and perioperative hypertension (RR 2.40); no differences in pain scales, MMSE, hallucinations/nightmares.

Methodological Strengths

  • PROSPERO-registered systematic review with comprehensive database search
  • Included only RCTs; RoB 2 assessment and heterogeneity/publication bias analyses

Limitations

  • Substantial heterogeneity for some outcomes; dosing and perioperative contexts varied
  • Predominantly short-term outcomes; limited cardiovascular stratification

Future Directions: Standardize dosing/timing regimens, stratify cardiovascular risk, and conduct multicenter RCTs powered for delirium and hemodynamic safety trade-offs in geriatric surgery.

BACKGROUND: Postoperative delirium (POD), a common complication in older surgical patients, has an incidence between 20 and 50%, highlighting the importance of effective intervention methods. Preventive methods available so far mainly focus on the reduction of well-known perioperative risks to prevent POD onset. Esketamine, a newly added therapeutic agent, has also exhibited the potential for POD incidence reduction and the improvement of patient outcomes. Previous meta-analyses and systematic reviews primarily focused on general adult patient groups; thus, the purpose of the current meta-analysis was specifically to examine the efficacy and safety outcomes of esketamine administration in surgical operations among elderly patients. METHODS: This study was registered with PROSPERO (CRD420251151647). A literature search was conducted in the Cochrane Library, PubMed, Embase, Ovid, Scopus, and Web of Science databases until 1 October 2025. Eligible studies were English-language randomized controlled trials (RCTs) involving surgical patients aged ≥60 and reporting esketamine-related POD outcomes. Two reviewers independently selected studies and extracted data. The study quality was assessed using the Cochrane risk of bias (RoB) 2 tool. Data were pooled using fixed- or random-effects models and reported as risk ratios (RRs) or standardized mean differences (SMDs) with 95% CI. Heterogeneity was evaluated using I2 statistics, and publication bias was assessed using funnel plots and Egger's test. RESULTS: A total of 13 RCTs involving 1,581 elderly surgical patients were analyzed. Esketamine significantly reduced the incidence of POD (RR = 0.58, 95% CI: 0.43-0.79), postoperative nausea and vomiting (RR = 0.57, 95% CI: 0.44-0.74), perioperative hypotension (RR = 0.47, 95% CI: 0.27-0.81), and opioid consumption during anesthesia induction (SMD = -0.43, 95% CI: -0.59 to -0.26). However, it increased dizziness (RR = 1.29, 95% CI: 1.03-1.62) and perioperative hypertension (RR = 2.40, 95% CI: 1.16-4.97). No significant differences were found in pain scales [visual analog scale (VAS) and Numerical Rating Scale (NRS)], cognitive function [Mini-Mental State Examination (MMSE)], or psychological events (hallucinations and nightmares). CONCLUSION: Although perioperative esketamine exhibits benefits across multiple recovery outcomes, particularly in reducing intraoperative opioid consumption during induction, highlighting its potential for optimizing analgesic strategies, caution is warranted regarding the elevated risk of perioperative hypertension in elderly patients. The substantial heterogeneity observed in certain outcomes necessitates further validation. Therefore, current evidence does not yet support its routine clinical application. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/PROSPERO/view/CRD420251151647, identifier CRD420251151647.

3. Comparison of SEEKflex and Stylet for double-lumen tube intubation: a multicenter randomized controlled trial.

71Level IRCT
International journal of surgery (London, England) · 2026PMID: 41729697

In 140 thoracic surgery patients, SEEKflex-assisted left-sided DLT intubation reduced 24-hour sore throat (17% vs 33%) and hoarseness (26% vs 41%), as well as tracheal injury (10% vs 24%) and vocal cord injury (6% vs 17%), compared with a stylet under videolaryngoscopy.

Impact: This multicenter RCT provides direct comparative evidence for a device strategy that reduces mucosal and vocal cord injury during DLT placement, a high-risk airway procedure in thoracic anesthesia.

Clinical Implications: When available, consider SEEKflex-assisted DLT placement to reduce airway trauma and early postoperative throat symptoms; training and device access should be incorporated into thoracic anesthesia workflows.

Key Findings

  • Lower 24-hour sore throat (17% vs 33%; P=0.032) and hoarseness (26% vs 41%; P=0.049) with SEEKflex.
  • Reduced tracheal injury (10% vs 24%; P=0.025) and vocal cord injury (6% vs 17%; P=0.034) versus stylet.
  • No new sore throat/hoarseness on postoperative day 2; severity similar between groups.

Methodological Strengths

  • Multicenter randomized parallel-group design with standardized videolaryngoscopy approach
  • Systematic postoperative assessment of airway complications

Limitations

  • Non-blinded design for operators and outcome assessors may introduce bias for subjective symptoms
  • Moderate sample size and limited to left-sided DLTs; short follow-up

Future Directions: Confirm findings with blinded outcome assessment, extend to right-sided DLTs and diverse anatomies, and evaluate cost-effectiveness and training curves.

BACKGROUND: Tracheal injury, vocal cord injury, sore throat, and hoarseness are common complications of double-lumen tube (DLT) intubation. We try to make efforts to minimize these complications. Our objective is to test whether the use of Safe Easy Endotracheal kit-flexible (SEEKflex)-assisted DLT intubation reduces complications. METHODS: We conducted a multicenter, non-blinded, randomized, parallel-group clinical trial with the aim of comparing the use of SEEKflex versus Stylet in DLT intubation under videolaryngoscopy. Between January 2023 and May 2024, patients aged 18-75 years who required a left-sided DLT to maintain pulmonary isolation during thoracic surgery. We randomly assigned 140 patients to two groups in a 1:1 ratio: SEEKflex combined with videolaryngoscopy group (SEEKflex group) and Stylet combined with videolaryngoscopy group (Stylet group). RESULTS: The incidence of sore throat and hoarseness at 24 h postoperatively was significantly higher in the Stylet group than in the SEEKflex group (sore throat, 33% vs 17%, P = 0.032, hoarseness, 41% vs 26%, P = 0.049); however, there was no significant difference in severity between the two groups. No patients developed new sore throat or hoarseness on postoperative day 2, and the incidence and severity of sore throat and hoarseness were similar between the two groups. The incidence of tracheal injury was higher in the Stylet group than in the SEEKflex group (24% vs 10%, P = 0.025). After examining all participants, 12 patients in the Stylet group and 4 patients in the SEEKflex group experienced vocal cord congestion or edema. The incidence of vocal cord injury was higher in the Stylet group compared to SEEKflex group (17% vs 6%, P = 0.034). CONCLUSIONS: SEEKflex-assisted DLT intubation reduces complications.