Skip to main content
Daily Report

Daily Anesthesiology Research Analysis

05/01/2025
3 papers selected
3 analyzed

Three studies stand out in anesthesiology: a prospectively validated decision tool (Expect-It) markedly improved first-attempt tracheal intubation success and recognition of indications for camera-assisted and awake intubation; an ESAIC consensus statement provides pragmatic, evidence-informed recommendations for intra-operative hemodynamic monitoring and management; and a randomized trial shows remimazolam does not potentiate rocuronium-induced neuromuscular block beyond propofol, unlike sevofl

Summary

Three studies stand out in anesthesiology: a prospectively validated decision tool (Expect-It) markedly improved first-attempt tracheal intubation success and recognition of indications for camera-assisted and awake intubation; an ESAIC consensus statement provides pragmatic, evidence-informed recommendations for intra-operative hemodynamic monitoring and management; and a randomized trial shows remimazolam does not potentiate rocuronium-induced neuromuscular block beyond propofol, unlike sevoflurane.

Research Themes

  • Airway management decision support and predictive planning
  • Intra-operative hemodynamic monitoring and individualized goal-directed therapy
  • Interactions between anesthetic maintenance agents and neuromuscular blockade

Selected Articles

1. Decision-Making Tool for Planning Camera-Assisted and Awake Intubation in Head and Neck Surgery.

78.5Level IICohort
JAMA otolaryngology-- head & neck surgery · 2025PMID: 40310618

A prospectively developed and validated airway decision tool (Expect-It) predicted when camera-assisted and awake intubation were appropriate with high accuracy, substantially outperforming non-algorithmic planning in sensitivity while maintaining specificity. Implementation was associated with higher first-attempt intubation success and fewer failed direct laryngoscopies.

Impact: It operationalizes multi-source airway risk data into a validated algorithm that improved real-world intubation outcomes, addressing a key patient safety domain in anesthesiology.

Clinical Implications: Use of Expect-It can guide preoperative airway planning, prompting camera-assisted and awake strategies when indicated to increase first-attempt success and reduce failed direct laryngoscopy. Integration into pre-op assessment workflows or EHRs may standardize difficult airway preparation.

Key Findings

  • AUC 0.86 for predicting appropriate camera-assisted intubation and 0.97 for appropriate awake intubation.
  • Sensitivity vs. clinical standard: 88% vs 35% (camera-assisted) and 97% vs 29% (awake); specificity noninferior (≥97%).
  • Post-implementation: first-attempt success increased 73%→82% (OR 1.72), failed direct laryngoscopy decreased 8%→2% (OR 0.18).

Methodological Strengths

  • Prospective two-stage development/validation with multivariable regularized regression.
  • Objective performance metrics (AUC, sensitivity/specificity) and pre-post clinical outcome comparison.

Limitations

  • Single-center study; external validation across diverse settings is needed.
  • Before-after comparison may be susceptible to temporal and implementation biases.

Future Directions: External multicenter validation, integration into clinical decision support within EHRs, and evaluation of algorithm-driven training effects on airway management.

IMPORTANCE: Indication criteria for camera-assisted and awake tracheal intubation are vague. It is unknown if diagnostic and clinical data from multiple sources, such as transnasal videoendoscopy or symptoms for pharyngolaryngeal lesions, might improve preanesthesia airway management planning and decision-making in patients undergoing head and neck surgery. OBJECTIVE: To develop and validate a new decision-making tool (Evidence-Based Algorithm for the Expected Difficult Intubation [Expect-It]) and show noninferiority to the clinical standard (nonalgorithm-based decision-making). DESIGN, SETTING, AND PARTICIPANTS: This single-center study prospectively developed and validated a decision-making tool with a 2-stage design that included anesthetic cases from patients undergoing head and neck surgery between May 1, 2021, and January 29, 2022. Data were analyzed between August 2021 (first stage) and December 2023. EXPOSURES: Airway-related risk factors from 4 domains (previous intubation difficulties, physical examination, physician's rating of difficult airway indicators, and pharyngolaryngeal lesions/transnasal videoendoscopy findings) were preoperatively assessed. During airway management planning, physicians proposed a first-line tracheal intubation technique (camera-assisted or direct laryngoscopy) and strategy (awake or asleep tracheal intubation). In the development cohort, these proposals were nonalgorithm-based (clinical standard); in the validation cohort, they relied on the Expect-It decision-making tool. MAIN OUTCOMES AND MEASURES: Regularized regression was used to select potentially predictive airway-related risk factors (covariables). The final decision-making tool is a combined score originating from 2 multivariable logistic regression models that predict 2 different primary outcomes: the most appropriate (1) tracheal intubation technique (camera-assisted or direct laryngoscopy) and (2) strategy (awake or asleep), as determined by the anesthesiologists after tracheal intubation. RESULTS: Of 1201 patients (mean [SD] age, 50.3 [19.0] years; 695 [58%] male), 1282 anesthetic cases were included in the analysis: 602 in the development and 680 in the validation cohort. The area under the curve of the decision-making tool was 0.86 (95% CI, 0.81-0.90) to predict appropriate camera-assisted and 0.97 (95% CI, 0.96-0.99) to predict appropriate awake tracheal intubation in the development cohort. The sensitivity of the Expect-It tool to predict both appropriate camera-assisted and awake tracheal intubation was superior compared to the clinical standard (camera-assisted: 88% [95% CI, 81%-93%] vs 35% [95% CI, 27%-44%], respectively; awake tracheal intubation: 97% [95% CI, 81%-100%] vs 29% [95% CI, 15%-50%], respectively), and specificity was noninferior to the clinical standard (camera-assisted: 97% [95% CI, 96%-98%] vs 96% [95% CI, 93%-97%], respectively; awake tracheal intubation: 100% [95% CI, 99%-100%] vs 98% [95% CI, 97%-99%], respectively). After tool implementation, the first-attempt success rate increased from the development to validation cohort (437 [73%] vs 557 [82%], respectively; odds ratio, 1.72 [95% CI, 1.32-2.22]), while failed direct laryngoscopy decreased from the development to validation cohort (45 [8%] vs 10 [2%], respectively; odds ratio, 0.18 [95% CI, 0.09-0.37]). CONCLUSIONS AND RELEVANCE: In this study, the Expect-It tool for airway management planning was prospectively developed and validated. The tool was found to support airway management planning accurately and may serve as a precursor for intelligent algorithms.

2. Intra-operative haemodynamic monitoring and management of adults having noncardiac surgery: A statement from the European Society of Anaesthesiology and Intensive Care.

70.5Level VSystematic Review
European journal of anaesthesiology · 2025PMID: 40308048

ESAIC experts recommend maintaining intra-operative MAP ≥60 mmHg, identifying and treating causes of hypotension, selectively monitoring stroke volume/cardiac output in high-risk or high-risk surgery patients, avoiding routine maximization of flow variables, and administering fluids only when clinical/metabolic signs of hypovolemia or hypoperfusion exist. Depth of anesthesia monitoring and optimization are also advised.

Impact: Provides pragmatic, evidence-informed guidance to standardize intra-operative hemodynamic care, directly influencing broad anesthetic practice and patient safety.

Clinical Implications: Adopt MAP-based targets (≥60 mmHg), use cause-directed therapy for hypotension, selectively apply CO/SV monitoring to high-risk cases, avoid chasing maximal flow, and give fluids based on hypovolemia/perfusion evidence rather than fluid responsiveness alone. Incorporate depth of anesthesia monitoring to titrate hypnotics/analgesics.

Key Findings

  • Maintain intra-operative MAP above 60 mmHg and treat underlying causes of hypotension.
  • Selective CO/SV monitoring for high-risk patients or high-risk surgeries; avoid routine maximization of flow variables.
  • Administer fluids based on clinical/metabolic signs of hypovolemia or hypoperfusion, not fluid responsiveness alone; optimize anesthetic depth.

Methodological Strengths

  • Multidisciplinary international expert panel with transparent recommendations.
  • Evidence-informed synthesis addressing monitoring, targets, and interventions.

Limitations

  • Consensus guidance rather than randomized evidence; heterogeneity of supporting studies.
  • No formal systematic review/meta-analysis protocol detailed.

Future Directions: Prospective implementation studies to test protocolized MAP targets and selective CO/SV monitoring, and trials adjudicating fluid strategies incorporating perfusion markers.

This article was developed by a diverse group of 25 international experts from the European Society of Anaesthesiology and Intensive Care (ESAIC), who formulated recommendations on intra-operative haemodynamic monitoring and management of adults having noncardiac surgery based on a review of the current evidence. We recommend basing intra-operative arterial pressure management on mean arterial pressure and keeping intra-operative mean arterial pressure above 60 mmHg. We further recommend identifying the underlying causes of intra-operative hypotension and addressing them appropriately. We suggest pragmatically treating bradycardia or tachycardia when it leads to profound hypotension or likely results in reduced cardiac output, oxygen delivery or organ perfusion. We suggest monitoring stroke volume or cardiac output in patients with high baseline risk for complications or in patients having high-risk surgery to assess the haemodynamic status and the haemodynamic response to therapeutic interventions. However, we recommend not routinely maximising stroke volume or cardiac output in patients having noncardiac surgery. Instead, we suggest defining stroke volume and cardiac output targets individually for each patient considering the clinical situation and clinical and metabolic signs of tissue perfusion and oxygenation. We recommend not giving fluids simply because a patient is fluid responsive but only if there are clinical or metabolic signs of hypovolaemia or tissue hypoperfusion. We suggest monitoring and optimising the depth of anaesthesia to titrate doses of anaesthetic drugs and reduce their side effects.

3. Comparative potentiating effects of remimazolam, propofol and sevoflurane on rocuronium-induced neuromuscular block: a randomized controlled trial.

68Level IRCT
Journal of anesthesia · 2025PMID: 40307489

In 90 analyzed patients, time to first PTC did not differ among remimazolam, propofol, and sevoflurane. Sevoflurane prolonged time to TOF count reappearance versus propofol, whereas remimazolam behaved similarly to propofol. Free rocuronium concentration at first PTC was lower with remimazolam than propofol, yet overall potentiation remained weaker than sevoflurane.

Impact: Clarifies neuromuscular interaction profiles of a newer benzodiazepine (remimazolam) versus established agents, informing agent selection and dosing for safe neuromuscular management.

Clinical Implications: Remimazolam can be expected to have neuromuscular block potentiation similar to propofol and less than sevoflurane, supporting its use where rapid recovery and predictable reversal are desired. Quantitative neuromuscular monitoring remains essential.

Key Findings

  • No difference among groups in time from rocuronium to first PTC reappearance.
  • Sevoflurane significantly prolonged time to TOF counts 1 and 2 compared with propofol; no significant differences between sevoflurane and remimazolam.
  • Free rocuronium concentration at first PTC was lower with remimazolam than propofol, yet overall potentiation was weaker than sevoflurane.

Methodological Strengths

  • Randomized controlled design with electromyography-based quantitative neuromuscular monitoring.
  • Concurrent measurement of free plasma rocuronium concentrations.

Limitations

  • Single-center RCT with modest sample size; not powered for rare adverse events.
  • Between-group anesthetic depth and other intraoperative variables may confound neuromuscular recovery kinetics.

Future Directions: Larger multicenter RCTs examining diverse surgical populations and integrating reversal agents and recovery endpoints (e.g., TOF ratio ≥0.9 time, PACU events).

BACKGROUND: Remimazolam is a new type of ultra-short-acting benzodiazepine. The aim of this study was to investigate the effects of remimazolam, propofol and sevoflurane anesthesia on rocuronium-induced neuromuscular block. METHODS: Ninety-nine consenting patients were randomly assigned to a remimazolam group (R-group), sevoflurane group (S-group), or propofol group (P-group). Train-of-four (TOF) responses evoked on the abductor digiti minimi muscle to ulnar nerve stimulation following bolus administration of 0.9-mg/kg rocuronium were monitored with electromyography-based neuromuscular monitor. The primary outcomes were times from administration of rocuronium to first reappearance of post-tetanic count (PTC). Free plasma concentrations of rocuronium were concurrently measured at these events. RESULTS: Ninety patients were analyzed. No significant differences were seen in time to first PTC among the three groups. Mean (± standard deviation) and median (inter-quartile range) times for the reappearance of TOF counts 1 and 2 were significantly prolonged in S-group [50.7 ± 13.9 min, P = 0.043 and 61.6 (54.3-78.0) min, P = 0.020, respectively], when compared with P-group [42.6 ± 10.3 min and 52.9 (45.4-58.8) min, respectively]. However, no significant differences were seen between S-group and R-group. Median (inter-quartile range) free plasma concentration of rocuronium measured at first PTC was significantly lower in R-group [1255 (1126-1717) ng/mL] than in P-group [1717 (1592-1961) ng/mL, P = 0.031]. CONCLUSIONS: These results suggest that the potentiating effects of remimazolam on rocuronium-induced neuromuscular block are weaker than those of sevoflurane and similar to those of propofol.